A stimulation electrode assembly configured to be positioned relative to a patient for an operative procedure is disclosed. An evoked stimulation response may be sensed by a sensor near a portion of a subject. The evoked response may be sensed by an electrode and determined with a monitoring system. The evoked response may additionally and/or alternatively be sensed with a motion sensor. A position sensor may be provided to measure or determine whether the sensor has moved during a procedure.

According to one aspect, an implantable medical device may include an anchor assembly configured to anchor the medical device to a body lumen. The implantable medical device may also include a capsule. The capsule may include a pH sensor. The pH sensor may be configured to measure a pH of contents within the body lumen. The capsule may also include a power source, a controller, and an impedance sensor. The impedance sensor may be configured to measure an impedance within the body lumen.

A system for performing a diagnostic or therapeutic procedure within a subject includes a device having a distal portion configured for insertion within a lumen or duct of the subject, the device including an elongate body having a longitudinal axis, the elongate body comprising a polymeric material and having a proximal end and a distal end, one or more electrically-conductive tracings carried on a first surface of the elongate body and configured to carry a signal, and one or more conductors embedded within the polymeric material and configured to carry a signal.

A filming method of probe by filling way and the probe made by the filming method, the method includes following steps: spraying hydrophilic matrix material on the rigid member; injecting liquid polyethylene glycol into the inner, letting the polyethylene glycol coagulate; cutting out the solid polyethylene glycol, letting the cutting surface and the perimeter of the rigid member to be formed in a smooth plane; letting the wedge end of the rigid member insert a liquid latex vertically for immersion, picking up the rigid member and dripping residue, air drying the adhesive layer of the rigid member; upward setting the wedge end of the rigid member, and letting the latex film be heated, melting the solid polyethylene glycol and letting the polyethylene glycol drain away. The method can minimize the nonlinear deviation, simplify the technological process, improves product quality and manufacturing efficiency.

The present invention relates to a system (1; 1A) for use in connection with mechanical ventilation of a patient (3), provided by a ventilator (5). The system comprises a sensor arrangement (7; 7A; 7B) configured to register at least one signal (S.sub.LP; S.sub.LP(TA), S.sub.LP(CT); S.sub.e1-5; S.sub.e11-12), herein referred to as LP signal, related to muscular activity of at least one muscle (17, 19) in the laryngopharyngeal region (9) of said patient (3). Furthermore, the system comprises at least one control unit (11; 11A, 11B) configured to control the operation of said ventilator (5) based on said at least one LP signal, and/or to cause display of information related to said at least one LP signal on a display unit (13A, 13B) for monitoring said patient (3) and/or the operation of the ventilator (5).

An apparatus for monitoring for accumulation of lung fluid comprises a feeding tube having first electrode(s) positioned thereon for electrical contact with tissue of an esophagus of a target patient including a lower esophageal sphincter (LES) and/or tissue in proximity to the LES, second electrode(s) sized and shaped for contacting skin of the target patient, and a non-transitory memory having stored thereon code instructions for applying alternating current(s) to pair(s) of first and second electrodes, measuring a voltage over the pair(s), and computing an estimate of a change of lung fluid relative to a baseline in lung(s) of the target patient according to the applied alternating current and measured voltage, wherein the applying, the measuring, and the computing the estimate of the change in lung fluid are iteratively executed for monitoring the target patient for accumulation of lung fluid while the feeding tube is in use.

In a method and system for use with a ventilator for mechanical ventilation of a patient, a sensor arrangement registers at least one signal related to muscular activity of at least one muscle in the laryngopharyngeal region of the patient. This signal is provide to a computer, which controls the operation of the ventilator based thereon, and/or causes display of information related to the signal in order monitor the patient and/or operation of the ventilator.

A stimulation electrode assembly configured to be positioned relative to a patient for an operative procedure is disclosed. An evoked stimulation response may be sensed by a sensor near a portion of a subject. The evoked response may be sensed by an electrode and determined with a monitoring system. The evoked response may additionally and/or alternatively be sensed with a motion sensor. A position sensor may be provided to measure or determine whether the sensor has moved during a procedure.

A system for performing a diagnostic or therapeutic procedure within a subject includes a device having a distal portion configured for insertion within a lumen or duct of the subject, the device including an elongate body having a longitudinal axis, the elongate body comprising a polymeric material and having a proximal end and a distal end, one or more electrically-conductive tracings carried on a first surface of the elongate body and configured to carry a signal, and one or more conductors embedded within the polymeric material and configured to carry a signal.

There is provided a system, comprising: internal probe(s) for transmitting and/or receiving an RF signal, the internal probe(s) set to be mounted on an elongated guiding element set for insertion via the pharynx into a tract of a patient, the internal probe(s) and elongated guiding element are configured to be directly inserted into the tract independently of another guiding device; external probe(s) which is set to be positioned in a location outside the body for transmitting and/or receiving an RF signal; a processing unit configured to analyze an RF signal transmitted between transducer(s) of the internal probe(s) and transducer(s) of the external probe(s), propagating via tissue(s) of the patient between walls of the tract and a skin layer of the patient, to estimate at least one dielectric property of the tissue(s); wherein the RF signals are unsuitable for generating anatomical images of the tissue(s).