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Небесная энциклопедия

Космические корабли и станции, автоматические КА и методы их проектирования, бортовые комплексы управления, системы и средства жизнеобеспечения, особенности технологии производства ракетно-космических систем

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Мониторинг СМИ

Мониторинг СМИ и социальных сетей. Сканирование интернета, новостных сайтов, специализированных контентных площадок на базе мессенджеров. Гибкие настройки фильтров и первоначальных источников.

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Форма поиска

Поддерживает ввод нескольких поисковых фраз (по одной на строку). При поиске обеспечивает поддержку морфологии русского и английского языка
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Применить Всего найдено 7805. Отображено 200.
24-01-2020 дата публикации

УСТРОЙСТВО ДЛЯ ОТБОРА ПРОБ, СПОСОБ ПОЛУЧЕНИЯ ПРОБЫ ЖЕЛУДОЧНО-КИШЕЧНОГО ТРАКТА ЖИВОТНОГО

Номер: RU2712026C2

Группа изобретений относится к медицинской технике. Устройство для отбора проб содержит корпус, содержащий камеру, отверстие, средство приведения в действие и отдельный отсек. Отдельный отсек закреплен с возможностью разъединения внутри корпуса с помощью удерживающего средства. Средство приведения в действие обеспечивает возможность втягивания внутреннего вещества через отверстие в камеру и одновременного выталкивания отдельного отсека вдоль корпуса до тех пор, пока отдельный отсек не выталкивается из корпуса устройства для отбора проб, тем самым создавая увеличенное пространство или объем для приема и хранения образца внутри камеры устройства для отбора проб. Средство приведения в действие привязано к закрывающему средству и выполнено с возможностью перекрытия отверстия закрывающим средством при перемещении средства приведения в действие. Удерживающее средство представляет собой крепежное средство и/или реагирующий на изменения внешней среды устройства материал. Отдельный отсек содержит ...

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20-03-2003 дата публикации

СПОСОБ ОПРЕДЕЛЕНИЯ ЖИЗНЕСПОСОБНОСТИ КИШКИ И ОПТИМАЛЬНЫХ ГРАНИЦ РЕЗЕКЦИИ ПРИ СТРАНГУЛЯЦИОННОЙ КИШЕЧНОЙ НЕПРОХОДИМОСТИ

Номер: RU2200472C2

Изобретение может быть использовано в медицине, в частности в хирургии. Лазерной доплеровской флоуметрией исследуют микроциркуляцию кишки. Кишку признают жизнеспособной, если после устранения причины странгуляции и проведения реабилитационных мероприятий перфузия кишечной стенки составляет 30 мл/мин/100 г ткани и выше для тонкой кишки, 20 мл/мин/100 г ткани - для толстой кишки. При показателях ниже 30 мл/мин/100 г ткани для тонкой и ниже 15 мл/мин/100 г ткани для толстой кишки проводят резекцию, которую осуществляют проксимальнее и дистальнее некротизированного участка, в зонах с нормальными показателями микроциркуляции для данного отдела кишечника, которые, в среднем, на приводящей петле регистрировались в 10±3,4 см, а на отводящей петле - в 5,1±2,1 см от места странгуляции. Способ позволяет повысить точность и информативность исследования. 1 з.п.ф-лы.

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20-06-2016 дата публикации

КЛИНИКО-СОНОСКОПИЧЕСКАЯ ШКАЛА ДЛЯ ДИАГНОСТИКИ ОСТРОГО АППЕНДИЦИТА

Номер: RU2587649C1

Изобретение относится к медицине, в частности к хирургии, и может быть использовано при диагностике острого аппендицита. Учитывают наличие положительных симптомов Кохера, Щеткина-Блюмберга в правой подвздошной области, Бартомье-Михельсона, наличие тошноты и/или рвоты, количества лейкоцитов в общем анализе крови - 10*10/л и более, соноскопического выявления несжимаемого аппендикса диаметром 7 мм и более, наличие ультразвуковых признаков неаппендикулярной острой патологии органов брюшной полости и/или соноскопическое выявление сжимаемого аппендикса, диаметром менее 7 мм. Присваивают баллы: при положительном симптоме Кохера: + «плюс» 1,5 балла; положительный симптом Щеткина-Блюмберга в правой подвздошной области + «плюс» 1,5 балла; положительный симптом Бартомье-Михельсона + «плюс» 1,5 балла; наличие тошноты и/или рвоты + «плюс» 1 балл; увеличение количества лейкоцитов в общем анализе крови до 10×10/л и более + «плюс» 1,5 балла; соноскопическое выявление несжимаемого аппендикса диаметром 7 ...

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20-12-2007 дата публикации

ДИАГНОСТИЧЕСКИЙ ЗОНД И КОМПЛЕКТ ДЛЯ ТОНОМЕТРИЧЕСКОГО ИССЛЕДОВАНИЯ ДЫХАТЕЛЬНОЙ НЕДОСТАТОЧНОСТИ И НЕДОСТАТОЧНОСТИ РЕГИОНАЛЬНОГО КРОВОСНАБЖЕНИЯ ОРГАНИЗМА

Номер: RU2006119474A
Принадлежит:

... 1. Тонометрическое устройство (20) для диагностики дыхательной недостаточности и недостаточности регионарного кровоснабжения тканей у больных, содержащее дистальный конец (22) для введения в желудочно-кишечный тракт тела пациента, участок (24), предназначенный для введения в тело пациента, и участок (3) для закрепления положения устройства на теле пациента, где участок (24), предназначенный для введения в тело пациента, содержит первую трубку (1), к которой присоединена дополнительная трубка (4), отличающееся тем, что оно содержит вторую трубку (2), расположенную по существу параллельно первой трубке (1) и прикрепленную к ней, где дистальный конец (22) второй трубки (2) соединен с возможностью сообщения с первой трубкой (1), и первая трубка (1) и вторая трубка (2) изготовлены из материала, легко проницаемого для газов, в особенности для углекислого газа, однако по существу непроницаемого для жидкостей организма и других субстанций, предпочтительно из кремнийорганического каучука, и дополнительная ...

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17-04-2002 дата публикации

Solid-state sensor for sphincter pressure measurement

Номер: GB0000204980D0
Автор:
Принадлежит:

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29-06-2016 дата публикации

Digestive profiling system

Номер: GB0201608365D0
Автор:
Принадлежит:

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28-09-1994 дата публикации

Substrate measurement by infrared spectroscopy

Номер: GB0009415869D0
Автор:
Принадлежит:

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15-09-2007 дата публикации

DEVICE FOR THE MEASUREMENT OF THE DIFFERENCE OF POTENTIAL OF THE INTESTINE

Номер: AT0000369789T
Принадлежит:

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15-02-2012 дата публикации

CATHETER FOR USE IN A SYSTEM FOR THE MONITORING OF SCHLEIMHAUTSCHÄDEN OF VISCOUS HOLLOW ORGANS

Номер: AT0000541509T
Принадлежит:

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15-01-1996 дата публикации

TONOMETRI CATHETER DEVICE AND PROCEDURE WITH REMOTE SENSOR

Номер: AT0000132719T
Принадлежит:

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15-02-1996 дата публикации

TONOMETRI CATHETER COMBINATION

Номер: AT0000133047T
Принадлежит:

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15-04-2004 дата публикации

DEVICE FOR REFLEKTROMETRI INVESTIGATION AND MEASUREMENT OF BODY CAVITIES

Номер: AT0000262303T
Принадлежит:

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09-08-2018 дата публикации

ANALYZING AND MAPPING ECG SIGNALS AND DETERMINING ABLATION POINTS TO ELIMINATE BRUGADA SYNDROME

Номер: AU2018200564A1
Принадлежит: Spruson & Ferguson

A system and method for Brugada syndrome epicardial ablation comprising preparing an endocardial duration map; preparing a baseline epicardial duration map comprising at least one or more areas of delimination; and when some of the areas of delimination are greater than 200ms, performing epicardial ablation of the areas of delimination greater than 200ms. The method may further comprise preparing an updated epicardial duration map after performing epicardial ablation, and determining whether or not a BrS pattern appears in the updated epicardial duration map; and when the BrS pattern appears, performing epicardial ablation. The method may further comprise preparing an updated epicardial duration map after performing epicardial ablation, and determining whether or not an abnormal EGM exists in the updated epicardial duration map; and when the abnormal EGM exists, performing epicardial ablation. The method may further comprise preparing an updated epicardial map comprising maintaining anatomical ...

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03-09-2020 дата публикации

Gas sensor nanocomposite membranes

Номер: AU2020220100A1
Принадлежит: FPA Patent Attorneys Pty Ltd

A gas permeable, liquid impermeable membrane for use with gas sensors in which the membrane consists of a film forming polymer which incorporates one or more 5 nanoparticles selected to improve one or more of the following the permeability to gases, to selectively impede or exclude permeation by some gases while facilitating the passage of selected gases through the membrane, to inhibit microbial growth on the membrane. The membranes are useful in capsules adapted to be introduced into the stomach and G1 tract of a mammal which consists of a capsule shaped container 0 consisting of a wall material capable of being bio compatible with the G1 tract and being adapted to protect the electronic and sensor devices contained in the capsule. The capsule contains gas composition sensors, pressure and temperature sensors, a micro controller, a power source and a wireless transmission device. The microprocessor is programmed to receive data signals from the sensors and convert the signals into gas ...

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16-08-2007 дата публикации

Gastro-intestinal device and method for treating addiction

Номер: AU2007212404A1
Принадлежит:

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02-03-2006 дата публикации

System and method for colon wall extraction in the presence of tagged fecal matter or collapsed colon regions

Номер: AU2005277835A1
Автор: JEREBKO ANNA, ANNA JEREBKO
Принадлежит:

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01-11-2004 дата публикации

METHOD AND APPARATUS FOR VERIFYING DATA MEASURED BY SEVERAL MEANS IN REAL-TIME

Номер: AU2003221104A1
Автор: MO SEUNG-KEE, SEUNG-KEE MO
Принадлежит:

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28-10-2002 дата публикации

Analysis of eating habits

Номер: AU2002255245A1
Принадлежит:

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22-05-2014 дата публикации

Ingestible circuitry

Номер: AU2009281876B2
Принадлежит:

The present invention provides for safe and reliable electronic circuitry that can be employed in ingestible compositions. The ingestible circuitry of the invention includes a solid support; a conductive element; and an electronic component. Each of the support, conductive element and electronic component are fabricated from an ingestible material. The ingestible circuitry finds use in a variety of different applications, including as components of ingestible identifiers, such as may be found in ingestible event markers, e.g., pharma-informatics enabled pharmaceutical compositions.

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14-09-1995 дата публикации

An analyzing apparatus and method

Номер: AU0002332295A
Принадлежит:

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17-09-1985 дата публикации

PATIENT MONITORING APPARATUS

Номер: CA1193504A
Принадлежит: ANTEC SYSTEMS, ANTEC SYSTEMS LIMITED

PATIENT MONITORING APPARATUS A method of monitoring the depth of anaesthesia of a patient, comprising stimulating contractions in the oesophagus of the patient, for example using an inflatable oesophageal balloon, obtaining signals inductive of the oesophageal contractions using a sensor, and deriving from the signals an output indicative of the rate of occurrence of signals having a magnitude greater than a preset threshold value, and apparatus for carrying out the method. An alternative aspect comprises assigning a score value to each of a plurality of different bodily functions of a patient, for example heart rate, blood pressure, degree of sweating, and formation of tears, the said score values being indicative of a depth of anaesthesia or sedation, summing the score values, and producing an output from the summed score values indicative of the amount of anaesthetic to be fed to the patient.

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18-06-2020 дата публикации

ON-SITE DETECTION OF PARASITIC INFECTION OF MAMMALS

Номер: CA3122897A1
Принадлежит:

A portable kit for generating a digital image of a faecal sample suitable for microscopic analysis, comprises a faecal sample preparation device configured to receive a faecal sample and a faecal flotation fluid, filter a suspension comprising the faecal sample and the faecal flotation fluid to provide a filtrate, a translucent faecal sample support, and a portable digital imaging module. The portable digital imaging module comprises a housing, a camera/microscopic lens assembly configured to generate a digital image of the faecal sample on the sample support, an illumination system, a seat for receiving the faecal sample support disposed between the camera/microscopic lens assembly and illumination system, a memory for storing the digital image, a communication system for communicating the digital image to an off-site image processing module via a communications network, and a battery operatively connected to the camera and microscopic lens assembly, memory and communication system.

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22-02-2018 дата публикации

SAMPLING SYSTEMS AND RELATED MATERIALS AND METHODS

Номер: CA0003034263A1
Принадлежит: SMART & BIGGAR

Sampling systems that include an absorbent material a preservative, such as an analyte preservative, as well as related materials and methods, are disclosed.

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29-03-2018 дата публикации

METHODS AND SYSTEMS FOR ADAPTIVE TREATMENT OF DISORDERS IN THE GASTROINTESTINAL TRACT

Номер: CA0003037818A1
Принадлежит: BHOLE IP LAW

A system and a method for treatment of a disorder in a gastrointestinal tract of a subject, using a treatment protocol, the treatment protocol being based at least in part on data relating to other subjects and their responses to treatment with various treatment protocols.

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14-06-2018 дата публикации

GASTROINTESTINAL TRACT DETECTION METHODS, DEVICES AND SYSTEMS

Номер: CA0003045296A1
Принадлежит: SMART & BIGGAR

The present disclosure relates to gastrointestinal (GI) tract detection methods, devices and systems.

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14-06-2018 дата публикации

GASTROINTESTINAL TRACT DETECTION METHODS, DEVICES AND SYSTEMS

Номер: CA0003044526A1
Принадлежит: SMART & BIGGAR

The present disclosure relates to gastrointestinal (GI) tract detection methods, devices and systems.

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04-10-2018 дата публикации

LOCALIZATION SYSTEMS AND METHODS FOR AN INGESTIBLE DEVICE

Номер: CA0003055762A1
Принадлежит: SMART & BIGGAR LLP

Ingestible devices are disclosed that provide very high localization accuracy for the devices when present in the GI tract of a body. Related systems and methods are also disclosed.

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21-06-2018 дата публикации

TREATMENT OF A DISEASE OF THE GASTROINTESTINAL TRACT WITH A TNF INHIBITOR

Номер: CA0003045307A1
Принадлежит: SMART & BIGGAR

This disclosure features methods and compositions for treating diseases of the gastrointestinal tract with a TNF inhibitor.

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10-01-2013 дата публикации

SYSTEM AND METHOD FOR PREDICTING THE VIABILITY OF A BODY TISSUE IN A PATIENT, AND MEASURING DEVICE USED THEREIN

Номер: CA0002839838A1
Принадлежит:

The invention relates to a system for predicting the viability of a body tissue in a patient. The system comprises a computing device (1), and a first pressure measuring device (2) for measuring local perfusion pressure in the body tissue of the patient. This measuring device is connected to the computing device. A second pressure measuring device (5) is provided for measuring the systemic perfusion pressure of the patient, said second pressure measuring device being connected to the computing device. A feedback indicator (6) is connected to the computing device and is adapted to indicate the viability of the tissue calculated by the computing device on the basis of the measured local and systemic perfusion pressures. The invention also includes a method of predicting the viability of the body tissue and to the first pressure measuring device.

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23-12-2009 дата публикации

SYSTEM AND METHOD OF EVALUATING A SUBJECT WITH AN INGESTIBLE CAPSULE

Номер: CA0002724890A1
Принадлежит:

A computerized method of analyzing measurements obtained from the gastrointestinal tract of subject comprising the steps of providing an ingestible capsule (20) having a sensor (22, 23, 24) for measuring a parameter of the gastrointestinal tract of a subject, having a subject ingest (118) the capsule, recording (130) measurements from the sensor as the capsule passes through the gastrointestinal tract of the subject, transmitting (131, 122) the measurements to a processor (31), conditioning (132) the measurements to provide data as a function of a time interval, plotting (133) the data on a display (32), providing a query (205, 216, 234), on the display, receiving input (207, 218, 237) from a user in response to the query, setting a marker (50-53) on the plot (40) at a location as a function of the input, and determining (238) a capsule transit time for a selected portion of the gastrointestinal tract as a function of the location of the marker.

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15-12-2014 дата публикации

sphincter test catheter.

Номер: CH0000708172A2
Автор: SCHLUMPF PETER
Принадлежит:

Der erfindungsgemässe Sphincterprüfkatheter besteht aus einem Katheterkörper (3) dessen proximales Ende eine Sonde (2) bildet. Im Katheterkörper (3), verlaufen entsprechende elektrische Leiter (5) die zu einer Aufzeichnungseinheit (4) führen. Der erfindungsgemässe Sphincterprüfkatheter enthält immer mindestens einen Drucksensor (10) und einen Lagesensor (11) in Kombination mit entweder einem pH-Wert-Sensor (12) oder einem Impedanzsensor (14). Die Kombination ist davon abhängig, welchen Sphincter man überwachen will. Zur Überwachung des unteren Ösophagus Sphincter wird der Lagesensor mit einem pH-Wert-Sensor kombiniert, während bei der Überwachung des Sphincter Urethra der Lagesensor mit einem Impedanzsensor kombiniert wird.

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15-02-2021 дата публикации

Sphincterprüfkatheter.

Номер: CH708172B1
Принадлежит: UNISENSOR AG, Unisensor AG

Der erfindungsgemässe Sphincterprüfkatheter besteht aus einem Katheterkörper (3) dessen proximales Ende eine Sonde (2) bildet. Im Katheterkörper (3) verlaufen entsprechende elektrische Leiter (5) die zu einer Aufzeichnungseinheit (4) führen. Der erfindungsgemässe Sphincterprüfkatheter enthält immer mindestens einen Drucksensor (10) und einen Lagesensor (11) in Kombination mit entweder einem pH-Wertsensor (12) oder einem Impedanzsensor (14). Die Kombination ist davon abhängig, welchen Sphincter man überwachen will. Zur Überwachung des unteren Ösophagus Sphincter wird der Lagesensor mit einem pH-Wertsensor kombiniert, während bei der Überwachung des Sphincter Urethra der Lagesensor mit einem Impedanzsensor kombiniert wird.

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19-02-1999 дата публикации

PROBE CAPTRICE OF MANOMETRY ANO-RECTALE HAS THREE SMALL BALOONS AND DEVICE Of BLOWING AND MEASUREMENT FOR SA STARTING.

Номер: FR0002673524B1
Автор:
Принадлежит:

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22-04-1988 дата публикации

DISPOSITIF DE SURVEILLANCE DE L'ACTIVITE D'UN ORGANE DU CORPS HUMAIN

Номер: FR0002605210A
Принадлежит:

L'INVENTION CONCERNE UN DISPOSITIF DE SURVEILLANCE DE L'ACTIVITE D'UN ORGANE DU CORPS HUMAIN. LE DISPOSITIF COMPREND DES MOYENS DE TRAITEMENT 9 DE VALEURS NUMERIQUES ENREGISTREES DANS DES MOYENS DE MEMORISATION 14 D'UN PROCESSEUR 13. CES VALEURS NUMERIQUES CORRESPONDENT AUX VALEURS ANALOGIQUES D'UN SIGNAL DIFFERENTIEL FOURNI PAR DES MOYENS D'AMPLIFICATION ET DE FILTRAGE 3 DE SIGNAUX D'ACTIVITE FOURNIS PAR DES CAPTEURS 1, 2. LES MOYENS DE MEMORISATION CONTIENNENT UN PROGRAMME POUR TRAITER LES VALEURS NUMERIQUES PAR ECHANTILLONNAGE SUR CHAQUE PERIODE T D'UNE SUCCESSION DE PERIODES DECALEES D'UN INTERVALLE DE TEMPS PREDETERMINE D T. LE PROGRAMME COMMANDE LE CALCUL DE LA TRANSFORMEE DE FOURIER DE CES VALEURS, SUR CHAQUE PERIODE T. ON OBTIENT LE SPECTRE DE FREQUENCES DU SIGNAL D'ENTREE SUR CHAQUE INTERVALLE D T. LE PROCESSEUR RECHERCHE SUR CHAQUE INTERVALLE, LE PIC DU SPECTRE RELATIF A L'ORGANE A ETUDIER, AINSI QUE LE MAXIMUM D'AMPLITUDE DE CE PIC. LE PROCESSEUR FOURNIT UN SIGNAL REPRESENTATIF ...

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22-08-2014 дата публикации

FILTER DEVICE FOR DETECTION OF FOOD WITH A MOUTH COVERED

Номер: FR0003002359A1
Автор: LEPINE JACQUES
Принадлежит: SLOW CONTROL

Dispositif de filtrage de détection de mise en bouche (B) d'aliments (A) par une fourchette à détection capacitive comprenant un manche (10) et des dents (30), les dents sont en contact avec un circuit de détection capacitive (11) de la mise en bouche de fourchette, un circuit de traitement électronique de traitement des données (12) gère les détections de mise en bouche des aliments caractérisé en ce que un dispositif de mesure d'inclinaison et de mouvement de fourchette (13) dans le manche analyse l'inclinaison du manche de fourchette et le déplacement vertical du manche de fourchette et filtre le déclenchement d'alarme d'alerte dans des conditions d'inclinaison spécifiques du manche de fourchette vers le bas et dans des conditions spécifiques d'historique d'accélération de la fourchette selon l'axe vertical ...

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11-10-2005 дата публикации

ACTIVE DRUG DELIVERY IN THE GASTROINTESTINAL TRACT

Номер: KR1020050098277A
Автор: GROSS YOSSI, SELA YORAM
Принадлежит:

Apparatus (100) for drug (36, 106) administration is provided, including an ingestible capsule (30, 102). The capsule (30, 102) includes a drug (36, 106), stored by the capsule (30, 102). An environmentally-sensitive mechanism (e.g., coating 104) is adapted to change a state thereof responsive to a disposition of the capsule (30, 102) within a gastrointestinal tract of a subject. A driving mechanism (e.g., driving mechanism 108), in response to a change of state of the environmentally-sensitive mechanism, is adapted to drive the drug (36, 106) directly through an endothelial layer of the gastrointestinal tract. © KIPO & WIPO 2007 ...

