Abstract: A device for supporting determination of return of spontaneous circulation, ROSC, during an associated cardiopulmonary resuscitation, CPR, procedure which is being performed on an associated patient. A sensor is used to sense a physiological signal of the patient. Frequency analysis of the signal is carried out to extract dominant fundamental frequency components in the signal. From this analysis it is possible to determine that there has been a potential ROSC.

Abstract: A device is configured for tracking e.g. the diastolic blood pressure in a patient. The device applies a pressure to a body part, e.g. by use of an inflatable cuff. By performing repeated and alternating pressure changes in the cuff, a specific feature of a signal that relates to the diastolic blood pressure can be tracked and possibly measured. The device may have particular use in conjunction with cardiopulmonary resuscitation devices.

Abstract: The present invention relates to a device, system and method for determining pulse pressure variation of a subject. To enable more reliably determining pulse pressure variation of a subject the device comprises a signal input (11) configured to obtain an input signal representing a hemodynamic signal of the subject, a processor (12) configured to process the input signal and compute a pulse pressure variation and a signal output (13) configured to output the computed pulse pressure variation. The pulse pressure variation is computed by deriving a pulse height signal from the input signal, deriving a pulse height baseline and a de-trended pulse height signal from the pulse height signal as the ratio between the difference between extrema of the de-trended pulse height signal and the respective value of the pulse height baseline signal, and computing the pulse pressure variation from the de-trended pulse height signal and the pulse height baseline.

Abstract: The invention provides a magnetic inductive sensing device (30) comprising a loop antenna (10) for inductively coupling with electromagnetic (EM) signals emitted from a medium in response to stimulation of the medium with electromagnetic excitation signals. The device includes an electromagnetic shield (36) element which is arranged such as to intercept electromagnetic signals travelling to or from the antenna. The shield element is formed of conductive material such as to block electrical field components of incident signals but further incorporates a non-conductive gap in the material so as to prevent the formation of eddy currents. A loop of the antenna is broken by an opening, the opening being bridged by a capacitor, and the device comprises a signal processing means which is electrically coupled to the antenna via only a single point of the antenna, located to one side of the opening.

Abstract: The invention provides a magnetic inductive sensing system for sensing electromagnetic signals emitted from a body in response to electromagnetic excitation signals applied to the body. The electromagnetic signals are generated and sensed by the same loop resonator which comprises a single-turn loop antenna and a tuning capacitor. The loop antenna of the resonator and a signal generation means for exciting the resonator to generate excitation signals are together configured so as to optimize the value of a ratio between the radial frequency of the generated electromagnetic excitation signals and a reference frequency of the antenna, where the reference frequency is the frequency for which one wavelength of the generated excitation signals (waves) matches the circumferential length of the antenna. This ratio, which corresponds to a normalized radial frequency of the generated excitation signals, is maintained between a value of 0.025 and 0.50.

Abstract: A device (10, 10?, 10?) includes a light source (12) and a light detector (14) spaced from, and in communication with, the light source (12). An electronic processor (18) is programmed to compute pulse oximetry data from output of the light detector (14). A clamping member (26) is included, on or in which the light source (12) and the light detector (14) are disposed. The clamping member (26) is configured for attachment to a human body part with the body part disposed between the light source (12) and the light detector (14) such that light from the light source (12) passes through the body part to reach the light detector (14). The clamping member (26) is configured to attach to the body part by transitioning from a first stable state to a second stable state via a compression force applied to the clamping member (26).

Abstract: The present invention relates to a device for measuring a physiological parameter of a human limb such as peripheral capillary oxygen saturation. The device comprises a body comprising a first body part and a second body part, which are movable relative to each other to define an opening with an adjustable size for receiving the limb therein, and a physiological sensor for interacting with the limb received in the opening, the sensor being attached to the body, wherein the first and second body parts are slidable or twistable relative to each other while at least partially engaging or intersecting each other, or wherein the first and second body parts are configured to form a clip having an L-shaped end section for at least partially enclosing the limb received in the opening, in order to adjust the size of the opening.

