39 results about "Septal formation" patented technology

A method for detecting and closing the patent foramen ovale including the steps of locating a His bundle, plane of the interatrial septum, and coronary sinus ostium in a patient; identifying a fossa ovalis on the basis of one or more predetermined distances between the fossa ovalis and the His bundle, the plane of the interatrial septum, and the coronary sinus ostium; locating a patent foramen ovale by probing the junction between the fossa ovalis and a limbus of the fossa ovalis; and causing injury to the surfaces of at least one of a septum primum and a septum secundum within the patent foramen ovale. Another method includes the steps of locating a tunnel of a patent foramen ovale by probing the junction between a fossa ovalis and a limbus of the fossa ovalis and causing injury to the surfaces of at least one of a septum primum and a septum secundum within the tunnel of the patent foramen ovale by applying energy to at least one of the septum primum and the septum secundum. Apparatuses to perform these methods are also provided.

Positioning of the distal end of a catheter at a desired location, for example, in the desired atrium of a patient's heart, can be determined or verified through measurement of blood gas values proximate to the distal end. In one embodiment, an oximeter is used to monitor oxygen saturation, for example, to distinguish between de-oxygenated venous blood and well-oxygenated arterial blood. Optical signals may be transmitted to the distal end of the catheter and received therefrom via optical fibers. Specifically, a catheter (300) has a number of optical fiber ends (308, 310 and 312) disposed at a distal end (304) thereof. A first fiber end (310) transmits the red and infrared optical signals. Fiber ends (308 and 312) are used for detecting reflected optical signals. The optical signals are then processed by a detector and an oximeter instrument to provide oxygen saturation readings that can indicate the position of the distal end of the catheter within the patient's heart or successful penetration of the interatrial septum.

What is proposed is a method for the catheterization of the coronary arteries in which a catheter is introduced via the venous system into the right atrium, then passed through the interatrial septum and introduced into the left atrium, followed by the left ventricle, and into the ascending aorta to the opening of the coronary arteries, and also a catheter for the implementation of this method.

A method of identifying the fossa ovalis in a patient by positioning one or more electrodes against the tissue of the interatrial septum of the patient and acquiring unipolar and/or bipolar electrograms of the tissue of the interatrial septum while moving the electrodes to a plurality of positions against the tissue of the interatrial septum. The fossa ovalis is identified on the basis of unipolar voltage reduction, signal fractionation, broadened signal, reduced signal slew rate, reduced local myocardial impedance, increased phase angle and/or increased pacing threshold. An apparatus for identify the fossa ovalis is also provided.

The invention relates to a puncture needle component which comprises a puncture needle, a navigation guide wire, a sheathing tube with a dilator and a three-dimensional positioning and orienting device. The navigation guide wire is arranged inside the puncture needle to form an integrated guide-wire-shaped solid core puncture needle which is connected with the sheathing tube and the three-dimensional positioning and orienting device. The puncture needle component can be used for completing interventricular septum puncture and interatrial septum puncture through a venipuncture approach, the problems of the prior art can be solved effectively, unlimited selecting of surrounding blood vessel approaches of a pre-operation position can be realized, spatial position selecting of a puncture target can be limited effectively while moving direction of a needle tip of the puncture needle can be positioned accurately and objectively, and two steps of puncture spacing of the puncture needle and building of a guide wire rail can be completed in one step; the puncture needle component is safe, simple and convenient to operate, operating technical difficulty is lowered substantially, operating technical error risk is avoided completely, and risks such as perforation of free ventricular wall and cardiac tamponade are avoided fully.

The invention discloses a wireless atrial pacing device implanted through a catheter. The device comprises a waist part provided with a left disk, a right disk and two disks on the two sides, wherein the disks are in bowl shapes, the waist part is cylindrical, the diameter of each disk is larger than that of the waist part, and a wireless pacemaker host is implanted in the waist part; the left disk, the right disk and the cylindrical support waist part are braided and connected into a whole through nitinol. Through the device, physiological atrial pacing on the basis of the wireless technology is realized, the disks enable the pacemaker to be fixed to the interatrial septum of the atrium more firmly, and an electrode is more closely attached to the interatrial septum tissue; the net-shaped cylindrical support waist part is formed by braiding nitinol wires, the two sides of the support are provided with the left disk and the right disk, the wireless pacemaker host is implanted in the cylindrical support waist part, and containing space and supporting are provided for the pacemaker host; the electrode at the head end of the wireless pacemaker host stretches towards the two side disks, the tail end of the electrode is connected with four metal electrodes located on the inner sides of the disks, and the electrode is in contact with the interatrial septum tissue, so that atrial pacing is realized.

