Distally loaded sheath and loading funnel

Abstract

A heart valve delivery system may include a handle, a shaft having a proximal end fixedly connected to the handle and extending distally along an axis away from the handle to a free end, and a tube surrounding the shaft. The tube may have a proximal end connected to the handle and extend distally along the axis away from the handle to a distal end. The tube may be axially movable relative to the shaft and the handle between a fully extended position at which the tube extends distally farther than the shaft, and a fully retracted position at which the shaft extends distally farther than the tube. The system may include an inserter for guiding insertion of the tube. In addition or in alternative to the inserter, the system may include a funnel for loading the prosthetic valve into the tube.

Description

BACKGROUND

Valvular heart disease, and specifically aortic and mitral valve disease, is a significant health issue in the United States. Annually, approximately 90,000 valve replacements are performed in the United States. Traditional valve replacement surgery, the orthotopic replacement of a heart valve, is an “open heart” surgical procedure. Briefly, the procedure necessitates a surgical opening of the thorax, initiation of extra-corporeal circulation with a heart-lung machine, stopping and opening the heart, excision and replacement of the diseased valve, and re-starting of the heart. While valve replacement surgery typically carries a 1-4% mortality risk in otherwise healthy persons, a significantly higher morbidity is associated with the procedure, largely due to the necessity for extra-corporeal circulation. Further, open heart surgery is often poorly tolerated in elderly patients. Thus, if the extra-corporeal component of the procedure could be eliminated, morbidities and cost of valve replacement therapies would be significantly reduced.

While replacement of the aortic valve in a transcatheter manner is the subject of intense investigation, lesser attention has been focused on the mitral valve. This is in part reflective of the greater level of complexity associated with the native mitral valve and thus a greater level of difficulty with regard to inserting and anchoring the replacement prosthesis.

Recent developments in the field have provided devices and methods for mitral valve replacement with reduced invasion and risk to the patient. However, due to factors including the need to maintain hemostatic pressure and avoid air embolism, such devices have complex designs and require time, space, and labor intensive loading procedures. Accordingly, there is a need for simplified devices and methods for loading and delivering replacement heart valves, particularly replacement mitral valves.

BRIEF SUMMARY

In some arrangements, a heart valve delivery system may include a handle, a shaft having a proximal end fixedly connected to the handle and extending distally along an axis away from the handle to a free end, and a tube surrounding the shaft. The tube may have a proximal end connected to the handle and extend distally along the axis away from the handle to a distal end. The tube may be axially movable relative to the shaft and the handle between a fully extended position at which the tube extends distally farther than the shaft, and a fully retracted position at which the shaft extends distally farther than the tube.

In further arrangements, a heart valve delivery system may include a handle, a tube, a distal nose, an inserter, and/or a funnel. The handle may have a longitudinally extending slot, a cavity, an annular adjustor with interior threading, and a pin block bounding an end of the cavity, the pin block including a bore and a set screw extending into the bore. The shaft may have a proximal end fixedly connected to the handle and extending distally along an axis away from the handle to a free end. The shaft may further have a shaft lumen extending from the proximal end to the distal end, and a retainer located at the free end and including an interior space in communication with the shaft lumen. The tube may surround the shaft, the tube having a proximal end connected to the handle and extending distally along the axis away from the handle to a distal end and having a tube lumen extending from the proximal end of the tube to the distal end of the tube, the tube being axially movable relative to the shaft and the handle between a fully extended position at which the tube extends distally farther than the shaft, and a fully retracted position at which the shaft extends distally farther than the tube. The distal nose may be fixedly connected to the proximal end of the tube. The inserter may have a tubular sheath with an inner diameter greater than an outer diameter of the tube. The inserter may be releasably couplable to the distal nose to restrain axial movement of the inserter relative to the tube. The funnel may include a first portion having an inner diameter equal to an inner diameter of the tube, a second portion having an inner diameter greater than the inner diameter of the first portion, and a loading lumen extending from the first portion through the second portion.

Methods of implanting a prosthetic heart valve into a patient's heart using the heart valve delivery system are also disclosed.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is an exploded view of an exemplary prosthetic cardiovascular valve.

FIG. 2 is an opened and flattened view of an unexpanded inner frame of the prosthetic valve.

FIGS. 3 and 4 are side and bottom views, respectively, of the inner frame of FIG. 2 in an expanded configuration.

FIG. 5 is an opened and flattened view of an unexpanded outer frame of the prosthetic valve.

FIGS. 6 and 7 are side and top views, respectively, of the outer frame of FIG. 5 in an expanded configuration.

FIGS. 8-10 are side, front, and top views, respectively, of an assembly of the inner frame of FIGS. 2-4 and the outer frame of FIGS. 5-7.

FIG. 11 is a longitudinal cross-sectional view of a device for deploying the prosthetic valve.

FIG. 12A is a side view of an inserter for the deploying device of FIG. 11.

FIG. 12B is an end view of the inserter of FIG. 12A.

FIGS. 13A and 13B illustrate aligning and coupling the deploying device of FIG. 11 to the inserter of FIG. 12A.

