WO2024258844A1 - Joints de revêtement de lumière et méthodes associées pour appareils de pose d'implant prosthétique - Google Patents

Joints de revêtement de lumière et méthodes associées pour appareils de pose d'implant prosthétique Download PDF

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Publication number
WO2024258844A1
WO2024258844A1 PCT/US2024/033390 US2024033390W WO2024258844A1 WO 2024258844 A1 WO2024258844 A1 WO 2024258844A1 US 2024033390 W US2024033390 W US 2024033390W WO 2024258844 A1 WO2024258844 A1 WO 2024258844A1
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WO
WIPO (PCT)
Prior art keywords
lumen liner
control wire
seal
lumen
coil
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US2024/033390
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English (en)
Inventor
Kurt Kelly Reed
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Edwards Lifesciences Corp
Original Assignee
Edwards Lifesciences Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Edwards Lifesciences Corp filed Critical Edwards Lifesciences Corp
Publication of WO2024258844A1 publication Critical patent/WO2024258844A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02—Prostheses implantable into the body
    • A61F2/24—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body
    • A61F2/2427—Devices for manipulating or deploying heart valves during implantation
    • A61F2/2436—Deployment by retracting a sheath
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00—Catheters; Hollow probes
    • A61M25/0009—Making of catheters or other medical or surgical tubes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00—Catheters; Hollow probes
    • A61M25/0043—Catheters; Hollow probes characterised by structural features
    • A61M25/0045—Catheters; Hollow probes characterised by structural features multi-layered, e.g. coated
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00—Catheters; Hollow probes
    • A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
    • A61M25/0105—Steering means as part of the catheter or advancing means; Markers for positioning
    • A61M25/0133—Tip steering devices
    • A61M25/0147—Tip steering devices with movable mechanical means, e.g. pull wires

Definitions

  • the present disclosure relates to delivery apparatuses for implantable prosthetic devices.
  • the human heart can suffer from various valvular diseases. These valvular diseases can result in significant malfunctioning of the heart and ultimately require repair of the native valve or replacement of the native valve with an artificial valve.
  • repair devices e.g., stents
  • artificial valves e.g., stents
  • Percutaneous and minimally- invasive surgical approaches are used in various procedures to deliver prosthetic medical devices to locations inside the body that are not readily accessible by surgery or where access without surgery is desirable.
  • a prosthetic heart valve can be mounted in a crimped state on the distal end of a delivery apparatus and advanced through the patient’s vasculature (e.g., through a femoral artery and the aorta) until the prosthetic heart valve reaches the implantation site in the heart.
  • the prosthetic heart valve is then expanded to its functional size, for example, by inflating a balloon on which the prosthetic valve is mounted, actuating a mechanical actuator that applies an expansion force to the prosthetic heart valve, or by deploying the prosthetic heart valve from a sheath of the delivery apparatus so that the prosthetic heart valve can self-expand to its functional size.
  • the prosthetic heart valve and/or a prosthetic docking device for supporting the prosthetic heart valve delivered to the implantation site via a steerable delivery apparatus can include a flexible tube and one or more control wires disposed in respective control wire lumens supported by the flexible tube. It is desirable to manufacture such steerable catheters such that no unwanted material enters the control wire lumens. Accordingly, there is a need for steerable catheters with lumen liner seals and associated methods.
  • Described herein delivery apparatuses for prosthetic implants e.g., prosthetic heart valves
  • the disclosed delivery apparatuses and methods can, for example, provide protection against unwanted material entering one or more lumens of the delivery apparatus during manufacture thereof.
  • the devices and methods disclosed herein can, among other things, overcome one or more of the deficiencies of typical prosthetic heart valves and their delivery apparatus.
  • a delivery apparatus for a prosthetic implant can comprise a handle and one or more shafts coupled to the handle.
  • a shaft for a delivery apparatus can comprise a lumen through which one or more other components of the delivery apparatus (e.g., a control wire) and/or a prosthetic implant can be disposed.
  • a control wire e.g., a control wire
  • a prosthetic implant e.g., a prosthetic implant
  • a lumen liner seal can used to form an at least substantially fluid- tight seal between a lumen liner and one or more other components of the shaft of the delivery apparatus.
  • a delivery apparatus can comprise a lumen liner seal that forms an at least substantially fluid-tight seal between a control wire lumen liner and a coil stopper.
  • the lumen liner seal is at least substantially tubular.
  • the lumen liner seal is configured to transition from an expanded configuration to a contracted configuration.
  • the lumen liner seal is formed of a heat-shrink material.
  • a steerable delivery apparatus for delivering a device to a native valve of a patient’s heart comprises a flexible tube at least partially defining a main lumen, a control wire lumen liner at least partially defining a control wire lumen, a control wire disposed within the control wire lumen, a coil sleeve disposed around the control wire, a coil stopper abutting the coil sleeve, and a lumen liner seal surrounding an end of the control wire lumen liner and a portion of the coil stopper such that the lumen liner seal forms an at least substantially fluid-tight seal between the control wire lumen liner and the coil stopper.
  • a delivery apparatus comprises one or more of the components recited in Examples 1-20 below.
  • a method of manufacturing a steerable delivery apparatus can comprise positioning a lumen liner seal over a portion of a component that at least partially defines a lumen.
  • a method of manufacturing a steerable delivery apparatus can comprise positioning a lumen liner seal over a portion of each of a control wire lumen liner and a coil stopper and transitioning the lumen liner seal to a contracted configuration in which the lumen liner seal forms an at least substantially fluid-tight seal between the control wire lumen liner and the coil stopper.
