Technology facilitates dynamic variability of head impact data recordal, for example, in the context of instrumented mouthguard devices. Some embodiments have been developed to facilitate an event recoding protocol that dynamically adjusts event recoding parameters thereby to provide appropriate data for both “short” and “prolonged” impact events. For example, various embodiments include methods for recording impact events in respect of an instrumented mouthguard device, such methods including dynamically adjusting a period of time for which event data is recorded for a given event responsive to length of time for which an over-threshold condition persists.

Technologies and implementations for a wearable healthcare system, which may be worn by a person. The wearable healthcare systems may include one or more motion sensors. A motion analysis modules may be included in the wearable healthcare system, which may be configured to determine physical activities and intensity of the physical activities of the person.

A method for time-synchronizing waveforms from different patient monitors that does not require devices to have high-precision synchronized clocks or to be coupled to a triggering synchronization signal generator. Comparable signals may be obtained from different devices either by placing selected sensors from the devices in the same locations, or by filtering signals from one device to obtain a signal comparable to signals from another device. Filtering may for example transform waveforms into independent components and identify a component that matches a signal from another device. The comparable signals may then be transformed into frequency variation curves, such as time intervals between peak values, to facilitate detection of the time shift between the signals. Cross correlation of the frequency variation curves may be used to locate the precise time shift between the signals. Use of frequency variation curves may be more robust than directly comparing and correlating the original signals.

Apparatus and methods are described including identifying that a subject suffers from sleep apnea. Positive airway pressure (PAP) is applied to the subject via a mask placed on a face of the subject. A respiratory-related parameter of the subject is sensed, while the mask is on the face of the subject, and a need of the subject for respiratory support is assessed, responsively to the respiratory-related parameter. In accordance with the assessed need, the mask is configured to regulate the PAP provided to the subject's face. Other applications are also described.

An apparatus that includes a partial power source including a first material and a second material, the partial power source configured to generate, upon contact with a conducting medium, a potential difference between the first material and the second material to provide power to a control device, and generate, using the first material and the second material, a current flow within the conducting medium, the current flow including information encoded based on a variable conductance between the first material and the second material.

An apparatus including a main processing unit. The apparatus further including a precordial patch coupled to the main processing unit, the precordial patch having a plurality of sensors for detecting heart sounds and cardiac electrical signals (ECG). The apparatus further including a probe coupled to the main processing unit, the probe having a sensor for detecting oxygen saturation of blood circulating through a human. A method is further described including simultaneously measuring and analyzing heart sounds, cardiac electrical signals (ECG) and oxygen saturation of blood circulating through a human. The method further includes performing an algorithm to determine the presence of a significant congenital heart disease and displaying management recommendations based on results of the algorithm.

Methods and Devices to monitor the level of at least one analyte are provided.

Systems and methods described provide dynamic and intelligent ways to change the required level of user interaction during use of a monitoring device. The systems and methods generally relate to real time switching between a first or initial mode of user interaction and a second or new mode of user interaction. In some cases, the switching will be automatic and transparent to the user, and in other cases user notification may occur. The mode switching generally affects the user’s interaction with the device, and not just internal processing. The mode switching may relate to calibration modes, data transmission modes, control modes, or the like.

A method and system are disclosed for use in monitoring/screening/diagnosing sleep or wake state of a subject or patient. The method generally includes monitoring the patient's activity during one or more sleep sessions comprising a plurality of intervals known as epochs. The sleep/wake state of the subject is determined during each epoch of the session using actigraphy data obtained during the monitoring session. The actigraphy data provides information about the activity of a patient during an epoch. The sleep or wake state is determined based on a ratio of the activity count during an epoch to the activity count during a preceding epoch. If the ratio is greater than a first activity threshold, then a “wake” indication may be provided by, for example, the system. Alternatively, or additionally, a “wake” indication may be determined if the activity count during the epoch is greater than a threshold.

A system for monitoring medical conditions including pressure ulcers, pressure-induced ischemia and related medical conditions comprises at least one sensor adapted to detect one or more patient characteristic including at least position, orientation, temperature, acceleration, moisture, resistance, stress, heart rate, respiration rate, and blood oxygenation, a host for processing the data received from the sensors together with historical patient data to develop an assessment of patient condition and suggested course of treatment, including either suspending or adjusting turn schedule based on various types of patient movement. Compliance with Head-of-Bed protocols can also be performed based on actual patient position instead of being inferred from bed elevation angle. The sensor can include bi-axial or tri-axial accelerometers, as well as resistive, inductive, capacitive, magnetic and other sensing devices, depending on whether the sensor is located on the patient or the support surface, and for what purpose.