A patient monitoring system includes: a biomedical sensor including: a transducer configured to produce a signal corresponding to a biological function; a sensor converter configured to convert the signal to a converted signal; and a transmitter configured to produce a communication, based on the converted signal, that is indicative of one or more values of the biological function, and to send the communication wirelessly; and a base station including: a receiver configured to receive the communication wirelessly and to produce a receiver output signal; a base station interface configured to produce a base station output signal indicative of the one or more values of the biological function; and at least one output port to receive the base station output signal and configured to be hard-wire connected to a display that is configured to display information indicative of the biological function.

Photoacoustic and/or acousto-optical techniques may be used to transabdominally perform fetal oximetry and/or trans-abdominal fetal pulse oximetry. In some cases, a composite acoustic signal that has emanated from an abdomen of a pregnant mammal may be received by a processor from, for example, an ultrasonic detector and/or microphone positioned on, or near, a pregnant mammal's abdomen and the composite acoustic signal may result from an optical signal incident on the pregnant mammal's abdomen and a fetus contained therein. A portion of the composite acoustic signal that was incident on the fetus may be isolated from the composite acoustic signal and then analyzed to determine a fetal hemoglobin oxygen saturation level and/or a fetal tissue oxygen saturation level.

A detection probe and a fetal monitor. The detection probe comprises a probe body (2) and a mounting structure (1), detachably mounted on the probe body (2) and having a heart rate sensor for heart rate detection, a socket (4) for data transmission, and a lead line (5) for connecting the heart rate sensor and the socket (4) arranged thereon. A variety of functions can be achieved by means of a single detection device and thus the degree of integration is high; moreover, when the heart rate sensor is failed or aged, because the mounting structure (1) can be separated from the probe body (2), it is only necessary to repair and replace a corresponding part, so that the maintenance is convenient and the cost is reduced. Furthermore, the mounting structure (1) can also product the probe body (2) to some extent, and thus the anti-dropping capability of the detection probe is improved.

An endoscope includes an insertion portion including a distal end portion in which an image pickup unit is disposed, the insertion portion being configured to be inserted into an organ of a subject, an operation portion disposed at a proximal end of the insertion portion, and a sensor disposed in the operation portion, the sensor being configured to detect a pressure of a fluid in a flow passage passing through from the operation portion to a first opening of the distal end portion, the flow passage being configured to allow the fluid flowed into the operation portion to be flowed out from the first opening.

In part, the disclosure relates to a safety monitor and related methods to evaluate and manage intrapartum uterine contractions induced or augmented by Pitocin or other contraction inducing agents. The systems and methods include measuring a contraction parameter that may include one or more of frequency, strength, and duration of uterine contractions through a measurement device connected to a monitor. The systems and methods are programmed to stop the pump-based administration of a contraction inducing agent. Various lock out protocols and control over the ability to re-start a given pump are also described herein.

The present invention provides a method for monitoring the actual pressure exerted by the interior wall of a biological channel at different locations along the length of said biological channel. The method comprises: i) introducing into the lumen of the biological channel a device comprising an elongated tube and at least two expandable means located at a predetermined distance on said elongated tube; ii) inflating each of the expandable means to its contact pressure (Pc); and iii) measuring the internal pressure in each expandable means, wherein when said internal pressure is greater than Pc, the actual pressure exerted by the interior wall of the biological channel is equal to the difference between said internal pressure and Pc.

A sensor interface system for providing a connection between at least one sensor and a maternal-fetal monitor, wherein the interface system converts electrical muscle activity captured by the sensor(s) into uterine activity data signals for use by the maternal-fetal monitor. The sensor interface system of the invention preferably includes a conversion means for converting the signals from the sensor(s) into signals similar to those produced by a tocodynamometer.

A method of determining a pressure of a body cavity with a controller of a fluid management system includes determining a pressure and a volume of a cuff disposed about a collapsible bag, determining a volume of the collapsible bag based on the pressure and the volume of the cuff, and determining a pressure of the collapsible bag based on the volume of the collapsible bag. The method also includes calculating a fluid flow from the collapsible bag into a body cavity from the collapsible bag and determining a pressure of the body cavity based on the fluid flow.

A patient monitoring system includes: a biomedical sensor including: a transducer configured to produce a signal corresponding to a biological function; a sensor converter configured to convert the signal to a converted signal; and a transmitter configured to produce a communication, based on the converted signal, that is indicative of one or more values of the biological function, and to send the communication wirelessly; and a base station including: a receiver configured to receive the communication wirelessly and to produce a receiver output signal; a base station interface configured to produce a base station output signal indicative of the one or more values of the biological function; and at least one output port to receive the base station output signal and configured to be hard-wire connected to a display that is configured to display information indicative of the biological function.

An apparatus (10) is for use in monitoring uterine contractions. Means are provided for separately detecting (18) solid (e.g. flush) contact of at least a portion of a sensor unit (14) of the apparatus on the abdomen, and for a detecting (20) an initial starting pressure, or a baseline pressure, between the sensor unit and the abdomen. A controller (24) is arranged to first sense contact of said at least portion of the sensor unit on the abdomen, and then responsive to the contact detection, detect the starting pressure using an integrated pressure sensor. The same pressure sensor is preferably used for monitoring the uterine contractions. The starting pressure provides a direct or indirect measure or indication of the tension of a belt which is arranged in use to hold the apparatus against the abdomen of the subject. By sensing the starting pressure, for example directly responsive to abdomen contact being sensed, this initial pressure value, or derivative therefore, can be used as a direct or indirect indication of the belt tension.