  • the positioning the control wire lumen liner comprises positioning such that the control wire lumen liner extends over a portion of the coil stopper.
  • the method comprises positioning a coil sleeve around a control wire within the control wire lumen liner, and the positioning the lumen liner seal comprises positioning such that the lumen liner seal extends partially over the coil sleeve.
  • the positioning the lumen liner seal is performed with the lumen liner seal in an expanded configuration, in which the lumen liner seal is sized to be slid over the control wire lumen liner, and the transitioning the lumen liner seal to the contracted configuration comprises radially shrinking the lumen liner seal such that the lumen liner seal is restricted from translating relative to the control wire lumen liner.
  • the method comprises reflowing a thermoplastic elastomer to form a flexible tube around at least a portion of the control wire lumen liner
  • a method of manufacturing a steerable delivery apparatus comprises positioning a control wire lumen liner proximate to a coil stopper, positioning a lumen liner seal over a portion of each of the control wire lumen liner and the coil stopper, and transitioning the lumen liner seal to a contracted configuration in which the lumen liner seal forms an at least substantially fluid-tight seal between the control wire lumen liner and the coil stopper.
  • a method of manufacturing a steerable delivery apparatus comprises one or more of the elements recited in Examples 21-38 below.
  • FIG. 1 is a partial perspective view of a delivery device for implanting a prosthetic anchoring device at a native valve of a heart using a transseptal technique according to an example.
  • FIG. 2 is a schematic partial cross-sectional side view of a steerable delivery apparatus including a control wire, two lumen liner seals, and a proximal coil sleeve according to an example.
  • FIG. 3 is a schematic side view of a portion of a steerable delivery apparatus prior to formation of a flexible tube according to an example.
  • FIG. 4 is a schematic side view of the portion of the steerable delivery apparatus of FIG. 3 with a proximal lumen liner seal and a distal lumen liner seal loosely positioned relative to a coil stopper according to an example.
  • FIG. 5 is a schematic partial cross-sectional side view of the steerable delivery apparatus of FIG. 2 detailing the region labeled 5 in FIG. 2.
  • FIG. 6 is a schematic cross-sectional end view of the steerable delivery apparatus of FIG. 2 as viewed along the line 6-6 in FIG. 2.
  • FIG. 7 is a schematic cross-sectional end view of the steerable delivery apparatus of FIG. 2 as viewed along the line 7-7 in FIG. 2.
  • FIG. 8 is a schematic partial cross-sectional side view of a steerable delivery apparatus including a control wire, two lumen liner seals, and two coil sleeves according to an example.
  • FIG. 9 is a schematic side view of a steerable delivery apparatus including two control wires according to an example.
  • FIG. 10 is a schematic side view of a portion of the steerable delivery apparatus of FIG. 9.
  • FIG. 11 is a schematic cross-sectional end view of the steerable delivery apparatus of FIG. 9 as viewed along the line 11-11 in FIG. 9.
  • FIG. 12 is a schematic cross-sectional end view of the steerable delivery apparatus of FIG. 9 as viewed along the line 12-12 in FIG. 9.
  • FIG. 13 is a schematic cross-sectional end view of the steerable delivery apparatus of FIG. 9 as viewed along the line 13-13 in FIG. 9.
  • proximal refers to a position, direction, or portion of a device that is closer to the user and further away from the implantation site.
  • distal refers to a position, direction, or portion of a device that is further away from the user and closer to the implantation site.
  • proximal motion of a device is motion of the device away from the implantation site and toward the user (e.g., out of the patient’s body)
  • distal motion of the device is motion of the device away from the user and toward the implantation site (e.g., into the patient’s body).
  • the term “approximately” and “about” means the listed value and any value that is within 10% of the listed value.
  • “about 1 mm” means any value between about 0.9 mm and about 1.1 mm, inclusive.
  • a steerable delivery apparatus (sometimes referred to as a steerable catheter) that can be used to navigate a subject’s vasculature to deliver an implantable, expandable medical device (e.g., a prosthetic heart valve), tools, agents, or other therapy to a location within the body of a subject.
  • an implantable, expandable medical device e.g., a prosthetic heart valve
  • tools, agents, or other therapy to a location within the body of a subject.
  • procedures in which the steerable catheters are useful include neurological, urological, gynecological, fertility (e.g., in vitro fertilization, artificial insemination), laparoscopic, arthroscopic, transesophageal, transvaginal, transvesical, transrectal, and procedures including access in any body duct or cavity.
  • implants including stents, grafts, embolic coils, and the like; positioning imaging devices and/or components thereof, including ultrasound transducers; and positioning energy sources, for example, for performing lithotripsy, RF sources, ultrasound emitters, electromagnetic sources, laser sources, thermal sources, and the like.
  • the steerable catheter can include a flexible tube and one or more control wires disposed in respective control wire lumens supported by the flexible tube. It is desirable to manufacture such steerable catheters such that no unwanted material enters the control wire lumens.
  • FIG. 1 shows an exemplary delivery device 10 including a steerable delivery apparatus 30 partially enclosed within a guide sheath 20.
  • the steerable delivery apparatus 30 is positioned for installing an anchoring device 40 at a native mitral valve annulus 50 using a transseptal technique.
  • the same or similar delivery device also can be used to implant a prosthetic heart valve and/or docking device within the pulmonary artery for replacing the function of a diseased pulmonary valve, such as disclosed in U.S. Patent Application Publication No. 2017/0231756, which is incorporated by reference herein.