FIGS. 14A-14E illustrate a method of delivering the prosthetic valve into a heart using the delivery device of FIG. 11 and the inserter of FIG. 12A.

FIG. 15 is a side view of a funnel for loading the prosthetic valve into a second arrangement of the deploying device of FIG. 11.

FIGS. 16A and 16B are opposite end views of the funnel of FIG. 15.

FIG. 17 is a longitudinal cross-sectional view of the funnel of FIG. 15 assembled to the deploying device of FIG. 11 according to the second arrangement.

FIG. 18A is a perspective view of a bridge for connecting the funnel to the deploying device.

FIG. 18B is a transverse cross-sectional view of the bridge.

FIGS. 19A-19C are transverse cross-sectional views of various embodiments of the funnel.

FIG. 20 illustrates a method of delivering the prosthetic valve into a heart using the deploying device according to the second arrangement.

DETAILED DESCRIPTION

As used herein, the term “proximal,” when used in connection with a delivery device or components of a delivery device, refers to the end of the device closer to the user of the device when the device is being used as intended. On the other hand, the term “distal,” when used in connection with a delivery device or components of a delivery device, refers to the end of the device farther away from the user when the device is being used as intended. As used herein, the terms “substantially,” “generally,” “approximately,” and “about” are intended to mean that slight deviations from absolute are included within the scope of the term so modified.

An exemplary prosthetic heart valve 110 as may be used with various embodiments of the present disclosure is shown in an exploded view in FIG. 1. Valve 110 includes an inner structure or assembly 112 and an outer structure or assembly 114. Valve 110 may be coupled to a tether 160 and a collapsible tether anchor 154.

Inner assembly 112 includes an inner frame 140, outer cylindrical wrap 152, and leaflet structure 136 (including articulating leaflets 138 that define a valve function). Leaflet structure 136 may be sewn to inner frame 140, and may use parts of inner frame 140 for this purpose. Inner assembly 112 is disposed and secured within outer assembly 114, as described in more detail below.

Outer assembly 114 includes outer frame 170. Outer frame 170 may also have in various embodiments an outer frame cover of tissue or fabric (not pictured), or may be left without an outer cover to provide exposed wireframe to facilitate in-growth of tissue. Outer frame 170 may also have an articulating collar or cuff (not pictured) covered by a cover 148 of tissue or fabric.

Tether 160 is connected to valve 110 by inner frame 140. Thus, inner frame 140 includes tether connecting or clamping portion 144 by which inner frame 140, and by extension valve 110, is coupled to tether 160.

Inner frame 140 is shown in more detail in FIGS. 2-4. Inner frame 140 can be formed from a milled or laser-cut tube of a shape-memory material such as, for example, nitinol. Inner frame 140 is illustrated in FIG. 2 in an undeformed, initial state, i.e., as milled or laser-cut, but cut longitudinally and unrolled into a flat sheet for ease of illustration. Inner frame 140 is shown fully deformed, i.e., to the final, deployed configuration, in the side view and bottom view in FIGS. 3 and 4, respectively. Inner frame 140 can be divided into four portions corresponding to functionally different portions of inner frame 140 in final form: apex portion 141, body portion 142, strut portion 143, and tether clamp portion 144. Strut portion 143 includes six struts, such as strut 143A, which connect body portion 142 to tether clamp portion 144. A greater or lesser number of struts is contemplated herein.

Connecting portion 144 includes longitudinal extensions of the struts, connected circumferentially by pairs of micro-V's. Connecting portion 144 is configured to be radially collapsed by application of a compressive force, which causes the micro-V's to become more deeply V-shaped, with the vertices moving closer together longitudinally and the open ends of the V shapes moving closer together circumferentially. When collapsed, connecting portion 144 can clamp or grip one end of tether 160, either connecting directly onto a tether line (e.g., braided filament line) or onto an intermediate structure, such as a polymer or metal piece that is, in turn, firmly fixed to the tether line. The foregoing is merely exemplary and other techniques can be used to connect tether 160 to connecting portion 144.

In contrast to connecting portion 144, apex portion 141 and body portion 142 are configured to be expanded radially. Strut portion 143 forms a longitudinal connection, and radial transition, between the expanded body portion 142 and the compressed connecting portion 144.

Body portion 142 includes six longitudinal posts, such as post 142A, although the body portion may include a greater or lesser number of such posts. The posts can be used to attach leaflet structure 136 to inner frame 140, and/or can be used to attach inner assembly 112 to outer assembly 114, such as by connecting inner frame 140 to outer frame 170. In the illustrated example, posts 142A include apertures 142B through which connecting members (such as suture filaments and/or wires) can be passed to couple the posts to other structures.

Outer frame 170 of valve 110 is shown in more detail in FIGS. 5-7. Outer frame 170 can be formed from a milled or laser-cut tube of a shape-memory material such as, for example, nitinol. Outer frame 170 is illustrated in FIG. 5 in an undeformed, initial state, i.e., as milled or laser-cut, but cut longitudinally and unrolled into a flat sheet for ease of illustration. Outer frame 170 can be divided into a coupling portion 171, a body portion 172, and a cuff portion 173, as shown in FIG. 5. Coupling portion 171 includes multiple openings or apertures 171A by which outer frame 170 can be coupled to inner frame 140, as discussed in more detail below.

