A leadless wireless ECG measurement system for measuring of bio-potentials includes at least one multi-contact bio-potential electrode assembly adapted for attachment to the patient's body to measure ECG. A processing unit is configured to produce a transfer function which computes estimated long-lead ECG signals based on the measured short-lead ECG signals from the plurality of contact points. This invention describes calibration process of short-lead ECG with standard lead ECG without requiring use of lead wires, only using a flexibly moving body part (finger) to calibrate patch. The invention describes use of algorithms for biopotential signal separation from mixed sources. The invention describes use of signal separation for identification of abnormal signals and the localization of biopotential source tissue. This invention describes effective biopotential evoked potential stimulation. The invention also describes biopotential neutralization of undesired biopotential.

A sensor device is described that includes a dry electrode, a pressure sensor, and a communication apparatus. The dry electrode is configured to be placed adjacent to a belly of a pregnant patient. The pressure sensor is coupled to the dry electrode to sense pressure within the belly. The sensed pressure indicates counts of physiological activities of a fetus within the pregnant patient over a period of time. The communication apparatus is coupled to the pressure sensor and the dry electrode. The communication apparatus is configured to transmit data characterizing the counts of the plurality of physiological activities to a cloud computing server for generating an assessment of health of the fetus.

A sensor device is described that includes a dry electrode, a pressure sensor, and a communication apparatus. The dry electrode is configured to be placed adjacent to a belly of a pregnant patient. The pressure sensor is coupled to the dry electrode to sense pressure within the belly. The sensed pressure indicates counts of physiological activities of a fetus within the pregnant patient over a period of time. The communication apparatus is coupled to the pressure sensor and the dry electrode. The communication apparatus is configured to transmit data characterizing the counts of the plurality of physiological activities to a cloud computing server for generating an assessment of health of the fetus.

Described herein are systems and methods for contraction monitoring. For example, a system for contraction monitoring includes an electrode patch including at least two electrodes, and a sensor module configured to be connected to the electrode patch. In some embodiments, the sensor module includes a signal acquisition module, a signal processing module, a power management module, a sensor control module, and a memory module and/or a data transmission module. In some embodiments, a method for contraction monitoring includes measuring, using the signal acquisition module, bio-potential signals by providing at least two electrodes on the abdomen of a pregnant woman. In some embodiments, a method for contraction monitoring includes processing, using the signal processing module, the bio-potential signal to extract electrohysterogram signals, maternal electrocardiogram signals and fetus electrocardiogram signals, and processing, using the signal processing module, the individual signals to extract uterine contraction.

A seamless, smart fetal monitoring garment and methods of using thereof. The system includes a knitted or interwoven garment having a multiplicity of conductive textile electrodes for sensing maternal and fetal electrical vital signals. The maternal and fetal electrical vital signals are selected from a group including maternal heart rate, fetal heart rate and electromyogram (EMG) activities including uterine activities. The method includes wearing the garment, acquiring electrical mixed common, maternal and fetal vital signals from surface region of a pregnant woman, using the plurality of textile electrodes, optimally weighted summing-up the acquired signals, analyzing the summed-up signals to thereby extract the maternal signal and the fetal signal, including determining their heart rates, and including detecting health hazards and in some embodiments, including detecting a uterine contraction sequence suggesting the need to be hospitalized for birth giving.

The invention concerns a multi-electrode patch for abdominal electrophysiological detection. The patch has a flexible substrate interconnecting multiple electrodes and a module unit for removably engaging with an electronic readout device for detecting a maternal and/or fetal electrophysiological signal from the electrodes. The module has a mechanical module unit for removable mechanical engagement with a housing of the readout device, and an electrical module unit for making an electrical connection from the electrodes to the readout device. Engaging the patch with the readout device comprises engaging both the mechanical module unit and the electrical module unit. The patch may be flexible in a manner that allows variation in the relative positioning between the electrodes. The patch and/or electronic readout device may comprise a security device for communication of an authentication code.

An electrical stimulation and bio-potential measurement device is provided. The electrical stimulation and bio-potential measurement device comprises at least one electrode module which comes into contact with the scalp of a user, a current supply unit, connected to the at least one electrode module, for supplying a current to the at least one electrode module so that the at least one electrode module can apply electrical stimulation to the user, and a signal processing unit, connected to the at least one electrode module, for processing bio-potential signals detected by the at least one electrode module, wherein the current supply unit comprises at least one switch which is arranged between the at least one electrode module and a voltage source for supplying the current.

A trans-abdominal non-invasive fetal blood oxygen saturation detection device comprises a trans-abdominal fetal oximeter and a signal detection assembly connected to the trans-abdominal fetal oximeter. The trans-abdominal oximeter comprises a signal processing controller. The signal detection assembly comprises a light-emitting light source device and a light receiving device, wherein the light-emitting light source device, the light receiving device and a reference signal detection device are all connected to the signal processing controller. The light-emitting light source device irradiates two or more different wavelengths of light into the abdominal cavity of a pregnant woman. The light receiving device comprises a plurality of light receivers respectively placed at a plurality of different positions outside the abdominal cavity of the pregnant woman, and is configured to collect a plurality of optical signals related to the fetal blood oxygen saturation, which are scattered and reflected back from the abdominal cavity of the pregnant woman through the plurality of light receivers, synthesize the optical signals into an optical signal sum related to the fetal blood oxygen saturation and then output it to the signal processing controller, such that the intensity of the received optical signals is improved.

An electrode includes a cutaneous contact for sensing electrocardiogram signals from a pregnant human subject, the electrocardiogram signals containing fetal electrocardiogram signals; a connector in contact with the cutaneous contact for transmission of the electrocardiogram signals from the cutaneous contact to a destination; and a cushion including a cavity, the cushion configured such that the cavity faces the pregnant human subject when in use, the cutaneous contact being coupled to the cushion such that the cutaneous contact is positioned within the cavity, the cushion and the cutaneous contact configured to allow the cutaneous contact to be an electrical interface with skin of the subject when the electrode is in use, the cavity being configured to receive and retain therein an amount of a conductive wetting substance sufficient to provide a skin-electrode impedance of less than 150 k when the electrocardiogram signals are at frequencies of 10 Hz or less.

The present invention provides a medical electrode, which comprises an annular adhesive pad (203) to be attached to a living being, a conductive pad (205) disposed in the central hole (207) of the annular adhesive pad, a first conductive snap element (209), a conductive element (211) and a sealing film (213). The conductive element (211) is configured to establish electrical communication between the conductive pad (205) and the first conductive snap element (209) and the sealing film (213) is attached to the annular adhesive pad (203) and to fix at least a portion of the conductive element (211) between the annular adhesive pad (203) and the sealing film (213). The flexibility and/or length of the conductive element is chosen to be large enough so as to allow the first conductive snap element (209) to move without causing the conductive pad (205) to move, resulting in reliable electrical contact between the conductive pad and the skin of the living being.