  • the same or similar delivery device also can be used to implant a prosthetic heart valve and/or docking device within the superior or inferior vena cava for replacing the function of a diseased tricuspid valve, such as disclosed in U.S. Patent Application Publication No. 2019/0000615, which is incorporated by reference herein.
  • the prosthetic valve For implanting a prosthetic valve within the native aortic valve via a transfemoral delivery approach, the prosthetic valve is mounted in a radially compressed state along the distal end portion of a delivery apparatus.
  • the prosthetic valve and the distal end portion of the delivery apparatus are inserted into a femoral artery and are advanced into and through the descending aorta, around the aortic arch, and through the ascending aorta.
  • the prosthetic valve is positioned within the native aortic valve and radially expanded (e.g., by inflating a balloon, actuating one or more actuators of the delivery apparatus, or deploying the prosthetic valve from a sheath to allow the prosthetic valve to self-expand).
  • a prosthetic valve can be implanted within the native aortic valve in a transapical procedure, whereby the prosthetic valve (on the distal end portion of the delivery apparatus) is introduced into the left ventricle through a surgical opening in the chest and the apex of the heart and the prosthetic valve is positioned within the native aortic valve.
  • a prosthetic valve (on the distal end portion of the delivery apparatus) is introduced into the aorta through a surgical incision in the ascending aorta, such as through a partial J- stemotomy or right parasternal mini- thoracotomy, and then advanced through the ascending aorta toward the native aortic valve.
  • the prosthetic valve is mounted in a radially compressed state along the distal end portion of a delivery apparatus.
  • the prosthetic valve and the distal end portion of the delivery apparatus are inserted into a femoral vein and are advanced into and through the inferior vena cava, into the right atrium, across the atrial septum (through a puncture made in the atrial septum), into the left atrium, and toward the native mitral valve.
  • a prosthetic valve can be implanted within the native mitral valve in a transapical procedure, whereby the prosthetic valve (on the distal end portion of the delivery apparatus) is introduced into the left ventricle through a surgical opening in the chest and the apex of the heart and the prosthetic valve is positioned within the native mitral valve.
  • the prosthetic valve is mounted in a radially compressed state along the distal end portion of a delivery apparatus.
  • the prosthetic valve and the distal end portion of the delivery apparatus are inserted into a femoral vein and are advanced into and through the inferior vena cava, and into the right atrium, and the prosthetic valve is positioned within the native tricuspid valve.
  • a similar approach can be used for implanting the prosthetic valve within the native pulmonary valve or the pulmonary artery, except that the prosthetic valve is advanced through the native tricuspid valve into the right ventricle and toward the pulmonary valve/pulmonary artery.
  • Another delivery approach is a transatrial approach whereby a prosthetic valve (on the distal end portion of the delivery apparatus) is inserted through an incision in the chest and an incision made through an atrial wall (of the right or left atrium) for accessing any of the native heart valves. Atrial delivery can also be made intravascularly, such as from a pulmonary vein. Still another delivery approach is a transventricular approach whereby a prosthetic valve (on the distal end portion of the delivery apparatus) is inserted through an incision in the chest and an incision made through the wall of the right ventricle (typically at or near the base of the heart) for implanting the prosthetic valve within the native tricuspid valve, the native pulmonary valve, or the pulmonary artery.
  • the delivery apparatus can be advanced over a guide wire previously inserted into a patient’s vasculature.
  • the disclosed delivery approaches are not intended to be limited. Any of the prosthetic valves disclosed herein can be implanted using any of various delivery procedures and delivery devices known in the art.
  • any of the systems, devices, apparatuses, etc. herein can be sterilized (for example, with heat/thermal, pressure, steam, radiation, and/or chemicals, etc.) to ensure they are safe for use with patients, and any of the methods herein can include sterilization of the associated system, device, apparatus, etc. as one of the steps of the method.
  • heat/thermal sterilization include steam sterilization and autoclaving.
  • radiation for use in sterilization include, without limitation, gamma radiation, ultra-violet radiation, and electron beam.
  • chemicals for use in sterilization include, without limitation, ethylene oxide, hydrogen peroxide, peracetic acid, formaldehyde, and glutaraldehyde. Sterilization with hydrogen peroxide may be accomplished using hydrogen peroxide plasma, for example. Examples of the Disclosed Technology
  • FIG. 2 depicts a distal region of an example of a steerable delivery apparatus 100.
  • the steerable delivery apparatus 100 includes a flexible tube 110 that at least partially defines a main lumen 112.
  • the main lumen 112 can be sized and/or otherwise configured to accommodate a prosthetic implant (e.g., the anchoring device 40 of FIG. 1 and/or a prosthetic heart valve) for delivery to a target implantation site.
  • the steerable delivery apparatus 100 additionally includes a distal anchor ring 172 and a control wire 150 terminating at and fixedly coupled to the distal anchor ring 172 such that applying tension to the control wire 150 causes the flexible tube 110 to bend in a controlled manner.
  • the steerable delivery apparatus 100 includes a proximal control wire lumen liner 120 at least partially defining a proximal control wire lumen 122 as well as a distal control wire lumen liner 130 at least partially defining a distal control wire lumen 132.
  • the control wire 150 extends through each of the proximal control wire lumen 122 and the distal control wire lumen 132.
  • the steerable delivery apparatus 100 additionally includes a proximal coil sleeve 160 disposed within the proximal control wire lumen 122 and around the control wire 150.