Cuff portion 173 may include an indicator 174. In one example, indicator 174 is simply a broader portion of the wire frame element of cuff portion 173, i.e., indicator 174 is more apparent in radiographic or other imaging modalities than the surrounding wireframe elements of cuff portion 173. In other examples, indicator 174 can be any distinguishable feature (e.g., protrusion, notch, etc.) and/or indicia (e.g., lines, markings, tic marks, etc.) that enhance the visibility of the part of cuff portion 173 on which it is formed, or to which it is attached. Indicator 174 can facilitate the implantation of the prosthetic valve by providing a reference point or landmark that the operator can use to orient and/or position the valve (or any portion of the valve) with respect to the native valve annulus or other heart structure. For example, during implantation, an operator can identify (e.g., using echocardiography) indicator 174 when the valve 110 is situated in a patient's heart. The operator can therefore determine the location and/or orientation of the valve and make adjustments accordingly.

Outer frame 170 is shown fully deformed, i.e., to the final, deployed configuration, in the side view and top view in FIGS. 6 and 7, respectively. As best seen in FIG. 7, the lower end of coupling portion 171 forms a roughly circular opening (identified by “O” in FIG. 7). The diameter of this opening preferably corresponds approximately to the fully deformed diameter of body portion 142 of inner frame 140, to facilitate the coupling together of these two components of valve 110.

Outer frame 170 and inner frame 140 are shown coupled together in FIGS. 8-10 in front, side, and top views, respectively. The two frames collectively form a structural support for a prosthetic valve, such as valve 110 in FIG. 1. The frames support the valve leaflet structure 136 in the desired relationship to the native valve annulus, support the coverings for the two frames to provide a barrier to blood leakage between the atrium and ventricle, and couple to the tether 160 (by the inner frame 140) to aid in holding the prosthetic valve in place in the native valve annulus by the connection of the free end of the tether and tether anchor 154 to the ventricle wall, as described more fully below. The two frames are connected at six coupling points (representative points are identified as “C”). In this embodiment, the coupling of the frames is implemented with a mechanical fastener, such as a short length of wire, passed through an aperture 171A in coupling portion 171 of outer frame 170 and a corresponding aperture 142B in a longitudinal post 142A in body portion 142 of inner frame 140. Inner frame 140 is thus disposed within the outer frame 170 and securely coupled to it.

FIG. 11 shows an exemplary device 210 for delivering valve 110 to the native valve annulus and deploying the valve. Device 210 includes a handle 212 and a tube 214 extending distally along axis X from handle 212. A distal nose 216 is integrally formed with or fixedly connected to a proximal end of tube 214 and extends into handle 212. Tube 214 and distal nose 216 are movable together at least axially relative to handle 212, but tube 214 and distal nose 216 are mutually connected to be axially immovable relative to one another. Distal nose 216 includes an externally threaded shaft 218, which extends along axis X into handle 212 and is engaged with an axial adjustor 220. Adjustor 220 is an internally threaded ring rotatably connected to handle 212 and centered on axis X. Adjustor 220 may be rotated about axis X and about threaded shaft 218 while handle 212 is held immobile to extend or retract distal nose 216 relative to handle 212, thereby moving tube 214 between a fully extended position, shown in FIG. 11, and a fully retracted position in which threaded shaft 218 extends into cavity 222 provided within handle 212.

Device 210 includes a pin block 224 at a proximal end of handle 212, which may limit axial movement of distal nose 216 and tube 214. For example, the fully retracted position may be a position at which the proximal end of threaded shaft 218 abuts a distal surface of pin block 224. Pin block 224 has a threaded bore 228 extending in a direction generally perpendicular to axis X. A set screw 226 in bore 228 may be adjusted radially to selectively engage or disengage tether anchor 154 or tether 160 of valve 110, which may extend across bore 228.

A shaft 230 positioned in handle 212 has one end mounted to pin block 224 and extends distally along axis X where it is telescopically received within tube 214. A retainer 232 disposed at a distal end of shaft 230 has an interior space 234 for accommodating and supporting part of valve 110. For example, valve 110 may be loaded in device 210 such that part or all of any one of or any combination of inner frame 140, clamping portion 144, or tether 160 are disposed within the interior space 234 of retainer 232. Shaft 230 further includes a lumen 236 extending through its entire length that communicates at one end with bore 228 and at the other end with interior space 234, thereby enabling tether 160 to extend from a valve 110 loaded distally of retainer 232 to bore 228. In this example, shaft 230 is axially immovable relative to handle 212, such that the retainer 232 at the distal end of shaft 230 is at a fixed position relative to handle 212. However, any axial movement of tube 214 and distal nose 216 relative to handle 212 will result in a similar movement of tube 214 and distal nose 216 relative to shaft 230. Thus, as tube 214 is retracted proximally, the distal end of tube 214 will move closer to retainer 232, and as tube 214 is extended distally, the distal end of tube 214 will move farther from retainer 232.

