A system, computer program product and method for facilitating concurrent monitoring of multiple obstetrics patients over a data network are proposed. Data conveying pregnancy progression information, including maternal and fetal vital sign information associated with the obstetrics patients, is received and processed to derive criticality levels for the obstetrics patients. As a first feature, notification data related to a particular obstetrics patient may be selectively transmitted to a medical expert based on different conditions including for example an associated criticality level exceeding a threshold and/or receipt of a consultation request. As a second feature, used together or separately from the first, a graphical user interface (GUI) may present a user with an ordered list of obstetrics patients dynamically adaptable based on the criticality levels. The GUI allows a user to select an obstetrics patient from the list and then adapts the GUI to present an expanded set of pregnancy progression information related to the selected obstetrics patient. Optionally, the GUI may also provide a tool allowing the user to cause a notification to be transmitted to a medical expert over the data network.

There is provided a system of transmitting partograph information and analyzing the same comprising a client device adapted to receive partograph information as inputs; the inputs transmittable to a partograph processing server via a wireless communication network; wherein the partograph processing server is configured to receive the partograph information; conform the partograph information to a standardized format and disseminate the partograph information to at least one computer device. Preferably, the partograph processing server further comprises an analyzer to analyze the partograph information for one or more abnormality condition and provides an alert to the at least one computer device and the client device. Alternatively, the analyzer is installed in the client device in the form of a software application.

An infrasonic stethoscope for monitoring physiological processes of a patient includes a microphone capable of detecting acoustic signals in the audible frequency bandwidth and in the infrasonic bandwidth (0.03 to 1000 Hertz), a body coupler attached to the body at a first opening in the microphone, a flexible tube attached to the body at a second opening in the microphone, and an earpiece attached to the flexible tube. The body coupler is capable of engagement with a patient to transmit sounds from the person, to the microphone and then to the earpiece.

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.

There is provided a device (100) for placement on the abdomen (102) of a subject to measure uterine contractions of the subject and a fetal heart rate. The device (100) comprises a rigid base (104) for placement on the abdomen (102) of the subject and a cover (106) configured to connect to the rigid base (104). The cover (106) comprises a flexible portion moveable in response to uterine contractions of the subject. The device (100) further comprises a fetal heart rate sensor (108) mounted on the rigid base (104) and configured to measure the fetal heart rate. The device (100) also comprises a uterine contractions sensor (110) located within the device (100) and configured to measure the uterine contractions of the subject.

One aspect of the invention provides a fetal pulse oximeter including: a shape-memory member adapted and configured to expand outward and define a loop when advanced out of a cannula; one or more light sources mounted on the shape memory member and facing toward a center of the loop, the one or more light sources adapted and configured to generate red and infrared light; and a photodiode mounted on the shape memory member and facing toward a center of the loop. Another aspect of the invention provides a method for measuring recording pulse and blood oxygen saturation. The method includes: advancing the fetal pulse oximeter as described herein out of a cannula within a placenta; allowing the shape-memory member to expand outward; and placing the loop over a limb.

An apparatus for monitoring an obstetrics patient during labour is provided. The apparatus receives a contraction signal conveying information related to occurrences of uterine contractions over time and processes his signal to derive a sequence of rates of uterine contractions over time. The apparatus also implements a Graphical User Interface (GUI) presenting a tracing of at least part of the sequence of rates of uterine contractions over time along with a threshold rate of uterine contractions GUI is dynamically adapted over time based on the contraction signal received. The sequence of rates of uterine contractions derived over time is also processed to detect occurrences of anomalous contraction rates and to identify one or more portions of the tracing corresponding to sustained anomalous contraction rate segments during which anomalous contraction rates have persisted for time durations exceeding a pre-determined time duration. The GUI is configured to trigger an alarm event in response to identification of a specific sustained anomalous contraction rate segment.

A system for monitoring fetal health data and mother health data comprises a belly-covering garment that is configured to at least partially cover a belly and to hold one or more sensor modules directly adjacent to the belly. One or more sensor modules disposed within the belly-covering garment. The one or more sensor modules comprise a pulse-oximeter sensor that gathers pulse oximetry data from the mother through contact with the belly. The one or more sensor modules also comprise an accelerometer sensor that gathers movement data from the mother. Additionally, the one or more sensor modules comprise a fetal sensor that gathers health data from a fetus within the belly.

Systems, methods, and computer-readable media are provided for displaying on a user display device alarm-triggering events detected by the medical device based on the location of the user display device. The method comprises receiving alarm-triggering patient data from a medical device and determining the physical location of first and second user display devices. The method further comprises determining that the physical location of the first user display device is designated to have an alarm displayed, and that the physical location of the second user display device is not designated to have an alarm displayed. In response to these determinations, the content of the alarm is displayed on the first user display device.

A system, computer program product and method for facilitating concurrent monitoring of multiple obstetrics patients over a data network are proposed. Data conveying pregnancy progression information, including maternal and fetal vital sign information associated with the obstetrics patients, is received and processed to derive criticality levels for the obstetrics patients. As a first feature, notification data related to a particular obstetrics patient may be selectively transmitted to a medical expert based on different conditions including for example an associated criticality level exceeding a threshold and/or receipt of a consultation request. As a second feature, used together or separately from the first, a graphical user interface (GUI) may present a user with an ordered list of obstetrics patients dynamically adaptable based on the criticality levels. The GUI allows a user to select an obstetrics patient from the list and then adapts the GUI to present an expanded set of pregnancy progression information related to the selected obstetrics patient. Optionally, the GUI may also provide a tool allowing the user to cause a notification to be transmitted to a medical expert over the data network.