  • the proximal coil sleeve 160 can serve to protect the control wire 150 and to prevent the proximal control wire lumen liner 120 and/or the flexible tube 110 from compressing, foreshortening, or buckling when the control wire 150 is pulled. In this manner, the proximal coil sleeve 160 can provide for an anti-whipping or anti-bending effect through the steerable delivery apparatus 100 when the control wire 150 is operated, thereby allowing for full, controlled torqueability of the steerable delivery apparatus 100.
  • the steerable delivery apparatus 100 additionally includes a proximal anchor ring 170 disposed in the flexible tube 110 and a coil stopper 180 extending through the proximal anchor ring 170.
  • the coil stopper 180 abuts the proximal coil sleeve 160 and is fixedly coupled to the proximal anchor ring 170. In this manner, the proximal anchor ring 170 and the coil stopper 180 operate to restrict the proximal coil sleeve 160 from translating in a distal direction beyond the coil stopper 180.
  • the proximal anchor ring 170 is positioned on a distal side of the proximal control wire lumen liner 120 and on a proximal side of the distal control wire lumen liner 130.
  • each of the proximal control wire lumen liner 120 and the distal control wire lumen liner 130 extends partially over the coil stopper 180.
  • the outer diameter of the coil stopper 180 can be smaller than the inner diameter of each of the proximal control wire lumen liner 120 and the distal control wire lumen liner 130, thus permitting the ingress of undesired material within the proximal control wire lumen 122 and/or the distal control wire lumen 132.
  • a traditional method of manufacturing the steerable delivery apparatus 100 can include positioning the proximal control wire lumen liner 120 and the distal control wire lumen liner 130 relative to the coil stopper 180 and subsequently reflowing a thermoplastic elastomer (e.g., PEBAX®) over a coiled or braided tube to form the flexible tube 110.
  • a thermoplastic elastomer e.g., PEBAX®
  • FIG. 3 illustrates a portion of the steerable delivery apparatus 100 centered on the proximal anchor ring 170 in a configuration prior to formation of the flexible tube 110.
  • thermoplastic elastomer of the flexible tube 110 can enter the proximal control wire lumen 122 and the distal control wire lumen 132 during reflow of the thermoplastic elastomer.
  • Introducing such material into the proximal control wire lumen and/or the distal control wire lumen 132 may, in some instances, introduce a source of friction to affect the function of the control wire 150 and/or of the proximal coil sleeve 160.
  • such material may, in some instances, produce a bump that protrudes into the main lumen 112, which may potentially impeding the ability of a prosthetic implant (or other component, e.g., a guide wire) to slide freely through the steerable delivery apparatus 100.
  • the steerable delivery apparatus 100 additionally includes a proximal lumen liner seal 140 and a distal lumen liner seal 142 to seal the proximal control wire lumen liner 120 and the distal control wire lumen liner 130 against the coil stopper 180.
  • the proximal lumen liner seal 140 surrounds a distal end of the proximal control wire lumen liner 120 and a portion of the coil stopper 180 distal to the distal end of the proximal control wire lumen liner 120 and is sealed against each of the proximal control wire lumen liner 120 and the coil stopper 180.
  • the distal lumen liner seal 142 surrounds a proximal end of the distal control wire lumen liner 130 and a portion of the coil stopper 180 proximal to the proximal end of the distal control wire lumen liner 130 and is sealed against each of the distal control wire lumen liner 130 and the coil stopper 180.
  • the proximal lumen liner seal 140 forms an at least substantially fluid-tight seal between the proximal control wire lumen liner 120 and the coil stopper 180
  • the distal lumen liner seal 142 forms an at least substantially fluid- tight seal between the distal control wire lumen liner 130 and the coil stopper 180.
  • the present disclosure generally is directed to examples in which the disclosed lumen liner seals (e.g., the proximal lumen liner seal 140 and/or the distal lumen liner seal 142) are sealed against lumen liners (e.g., the proximal control wire lumen liner 120 and/or the distal control wire lumen liner 130) that at least partially define respective lumens, this is not required of all examples.
  • the disclosed lumen liner seams can be sealed against structures that do not themselves directly define and/or line respective lumens, such as a tube, conduit, liner, etc. that is layered over a lumen liner as disclosed herein.
  • FIG. 2 and the associate discussion herein pertains to an example in which the steerable delivery apparatus 100 includes each of the proximal lumen liner seal 140 and the distal lumen liner seal, this is not required of all examples.
  • the steerable delivery apparatus 100 can include only the proximal lumen liner seal 140 or the distal lumen liner seal 142 (e.g., sealed against a selected coil stopper 180 thereof).
  • each of the proximal lumen liner seal 140 and the distal lumen liner seal 142 can have any suitable form and/or configuration for forming seals as discussed herein.
  • each of the proximal lumen liner seal 140 and the distal lumen liner seal 142 can be substantially tubular, and/or can be formed of a heat-shrink material such as a thermoplastic polymer.
  • each of the proximal lumen liner seal 140 and the distal lumen liner seal 142 can be formed of polyethylene terephthalate (PET).
  • each of the proximal lumen liner seal 140 and the distal lumen liner seal 142 can be loosely positioned over the coil stopper 180 and subsequently shrunk, such as by applying heat, to conform to the coil stopper 180, the proximal control wire lumen liner 120, and the distal control wire lumen liner 130. It is desirable, however, that each of the proximal lumen liner seal 140 and the distal lumen liner seal 142 be formed of a material that does not melt or otherwise introduce a fluid path therethrough when subject to the heat of the flexible tube reflow process.
  • Each of the proximal lumen liner seal 140 and the distal lumen liner seal 142 can have any suitable thickness, such as a thickness that is sufficiently small to avoid restricting motion of any devices within the main lumen 112.