In the fully extended position, tube 214 extends distally beyond a distal-most point of the retainer 232 such that shaft 230 and retainer 232 are entirely contained within handle 212 and tube 214. When tube 214 is in the fully retracted position, retainer 232 and part of shaft 230 extend distally out of tube 214. A valve 110 loaded within the distal end of tube 214 would be radially constrained while tube 214 is in an extended position overlying the valve, but would be free to expand upon movement of tube 214 to a retracted position in which the valve is exposed. Valve 110 may therefore be deployed after being collapsed and loaded into the distal end of tube 214 by moving tube 214 from the fully extended position to a retracted position while shaft 230 and valve 110 remain in a fixed position. Such a method of deployment provides a significant degree of control to a surgeon operating device 210, as device 210 can be manipulated to position and maintain valve 110 at an intended implanting location prior to and throughout deployment.

Materials envisioned for construction of device 210 are generally sufficiently rigid or semi-rigid to allow manipulation of device 210 without flexure, while also being biocompatible. Examples of such materials include stainless steel and polyetheretherketone (PEEK), which may be used to form any combination of the components of device 210 described above. For example, as described more fully below tube 214 and shaft 230 may be constructed from stainless steel, while retainer 232 may be constructed from PEEK. The use of other biocompatible metals and polymers and combinations thereof is also contemplated.

FIGS. 12A and 12B illustrate an inserter 238 including a sheath 240 and a collar 242. Sheath 240 is cannular and has an inner diameter slightly larger than the outer diameter of tube 214. Collar 242 is attached to or integrally formed with the proximal end of sheath 240 and includes features, such as a passive seal or valve (not pictured), for maintaining hemostatic pressure and preventing air emboli when inserter 238 is inserted into a patient's heart. Port 244, for example, extends from collar 242 in a direction transverse to sheath 240 and may include a pressure regulating valve or may be connected to external pressure regulating apparatus. In addition or in the alternative, port 244 may provide a passageway for the introduction and removal of ancillary instruments. For example, a dilator (not shown), such as a saline balloon, may be inserted through port 244 and out from the distal end of sheath 240 to provide an atraumatic tip while inserter 238 is advanced within a patient.

Turning to FIGS. 13A and 13B with continued reference to FIGS. 12A and 12B, the distal end of tube 214 may be inserted through collar 242 and into the proximal end of sheath 240, and inserter 238 may then be coupled to device 210 to maintain full coverage of tube 214 by sheath 240. Collar 242 and distal nose 216 include features for releasably coupling inserter 238 to delivery device 210. More particularly, collar 242 includes a clamp screw 246 and first coupling features 248, while distal nose 216 includes distally extending second coupling features 250 for engaging first coupling features 248. In one embodiment, second coupling features 250 may be semi-rigid, elastically deformable tapered hook arms, and first coupling features 248 may be complimentary recesses within collar 242, with each recess including a shoulder for engaging a hook arm. As tube 214 is advanced to a fully covered position within sheath 240, second coupling features 250 are advanced into first coupling features 248 such that second coupling features 250 deform slightly before snapping into hooked engagement with first coupling features 248. Tightening clamp screw 246 against tube 214 secures sheath 240 to tube 214. In alternative embodiments, first and second coupling features 248, 250 may be reversed, with first coupling features 248 on distal nose 216 and second coupling features on collar 242. Still further, any type of releasable coupling features other than those described above may be used to mutually engage and restrain relative axial movement between tube 214 and sheath 240 after tube 214 has been fully advanced into sheath 240.

As collar 242 is directly coupled to distal nose 216, the retraction or extension of tube 214 and distal nose 216 will result in a corresponding retraction or extension of inserter 238. To accommodate the retraction of inserter 238, collar 242 has a diameter that is similar to or smaller than the diameter of distal nose 216 so that collar 242 will be receivable within the distal end of handle 212. Additionally, handle 212 includes a slot 252 extending proximally from the distal end of handle 212 to accommodate port 244 as tube 214 and inserter 238 are retracted. Handle 212 includes a second slot (not visible in the views provided by the Figures), to accommodate clamp screw 246 as tube 214 and inserter 238 are retracted. The fully retracted position may be the point at which port 244 abuts the proximal end of slot 252.

FIGS. 14A-14E schematically illustrate the delivery of prosthetic heart valve 110 into heart 310 using delivery device 210 and inserter 238. As shown in FIG. 14A, a distal end of sheath 240 is inserted into heart 310 near the apex 314 of the heart 310. Sheath 240 is advanced through ventricle 318 of the heart 310 toward native valve 322 to be replaced. In one embodiment of the delivery process, ventricle 318 may be the left ventricle and valve 322 may be the mitral valve. Dilator 254, such as a saline balloon, may extend from the distal end of sheath 240 to serve as an atraumatic tip to prevent injury to cardiac tissue, such as chordae tendineae or myocardium, as sheath 240 advances. Turning to FIG. 14B, inserter 238 may be advanced until the distal end of sheath 240 extends at least partially through native valve 322 into atrium 326. At this point, dilator 254 may be removed, for example, through port 244 and the distal end of tube 214 of device 210 may be inserted through collar 242 and into the proximal end of sheath 240. Prosthetic valve 110 is loaded in the distal end of tube 214, with tether 160 extending proximally through the lumen 236 of shaft 230 from valve 110 to tether anchor 154, which is retained at the proximal end of handle 212 by set screw 226.

