An oximetry device sealed in a sheath directs a user to allow the oximetry device to make oximetry readings at a number of different tissue locations of a patient and average two or more of the oximetry readings by directing the lifts and placements of the oximetry device and sheath to and from the different tissue locations and detecting the lift and placements. The averages are generated and displayed on a display of the device for the oximetry readings if the lifts are made while use directions for the lifts are displayed on a display of the oximetry device. The averages are not generated if the lifts are not made while the user directions for the lifts are not displayed. The averages are simultaneously displayed with the oximetry readings which are instantaneous measurement for patient tissue.

A system for evaluating a cardiac pumping function includes an oximeter which is attached to a patient for the purpose of recording a pulse oximeter waveform. A computer is connected to the oximeter to receive metric information from the waveform. With this information, the computer determines the value and location of a second derivative acceleration, d.sup.2A/dt.sup.2 in the waveform, which indicates the rate of rise/fall of the waveform. A comparator in the computer then compares this with the value and location of maximum second derivative acceleration, d.sup.2A/dt.sup.2, in earlier waveforms. With this comparison, the computer identifies a trend which can be clinically used to evaluate the efficacy of a cardiac pumping function.

The invention provides a body-worn system that continuously measures pulse oximetry and blood pressure, along with motion, posture, and activity level, from an ambulatory patient. The system features an oximetry probe that comfortably clips to the base of the patient's thumb, thereby freeing up their fingers for conventional activities in a hospital, such as reading and eating. The probe secures to the thumb and measures time-dependent signals corresponding to LEDs operating near 660 and 905 nm. Analog versions of these signals pass through a low-profile cable to a wrist-worn transceiver that encloses a processing unit. Also within the wrist-worn transceiver is an accelerometer, a wireless system that sends information through a network to a remote receiver, e.g. a computer located in a central nursing station.

An electrocardiography monitor is provided. A sealed housing includes one end wider than an opposite end of the sealed housing. Electronic circuitry is provided within the sealed housing. The electronic circuitry includes an electrographic front end circuit to sense electrocardiographic signals and a micro-controller interfaced to the electrocardiographic front end circuit to sample the electrocardiographic signals. A buzzer within the housing outputs feedback to a wearer of the sealed housing.

This relates to one or more integrated photodiodes on a back surface of a PPG device. The one or more integrated photodiodes can reduce the gap between one or more windows and the active area of the photodiode(s) to increase the PPG signal strength without affecting the depth of light penetration into skin tissue. In some examples, the photodiode stackup can contact the surface of the windows. In some examples, the photodiode stackups can exclude a separate substrate. In some examples, the photodiode stackup can be deposited on the inner surface of the windows opposite the outer surface of the device. In some examples, the photodiode stackup can be deposited on the back surface and/or outer surface of the device. In this manner, PPG sensors can be included in the device without the need for extra layers and measurement accuracy can be improved due to lower light loss.

The present invention relates to a device (100), system (500) and method for determining SpO2 (160) of a subject. Two types of PPG measurements, widefield PPG with a homogenous illumination and/or a spot pattern and radial PPG with a spot illumination, are used to quantify the discrepancy in penetration depths for electromagnetic radiation in the red spectral range and infrared spectral range. This discrepancy in penetration depth is then used to find a more stable ratio signals of ratios, RR, and thus a more accurate SpO2 (160).

A measurement device is provided that has a contact surface that comes into contact with a measurement portion of a living body. The measurement device includes a biosensor disposed on the contact surface and has a detection surface that acquires biological information. Moreover, a suction portion is provided that sucks the living body from one or multiple suction holes provided in the contact surface on a periphery of the detection surface of the biosensor.

A blood pressure monitor configured to removably mount to a cuff in a substantially symmetrical position with respect to a width of the cuff can include a housing defining an interior, a first port, and a second port. The first port can: secure to a first prong of the cuff when the cuff is mounted in a first orientation; receive and secure to a second prong of the cuff when the cuff is mounted in a second orientation; and enable fluid communication between the interior and at least one of a first fluid passage within the first prong and a second fluid passage within the second prong. The second port can: secure to the second prong of the cuff when the cuff is mounted in the first orientation; and receive and secure to the first prong of the cuff when the cuff is mounted in the second orientation.

Vision-based stimulus monitoring and response systems and methods are presented, wherein detection, via image(s) of a patient through an external stimulus, such as a caregiver, prompts analysis of the response of the patient, via secondary patient sensors or via analysis of patient image(s), to determine an autonomic nervous system (ANS) state.

A device for improving cognitive and functional capabilities by means of hypoxic and hyperoxic gas mixtures. An air splitter (5) separates oxygen and nitrogen and feeds these gases to a mixer (4), whose mixing rate is determined by feed back from a bio feedback regulator and an oximeter. The oximeter is connected to a finger piece sensor or pulse meter, and/or an ear-piece sensor for receiving inpute from a patient. The gas mixer feeds an adjusted oxygen and nitrogen mixture to the patient by way of a mouthpiece connected to the mixer.