Annulus plane catheter
11534574 ยท 2022-12-27
Inventors
Cpc classification
A61M25/0147
HUMAN NECESSITIES
A61M25/0074
HUMAN NECESSITIES
A61M2025/0034
HUMAN NECESSITIES
A61F2/2427
HUMAN NECESSITIES
A61M25/003
HUMAN NECESSITIES
A61M25/0041
HUMAN NECESSITIES
A61M25/0026
HUMAN NECESSITIES
A61M2025/0175
HUMAN NECESSITIES
A61M25/0152
HUMAN NECESSITIES
International classification
A61F2/24
HUMAN NECESSITIES
Abstract
A coaxial multilumen annulus plane catheter, including an outer pigtail catheter enclosing one or two additional lumens, each housing either a slidable shaped wire or a second pigtail catheter shaped to fit into a wide range of annulus diameters and/or depths. In embodiments, the device may include a catheter delivery handle with thumb/finger-actuated sliders that extend or retract the shaped wires and are sized to enable side-to-side or radial motion, imparting a torque to the pre-shaped wires which translates the length of the wires to enable individually controlled rotation or sweep of each wire to accommodate different annulus diameters. The delivery handle includes hemostasis controls and flush ports. In other embodiments, a handle is obviated by direct lumen axial and rotational control at a proximal end.
Claims
1. A coaxial multilumen annulus plane catheter, comprising: a first pigtail catheter having a primary shaft, a distal primary curve, a secondary curve, and a proximal end, and a catheter side port in said secondary curve; a second pigtail catheter axially and slidably disposed within said primary shaft of said first pigtail catheter, said second pigtail catheter having a distal primary curve, a secondary curve, and a proximal end extending beyond said proximal end of said first pigtail catheter; a guide wire axially and slidably disposed within said second pigtail catheter, said guide wire having a curved distal end and a proximal end extending beyond said proximal end of said second pigtail catheter; and first and second control fittings, wherein the first control fitting is disposed on the proximal end of said first pigtail catheter and the second control fitting is disposed on the proximal end of said second pigtail catheter.
2. The coaxial multilumen catheter of claim 1, wherein said first and second control fittings each include hemostasis valves.
3. The coaxial multilumen catheter of claim 2, wherein said first and second control fittings each include flush ports.
4. The coaxial multilumen catheter of claim 1, wherein said first and second control fittings each include flush ports.
5. The coaxial multilumen catheter of claim 1, wherein said first and second pigtail catheters may be rotated independently of one another and in opposing directions to each other.
Description
BRIEF DESCRIPTION OF SEVERAL VIEWS OF THE DRAWINGS
(1) The invention will be better understood and objects other than those set forth above will become apparent when consideration is given to the following detailed description thereof. Such description makes reference to the annexed drawings wherein:
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DETAILED DESCRIPTION OF THE INVENTION
(25) Referring generally to
(26) As seen in
(27) Thus, and referring now to
(28) The outer tubular member extends distally to a distal end portion 60, from which a pigtail catheter 62 extends, and where pre-shaped wires 64, 66 extend from and retract into distal wire ports 68, 70, respectively. Distal (end) portions of the pigtail catheter may include side ports to promote contrast injection distribution, and the pre-shaped wires each have radiopaque markers, not shown but well understood in the art (radiopaque polymer materials may be employed instead of radiopaque coatings). The pre-shaped wires may be sufficiently dense to be easily seen using fluoroscopy and thus to eliminate the need for additional radiopaque coatings or materials.
(29) The handle includes first and second (respectively, upper and lower) halves 72, 74, joined at their respective perimeter edges 76, 78, and secured together with assembly screws 80. The handle has a proximal end 82 and a distal end 84. Interior handle structure includes a medial boss 86 positioned at or near the center of the handle interior and a distal boss 88 at the distal end. The medial boss partitions the housing interior into a proximal half 46a and a distal half 46b. Recesses in the medial boss 86a, 86b, 86c, of the upper half of the housing, and complementary recesses in the housing lower half (not shown), as well as recesses 88a, 88b, 88c in the housing upper half of the distal boss 88, and the complementary recesses (not shown) in the housing lower half, provide spaces and surfaces for capturing the ends of slider rods 90, 92. Control sliders 94, 96, are slidably disposed on the control rods. The bosses also capture and center the outer tubular member 50 of the multilumen catheter 44.
(30) The slider controls each include a sleeve 98, 100 slidingly disposed around the slider rods and thus disposed interiorly in the housing, external buttons 102, 104, and planar blades 106, 108 joining the sleeves and the external buttons. The external buttons preferably include surface features 110, 112, such as knurling or ridges, to enhance slip-free finger engagement, and they include curvature generally matching the curvature along the exterior side 114 of the first half 72 of the housing.
