Aspects of the instant disclosure relate to an elongated medical device. In particular, the instant disclosure relates to apparatuses for sensing contact force. In various embodiments, a force sensing element including a tip and a catheter shaft, wherein the tip is configured to move relative to the shaft when an external force is applied to the tip comprising a transmitter configured to transmit a transmitter signal when external force is applied to the tip, a first plurality of sensors and a second plurality of sensors positioned proximate the transmitter, wherein each of the sensors is configured to receive the transmitter signal and the first plurality of sensors is longitudinally offset from the second plurality of sensors.

Disclosed is a system and method for in-situ and instantaneous measurement of a pressure gradient by real-time localized pressure measurement with two or more pressure sensors, operating with respect to blood pressure gradient across the aortic valve, or other heart valves, and associated regurgitation of blood flow due to leakage resulting from insufficient valve closure. The system includes a multi-sensor catheter, with sensors arranged along the length of the distal segment of the catheter body, spaced apart to provide simultaneous pressure measurement on either side of the valves of the heart, in addition to one or more lumina in the core of the catheter that will provide a path for introduction of diagnostic fluids which flow out through a multitude of holes in the body of the distal segment of the catheter body.

A catheter comprises an elongated catheter body, a control handle, and a hollow tip electrode having a radially-symmetrical shell defining a cavity surrounding a center inner location from which light is emitted to pass through a plurality of openings formed in the shell for interaction with tissue and/or fluid, such as blood, outside of and in contact with the shell. Light interacting with tissue is reflected back into the cavity for collection whereas light interacting with fluid, such as blood, is absorbed. By analyzing the light collected in the cavity, a determination is made as to a ratio of light reflected by tissue versus light absorbed by fluid for indicating the amount of contact between the tip electrode and tissue. Alternatively, fluorescence may similarly be employed (light is emitted at one wavelength and detected at one or more different wavelengths) since tissue and blood have different fluorescence properties at various wavelengths. An integrated ablation and spectroscopy system further comprises an RF generator, a light source and a light analyzer adapted to analyze the light collected in the cavity.

Methods, systems, devices, assemblies and apparatuses for treatment of hypertension in a patient using renal denervation. The therapeutic assembly includes an energy delivery element. The energy delivery element is configured to provide renal denervation energy to a nerve within a blood vessel of a patient. The therapeutic assembly includes a controller. The controller is coupled to the energy delivery element. The controller is configured to determine that the hypertension in the patient is orthostatic. The controller is configured to apply renal denervation energy to the patient using the energy delivery element.

An expandable electrode assembly for use in a cardiac mapping procedure includes multiple bipolar electrode pairs including a first electrode located on an outer surface and a second electrode located on an inner surface of the individual splines forming the expandable electrode assembly. Such an electrode arrangement may produce improved electrical activation signals which may be used to produce a more accurate map of the electrical activity of a patient's heart.

Methods, systems, devices, assemblies and apparatuses for treatment of hypertension in a patient using renal denervation. The therapeutic assembly includes an energy delivery element. The energy delivery element is configured to provide renal denervation energy to a nerve within a blood vessel of a patient. The therapeutic assembly includes a controller. The controller is coupled to the energy delivery element. The controller is configured to determine that the hypertension in the patient is orthostatic. The controller is configured to apply renal denervation energy to the patient using the energy delivery element.

Apparatus comprises: (a) a longitudinal member (32), having a distal portion (34); (b) a plurality of electrodes (38) disposed on the distal portion of the longitudinal member, such that a first electrode (38a) of the plurality of electrodes is disposed distally along the longitudinal member from a second electrode (38b) of the plurality of electrodes; and (c) a controller (40). The controller comprises an actuator, and circuitry (42) electrically connected to the electrodes via the longitudinal member. The actuator is configured to move the longitudinal member in discrete incremental movements such that for each incremental movement, (i) before the incremental movement the first electrode is disposed in a starting position, (ii) during each incremental movement the actuator moves second electrode toward the starting position, and (iii) at the end of each incremental movement the second electrode is stationary at the starting position.

A method and system capable of identifying ectopic foci, rotors, or conduction pathways involved in reentrant arrhythmias within cardiac tissue, and then treating identified ectopic foci, rotors, and/or pathways with either lethal or sub-lethal temperatures. The system includes a medical device having one or more mapping elements and one or more treatment elements, and a computer programmable to identify ectopic foci and rotors based at least in part on signals received from the one or more mapping elements at one or more locations.

An apparatus includes an instrument that comprises an elongated, flexible body including an inner surface and an outer surface, wherein the inner surface is shaped to define a lumen extending through at least a portion of the elongated, flexible body. The instrument further comprises a plurality of portions extending along a length of the elongated, flexible body. The apparatus further comprises a radiopaque material incorporated into a first portion of the plurality of portions and a second portion of the plurality of portions, wherein the radiopaque material is incorporated into the first portion such that the first portion has a first radiopacity, and the radiopaque material is incorporated into the second portion such that the second portion has a second radiopacity, wherein the first radiopacity is different from the second radiopacity.

Provided is a catheter that is manufacturable in a simplified fashion. The catheter 1 includes: a catheter tube 11 including a tip-flexible part 11A that has an inner tube (first tube 61) and a plurality of divided tube members 620 to 625 that are disposed on outer circumference of the inner tube and independent of each other; one or a plurality of metal rings disposed in the tip-flexible part 11A; one or a plurality of temperature sensors disposed corresponding to the one or the plurality of metal rings; and a handle 12 attached at a base end of the catheter tube 11. A rate of a thickness of the metal ring to an outer diameter of the metal ring is 7.5% or greater. The metal ring and the plurality of divided tube members 621 to 625 are both so disposed in the tip-flexible part 11A as to be fitted on an outer circumferential surface of the inner tube side by side in an axial direction of the catheter tube 11.