In the rapidly progressive field of structural heart, there are several different wires available for the delivery of transcatheter valves. The new and unique combination of a microcatheter and movable core wire to function as a structural wire is described in U.S. Publication No. 2018/0161549 A1. The materials and technology of this device make it ideally suited for cardiac pacing as well as device delivery.
During transcatheter valve placement, rapid cardiac pacing is required for the proper and safe positioning of the valve. In most cases of transcatheter valve placement, the cardiac pacing is performed by placing a separate pacing wire in the right ventricle. This pacing approach requires a separate vascular puncture. A bipolar wire that is often balloon tipped for floatation is advanced through the venous system into the right ventricle.
A microcatheter structural wire according to the present disclosure performs the pacing function without requiting a separate vascular puncture. Pacing will be in a unipolar mode, which differentiates it from the present pacing devices used in structural heart. Unipolar cardiac pacing generally results in better stimulation characteristics compared to bipolar pacing. Bipolar pacing has a lower potential for skeletal muscle stimulation. With the unipolar pacing, the distal section of the wire will serve as the cathode and a conductive skin patch will serve as the anode. These cathode and anode circuits are connected to the pacemaker generator.
The present microcatheter structural wire consists of a polyimide microcatheter, a specially engineered moveable core wire, and a flexible distal metal tip. The core wire is designed to interact with the performed distal end of the microcatheter. This dynamic interaction controls the shape of the distal end of the microcatheter structural wire system.
This version of the previously designed microcatheter structural wire can function as a unipolar pacing wire as well as a wire for deployment of the structural heart devices. Designing pacing capacity into the wire will eliminate the use of a separate transvenous pacing system, which adds to the time, risk, and expense of the medical procedure. Having the guidewire function as the cardiac pacing wire will significantly simplify the procedure. Making things simple is usually in the best interest of the patient.
A proximal opening 107 of the microcatheter structural wire 101 receives the core 102, which slides within the microcatheter structural wire 101 to advance and retract in the direction indicated by directional arrow 120.
The microcatheter structural wire 101 comprises a generally straight main shaft 103 that is hollow to receive the core 102. The microcatheter structural wire 101 further comprises an expandable distal loop 105. The distal loop 105 is disposed at a distal end 106 of the microcatheter structural wire 101. The distal end 106 of the microcatheter structural wire 101 is closed in the illustrated embodiment, and not open like typical microcatheters. The distal end 106 is formed from flexible metal in one embodiment.
The core 102 is designed to interact with the distal end 106 of the microcatheter. This dynamic interaction controls the shape of the distal loop 105 of the microcatheter structural wire, as further discussed herein. The core 102 further comprises a proximal core end 104.
The main shaft 103 of the microcatheter structural wire 101 is formed from kink-resistant, thin-walled, semi-rigid tube that is 0.035 inches in outer diameter and 0.028 inches in inner diameter in one embodiment. The main shaft 103 comprises an inner and outer layer of plastic, and a middle layer of braided metal within the plastic of the guidetube, as further discussed below with respect to
In the illustrated embodiment, the body of the distal loop makes about one and one half loops. An outer diameter of the distal loop in this configuration may be about 3.0 centimeters in one embodiment.
When the core 102 is advanced such that its tip (not shown) enters the distal loop 105, the tip contacts an inner surface of the distal loop 105 and causes the diameter of the distal loop 105 to increase. By advancing or retracting the core 102, the size of the distal loop 105 may be enlarged or decreased. Further, the distal loop 105 may fully straighten upon advancement of the core 102 as well. For insertion of the microcatheter 101 into the patient's heart, the core is generally fully advanced to straighten the core. After the microcatheter is in place in the left ventricle, the core is retracted enough that it no longer acts to straighten the distal loop 105, and the distal loop 105 is deployed.
The main shaft 103 comprises a conductive collar 110 where the braided metal layer of the microcatheter is exposed near the proximal end 107 of the microcatheter 101. In this regard, the plastic outer layer is removed in a small section of the main shaft 103 so that the conductive metal braid can be attached to a cathode, as further discussed herein. In one embodiment, the conductive collar is disposed about 10 cm from the proximal end 107 of the microcatheter 101.
