A wearable device and the accompanying method for the determination of continuous pulsatile BP are described. The absolute values can be obtained in the initial phase and how a transfer function can transform the BP-signal obtain at the finger or wrist to correct BP-values corresponding to the brachial artery and at heart level. The wearable device contains an orthostatic level-correcting element, which can measure the vertical distance between heart level and finger/wrist level, where the actual measurement takes places. The wearable device may be in the form of a ring, a watch, or a bracelet. Further, the wearable device has elements for wirelessly transmitting signals to host devices such as a smart phone, tablet or other computers.

A health monitoring device is provided. The health monitoring device includes a wearable component, an optical monitoring module and an air-bag positioning assembly. The wearable component is worn on a body part of a subject and is contacted with a skin tissue. The optical monitoring module is disposed inside the wearable component and includes a driving controller, an optical sensor and at least one light-emitting element. A light source emitted by the light-emitting element irradiates on the skin tissue. The optical sensor receives a reflection light and generates a sensing signal accordingly. The driving controller converts the sensing signal into health data information and outputs the health data information. By the air-bag positioning assembly, the wearable component is securely worn on the body part of the subject, and the optical sensor is attached on the skin tissue of the subject for accurately monitoring the health data information.

The invention relates to a method and a measuring device for continuously non-invasively determining at least one cardiovascular parameter, preferably the arterial blood pressure, at an extremity containing an artery, the measuring device comprising a receiving element that can be attached to the extremity and is suited to at least partly surround the extremity, and comprising a flexible bubble which is supported on the receiving element, acts on the extremity and is filled with a fluid. According to the invention, an actuator which is suited to vary the pressure in the flexible bubble is placed in or on the receiving element, and the flexible bubble includes a pressure sensor which is in contact with the fluid in the flexible bubble and which is suited to continuously measure the absolute pressure value. The measuring device further comprises a unit suited to measure the pulsations generated by the volume flow in the artery, and a control unit having two different modes of operation, i.e. a measuring phase and an interpolation phase.

A pulse wave signal expressing a pulse is obtained by detecting a pulse of a measurement subject using a pulse wave sensor. The pulse wave signal is stored in a storage unit. A frequency spectrum of the pulse wave signal is found by converting the time-domain pulse wave signal stored in the storage unit into the frequency domain. It is determined whether or not the measurement subject is at rest by finding a frequency range, within a predetermined total frequency range the pulse rate of a person can take on, in which an intensity of a frequency component of the frequency spectrum exceeds a first threshold, and finding whether or not a ratio of the frequency range with respect to the total frequency range is less than a second threshold. A pulse rate from the point in time when the measurement subject has been determined to be at rest is found as the measurement subject's at-rest pulse rate.

A time-resolved measurement of blood pressure, arterial elasticity, pulse wave, pulse wave transit time and pulse wave velocity, a cardiac output, and/or changes in cardiac output of a human or animal body, using a pressure sensor unit while being pressed against the skin. The unit is an air and/or gas pressure sensor, and is configured to change at least one electrical conductance and/or resistance when subjected to pressure. The unit has at least two conductor trace arrays, particularly conductor trace networks, and a functional polymer that is compressed when subjected to pressure, and produces and/or alters contact between the conductor trace arrays. Alternatively, the unit has at least two conductive layers with a gap therebetween, and is configured such that the gap becomes compressed when subjected to pressure, and/or such that the capacitance of the assembly composed of the two conductive layers is changed as a result.

The present invention relates to wearable devices for monitoring of vital signs. More specifically, the present invention relates to a one-piece wearable device for mounting on the upper arm of the patient and monitoring of multi-parameter vital signs without any attached cable.

In one implementation, a multi-vital-sign smartphone system detects multiple vital signs from sensors such as a digital infrared sensor, a photoplethysmogram (PPG) sensor and at least one micro dynamic light scattering (mDLS) sensor, and thereafter in some implementations the vital signs are transmitted to, and stored by, an electronic medical record system.

A expandable multi-physiological parameter monitoring ring, comprising a microprocessor module (1) and an internal sensor module (3) connected to the microprocessor module (1), and further comprising an external module interface (4) detachably connected to the microprocessor module (1) and used for connecting an external sensor module (5). The microprocessor module (1) is configured to: when the external module interface (4) is connected to the external sensor module (5), obtain measurement signals from the external sensor module (5) and the internal sensor module (3), and process the measurement signals to obtain a difference between a measurement signal of the external sensor module (5) and a measurement signal of the internal sensor module (3); and when the external module interface (4) is not connected to the external sensor module (5), calibrate, according to the difference, a physiological parameter obtained by the internal sensor module (3). The monitoring ring can improve accuracy of physiological parameter measurement at a fingertip, and can implement low load, portability, and comfort.

A method of detecting atrial fibrillation includes detecting a pulse signal to obtain a time pulse waveform and converting it to an energy spectrum waveform via Fast Fourier Transform. The energy spectrum waveform includes a first frequency region, a second frequency region, and a third frequency region. The number of spikes in each frequency region was calculated and the heart indexes of the first, second, and third frequency regions were obtained, which were the first heart index, the second heart index, and the third heart index. And by the sum of the three heart index values and the first heart index to determine the possibility of atrial fibrillation. An apparatus for detecting atrial fibrillation is also provided, whereby the user can determine the possibility and predicting atrial fibrillation by simple measurement of blood pressure at home.

A light emitting unit emits first light and second light having different wavelengths. A photoreception unit outputs first and second signals depending on photoreception intensities of the first and second light transmitted through or reflected by biological tissue. A processing period setting unit extracts a signal cycle corresponding to the cardiac cycle for the first or second signal and sets a processing period in a first part dominantly affected by arterial blood flowing to the tissue or a second part dominantly affected by venous blood flowing from the tissue in the signal cycle. First and second change amount acquisition units obtain first and second change amounts corresponding to the attenuation change amounts of the first and second light from the first and second signals in the processing period. A concentration calculation unit calculates the concentration of light absorbing substance in blood from the first and second change amounts.