Abstract: The invention relates to a system and a method for determining a severity of a respiratory disease of a patient. The patient is instructed by a system to recite a phrase. The system receives the phrase recited by the patient as acoustic signal and analyzes the acoustic signal with respect to a severity of a respiratory disease. The result of the analysis is provided, which is indicative for the severity of the respiratory disease of the patient.

Abstract: A system determines a risk level of a respiratory attack of a user of the system. The system comprises part of a network of systems, and it reports information to, and receives information from, the network. The system comprises a local activity monitoring device for tracking the physical activity level of the user. Location information and activity levels in respect of other users of the network of systems are received, relating to when they have suffered a respiratory attack. A warning can then be given to the user which takes account of the location of the user and the activity level or planned activity level of the user, and the received location information and activity levels in respect of other users.

Abstract: Various methods and apparatus disclosed herein relate to apparatus and techniques for harvesting energy from operation of a pill pack, and utilizing that energy for various purposes. In various embodiments, an energy harvesting apparatus configured to receive a pill pack (104, 304) is disclosed. An energy harvesting apparatus in accordance with various embodiment may include a housing (102, 302), where the housing is configured to receive a pill pack (104, 304), and an electrical generator incorporated into the housing (102, 302), where the electrical generator converts motion associated with compression of at least one blister (1031-n, 3031-n) of the pill pack (104, 304) expelling one or more pills (1051-n, 3051-n) from the pill pack into electrical energy, where the electrical energy is used to collect one or more data points associated with operation of the pill pack during the expelling of the one or more pills.

Abstract: A computer-implemented method and corresponding output generator for handling alarm events, generated by a subject/patient monitoring device, and generating clinician-perceptible outputs indicative of the alarm events. Alarm events are divided into non-actionable and actionable alarm events. Information on non-actionable alarm events is stored. Stored information on non-actionable alarm events is contained in a clinician-perceptible output generated in response to detecting an actionable alarm event.

Abstract: A blood pressure monitoring system is for mounting around a body limb or digit, in which an array of electroactive material actuators provides an inward force. One or more electroactive material actuators are identified which are best located for performing blood pressure monitoring and these are then used to apply a pressure. By performing pulse monitoring while controlling the identified one or more electroactive material actuators, the blood pressure may be determined.

Abstract: A breast pump device (1) comprises an expression kit (2) and a vacuum unit (3) configured to realize a pressure cycle in the expression kit (2). For the purpose of determining one or more milk expression characteristics such as total volume of expressed milk, the device (1) is equipped with an acoustic milk expression assessment system (6) including an acoustic sensor (61) and a processor (62) configured to process an acoustic signal received from the sensor (61) during operation of the device (1) when a receptacle (4) is used with the device (1) for receiving expressed milk. By recording sound during a pumping session, it is possible to determine a value of a time duration of a free fall of droplets of expressed milk from the expression kit (2) to the receptacle (4), which can be taken as a measure of a number of interesting milk expression characteristics.

Abstract: A system for analysis of the upper airway has a sensor arrangement with at least two sensor positions provided along a flow path leading to the mouth and/or nose of a user (4). A relation is derived between sensor signals at the two locations, and this is interpreted to detect at least the presence of upper airway obstructions, and preferably also the location and/or extent of such obstructions. The system is adapted to distinguish between inhalation and exhalation using the acoustic sensor arrangement signals at the first and second locations.

Abstract: The present invention relates to a device for monitoring an eye of a subject, comprising: a transparent carrier for being in contact with the eye of the subject; and a photosensor facing the eye of the subject for receiving light reflected from the eye of the subject and for determining a light intensity of the received light, wherein the photosensor is arranged on the transparent carrier; and wherein the photosensor includes one of: a plurality of photodetectors arranged in the form of a two-dimensional array and spaced apart from one another for allowing incident light to pass between the photodetectors to enter the eye of the subject wherein the plurality of photodetectors is arranged in a plurality of rows of photodetectors or in a plurality of concentric circles substantially covering the iris and the pupil of the eye of the subject; and a single large area photodetector covering an iris and a pupil of the eye of the subject.

Abstract: Various methods and apparatus disclosed herein relate to apparatus and techniques for harvesting energy from operation of a syringe, and utilizing that energy for various purposes. In various embodiments, a method (400) for harvesting and using electrical energy during operation of a syringe (100, 300) may include: operating (402) the syringe, wherein operating includes displacing a plunger (112) of the syringe to draw fluid into a reservoir (114) of the syringe or expel fluid from the reservoir of the syringe; converting (404), by an electrical generator (120, 122) that is integral with the syringe, motion associated with displacing the plunger into electrical energy; and using (406) at least some of the electrical energy to at least temporarily store, in a memory component (136) integral with the syringe, one or more data points associated with operation of the syringe.

Abstract: The present invention relates to a device, system and method for detection of pulse and/or pulse-related information of a patient.

Abstract: A method for use in detecting and monitoring effects experienced by a subject taking a first drug, drug A, and at least one other substance, substance B, the method comprising: (a) obtaining a plurality of measured values of a physiological characteristic of the subject over a time period; (b) comparing the measured values to a predefined signature, the drug A signature, associated with the first drug, and thereby calculating a measure, Adiff, of the difference between the measured values and the drug A signature; (c) comparing the measured values to a predefined signature, the substance B signature, associated with the at least one other substance, and thereby calculating a measure, Bdiff, of the difference between the measured values and the substance B signature; (d) comparing the measured values to a predefined signature, the DO signature, associated with a desired physiological state of the subject, and thereby calculating a measure, DOdiff, of the difference between the measured values and the DO signat

Abstract: An inflatable tourniquet system for arterial blood occlusion of a leg or arm, e.g. after injury or for surgery. A tourniquet (TQ) is to be manually fastened around the limb by a user, e.g. a first aid helper, e.g. an untrained person. A manual inflator (B) is used to inflatable the tourniquet to apply pressure for occlusion of arterial blood flow to the limb. An electric circuit (CC) measures an electrical input from a length sensor (C), e.g. an electric conductor, and to determine a value (R), e.g. electric resistance, indicative of circumference of the limb accordingly, when the tourniquet has been fastened around the limb. A blood pressure measuring circuit (BP) automatically determines a systolic blood pressure (SBP) in response to input from a pressure sensor (PS) arranged to measure a pressure (PR) of the tourniquet.