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03-07-2014 дата публикации

DEVICE, SYSTEM AND METHOD FOR IN-VIVO DETECTION OF BLOOD IN GASTROINTESTINAL FLUIDS

Номер: WO2014102791A2
Принадлежит:

In-vivo devices, systems and methods can be for the detection of blood within in-vivo fluids. The in-vivo devices include a gap or passage, which remains in contact with bodily fluids, and through which the fluids pass when the device is in-vivo. The devices further include illumination sources on a first side of the gap or passage for irradiating in-vivo fluids that pass through the gap or passage. The devices further include a light detector positioned on a second side of the gap/passage opposite to the first side and facing the illumination sources, for detecting light from the illumination sources that passes through the in-vivo fluids.

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21-12-2007 дата публикации

DEVICE, SYSTEM AND METHOD FOR MEASUREMENT AND ANALYSIS OF CONTRACTILE ACTIVITY

Номер: WO2007144879A1
Принадлежит:

A method and system for determining intestinal dysfunction condition are provided by classifying and analyzing image frames captured in-vivo. The method and system also relate to the detection of contractile activity in intestinal tracts, to automatic detection of video image frames taken in the gastrointestinal tract including contractile activity, and more particularly to measurement and analysis of contractile activity of the GI tract based on image intensity of in vivo image data.

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22-01-2004 дата публикации

METHOD AND APPARATUS FOR THE DETECTION OF THE PRESENCE OF A BACTERIA IN THE GASTROINTESTINAL TRACT OF A SUBJECT

Номер: WO2004006766A3
Автор: PAN, Li
Принадлежит:

The present invention generally relates to a method and an apparatus to detect the presence of a bacteria in a subject. More particularly, the method is directed toward the detection of a bacteria which is associated with catalyzing urea to carbon dioxide and ammonia when present in the gastrointestinal tract of a subject. The method comprises administering urea to a subject, obtaining a fluid sample from the subject after the administration of the urea and then determining the presence or amount of ammonia gas in the fluid sample. The apparatus facilitates ease of implementing the method and facilitates accuracy and speed of obtaining the test result.

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18-06-1987 дата публикации

INGESTABLE MODULE FOR THE FUNCTIONAL EXPLORATION OF THE DIGESTIVE TRACT

Номер: WO1987003465A1
Автор: LAMBERT, Alain
Принадлежит:

An ingestable module for the functional exploration of the digestive tract is configured like an elongate capsule (1) having a small diameter and comprising a displacement measuring means (2) delivering displacement pulses to an electronic emitter circuit (3) for transmission of data to a corresponding outer receiver, and an electric power source (4) for the supply of the circuit (3).

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26-06-2003 дата публикации

ENDOSCOPIC MEASUREMENT OF MYOELECTRICAL ACTIVITY FROM INTRA-ABDOMINAL ORGANS

Номер: WO2003051194A1
Автор: KOCH, Kenneth, L.
Принадлежит:

A catheter structure (10) includes an elongated tube structure (16) having distal and proximal ends and an axis. Electrodes (22) are associated with the tube structure (16) and are constructed and arranged to be moved from a retraced position substantially within the tube structure (16) to an extended position extended directly outwardly from the distal end (18) of the tube structure (16) and generally in the direction of the axis. The electrodes (22) are constructed and arranged to obtain signals relating to myoelectrical activity of an intra-abdominal organ. Actuating structure (34, 36) is operatively associated with the electrodes (22) to move the electrodes between the extended and retraced positions.

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13-04-2000 дата публикации

METHOD AND APPARATUS FOR MEASURING OF INTESTINAL POTENTIAL DIFFERENCE

Номер: WO2000019893A1
Автор: SJÖVALL, Henrik
Принадлежит:

L'invention concerne un procédé et un appareil servant à générer un signal de différence de potentiel (DP) à travers la muqueuse, ledit signal n'étant pratiquement pas affecté par les activités motrices intestinales, et ce grâce à la réduction du signal DP sur la base des variations dans le temps du signal de pression intraluminale (PI). L'invention concerne également de différentes applications de ce signal telles que la mesure de la résistance périphérique globale, la détection d'anomalies dans le système nerveux entérique et la détection de lésions dans la barrière muqueuse.

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11-12-1997 дата публикации

VIDEO DATA REPRESENTATION OF PHYSIOLOGICAL DATA

Номер: WO1997046972A1
Принадлежит:

A system for patient diagnostic testing includes the physiological data output is in a two dimensional graphical format. Optionally, the report includes imaging data. Color is a dimension provided to the graphical presentation of normal patient data in horizontal and vertical dimensions (Fig. 7). Detrusor pressures are obtained. One detrusor pressure is the difference between average data points of the bladder and rectal pressures. The other is obtained by subtracting curve fitted rectal and bladder pressures (Fig. 4). The displayed data is a presentation including bladder capacity information, pressure characteristics, and data as a function of volume such that bladder volume is indicated (Fig. 8).

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10-07-2008 дата публикации

Enteral Feeding Catheter, Computer System and Computer Program for Operating the Feeding Catheter

Номер: US2008167607A1
Принадлежит:

The invention relates to an enteral feeding catheter ( 1 ) for channelling flowable nutrient into a patient's digestive tract, such as into patients stomach, duodenum or jejunum, said catheter having a first lumen ( 2 ), having an opening ( 3 ) for connecting it to a supply for of nutrient and channelling said nutrient from the proximal end (P) to the distal end (D), the distal end (D) of the first lumen ( 2 ) being provided with several radial outlets ( 4 ) for the exit of said nutrient into patient's digestive tract, the catheter ( 1 ) further comprising a second lumen ( 7 ), for being connected to a source/sink of gas ( 26 ) and a gas pressure gauge ( 24 ) at its proximal end and being connected to an inflatable and deflatable distal balloon ( 6 ) provided on the catheter ( 1 ) near the distal end (D). The invention refers also to a computer system and computer program to operate said feeding catheter.

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16-08-2012 дата публикации

MULTI-FOCUS OPTICAL-RESOLUTION PHOTOACOUSTIC MICROSCOPY WITH ULTRASONIC ARRAY DETECTION

Номер: US20120204648A1
Принадлежит: Washington University in St. Louis

A probe for use with an imaging system, including a scanning device configured to receive a first light beam from a light source, a beam-divider configured to split the first light beam into a plurality of second light beams, and a focusing device configured to focus each of the second light beams on respective locations in an object of interest.

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03-07-2008 дата публикации

System and Method for Acoustic Information Exchange Involving an Ingestible Low Power Capsule

Номер: US2008161660A1
Принадлежит:

A method of communicating with an ingestible capsule includes detecting the location of the ingestible capsule, focusing a multi-sensor acoustic array on the ingestible capsule, and communicating an acoustic information exchange with the ingestible capsule via the multi-sensor acoustic array. The ingestible capsule includes a sensor that receives a stimulus inside the gastrointestinal tract of an animal, a bidirectional acoustic information communications module that transmits an acoustic information signal containing information from the sensor, and an acoustically transmissive encapsulation that substantially encloses the sensor and communications module, wherein the acoustically transmissive encapsulation is of ingestible size. The multi-sensor array includes a plurality of acoustic transducers that receive an acoustic signal from a movable device, and a plurality of delays, wherein each delay is coupled to a corresponding acoustic transducer. Each delay may be adjusted according to ...

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26-08-2004 дата публикации

Method and device for locating visceral constrictions

Номер: US20040167426A1
Автор: Gaston Vantrappen
Принадлежит:

A method and device are provided for determination of the location of an anatomical or functional constriction of a hollow body organ, such as the lower esophageal sphincter (LES) in the gastroesophageal junctional segment, or constrictions in other tubular organs of the body such as other parts of the gastrointestinal tract, the pancreatico-biliary tract, the genito-urinary tract, and blood vessels.

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23-05-1995 дата публикации

Apparatus for the invasive use of oximeter probes

Номер: US0005417207A1
Принадлежит: Sensor Devices, Inc.

A reflectance oximeter probe is suitably disposed at a distal end of an elongated, substantially flat, semi-rigid chassis configured for insertion into an anatomical canal, for example in the esophagus, rectum or vaginal cavity of a human patient. The reflectance probe may also be suitably employed in many veterinary applications. An electrical connector extends from a proximal end of the chassis and terminates at a plug configured for mechanical and electrical connection to a pulse oximeter box. The reflectance probe includes first and second LED's mounted to an emitter assembly and a detector assembly spaced apart from and mounted substantially coplanar with respect to the emitter assembly. The reflectance probe generates and transmits signals to the oximeter box, the signals indicative of the dynamic oxygen saturation level of the blood perfused mucus membrane tissue.

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20-07-1999 дата публикации

Anorectal probe apparatus having at least one muscular activity sensor

Номер: US0005924984A1
Автор: Rao; Satish
Принадлежит: University of Iowa Research Foundation

An apparatus for sensing muscular activity of the rectosigmoid region, rectum, and the anorectal canal of a subject is disclosed. This apparatus includes an elongate probe having a distal end opposing a proximal end which is configured for insertion into the patient's anorectal canal and includes a pressure sensor, an electromyography sensor, and a stimulus balloon. Multiple pressure sensors may be included to evaluate muscular activity in the anorectal canal. In addition, pressure sensors may be distributed along the length of the probe to simultaneously measure the response of other portions of the anorectal canal besides the anal sphincter muscle. A pressure sensor is also located inside the stimulus balloon for monitoring intraballoon pressure.

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26-08-2004 дата публикации

Method and device for locating visceral constrictions

Номер: US2004167426A1
Автор:
Принадлежит:

A method and device are provided for determination of the location of an anatomical or functional constriction of a hollow body organ, such as the lower esophageal sphincter (LES) in the gastroesophageal junctional segment, or constrictions in other tubular organs of the body such as other parts of the gastrointestinal tract, the pancreatico-biliary tract, the genito-urinary tract, and blood vessels.

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26-01-2017 дата публикации

Systems and Methods for Enabling Appetite Modulation and/or Improving Dietary Compliance Using an Electro-Dermal Patch

Номер: US20170021171A1
Принадлежит:

A wearable device for suppressing appetite or hunger in a patient includes a microprocessor, electrical stimulator and at least one electrode configured to deliver electrical stimulation to the epidermis, through a range of 0.1 mm to 10 mm or a range of 0.1 mm to 20 mm of the dermis, of a T2 frontal thoracic dermatome to a T12 frontal thoracic dermatome or meridian of the patient and/or front or back, C5-T1 dermatome across the hand and/or arm, and/or the upper chest regions. The device includes a pad, in which the electrode is disposed, for secure placement of the device on a skin surface of a patient. The device is adapted to provide electrical stimulation as per stimulation protocols and to communicate wirelessly with a companion control device configured to monitor and record appetite patterns of the patient. The control device is also configured to monitor, record, and modify stimulation parameters of the stimulation protocols.

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20-11-2014 дата публикации

SYSTEM AND METHOD FOR ACOUSTIC INFORMATION EXCHANGE INVOLVING AN INGESTIBLE LOW POWER CAPSULE

Номер: US20140343378A1
Принадлежит: INNURVATION, INC.

A method of communicating with an ingestible capsule includes detecting the location of the ingestible capsule, focusing a multi-sensor acoustic array on the ingestible capsule, and communicating an acoustic information exchange with the ingestible capsule via the multi-sensor acoustic array. The ingestible capsule includes a sensor that receives a stimulus inside the gastrointestinal tract of an animal, a bidirectional acoustic information communications module that transmits an acoustic information signal containing information from the sensor, and an acoustically transmissive encapsulation that substantially encloses the sensor and communications module, wherein the acoustically transmissive encapsulation is of ingestible size. The multi-sensor array includes a plurality of acoustic transducers that receive an acoustic signal from a movable device, and a plurality of delays, wherein each delay is coupled to a corresponding acoustic transducer. Each delay may be adjusted according to ...

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04-07-2023 дата публикации

System and method for an ingestible physiological monitor

Номер: US0011690550B2

In accordance with some non-limiting examples of the disclosed subject matter, an ingestible system configured to acquire physiological information from an interior of a subject is provided, comprising a substrate and at least one physiological sensor. The at least one “physiological sensor can be coupled to the substrate and configured to capture physiological data from at least one of an internal area or an orientation in a digestive tract of the subject. The system can include a controller coupled to the substrate and configured to receive the physiological data and prepare the physiological data for one of transmission from the subject or analysis of the physiological data. The substrate, including the at least one physiological sensor and the controller coupled thereto can be configured to self-orient within the digestive tract of the subject, during ingestion of the system by the subject.

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31-10-2023 дата публикации

Animal health assessment

Номер: US0011803962B2
Принадлежит: DIG LABS CORPORATION

The present teachings generally include techniques for characterizing the health of an animal (e.g., gastrointestinal health) using image analysis (e.g., of a stool sample) as a complement, alternative, or a replacement to biological specimen sequencing. The present teachings may also or instead include techniques for personalizing a health and wellness plan (including, but not limited to, a dietary supplement such as a customized formula based on a health assessment), where such a health and wellness plan may be based on one or more of the health characterization techniques described herein. The present teachings may also or instead include techniques or plans for continuous care for an animal, e.g., by executing health characterization and heath planning techniques in a cyclical fashion. A personalized supplement system (e.g., using a personalized supplement, personalized dosing device, and personalized packaging) may also or instead be created using the present teachings.

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19-05-2010 дата публикации

Номер: JP0004465187B2
Автор:
Принадлежит:

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20-06-2011 дата публикации

СПОСОБ ОПРЕДЕЛЕНИЯ ЖИЗНЕСПОСОБНОСТИ ТКАНИ КИШКИ ПРИ СТРАНГУЛЯЦИОННОЙ КИШЕЧНОЙ НЕПРОХОДИМОСТИ

Номер: RU2421144C1

Изобретение относится к медицине, а именно к хирургии брюшной полости, и предназначено для определения жизнеспособности кишки при странгуляционной кишечной непроходимости. Определяют значение контролируемого параметра - индекса биоэлектромагнитной реактивности (БЭМР) в исследуемой зоне кишки на ишемизированном и заведомо здоровом участках кишки. Сравнивают полученные результаты. В результате сравнения вычисляют значение индекса функционального состояния кишки (ИФСК), который представляет собой взятое в абсолютных единицах значение разницы между индексом БЭМР, измеренным на заведомо здоровом неизмененном участке стенки кишки, и значением индекса БЭМР, измеренным на ишемизированном участке стенки кишки. Если значение ИФСК находится в пределах от 4,4 до 73,3, то констатируют состояние тканей кишки как компенсированное. Способ позволяет повысить достоверность определения жизнеспособности кишки.

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10-08-2009 дата публикации

ДИАГНОСТИЧЕСКИЙ ЗОНД И КОМПЛЕКТ ДЛЯ ТОНОМЕТРИЧЕСКОГО ИССЛЕДОВАНИЯ ДЫХАТЕЛЬНОЙ НЕДОСТАТОЧНОСТИ И НЕДОСТАТОЧНОСТИ РЕГИОНАРНОГО КРОВОСНАБЖЕНИЯ ОРГАНИЗМА

Номер: RU2363371C2

Изобретение относится к медицине. Устройство (20) содержит дистальный конец (22) для введения в желудочно-кишечный тракт тела пациента, участок (24), предназначенный для введения в тело пациента, и участок (3) для закрепления положения устройства на теле пациента. Участок (24), предназначенный для введения в тело пациента, содержит первую трубку (1), к которой присоединена дополнительная трубка (4). Устройство содержит вторую трубку (2), расположенную, по существу, параллельно первой трубке (1) и прикрепленную к ней. Дистальный конец (22) второй трубки (2) соединен с возможностью сообщения с первой трубкой (1). Первая трубка (1) и вторая трубка (2) изготовлены из материала, легко проницаемого для газов, в особенности для углекислого газа, непроницаемого для жидкостей организма и других субстанций. Дополнительная трубка (5) соединена со второй трубкой (2). Внешний диаметр трубок (1, 2) изменяется в диапазоне от 1 до 4 мм, а толщина стенки изменяется от 0,3 до 1,0 мм. Комплект содержит тонометрическое ...

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20-02-2005 дата публикации

СПОСОБ ОПРЕДЕЛЕНИЯ НАРУЩЕНИЙ ЖИЗНЕСПОСОБНОСТИ ОРГАНОВ И ТКАНЕЙ ЖЕЛУДОЧНО-КИШЕЧНОГО ТРАКТА

Номер: RU2003126275A
Принадлежит:

Способ определения нарушений жизнеспособности органов и тканей желудочно-кишечного тракта, включающий определение функциональных параметров в исследуемом участке органа, отличающийся тем, что в качестве функциональных параметров определяют амплитуду пульсовых осцилляций, период моторной волны и показатель тканевой оксигенации, при этом измерение амплитуды пульсовых осцилляций и показателя тканевой оксигенации в исследуемом участке проводят в период не менее одной моторной волны и при значениях одной и более амплитуд пульсовых осцилляций менее 2 мм и показателя тканевой оксигенации менее 80% судят о нарушениях жизнеспособности исследуемого участка, а при отсутствии моторики в исследуемом участке одновременно определяют период моторной волны в смежном интактном участке и при значениях одной и более амплитуд пульсовых осцилляций менее 2 мм и показателя тканевой оксигенации менее 80% в исследуемом участке за период одной моторной волны в смежном интактном участке судят о нарушениях жизнеспособности ...

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16-05-2012 дата публикации

Verfahren zur Gewinnung medizinisch relevanter Daten aus dem Gastrointestinaltrakt eines Menschen oder eines Tieres sowie eine dafür geeignete Darreichungsform

Номер: DE102004016694B4
Принадлежит: SIEMENS AG

Verfahren zur Gewinnung medizinisch relevanter physikalischer, chemischer oder elektrochemischer, zu diagnostischen Zwecken verwertbarer Daten aus dem Gastrointestinaltrakt eines Patienten, bei dem diesem ein zur Überwachung einer Medikamentierung in eine insgesamt feste oder eine feste Hülle (1) aufweisende Darreichungsform integrierter und von einer biokompatiblen, für hochfrequente elektromagnetische Strahlung durchlässigen Schutzschicht (4) umgebener, dem Patienten datentechnisch zugeordneter Transponder (3) oral verabreicht wird und von diesem während oder nach der Passage durch den Gastrointestinaltrakt ausgesandte Signale mit Hilfe eines Lesegeräts (16) empfangen werden, wobei die feste oder eine feste Hülle (1) aufweisende Darreichungsform ein Medikament enthält, das durch Auflösung der Darreichungsform im Gastrointestinaltrakt des Patienten freigesetzt wird.

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02-12-2010 дата публикации

Gastroscope i.e. flexible endoscope, for examining e.g. gastric acid, on upper gastrointestinal tract for Helicobacter pylori of patient, has sensor with electrodes, where change in electric variable is measured between electrodes

Номер: DE102009023056A1
Принадлежит:

The gastroscope (1) has an insertion tube (2) in which a working channel (3) is arranged, and a sensor (4) guided in the working channel via a guide wire (5). The sensor has an electrode (6) made of an acid-fast noble metal, and another electrode (7) made of silver. An electrical voltage is applied between the electrodes and a change in an electric variable e.g. electrical current or electric resistance, is measured between the electrodes when ammonia is present. The former electrode is made of platinum or gold, and the latter electrode is made of silver chloride layer.

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02-04-1997 дата публикации

Method and apparatus for analyzing a sample

Номер: GB0002271635B
Принадлежит: INSTRUMENTARIUM CORP, * INSTRUMENTARIUM CORP

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10-10-1984 дата публикации

Probe with variable geometry for measuring the radial strains in a sphincter of a living organism

Номер: GB0002137499A
Принадлежит:

A probe for studying the visco-elastic behavior of sphincters of living organisms is comprised of an expansible head formed by three articulated groups disposed radially at 120 DEG intervals about a central axis. Each of the articulated groups is composed of a cross-piece which interconnects a rigid member, carrying a strain gauge on its outer surface, to the central axis. The cross-pieces are articulated at one end about the opposite ends of the rigid member and are articulated at the other end about two blocks which are carried by the central axis. The cross-pieces are constructed such that rotation of the central axis causes the distance between the rigid elements and the central axis to vary. A flexible shaft couples the central axis to a motor.

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22-10-2014 дата публикации

Biomarker

Номер: GB0201416015D0
Автор:
Принадлежит:

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27-10-1976 дата публикации

MULTIPURPOSE OESOPHAGEAL PROBE

Номер: GB0001454066A
Автор:
Принадлежит:

... 1454066 Oesophageal probes VITAL SIGNS INC 3 Jan 1975 244/75 Heading A5R An endo-oesophageal probe 10 for monitoring at least one body condition, comprises an elongate plastics tube 12 of which a first end 16, which is to be inserted into the lower part of the oesophagus through a body cavity, is openended and provided with a plurality of apertures 18 in its wall, said open first end and said apertures being covered by a fluid-tight sleeve 20 which constitutes a diaphragm offering in comparison to the tube wall a lower resistance to the coupling of sound or detection of temperature therethrough; a detector 32 or 38, disposed in or on the tube towards said first end, for monitoring a body condition through electrical connections 34 or 48 housed within the cavity of the tube; the other end of the tube being fitted with means 28 for externally communicating sound or other signals indicative of a monitored condition. As shown there are provided detectors for temperature 32 and ECG 38. The tube ...

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15-02-2008 дата публикации

EQUIPMENT FOR THE REGULATION OF DISTURBANCES OF THE PERFUSION OF A PATIENTENS

Номер: AT0000383810T
Принадлежит:

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15-05-2002 дата публикации

PROCEDURE AND DEVICE FOR THE PRIMARILY AMBULATORY COLLECTION OF DIGESTING PARAMETERS

Номер: AT0000216773T
Принадлежит:

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15-10-2003 дата публикации

MARKER FOR THE DETERMINATION OF ITS POSITION IN A CAVITY WITHIN THE ORGANISM OF AN ORGANISM

Номер: AT0000250895T
Принадлежит:

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07-09-2006 дата публикации

Ingestible device

Номер: AU2002226655B2
Принадлежит:

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03-12-2015 дата публикации

Gastrointestinal neuromodulation and associated systems and methods

Номер: AU2013230774B2
Принадлежит:

Methods for treating gastrointestinal conditions, conditions associated with sympathetic and/or parasympathetic activity in the gastrointestinal organs, and conditions associated with central sympathetic and/or parasympathetic activity in a patient with therapeutic gastrointestinal neuromodulation and associated systems and methods are disclosed herein. One aspect of the present technology is directed to methods that at least partially inhibit sympathetic neural activity in nerves proximate a gastrointestinal artery of a gastrointestinal organ of a patient. Sympathetic drive in the patient can thereby be reduced in a manner that treats the patient for the gastrointestinal condition. Gastrointestinal sympathetic nerve activity can be modulated along afferent and/or efferent pathways. The modulation can be achieved, for example, using an intravascularly positioned catheter carrying a therapeutic assembly, e.g., a therapeutic assembly configured to use electrically-induced, thermally-induced ...