Abstract: An optical source for guiding light to a target of a patient includes at least one light source configured to emit red light and infrared light. The at least one light source is embedded within a light-conducting sheet. A photodistributor is spaced from the at least one light source. The photodistributor includes a light-emitting surface and at least one light-receiving surface optically coupled to the light-conducting sheet. The photodistributor is configured to discharge at least a portion of the emitted red light and at least a portion of the emitted infrared light into a target.

Abstract: A device (10, 10?, 10?) includes a light source (12) and a light detector (14) spaced from, and in communication with, the light source (12). An electronic processor (18) is programmed to compute pulse oximetry data from output of the light detector (14). A clamping member (26) is included, on or in which the light source (12) and the light detector (14) are disposed. The clamping member (26) is configured for attachment to a human body part with the body part disposed between the light source (12) and the light detector (14) such that light from the light source (12) passes through the body part to reach the light detector (14). The clamping member (26) is configured to attach to the body part by transitioning from a first stable state to a second stable state via a compression force applied to the clamping member (26).

Abstract: A wearable gear (100) for holding a physiological sensor for monitoring a subject, such as a pulse oximeter. Said wearable gear being configured to automatically adjust the maximal length such that the predefined tension is obtained regardless of the size of the body part of the subject. The wearable gear comprises a tensioning element (102) having a maximal length, a holding unit for holding the physiological sensor, the wearable gear further comprises a tension mechanism for tensioning the tensioning element to a predefined tension when at least partially around a body part of the subject, wherein the tension mechanism comprises i) a first part comprising a resilient material, and ii) a second part comprising a non-resilient material, and wherein the first part and the second part mechanically cooperate with each other to automatically adjust the maximal length such that the predefined tension is obtained regardless of the size of the body part.

Abstract: A device for supporting determination of return of spontaneous circulation, ROSC, during an associated cardiopulmonary resuscitation, CPR, procedure which is being performed on an associated patient. A sensor is used to sense a physiological signal of the patient. Frequency analysis of the signal is carried out to extract dominant fundamental frequency components in the signal. From this analysis it is possible to determine that there has been a potential ROSC.

Abstract: When measuring SpO2 in a patient, a nasal oximeter is inserted into the patient's nose and comprises a source pad (14) and a detector pad (18) that are positioned at a predetermined location on either side of the nasal septum. The source pad and detector pad are biased toward each other to provide a clamping force on the nasal septum sufficient to permit SpO2 measurement without causing tissue necrosis. Clamping force is supplied by means of a spring type device, an expandable material, or the like.

Abstract: A device for supporting determination of return of spontaneous circulation, ROSC, during an associated cardiopulmonary resuscitation, CPR, procedure which is being performed on an associated patient. A sensor is used to sense a physiological signal of the patient. Frequency analysis of the signal is carried out to extract dominant fundamental frequency components in the signal. From this analysis it is possible to determine that there has been a potential ROSC.

Abstract: The invention relates to a device configured for tracking e.g. the diastolic blood pressure in a patient. The device applies a pressure to a body part, e.g. by use of an inflatable cuff. By performing repeated and alternating pressure changes in the cuff a specific feature of a signal that relates to the diastolic blood pressure can be tracked and possibly measured.

Abstract: There is provided a device (100) and method for determining a total probability (Ptot) of Return of Spontaneous Circulation (ROSC) during an associated CPR procedure, which is being performed on an associated patient, comprising an input for receiving a set of photoplethysmograpy data (328, 330) having been obtained from the associated patient during the CPR procedure, and a processor (112) being arranged for carrying out one or more processes according to one or more predetermined algorithms (321, 322, 323, 324) so as to calculate the total probability (Ptot) of ROSC based on the one or more parameters, wherein the one or more processes are each, and/or in combination, being arranged for overcoming challenges derived from the CPR process, such as arbitrary signals not related to return of spontaneous circulation. In embodiments, the device and method relies on a plurality of processes in determining the total probability of ROSC.

Abstract: An optical source for guiding light to a target of a patient includes at least one light source configured to emit red light and infrared light. The at least one light source is embedded within a light-conducting sheet. A photodistributor is spaced from the at least one light source. The photodistributor includes a light-emitting surface and at least one light-receiving surface optically coupled to the light-conducting sheet. The photodistributor is configured to discharge at least a portion of the emitted red light and at least a portion of the emitted infrared light into a target.