A vaginal ring sensor device adapted to be placed within the vaginal vault of a user, the device including a ring body, at least one through hole that passes through the ring body, and at least one biosensor structured and arranged to sense and/or measure a parameter of vaginal fluid as such fluid passes through the at least one through hole.

The present disclosure relates to a maternal monitoring transducer (20), comprising a housing (60), a substrate board (72), particularly a PCB (70), disposed in the housing (60) and comprising control components (74), and a displacement measurement arrangement (76) comprising a displacement-sensitive structure (78) that is arranged to detect deformations of a deflectable measurement section (80) of the substrate board (72), wherein the maternal monitoring transducer (20) supplies a signal that is representative of maternal motion. The disclosure further relates to a method of operating a maternal monitoring transducer (20).

A micro-device and system for monitoring cervical tissue includes micro-circuitry for simulating electrochemical impedance spectroscopy and a system for monitoring the physiological condition of the cervical tissue.

A system and method for monitoring a plurality of parameters of a user that includes receiving the plurality of parameters of the user from a vital signs recording device, identifying at least one abnormal value based on at least one parameter of the plurality of parameters, the at least one parameter being at least one of below a normal range and above a normal range, sending at least one alarm based on the at least one abnormal value to a remote facility, and displaying the at least one alarm continuously on a display device in the remote facility on a condition that the at least one parameter is at least one of below the normal range and above the normal range.

A vaginal ring sensor device adapted to be placed within the vaginal vault of a user, the device including a ring body, at least one through hole that passes through the ring body, and at least one biosensor structured and arranged to sense and/or measure a parameter of vaginal fluid as such fluid passes through the at least one through hole.

A decision support tool is provided for predicting the neonatal vitality scores of a fetus during delivery, the scores being an indicator of future health for the infant anticipated to be born within a future time interval, measured as time to birth. The predicted neonatal vitality score is determined from measurements of physiological variables monitored during labor, such as uterine activity and fetal heart rate. Fetal heart rate variability and patterns may be detected and computed using the monitored physiological variables, and neonatal vitality scores may be predicted based, at least in part, on the variability metrics and fetal heart rate patterns. Scores may be predicted for different delivery methods, such as vaginal delivery or cesarean delivery, for different time-to-birth intervals. In this way, these scores may be used for decision support for care plans during labor, such as increased monitoring and/or modifying the delivery type.

A system for monitoring a fetus in a pregnant woman, and/or the maternal health risk for pregnancies complicated by such as pre-eclampsia and hypertensive disorders is configured to be worn by the pregnant woman, preferably so as to allow monitoring during daily life, e.g. in the form of an adhesive patch. The unit has a sound sensor, e.g. a microphone or accelerometer, to be positioned on the skin of the abdominal area so as to detect a vascular sound from umbilical arteries of the fetus or from the uterine arteries of the pregnant woman. The sound sensor is functionally connected to a processing unit which executes a processing algorithm on the captured vascular sound and extracts a signal parameter accordingly. The processing unit then communicates the signal parameter, e.g. using an audio signal, a visual display or by means of a wired or a wireless data signal.

A apparatus for automatically detecting a pregnancy status of a patient include a patch for adhering to human skin, a uterine contraction sensor, such as electromyography (EMG), coupled to the patch with at least two electrodes, and an inertial sensor for sensing fetal movement, or Fetal Heart Rate (FHR) sensor, such as Fetal EKG or a Doppler Ultrasound. An electronic circuit is coupled to the patch, the EMG sensor and the inertial sensor, and/or FHR sensor. The circuit provides an output based on a uterine contraction signal from the EMG sensor (or Doppler ultrasound) correlated in time to a fetal movement, and/or fetal heart rate. The apparatus may include a thermometer to aid in automatically providing an indication of a pregnancy complication or ovulation status of the patient, based on the output.

The present invention relates to a pregnancy monitoring system, the system comprising a fetal monitoring transducer (20) arranged to detect fetal medical condition information; and a control device (48) comprising a motion assessment unit (50) and a signal output unit (52); wherein the fetal monitoring transducer (20) is arranged to detect fetal movement indicative information, wherein the motion assessment unit (50) is arranged to process fetal movement grading information, in addition to the fetal movement indicative information, wherein the signal output unit (52) is arranged to simultaneously output a fetal condition signal, particularly a fetal heart rate signal, and an augmented fetal movement signal based on the fetal movement indicative information and the fetal movement grading information, wherein a characteristic property of the original fetal movement information is still present in the augmented fetal movement signal. The disclosure further relates to a corresponding pregnancy monitoring method.

Sensor-based systems, devices, and methods are disclosed for monitoring for an aortocaval compression condition in a pregnant woman. A sensor device may be secured directly or indirectly to the woman, which may collect various sensor data related to the woman and/or the fetus. The device may determine a physical orientation of the woman (e.g., upright and/or lateral tilt angles of the woman) and/or biometric parameter(s) of the woman and/or fetus based on the collected sensor data, identify an aortocaval compression condition based on the determined orientation of the woman and/or biometric parameter(s) of the woman and/or fetus, and generate a repositioning alert via an alert mechanism. The disclosed concepts may be implemented, for example, as a personal home-use device, or as a broader system in a hospital or other medical facility, e.g., for monitoring and displaying aortocaval compression related information for multiple patients and/or facilitating patient turn protocols.