  • each of the proximal lumen liner seal 140 and/or the distal lumen liner seal 142 can have a thickness that is approximately 0.002-0.007 inches.
  • each of the proximal lumen liner seal 140 and the distal lumen liner seal 142 can have any suitable length, such as a length that facilitates positioning each lumen linear seal proximate the proximal anchor ring 170 while ensuring sufficient overlap with the corresponding control wire lumen liner.
  • each of the proximal lumen liner seal 140 and/or the distal lumen liner seal 142 can have a length that is approximately 2-15 millimeters (mm).
  • FIGS. 4-5 illustrate a sequence by which the proximal lumen liner seal 140 and the distal lumen liner seal 142 can be attached to the proximal control wire lumen liner 120, the distal control wire lumen liner 130, and the coil stopper 180.
  • FIG. 4 shows the proximal lumen liner seal 140 loosely positioned over the proximal control wire lumen liner 120 and a proximal portion of the coil stopper 180 and shows the distal lumen liner seal 142 loosely positioned over the distal control wire lumen liner 130 and a distal portion of the coil stopper 180.
  • FIG. 4 shows the proximal lumen liner seal 140 loosely positioned over the proximal control wire lumen liner 120 and a proximal portion of the coil stopper 180 and shows the distal lumen liner seal 142 loosely positioned over the distal control wire lumen liner 130 and a distal portion of the coil stopper 180.
  • FIG. 4 shows the proxi
  • proximal lumen liner seal 140 may be described as illustrating each of the proximal lumen liner seal 140 and the distal lumen liner seal 142 in an expanded configuration, in which the proximal lumen liner seal 140 may be slid over the proximal control wire lumen liner 120 and the coil stopper 180 and the distal lumen liner seal 142 may be slid over the distal control wire lumen liner 130 and the coil stopper 180.
  • FIG. 5 shows the proximal lumen liner seal 140 shrunk (i.e., contracted) onto the proximal control wire lumen liner 120 and the proximal portion of the coil stopper 180 and shows the distal lumen liner seal 142 shrunk (i.e., contracted) onto the distal control wire lumen liner 130 and the distal portion of the coil stopper 180.
  • FIG. 5 additionally shows the flexible tube 110 in cross-section surrounding the proximal anchor ring 170, and thus represents a detail view of the region labeled 5 in FIG. 2.
  • FIG. 5 may be described as illustrating each of the proximal lumen liner seal 140 and the distal lumen liner seal 142 in a contracted configuration, in which the proximal lumen liner seal 140 forms the substantially fluid-tight seal between the proximal control wire lumen liner 120 and the coil stopper 180 and the distal lumen liner seal 142 form the at least substantially fluid-tight seal between the distal control wire lumen liner 130 and the coil stopper 180.
  • the proximal lumen liner seal 140 can be transitioned from the expanded configuration to the contracted configuration by radially shrinking the proximal lumen liner seal 140 such that the proximal lumen liner seal 140 is restricted from translating relative to the proximal control wire lumen liner 120.
  • a transition from the configuration of FIG. 4 to the configuration of FIG. 5 can be performed by first transitioning the proximal lumen liner seal 140 and/or the distal lumen liner seal 142 to the contracted configuration (such as by application of heat) and subsequently reflowing the thermoplastic elastomer material to form the flexible tube 110.
  • reflowing the thermoplastic elastomer material and transitioning each lumen liner seal to the contracted configuration can be performed at least partially concurrently.
  • the reflowing of the thermoplastic elastomer material to form the flexible tube 110 can cause the proximal lumen liner seal 140 and/or the distal lumen liner seal 142 to transition to the contracted configuration.
  • Each of the proximal lumen liner seal 140 and the distal lumen liner seal 142 can be positioned in any suitable configuration to seal each respective control wire lumen liner to the coil stopper 180.
  • each of the proximal lumen liner seal 140 and/or the distal lumen liner seal 142 can extend axially beyond the ends of the coil stopper 180.
  • the proximal lumen liner seal 140 can also at least partially axially overlap the proximal coil sleeve 160.
  • proximal lumen liner seal 140 and/or of the distal lumen liner seal 142 can axially overlap with the coil stopper 180.
  • FIG. 6 is a cross-sectional view of the steerable delivery apparatus 100 as viewed along the line 6-6 in FIG. 2 and illustrates the configuration of the control wire 150 and the coil stopper 180 relative to the proximal anchor ring 170 and the flexible tube 110.
  • FIG. 7 is a cross-sectional view of the steerable delivery apparatus 100 as viewed along the line 7-7 in FIG. 2 and illustrates the control wire 150 and the proximal coil sleeve 160 received within the proximal lumen liner seal 140.
  • FIG. 7 illustrates the proximal control wire lumen liner 120 as extending partially into the main lumen 112, it also is within the scope of the present disclosure that the proximal control wire lumen liner 120 can be fully contained within the thickness of the flexible tube 110 such that the main lumen 112 is at least substantially cylindrical.
  • FIG. 8 illustrates a portion of a steerable delivery apparatus 200, which is at least substantially similar to the steerable delivery apparatus 100 of FIG. 5.
  • components illustrated in FIG. 8 and labeled with a reference numeral beginning with a first digit of 2 can share any suitable features, attributes, etc. with corresponding components beginning with a first digit of 1 in FIG. 5 (i.e., components with reference numerals whose second and third digits are the same), even when such reference numerals are not specifically referenced here.
  • the anchor ring 270 of FIG. 8 can be similar to and/or analogous to the proximal anchor ring 170 of FIG. 5.