Tube 214 may be advanced distally through sheath 240 while inserter 238 is held stationary until the distal nose 216 of handle 212 reaches collar 242 and second coupling features 250 engage in first coupling features 248 to couple device 210 to inserter 238. At this juncture, the distal end of tube 214 will be positioned such that prosthetic valve 110 is disposed at least partially within the annulus of native valve 322, as shown in FIG. 14C. Tube 214 is next retracted along with inserter 238 by rotating adjustor 220 relative to handle 212 in the example illustrated in FIG. 14D. The retraction of tube 214 and inserter 238 relative to stationary shaft 230 moves the open distal ends of tube 214 and shaft 240 toward prosthetic valve 110. When tube 214 and inserter 238 are in the fully retracted position, retainer 232 and part of shaft 230 will protrude distally from tube 214 and sheath 240, and prosthetic valve 110 will no longer be constrained. Prosthetic valve 110 will then expand or unfold into an implanted position within the annulus of native valve 322.

Finally, tether anchor 154 is released by loosening set screw 226 and retracting device 210 and inserter 238, whereupon tether 160 and tether anchor 154 are pulled distally through the lumen 236 of shaft 230 toward and out from retainer 232. Upon its release from lumen 236, tether anchor 154 will expand and seat against an outer surface of heart 310 at apex 314, as shown in FIG. 14E. Prosthetic valve 110 will then settle into a final position and will be prevented from displacement by tether anchor 154.

FIG. 15 shows a loading funnel 256 according to another aspect of the disclosure. Funnel 256 has a distal end 258, a proximal end 260, and a plurality of apertures 262, which may be fastener apertures, near proximal end 260. Apertures 262 may be used to hold funnel 256 in place relative to device 210 throughout loading.

FIGS. 16A and 16B illustrate funnel 256 from distal end 258 and proximal end 260, respectively. Funnel 256 defines a tapered loading space 264 that opens at distal end 258 and tapers toward proximal end 260. A loading lumen 266 extends along the interior of funnel 256 between distal end 258 and proximal end 260.

Turning to FIG. 17, funnel 256 may be aligned along axis X and assembled to the distal end of tube 214. Loading space 264 tapers to an inner diameter at a step 270 that is equal or approximately equal to the inner diameter of tube 214. A fitting portion 268 extending from proximal end 260 to step 270 has a slightly larger inner diameter that is equal or approximately equal to the outer diameter of tube 214. Inserting tube 214 into fitting portion 268 therefore creates a smooth transition from loading space 264 to the interior of tube 214. The smooth transition allows prosthetic valve 110 to be safely loaded into tube 214. For example, with tube 214 in the fully retracted position and funnel 256 located at the distal end of tube 214, prosthetic valve 110 may be folded or compressed within loading space 264 with tether 160 extending through proximal end 260 and shaft 230 such that tether anchor 154 is fixed at the proximal end of device 210 as described above. Advancing tube 214 to the fully extended position pushes funnel 256 away from handle 212 and further compresses prosthetic valve 110 as it is drawn proximally through funnel 256 and into the distal end of tube 214.

Loading lumen 266 follows the tapered contour of loading space 264 but otherwise extends straight from fitting portion 268 to distal end 258. Its straight configuration enables loading lumen 266 to function as a guide to prevent rotation of prosthetic valve 110 while prosthetic valve 110 is being loaded into tube 214. For example, prosthetic valve 110 may be constructed or folded with a dent or groove complementary in shape to loading lumen 266 such that the dent or groove remains aligned with loading lumen 266 as funnel 256 moves relative to prosthetic valve 110.

Additionally, loading lumen 266 provides a guide for loading a balloon, such as dilator 254 described above, into device 210. For example, tube 214 may have a separate tube lumen 274 that is alignable with loading lumen 266 when tube 214 is assembled to funnel 256. Tube lumen 274 may or may not extend to the distal end of tube 214. In arrangements in which tube lumen 274 does not extend to the distal end of tube 214, as illustrated in FIG. 17, any balloon or dilator 254 deployed from tube lumen 274 would expand to occupy an entire diameter of tube 214 in the space between the distal end of tube lumen 274 and the distal end of tube 214. As a result of dilator 254 occupying the entire diameter of tube 214, any portion of dilator 254 protruding from distal end of tube 214 would tend to be centered on axis X.