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06-04-2006 дата публикации

DEVICE AND METHOD FOR TREATING WEIGHT DISORDERS

Номер: CA0002582929A1
Автор: KARASIK, YAEL
Принадлежит:

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12-08-2004 дата публикации

ACTIVE DRUG DELIVERY IN THE GASTROINTESTINAL TRACT

Номер: CA0002514392A1
Автор: SELA, YORAM, GROSS, YOSSI
Принадлежит:

Apparatus (100) for drug (36, 106) administration is provided, including an ingestible capsule (30, 102). The capsule (30, 102) includes a drug (36, 106), stored by the capsule (30, 102). An environmentally-sensitive mechanism (e.g., coating 104) is adapted to change a state thereof responsive to a disposition of the capsule (30, 102) within a gastrointestinal tract of a subject. A driving mechanism (e.g., driving mechanism 108), in response to a change of state of the environmentally-sensitive mechanism, is adapted to drive the drug (36, 106) directly through an endothelial layer of the gastrointestinal tract.

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13-04-2010 дата публикации

INDEX AND METHOD OF USE OF ADAPTED FOOD COMPOSITIONS FOR DYSPHAGIC PERSONS

Номер: CA0002568650C
Принадлежит: PROPHAGIA INC.

The present invention provides a method in which a quantitative and descriptive approach is used to adapt the food texture in the clinical management of dysphagia. There is provided a new index, ST index, and method of use for determining and modulating the physical characteristics of foods in a manner to allow the food composition at serving temperature to have a desired combination of firmness, adhesiveness, springiness and cohesiveness to overcome dysphagia-related problems.

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18-08-2009 дата публикации

METHOD AND APPARATUS FOR MEASURING OF INTESTINAL POTENTIAL DIFFERENCE

Номер: CA0002343323C
Автор: SJOVALL, HENRIK
Принадлежит: HENDEVO AB

The present invention relates to a method and an apparatus for producing a transmucosal potential difference (PD) signal essentially being unaffected by intestinal motor activities. This is accomplished by reducing the PD signal based on time variations in the intraluminal pressure (IP) signal. The invention also relates to different applications of such a signal, such as measurement of the total peripheral resistance (TPR), detection of abnormalities in the enterical nervous system, detection of damages in the mucosal barrier.

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30-07-2020 дата публикации

DEVICE FOR MEASURING A CONGESTION OF THE DIGESTIVE TRACT

Номер: CA3126786A1
Принадлежит:

Un dispositif de mesure (1) de congestion du tractus digestif comprend au moins un boîtier (2), un générateur de courant (30) et un moyen de mesure de différence de potentiel (31) logés dans ledit boîtier, et un jeu d'électrodes (3) comportant au moins deux électrodes raccordées électriquement, indépendamment l'une de l'autre, au générateur de courant (30) et/ou au moyen de mesure de différence de potentiel (31) aux bornes des électrodes, chaque électrode du jeu (3) d'électrodes étant configurée pour émettre un courant électrique et/ou permettre la mesure d'une différence de potentiel électrique. Le jeu (3) d'électrodes est configuré pour générer au moins une boucle de circulation (13) du courant électrique circulant au moins au travers d'un tissu du tractus gastro-intestinal (14) de l'utilisateur et pour permettre la mesure d'une différence de potentiel électrique relatif au tissu du tractus gastro-intestinal, le dispositif de mesure (1) de bio-impédance du tractus digestif comprenant ...

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24-03-2016 дата публикации

DEVICE

Номер: CA0002961307A1
Принадлежит:

The present invention relates to a sampling device. The sampling device comprises a separate compartment that is ejected creating an increased space or volume for a sample to be stored The sampling device of the present invention is suitable for collecting a sample in an aquaculture environment, enclosed system or in the gastrointestinal tract of a human or an animal. The invention also relates to a method of orally administering the device to an animal and recovering the device to carry out analysis on the collected sample for diagnosing the health of the gastrointestinal tract and determining nutrient absorption and digestibility.

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01-09-2016 дата публикации

SYSTEMS AND METHODS FOR ENABLING APPETITE MODULATION AND/OR IMPROVING DIETARY COMPLIANCE USING AN ELECTRO-DERMAL PATCH

Номер: CA0002977584A1
Принадлежит:

A wearable device for suppressing appetite or hunger in a patient includes a microprocessor, electrical stimulator and at least one electrode configured to deliver electrical stimulation to the epidermis, through a range of 0.1mm to 10 mm or a range of 0.1 mm to 20 mm of the dermis, of a T2 frontal thoracic dermatome to a T12 frontal thoracic dermatome or meridian of the patient and/or front or back, C5 - T1 dermatome across the hand and/or arm, and/or the upper chest regions. The device includes a pad, in which the electrode is disposed, for secure placement of the device on a skin surface of a patient. The device is adapted to provide electrical stimulation as per stimulation protocols and to communicate wirelessly with a companion control device configured to monitor and record appetite patterns of the patient. The control device is also configured to monitor, record, and modify stimulation parameters of the stimulation protocols.

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24-07-2008 дата публикации

ORAL DRUG CAPSULE COMPONENT INCORPORATING A COMMUNICATION DEVICE

Номер: CA0002671332A1
Принадлежит:

An improved upper capsule portion (62) of an oral drug delivery capsule ( 60) that includes an upper capsule portion (62) and a lower cup shaped capsu le portion (64), the lower cup shaped capsule portion (64) containing a medi cal formulation (66), the lower capsule portion (64) being made of a materia l that disperses in gastrointestinal fluid, the lower capsule portion (64) h aving a mouth, the upper capsule portion (62) dimensioned to engage with the mouth of the lower capsule portion (64). The improvement is the positioning of a communication device, such as an RFID tag (9O)1 on or integrally with the upper capsule portion (62) so that the communication device can communic ate that the oral drug delivery capsule has been ingested. An alternate embo diment with an improved lower capsule portion is also disclosed.

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16-08-2007 дата публикации

GASTRO-INTESTINAL DEVICE AND METHOD FOR TREATING ADDICTION

Номер: CA0002641625A1
Принадлежит:

A device and a method for treating a medical condition include a reversible member disposed in a patient's gastro-intestinal tract, and a dispensing member coupled to the reversible member that delivers a drug and/or a noxiou s when a predetermined substance is detected. In a different embodiment, the device and method of the present invention include a polymer infused with a drug and disposed into a preformed shell inside the gastric space, where it expands and hardens, releasing the drug over time. Both the casing and the polymer may be biocompatible. The present invention enables the slow-release of anti-addictive agents without patient tampering and with the appropriate dosage. Ancillary systems such as sensors, actuators, refill and recharge ports, and communication and data processing units may also be included. ...

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01-02-2007 дата публикации

MULTI MODAL SPECTROSCOPY

Номер: CA0002658811A1
Принадлежит:

The present invention relates to multimodal spectroscopy (MMS) as a clini cal tool for the in vivo diagnosis of disease in humans. The MMS technology combines Raman and fluorescence spectroscopy. A preferred embodiment involve s diagnosis cancer of the breast and of vulnerable atherosclerotic plaque, e sophageal, colon, cervical and bladder cancer. MMS is used to provide a more comprehensive picture of the metabolic, biochemical and morphological state of a tissue than afforded by either Raman or fluorescence and reflectance s pectroscopies alone.

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17-09-1985 дата публикации

PATIENT MONITORING APPARATUS

Номер: CA0001193504A1
Принадлежит: STEWART, MICHAEL I.

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19-09-1995 дата публикации

MAGNETIC OPERATING TABLE

Номер: CA0002117743A1
Принадлежит:

A novel operating table system is provided herein. The operating table system includes a table formed of nonmagnetic material. A support is provided for such table. Magnetic means are provided for applying a magnetic field around a defined area of the table. The magnetic means includes one pole below the table and a second pole disposed a selected spaced-distance above the table.

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20-11-2007 дата публикации

METHOD AND DEVICE FOR ASSESSING PERFUSION FAILURE IN A PATIENT

Номер: CA0002304534C

A device for assessing impairment of blood circulation in a patient, such as that in perfusion failure, by measurement of pCO2 (partial pressure of carbon dioxide) in the upper digestive and/or respiratory tract of the patient comprises a carbon dioxide sensor (22; 104) introduced into the upper digestive and/or respiratory tract of a patient, without passing the sensor beyond the patient's epiglottis. The carbon dioxide sensor is placed adjacent a mucosal surface, preferably within the patient's mouth or inside the patient's nose. By lack of passage into the throat and esophagus, discomfort is substantially avoided and the potential for injury minimized.

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19-01-2012 дата публикации

High-throughput production of ingestible event markers

Номер: US20120011699A1
Принадлежит: Proteus Biomedical Inc

High-throughput ingestible event marker manufacturing systems are provided. The systems include an assembly unit configured to stably associate an ingestible event marker with a carrier to produce a product. Also provided are manufacturing methods to produce such products which include assembling an ingestible event marker with an assembly unit configured to stably associate an ingestible event marker with a carrier.

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09-02-2012 дата публикации

Catheter, a balloon catheter and a method and apparatus for monitoring the transverse cross-section of a stoma

Номер: US20120035642A1
Принадлежит: Flip Technologies Ltd

A balloon catheter ( 1 ) comprises a catheter ( 2 ) and a balloon ( 6 ) located on the distal end of the catheter. A pair of stimulating electrodes ( 15 ) for receiving a constant current stimulating signal when the balloon ( 6 ) is inflated with an electrically conductive medium and a plurality of sensing electrodes ( 16 ) for producing voltage response signals are located on the catheter ( 2 ). The voltage response signals are indicative of the values of the transverse cross-sectional area of the balloon ( 6 ) adjacent the sensing electrodes ( 16 ). A first lumen < 9 ) accommodates the inflating medium to and from the balloon ( 6 ), and a second lumen ( 19 ) accommodates electrically conductive wires ( 18 ) to the stimulating and sensing electrodes ( 15,16 ). A pressure sensing dement ( 21 ) is located in a protective housing ( 22 ) in the second lumen ( 19 ), and communicates through a communicating opening ( 26 ) in the protective housing ( 22 ) and through a communicating port ( 24 ) in the catheter ( 2 ) with a hollow interior region ( 7 ) of the balloon ( 6 ).

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05-04-2012 дата публикации

Diagnostic device and method for sensing hydration state of a mammalian subject

Номер: US20120083711A1
Принадлежит: HYDRADX Inc

Timed sensing of collection of saliva in a liquid collection element of predetermined volumetric capacity may be used to determine salivary secretion rate, as may be indicative of state of euhydration or dehydration. Sensing of salivary flow rate may be further augmented by sensing concentration of at least one analyte in saliva (e.g., with an immunochromatographic assay performed in a lateral flow device) in order to determine a state of euhydration or dehydration. Production of saliva may be stimulated, and collected saliva may be analyzed to generate an analyte detection signal that indicative of presence and/or correlative of concentration of at least one analyte in the collected saliva to sense a state of euhydration or dehydration.

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24-05-2012 дата публикации

Orifice probe apparatus and a method of use thereof

Номер: US20120130281A1
Автор: Nicholas Ahn
Принадлежит: Individual

An orifice probe, particularly for detecting if a patient has or has a risk of having cauda equina syndrome and a method for using same, the probe having a body for insertion into the anus of a patient, a sensing device for measuring at least one of the rectal tone and perianal or rectal sensation, and an output device for yielding at least one of the measurement of the rectal tone of the patient and whether the patient has perianal or rectal sensation.

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31-05-2012 дата публикации

Methods and devices for providing information useful in the diagnosis of abnormalities of the gastrointestinal tract

Номер: US20120136209A1

Disclosed are methods useful for providing information useful in the diagnosis of gastrointestinal abnormalities as well as ingestible devices useful for providing information useful in the diagnosis of gastrointestinal abnormalities.

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05-07-2012 дата публикации

System for continuous measuring, recording and monitoring of the splanchnic tissue perfusion and the pulmonary physiological dead space, and use thereof

Номер: US20120172683A1
Принадлежит: Individual

The present invention relates to a new system for measuring, recording and monitoring the splanchnic tissue perfusion and the pulmonary physiological dead space in an automated way, both continuously and intermittently, and in real time, which is easy to manage and generates information easy to interpret. Said system comprises at least four measuring devices of medical parameters, connected to a device receiving, converting, storing, integrating, processing, and allowing the management and display of the data recorded in the measurements and the parameters estimated by the same. For this purpose, said device comprises a specific computer program of estimation of parameters related to the measurement of the splanchnic tissue perfusion and the pulmonary physiological dead space, from the data derived from the measuring devices. Likewise, the present invention is related to the use of a device for measuring, recording and monitoring of the splanchnic tissue perfusion and the pulmonary physiological dead space.

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26-07-2012 дата публикации

Retrofittable aspiration prevention mechanism for patients

Номер: US20120191038A1
Автор: Allen Gerber
Принадлежит: Individual

A device is employed that can be retrofit onto existing feed pumps to remediate the problem of fluid aspiration in patients being fed through a feeding tube from the pump. In one embodiment the feeding pump is plugged into the device which is plugged into a power outlet. A patient angle sensor triggers power cutoff to the pump and stoppage of fluid flow. The angle sensor and operating program may be part of a smart phone. Power to the pump may be shut off due to a Bluetooth signal from the smart phone to a Bluetooth controlled power strip into which the pump is plugged to receive power.

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09-08-2012 дата публикации

POSITIONING SYSTEM, APPARATUS, AND METHOD FOR WIRELESS MONITORING OF ESOPHAGEAL pH VALUE

Номер: US20120203084A1

A positioning system, an apparatus, and a method for wireless monitoring of esophageal pH value. The positioning system includes an internal transmitting apparatus and an external recording apparatus. The external recording apparatus includes a second element, and the second element of the external recording apparatus cooperates with a first element of the internal transmitting apparatus. If the external recording apparatus detects that the internal transmitting apparatus is not located in the preset region, alerting action is conducted under the control of a micro-processor. The external recording apparatus periodically detects the intensity of a signal received by a second wireless transceiver module, under the control of the micro-processor, and if the signal intensity is not within the preset range, the alerting action is conducted under the control of the micro-processor.

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23-08-2012 дата публикации

Feedback Systems and Methods for Communicating Diagnostic and/or Treatment Signals to Enhance Obesity Treatments

Номер: US20120214140A1
Принадлежит: IntraPace Inc

Feedback systems and methods communicate implanted sensor-based feedback signals to promote behavior modifications that ameliorate obesity and other eating disorders. The system and methods described may also be applicable to any treatment in which presenting feedback regarding patients' eating and exercise habits is desired. The present invention provides a method and system for treating a patient by collecting ingestion and exercise information about the patient from an implanted sensor and communicating the collected information to the patient, his or her physician and/or other health care providers. In some embodiments, stimulation of the patient's stomach is also provided to reduce caloric intake. In some embodiments, the collected data is transmitted to a central server. Further embodiments may provide access to additional information in conjunction with the collected patient information, such as a calorie database, an exercise planner, and so forth, with the data optionally being used within a social networking system.

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06-09-2012 дата публикации

Meibomian gland imaging

Номер: US20120226156A1
Принадлежит: TearScience Inc

A method of evaluating dry eye in humans wherein the flow of naturally occurring secretion to the eye is reduced or stopped due to the presence of an obstruction of a meibomian gland in the eyelid involves applying a pressure to the eyelid that mimics pressure applied during blinking; and simultaneously imaging the glands to diagnose the condition of the meibomian gland. This abstract is not to be considered limiting, since other embodiments may deviate from the features described in this abstract.

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13-09-2012 дата публикации

Bariatric device and method for weight loss

Номер: US20120232577A1
Принадлежит: Allergan Inc

A bariatric device for use in inducing weight loss, comprising a cardiac element, a pyloric element, and a connecting element between the two other elements, wherein the connecting element provides structure between the cardiac and pyloric elements, keeping them largely in place and at least intermittently touching and applying pressure to the stomach's cardiac, adjacent fundic and pyloric regions, respectively, which produces a satiety signal to the user, giving the recipient a feeling of fullness and reducing his or her hunger feelings. Alternatively, the cardiac and pyloric elements may be symmetrical, so that the device can orient itself either way in the stomach and still achieve the weight loss function.

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20-09-2012 дата публикации

Detector and Method for Detection of H. Pylori

Номер: US20120237968A1
Автор: Anastasia Rigas
Принадлежит: Individual

An inexpensive, portable, hand held, point-of-care, non-invasive breath-analyzer for the detection of H. Pylori in adults and children by measuring ammonia in breath using a polyaniline-carbon nanotube sensor.

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27-09-2012 дата публикации

Strain compensation for pressure sensors

Номер: US20120245864A1
Принадлежит: MEDTRONIC INC

A pressure sensing system provides signals representative of a magnitude of pressure at a selected site. A sensor module includes a first transducer producing a first signal having an associated first response to pressure and strain applied to the sensor module and a second transducer producing a second signal having an associated second response to pressure and strain applied to the sensor module. A calculated pressure, a bending pressure error and a bend-compensated pressure are computed in response to the first signal and the second signal.

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18-10-2012 дата публикации

Methods for diagnosing meibomian gland dysfunction

Номер: US20120265101A1
Принадлежит: TearScience Inc

Methods of diagnosing meibomian gland dysfunction are disclosed. The methods may be standardized and provide an accurate diagnosis of whether meibomian gland dysfunction exists. In one embodiment, a method is provided that utilizes an evaluation tool to apply a force for a preselected period of time to at least one of a plurality of meibomian glands in two or more regions of a plurality of regions of an eyelid. A grade is assigned to the at least one meibomian gland of the plurality of meibomian glands in each of the two or more regions based on any secretion that is expressed from each meibomian gland. In this manner, a plurality of meibomian gland secretion grades is obtained. The plurality of meibomian gland secretion grades is indicative of the presence of meibomian gland dysfunction.

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15-11-2012 дата публикации

Mask on monitor hernia locator

Номер: US20120289811A1
Автор: Emily Davis, Frank Viola
Принадлежит: TYCO HEALTHCARE GROUP LP

A method of tracking the location of a hernia defect is disclosed, the method including providing a display device, a camera adapted to transmit an image to the display device, a marking surface disposed on the display device and a marker adapted to alter the marking surface when applied to the marking surface. The method includes receiving an image of a hernia defect from the camera and displaying the received image on the display device and marking the shape and position of the hernia defect on the marking surface by applying the marker to the marking surface. Alternatively the display device may be marked by executing by the processor a computer program to mark the shape and position of the hernia defect on the display device.

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27-12-2012 дата публикации

System for Non-Invasive Assay of Liver Function

Номер: US20120330116A1
Принадлежит: Cardiox Corp

A system, method and apparatus are disclosed for using a transcutaneous detection system to measure the quantity of a circulating organ activity detection analyte in the blood, and thereby assay the activity of an organ. A preferred organ for assay is the human liver and a preferred indicator is indocyanine green (ICG) dye The procedure is under the control of a monitor/controller having a visual display and capable of providing cues to the operator. A sensor array apparatus for use in conjunction with the system monitor/controller is configured for increased sensitivity of assaying organ function.

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03-01-2013 дата публикации

Systems and Methods for Alcohol Consumption Monitoring

Номер: US20130006066A1
Автор: Donald A. Melton
Принадлежит: BI Inc

Various embodiments of the present inventions are related to monitoring physical characteristics of a monitored individual including, but not limited to, alcohol consumption by the monitored individual.

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07-02-2013 дата публикации

System and method for mapping gastro-intestinal electrical activity

Номер: US20130035576A1
Принадлежит: Auckland Uniservices Ltd

A gastro-electrical activity mapping system and comprises a catheter insertable through a natural orifice into the gastro-intestinal (GI) tract and comprising an array of electrodes for contacting an interior surface of a section of the GI tract to detect electrical potentials at multiple electrodes, and a signal analysis and mapping system arranged to receive and process electrical signals from multiple electrodes of the array and spatially map GI smooth muscle electrical activity as an activation time map, a velocity map, or an amplitude map, which may be in the form of contour plots and may be mapped on an anatomical computer model of at least the section of the GI tract and may be animated. A GI mapping method and catheter are also claimed.

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28-02-2013 дата публикации

Cystic fibrosis diagnostic device and method

Номер: US20130053673A1
Автор: Philippe Brunswick
Принадлежит: Impeto Medical SAS

A method for detecting cystic fibrosis is disclosed, which is performed in a system comprising an anode and a cathode placed on different regions of the patient body, and an adjustable DC source, which is controlled in order to feed the anode with a DC current. The method includes applying DC voltage pulses of varying voltage values to the anode for given durations allowing the stabilization of electrochemical phenomena in the body in the vicinity of the electrodes, collecting data representative of the current between the electrodes, and of the potentials of the electrodes, for the different DC voltages, and from the data, computing data representative of the electrochemical skin conductance of the patient, and reconciling the latter data with reference data obtained in the same conditions on patients suffering or not from cystic fibrosis, and identifying the patient as suffering or not from cystic fibrosis.