Abstract: A breastfeeding supporting system and a corresponding method are disclosed, the breastfeeding supporting system (1) comprising a nipple shield (10) adapted to be positioned at least partly over the areola and nipple of a breast of a breastfeeding woman, a capacitive pressure sensing unit (20) for sensing a capacity of at least part of a surface of the nipple shield, a processing unit (40) adapted to process the sensed surface capacity to derive at least one parameter of an infant interacting with the nipple of the breastfeeding woman. The breastfeeding supporting system and corresponding method eliminate at least some concerns related to breastfeeding.

Abstract: A hands-free cardiopulmonary resuscitation (CPR) guidance method (40) for a system including a head-mountable computing device (100) comprising a processor (110) and at least one display module (106, 106?) arranged to be viewed by the wearer (20) of the head-mountable computing device when wearing the device is disclosed that allows a rescuer to receive CPR guidance without losing sight of the victim. The method comprises receiving (420), on said processor, a first signal conveying vital signs information from at least one sensor (200, 210) for monitoring vital signs of a patient (10), wherein a sensor (210) of the at least one sensor is integrated in the head-mountable computing device (100); processing said first signal on said processor to obtain the vital signs information; and displaying (422) CPR guidance on said at least one display module in response to the processed vital signs information. A computer program product and a CPR guidance system are also disclosed.

Abstract: The present invention relates to a device (10) and method for non-invasively measuring a hydration state of a living being (62). To improve with respect to the convenience-to-use, the cost-effectiveness and the accuracy of the delivered results, the proposed device comprises a first light source (14) for emitting light of a first wavelength into a tissue portion (12) of the living being (62), polarization means (18) for polarizing at least part of the emitted light prior to an interaction of the emitted light with the tissue portion (12), a first light detector (26) for detecting polarized light of the first wavelength reflected at the tissue portion (12) and processing means (32) configured to derive a tissue hydration parameter from the detected reflected polarized light and to determine a body hydration index based on said tissue hydration parameter.

Abstract: A device and method for monitoring pain of a user (50) are presented. The device (10) comprises a receiving unit (12) for receiving an accelerometer signal (38) from an accelerometer sensor (30) worn by the user (50), wherein the accelerometer signal (38) comprises components of a pulse signal (20) and a respiration signal (22); and a processing unit (14) configured to: derive the pulse signal (20) and the respiration signal (22) from the accelerometer signal (38); adapt the pulse signal (20) based on the respiration signal (22) in order to obtain a corrected pulse signal (40); and derive a pain descriptor based on the corrected pulse signal (40).

Abstract: The invention provides amongst others kit of parts (1000) comprising a container (200) comprising a container enclosure (210), the container enclosure (210) comprising a container enclosure internal face (211), and a container closure (220), the container closure (220) comprising a container closure internal face (221), wherein one or more of the container enclosure internal face (211) and the container closure internal face (221) comprises a CO2 detector (100), and wherein one or more of the container enclosure (210) and the container closure (220) comprise a light transmissive part (233) for external visual inspection of the CO2 detector (100).

Abstract: The present invention relates to a device for monitoring an eye of a subject, comprising: a transparent carrier for being in contact with the eye of the subject; and a photosensor facing the eye of the subject for receiving light reflected from the eye of the subject and for determining a light intensity of the received light, wherein the photosensor is arranged on the transparent carrier; and wherein the photosensor includes one of: a plurality of photodetectors arranged in the form of a two-dimensional array and spaced apart from one another for allowing incident light to pass between the photodetectors to enter the eye of the subject wherein the plurality of photodetectors is arranged in a plurality of rows of photodetectors or in a plurality of concentric circles substantially covering the iris and the pupil of the eye of the subject; and a single large area photodetector covering an iris and a pupil of the eye of the subject.

Abstract: A system for analysis of the upper airway has a sensor arrangement with at least two sensor positions provided along a flow path leading to the mouth and/or nose of a user (4). A relation is derived between sensor signals at the two locations, and this is interpreted to detect at least the presence of upper airway obstructions, and preferably also the location and/or extent of such obstructions. The system is adapted to distinguish between inhalation and exhalation using the acoustic sensor arrangement signals at the first and second locations.

Abstract: A hands-free cardiopulmonary resuscitation (CPR) guidance method (40) for a system including a head-mountable computing device (100) comprising a processor (110) and at least one display module (106, 106?) arranged to be viewed by the wearer (20) of the head-mountable computing device when wearing the device is disclosed that allows a rescuer to receive CPR guidance without losing sight of the victim. The method comprises receiving (420), on said processor, a first signal conveying vital signs information from at least one sensor (200, 210) for monitoring vital signs of a patient (10), wherein a sensor (210) of the at least one sensor is integrated in the head-mountable computing device (100); processing said first signal on said processor to obtain the vital signs information; and displaying (422) CPR guidance on said at least one display module in response to the processed vital signs information. A computer program product and a CPR guidance system are also disclosed.