Dilator 254 may be loaded through loading lumen 266 and into separate tube lumen 274 simultaneously with and in a similar manner to prosthetic valve 110. Loading a balloon dilator 254 into device 210 may obviate the need for inserter 238 in that tube 214 may be advanced within the patient with an atraumatic tip provided by the balloon, and, when no longer needed, the balloon may be withdrawn through tube lumen 274 while tube 214 is held stationary. Prosthetic valve 110 may then be deployed by retracting tube 214 proximally as described above. Certain arrangements of device 210 configured for use with funnel 256 are therefore used without inserter 238. For example, certain arrangements of device 210 configured for use with funnel 256 do not include features for accommodating inserter 238, such as cavity 222, slot 252, or second coupling features 250, and may have an adjustor 220 of a linear rather than rotating design. Similarly, certain arrangements of device 210 configured for use with inserter 238 are incompatible with funnel 256 and do not include tube lumen 274.

Turning to FIG. 18A, a bridge 272 may be used to align funnel 256 with, and secure funnel 256 to, tube 214. Bridge 272 has a bridge lumen 276 extending therethrough with an inner diameter equal to the inner diameters of loading lumen 266 and tube lumen 274. As shown in FIG. 17, loading lumen 266 does not extend flush to proximal end 260 of funnel 256, so bridge 272 and bridge lumen 276 act to connect loading lumen 266 to tube lumen 274 for loading a dilator 254 into tube 214. Bridge 272 may further include laterally extending wings 278 (FIG. 18B), which may fit corresponding slots or grooves (not illustrated) in tube 214 and funnel 256.

FIGS. 19A-19C illustrate transverse cross-sections of funnel 256 taken approximately through a midpoint of funnel 256 according to various embodiments. Loading lumen 266 may be disposed entirely within loading space 264 as illustrated in FIGS. 16A, 17 and 19A. Alternatively, loading lumen 266 may be disposed only partially within loading area 264 and partially within the wall of funnel 256 as shown in FIG. 19B, or entirely outside of loading space 264 as illustrated in FIG. 19C. In any of the foregoing examples, tube lumen 274 may be disposed within or outside of tube 214 to match the relationship of loading lumen 266 to loading space 264.

Certain arrangements of device 210 configured for use with funnel 256 may therefore be used to deliver prosthetic valve 110 in a manner similar to the process illustrated in FIGS. 14A-14E. In such a process, dilator 254 may be inflated to extend from the distal end of tube lumen 274 to enable atraumatic insertion of the distal tip of tube 214 into ventricle 318, then through native valve 322 into atrium 326, as shown in FIG. 20. In such arrangement of device 210, a tube lumen port 280 in fluid communication with tube lumen 274 extends laterally from device 210. Tube lumen port 280 can be used to add or remove fluid within dilator 254. Tube lumen port 280 is accommodated by slot 252 in the same manner as port 244. Thus, after insertion of the distal tip of tube 214 to the proper depth within atrium 326 and withdrawal of dilator 254 into tube lumen 274 by evacuation of fluid from tube lumen port 280, delivery of prosthetic valve 110 can be achieved by steps like those described above with regard to FIGS. 14D and 14E. Particularly, adjustor 220 is rotated to withdraw tube 214, thus leaving prosthetic valve 110 free to expand and seat in its intended permanent position, similar to the step illustrated in FIG. 14D. Tether anchor 154 is then released by loosening set screw 226, and device 210 is removed to result in the same arrangement of valve 110 within heart 310 as shown in FIG. 14E.

