A system for treating atrial dysfunction, including heart failure and/or atrial fibrillation, that includes one or more pressurizing elements and control circuitry. The one or more pressurizing elements can comprise one or more balloons and can be configured to be positioned in the left atrium, and optionally the pulmonary artery, of a patient's heart. The one or more pressurizing elements can be coupled to one or more positioning structures that can be configured to position the one or more pressurizing elements in the left atrium, and optionally the pulmonary artery. The control circuitry can be configured to operate the one or more pressurizing elements to decrease or increase pressure and/or volume in the left atrium, and optionally the pulmonary artery, in accordance with different phases of the cardiac cycle. The control circuitry can be further configured to operate the one or more pressurizing elements to generate coordinated pressure modifications in the left atrium, and optionally the pulmonary artery.

Provided is a guide wire including a detection portion, a housing, and a distal end side-covering. The detection portion includes a detection element configured to detect information about a vessel from inside of the vessel, and includes an extension portion extending from the detection element toward a proximal end side of the guide wire. The extension portion is configured to transmit the detected information. The housing includes a first accommodating portion housing the detection element, and includes a second accommodating portion housing the extension portion. The distal end side-covering covers the second accommodating portion. A distal end portion of the distal end side-covering is connected to a proximal end portion of the first accommodating portion.

This disclosure is related to devices, systems, and techniques for performing patient parameter measurements. In some examples, a medical device system includes an optical sensor configured to measure ambient light and a tissue oxygen saturation parameter and processing circuitry configured to determine that a current measurement of the tissue oxygen saturation parameter is prompted and control the optical sensor to perform an ambient light measurement associated with the current measurement of the tissue oxygen saturation parameter. The processing circuitry is further configured to determine, based on the ambient light measurement, at least one of whether to control the optical sensor to perform the current measurement of the tissue oxygen saturation parameter, when to control the optical sensor to perform the current measurement of the tissue oxygen saturation parameter, or whether to include the current measurement of the tissue oxygen saturation parameter in a trend of the tissue oxygen saturation parameter.

Dual sensor system for continuous blood pressure monitoring during transcatheter heart valve therapies (TVT), such as transcatheter aortic valve replacement (TAVR) or transcatheter mitral valve replacement (TMVR), comprises a controller, a support guidewire for TVT containing a first Fabry-Prot (FP) optical pressure sensor near its distal end, and a pigtail catheter for delivery of contrast medium containing a second FP optical pressure sensor near its distal end. For example, for TAVR, the support guidewire is positioned to place the first optical pressure sensor within the left ventricle (LV) for monitoring LV pressure, the pigtail catheter is positioned in the aorta to place the second optical pressure sensor in the ascending aorta for direct measurement of pressure in the aorta, downstream of the aortic valve, enabling continuous monitoring of blood pressure at both sensor locations during TAVR. The controller may be configured to interface with standard patient monitoring systems.

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.

A medical device system may include a guidewire including a distal pressure sensor and a proximal end. A connector cable may be coupled to the proximal end of the guidewire and may have a proximal end. A signal conditioning unit may be coupled to the proximal end of the connector cable. One or more of the guidewire, the connector cable, and the signal conditioning unit may include an optical fiber having a core with a tapered outer diameter.

Method for determining a blood pressure value including the steps of: providing a pulsatility signal, determining a time-related feature and a normalized amplitude-related feature on the basis of the pulsatility signal; and calculating a blood pressure value on the basis of a blood pressure function depending on the time-related feature, the normalized amplitude-related feature and function parameters.

There is described a pressure guidewire. It comprises a sensor housing and a sensor assembly embedded in the sensor housing and comprising a pressure sensor. There is a band to support the pressure sensor assembly, the band being embedded inside the sensor housing and fixed to the pressure sensor assembly for holding the pressure sensor inside the sensor housing.

A combined OCT/pressure sensor system includes an optical cable comprising a single-mode core and a multi-mode core. An OCT optical imaging sensor near a distal end of the optical cable can be inserted into a lumen of a living being. First light exiting a distal end of the single-mode core illuminates an interior of the lumen. The OCT optical imaging sensor acquires image information about the interior of the lumen and transmits an optical signal carrying the image information into the distal end of the single-mode core, toward a proximal end of the single-mode core. An optical pressure sensor attached near the OCT optical imaging sensor receives second light from the distal end of the optical cable, senses ambient pressure within the lumen and transmits an optical signal indicative of the ambient pressure into a distal end of the multi-mode core, toward a proximal end of the multi-mode core.

A system and apparatus comprising a multisensor guidewire for use in interventional cardiology, e.g., Transcatheter Valve Therapies (TVT), comprises a plurality of optical sensors for direct measurement of cardiovascular parameters, e.g. transvalvular blood pressure gradients. The guidewire has flexibility and stiffness characteristics for use as a support guidewire for TVT, e.g. for Transcatheter Aortic Valve Implantation (TAVI), comprises multiple optical pressure sensors and respective optical fibers, and a pre-formed three-dimensional flexible tip, e.g. in the form of a helix. The three-dimensional pre-formed tip is configured to assist with anchoring the guidewire within one of the ventricles and atria of the heart, or within the pulmonary artery or aorta, during interventional cardiology procedures.