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11-04-2013 дата публикации

DETECTION AND TREATMENT OF ABNORMAL ESOPHAGEAL SPHINCTER FUNCTIONALITY

Номер: US20130090573A1
Автор: Shaker Reza
Принадлежит:

An esophageal device is used to recognize, diagnose, characterize, or relieve an impact of an abnormal or defective UES anatomy, physiology, or functionality. In one implementation, the esophageal device measures a UES response to esophageal fluid infusion to detect or characterize an abnormality or defective UES anatomy, physiology, or functionality. An Upper Esophageal Sphincter compression device is used to increase intra-luminal pressure within the Upper Esophageal Sphincter of a patient in order relieve an impact of an abnormal or defective UES anatomy, physiology, or functionality. 1. An esophageal device for diagnosing Upper Esophageal Sphincter (UES) pathology , the esophageal device comprising:(a) a intra-luminal pressure sensor configured to measure UES pressure when the intra-luminal pressure sensor is located within an Upper Esophageal Sphincter of a patient; tubing configured for insertion into an esophagus of a patient;', 'a pump configured to inject fluid into the tubing, wherein, when the tubing is inserted into the esophagus, injection of the fluid invokes a pharyngeal reflux in the patient; and', 'a controller configured to control a pump pressure of the pump;, '(b) a fluid infusion device including(c) an output device;and receiving indicia about the UES pressure measured by the intra-luminal pressure sensor when the pharyngeal reflux occurs in the patient;', 'comparing the received said UES pressure of the patient with a predetermined said UES pressure, wherein the predetermined said UES pressure is determined from at least one said UES pressure of a corresponding control subject when the corresponding control subject experiences pharyngeal reflux; and', 'transmitting a result of the comparison to the output device accessible by a health care provider diagnosing the patient., '(d) an article of manufacture communicatively coupled with the output device, the article of manufacture including a processor and a non-transitory computer readable medium ...

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18-04-2013 дата публикации

METHODS AND DEVICES FOR DETECTING BOWEL PERFORATION

Номер: US20130096399A1
Принадлежит:

The present disclosure relates to methods and devices to detect perforation of the bowel, for example, resulting from surgical procedures, such as laparoscopy, diagnostic procedures, such as colonoscopy, medical conditions, such as diverticulitis, and trauma. The present disclosure also relates to filtration systems and electrical connector assemblies for use in the methods and devices. 1. A bowel perforation detection device comprising:a sample delivery unit comprising an aspirate filtering means;a sensing unit comprising a gas-detecting means, a pump, a processor, and a display; anda connecting means connecting the sample delivery unit and the sensing unit.2. The device of wherein said aspirate filtering means comprises a first filter and a second filter.3. The device of wherein said first filter is a hydrophobic porous membrane filter having pore sizes ranging from about 100 microns to about 500 microns.4. The device of wherein said second filter is a hydrophobic filter having minimum pore size of 0.2 microns or a hydrophilic filter having a minimum pore size of 0.01 microns.5. The device of wherein said aspirate filtering means comprises:an outer housing section;an inner tubing section, a portion of which is perforated;a sleeve comprising an absorbent wicking material disposed between the perforated tubing and the outer housing;a hydrophobic liquid filter having pore sizes ranging from about 100 microns to about 500 microns; anda gas/microbial filter.6. The device of wherein said sample delivery unit further comprises a one-way valve in the tubing.7. The device of wherein said gas-detecting means is selected from the group consisting of contact gas sensors claim 1 , non-contact gas sensors claim 1 , and combinations thereof.8. The device of wherein said gas-detecting means is selected from the group consisting of a carbon dioxide gas sensor claim 1 , a methane gas sensor claim 1 , a hydrogen gas sensor claim 1 , a sulfide gas sensor claim 1 , a nitrogen gas ...

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18-04-2013 дата публикации

METHOD AND APPARATUS FOR DETERMINING FLOW RATES OF EXCRETED OR SECRETED BODY FLUIDS

Номер: US20130096461A1
Автор: SELLA Yoav
Принадлежит:

The invention relates to an apparatus and method to determine and monitor the flow rates and volume of fluids excreted or secreted by the body. The invention achieves the above objects by providing an apparatus comprising; a measuring unit comprising a conduit made of a material having a low thermal conductivity and supporting at least two thermistors; an upstream thermistor serving as a compensation thermistor and a downstream thermistor located as far downstream as possible from said upstream thermistor and pre-heated to and kept at pre-defined temperature which is warmer than the fluid temperature to be metered; and means for applying small electric voltages to the thermistors to enable generation of an electric signal; and a control and display unit being operatively connected to the measuring unit. 1. An apparatus for determining the flow rate and amount of a selected secreted or excreted body fluid , comprising:a) a measuring unit comprising a conduit made of a material having a low thermal conductivity and supporting at least two thermistors; an upstream thermistor serving as a compensation thermistor and a downstream thermistor located as far downstream as possible from said upstream thermistor and pre-heated to a temperature which is warmer than the fluid temperature;b) means for applying constant small electric voltages to said thermistors to enable generation of electric signals, said signals flowing through said upstream thermistor being sufficiently low to prevent substantial heating of said thermistor; andc) a control and display unit being operatively connected to said measuring unit, said control unit including means for calculating the difference between the electrical resistance of said upstream and said downstream thermistors and then calculating the flow rate based on the electrical signal difference, the flow rate being a function of the body fluid flow rate and then calculating the accumulated amount of fluid based on the internal cross section ...

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02-05-2013 дата публикации

Arrangement and method for navigating an endoscopic capsule

Номер: US20130109920A1
Принадлежит: SIEMENS AG

An arrangement for navigating an endoscopic capsule includes an external first magnetic field with a first magnetic flux density for moving the endoscopic capsule. The arrangement also includes at least one sensor coil pair outside of the endoscopic capsule for determining a position and/or orientation of the endoscopic capsule. The at least one sensor coil par includes a first sensor coil and a second sensor coil. The first sensor coil and the second sensor coil are electrically connected to one another and arranged at locations with the same first magnetic flux density.

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16-05-2013 дата публикации

DEVICE, SYSTEM AND METHOD FOR MEASUREMENT AND ANALYSIS OF CONTRACTILE ACTIVITY

Номер: US20130123586A1
Принадлежит: GIVEN IMAGING LTD.

A method and system for determining intestinal dysfunction condition are provided by classifying and analyzing image frames captured in-vivo. The method and system also relate to the detection of contractile activity in intestinal tracts, to automatic detection of video image frames taken in the gastrointestinal tract including contractile activity, and more particularly to measurement and analysis of contractile activity of the GI tract based on image intensity of in vivo image data. 1. A method for analysis of contractile activity of the gastrointestinal (GI) tract in an in-vivo image stream , the method comprising:receiving a stream of image frames from an in-vivo imaging device;measuring a property of each image frame of a plurality of image frames of said stream;classifying said plurality of image frames into frame classifications based on the measured property, said frame classifications selected from at least turbid frames, wall frames, wrinkle pattern frames and static frames; andanalyzing the properties of the classified image frames to determine contractile activity in the image stream.2. A method for analysis of contractile activity of the gastrointestinal (GI) tract in an in-vivo image stream , the method comprising:receiving a stream of image frames from an in-vivo imaging device;measuring a property of each image frame of a plurality of image frames of said stream;detecting turbid frames in said plurality of image frames based on the measured property; andanalyzing the turbid frames to determine contractile activity in the image stream.3. The method of wherein analyzing the turbid frames comprises at least one of:determining a percentage of turbid frames in the image stream or in a portion thereof,determining a percentage of turbid frames that are also static frames, determining a percentage of tunnel frames in parts of the image stream which are not turbid and determining a static level of images in parts of the image stream which are not turbid.4. ...

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06-06-2013 дата публикации

MULTI-MODAL IMAGING OF BLOOD FLOW

Номер: US20130144140A1
Принадлежит:

The application features methods, devices, and systems for measuring blood flow in a subject. The computer-implemented methods include receiving functional magnetic resonance imaging (fMRI) data that provides information on at least one of volume or oxygenation of blood at one or more locations in a body over a first predetermined length of time. The methods also include receiving near-infrared spectroscopic (NIRS) imaging or measurement data representing at least one of blood concentration or oxygenation at a first portion of the body over a second predetermined length of time. The methods further include deriving, from the fMRI data corresponding to a second portion of the body, a time varying data set representing changes in blood oxygenation or volume or both blood oxygenation and volume at the second portion over the first predetermined length of time and determining, by a computing device, a time delay and a value of a similarity metric corresponding to a part of the spectroscopic imaging data that most closely matches the time varying data set. The time delay represents a difference between a first time in which blood flows from a third portion in the body to the first portion and a second time in which blood flows to the second portion from the third portion. The value of the similarity metric represents an amount of blood at the second portion. An estimate of a characteristic of at least one of blood flow or blood volume in the second portion at a given time is determined based on the time delay and the value of the similarity metric. 136-. (canceled)37. A computer-implemented method for measuring at least one of blood flow or volume in a subject , the method comprising:receiving functional magnetic resonance imaging (fMRI) data that provides information on at least one of volume or oxygenation of blood at one or more locations in a body over a first predetermined length of time;receiving spectroscopic measurement data representing at least one of blood ...

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13-06-2013 дата публикации

BIO-DIAGNOSTIC TESTING SYSTEM AND METHODS

Номер: US20130149714A1
Принадлежит:

An implantable diagnostic device in accordance with the present disclosure includes a probe assembly that can be implemented in a variety of ways. A few example implementations include: a needle inside which is located a bio-sensor chip (the needle being insertable into a human being); a compact package containing the bio-sensor chip (the compact package configured for placement inside a catheter); or a silicon-based bio-sensor package configured for insertion into a vein. 1. A bio-diagnostic system comprising:a probe assembly configured for insertion into an animate object, the probe assembly comprising:an optical waveguide configured for propagating a light beam; andan optical resonator incorporating a capture agent placed upon a binding site that is exposed to a fluid, the optical resonator configured to receive at least a portion of the propagated light beam and generate therefrom, a first resonant wavelength when no binding reaction is present at the binding site, and a second resonant wavelength when a binding reaction is present at the first binding site, the binding reaction modifying a refractive index of the optical resonator.2. The bio-diagnostic system of claim 1 , wherein the probe assembly is at least one of: a) a needle comprising a first bio-sensor chip that includes the optical waveguide and the first optical resonator claim 1 , b) a catheter comprising a second bio-sensor chip that includes the optical waveguide and the first optical resonator claim 1 , or c) a third bio-sensor chip configured for insertion into the vein claim 1 , the third bio-sensor chip comprising the optical waveguide and the first optical resonator.3. The bio-diagnostic system of claim 2 , wherein at least one of the needle or the catheter is a part of an intravenous (IV) apparatus.4. The bio-diagnostic system of claim 2 , wherein the needle has a sub-mm diameter.5. The bio-diagnostic system of claim 4 , wherein the fluid is one of: blood claim 4 , lymphatic fluid claim 4 , ...

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13-06-2013 дата публикации

SURGICAL TISSUE MONITORING SYSTEM

Номер: US20130150694A1
Автор: Beetel Robert, Viola Frank
Принадлежит: COVIDIEN LP

A tissue monitoring system includes an introducer having an inflatable section and a plurality of electrodes disposed thereon. The electrodes are alternatively connected to an electrode contact system which includes at least one signal line and at least one measurement line for taking readings about a circumferential segment of tissue encompassed by the electrodes. 1. A method of monitoring tissue comprising:placing an introducer having an inflatable section and a plurality of electrodes disposed about the inflatable section adjacent to a section of tissue;distending the first inflatable section of the introducer;imposing an electrical signal on the tissue using a subset of the plurality of electrodes selected for an electrode contact system;measuring a resulting potential with the subset of the plurality of electrodes of the electrode contact system; andshifting the electrode contact system to alternate placement of the electrode contact system within the tissue.2. The method of claim 1 , wherein the step of shifting the electrode contact system includes electronically shifting each contact of the electrode contact system to encompass a different subset of the plurality of electrodes.3. The method of claim 2 , wherein electronically shifting each contact includes shifting each contact to an adjacent electrode on the inflatable section of the introducer.4. The method of claim 1 , wherein the introducer further includes a shaft extending through the introducer claim 1 , and wherein the step of shifting the electrode contact system includes rotating the shaft to shift the electrode contact system clockwise or counterclockwise around a circumferential segment of the tissue.5. The method of claim 1 , further comprising repeating the step of shifting the electrode contact system until an entire circumference of the tissue is characterized.6. The method of claim 1 , wherein the step of imposing an electrical signal includes attaching two electrodes of the subset of the ...

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27-06-2013 дата публикации

Noninvasive detection of meconium in amniotic fluid

Номер: US20130165816A1
Автор: Gideon Mor
Принадлежит: Individual

Meconium stained amniotic fluid can indicate intrauterine fetal distress. The invention provides a system and method for detecting meconium in released amniotic fluid in pregnant women, including a collection body such as a hygienic pad, having a meconium detector. This invention is designed to be employed mainly by a lay person at home; it also may provide possible etiologies for fetal distress.

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27-06-2013 дата публикации

Devices and systems to size a luminal organ

Номер: US20130165818A1
Автор: Ghassan S. Kassab
Принадлежит: Individual

Devices and systems to size a luminal organ. At least some embodiments include a catheter comprising an outer elongate tube, an inner elongate tube disposed within the outer elongate tube, a proximal balloon attached to the outer elongate tube, a distal balloon having a first end attached to the outer elongate tube and a second end attached to the inner elongate tube, electrodes positioned on the outer elongate tube, and a pressure transducer positioned on the outer elongate tube.

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11-07-2013 дата публикации

DEVICE FOR APPLYING A PNEUMATIC PRESSURE STIMULUS IN THE NASAL FOSSAE AND EUSTACHIAN TUBE AT THE TIME OF DEGLUTITION

Номер: US20130178716A1
Принадлежит: La Diffusion Technique Francaise

Apparatus for automatically applying a pneumatic overpressure phase, of a value of between 5 and 100 hPa in the Eustachian tube and/or in the nasal fossae of a patient through at least one nostril at the moment of swallowing, includes a gas generator, a gas reservoir, a detection-fluid and control circuit communicating with the gas reservoir and gas generator and leading to a sealed plug in the nostrils forming part of a nosepiece equipped with a control nozzle, a device for measuring at least one characteristic value of a flow of gas during swallowing, a device for automatically comparing the characteristic value with at least one pre-set value, and a device for informing the patient whether the swallowing action is being correctly performed. 1. Device for automatically applying a pneumatic overpressure phase , of a value of between 5 and 100 hPa in a Eustachian tube and/or in a nasal fossae of a patient through at least one nostril at a moment of swallowing , the device comprising a gas generator , a gas reservoir and a detection-fluid and control circuit communicating with the gas reservoir and the gas generator and leading to a sealed plug of a nosepiece equipped with a control nozzle for placement in nostrils; first means for measuring at least one characteristic value of a flow of gas during swallowing , second means for automatically comparing the characteristic value with at least one pre-set value , and third means for informing the patient whether the swallowing action is being correctly performed.2. Device according to claim 1 , wherein the first means comprises means for measuring variation of the flow and/or duration of the variation of the flow on swallowing and the second means comprises means for automatically comparing value of the variation of the flow and/or the duration of the variation of the flow with at least one pre-set value of variation of flow and/or with at least one pre-set duration of variation of flow.3. Device according to claims 1 , ...

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11-07-2013 дата публикации

VIVO DETERMINATION OF ACIDITY LEVELS

Номер: US20130178721A1
Автор: Bird Uzi, Livshits David
Принадлежит: DELAVAL HOLDING AB

A bolus for use in a ruminant animal's reticulum includes a cavity () configured to receive ruminal fluids present in the stomach. The cavity has walls () of a dielectric material and is encircled by a coil member (), which is configured to subject the ruminal fluids to an electro-magnetic field. A Sensor element () measures the electromag-netic field's influence on the ruminal fluids and thus register an electromagnetic property representative of an acidity level of said fluids. A transmitter () transmits a wireless output signal (SD) reflecting the acidity measure. 113-. (canceled)14100. A bolus for introducing into a ruminant animal's (A) reticulum (R) and for ongoing measurement of an acidity level of an animal's stomach fluids , the bolus () comprising:{'b': '100', 'a housing () having an outermost surface exterior wall;'}{'b': 1', '2', '110, "a cavity defined by a portion of the exterior wall of the housing, the cavity (C, C) having a wall of dielectric material and at least a first opening for receiving ruminal fluids into the cavity, the wall defining a dielectric conduit (), the first opening being an unobstructed opening freely allowing the ruminal fluids from the animal's (A) reticulum (R) to be received into the cavity;"}{'b': '310', 'a power generator () that generates electric power within a spectral range;'}{'b': 120', '110', '120, 'a sensor coil () encircling the dielectric conduit () and powered by the power generator, the sensor coil () configured to subject the received ruminal fluids (L) within the cavity to an electromagnetic field (B) within the spectral range;'}{'b': 320', '120, 'a processor () connected to the sensor coil () to measure, under influence of the electromagnetic field (B), an electromagnetic property (z) of the ruminal fluids (L),'}{'b': '320', 'sub': 'pH', 'wherein from the measure of the electromagnetic property (z), the processor () determines an acidity measure (M) of an acidity level of the ruminal fluids (L); and'}{'b': 410 ...

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11-07-2013 дата публикации

Functional eeg imager

Номер: US20130178757A1
Принадлежит: Norconnect Inc

A system for identifying the connectivity between different brain regions to determine the functional role of brain regions in various human and animal actions.

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25-07-2013 дата публикации

DEVICE FOR MEASURING ORAL CAVITY PRESSURE, PRESSURE MEASURING PROBE

Номер: US20130190656A1
Автор: TOYOTA Koichiro
Принадлежит: JMS CO., LTD.

A device for measuring oral cavity pressure includes the following: a pressure measuring probe having a configuration in which a balloon made of an elastic material is supported by a balloon base ; a communicating member having an inner bore that communicates with the inside of the balloon via the balloon base to transmit the air pressure in the balloon; and a pressure detecting unit that is connected to the rear end of the communicating member and detects the transmitted air pressure. The balloon includes a pressure receiving portion that forms a cavity and a balloon tubular portion that communicates with the inside of the pressure receiving portion, and the balloon is joined to the front end portion of the balloon base with the balloon tubular portion. The balloon base has a rib that protrudes outward along the outer circumferential direction of the front end portion on the balloon side. The device for measuring oral cavity pressure uses the pressure measuring probe including a flat balloon and allows the balloon to be inserted into the oral cavity in an appropriate state, and thus stably can ensure good measurement accuracy. 1. A device for measuring oral cavity pressure comprising:a balloon that is made of an elastic material;a tubular member that supports the balloon at a front end and has an inner bore that communicates with an inside of the balloon to transmit an air pressure in the balloon; anda pressure detecting unit that is connected to a rear end of the tubular member via a connecting tube and detects the transmitted air pressure,wherein the balloon includes a pressure receiving portion that forms a cavity and a balloon tubular portion that communicates with an inside of the pressure receiving portion, and the balloon is joined to a front end portion of the tubular member with the balloon tubular portion,wherein the tubular member is divided into a balloon base to which the balloon tubular portion is joined, and a probe mounting member to a front end of ...

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01-08-2013 дата публикации

NEURAL MONITORING METHODS AND SYSTEMS FOR TREATING UPPER AIRWAY DISORDERS

Номер: US20130197321A1
Автор: Wilson Willard
Принадлежит: NEUROSTREAM TECHNOLOGIES G.P.

Methods and systems for monitoring, preventing and/or treating upper airway disorders such as apnea, dysphagia, reflux and/or snoring are described. The methods and systems monitor the upper airway disorders by processing one or more neural signals obtained from one or more upper airway afferents. Upper airway disorders are prevented and/or treated by delivering one or more stimulations to one or more reflex-related afferents, efferents, muscles, and sensory receptors to manipulate the threshold and/or trigger an upper airway reflex including, but not limited to a swallow reflex and/or a negative-pressure reflex. 1. A method for monitoring a condition in a subject , the method comprising:obtaining one or more neural signals from one or more upper airway afferents of the subject;processing each of the one or more neural signals to obtain at least one neural activity profile, each neural activity profile characterized by at least one of: a neural signal timing, a neural signal amplitude, a neural signal phase, a neural signal position, a neural signal conduction velocity, and any combination thereof;comparing each of the at least one neural activity profiles to one or more activity criteria to associate each neural activity profile with an associated activity type chosen from a respiratory activity type, a deglutition activity type, a vibration activity type, a reflux activity type, and any combination thereof; a respiratory state comprising respiratory timing, respiratory amplitude, respiratory phase, respiratory location, and any combination thereof;', 'a deglutition state comprising solid contact, fluid contact, contact velocity, contact timing, contact amplitude, contact pressure, contact texture, contact temperature, a presence of a unswallowed bolus, and any combination thereof;', 'a vibration state comprising vibration timing, vibration amplitude, vibration phase, vibration location, vibration pattern, and any combination thereof; and', 'a reflux state ...

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01-08-2013 дата публикации

FIDUCIAL PLACEMENT SYSTEM AND SPLAYED STYLET

Номер: US20130197356A1
Принадлежит: Cook Medical Technologies Inc

A fiducial deployment system may include one or more of a needle including a dimpled retention structure configured to releasably retain a plurality of fiducials, each of which includes a central aperture (which may be embodied as a groove or similar opening); a retention/deployment stylet that traverses through each fiducial's central aperture and releasably engages a distalmost fiducial of the plurality of fiducials with a splayed distal stylet end; a pusher cannula member; and echogenic dimpling and/or other echogenic-enhancing features on at least a distal portion of the needle. 1. A fiducial deployment system comprising: a generally tubular cannula body defining a needle lumen disposed through at least a lengthwise portion of the cannula body and', 'a distal needle end opening at a distal end of the needle lumen;', 'a distal needle end region, the distal end region comprising'}], 'a needle including'}at least one fiducial comprising a fiducial body slidably disposed in the needle lumen, which fiducial body includes a fiducial aperture extending longitudinally therethrough;a pusher slidably disposed longitudinally through the needle lumen proximal of and contacting the at least one fiducial, where the pusher is configured to advance the at least one fiducial out of the distal needle end opening; anda stylet extending longitudinally through a portion of the needle lumen and the aperture of the at least one fiducial,wherein the stylet includes at least one splayed distal end portion that is biased apart to engage a distal end surface of the at least one fiducial and that is sufficiently collapsible to pass through a cross-sectional area of the fiducial aperture, such that the stylet is configured to releasably retain the at least one fiducial.2. The fiducial deployment system of claim 1 , where the pusher is embodied as a pusher cannula including a pusher lumen longitudinally disposed therethrough claim 1 , through which a portion of the stylet slidably extends.3. ...