To summarize the foregoing, disclosed is a heart valve delivery system including a handle; a shaft having a proximal end fixedly connected to the handle and extending distally along an axis away from the handle to a free end; and a tube surrounding the shaft, the tube having a proximal end connected to the handle and extending distally along the axis away from the handle to a distal end, the tube being axially movable relative to the shaft and the handle between a fully extended position at which the tube extends distally farther than the shaft, and a fully retracted position at which the shaft extends distally farther than the tube; and/or the heart valve delivery system may further include a distal nose fixedly connected to the proximal end of the tube, the distal nose including a threaded shaft extending proximally into the handle; and an internally threaded adjustor ring rotatably connected to the handle and threadedly connected to the threaded shaft such that rotation of the adjustor ring relative to the handle axially moves the tube between the fully extended position and the fully retracted position; and/or the heart valve delivery system may further include a retainer located at the free end of the shaft and having an interior space extending proximally from a distal end of the retainer; and/or a lumen may extend continuously from the proximal end of the shaft to the free end of the shaft; and/or the heart valve delivery system may further include a pin block at a proximal end of the handle; a bore extending through the pin block; and a locking element selectively movable to impinge upon or clear the bore; and/or the heart valve delivery system may further include an inserter having a tubular sheath with an inner diameter greater than an outer diameter of the tube; and a distal nose fixedly connected to the proximal end of the tube, the distal nose being couplable to the inserter to restrain axial movement of the inserter relative to the tube; and/or the inserter may include a port near a proximal end of the inserter, the port being in communication with an interior of the sheath and extending transverse to the sheath; and/or the heart valve delivery system may further include a storage lumen extending axially along the tube; and a funnel, the funnel including a first portion having an inner diameter equal to an inner diameter of the tube; a second portion having an inner diameter greater than the inner diameter of the first portion; and a loading lumen extending from the first portion through the second portion; and/or the heart valve delivery system may further include a bridge having a lumen extending therethrough, the lumen having a diameter at a first end equal to an inner diameter of the storage lumen and a diameter at another end equal to an inner diameter of the loading lumen; and/or the tube may include tube slots, the funnel may include funnel slots, and the bridge may include laterally extending wings that fit within the tube slots and the funnel slots such that the bridge may be received simultaneously in both the tube slots and the funnel slots to align the loading lumen with the channel and the storage lumen and to restrain rotation of the funnel about the axis relative to the tube; a method of implanting a prosthetic heart valve into a patient's heart using the heart valve delivery system may include inserting a distal end of the sheath into the heart; and inserting a distal end of the tube into the sheath; and/or the method may further include coupling the distal nose to the sheath; and retracting the tube to the fully retracted position; and/or the method may further include inflating a balloon disposed within the sheath such that part of the inflated balloon extends outward from the distal end of the sheath while advancing the sheath through the heart; and deflating the balloon and removing the balloon from the sheath prior to inserting the distal end of the tube into the sheath; and/or the method may further include loading a prosthetic heart valve into the tube before inserting the tube into the sheath; and/or the step of loading the prosthetic heart valve may include securing an anchor of the prosthetic heart valve to the handle; and/or the method may further include removing the sheath and the tube from the heart; and tightening the anchor against an outside of the heart after removing the sheath and the tube from the heart; and/or a method of loading a prosthetic heart valve into the heart valve delivery system may include axially aligning the first portion of the funnel with the distal end of the tube; rotationally aligning the loading lumen of the funnel with the storage lumen along the tube; disposing a prosthetic heart valve within the funnel and at a distal end of the shaft while the tube is in the fully retracted position; securing an anchor of the prosthetic heart valve to the handle to restrain relative movement between the prosthetic heart valve and the handle, the prosthetic heart valve being connected to the anchor by a tether extending through the tube; and extending the tube from the fully retracted position to the fully extended position; and/or the method may further include loading a balloon in the loading lumen and connecting the balloon to the handle to restrain motion of the balloon relative to the handle prior to moving the tube from the fully retracted position to the fully extended position; and/or the method may further include slotting a bridge into both the tube and the funnel during the step of axially aligning the first portion of the funnel with the distal end of the tube; and/or the step of disposing a prosthetic heart valve within the funnel may include folding the prosthetic heart valve to form a groove in the prosthetic heart valve complementary to a shape of the loading lumen and aligning the groove with the loading lumen.

Also disclosed is a heart valve delivery system including a handle having a longitudinally extending slot, a cavity, an annular adjustor with interior threading, and a pin block bounding an end of the cavity, the pin block includes a bore and a set screw extending into the bore; a shaft having a proximal end fixedly connected to the handle and extending distally along an axis away from the handle to a free end, the shaft having a shaft lumen extending from the proximal end to the distal end, and a retainer located at the free end and including an interior space in communication with the shaft lumen; a tube surrounding the shaft, the tube having a proximal end connected to the handle and extending distally along the axis away from the handle to a distal end and having a tube lumen extending from the proximal end of the tube to the distal end of the tube, the tube being axially movable relative to the shaft and the handle between a fully extended position at which the tube extends distally farther than the shaft, and a fully retracted position at which the shaft extends distally farther than the tube; a distal nose fixedly connected to the proximal end of the tube; an inserter having a tubular sheath with an inner diameter greater than an outer diameter of the tube, the inserter being releasably couplable to the distal nose to retrain axial movement of the inserter relative to the tube; and a funnel including a first portion having an inner diameter equal to an inner diameter of the tube, a second portion having an inner diameter greater than the inner diameter of the first portion, and a loading lumen extending from the first portion through the second portion.

Although the invention herein has been described with reference to particular embodiments, it is to be understood that these embodiments are merely illustrative of the principles and applications of the present invention. It is therefore to be understood that numerous modifications may be made to the illustrative embodiments and that other arrangements may be devised without departing from the spirit and scope of the present invention as defined by the appended claims.

Claims

1. A heart valve delivery system, comprising: a handle;a shaft having a proximal end fixedly connected to the handle and extending distally along an axis away from the handle to a free end;a tube surrounding the shaft, the tube having a proximal end connected to the handle and extending distally along the axis away from the handle to a distal end, the tube being axially movable relative to the shaft and the handle between a fully extended position at which the tube extends distally farther than the shaft, and a fully retracted position at which the shaft extends distally farther than the tube; anda funnel, the funnel including: a first portion having an inner diameter equal to an inner diameter of the tube;a second portion having an inner diameter greater than the inner diameter of the first portion; anda tapered loading space extending between the first portion and the second portion,wherein the funnel includes only a single protruding guide surface on the tapered loading space, the single protruding guide surface extending in a straight direction from the first portion to the second portion, the single protruding guide surface configured to prevent rotation of a prosthetic heart valve being loaded into the tube through the funnel.

2. The heart valve delivery system of claim 1, further comprising: a distal nose fixedly connected to the proximal end of the tube, the distal nose including a threaded shaft extending proximally into the handle; andan internally threaded adjustor ring rotatably connected to the handle and threadedly connected to the threaded shaft such that rotation of the adjustor ring relative to the handle axially moves the tube between the fully extended position and the fully retracted position.