The main shaft 103 further comprises a plurality of distal conductive patches 111a, 111b and 111c where the braided metal layer is also exposed. In the illustrated embodiment, the distal conductive patches 111a, 111b and 111c are rectangular areas extending partially around a circumference of the distal end 105 where the plastic outer layer is removed. The purpose of the distal conductive patches is to contact the inside of the patient's left ventricle and provide a pacing function, as further discussed herein. The distal conductive patches 111a, 111b, and 111c are located on the outer curvature of the distal loop 105.
Each of the distal conductive patches 111a, 111b and 111c is a rectangular area about 2-3 cm long in one embodiment. The illustrated embodiment has three distal conductive patches 111a, 111b, and 111c as shown, to provide good conductivity to the patient's heart. Other sizes and numbers of conductive patches are possible, provided that they provide sufficient conductivity.
In operation of the unipolar pacing system according to the present disclosure, the cathode will be the exposed braided metal layer at the distal conductive patches 111a, 111b, and 111c. The electrical current connection will be at the exposed braid of the conductive collar 110. In this regard, a wire and clip (not shown) may be attached to the conductive collar 110, and this connection will be the negative polarity (cathode) of the unipolar pacing system.
The anode (positive) part of the system will consist of a wire attached to a conductive skin patch, as further discussed herein with respect to
As discussed above, the cathode for the pacing is the exposed braided metal layer at the distal conductive patches 111 in the left ventricle of the patient. The electrical current connection will be at the exposed braid of the conductive collar 110. The anode (positive) part of the system will consist of a wire (not shown) attached to a conductive skin patch 502. This patch 502 will be applied to the skin on the left side of the chest not far from the left ventricular apex. The electron flow will be from the cathode to the anode.
The electric wires from the cathode and anode will be connected to a pacemaker generator (not shown). When the necessary pacing is completed, the cathode wire/clip is easily removed from the proximal end of the microcatheter.
An alternative design is to use metal conductive collars on the distal loop of the microcatheter in place of just having exposed braid. These collars will be on the outer layer of the microcatheter and electrically connected to the braided metal layer. The collars will provide strength to the microcatheter and an improved surface contact area. A similar collar will be on the proximal end of the microcatheter for the connection with the pulse generator wire.
This disclosure may be provided in other specific forms and embodiments without departing from the essential characteristics as described herein. The embodiments described are to be considered in all aspects as illustrative only and not restrictive in any manner.
This application claims priority to U.S. Provisional Patent Application No. 62/958,411, entitled “Microcatheter Structural Wire with Pacing Function,” and filed on Jan. 8, 2020. This application is further a continuation-in-part of, and claims priority to, U.S. Non-provisional application Ser. No. 15/890,767, entitled “Hybrid Microcatheter Guidewire, and filed on Feb. 7, 2018, which is a continuation-in-part of, and claims priority to, U.S. Non-provisional application Ser. No. 15/602,463, entitled “Microtube Guide,” and filed on May 23, 2017, which claims priority to Provisional Patent Application U.S. Ser. No. 62/340,111, entitled “Microtube Guide” and filed on May 23, 2016, which is fully incorporated herein by reference. U.S. Non-provisional application Ser. No. 15/602,463 is a continuation-in-part of, and claims priority to, U.S. Non-provisional application Ser. No. 15/445,272, entitled “TAVR Valve Guidewire and Guidetube with Adjustable Distal Loop,” and filed on Feb. 28, 2017, which claims priority to U.S. Provisional Patent Application Ser. No. 62/301,270, entitled “TAVR Valve Guidewire and Guidetube with Adjustable Distal Loop” and filed on Feb. 29, 2016. These patent applications are fully incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| 62958411 | Jan 2020 | US | |
| 62340111 | May 2016 | US | |
| 62301270 | Feb 2016 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15890767 | Feb 2018 | US |
| Child | 17144638 | US | |
| Parent | 15602463 | May 2017 | US |
| Child | 15890767 | US | |
| Parent | 15445272 | Feb 2017 | US |
| Child | 15602463 | US |