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01-08-2013 дата публикации

Estimation of distances and size of lesions in the colon with an imaging capsule

Номер: US20130197360A1
Автор: Gideon Baum, Yoav Kimchy
Принадлежит: Check Cap Ltd

A method of estimating distances in a colon of a subject, including: orally administering to a subject a contrast agent, orally administering an imaging capsule to the subject, emitting radiation from the imaging capsule at a location in the colon, detecting photons that are returned from an interaction of the radiation with an inner wall of the colon and contents of the colon, summating the detected photons with energies corresponding to X-ray florescence interactions to form a first count, summating the detected photons with energies corresponding to Compton back-scattering interactions to form a second count, determining the distance from the imaging capsule to the inner wall of the colon and a concentration of the contrast agent at the location of the imaging capsule in the colon using the values of the first count and the second count.

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08-08-2013 дата публикации

System to diagnose the function of intrinsic sphincters

Номер: US20130204313A1
Принадлежит: Pneumoflex Systems LLC

A system treats at least one of the urethral and anal sphincters. A muscle contraction device is located on at least one of the urethral and anal sphincters. A controller is connected to the muscle contraction device and operative to transmit control signals to the muscle contraction device located on at least one of the urethral and anal sphincters to contract the muscle during an inspiratory phase of respiration.

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22-08-2013 дата публикации

METHODS AND COMPOSITIONS FOR NON-INVASIVE, DYNAMIC IMAGING OF INTESTINAL MOTILITY

Номер: US20130216482A1

Described are methods and composition for use in non-invasive imaging of intestinal structure and function. These methods can be used to identify, diagnose, assess, monitor and direct therapies for gastrointestinal diseases and disorders. Embodiments of the methods utilize highly sensitive optical imaging and fluorescent spectroscopy techniques to track or monitor packets of organic dye excreted in bile into the intestinal tract to provide quantitative information regarding intestinal propulsion and function. 1. A method of non-invasively imaging gastrointestinal motility in a subject having an abdominal surface and a gastrointestinal tract , the method comprising:a) selecting a subject that has been administered an animal foodstuff comprising at least one auto fluorescent compound;b) illuminating the abdominal surface with an excitation light to excite the auto fluorescent compound;c) continuously, non-invasively detecting fluorescent emissions from the auto fluorescent compound to image at least a region of the gastrointestinal tract of the subject;d) capturing a plurality of images of said one or more regions of the gastrointestinal tract of the subject, based on said detected auto fluorescent emissions; ande) tracking in vivo propulsion of said auto fluorescent compound through the one or more regions of the gastrointestinal tract, based on said captured images.2. The method of claim 1 , wherein (a) selecting a subject comprises:i) administering an animal foodstuff comprising at least one auto fluorescent compound to the subject; andii) allowing sufficient time for said foodstuff to enter into the gastrointestinal tract of the subject;3. The method of claim 1 , wherein the auto fluorescent compound has an excitation wavelength ranging from about 700 nm to about 900 nm.4. The method of claim 1 , wherein (c) comprises using an intensified charge-coupled camera.5. The method of claim 1 , wherein (b) comprises illuminating the tissue surface with an excitation light ...

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22-08-2013 дата публикации

Method of generating elasticity data, elasticity data generating apparatus, and elasticity image generating system based thereon

Номер: US20130217994A1
Принадлежит: Individual

A method of generating elasticity data, an elasticity generating apparatus, and an elasticity image generating system based thereon is provided. The method of generating elasticity data includes receiving first elasticity data of a region of interest (ROI) in a subject, the first elasticity data indicating elasticity corresponding to a predetermined degree of deformation, receiving second elasticity data of a local region of the ROI in the subject, the second elasticity data indicating elasticity corresponding to a local degree of deformation that is greater than the predetermined degree of deformation, and generating third elasticity data of the ROI in the subject based on the received first elasticity data and second elasticity data, the third elasticity data indicating elasticity corresponding to a global degree of deformation that is greater than the predetermined degree of deformation.

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22-08-2013 дата публикации

METHODS FOR DIAGNOSIS OF COLORECTAL CANCER

Номер: US20130218023A1
Принадлежит: THE JOHNS HOPKINS UNIVERSITY

Methods and systems for use of phenotypic markers, principally oral mucosal vascular density alone or in combination with detection of other markers, to identify individuals afflicted with or having an increased risk of hereditary colorectal cancer, especially familial adenomatous polyposis, are disclosed. 1. A method for diagnosing familial adenomatous polyposis (FAP) or an increased risk of FAP in a test subject believed to be at risk for such cancer , the method comprising:(a) positioning a sampling area of the oral mucosa of the test subject in a system for measuring the oral mucosal vascular density (OMVD);(b) transilluminating the sampling area of the oral mucosa of the test subject with a light source from the system in a range of wavelengths from 470 nm to 700 nm for a period of time;(c) obtaining at least one or more images of the illuminated sampling area of the test subject using a camera from the system;(d) storing the at least one or more images of (c) on an electronic storage device on a computer;(e) analyzing the at least one or more images of the test subject stored on the electronic storage device to provide an oral mucosal vascular density (OMVD) value from a selected portion of the one or more images; and(f) comparing the OMVD values of the at least one or more images of the test subject to one or more OMVD values of one or more control subjects which are not afflicted with colorectal cancer; and(g) diagnosing the test subject has having adenomatous polyposis (FAP) or an increased risk of FAP when there is found a statistically significant increase in OVMD value in the test subject when compared to the one or more control subjects.26.-. (canceled)7. The method of claim 1 , further comprising analysis of oral mucosal reflectance (OMR) in the one or more subjects compared to controls.8. (canceled)9. The method of claim 7 , wherein the difference between the OMR measurements in the one or more subjects does not differ from the OMR measurements in the ...

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19-09-2013 дата публикации

ELECTRONICS FOR DETECTION OF A CONDITION OF TISSUE

Номер: US20130245388A1
Принадлежит:

Apparatus are provided for monitoring a condition of a tissue based on a measurement of an electrical property of the tissue. In an example, the electrical property of the tissue is performed using an apparatus disposed above the tissue, where the apparatus includes at least two conductive structures, each having a non-linear configuration, where the at least two conductive structures are disposed substantially parallel to each other. In another example, the electrical property of the tissue is performed using an apparatus disposed above the tissue, where the apparatus includes at least one inductor structure. 1. An apparatus for monitoring a condition of a tissue , the apparatus comprising:at least two conductive structures disposed above the tissue, wherein each of the at least two conductive structures has a non-linear configuration, and wherein the at least two conductive structures are disposed substantially parallel to each other;at least two brace structures, each disposed substantially perpendicularly to the orientation of the at least two parallel conductive structures, and each being in electrical communication with at least one of the at least two parallel conductive structures; andat least one spacer structure that is physically coupled at each end to a portion of each of the at least two brace structures, such that a substantially uniform separation is maintained between the at least two brace structures,wherein a measure of an electrical property of the tissue using the apparatus provides an indication of the condition of the tissue.2. The apparatus of claim 1 , wherein the condition of the tissue is a hydration state of the tissue claim 1 , a volume of sweat lost claim 1 , a mechanical property of the tissue claim 1 , a disease state of the tissue claim 1 , or a level of SPF protection of the tissue.3. The apparatus of claim 1 , wherein each of the at least two conductive structures has a zig-zag conformation claim 1 , a serpentine configuration claim ...

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19-09-2013 дата публикации

Statistical, Noninvasive Measurement of Intracranial Pressure

Номер: US20130245397A1
Принадлежит: University of Colorado

Tools and techniques for the rapid, continuous, invasive and/or noninvasive measurement, estimation, and/or prediction of a patient's intracranial pressure. In an aspect, some tools and techniques can predict the onset of conditions such as herniation and/or can recommend (and, in some cases, administer) a therapeutic treatment for the patient's condition. In another aspect, some techniques employ high speed software technology that enables active, long term learning from extremely large, continually changing datasets. In some cases, this technology utilizes feature extraction, state-of-the-art machine learning and/or statistical methods to autonomously build and apply relevant models in real-time.

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26-09-2013 дата публикации

Device and System for Sensing Medically Relevant Information from the Mouth

Номер: US20130253286A1
Автор: Gene Yevgeny Fridman
Принадлежит: JOHNS HOPKINS UNIVERSITY

An intraoral multisensor device includes a mouthpiece, a plurality of sensors at least one of attached to or integrated with the mouthpiece, and a data communications unit configured to receive signals from the plurality of sensors. The mouthpiece has a form to permit stable arrangement at least partially within a person's mouth such that it can remain for hands-free sensing of a plurality of biological parameters. Also, an intraoral multisensor system includes an intraoral multisensor device and a data processing device adapted to communicate with the intraoral multisensor device.

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31-10-2013 дата публикации

Method for diagnosing the function of intrinsic sphincters

Номер: US20130289363A1
Принадлежит: Pneumoflex Systems LLC

A method for treating at least one of the urethral and anal sphincters in a patient includes inducing an involuntary reflex cough event within the patient to determine whether a dysfunction exists in at least one of the urethral and anal sphincters. If a dysfunction is determined to exist, then contracting a muscle located at one of at least the urethral and anal sphincters during an inspiratory phase of respiration.

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31-10-2013 дата публикации

Device for Measuring and Analyzing Electromyography signals

Номер: US20130289434A1
Принадлежит: NATIONAL CHIAO TUNG UNIVERSITY

A device is for measuring and analyzing electromyography signals obtained from a target body part that is divided into an unhealthy-side muscle group and a healthy-side muscle group, and includes an unhealthy-side measuring electrode unit to be disposed on the unhealthy-side muscle group for measuring an electromyography signal therefrom so as to generate unhealthy-side measured data, a healthy-side measuring electrode unit to be disposed on the healthy-side muscle group for measuring an electromyography signal therefrom so as to generate healthy-side measured data, and a control unit determining a correlation between the unhealthy-side measured data and the healthy-side measured data. 1. A device for measuring and analyzing electromyography signals obtained from a target body part that is divided into an unhealthy-side muscle group and a healthy-side muscle group , said device comprising:an unhealthy-side measuring electrode unit adapted to be disposed on the unhealthy-side muscle group and for measuring an electromyography signal from the unhealthy-side muscle group so as to generate unhealthy-side measured data;a healthy-side measuring electrode unit adapted to be disposed on the healthy-side muscle group and for measuring an electromyography signal from the healthy-side muscle group so as to generate healthy-side measured data; anda control unit connected electrically to said unhealthy-side measuring electrode unit and said healthy-side measuring electrode, and determining a correlation between the unhealthy-side measured data and the healthy-side measured data.2. The device as claimed in claim 1 , the unhealthy-side muscle group including unhealthy-side orbicularis oris (OO) muscles claim 1 , the healthy-side muscle group including healthy-side orbicularis oris (OO) muscles claim 1 , wherein:said unhealthy-side measuring electrode unit includes a first unhealthy-side measuring electrode that is to be disposed on the unhealthy-side OO muscles and that is for ...

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07-11-2013 дата публикации

METHODS FOR ASSESSING SWALLOWING MOTOR FUNCTION

Номер: US20130296662A1
Принадлежит:

The present invention relates to methods for assessing swallowing motor function in a subject. The methods rely on obtaining intraluminal impedance and pressure measurements from the pharynx and/or esophagus of the subject during clearance of a bolus from the mouth and/or throat of the subject. The intraluminal impedance and pressure measurements are combined to derive a value for one or more pressure-flow variables in the pharynx and/or esophagus of the subject. The value of the one or more pressure-flow variables is compared to a predetermined pharyngeal and/or esophageal reference value for the one or more pressure-flow variables in order to provide an assessment of swallowing motor function in the subject. The intraluminal impedance and pressure measurements can also be combined to generate a swallow risk index for the subject or to generate an obstructive risk index for the subject based on a combination of a value of more than one pressure-flow variable in the pharynx and/or esophagus of the subject. In this way, swallowing motor function in the subject can be assessed by comparing the swallow risk index or obstructive risk index for the subject to a predetermined reference swallow index or predetermined reference obstructive index, respectively. Products which make use of these methods are also encompassed by the present invention. 1. A method for assessing swallowing motor function in a subject , the method including:(a) accessing intraluminal impedance measurements and pressure measurements obtained from the pharynx and/or esophagus of the subject during clearance of a bolus from the mouth and/or throat of the subject;(b) combining and analysing the intraluminal impedance and pressure measurements to derive a value for one or more pressure-flow variables in the pharynx and/or esophagus of the subject; and(c) assessing swallowing motor function in the subject by comparing the value of the one or more pressure-flow variables with a predetermined pharyngeal ...

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21-11-2013 дата публикации

Apparatuses and methods for diagnosing swallowing dysfunction

Номер: US20130310661A1
Принадлежит: Nestec SA

The present disclosure is directed to apparatuses and methods for diagnosing a swallowing dysfunction. The apparatuses may include a multi-parametric dysphagia analysis system in a plastic foil. The analysis systems may be smart sensing systems that are flexible, lightweight, and based on substrates having low-cost printed electronics technologies thereon. The methods may include measurement and classification of non-invasive parameters that may be indicative of a swallowing dysfunction or the probability of same. In a general embodiment, the methods include placing a sensor on a patient for measurement of at least one parameter associated with the patient's swallowing profile. The measured parameter is then analyzed and compared with several known normal and dysphagic swallowing profiles to provide an indication of the probability of an underlying swallowing dysfunction.

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05-12-2013 дата публикации

Device for diagnosing condition of liver and method of examining condition of liver

Номер: US20130324821A1
Принадлежит: Nagoya University NUC

The diagnostic device disclosed in this application is a device for diagnosing liver condition. The diagnostic device comprises a nitric oxide sensor and an information output unit. The nitric oxide sensor can be brought into contact with hepatocytes making up the liver and detects the concentration of nitric oxide produced by the hepatocytes. The information output unit, based on the nitric oxide concentration detected by the nitric oxide sensor, outputs information for diagnosing the condition of the liver. The information output unit can, for example, output a graph showing the change over time in the nitric oxide concentration detected by the nitric oxide sensor.

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26-12-2013 дата публикации

Endoscope apparatus and medical system

Номер: US20130345513A1
Принадлежит: OLYMPUS MEDICAL SYSTEMS CORP

An endoscope apparatus includes: a light source apparatus that emits light in a wavelength band including a first wavelength band for exciting a first fluorescent substance and a second wavelength band; an image pickup section that picks up an image of first fluorescence emitted when the first fluorescent substance is excited and an image of second fluorescence emitted when a second fluorescent substance provided on a treatment instrument is excited, to generate a fluorescence image; an information storing section that stores shape information including information on a shape of the second fluorescent substance; and an operation section that performs an operation to estimate an actual size of a region in which the first fluorescence is generated, based on a scaling factor calculated based on the shape information and a size of a draw region of the second fluorescence, and a size of a draw region of the first fluorescence.

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02-01-2014 дата публикации

Non-Invasive Method for Assessing the Presence or Severity of Liver Fibrosis Based on a New Detailed Classification

Номер: US20140005500A1

The present invention relates to a non-invasive method for assessing the presence and/or severity of a lesion in an organ of an animal, including a human, said method comprising carrying out at least one non-invasive test resulting in a value, preferably a score result, and positioning the at least one value or score result in a class of a detailed classification, such as, for example, a detailed classification based on population percentiles, or on a reliable diagnostic interval (RDI), to be crossed with another RDI. The present invention also relates to a device, preferably a meter, carrying out the non-invasive method of the invention.

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23-01-2014 дата публикации

BREATH TEST DEVICE AND METHOD

Номер: US20140024953A1
Принадлежит: EXALENZ BIOSCIENCE LTD.

There is provided a method of evaluating a liver condition of a subject, the method includes computing a fluctuation parameter from a liver breath test based on at least one of a percentage dose recovery (PDR) curve and a delta over baseline (DOB) curve of an isotope labeled methacetin, or a salt or a derivative thereof, and evaluating at least one liver condition of the subject, based at least on the fluctuation parameter. There is provided herein a method of evaluating a liver condition of a subject, the method includes computing a hepatic impairment score based at least on a breath test related parameter and on a demographic parameter. 196-. (canceled)97. A method for evaluating a liver condition of a subject , the method comprising:sensing an isotope level of a metabolic product of labeled methacetin or a salt or a derivative thereof in a breath of the subject; andreceiving data indicative of the isotope level of the metabolic product of labeled methacetin; andevaluating hepatic venous pressure gradient (HVPG) by a percentage dose recovery (PDR) curve and/or a delta over baseline (DOB) curve of an isotope labeled methacetin, or a salt or a derivative thereof and/or evaluating a number of shunts as detected by a physiological noise in a percentage dose recovery (PDR) curve and/or a delta over baseline (DOB) curve of an isotope labeled methacetin, or a salt or a derivative thereof, in comparison to a smooth curve.98. The method of claim 97 , wherein the isotope labeled methacetin claim 97 , or a salt or a derivative thereof comprises carbon-13 claim 97 , carbon-14 claim 97 , oxygen-18 or any combination thereof.99. The method of claim 97 , wherein the liver condition comprises a liver related disease claim 97 , malfunction claim 97 , injury claim 97 , transplantation claim 97 , abnormality claim 97 , fat accumulation claim 97 , increased metabolism claim 97 , decreased metabolism or a combination thereof.100. The method of claim 97 , further comprising to follow- ...

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30-01-2014 дата публикации

Non-invasive device for diagnosing gastroesphageal reflux

Номер: US20140031720A1
Принадлежит: Michigan State University MSU

The present invention provides compositions and methods useful in the diagnosis and management of Gastroesophageal Reflux. Specifically, the inventions provide a device and methods of using the device for accurately, quantitatively, and non-invasively diagnosing Gastroesophageal reflux disease (GERD) in both patients at risk for GERD and patients demonstrating reflux-like symptoms. In particular, the inventions relate to detecting and analyzing upward esophageal movements in patients, such as human infants, children, and adults.

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06-02-2014 дата публикации

BARIATRIC INSTRUCMENT OR ACCESSORY WITH SENSORS

Номер: US20140039278A1
Автор: Birk Janel A.
Принадлежит: ALLERGAN, INC.

A bariatric instrument or accessory with sensors used for sensing or monitoring parameters related to a patient during the placement, adjustment or in vivo duration of a bariatric or intraluminal device such as a balloon, stent, feeding tube or other. The instrument or accessory may sense parameters from direct patient contact, non-patient contact such as intraluminal data, or indirect patient contact. The instrument could be used during placement and adjustment of a device. The accessory could be attached to a bariatric or intraluminal device for the placement or adjustment of a bariatric device, or could be left on the bariatric device for in vivo placement. 1. A bariatric instrument for sensing one or more parameters in connection with a separate bariatric device , comprising:a sensor capable of producing signals in response to a parameter within the gastrointestinal tract,an arm coupled with the sensor,a central shaft with proximal and distal ends, the distal end coupled with the arm, the central shaft being long enough for the sensor and arm to reach the target area in the approximate location of the separate bariatric device and for the proximal end to be accessible through the mouth of the patient.2. The bariatric instrument for sensing one or more parameters in connection with a separate bariatric device of claim 1 , wherein the sensor does not contact the patient's tissue.3. The bariatric instrument for sensing one or more parameters in connection with a separate bariatric device of claim 1 , wherein the sensor is communicatively coupled with a transmitter capable of transmitting the sensor signals claim 1 , a receiver capable of receiving signals from an outside source claim 1 , and a memory module that is capable of storing the signal data from the sensor.4. The bariatric instrument for sensing one or more parameters in connection with a separate bariatric device of claim 3 , further comprising an external controller that communicates with the sensor.5. ...

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20-02-2014 дата публикации

SINGLE SCAN MULTI-PROCEDURE IMAGING

Номер: US20140050383A1
Принадлежит: KONINKLIJKE PHILIPS ELECTRONICS N.V.

A method includes receiving a signal indicative of a single user selected imaging protocol for scanning a patient. The imaging protocol includes parameters for two or more of a bone mineral density, a fat composition, or an aortic calcium imaging procedures. The method further includes performing a single scan of the patient using the single user selected protocol. The method further includes generating a single set of image data for the two or more of a bone mineral density, a fat composition, or an aortic calcium imaging procedures. 1. A method , comprising:receiving a signal indicative of a single user selected imaging protocol for scanning a patient,wherein the imaging protocol includes parameters for two or more of a bone mineral density, a fat composition, or an aortic calcium imaging procedures;performing a single scan of the patient using the single user selected protocol; andgenerating a single set of image data for the two or more of the bone mineral density, the fat composition, or the aortic calcium imaging procedures.2. The method of claim 1 , further comprising:receiving a signal indicative of one or more user selected analysis algorithms, wherein the one or more user selected analysis algorithms include at least two of a bone mineral density algorithm, a fat composition algorithm, or an aortic calcium algorithm; andprocessing the single set of image data using the one or more user selected analysis algorithms, producing a processing result.3. The method of claim 2 , wherein the processing result includes at least one of a bone mineral density image claim 2 , a fat composition algorithm image claim 2 , or an aortic calcium image.4. The method of claim 3 , further comprising:concurrently displaying the at least one of the bone mineral density image, the fat composition algorithm image, or the aortic calcium image in a same view port of a graphical user interface.5. The method of claim 3 , further comprising:concurrently displaying the at least one of ...

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20-02-2014 дата публикации

Apparatus for physiological and environmental monitoring with optical and footstep sensors

Номер: US20140051948A1
Принадлежит: Valencell, Inc.

Wearable apparatus for monitoring various physiological and environmental factors are provided. Real-time, noninvasive health and environmental monitors include a plurality of compact sensors integrated within small, low-profile devices, such as earpiece modules. Physiological and environmental data is collected and wirelessly transmitted into a wireless network, where the data is stored and/or processed.