3. The heart valve delivery system of claim 1, further comprising a retainer located at the free end of the shaft and having an interior space extending proximally from a distal end of the retainer.

4. The heart valve delivery system of claim 1, wherein a lumen extends continuously from the proximal end of the shaft to the free end of the shaft.

5. The heart valve delivery system of claim 4, further comprising: a pin block at a proximal end of the handle;a bore extending through the pin block; anda set screw selectively movable to impinge upon or clear the bore.

6. The heart valve delivery system of claim 1, further comprising: an inserter having a tubular sheath with an inner diameter greater than an outer diameter of the tube; anda distal nose fixedly connected to the proximal end of the tube, the distal nose being couplable to the inserter to restrain axial movement of the inserter relative to the tube.

7. The heart valve delivery system of claim 6, wherein the inserter includes a port near a proximal end of the inserter, the port being in communication with an interior of the sheath and extending transverse to the sheath.

8. The heart valve delivery system of claim 1, further comprising: a storage lumen extending axially along the tube; andthe funnel including a loading lumen extending from the first portion through the second portion, the loading lumen being positioned within the single protruding guide surface.

9. The heart valve delivery system of claim 8, further comprising a bridge having a lumen extending therethrough, the lumen having a diameter at a first end equal to an inner diameter of the storage lumen and a diameter at another end equal to an inner diameter of the loading lumen.

10. The heart valve delivery system of claim 9, wherein the bridge includes laterally extending wings such that the bridge may align the loading lumen with the storage lumen and restrain rotation of the funnel about the axis relative to the tube.

11. A method of implanting a prosthetic heart valve into a patient's heart using the heart valve delivery system of claim 6, comprising: inserting a distal end of the sheath into the heart; andinserting a distal end of the tube into the sheath.

12. The method of claim 11, further comprising: coupling the distal nose to the sheath; andretracting the tube to the fully retracted position.

13. The method of claim 11, further comprising: inflating a balloon disposed within the sheath such that part of the inflated balloon extends outward from the distal end of the sheath while advancing the sheath through the heart; anddeflating the balloon and removing the balloon from the sheath prior to inserting the distal end of the tube into the sheath.

14. The method of claim 11, further comprising: loading the prosthetic heart valve into the tube before inserting the tube into the sheath.

15. The method of claim 14, wherein the step of loading the prosthetic heart valve includes securing an anchor of the prosthetic heart valve to the handle.

16. The method of claim 15, further comprising: removing the sheath and the tube from the heart; andtightening the anchor against an outside of the heart after removing the sheath and the tube from the heart.

17. A method of loading a prosthetic heart valve into the heart valve delivery system of claim 8, comprising: axially aligning the first portion of the funnel with the distal end of the tube;rotationally aligning the loading lumen of the funnel with the storage lumen along the tube;disposing a prosthetic heart valve within the funnel and at a distal end of the shaft while the tube is in the fully retracted position;securing an anchor of the prosthetic heart valve to the handle to restrain relative movement between the prosthetic heart valve and the handle, the prosthetic heart valve being connected to the anchor by a tether extending through the tube; andextending the tube from the fully retracted position to the fully extended position.

18. The method of claim 17, further comprising loading a balloon in the loading lumen and connecting the balloon to the handle to restrain motion of the balloon relative to the handle prior to moving the tube from the fully retracted position to the fully extended position.

19. The method of claim 17, wherein the step of disposing the prosthetic heart valve within the funnel includes folding the prosthetic heart valve to form a groove in the prosthetic heart valve complementary to a shape of the loading lumen and aligning the groove with the loading lumen.

20. A heart valve delivery system, comprising: a handle having a longitudinally extending slot, a cavity, an annular adjustor with interior threading, and a pin block bounding an end of the cavity, the pin block including a bore and a set screw extending into the bore;a shaft having a proximal end fixedly connected to the handle and extending distally along an axis away from the handle to a free end, the shaft having a shaft lumen within the shaft from the proximal end to the distal end, and a retainer located at the free end and including an interior space in communication with the shaft lumen;a tube surrounding the shaft, the tube having a proximal end connected to the handle and extending distally along the axis away from the handle to a distal end and having a tube lumen extending from the proximal end of the tube to the distal end of the tube, the tube being axially movable relative to the shaft and the handle between a fully extended position at which the tube extends distally farther than the shaft, and a fully retracted position at which the shaft extends distally farther than the tube;a distal nose fixedly connected to the proximal end of the tube;an inserter having a tubular sheath with an inner diameter greater than an outer diameter of the tube, the inserter being releasably couplable to the distal nose to restrain axial movement of the inserter relative to the tube; anda funnel including a first portion having an inner diameter equal to an inner diameter of the tube, a second portion having an inner diameter greater than the inner diameter of the first portion, and a tapered loading space extending between the first portion and the second portion;wherein the funnel includes only a single protruding guide surface on the tapered loading space, the single protruding guide surface extending in a straight direction from the first portion to the second portion, the single protruding guide surface configured to prevent rotation of a prosthetic heart valve being loaded into the tube through the funnel.