A transseptal insertion device includes a sheath that defines a lumen and has a distal end that is closest to the cardiac interatrial septum of a patient, at least one balloon connected to the distal end of the sheath, in which the at least one balloon, when inflated, overhangs and extends past the distal end of the sheath, preventing accidental puncturing of the cardiac interatrial septum and stabilizing the transseptal insertion device against fossa ovalis of the cardiac interatrial septum, and a dilator positioned within the lumen. The dilator has a distal end and is capable of precisely puncturing the cardiac interatrial septum without the use of a needle or other sharp instrument. The at least one balloon is connected to at least one hypotube through which the at least one balloon is inflated or deflated by gas or fluid flowing through the at least one hypotube.

The invention discloses a device for a left auricle ligation. The device comprises an epitheca tube, an endotheca tube, guide wires, a spiral device, a knotting and sewing device and a cutting device. The epitheca tube reaches a left auricle through a vein blood vessel. The endotheca tube is used for interatrial septum puncturing and positioning the guide wires in the left auricle. The guide wires are used for being introduced into a minimally invasive surgery device. The spiral device is used for being connected with the tip of the left auricle. The knotting and sewing device is used for knotting and sewing the tip of the left auricle. The cutting device is used for cutting the knotted part of the tip of the left auricle. The caliber of the epitheca tube is larger than that of the endotheca tube. The device has the benefits that the part, prone to cause thrombus, in the left auricle is cut, so that the hidden danger of stroke is eliminated thoroughly; the guide wires are arranged in the endotheca tube to reduce the danger that the tip of the left auricle is mistakenly punctured by the epitheca tube; the whole operation is conducted in a vein blood vessel, and a thoracotomy is not needed, so that the invasive surgery is reduced, and the postoperative recovery time is shortened; and since the left auricle is cut, the problem of related complications caused by left atrial appendage occluder at present is solved.

The present disclosure provides embodiments of an assembly that can be used in a method for improving coaptation of the anterior and posterior mitral valve leaflets by applying a remodeling force to the posterior leaflet. In particular embodiments, the assembly includes an elongate delivery catheter having at least one lumen and an elongate flexible tension member having first and second ends. Thetension member is deployable from the delivery catheter. The assembly further includes a closure member configured to be implanted in the interatrial septum of a patient' s heart, and a deployable fastener configured to be secured on the tension member adjacent to the closure member. Once secured to the heart, tension can be applied to the tension member in a direction superiorly and anteriorly toward the interatrial septum, providing a remodeling force pulling the posterior leaflet superiorly and anteriorly to improve coaptation with the anterior leaflet.

The invention relates to the technical field of medical instruments, and particularly discloses an atrial septal stoma device which comprises a first sheath tube, and the far end of the first sheath tube is connected with a supporting piece; the second sheathing canal sleeves the first sheathing canal, and the far end of the second sheathing canal is connected with a cutting assembly; the handle assembly is connected with the near ends of the first sheathing canal and the second sheathing canal and used for controlling axial movement of the first sheathing canal relative to the second sheathing canal so as to drive the supporting piece to be away from or close to the cutting assembly. According to the arrangement, the supporting piece can penetrate through the pre-opening hole in the atrial septum before the atrial septum tissue is cut, and the supporting piece in the contraction state and the cutting assembly can clamp the atrial septum tissue needing to be cut through movement of the first sheath tube; and the supporting piece is controlled to pull the cut tissue into the inner cavity of the cutting assembly and block the far-end opening of the cutting assembly. The situation that when the cutting assembly retreats out of the body from the interatrial septum, cut tissue is scattered into the body and embolism is formed is avoided.

The invention provides a puncture assembly suitable for atrial septum, and the assembly comprises an outer sheath, a dilator and a puncture needle; the dilator is sleeved in the outer sheath, the puncture needle is sleeved in the dilator, the head end of the puncture needle is a puncture head with a variable state, the puncture head is in a closed cone shape when the puncture head is located in the dilator, the puncture head is separated from the dilator after puncturing the interatrial septum, and the puncture head is in an open blunt end shape. The puncture head part of the puncture needle extends out of the dilator, at the moment, the puncture head is in a closed (closed) state, and then the whole puncture head is conical, so that puncture is facilitated; when the puncture head punctures the interatrial septum, the puncture head is separated from the dilator, and at the moment, the fork part can be opened and is in a blunt end shape due to the loss of the constraint of the check block, so the puncture state can be changed immediately; the puncture head is not enough to puncture the atrium wall, tissues such as the heart cannot be punctured, and the inner wall of the left atrium is prevented from being damaged.

The embodiment of the invention provides an atrial septum blood flow channel creating device. The device comprises a clamping mechanism used for clamping and positioning the atrial septum from the two ends of the atrial septum; the cutting pipe can axially move relative to the clamping mechanism and is used for cutting off part of the interatrial septum from the interatrial septum clamped by the clamping mechanism, so that a blood flow channel is formed in the interatrial septum. Therefore, the blood flow of the interatrial septum can be kept smooth for a long time and an implant does not need to be arranged on the interatrial septum.