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20-02-2014 дата публикации

TOUCH SCREEN MEDICAL DIAGNOSTIC DEVICE AND METHODS

Номер: US20140052017A1
Автор: Kapoor Trishul
Принадлежит:

A capacitive touch screen device forms a capacitance between a body part of a user and a sensor layer. The sensor layer of the device includes capacitive sensors that allow a current to flow to the body part from the device when contact is made. The body part contacts the device through a bodily fluid. The current drawn is measured and a value for the bodily fluid is determined. This value is compared against known values to diagnose a possible medical condition or to infer characteristics of the bodily fluid. 120-. (canceled)21. A method for determining a possible medical condition using a touch screen device by measuring electro-physiological properties of the skin , the method comprising:contacting a body part with sweat glands to the device;drawing a current from the device to the body part through the sweat glands;performing an analysis on a dermal conductivity based on the sweat glands through a measurement corresponding to the current drawn from the device; andindicating whether a probability for a medical condition exists based on the analysis.22. The method of claim 21 , further comprising measuring the current drawn from the device.23. The method of claim 21 , further comprising comparing the measurement to a range of values to indicate the probability of the medical condition.24. The method of claim 21 , wherein the medical condition includes cystic fibrosis.25. The method of claim 21 , further comprising adding an attachment to the layer of the device claim 21 , wherein the attachment contact the sweat glands.26. The method of claim 21 , further comprising creating a capacitance between the body and a sensor layer of the device to generate the current.271. The method of claim claim 21 , wherein the measurement corresponds to a resistance or conductivity value of the sweat glands.28. A method for determining a potential medical condition using a touch screen device claim 21 , the method comprising:drawing a current from the device to a body part of a user ...

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27-02-2014 дата публикации

METHOD DEVICE AND SYSTEM FOR MONITORING LUNG VENTILATION

Номер: US20140058274A1
Принадлежит:

A method of monitoring lung ventilation of a subject is disclosed. The method comprises recording signals from a plurality of sensing location on the chest of the subject, at least a portion of the signals being indicative of a local motion of the chest at a respective sensing location. The method further comprises operating a data processing system to analyze the signals such as to determine a status of the ventilation, thereby to monitor the lung ventilation of the subject. 1. A method comprising:receiving signals from a plurality of sensing locations on a chest of a subject, at least a portion of said signals being indicative of a local motion of said chest at a respective sensing location, and continuously monitoring ventilation and functional volume changes of the chest using data of the local motion of the chest.2. A method comprising:receiving signals from a plurality of sensing locations on a chest of a subject, at least a portion of said signals being indicative of a local motion of said chest at a respective sensing location, and continuously monitoring ventilation and heart function using data of the local motion of the chest.3. A method comprising:receiving signals from a plurality of sensing locations on a chest of a subject, at least a portion of said signals being indicative of a local motion of said chest at a respective sensing location,receiving signals from an epigastric location of the subject,and detecting an air leak to an esophagus of the subject. This application is a continuation of U.S. patent application Ser. No. 12/162791, filed Jul. 31, 2008, now U.S. Pat. No. 8,226,571.In the medical treatment of patients requiring breathing assistance, it is common to insert an endotracheal or nasotracheal tube into the trachea of the patient, by way of the mouth, nose or any other surgically created opening. One end of the tube is connected to a ventilator which periodically forces air into the lungs through the tube. In big children and adult ...

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27-02-2014 дата публикации

SYSTEM AND METHOD FOR GASTRO-INTESTINAL ELECTRICAL ACTIVITY

Номер: US20140058282A1
Принадлежит:

A gastro-electrical activity mapping system and method may comprise a catheter insertable through a natural orifice into the gastro-intestinal (GI) tract and comprising an array of electrodes for contacting an interior surface of a section of the GI tract to detect electrical potentials at multiple electrodes, and comprises a signal analysis and mapping system arranged to receive and process electrical signals from multiple electrodes of the array and spatially map GI smooth muscle electrical activity as an activation time map, a velocity map, or an amplitude map, which may be in the form of contour plots and may be mapped on an anatomical computer model of at least the section of the GI tract and may be animated. 1. A gastrointestinal-electrical activity mapping and/or signal analysis system arranged to receive and process electrical signals from one or more electrodes and spatially map GI smooth muscle electrical activity at said section of the GI tract and/or identify as indicative of disease including (but not limited to) gastroparesis and/or functional dyspepsia or as useful in the diagnosis of disease mechanisms in gastro-oesophageal reflux disease , or nausea and vomiting disorders , and other gastro-intestinal motility disorders any one of or any of in combination:propagation of re-entrant or non re-entrant GI electrical activity upwardly within the GI tract, optionally at frequency above about 3.7 cycles per minute (cpm) or 4 cpm, as a result of a re-entrant propagation around the GI tract,propagation of re-entrant or non re-entrant GI electrical activity circumferentially within the GI tract other than at the normal pacemaker site in the stomach,propagation of re-entrant GI electrical activity substantially only circumferentially within the GI tract,propagation of non re-entrant GI electrical activity circumferentially within the GI tract at a velocity and/or amplitude higher than the normal (non re-entrant) GI electrical activity in the GI tract and/or at ...

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27-02-2014 дата публикации

Nerve monitoring system

Номер: US20140058284A1
Принадлежит: Innovative Surgical Solutions LLC

A neural monitoring system includes a stimulator configured to provide an electrical stimulus within an intracorporeal treatment area of a subject, an elongate sphincter contraction sensor, and a receiver in communication with the sphincter contraction sensor. The elongate sphincter contraction sensor includes an elongate device body configured to be inserted within a sphincter of the subject and a force sensor in mechanical communication with the elongate device body. The force sensor is configured to provide a mechanomyography output signal in response to a contact force applied against the elongate device body by the sphincter. The receiver is configured to receive the mechanomyography output signal from the elongate sphincter contraction sensor and provide an indicator to a user based on at least a portion of the output of the sphincter contraction sensor.

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27-02-2014 дата публикации

SYSTEM FOR MARKING A LOCATION FOR TREATMENT WITHIN THE GASTROINTESTINAL TRACT

Номер: US20140058317A1
Принадлежит: ENTRACK, INC.

A device and method for mapping, diagnosing and treating the intestinal tract is provided using a capsule passing through the intestinal tract. Further, a capsule tracking system is provided for tracking a capsule's location along the length of an intestinal tract as various treatment and/or sensing modalities are employed. In one variation, an acoustic signal is used to determine the location of the capsule. A map of sensed information may be derived from the pass of a capsule. Capsules may be subsequently passed through to treat the intestinal tract at a determined location along its length. One variation uses an electrical stimulation capsule to treat and/or diagnose a condition in the intestinal tract. 1. A system for the delivery of a drug to a gastrointestinal tract , the system comprising:a capsule sized to pass through an intestinal tract of a patient;a transmitter coupled to the capsule, the transmitter configured to transmit a tracking signal between the capsule and a location external to a patient's body to track a linear position of the capsule within the patient's intestinal tract as the capsule is passing through the intestinal tract;a reference signal generator coupled to the capsule, the reference signal generator configured to generate and transmit a reference signal for identifying a time of tracking signal origination;a drug delivery device configured to deliver drug to the intestinal tract; anda controller configured to actuate the drug delivery device as the capsule is passing through the intestinal tract at a desired position in the intestinal tract based on the capsule position within the intestinal tract.2. The system of wherein the drug delivery device comprises a pump.3. The system of claim 1 , wherein the drug delivery device comprises a valve or a solenoid.4. The system of claim 1 , wherein the controller is actuable responsive to an external signal.5. The system of claim 4 , wherein the drug delivery device includes an RF receiver for ...

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06-03-2014 дата публикации

METHOD AND APPARATUS FOR DETECTING INEFFECTIVE INSPIRATORY EFFORTS AND IMPROVING PATIENT-VENTILATOR INTERACTION

Номер: US20140066725A1
Принадлежит: RESMED LIMITED

A method and system for detecting an ineffective effort of a patient being mechanically ventilated by a ventilator comprises (i) monitoring a respiratory flow of air of the patient after said ventilator has cycled; (ii) creating a signal indicative of said flow; (iii) removing artefact from said signal; (iv) monitoring said signal for perturbations; and (v) determining that an ineffective effort has occurred when said perturbation is significant. 194-. (canceled)95. A method of detecting an ineffective effort of a patient being mechanically ventilated by a ventilator , the method comprising:monitoring a respiratory flow of air of the patient during expiration by the patient after said ventilator has cycled and before the ventilator has triggered;generating a signal indicative of said flow of the patient during expiration;outputting the generated signal to a processing system;determining a peak expiratory flow (PEF) of the patient based on the generated signal;calculating, via a processing system that includes at least one processor, a second derivative of the signal that is indicative of the respiratory flow;determining an occurrence of a significant declivity within the signal when the second derivative of the signal is greater than a negative threshold; anddetecting perturbations within the generated signal by classifying the perturbations between at least ineffective efforts and non-ineffective efforts based on determination of the occurrence of the significant declivity within the signal.96. The method of claim 95 , further comprising removing a signal representative of cardiogenic oscillation from the generated signal.97. The method of claim 95 , further comprising determining whether a cough has occurred.98. The method of claim 95 , further comprising modifying the generated signal by removing signals that are indicative of secretions.99. The method of claim 95 , further comprising applying a noise filter to the generated signal.100. The method of claim 95 , ...

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03-04-2014 дата публикации

Apparatus, systems and methods for monitoring and evaluating cardiopulmonary functioning

Номер: US20140094663A1
Принадлежит: Valencell, Inc.

Wearable apparatus for monitoring various physiological and environmental factors are provided. Real-time, noninvasive health and environmental monitors include a plurality of compact sensors integrated within small, low-profile devices, such as earpiece modules. Physiological and environmental data is collected and wirelessly transmitted into a wireless network, where the data is stored and/or processed.

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06-01-2022 дата публикации

Sensor system and method for continuous and wireless monitoring and analysis of heart sounds, circulatory effects and core temperature in organisms

Номер: US20220000376A1
Автор: Kjetil Meisal
Принадлежит: ONIO AS

A system and method for continuous readout is provided. The object of the invention is achieved by a contact surface for attaching to a surface of an organism, a sensor system in thermal, mechanical and electrical contact with the contact surface, a radio chip operatively connected to the sensor, wherein the radio chip will respond to an induced signal from a reader by reading data from the sensor and transmit said data, and method for operating the sensor wherein the data from the sensor system is compensated for environmental effects using comprising a second sensor for detecting at least one property from the group comprising ambient temperature, pressure, flow, level, proximity, displacement, bio, image, gas, chemical, acceleration, orientation, humidity, moisture, impedance, capacitance, force, electric, magnetic and mass, thus forming compensated data.

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02-01-2020 дата публикации

INTRABODY PROBE NAVIGATION BY ELECTRICAL SELF-SENSING

Номер: US20200000368A1
Принадлежит: Navix International Limited

Methods and systems for position determination are described for using an intrabody probe having a plurality of electrodes to generate a plurality of different electrical fields, and to also measure, using the plurality of electrodes, a measurement set (a Vmeasurement set) comprising a plurality of measurements of the plurality of different electrical fields while the probe remains in one position. From the Vmeasurement set, spatial position coordinates for the intrabody probe are estimated within an intrabody coordinate system, using an established mapping between previously observed Vmeasurement sets and positions in the intrabody coordinate system. Systems and methods for generating and selecting such mappings are also described. 1. A method of estimating an intrabody position of a probe having a plurality of electrodes , the method comprising:generating, from the intrabody position, a plurality of electrical fields using the plurality of electrodes;measuring, at the intrabody position and also using the plurality of electrodes, a position-identifying data set comprising a plurality of measurements of the plurality of electrical fields; andestimating a plurality of position coordinates defining the intrabody position within a spatial coordinate system, based on the position-identifying data set.2. The method of claim 1 , wherein measurements of the position-identifying data set measured by the plurality of electrodes differ at different positions of the probe claim 1 , due to interactions of electrical fields generated by the plurality of electrodes with the different electrical environment of different intrabody positions.3. The method of claim 1 , wherein the estimating comprises determining the position coordinates based on a mapping between position coordinates and position-identifying data sets.4. The method of claim 1 , wherein the measuring detects differences among position-identifying data sets measured by the plurality of electrodes at different ...

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03-01-2019 дата публикации

Systems Approach to Disease State and Health Assessment

Номер: US20190000378A1
Автор: Osorio Ivan
Принадлежит: FLINT HILLS SCIENTIFIC, L.L.C.

Methods, systems, and apparatus for assessing a state of an epilepsy disease or a comorbidity thereof are provided. The methods comprise receiving at least one autonomic index, neurologic index, stress marker index, psychiatric index, endocrine index, adverse effect of therapy index, physical fitness index, or quality of life index of a patient; comparing the at least one index to at least one reference value; and assessing a state of an epilepsy disease or a body system of the patient based on the comparison. A computer readable program storage device encoded with instructions that, when executed by a computer, perform the method described above is also provided. A medical device system capable of implementing the method described above is also provided. 1. A non-transitory computer readable program storage unit encoded with instructions that , when executed by a computer , perform a method for assessing a comorbidity associated with epilepsy , comprising:receiving at least one of a quality of life assessment and a physical fitness assessment;receiving at least one of an autonomic index and/or a neurologic index, or both;comparing at least one of the autonomic index and the neurologic index to at least one reference value associated with at least one of the autonomic index and the neurologic index;assessing a state of a body system of the patient based on the comparison and at least one of the quality of life assessment and the physical fitness assessment, wherein the body system comprises at least one of an autonomic system, a neurologic system, a psychiatric system, an endocrine system or subsystems of the foregoing; andproviding an output relating to the assessment, wherein the output comprises at least one of a body system stability, a body system improvement, a body system decline or a finding that a state of the body system cannot be determined, wherein the body system is a site of the comorbidity.2. The non-transitory computer readable program storage unit ...

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07-01-2016 дата публикации

Pressure Measuring System

Номер: US20160000366A1
Принадлежит:

A pressure measuring system, including a tube system having at least one first device for measuring pressure in a fluid. The at least one first device includes a coupling element, at least one pressure transducer and at least one measuring chamber, which can be filled with a fluid. Between the first device and the feed of the fluid, the tube system has a second device for regulating a fluid flow, the second device having a tube section through which fluid can flow and at least one tube clamp, which can be set in the regulation positions open, closed and perfused. 1. Pressure-measuring system , with at least one measuring lumen which can be filled with a fluid , comprising:at least one tube system for connecting a fluid reservoir to the at least one measuring lumen, and a mechanism for conveying the fluid through the at least one tube system, wherein the tube system includes at least one first device for measuring pressure in the fluid and having a coupling element, at least one pressure transducer and at least one measuring chamber which can be filled with fluid, wherein the coupling element mechanically connects the measuring chamber via a membrane with the measuring area of the pressure transducer and the measuring chamber has at least two connection points for a fluid flow,between the first device and the supply of the fluid, the tube system has a second device for regulating fluid flow with a tube section through which fluid can flow and has a least one tube clamp, andthe second device can be set to the regulation positions open, closed and perfused, wherein in the closed position the lumen of the tube section is completely closed and in the perfused position, through a spacer in the inside of the tube section the lumen is at least slightly open.2. Pressure-measuring system according to claim 1 , wherein the coupling element has a clamping edge which preferably has at least one rotatably borne pressing roller that can be connected to the coupling device and that ...

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07-01-2016 дата публикации

ENDOSCOPY CAPSULE AND METHOD OF PRODUCING AN ENDOSCOPY CAPSULE

Номер: US20160000375A1
Принадлежит:

An endoscopy capsule is provided for detecting a metabolic product of a bacterium located in a gastrointestinal tract, wherein the endoscopy capsule has a sensor unit with two electrodes and has a capsule shell that encloses a usable space, and wherein the electrodes are routed through the capsule shell. 1. An endoscopy capsule for detecting a metabolic product of a bacterium located in a gastrointestinal tract , the endoscopy capsule comprising:a sensor unit with two electrodes; anda capsule shell that encloses a usable space,wherein the electrodes are routed through the capsule shell.2. The endoscopy capsule as claimed in claim 1 , wherein the electrodes are needle-shaped.3. The endoscopy capsule as claimed in claim 1 , the wherein free ends of the electrodes protruding out from the capsule shell are rounded.4. The endoscopy capsule as claimed in claim 1 , wherein the capsule shell is in multiple parts cohesively bonded to one another.5. The endoscopy capsule as claimed in claim 1 , wherein the sensor unit comprises a semiconductor plate claim 1 , which lies in the usable space claim 1 , at least in parts at a distance from the capsule shell.6. The endoscopy capsule as claimed in claim 1 , wherein the sensor unit comprises an ammonia-sensitive sensor.7. The endoscopy capsule as claimed in claim 1 , wherein a position of a center of mass relative to a center of volume is predefined in such a way that claim 1 , starting from the position of the center of volume claim 1 , the center of mass is offset in a direction of the electrodes.8. The endoscopy capsule as claimed in claim 1 , wherein the endoscopy capsule is configured exclusively to detect ammonia in a gastrointestinal tract and has no functional units beyond this.9. The endoscopy capsule as claimed in claim 1 , wherein the capsule shell is made from a thermoplastic material.10. The endoscopy capsule as claimed in claim 1 , wherein the capsule shell is an injected molded part.11. A method for producing an ...

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04-01-2018 дата публикации

Systems and Methods for Enabling A Patient To Achieve A Weight Loss Objective Using An Electrical Dermal Patch

Номер: US20180000347A1
Принадлежит:

The disclosed wearable device modulates a patient's gastric emptying time and/or gastric retention time. The wearable device includes a microprocessor, electrical stimulator and at least one electrode configured to deliver electrical stimulation to the epidermis, through a range of 0.1 mm to 10 mm or a range of 0.1 mm to 20 mm of the dermis, of a T2 dermatome to a T12 dermatome or meridian of the patient, a C5 to a T1 dermatome across the hand and/or arm, and/or the upper chest regions. The device is adapted to provide electrical stimulation as per stimulation protocols and to communicate wirelessly with a companion control device configured to monitor and record appetite patterns of the patient. The control device is also configured to monitor, record, and modify stimulation parameters of the stimulation protocols. 1. A method of enabling a patient to achieve a weight loss objective , comprising:providing the patient with an electrical dermal patch comprising a housing, an electrical pulse generator positioned within the housing, and at least one electrode attached to said housing and in electrical communication with the electrical pulse generator, wherein said electrical pulse generator is configured to deliver electrical pulses having a pulse amplitude in a range of 5 mA to 45 mA;instructing the patient to secure the electrical dermal patch to the patient's skin;applying a plurality of stimulation sessions to the patient's skin using said electrical dermal patch over a duration of one week, wherein each of the plurality of stimulation sessions comprises said electrical pulses, wherein at least some of the plurality of stimulation sessions have a duration of at least 15 minutes, and wherein the plurality of stimulation sessions comprises at least one in said week; andinstructing the patient to repeatedly apply said plurality of stimulation sessions until said weight loss objective is achieved.2. The method of claim 1 , wherein each of said electrical pulses is ...

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04-01-2018 дата публикации

UPPER GASTROINTESTINAL BLEEDING MONITORING SYSTEM

Номер: US20180000358A1
Принадлежит:

An upper gastrointestinal bleeding monitoring system includes a detection device and a signal processing device to determine bleeding condition of an upper gastrointestinal tract by using relation of time and intensity ratios of RGB three primary colors. The detecting device is placed to the upper gastrointestinal tract of a patient via his/her mouth or nasal passage and then stay the upper gastrointestinal tract for several days for detection of bleeding. The signal processing device may receive and display signal from the detection device to help medical professionals check if bleeding occurs in an upper gastrointestinal tract. Moreover, a procedure of determination of bleeding in an upper gastrointestinal tract with the upper gastrointestinal bleeding monitoring system is described. 1. An upper gastrointestinal bleeding monitoring system , comprising:a detection device including a cable, a bleeding detecting device and a signal transmission module, wherein the bleeding detecting device is coupled to the signal transmission module with the cable and provided to output a time signal of RGB three primary colors; and a signal processing device including a signal display and receiving the time signal of RGB three primary colors from the bleeding detecting device, wherein the signal processing device analyzes an intensity ratio of the time signal of RGB three primary colors, determines bleeding condition according to the intensity ratio of the time signal of RGB three primary colors, provides bleeding alarm, and evaluates bleeding time.2. The upper gastrointestinal bleeding monitoring system according to claim 1 , wherein the position of the bleeding detecting device in an upper gastrointestinal tract can be adjusted by the cable.3. The upper gastrointestinal bleeding monitoring system according to claim 1 , wherein the bleeding detecting device is put into an upper gastrointestinal tract of a patient via his/her nasal passage or mouse.4. The upper gastrointestinal ...

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07-01-2021 дата публикации

Swallowing sensor device and methods of manufacturing the same

Номер: US20210000408A1
Автор: Hiroshi Miyaguchi
Принадлежит: Tohoku University NUC

A swallowing sensor device includes a sensor unit comprising a sensor and a device that wirelessly transmits information detected by the sensor and a board group formed by stacking a plurality of rigid boards. The board group includes a fist rigid board on which one part of the sensor unit is mounted, a second rigid board on which other part of the sensor unit except for the one part of the sensor unit is mounted, and a third rigid board being disposed between the first rigid board and the second rigid board and comprising a through-hole drilled thereon, the through-hole being configured to electrically connecting the one part and the other part.

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05-01-2017 дата публикации

Estimation device, program, estimation method, and estimation system

Номер: US20170000397A1
Автор: Shunji Mitsuyoshi

Includes an extraction unit that extracts first information on a physiological state of a subject and second information on at least one of an emotion and organ activity of the subject from information on a physiology of the subject; a calculation unit that obtains a degree of similarity between changes over time indicated by the first information and the second information which are extracted and calculates a shift amount from a predetermined state in which a homeostasis in the subject is maintained based on the obtained degree of similarity; and an estimation unit that estimates a pathology of the subject based on the calculated shift amount.

