A plethysmographic respiration processor is responsive to respiratory effects appearing on a blood volume waveform and the corresponding detected intensity waveform measured with an optical sensor at a blood perfused peripheral tissue site so as to provide a measurement of respiration rate. A preprocessor identifies a windowed pleth corresponding to a physiologically acceptable series of plethysmograph waveform pulses. Multiple processors derive different parameters responsive to particular respiratory effects on the windowed pleth. Decision logic determines a respiration rate based upon at least a portion of these parameters.

Embodiments described herein relate generally to biosensing garments, and in particular, to systems and methods for monitoring respiration in a biosensing garment, whereby an improved integration of the respiration monitoring circuit into the garment is achieved, resulting in improved signal quality and durability. In some embodiments, an apparatus includes an elongate member having a longitudinal axis and configured to be stretchable along its longitudinal axis. The elongate member includes a plurality of elastic members (e.g., a first elastic member, a second elastic member, and a third elastic member) that extend along the longitudinal axis. A conductive member is coupled to the first, second and third members, and forms a “curved” pattern along the longitudinal axis of the elongate member. The conductive member is configured to change from a first configuration to a second configuration as the elongate member stretches along its longitudinal axis.

The present disclosure relates to the field of medical monitoring, and, in particular, to non-contact detecting and monitoring of patient breathing. Systems, methods, and computer readable media are described for calculating a change in depth of regions in one or more regions of interest (ROI's) on a patient and assigning one or more visual indicators to the regions based on the calculated changes in depth of the regions over time. In some embodiments, one or more breathing parameter signals corresponding to the regions can be generated and/or analyzed. In these and other embodiments, the one or more visual indicators can be displayed overlaid onto the regions in real-time. In these and still other embodiments, the systems, methods, and/or computer readable media (i) can display one or more generated breathing parameter signals in real-time and/or (ii) can trigger an alert and/or an alarm when a breathing abnormality is detected.

The present invention provides a method of conducting a sleep analysis by collecting physiologic and kinetic data from a subject, preferably via a wireless in-home data acquisition system, while the subject attempts to sleep at home. The sleep analysis, including clinical and research sleep studies and cardiorespiratory studies, can be used in the diagnosis of sleeping disorders and other diseases or conditions with sleep signatures, such as Parkinson's, epilepsy, chronic heart failure, chronic obstructive pulmonary disorder, or other neurological, cardiac, pulmonary, or muscular disorders. The method of the present invention can also be used to determine if environmental factors at the subject's home are preventing restorative sleep.

Systems and methods for determining if a wearable photoplethysmography device is correctly positioned in operating to medical signs of a user by using a classifier to determine if a signal is valid or invalid. In some embodiments, in using the classifier to determine in a signal is valid or invalid, a lean method of linear computational complexity and minimal memory complexity is provided for determining at the wearable photoplethysmography device if it is correctly positioned. In some embodiments, in using the classifier minimal computational complexity is used in determining at the wearable photoplethysmography device if it is correctly positioned.

A swallowing medical device includes: an attachment unit configured to be attached to a target portion of a human body for a medical operation; a control unit configured to control the medical operation; and a storage configured to store use information regarding a use state over time of the attachment unit. The control unit executes a control for restricting use of the attachment unit on the basis of a fact that the use information does not satisfy a set condition for ensuring a characteristic of the attachment unit.

An apparatus and method for employing data from the person and from the environment where the person is situated facilitate the detection and prediction of severity of high altitude-induced Sleep Disordered Breathing (SDB, and specifically Central Sleep Apnea (CSA)). Longitudinal tracking of local barometric pressure and severity of SDB symptoms (objective or subjective or both) allow for prediction of occurrence of SDB (per altitude). Some of all of the data can be obtained from one or more wearable devices that may be worn by the person. Additionally, personalized mapping for dosing of medication (e.g. acetazolamide, low-flow oxygen therapy) to treat high altitude-induced SDB are provided, with recommended dosing provided to the person per altitude.

The present invention relates to a device, system and method for automatic and unobtrusive caloric intake detection. The device comprises a respiration input for obtaining a respiration signal indicating the subject's respiration, and an analysis unit for analyzing the obtained respiration signal in the frequency domain by determining one or more respiration signal features from the obtained respiration signal in the frequency domain related to changes in oxidation and by detecting changes of the one or more determined respiration signal features to detect periods of caloric intake by the subject.

The present invention provides a method of conducting a sleep analysis by collecting physiologic and kinetic data from a subject, preferably via a wireless in-home data acquisition system, while the subject attempts to sleep at home. The sleep analysis, including clinical and research sleep studies and cardiorespiratory studies, can be used in the diagnosis of sleeping disorders and other diseases or conditions with sleep signatures, such as Parkinson's, epilepsy, chronic heart failure, chronic obstructive pulmonary disorder, or other neurological, cardiac, pulmonary, or muscular disorders. The method of the present invention can also be used to determine if environmental factors at the subject's home are preventing restorative sleep.

A method of providing personalized PAP therapy recommendations to a patient includes: receiving in a controller patient information obtained from one or more electronic devices associated with the patient; analyzing the patient information with the controller; determining in the controller from the analyzing of the patient information personalized PAP therapy recommendations for the patient; and providing the personalized PAP therapy recommendations to the patient.