  • the steerable delivery apparatus 200 of FIG. 8 additionally includes a distal coil sleeve 262 disposed within the distal control wire lumen 230 around the control wire 250.
  • the distal lumen liner seal 242 extends over a distal end region of the coil stopper 280 and partially over the distal coil sleeve 262. This is not required, however, and it also is within the scope of the present disclosure that an entirety (e.g., a full length) of the proximal lumen liner seal 240 and/or of the distal lumen liner seal 242 can be positioned over the coil stopper 280.
  • FIGS. 9-13 illustrate aspects of another example of a steerable delivery apparatus 300 that can include lumen liner seals as disclosed herein.
  • FIGS. 2-8 illustrate aspects and/or regions of the steerable delivery apparatus 100 and the steerable delivery apparatus 200 including a single control wire 150/250
  • the steerable delivery apparatus 300 includes a first control wire 350 and a second control wire 352.
  • any components illustrated in FIGS. 9-13 and labeled with a reference numeral beginning with a first digit of 3 can share any suitable features, attributes, etc. with corresponding components beginning with a first digit of 1 in any of FIGS. 2-7 and/or with corresponding components beginning with a first digit of 2 in FIG. 8 (i.e., components with reference numerals whose second and third digits are the same), even when such reference numerals are not specifically referenced here.
  • the flexible tube 310 can be similar to and/or analogous to the flexible tube 110 and/or the flexible tube 210.
  • the steerable delivery apparatus 300 includes a flexible tube 310, a distal region of which encloses the first control wire 350 and the second control wire 352.
  • the first control wire 350 and the second control wire 352 can be configured to be independently tensioned to independently flex respective portions of the distal region of the flexible tube 310.
  • the steerable delivery apparatus 300 additionally includes a first anchor ring 370, a second anchor ring 372, and a third anchor ring 374.
  • FIG. 10 shows the steerable delivery apparatus 300 of FIG. 9 with the flexible tube 310 removed.
  • the first control wire 350 extends through each of the first anchor ring 370 and the second anchor ring 372 and terminates at the third anchor ring 374, to which it is fixedly coupled.
  • the second control wire 352 extends through the first anchor ring 370 and terminates at the second anchor ring 372, to which it is fixedly coupled.
  • a first coil stopper 380 extends through the first anchor ring 370 and a second coil stopper 382 extends through the second anchor ring 372.
  • the second coil stopper 382 abuts a first coil sleeve 360 extending around the first control wire 350, while the first coil stopper 380 abuts a second coil sleeve 364 extending around the second control wire 352.
  • the first control wire 350 and the second control wire 352 extend into a distal region of the flexible tube 310 to bend respective portions of the flexible tube 310 to steer the steerable delivery apparatus 300.
  • tensioning the first control wire 350 operates to bend a region of the flexible tube 310 between the second anchor ring 372 and the third anchor ring 374.
  • the first coil sleeve 360 is contained within a first proximal control wire lumen liner 320, while the second coil sleeve 364 is contained within a second proximal control wire lumen liner 324. While not specifically illustrated in FIG.
  • an interfaces between the first proximal control wire lumen liner 320 and the second coil stopper 382 and/or an interface between the second proximal control wire lumen liner 324 and the first coil stopper 380 can be sealed with corresponding lumen liner seals in a similar manner as the proximal lumen liner seals 140/240 or the distal lumen liner seal 242 disclosed herein.
  • any interface between the first coil stopper 380 and/or the second coil stopper 382 and a control wire lumen liner that does not enclose a coil sleeve can be sealed with a lumen liner seal in a similar manner as the distal lumen liner seal 142 disclosed herein.
  • FIGS. 11-13 The relative angular configuration of the first control wire 350 and the second control wire 352 is shown in FIGS. 11-13.
  • FIG. 11 is a cross-sectional view as viewed along the line 11-11 in FIG. 9
  • FIG. 12 is a cross-sectional view as viewed along the line 12- 12 in FIG. 9
  • FIG. 13 is a cross-sectional view as viewed along the line 13-13 in FIG. 9.
  • the first control wire 350 and the second control wire 352 are separated by an angle of approximately 90 degrees, and thus serve to bend respective portions of the flexible tube 310 through planes that are perpendicular to one another.
  • treatment techniques, methods, steps, etc. described or suggested herein or in references incorporated herein can be performed on a living animal or on a non-living simulation, such as on a cadaver, cadaver heart, anthropomorphic ghost, simulator (e.g., with the body parts, tissue, etc. being simulated), etc.
  • Example 1 A steerable delivery apparatus for delivering a device to a native valve of a patient’s heart, comprising: a flexible tube at least partially defining a main lumen; a control wire lumen liner at least partially defining a control wire lumen; a control wire disposed within the control wire lumen; a coil sleeve disposed around the control wire; a coil stopper abutting the coil sleeve; and a lumen liner seal surrounding an end of the control wire lumen liner and a portion of the coil stopper such that the lumen liner seal forms an at least substantially fluid-tight seal between the control wire lumen liner and the coil stopper.
  • Example 2 The steerable delivery apparatus of any example herein, particularly example 1 , wherein the control wire lumen liner extends partially over the coil stopper.
  • Example 3 The steerable delivery apparatus of any example herein, particularly any one of examples 1-2, wherein the lumen liner seal is at least substantially tubular.