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07-01-2021 дата публикации

MOISTURE-RESPONSIVE FILMS

Номер: US20210000455A1
Принадлежит:

A moisture-responsive film can include a complexing substrate and an iodine layer applied to the complexing substrate to form the moisture-responsive film. The moisture-responsive film can include a test area formed on a testing surface of the moisture-responsive film. 1. A system for detecting a moisture-related skin condition , the system comprising:a moisture-responsive film having a complexing substrate and an iodine layer disposed thereon, the iodine layer comprising a designated test area and a designated calibration area for detecting moisture on a skin surface of a user; andinstructions for directing the user to apply the moisture-responsive film to the skin surface for a predetermined period of time.2. The system of claim 1 , wherein the designated calibration area comprises one or more calibration marks.3. The system of claim 1 , further comprising a skin drying material.4. The system of claim 3 , wherein skin drying material comprises a water-absorbent fabric claim 3 , a paper-based towel claim 3 , a disposable towelette including a drying solvent claim 3 , or a combination thereof.5. The system of claim 3 , wherein instructions further direct the user to apply the skin drying material for a predetermined period of time prior to applying the moisture-responsive film to the skin surface.6. The system of claim 1 , wherein the predetermined period of time is in a range from 1 second to 300 seconds.7. The system of claim 1 , further comprising one or more water standards for application to the designated calibration area to prepare one or more calibration marks.8. The system of claim 1 , wherein designated test area comprises a plurality of test areas.9. The system of claim 1 , wherein the iodine layer is disposed on a first side of the complexing substrate claim 1 , and the moisture-responsive film further comprises a backing layer positioned on a second side of the complexing substrate opposite the first side.10. The system of claim 1 , wherein the ...

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02-01-2020 дата публикации

PHYSIOLOGICAL MONITORING DEVICES AND METHODS USING OPTICAL SENSORS

Номер: US20200000412A1
Принадлежит:

A monitoring device configured to be attached to a subject includes a photoplethysmography (PPG) sensor configured to measure physiological information from the subject, a blood flow stimulator, and a processor configured to process signals from the PPG sensor to determine a signal-to-noise level of the signals. In response to a signal-to-noise level determination, the processor is configured to instruct the blood flow stimulator to increase blood perfusion at a location where the PPG sensor is attached to the subject. The signal-to-noise level determination may be a determination that the signal-to-noise level is below a threshold level. The blood flow stimulator may be a heating element or light source configured to heat the location of the subject. 1. A monitoring device configured to be attached to a subject , the monitoring device comprising:a photoplethysmography (PPG) sensor configured to measure physiological information from the subject;a blood flow stimulator; andat least one processor configured to process signals from the PPG sensor to determine a signal-to-noise level of the signals, and wherein, in response to a signal-to-noise level determination, the at least one processor is configured to instruct the blood flow stimulator to increase blood perfusion at a location where the PPG sensor is attached to the subject.2. The monitoring device of claim 1 , wherein the signal-to-noise level determination is a determination that the signal-to-noise level is below a threshold level.3. The monitoring device of claim 1 , wherein the blood flow stimulator comprises a heating element configured to heat the location of the subject.4. The monitoring device of claim 1 , wherein the blood flow stimulator comprises a light source configured to heat the location of the subject.5. The monitoring device of claim 4 , wherein the light source comprises at least one LED.6. The monitoring device of claim 1 , wherein claim 1 , subsequent to instructing the blood flow ...

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04-01-2018 дата публикации

METHODS FOR ASSESSING SWALLOWING MOTOR FUNCTION

Номер: US20180000402A1

The present invention relates to methods for assessing swallowing motor function in a subject. The methods rely on obtaining intraluminal impedance and pressure measurements from the pharynx and/or esophagus of the subject during clearance of a bolus from the mouth and/or throat of the subject. The intraluminal impedance and pressure measurements are combined to derive a value for one or more pressure-flow variables in the pharynx and/or the esophagus of the subject. The value of the one or more pressure-flow variables is compared to a predetermined pharyngeal and/or esophageal reference value for the one or more pressure-flow variables in order to provide an assessment of swallowing motor function in the subject. The intraluminal impedance and pressure measurements can also be combined to generate a swallow risk index for the subject or to generate an obstructive risk index for the subject based on a combination of a value of more than one pressure-flow variable in the pharynx and/or esophagus of the subject. In this way, swallowing motor function in the subject can be assessed by comparing the swallow risk index or obstructive risk index for the subject to a predetermined reference swallow index or predetermined reference obstructive index, respectively. Products which make use of these methods are also encompassed by the present invention. 1. A method for assessing swallowing motor function in a subject , the method including:(a) accessing intraluminal impedance measurements and pressure measurements obtained from the pharynx, the esophagus or a combination of the pharynx and esophagus of the subject during clearance of a bolus from the mouth, the throat or a combination of the mouth and the throat of the subject; (i) using the intraluminal impedance measurements to generate an impedance waveform during clearance of the bolus, and using the pressure measurements to generate a pressure waveform during clearance of the bolus; and', '(ii) using the intraluminal ...

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04-01-2018 дата публикации

METHOD AND DEVICE FOR SWALLOWING IMPAIRMENT DETECTION

Номер: US20180000403A1
Принадлежит:

In a method and apparatus for swallowing impairment detection, a candidate executes one or more swallowing events, and dual axis accelerometry data is acquired representative thereof. Upon feature extraction and classification, vibrational data acquired in respect of each swallowing event is classified as indicative of one of normal or possibly impaired swallowing. 1. A device for identifying a possible swallowing impairment in a candidate during execution of a swallowing event , the device comprising:an accelerometer configured to acquire axis-specific vibrational data for an anterior-posterior (A-P) axis and a superior-inferior (S-I) axis of the candidate's throat, the axis-specific vibrational data is representative of the swallowing event; anda processing module that is a local or remote computing device operatively coupled to the accelerometer, the processing module configured for processing the axis-specific data to (i) extract therefrom distinct axis-specific features representative of the swallowing event, the distinct axis-specific features comprising at least one feature for the A-P axis different than the distinct axis-specific features for the S-I axis, the distinct axis-specific features further comprising at least one feature for the S-I axis different than the distinct axis-specific features extracted for the A-P axis, (ii) perform a comparison of the distinct axis-specific features against preset classification criteria defined for each of swallowing safety and swallowing efficiency, and (iii) classify the vibrational data as one of a first classification or a second classification based on the comparison of the distinct axis-specific features against the preset classification criteria defined for each of the swallowing safety and the swallowing efficiency.2. The device of claim 1 , wherein the second classification is indicative of at least one of a swallowing safety impairment or a swallowing efficiency impairment.3. The device of claim 1 , wherein ...

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04-01-2018 дата публикации

METHOD AND SYSTEM FOR DETECTING PACREACTIC TRAUMA

Номер: US20180000404A1
Автор: Jones Mark W.
Принадлежит:

A method and system are provided for detecting pancreatic trauma in a trauma patient during a surgical operation. The method includes positioning a detection device in contact with the patient's pancreas, applying a chemical indicator to the detection device after removing the detection device from the patient, and detecting a chemical reaction on the detection device that is indicative of the pancreas releasing an enzyme as a result of pancreatic trauma. 1. A method of detecting pancreatic trauma , said method comprising:positioning a detection device into contact with a pancreas during a surgical operation, wherein an outer surface of the detection device is coated or impregnated with a first chemical reactant that is reactive with a pancreatic enzyme;applying a chemical indicator containing a second chemical reactant to the outer surface of the detection device, wherein a product of the second chemical reactant with the first chemical reactant has a color that is visibly distinguishable from each of (i) a color of the first chemical reactant, (ii) a color of the pancreatic enzyme, and (iii) a color of a product of the first chemical reactant with the pancreatic enzyme; anddetecting trauma to the pancreas via the absence, at the outer surface of the detection device, of the color of the product of the first and second chemical reactants.2. The method of claim 1 , wherein the detection device comprises a surgical pad or sponge.3. The method of claim 1 , wherein the first chemical reactant comprises starch and the second chemical reactant comprises iodine.4. The method of claim 3 , wherein the chemical indicator comprises povidone-iodine.5. The method of claim 1 , wherein said applying the chemical indicator comprises spraying the chemical indicator in liquid form onto the outer surface of the detection device.6. The method of claim 1 , further comprising providing a kit containing two or more of the detection devices and two or more of the chemical indicators.7. A ...

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03-01-2019 дата публикации

A SKIN PATCH

Номер: US20190000427A1
Автор: Findlay Ewan, MURRAY Sara
Принадлежит:

The application relates to a chemical monitoring system comprising a skin patch for detecting an analyte in perspiration and a processor adapted to receive parameter data and to return an output indicative of a presence of an analyte in a subject's body based on the parameter data. The skin patch () includes a first layer () permeable to perspiration; a second layer () coupled to the first layer, the second layer being adapted to receive the perspiration; wherein a property of the second layer changes upon receiving the analyte; an electrical detector coupled to the second layer, adapted to detect parameter data indicative of the property o f the second layer; and a flexible electronic circuit () coupled to the second layer, comprising a readout circuit for reading parameter data from the electronic detector and a transmitter adapted to transmit the parameter data to a processor. 130-. (canceled)31. A chemical monitoring system comprising:a skin patch for detecting ethanol in perspiration, comprising a first layer permeable to perspiration; a second layer coupled to the first layer, the second layer being adapted to receive the perspiration; wherein a property of the second layer changes upon receiving ethanol; wherein the second layer is made at least in part of a film or matrix comprising Alcohol Oxidase; and an electrical detector coupled to the second layer, adapted to detect parameter data indicative of the property of the second layer; andthe system further comprising a processor adapted to receive the parameter data and to return an output indicative of a presence of ethanol in a subject's body based on the parameter data.32. The chemical monitoring system as claimed in claim 31 , comprising a housing comprising communication means; optionally wherein the housing is removably coupled to the skin patch.33. The chemical monitoring system as claimed in claim 32 , wherein the processor is located within the housing or wherein the processor is located in a device ...

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04-01-2018 дата публикации

MIGRAINE HEADACHE TRIGGER DETECTION PROCESSING

Номер: US20180000425A1
Автор: Hernacki Brian J.
Принадлежит:

Techniques and device configurations used in the detection of migraine triggers or similar human pain conditions are disclosed. In an example, a migraine trigger detection device collects data on ambient stimuli for a human subject, through various light, sound, or odor sensors. A computing device connected to the migraine trigger detection device receives and processes the data to correlate the detected stimuli with migraine symptoms of the human subject. Such correlation may be based on real-time data, data from a prior phase of the migraine, or data from other migraine episodes (e.g., to identify common triggers of migraines over time). Additionally, such correlation may be performed with use of a remote data processing system that receives the sensor data (or aggregated forms of data). In further examples, trigger reports, pain condition, time inputs, or migraine phase may be obtained through a graphical user interface of the computing device. 1. A computing device , comprising processing circuitry to:receive sensor data from a sensor device worn by a human subject, wherein the sensor data indicates respective conditions of a plurality of ambient stimuli occurring in proximity to the human subject;receive input from the human subject, wherein the input indicates a pain condition of the human subject;process the sensor data and the received input with a user-trained model to identify a trigger of the pain condition, wherein the trigger of the pain condition corresponds to a particular stimulus of the plurality of ambient stimuli; andgenerate output to the human subject, wherein the output indicates the trigger of the pain condition.2. The computing device of claim 1 ,wherein the pain condition of the human subject is a migraine headache,wherein the trigger of the pain condition relates to an environmental characteristic of the particular stimulus, andwherein the generated output includes an identification of the environmental characteristic of the particular ...

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04-01-2018 дата публикации

Methods and Systems for Pre-Symptomatic Detection of Exposure to an Agent

Номер: US20180000428A1
Принадлежит:

Systems and methods for predicting exposure to an agent. One or more features are extracted from physiological data. For each respective classifier, (i) the respective classifier is identified, wherein the respective classifier is trained using training data for a respective physiological state, (ii) the respective classifier is applied to the one or more features to obtain a classifier output that represents a likelihood of exposure, (iii) a respective first threshold is applied to the classifier output to determine a patient state classification, and (iv) the patient state classifications are aggregated across a number of time intervals to obtain an aggregate patient state classification for each classifier. The aggregate patient state classifications are combined across the plurality of classifiers to obtain a combined classification, and an indication that the patient has been exposed to the agent is provided when the combined classification exceeds a second threshold. 1. A method for predicting whether a patient has been exposed to an agent , the method comprising , for each respective time interval in a plurality of time intervals:(a) receiving, by at least one processor, physiological data regarding the patient that was recorded during the respective time interval;(b) extracting one or more features from the physiological data, wherein each feature is representative of the physiological data during the respective time interval; (i) identifying the respective classifier, wherein the respective classifier is trained using training data for a respective physiological state;', '(ii) applying the respective classifier to the one or more features to obtain a classifier output that represents a likelihood that the patient has been exposed to the agent;', '(iii) applying a respective first threshold to the classifier output to determine a patient state classification;', '(iv) aggregating the patient state classifications across a number of time intervals to obtain an ...

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05-01-2017 дата публикации

RAPID, REPRODUCIBLE, NON-INVASIVE PREDICTOR OF CADAVERIC DONOR LIVER GRAFT UTILIZATION

Номер: US20170000405A1
Автор: Zarrinpar Ali

A method for rapid, non-invasive assessment of liver function in a brain-dead donor, prior to procurement is presented. Quantitative assessment of liver function can be measured in brain-dead donors in the local donor service area prior to organ procurement by measuring indocyanine green plasma disappearance rates (ICG-PDR). This method can be performed with devices that use a non-invasive finger probe to obtain the ICG-PDR using pulse-densitometry. 1. A method for determining whether liver tissue will be acceptable for transplantation , the method comprising:(a) measuring indocyanine green plasma disappearance rates (ICG-PDR) in a brain-dead donor prior to organ procurement; and(b) designating liver tissue in the donor as acceptable for transplantation if the ICG-PDR is greater than about 18%.2. The method of claim 1 , further comprising designating the liver tissue as acceptable for transplantation if the ICG-PCR is greater than about 24%.3. The method of claim 1 , wherein ICG-PDR is measured non-invasively.4. The method of claim 3 , wherein ICG-PDR is measured using a PULSON LiMON liver function monitor.5. A method of determining whether liver tissue will be acceptable for transplantation claim 3 , the method comprising:(a) measuring indocyanine green plasma disappearance rates (ICG-PDR) in a brain-dead donor prior to organ procurement;(b) comparing measured ICG-PDR to a threshold; and(c) designating liver tissue in the donor as acceptable for transplantation if the ICG-PDR exceeds the threshold.6. The method of claim 5 , wherein the threshold is about 18%.7. The method of claim 5 , wherein the threshold is about 24%.8. The method of claim 5 , wherein ICG-PDR is measured non-invasively.9. The method of claim 8 , wherein ICG-PDR is measured using a PULSON LiMON liver function monitor. This application is a 35 U.S.C. §111(a) continuation of PCT international application number PCT/US2015/012582 filed on Jan. 23, 2015, incorporated herein by reference in its ...

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07-01-2021 дата публикации

TREATMENT OF SHORT BOWEL SYNDROME PATIENTS WITH COLON-IN-CONTINUITY

Номер: US20210000923A1
Принадлежит: SHIRE-NPS PHARMACEUTICALS, INC.

Intestinal absorption is enhanced in short bowel syndrome patients presenting with colon-in-continuity by treatment with a GLP-2 receptor agonist, such as teduglutide. 1. A method of treating an adult human patient having short bowel syndrome with at least 25% colon-in-continuity with remnant small intestine and who receives an amount of parenteral nutrition each week , said method comprising administering [Gly2]hGLP-2 to said patient using a dosing regimen effective to reduce or eliminate said weekly amount of parenteral nutrition received by said patient.2. The method as defined in claim 1 , wherein said patient has at least 30% colon-in-continuity with remnant small intestine.3. The method as defined in claim 2 , wherein said patient has at least 35% colon-in-continuity with remnant small intestine.4. The method as defined in claim 3 , wherein said patient has at least 40% colon-in-continuity with remnant small intestine.5. The method as defined in claim 4 , wherein said patient has at least 45% colon-in-continuity with remnant small intestine.6. The method as defined in claim 5 , wherein said patient has at least 50% colon-in-continuity with remnant small intestine.7. The method as defined in claim 6 , wherein said patient has at least 60% colon-in-continuity with remnant small intestine.8. The method as defined in claim 7 , wherein said patient has at least 70% colon-in-continuity with remnant small intestine.9. The method as defined in claim 8 , wherein said patient has at least 80% colon-in-continuity with remnant small intestine.10. The method as defined in claim 9 , wherein said patient has at least 90% colon-in-continuity with remnant small intestine.11. The method as defined in claim 1 , wherein the [Gly2]hGLP-2 is administered at a daily dose of from 30 to 150 μg/kg.12. A method of treating an adult human patient having short bowel syndrome with at least 25% colon-in-continuity with remnant small intestine and who receives parenteral nutrition each week ...

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13-01-2022 дата публикации

SWALLOWABLE CAPSULE, SYSTEM AND METHOD FOR MEASURING GASTRIC EMPTYING PARAMETERS

Номер: US20220008013A1
Автор: Imran Mir A.
Принадлежит:

Embodiments provide devices, systems and methods for measuring a gastric emptying (GE) parameter (GEP). Many embodiments provide a swallowable capsule having three electrodes one covered by a coating which remains in the stomach but is degraded in the small intestine (SI). The electrodes are coupled to circuitry such that when the capsule is in the stomach, current flow occurs between the first two electrodes generating a first signal and in the SI current flow occurs between the second and now uncovered third electrode generating a second signal. These two signals can be transmitted and analyzed externally or by an internal controller to determine a GEP e.g., GE time. The patient may wear an external device configured to receive and analyze the signals to determine GE time. Embodiments of the invention may be used to diagnose gastroparesis and provide patient's information on when to eat meals or administer insulin after eating. 1. (canceled)2. A swallowable capsule for measurement of a gastric emptying parameter in a gastro-intestinal (GI) tract of a patient , the capsule comprising:a first, second, and third electrode;a first circuit electrically coupled to the first and second electrodes, the first circuit configured to generate a first input signal based on a current flow between the first and second electrodes at a first location in the GI tract;a second circuit electrically coupled to the second and third electrodes, the second circuit configured to generate a second input signal based on a current flow between the second and third electrodes at a second location in the GI tract different from the first location; anda controller operatively coupled to the first and second circuits, wherein the controller is programmed to determine the gastric emptying parameter based on information relating to the first and second input signals.3. The capsule of claim 2 , wherein the first location is the stomach and the second location is the small intestine.4. The capsule ...

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04-01-2018 дата публикации

DETERMINING AND ENHANCING PRODUCTIVITY

Номер: US20180005160A1
Принадлежит:

Techniques and technologies for determining and enhancing productivity are described. In at least some embodiments, a system for includes a processing component operatively coupled to a memory; a productivity analyzer at least partially disposed in the memory, the productivity analyzer including one or more instructions that when executed by the processing component perform operations including: receive productivity data associated with usage of one or more productivity tools by at least one user during a time period; receive biometric data associated with one or more biometric aspects of the at least one user during the time period; analyze one or more aspects of the productivity data and the biometric data; and determine based on the analysis at least one productivity-related operation intended to enhance at least one productivity metric of the at least one user. 1. A system , comprising:a processing component operatively coupled to a memory; receive productivity data associated with usage of one or more productivity tools by at least one user during a time period;', 'receive biometric data associated with one or more biometric aspects of the at least one user during the time period;', 'analyze one or more aspects of the productivity data and the biometric data; and', 'determine based on the analysis at least one productivity-related operation intended to enhance at least one productivity metric of the at least one user., 'a productivity analyzer at least partially disposed in the memory, the productivity analyzer including one or more instructions that when executed by the processing component perform operations including2. The system of claim 1 , wherein the productivity analyzer configured to receive productivity data associated with usage of one or more productivity tools by at least one user during a time period comprises:a productivity analyzer configured to receive electronic messaging data associated with usage of an electronic messaging application by at ...

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02-01-2020 дата публикации

HYPERSPECTRAL IMAGING SENSOR

Номер: US20200005455A1
Принадлежит:

Systems, methods, and computer readable media for hyperspectral imaging are provided. An example hyperspectral imaging sensor system to identify item composition includes an imager to capture hyperspectral imaging data of one or more items with respect to a target. The example includes a sensor to be positioned with respect to the target to trigger capture of the image data by the imager based on a characteristic of the target. The example includes a processor to prepare the captured imaging data for analysis to at least: identify the one or more items; determine composition of the one or more items; calculate an energy intake associated with the one or more items; and classify the target based on the energy intake. 1. A hyperspectral imaging sensor system to identify item composition , the system comprising:an imager to capture hyperspectral imaging data of one or more items with respect to a target;a sensor to be positioned with respect to the target to trigger capture of the image data by the imager based on a characteristic of the target; and identify the one or more items;', 'determine composition of the one or more items;', 'calculate an energy intake associated with the one or more items; and', 'classify the target based on the energy intake., 'a processor to prepare the captured imaging data for analysis to at least2. The system of claim 1 , wherein the one or more items include food items.3. The system of claim 1 , wherein the characteristic of the target includes at least one of chewing or swallowing.4. The system of claim 1 , wherein the sensor includes at least one of a proximity sensor claim 1 , an inertial measurement unit claim 1 , or a light sensor.5. The system of claim 1 , wherein the imager is to capture both hyperspectral imaging data and red-green-blue imaging data to be fused into combined imaging data for analysis.6. The system of claim 1 , wherein the energy intake is based on caloric content of the one or more items to be determined by ...

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12-01-2017 дата публикации

Methods, systems and non-transitory computer-readable recording media for monitoring blood pressure in real time

Номер: US20170007136A1
Автор: Yeong Joon Gil
Принадлежит: Huinno Co Ltd

Methods, systems, and non-transitory computer-readable recording media for monitoring blood pressure are provided. The method includes calculating an estimate of deviations between every two pulse transit time (PTT) values measured at an interval of a first period, and estimating a PTT value to be measured the first period after a current time. The method also includes calculating an estimate of deviations between every two oxygen saturation values measured at an interval of a second period, and estimating an oxygen saturation value to be measured the second period after the current time. The method additionally includes calculating current systolic blood pressure and diastolic blood pressure based on an electrocardiogram (ECG) value measured at the current time, the estimated PTT value, and the estimated oxygen saturation value.

