One aspect of the apparatus comprising, a sensor configured to acquire a biological signal of a user, and a controller configured to, determine whether the biological signal is continuously outside a predetermined range for a first time period, after determining that the biological signal has been continuously outside the predetermined range for the first time period, then determine whether the biological signal is inside the predetermined range, and activate an alarm if the controller has determined that (i) the biological signal has been outside the predetermined range for the first time period, and (ii) the biological signal has been continuously inside the predetermined range for a second time period, the second time period being longer than the first time period.

A system or a method for assisting an individual to acclimatize to hot environment prior to being exposed to the hot environment using a measured heart rate with or without a measured skin temperature and/or a measured body core temperature. A Physiological Strain Index (PSI) or adaptive PSI (aPSI) is calculated for the individual to provide a target for the individual's exertion level such that an area under the calculated PSI/aPSI curve is used to determine the amount of heat acclimatization that has occurred for that particular training session and/or prior training sessions.

A self-inflating personal flotation device (SIPFD) configured to be worn by a wearer and aid the wearer automatically. The SIPFD may communicate with a global communication network and pressurized gas cartridge assembly based on a triggering event. The SIPFD may have a wearable data transmitter of a heartbeat device; a water depth device; and a geolocation device. The SIPFD may have a neck inflation device and a torso inflation device both connected to the pressurized gas cartridge assembly to enable the pressurized gas cartridge to inflate the neck and torso inflation devices when prompted. The prompt may be automatic or on request and be performed using an actuator mechanically communicating with the pressurized gas cartridge assembly to: (i) inflate the neck and torso inflation devices; and (ii) deflate the neck and torso inflation devices associated with a wearer.

Technologies and implementations for wearable healthcare devices are generally disclosed. An example method performed by a wrist-wearable device includes: detecting, by a sensor, a physiological parameter of a user; determining, by a processor based on the physiological parameter, that the user is experiencing atrial fibrillation (AF); outputting, by a display, a visual signal indicating that the user is experiencing the AF; and transmitting, by a transceiver to a first external computing device, a first wireless signal indicating that the user experienced the AF.

A method of detecting abnormal heartbeats includes providing a library of abnormal beat synthesis (ABS) filters, wherein each ABS filter corresponds to a specific cause of a cardiac problem. The method further includes obtaining an ECG of a normal heartbeat of a person and applying an ABS filter from the library of ABS filters to the ECG of the normal heartbeat of the person to generate a potential abnormal ECG. The method further includes monitoring a heartbeat of the person and classifying each heartbeat as either normal or abnormal.

A method for determining and responding in real-time to an increased risk of death relating to a patient with epilepsy is provided. The method includes receiving cardiac data and determining a cardiac index based upon the cardiac data. The method includes determining an increased risk of death associated with epilepsy if the indices are extreme, issuing a warning of the increased risk of death and logging information related to the increased risk of death. Also presented is a second method for determining and responding in real-time to an increased risk of death relating to a patient with epilepsy comprising receiving at least one of arousal data, responsiveness data or awareness data and determining an arousal index, a responsiveness index or an awareness index, where the indices are based on arousal data, responsiveness data or awareness data respectively. The second method includes determining an increased risk of death related to epilepsy if indices are extreme values, issuing a warning of the increased risk of death and logging information related to the increased risk of death. A computer readable program storage device is also provided. Also provided is a method for receiving body data, determining a cardiac, an arousal, a responsiveness, or a kinetic index, determining an increased or increasing risk of death over a first time window relating to a patient with epilepsy and issuing a warning and logging relevant information.

The present specification discloses systems and methods of patient monitoring in which multiple sensors are used to detect physiological parameters and the data from those sensors are correlated to determine if an alarm should, or should not, be issued, thereby resulting in more precise alarms and fewer false alarms. Electrocardiogram readings can be combined with invasive blood pressure, non-invasive blood pressure, and/or pulse oximetry measurements to provide a more accurate picture of pulse activity and patient respiration. In addition, the monitoring system can also use an accelerometer or heart valve auscultation to further improve accuracy.

This disclosure provides a monitoring apparatus and a statistical display method for physiological parameter(s) thereof. The method may include receiving statistical setting information including a time range, a time interval, a classification rule, and a target parameter, and the classification rule may define one or more types of the target parameter; obtaining N group of target parameter result corresponding to N time interval from a result of historical physiological parameter, where the N time interval is included in the time range, and the N group of target parameter result may be a physiological parameter result corresponding to the target parameter in the result of historical physiological parameter; counting the number of each type of the target parameter in the N group of target parameter result according to the classification rule, and obtaining N group of statistical result corresponding to the N time interval for each target parameter

The present specification discloses systems and methods of patient monitoring in which multiple sensors are used to detect physiological parameters and the data from those sensors are correlated to determine if an alarm should, or should not, be issued, thereby resulting in more precise alarms and fewer false alarms. Electrocardiogram readings can be combined with invasive blood pressure, non-invasive blood pressure, and/or pulse oximetry measurements to provide a more accurate picture of pulse activity and patient respiration. In addition, the monitoring system can also use an accelerometer or heart valve auscultation to further improve accuracy.

Method and apparatus are disclosed for monitoring of steering wheel engagement for autonomous vehicles. An example vehicle includes an autonomy unit configured to perform autonomous motive functions, a steering wheel, capacitive sensors coupled to the steering wheel, a second sensor configured to monitor an operator, and a controller. The controller is configured to detect a first heart rate via the capacitive sensors, detect a second heart rate via the second sensor, identify that an engagement-imitating device is coupled to the steering wheel responsive to determining that the first heart rate does not correlate with the second heart rate, and emit an alert responsive to determining that the engagement-imitating device is coupled to the steering wheel.