  • Example 4 The steerable delivery apparatus of any example herein, particularly any one of examples 1-3, wherein the lumen liner seal is configured to transition from an expanded configuration to a contracted configuration, wherein, when in the expanded configuration, the lumen liner seal may be slid over the control wire lumen liner and the coil stopper, and wherein, when in the contracted configuration, the lumen liner seal forms the substantially fluid-tight seal between the control wire lumen liner and the coil stopper.
  • Example 5 The steerable delivery apparatus of any example herein, particularly any one of examples 1-4, wherein the lumen liner seal is formed of a heat-shrink material.
  • Example 6 The steerable delivery apparatus of any example herein, particularly any one of examples 1-5, wherein the lumen liner seal comprises a thermoplastic polymer.
  • Example 7 The steerable delivery apparatus of any example herein, particularly any one of examples 1-6, wherein the lumen liner seal comprises polyethylene terephthalate (PET).
  • PET polyethylene terephthalate
  • Example 8 The steerable delivery apparatus of any example herein, particularly any one of examples 1-7, wherein the lumen liner seal extends partially over the coil sleeve.
  • Example 9 The steerable delivery apparatus of any example herein, particularly any one of examples 1-8, wherein an entirety of the lumen liner seal is positioned around the coil stopper.
  • Example 10 The steerable delivery apparatus of any example herein, particularly any one of examples 1 -9, further comprising an anchor ring disposed within the flexible tube, and wherein the coil stopper extends through and is fixedly coupled to the anchor ring.
  • Example 11 The steerable delivery apparatus of any example herein, particularly example 10, wherein the anchor ring is a proximal anchor ring, wherein the steerable delivery apparatus further comprises a distal anchor ring, and wherein the control wire is fixedly coupled to the distal anchor ring.
  • Example 12 The steerable delivery apparatus of any example herein, particularly example 11, wherein the control wire terminates at the distal anchor ring.
  • Example 13 The steerable delivery apparatus of any example herein, particularly any one of examples 1-12, wherein the control wire lumen liner is a proximal control wire lumen liner, wherein the control wire lumen is a proximal control wire lumen, and wherein the lumen liner seal is a proximal lumen liner seal surrounding a distal end of the proximal control wire lumen liner and a portion of the coil stopper distal to the distal end of the proximal control wire lumen liner.
  • Example 14 The steerable delivery apparatus of any example herein, particularly example 1 , wherein the coil sleeve is a proximal coil sleeve disposed within the proximal control wire lumen.
  • Example 15 The steerable delivery apparatus of any example herein, particularly example 14, wherein the proximal lumen liner seal extends partially over the proximal coil sleeve.
  • Example 16 The steerable delivery apparatus of any example herein, particularly any one of examples 1-12, wherein the control wire lumen liner is a distal control wire lumen liner, wherein the control wire lumen is a distal control wire lumen, and wherein the lumen liner seal is a distal lumen liner seal surrounding a proximal end of the distal control wire lumen liner and a portion of the coil stopper proximal to the proximal end of the distal control wire lumen liner.
  • Example 17 The steerable delivery apparatus of any example herein, particularly example 16, wherein the coil sleeve is a distal coil sleeve disposed within the distal control wire lumen.
  • Example 18 The steerable delivery apparatus of any example herein, particularly example 17, wherein the distal lumen liner seal extends partially over the distal coil sleeve.
  • Example 19 The steerable delivery apparatus of any example herein, particularly any one of examples 16-18, wherein the steerable delivery apparatus further comprises: a proximal control wire lumen liner at least partially defining a proximal control wire lumen; and a proximal lumen liner seal surrounding a distal end of the proximal control wire lumen liner and a portion of the coil stopper distal to the distal end of the proximal control wire lumen liner such that the proximal lumen liner seal forms an at least substantially fluid-tight seal between the proximal control wire lumen liner and the coil stopper.
  • Example 20 The steerable delivery apparatus of any example herein, particularly any one of examples 1-19, wherein the steerable delivery apparatus is sterilized.
  • Example 21 A method of manufacturing a steerable delivery apparatus, comprising: positioning a control wire lumen liner proximate to a coil stopper; positioning a lumen liner seal over a portion of each of the control wire lumen liner and the coil stopper; and transitioning the lumen liner seal to a contracted configuration in which the lumen liner seal forms an at least substantially fluid-tight seal between the control wire lumen liner and the coil stopper.
  • Example 22 The method of any example herein, particularly example 21, wherein the positioning the control wire lumen liner comprises positioning such that the control wire lumen liner extends over a portion of the coil stopper.
  • Example 23 The method of any example herein, particularly any one of examples 21-22, further comprising positioning a control wire within the control wire lumen liner.
  • Example 24 The method of any example herein, particularly example 23, wherein the positioning the control wire comprises positioning such that the control wire extends through the coil stopper.
  • Example 25 The method of any example herein, particularly any one of examples 23-24, further comprising positioning a coil sleeve around the control wire within the control wire lumen liner.
  • Example 26 The method of any example herein, particularly example 25, wherein the positioning the coil sleeve comprises positioning such that the coil sleeve abuts the coil stopper.
  • Example 27 The method of any example herein, particularly any one of examples 25-26, wherein the positioning the lumen liner seal comprises positioning such that the lumen liner seal extends partially over the coil sleeve.
  • Example 28 The method of any example herein, particularly any one of examples 25-26, wherein the positioning the lumen liner seal comprises positioning such that an entirety of the lumen liner seal is positioned around the coil stopper.
  • Example 29 The method of any example herein, particularly any one of examples 21-28, further comprising positioning the coil stopper within an anchor ring.
  • Example 30 The method of any example herein, particularly example 29, wherein the positioning the coil stopper within the anchor ring comprises fixedly coupling the coil stopper to the anchor ring.
