A system includes an endoscope configured for insertion into an internal body cavity and a fluid management system. The fluid management system includes a pump configured to pump fluid through the endoscope into the internal body cavity and a controller configured to determine a pressure within the internal body cavity based upon a current feedback signal received from the pump. A method includes supplying a drive signal to a pump to pump fluid into an internal body cavity, receiving a current feedback signal from the pump, and determining a pressure within the internal body cavity based on the current feedback signal.

The present invention relates to a device and a method for detecting a peak of an intracranial pressure (ICP) waveform using a morphological feature of an arterial blood pressure waveform. A peak extracting method of an ICP waveform using a morphological feature of an arterial blood pressure waveform according to an aspect of the present invention includes: extracting a pulse onset from a continuous ICP waveform based on systolic peak from arterial blood pressure waveform; dividing individual ICP waveforms in the continuous ICP waveform based on the pulse onset; deriving a derivative value from each of the ICP waveforms to extract a peak, a trough, and a flat; calculating latencies from the pulse onset extracted in each of the ICP waveforms to the extracted peaks to cluster peaks with a similar time interval and generate a peak cluster; searching a notch from each of the ICP waveforms based on the latency of a dicrotic notch of the arterial blood pressure waveform; and extracting P1, P2, and P3 peaks from each of the ICP waveforms by referring to the searched notch of the ICP.

The present invention relates to a device for measuring, recording, and acting in response to changes in air pressures encountered through the lumen of a connected needle. The device signals when it has been powered and signals when the device recognizes both pressures and pressure change rates indicative of synovial cavity joint penetration, such as knee joint penetration. Synovial cavity pressures detected and acted upon may either be supra- (positive) or sub-atmospheric (negative). Internal light emitting diodes and a laptop connected display are demonstrated as signaling and communication mechanisms. Methods for delivering medicaments into human and animal intra-articular cavities or joints such as synovial cavities are provided. Furthermore, methods for facilitating the diagnoses of joint effusion also are provided.

The present invention relates to a device for measuring, recording, and acting in response to changes in air pressures encountered through the lumen of a connected needle. The device signals when it has been powered and signals when the device recognizes both pressures and pressure change rates indicative of synovial cavity joint penetration, such as knee joint penetration. Synovial cavity pressures detected and acted upon may either be supra- (positive) or sub-atmospheric (negative). Internal light emitting diodes and a laptop connected display are demonstrated as signaling and communication mechanisms. Methods for delivering medicaments into human and animal intra-articular cavities or joints such as synovial cavities are provided. Furthermore, methods for facilitating the diagnoses of joint effusion also are provided.

In some embodiments, a self-monitoring intravenous catheter system is provided. An alarm controller is provided that receives signals representing a pH value, an oxygen saturation value, and a pressure value in proximity to the distal end of the catheter. By performing a fuzzy logic analysis of the values, the alarm controller is able to detect that the catheter is about to fail or has failed, and can cause alerts to be presented. In some embodiments, an intravenous catheter is provided that has a pH sensor and an oximeter disposed at a distal end of the catheter to obtain the pH value and oxygen saturation values analyzed by the alarm controller. Embodiments of the catheter and self-monitoring intravenous catheter system may be particularly useful in treating neonates, who are sensitive to catheter failure and are not capable of detecting the signs of failure themselves.

A system for in-vivo monitoring of intracranial pressure is provided. The system includes a probe and a controller. The probe includes optical emitters and optical detectors. The optical detectors detect light emitted by the optical emitters generate signals representative of the detected light. The controller includes memory and processor. The controller connects to the probe to energize the optical emitters and receiving signals from the optical detectors. The system may include modelling, extraction, and pressure prediction modules. The modelling module can relate intracranial pressure to features of an optical signal representative of a degree to which light input into a subject's skull is absorbed by the subject's brain. The extraction module can extract signal features from a signal derived from the optical signals output by the detectors. The pressure prediction module can input the signal features into the modelling module and output an indication of intracranial pressure.

Embodiments of the present invention relate to a system and method for measuring intracranial pressure (ICP). Embodiments of the present invention include emitting an electromagnetic wave into the temple area and/or inner ear of a patient and measuring ICP based on the characteristics of the reflected and/or transmitted electromagnetic wave scattered by the tissue and/or cavity. The characteristics may include variations in the electromagnetic wave corresponding to distortions by the cavity within the skull beneath the temple and/or the oval window within the patient's inner ear. Further, embodiments of the present invention include ICP is elevated in the patient. The present invention concentrates on measuring and quantifying the changes in transmission characteristics to determine changes in ICP.

An imaging capsule including, a radiation source, a collimator that provides a collimated beam from the radiation source, at least one detector configured to detect particles resulting from X-ray fluorescence and/or Compton backscattering in response to the collimated beam to reconstruct images of a user's gastrointestinal tract, wherein the imaging capsule is configured to identify an inflamed area, within the user's gastrointestinal tract, based on a count of the detected particles and initiate actions responsive to detecting the inflamed area.

Described herein is a safety system that works collectively with an automated fluid drain control apparatus and systems and clinical experts to establish protocols and methods for given patient populations to ensure that the drainage of fluid from patients is both safe and effective. It further enables the transportation of drain orders from systems external to the drain system and returns to them the drainage data on a periodic basis for inclusion into the patient chart.

Described herein is a safety system that works collectively with an automated fluid drain control apparatus and systems and clinical experts to establish protocols and methods for given patient populations to ensure that the drainage of fluid from patients is both safe and effective. It further enables the transportation of drain orders from systems external to the drain system and returns to them the drainage data on a periodic basis for inclusion into the patient chart.