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12-01-2017 дата публикации

CAPSULE AND METHOD FOR TREATING OR DIAGNOSING CONDITIONS OR DISEASES OF THE INTESTINAL TRACT

Номер: US20170007154A1
Автор: Imran Mir A.
Принадлежит:

A device and method for mapping, diagnosing and treating inflammatory disorders (such as Crohn's disease) or other diseases, disorders or conditions of the intestinal tract is provided using a capsule passing through the intestinal tract. Further, a capsule tracking system is provided for tracking a capsule's location along the length of an intestinal tract as various treatment and/or sensing modalities are employed. In one variation, an acoustic signal is used to determine the location of the capsule. A map of sensed impedance and or temperature may be derived from the pass of a capsule to diagnose the disorder or disease. The capsule or subsequently passed capsules may treat, further diagnose, or mark the intestinal tract at a determined location along its length. 1providing an autonomous capsule comprising an impedance sensor;sensing with the impedance sensor, an impedance of a portion of a gastrointestinal tract at a first impedance location along a length of the gastrointestinal tract;sensing with the impedance sensor, an impedance of a portion of a gastrointestinal tract at a second impedance location along a length of the gastrointestinal tract; anddetermining whether the impedance at the first impedance location is different from the impedance at the second impedance location by a predetermined difference.. A method for diagnosing an inflammatory gastrointestinal disorder comprising: This application is a continuation of U.S. application Ser. No. 13/215,182 filed Aug. 22, 2011, which is a divisional of U.S. application Ser. No. 10/744,558 filed Dec. 22, 2003 and issued as U.S. Pat. No. 8,005,536 on Aug. 23, 2011 which claims the benefit of Provisional Application Ser. No. 60/436,154, filed on Dec. 24, 2011, said U.S. application Ser. No. 10/744,558 is also a continuation-in-part of U.S. application Ser. No. 09/892,404 filed Jun. 26, 2001 and issued as U.S. Pat. No. 7,160,258 on Jan. 9, 2007; all of the aforementioned priority applications are hereby ...

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12-01-2017 дата публикации

CORRELATION OF SALIVA FLOW-RATE AND ORAL DRYNESS IN HYPERURICEMIA

Номер: US20170007172A1
Принадлежит:

Hyperuricemia has been studied extensively. However studies on salivary flow rate (SFR; ml/min) in unstimulated saliva (USS) and stimulated saliva (SS) conditions and oral dryness (OD) in subjects with hyperuricemia (HUS) have never been conducted. Current studies showed significantly decreased values in presence of OD (ODP) compared to absence of OD (ODA) in USS both for NUS (normouricemic subjects; p=0.0001) and HUS (p=0.0170). Furthermore, OD comparisons gave significantly decreased values in ODP compared to ODA in SS both for NUS (p=0.0049) and HUS (p=0.0444). In view of the significance in hyperuricemic subjects the “flow rate of unstimulated saliva (USS) and stimulated saliva (SS) decreases significantly in hyperuricemic subjects with oral dryness present (ODP)”. Conclusively, it is suggested that the salivary digestion affected in hyperuricemia can be diagnosed by investigating the salivary composition and flow rate. 1. A method to identify hyperuricemia in a subject , the method comprising:estimating a uric acid level of the subject in need of diagnosis for the hyperuricemia, the uric acid level being measured in a saliva or blood;categorizing the subject as hyperuricemic when the uric acid level is above 420 micromol/l and as normouricemic when the uric acid level is below 420 micromol/l;evaluating an absence or a presence of oral dryness of the subject;collecting an unsimulated saliva and a simulated saliva of the subject;estimating a flow-rate of the unsimulated saliva and a simulated saliva, the flow-rate being estimated based on the collected the unsimulated saliva and the simulated saliva; andcomparing oral dryness, the flow rate of an unsimulated saliva and a simulated saliva, and the hyperurecimia in a subject to diagnose hyperuricemic state in a subject.2. The method of claim 1 , further comprising evaluating salivary composition for diagnosis of the subject with or without hyperuricemia.3. The method of claim 1 , wherein oral dryness being ...

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12-01-2017 дата публикации

SYSTEM FOR SALIVA COLLECTION

Номер: US20170007215A1
Автор: PODOLY Erez
Принадлежит: SALVME, INC.

Disclosed herein are portable handheld devices for saliva collection for daily monitoring of salivary biomarkers of physiological conditions, the device comprising: a handheld handle comprising a saliva collector, the saliva collector comprising: a suction tip; a bi-directional pump electrically configurable for pumping towards two opposite directions; a saliva reservoir; a valve; a water reservoir, the water reservoir comprising an external filling lid; a reversible fluidic connection configurable in a connected and disconnected position; and a base accommodating the handheld handle, the base configurable to fluidly communicate with the handheld handle through at least the reversible fluidic connection, wherein the valve is electrically configured to allow fluid communication directly between at least two selected from: the saliva reservoir, the water reservoir, and the reversible fluidic connection, and wherein the bi-directional pump is electrically configurable to allow fluid communication directly between the suction tip and the saliva reservoir. 139-. (canceled)40. A portable handheld device for tooth brushing and saliva collection for daily monitoring of salivary biomarkers of physiological conditions of a subject , the device comprising: i) a suction tip;', 'ii) a bi-directional pump electrically configurable for pumping towards two opposite directions;', 'iii) a saliva reservoir;', 'iv) a valve;', 'v) a water reservoir, the water reservoir comprising an external filling lid;', 'vi) a reversible fluidic connection configurable in a connected position and a disconnected position; and, 'a) a handheld handle comprising a saliva collector, the saliva collector comprisingb) a base accommodating the handheld handle, the base configurable to fluidly communicate with the handheld handle through at least the reversible fluidic connection, wherein the valve is electrically configured to allow fluid communication directly between at least two elements selected from: ...

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14-01-2016 дата публикации

Methods, systems and devices for performing multiple treatments on a patient

Номер: US20160008050A1
Принадлежит: Fractyl Laboratories Inc

Methods, systems and devices for treating a patient include performing a first treatment to treat a first portion of tissue and performing a second treatment to treat a second portion of tissue. The second portion of tissue is treated at least twenty-four hours after the first portion of tissue is treated. In particular embodiments, the first portion of tissue includes duodenal tissue, and the second portion of tissue includes duodenal or other gastrointestinal tissue.

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11-01-2018 дата публикации

DATA COLLECTING HEAD GUARD SYSTEMS AND METHODS THEREOF

Номер: US20180007990A1
Принадлежит:

A head guard is provided. The head guard includes one or more sensors as part of an sensory input and communications system. The head guard wirelessly communicates data to remote computing devices for intelligent data collection. 1. A data collection system , comprising [ a stretchable fabric layer, and', 'a padding layer; and, 'a multi-layered sidewall, wherein the multi-layered sidewall forms a dome, wherein the dome defines a circular opening for a head of a wearer and a plurality of sensor ports, and wherein the multi-layered sidewall comprises, 'a removable cover system selectably attachable to the multi-layered sidewall, wherein the removable cover system has an inner surface and an outer surface, wherein a portion of the inner surface of the removable cover system is attachable to a portion of the dome to maintain the position of the removable cover system relative to the dome; and', a microcontroller,', 'a plurality of sensors that are each in communication with the microcontroller, wherein each of the plurality of sensors are removably received into a respective one of the plurality of sensors ports,', 'a communications unit, and', 'a local indicator, wherein the microcontroller is configured to activate the local indicator upon a detected impact in excess of a predefined magnitude, wherein the local indicator comprises any of a visual device and an audio device; and, 'a sensory input and communications system, wherein at least a portion of the sensory input and communications system is positioned between the cover system and the multi-layered sidewall, the sensory input and communications systems comprises], 'a head guard comprising for the data received from the head guard, determine athlete information associated with the data based on the source of the data;', 'group data based on one or more factors selected from the group of factors comprising sport, age, and geography; and', 'generate aggregated data reporting based on the grouped data., 'an activity ...

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14-01-2021 дата публикации

Saliva test strip and method

Номер: US20210007646A1
Принадлежит: MX3 Diagnostics Inc

A test strip for sampling a bodily fluid may include multiple layers of a substrate material, an adhesive between at least some of the multiple layers, and a microfluidic channel formed between at least some of the multiple layers. The test strip may further include multiple electrodes on one of the multiple layers, positioned and partially exposed within the microfluidic channel, an additional material positioned at or near an entrance to the microfluidic channel, to selectively limit the flow of at least one of bubbles or debris into the microfluidic channel, and at least one exit port in at least one of the multiple layers to allow for release of pressure from the test strip. In some embodiments, the test strip is a saliva analysis test strip. In some embodiments, the test strip includes multiple exit ports to prevent blockage of sample flow.

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14-01-2021 дата публикации

SWEAT MAPPING METHOD

Номер: US20210007655A1
Принадлежит:

A method for mapping sweat production from the human skin, said method comprising the application of a polydiacetylene (PDA) prepared from a derivative of a conjugated diynoic acid having at least 18 carbon atoms, wherein the PDA changes colour when exposed to sweat, but does not change colour when exposed to pure water. 1. A method for mapping sweat production from a human skin , comprising: 'wherein the PDA is a homopolymer of 3-(pentacosa-10,12-diynamido)propyl-imidazole or a salt thereof;', 'applying to the surface of the human skin of a polydiacetylene (PDA) prepared from a derivative of a conjugated diynoic acid having at least 18 carbon atoms;'}exposing the surface of the human skin to sweat; and 'wherein, when exposed to pure water, the PDA does not change colour.', 'mapping a colour change of the PDA;'}2. (canceled)3. (canceled)4. A method according to claim 1 , wherein the PDA changes its fluorescence spectrum when exposed to sweat.5. A method according to claim 1 , further comprising the step of assessing the relative performance of an antiperspirant active or formulation.6. A method according to claim 1 , wherein the PDA is applied on a flexible film.7. A method according to wherein the PDA is on the flexible film as a uniform layer of from 2 to 5 microns.8. A method according to claim 6 , wherein the PDA is on the flexible film at a level of from 0.2 to 0.8 mg/cm.9. A sweat mapping device comprising a flexible film with a PDA supramolecule applied to its surface claim 1 , the PDA as recited in .10. A method of manufacture of a sweat monitoring device claim 1 , the method comprising the steps of:(i) preparing a derivative of a conjugated diynoic acid having at least 18 carbon atoms,(ii) dissolving the derivative in a solvent and applying the resulting solution to the surface of a flexible film,(iii) evaporating the solvent from the flexible film, 'wherein the PDA is a homopolymer of 3-(pentacosa-10,12-diynamido)propyl-imidazole or a salt thereof.', '(iv) ...

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14-01-2021 дата публикации

SALIVA ASSESSING METHOD, DEVICE, AND SYSTEM

Номер: US20210007721A1
Принадлежит:

Various embodiments of a swab device, system, and method are provided for measuring and assessing saliva flow in the mouth of a person. In one embodiment, a system includes a swab device and a measuring device. The swab device includes a handle portion and a swab portion, the handle portion being elongated to extend between a proximal end and a distal end. The swab portion is coupled to a distal portion of the handle portion and is sized and configured to collect saliva from the mouth. The measuring device is sized and configured to measure an amount of the saliva collected with the swab portion, the measuring device including a nesting portion integrated therewith. Such nesting portion of the measuring device is sized and configured to receive the proximal end of the handle portion of the swab device to measure the saliva collected therewith. 1. A method for measuring saliva flow in a mouth of a person , comprising:clearing excess saliva from the mouth;inserting a swab into the mouth for a first predetermined period of time ranging between about 1 second and about 20 seconds; andmeasuring an amount of saliva captured by the swab by positioning the swab on a measuring device.2. The method according to claim 1 , further comprising determining whether the measured amount of saliva is below a standard healthy saliva amount.3. The method according to claim 1 , further comprising:maintaining the mouth in a closed position for a second predetermined period of time ranging between about 3 second and about 90 seconds;inserting a second swab into the mouth for a third predetermined period of time ranging between about 1 second and about 20 seconds; andmeasuring an amount of saliva captured by the second swab by positioning the second swab on the measuring device.4. A method for measuring saliva flow in a mouth of a person claim 1 , comprising:clearing excess saliva from the mouth;maintaining the mouth in a closed position for a first predetermined period of time ranging ...

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10-01-2019 дата публикации

SYSTEM AND METHOD FOR GASTRO-INTESTINAL ELECTRICAL ACTIVITY

Номер: US20190008442A1
Принадлежит:

A gastro-electrical activity mapping system and method may comprise a catheter insertable through a natural orifice into the gastro-intestinal (GI) tract and comprising an array of electrodes for contacting an interior surface of a section of the GI tract to detect electrical potentials at multiple electrodes, and comprises a signal analysis and mapping system arranged to receive and process electrical signals from multiple electrodes of the array and spatially map GI smooth muscle electrical activity as an activation time map, a velocity map, or an amplitude map, which may be in the form of contour plots and may be mapped on an anatomical computer model of at least the section of the GI tract and may be animated. 139-. (canceled)40. A gastrointestinal-electrical activity mapping or signal analysis system comprising a processor , a memory , and a program , wherein the program is stored in the memory and configured to be executed by the processor , the program including instructions for:(a) receiving and processing electrical signals from one or more electrodes contacting a surface of a section of a human GI tract;(b) spatially mapping GI smooth muscle electrical activity at said section of the human GI tract based on the received and processed electrical signals; and propagation of anatomical re-entrant or non re-entrant GI electrical activity upwardly within the GI tract as a result of circumferential re-entrant propagation circumferentially around the GI tract,', 'propagation of circumferential re-entrant or non re-entrant GI electrical activity circumferentially within the GI tract other than at a normal pacemaker site in a stomach,', 'propagation of circumferential re-entrant GI electrical activity circumferentially within the GI tract,', 'propagation of circumferential non re-entrant GI electrical activity circumferentially within the GI tract at a velocity, amplitude or both velocity and amplitude, higher than a normal (non re-entrant) GI electrical activity ...

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10-01-2019 дата публикации

SWEAT ELECTROLYTE LOSS MONITORING DEVICES

Номер: US20190008448A1
Принадлежит: Eccrine Systems, Inc.

Embodiments of the disclosed invention provide devices and methods to incorporate suspension-based, i.e., hydrogel-based and thixotropic compound-based, ion-selective electrodes and reference electrodes into a wearable sweat sensing device. Embodiments of this device are configured to monitor sweat electrolyte concentrations, trends, and ratios under demanding use conditions. The accompanying method includes use of the disclosed device to track fluid and electrolyte gain and loss in order to produce an electrolyte estimate, such as a sweat electrolyte concentration, a sweat electrolyte concentration trend, a sweat rate, or a concentration ratio between a plurality of electrolytes. 1. A sweat sensing device configured to be worn on an individual's skin , and that provides sweat electrolyte loss monitoring , comprising:one or more ion selective electrode sensors for measuring a characteristic of an analyte in a sweat sample;a reference electrode, wherein the reference electrode includes an electrode, a first suspension material containing a reference salt, a second suspension material containing a bridge salt, a reference port, and a reference membrane; and where the electrode is in fluidic communication with the first suspension material, the first suspension material is in fluidic communication with the second suspension material, the second suspension is in fluidic communication with the reference membrane, and the reference membrane is in fluidic communication with the reference port;a microfluidic channel, wherein said channel allows fluidic communication between the skin, the ion selective electrode sensors, and the reference port;one or more secondary sensors; anda user interface.2. The device of claim 1 , where the user interface is at least one of the following: one or more lights; a visual display; a sound generating component; a haptic component; a touchscreen; one or more buttons; an optical scanner; and a camera.3. The device of claim 1 , where the ion ...

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09-01-2020 дата публикации

DEVICES, SYSTEMS, AND METHODS FOR DETERMINING INFLAMMATION AND/OR FIBROSIS

Номер: US20200008736A1
Принадлежит: BOSTON SCIENTIFIC SCIMED, INC.

A method for evaluating a gastrointestinal tract of a subject may comprise using a sensor located in the subject to obtain data regarding qualities of a tissue of the gastrointestinal tract; using the obtained data, determining a measure of perfusion of blood in the tissue; using the obtained data, determining a measure of thickness of the tissue; using the measure of perfusion and the measure of thickness, determining a measure of inflammation of the tissue; and using one or more of the measure of perfusion, the measure of thickness, and the measure of inflammation, classifying a state of the tissue. 1. A method for evaluating a gastrointestinal tract of a subject , the method comprising:using a sensor located in the subject to obtain data regarding qualities of a tissue of the gastrointestinal tract;using the obtained data, determining a measure of perfusion of blood in the tissue;using the obtained data, determining a measure of thickness of the tissue;using the measure of perfusion and the measure of thickness, determining a measure of inflammation of the tissue; andusing one or more of the measure of perfusion, the measure of thickness, and the measure of inflammation, classifying a state of the tissue.2. The method of claim 1 , wherein classifying a state of the tissue includes classifying a fibrotic attribute of the tissue.3. The method of claim 1 , wherein the sensor is an optical sensor located in a lumen of the gastrointestinal tract.4. The method of claim 3 , wherein the measure of perfusion is a perfusion index claim 3 , wherein the perfusion index is a ratio of an amount of pulsatile light received by the sensor to an amount of total light received by the sensor.5. The method of claim 1 , wherein determining a measure of inflammation comprises:applying a first function to the measure of perfusion; andapplying a second function to the measure of thickness.6. The method of claim 5 , wherein determining a measure of inflammation further comprises adding ...

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09-01-2020 дата публикации

Information provision method, information processing system, information terminal, and information processing method

Номер: US20200008753A1

In order to objectively grasp a stress state of a user and to prevent postpartum depression, biological gas information is acquired via a network, where the biological gas information indicates a concentration of benzyl alcohol of the user and is obtained by a sensor that detects benzyl alcohol released from a skin surface of the user. From a memory storing information including an upper limit of a normal range of the concentration of benzyl alcohol per unit period, the information indicating the upper limit of the normal range is read out. When a frequency in the unit period with which the concentration of benzyl alcohol of the user exceeds the upper limit of the normal range is determined to have an increasing tendency based on the biological gas information obtained during a pregnancy period of the user, the information related to stress of the user is output to an information terminal of the user.

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14-01-2021 дата публикации

SYSTEMS, DEVICES AND METHODS FOR PERFORMING MEDICAL PROCEDURES IN THE INTESTINE

Номер: US20210008336A1
Принадлежит: Fractyl Laboratories, Inc.

A method for performing a medical procedure in an intestine of a patient is provided. The method comprises providing a system comprising: a catheter for insertion into the intestine, the catheter comprising: an elongate shaft comprising a distal portion; and a functional assembly positioned on the shaft distal portion and comprising at least one treatment element. The catheter is introduced into the patient, and target tissue is treated with the at least one treatment element. The target tissue comprises mucosal tissue of the small intestine, and the medical procedure can be configured to treat at least one of non-alcoholic fatty liver disease (NAFLD) or non-alcoholic steatohepatitis (NASH). 1. A method for performing a medical procedure in an intestine of a patient , comprising:providing a system comprising:a catheter for insertion into the intestine, the catheter comprising:an elongate shaft comprising a distal portion; anda functional assembly positioned on the shaft distal portion and comprising at least one treatment element;introducing the catheter into the patient; andtreating target tissue with the at least one treatment element, wherein the target tissue comprises mucosal tissue of the small intestine;wherein the medical procedure is configured to reduce liver fat in the patient.2. The method according to claim 1 , wherein the medical procedure is further configured to reduce and/or prevent fibrosis of the liver.3. The method according to claim 1 , wherein the medical procedure is further configured to treat Type 2 diabetes.4. The method according to claim 1 , wherein the medical procedure is further configured to treat a disease or disorder selected from the group consisting of: Type 2 diabetes; Type 1 diabetes; “Double diabetes”; gestational diabetes; hyperglycemia; pre-diabetes; impaired glucose tolerance; insulin resistance; and combinations thereof.5. The method according to claim 1 , wherein treating target tissue modifies at least one of (1) nutrient ...

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08-01-2015 дата публикации

DISCRETE IMAGING OF HEPATIC OXIDATIVE AND NITROSATIVE STRESS WITH TWO-CHANNEL NANOPARTICLES FOR IN VIVO DRUG SAFETY SCREENING

Номер: US20150011878A1
Принадлежит:

Encompassed are embodiments of activatable nanoprobes useful for in vivo longitudinal imaging of drug hepatotoxicity with oxidative and nitrosative stress as the safety biomarkers. Both HOand ONOOare important mediators of radical stress. Two channels of optical detection, intrinsically free from cross-talk, were engineered into superconducting polymer nanoparticles to generate chemiluminescence resonance energy transfer between the conjugated polymer matrix of the nanoparticle and an incorporated chemiluminescent substrate allowing for the luminescent detection of HOand fluorescence resonance energy transfer between the polymer matrix and an oxidation-degradable fluorophore for ratiometric detection of ONOO These nanoprobes have been applied for real-time in vivo monitoring of hepatotoxicity resulting from challenges from drugs. In addition to the ability of imaging the dose-dependence of oxidative and nitrosative stress, the positive detection of radical stress that precedes histological changes allow the early and longitudinal detection of drug-induced hepatotoxicity in vivo. 1. A bifunctional nanoprobe for detecting hepatic injury generating at least one of a reactive oxygen species and a reactive nitrogen species , said nanoprobe comprising: (a) a fluorescent superconducting polymer; and', '(b) a copolymer having a plurality of galactose moieties conjugated thereto, wherein the plurality of galactose moieties are disposed at the surface of the matrix core;, '(i) a matrix core comprising(ii) a chemiluminescent sensor that in the presence of hydrogen peroxide provides a chemical source of energy capable of inducing a detectable signal from a dye; and(iii) a fluorescent sensor that is decomposed when in the presence of a reactive oxygen or nitrogen species.2. The nanoprobe of claim 1 , wherein the fluorescent superconducting polymer is selected from the group consisting of: a poly(phenylene-vinylene) (PPV) derivative claim 1 , a polyfluorene (PF) derivative claim ...

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08-01-2015 дата публикации

Peristaltic sound detection apparatus, method for detecting peristaltic sound, and recording medium

Номер: US20150011912A1
Принадлежит: Sharp Corp, University of Yamanashi NUC

A peristaltic sound detection apparatus ( 10 ) includes matching coefficient calculation means for calculating a plurality of matching coefficients by individually matching a frequency spectrum of a biological sound and a plurality of standard frequency spectra of peristaltic sounds.

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