  • Example 31 The method of any example herein, particularly any one of examples 29-30, wherein the positioning the lumen liner seal comprises positioning such that an edge of the lumen liner seal is proximate to the anchor ring.
  • Example 32 The method of any example herein, particularly any one of examples 21-31, wherein the positioning the lumen liner seal comprises positioning such that a first portion of the lumen liner seal directly overlies the control wire lumen liner and such that a second portion of the lumen liner seal directly overlies the coil stopper.
  • Example 33 The method of any example herein, particularly any one of examples 21-32, wherein the positioning the lumen liner seal is performed with the lumen liner seal in an expanded configuration, in which the lumen liner seal is sized to be slid over the control wire lumen liner, and wherein the transitioning the lumen liner seal to the contracted configuration comprises radially shrinking the lumen liner seal such that the lumen liner seal is restricted from translating relative to the control wire lumen liner.
  • Example 34 The method of any example herein, particularly any one of examples 21-33, wherein the control wire lumen liner is a first control wire lumen liner positioned on a first side of the coil stopper, wherein the lumen liner seal is a first lumen liner seal, and wherein the method further comprises: positioning a second control wire lumen liner proximate to the coil stopper on a second side of the coil stopper; positioning a second lumen liner seal over a portion of each of the second control wire lumen liner and the coil stopper; and transitioning the second lumen liner seal to a contracted configuration in which the second lumen liner seal forms an at least substantially fluid-tight seal between the second control wire lumen liner and the coil stopper.
  • Example 35 The method of any example herein, particularly any one of examples 21-34, wherein the transitioning the lumen liner seal to the contracted configuration comprises applying heat to the lumen liner seal.
  • Example 36 The method of any example herein, particularly any one of examples 21-35, further comprising reflowing a thermoplastic elastomer to form a flexible tube around at least a portion of the control wire lumen liner.
  • Example 37 The method of any example herein, particularly example 36, wherein the transitioning the lumen liner seal to the contracted configuration is performed prior to the reflowing the thermoplastic elastomer.
  • Example 38 The method of any example herein, particularly example 36, wherein the transitioning the lumen liner seal to the contracted configuration and the reflowing the thermoplastic elastomer are performed at least partially concurrently.
  • Example 39 A method comprising sterilizing the apparatus of any example herein, particularly any one of examples 1 -20.

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  • Health & Medical Sciences (AREA)
  • Cardiology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Transplantation (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Media Introduction/Drainage Providing Device (AREA)

Abstract

La présente invention concerne des appareils de pose orientables avec des joints de revêtement de lumière et des méthodes associées. Dans un exemple, un appareil de pose orientable comprend un tube flexible, un revêtement de lumière de fil de commande définissant au moins partiellement une lumière de fil de commande, un fil de commande disposé à l'intérieur de la lumière de fil de commande, un manchon en spirale disposé autour du fil de commande, un bouchon de spirale venant en butée contre le manchon en spirale, et un joint de revêtement de lumière qui forme un joint d'étanchéité au moins sensiblement étanche aux fluides entre le revêtement de lumière de fil de commande et le bouchon de spirale. Dans un autre exemple, un procédé comprend le positionnement d'un revêtement de lumière de fil de commande à proximité d'un bouchon de spirale, le positionnement d'un joint de revêtement de lumière sur une partie de chacun du revêtement de lumière de fil de commande et du bouchon de spirale, et la transition du joint de revêtement de lumière vers une configuration contractée pour former un joint d'étanchéité au moins sensiblement étanche au fluide entre le revêtement de lumière de fil de commande et le bouchon de spirale.
PCT/US2024/033390 2023-06-12 2024-06-11 Joints de revêtement de lumière et méthodes associées pour appareils de pose d'implant prosthétique Ceased WO2024258844A1 (fr)

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US63/507,710 2023-06-12

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Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120123327A1 (en) * 2010-11-03 2012-05-17 Biocardia, Inc. Steerable endoluminal devices and methods
US20170231756A1 (en) 2016-02-05 2017-08-17 Edwards Lifesciences Corporation Devices and systems for docking a heart valve
US20190000615A1 (en) 2017-06-30 2019-01-03 Edwards Lifesciences Corporation Docking stations for transcatheter valves
EP3226956B1 (fr) * 2014-12-05 2021-03-31 Edwards Lifesciences Corporation Cathéter orientable à fil de traction
US20210251757A1 (en) 2018-11-20 2021-08-19 Edwards Lifesciences Corporation Deployment tools and methods for delivering a device to a native heart valve
US11382744B2 (en) 2016-12-16 2022-07-12 Edwards Lifesciences Corporation Steerable delivery catheter

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120123327A1 (en) * 2010-11-03 2012-05-17 Biocardia, Inc. Steerable endoluminal devices and methods
EP3226956B1 (fr) * 2014-12-05 2021-03-31 Edwards Lifesciences Corporation Cathéter orientable à fil de traction
US20170231756A1 (en) 2016-02-05 2017-08-17 Edwards Lifesciences Corporation Devices and systems for docking a heart valve
US11382744B2 (en) 2016-12-16 2022-07-12 Edwards Lifesciences Corporation Steerable delivery catheter
US20190000615A1 (en) 2017-06-30 2019-01-03 Edwards Lifesciences Corporation Docking stations for transcatheter valves
US20210251757A1 (en) 2018-11-20 2021-08-19 Edwards Lifesciences Corporation Deployment tools and methods for delivering a device to a native heart valve

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