(31) Each slider control sleeve includes a hole 98a, 100a, into which the proximal end 64a, 66a, of one of the pre-shaped wires is inserted and affixed. The slider controls move proximally and distally (i.e., longitudinally) in parallel longitudinal slots 116, 118, cut in the upper housing half 72 to move the distal ends 64, 66 into and out from the ports 68, 70. The slots are sized to allow arcuate (radial) motion of the slider controls of approximately 10-25 degrees. In this manner, the user may impart a torque to the proximal ends of the pre-shaped wires. The wires are fabricated from materials that will translate the torque the entire length of the wire, such that torque control inputs result in a rotational (sweeping) motion of the loop portions of the wires. This may be employed to explore the valve cusps to precisely locate each cusp nadir and in so doing the annulus plane.
(32) Looking now at the cross-sectional views of
(33) Looking next at
(34) Disposed within the proximal half 46a of the housing interior are components connecting the multilumen catheter with first and second flush ports 140, 142 to provide fluid paths for introducing solutions to prevent catheter occlusion and clot formation. The proximal end 150 of the multilumen catheter 44 fits through the female T-fitting 152, which includes an inlet 154 into which a feed tube 156 is inserted and is in fluid communication with the second flush port 142. Sealing of the first flush port and T-fitting 152 is accomplished by bonding the distal edge to the multi-lumen and proximally with an O-ring 160 and affixed keeper or cap 158. The flush port 140 components include the proximal end 150 bonded to the female end 148 of the flush port 140.
(35) Looking at
(36) Positioning of the annulus plane catheter in a schematic aortic valve can be seen in
(37) Looking next at
(38) In using the inventive device (coaxial lumens) to define the annulus plane, method steps include the insertion of the annulus plane catheter into an access introducer sheath and advancing the catheter tip to the valve annulus under fluoroscopic guidance. With the catheter tip near the annulus, the guidewire is retracted allowing the first pre-shaped pigtail catheter to form and be manipulated into the right coronary cusp RCC. Advancement of the second pigtail catheter is achieved through the side-port of the first catheter and manipulated accordingly into the left coronary cusp LCC. To complete the definition of the annulus plane, the guidewire is advanced through the side-port of the second catheter and manipulated into the non-coronary cusp NCC. [Noted: The multilumen catheter shown in
(39) It should be noted that the pre-shaped wires are each curved in two directions, including a first gentle curvature in a first direction, and a second curvature into the loop, wherein the loop and the direction of the first curvature lie in the same geometric plane. Accordingly, when extending the pre-shaped wires from the distal exit port, back and forth (lateral) movement of the wire in the plane of the loop can be effected by retracting and extending (respectively) the wire into and from the exit port. Combined with the radial movement effected by imparting a torque to the wire using the controls on the catheter handle, a user is able to sweep a broad region within the valve cusp to find and define the respective leaflet nadirs. The pre-shaped wires may include curvature in directions other than those listed previously to prevent interaction with other procedural elements or devices as needed. It should also be noted that this functionality also applies to the coaxial lumen catheter in that the pigtail catheters that engage into each cusp may be shaped either in a single plane curvature or each curved in multiple directions as previously described.
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(43) The advancement of the replacement valve delivery system may occur after determining the C-arm position for an orthogonal view of the annulus plane. The pre-shaped wires (or the pigtails in an alternative configuration, as discussed with respect to
(44) The annulus plane catheter is fabricated from materials commonly found in medical devices, including, among others, extrusions, shape memory wires, radiopaque materials, injection molded, and machined components. The inventive annulus plane catheter is compatible with standard-sized catheter sheaths and guidewires. The views show the outer tubular member with break lines indicating that it is not shown in its entirety. The characteristics of the structure are established on each side of the break lines, and the actual relative length is variable and tailored to the access point specific to the particular catheterization procedure.
(45) It should be noted, moreover, that it may be disadvantageous to make the catheter shaft outer diameter greater than 10 F, as most pigtail angiographic catheters are compatible with 5-7 F introducer sheaths. A smaller diameter is generally preferred for controlling hemostasis and promoting healing at vascular access sites.
(46) The above disclosure is sufficient to enable one of ordinary skill in the art to practice the invention, and provides the best mode of practicing the invention presently contemplated by the inventor. While there is provided herein a full and complete disclosure of the preferred embodiments of this invention, it is not desired to limit the invention to the exact construction, dimensional relationships, and operation shown and described. Various modifications, alternative constructions, changes and equivalents will readily occur to those skilled in the art and may be employed, as suitable, without departing from the true spirit and scope of the invention. Such changes might involve alternative materials, components, structural arrangements, sizes, shapes, forms, functions, operational features or the like.
(47) Therefore, the above description and illustrations should not be construed as limiting the scope of the invention, which is defined by the appended claims.