The present invention relates to the field of medical monitoring, and in particular non-contact monitoring of one or more physiological parameters in a region of a patient during surgery. Systems, methods, and computer readable media are described for generating a pulsation field and/or a pulsation strength field of a region of interest (ROI) in a patient across a field of view of an image capture device, such as a video camera. The pulsation field and/or the pulsation strength field can be generated from changes in light intensities and/or colors of pixels in a video sequence captured by the image capture device. The pulsation field and/or the pulsation strength field can be combined with indocyanine green (ICG) information regarding ICG dye injected into the patient to identify sites where blood flow has decreased and/or ceased and that are at risk of hypoxia.

Disclosed herein are in vivo non-invasive methods and devices for the measurement of the hemodynamic parameters and aortic valve conformance and compliance in a subject. The method requires measuring the peripheral pulse volume waveform (PVW), the peripheral pulse pressure waveform (PPW), and the peripheral pulse velocity waveform (PUW) from the same artery using a non-invasive device. The waveforms PPW and PUW are used to calculate the waveform dPdU which is used to determine aortic valve ejection volume, closure volume, and quality factor, as well as stroke volume and cardiac output. The disclosed methods and devices are useful in the diagnosis and treatment of aortic valve disease, disorders, and dysfunction.

Disclosed herein are in vivo non-invasive methods and devices for the measurement of the hemodynamic parameters and aortic valve conformance and compliance in a subject. The method requires measuring the peripheral pulse volume waveform (PVW), the peripheral pulse pressure waveform (PPW), and the peripheral pulse velocity waveform (PUW) from the same artery using a non-invasive device. The waveforms PPW and PUW are used to calculate the waveform dPdU which is used to determine aortic valve ejection volume, closure volume, and quality factor, as well as stroke volume and cardiac output. The disclosed methods and devices are useful in the diagnosis and treatment of aortic valve disease, disorders, and dysfunction.

A probe with a blood circulation sensor and a force or pressure sensor is placed against a patient. One part of the probe applies a force to another part of the probe which is pressed against the patient at one or more locations. The variation of a measure of blood circulation is recorded as a function of the applied pressure, thereby giving the operator a specific knowledge of the Tissue Perfusion Pressure (TPP), a measure of circulatory health, at each location.

A probe with a blood circulation sensor and a force or pressure sensor is placed against a patient. One part of the probe applies a force to another part of the probe which is pressed against the patient at one or more locations. The variation of a measure of blood circulation is recorded as a function of the applied pressure, thereby giving the operator a specific knowledge of the Tissue Perfusion Pressure (TPP), a measure of circulatory health, at each location.

A wearable device for detecting and/or measuring physiological information from a subject includes a housing, at least one optical emitter supported by the housing, at least one optical detector supported by the housing, a first light guide supported by the housing, a second light guide supported by the housing, a motion sensor supported by the housing, and a processor supported by the housing. The processor is configured to calculate footsteps, distinguish footsteps from heart beats, and to remove footstep motion artifacts from signals produced by the at least one optical detector. Also, the processor is configured to process signals produced by the at least one optical detector to determine subject heart rate and to produce integrity data about the subject heart rate. The process is further configured to generate a multiplexed output serial data string comprising the subject heart rate and the integrity data.

A wearable device for detecting and/or measuring physiological information from a subject includes a housing, at least one optical emitter supported by the housing, at least one optical detector supported by the housing, a first light guide supported by the housing, a second light guide supported by the housing, a motion sensor supported by the housing, and a processor supported by the housing. The processor is configured to calculate footsteps, distinguish footsteps from heart beats, and to remove footstep motion artifacts from signals produced by the at least one optical detector. Also, the processor is configured to process signals produced by the at least one optical detector to determine subject heart rate and to produce integrity data about the subject heart rate. The process is further configured to generate a multiplexed output serial data string comprising the subject heart rate and the integrity data.

A system (1) for estimating the brain blood volume and/or brain blood flow and/or depth of anesthesia of a patient, comprises at least one excitation electrode (110E) to be placed on the head (20) of a patient (2) for applying an excitation signal, at least one sensing electrode (110S) to be placed on the head (20) of the patient (2) for sensing a measurement signal caused by the excitation signal, and a processor device (12) for processing said measurement signal (VC) sensed by the at least one sensing electrode (110S) for determining an output indicative of the brain blood volume and/or the brain blood flow. Herein, the processor device (12) is constituted to reduce noise in the measurement signal (VC) by applying a non-linear noise-reduction algorithm. In this way a system for estimating the brain blood volume and/or the brain blood flow of a patient is provided which may lead to an increased accuracy and hence more exact estimates.

A blood pressure estimation device includes a display unit (10), a belt portion (20), a first contact electrode (61) and a second contact electrode (62) for detecting an electrocardiographic waveform, and a pulse wave sensor. The display unit (10) displays a blood pressure estimation result. The belt portion (20) is connected to the display unit (10) and surrounds a target measurement site. The pulse wave sensor includes a pulse wave detection unit (40E) that detects a pulse wave of an artery (91) passing through the target measurement site. The first contact electrode (61) and the pulse wave detection unit (40E) are provided on an inner circumferential portion (20a) of the belt portion (20). The second contact electrode (62) is provided on an outer circumferential portion (20b) of the belt portion (20). The first contact electrode (61) and the pulse wave detection unit (40E) are provided in a position where the first contact electrode (61) and the pulse wave detection unit (40E) are to be pressed against the target measurement site when the second contact electrode (62) is pressed from an outer circumferential side of the belt portion (20).

A blood pressure estimation device includes a display unit (10), a belt portion (20), a first contact electrode (61) and a second contact electrode (62) for detecting an electrocardiographic waveform, and a pulse wave sensor. The display unit (10) displays a blood pressure estimation result. The belt portion (20) is connected to the display unit (10) and surrounds a target measurement site. The pulse wave sensor includes a pulse wave detection unit (40E) that detects a pulse wave of an artery (91) passing through the target measurement site. The first contact electrode (61) and the pulse wave detection unit (40E) are provided on an inner circumferential portion (20a) of the belt portion (20). The second contact electrode (62) is provided on an outer circumferential portion (20b) of the belt portion (20). The first contact electrode (61) and the pulse wave detection unit (40E) are provided in a position where the first contact electrode (61) and the pulse wave detection unit (40E) are to be pressed against the target measurement site when the second contact electrode (62) is pressed from an outer circumferential side of the belt portion (20).