Vascular closure methods and apparatuses
A vascular closure device comprised of a sheath-delivered expandable, umbrella-like device with structural radial members with terminal and non-terminal hooks that engage the vessel wall. Unlike other vascular closure umbrella-type devices that effect closure by opening of the umbrella to cover an opening, the present invention effects closure of the aperture with closure of the umbrella. The closure can be maintained by a retainer lock that slides down the members, causing contraction, bringing the members into a compressed configuration (e.g., a parallel orientation of linear members) and the wound edges together, permitting immediate vascular closure and healing of the blood vessel. The device can be delivered and recovered by an intravascular sheath.
The present invention relates to methods and apparatuses for closing punctures and apertures in human and animal tissue and to methods and apparatuses for inserting such an apparatus into such tissue to perform such closure functions.
During angiography and related procedures, catheters are inserted through an incision or puncture in the skin and underlying tissues to access an artery or vein, typically in the groin, neck, or subclavian areas of a patient. The catheter can be inserted through a puncture in the blood vessel and guided to the desired site to perform interventional procedures such as angiography, angioplasty, plaque removal, and infusion of a therapeutic substance. After the procedure is completed and the catheter is removed from the patient, the access hole must be closed to prevent massive hemorrhage. This is conventionally achieved by applying pressure over the blood vessel manually and then by applying a pressure bandage, compressive weight, or clamp device. With conventional methods, the rate of post-puncture hemorrhage is high, which causes considerable complications. This complication is exacerbated by the concomitant use of anticoagulant medications such as heparin or warfarin and by antiplatelet drugs, which are commonly used to treat vascular disease.
Sutures have been used to close access puncture wounds in blood vessels. U.S. Pat. No. 5,613,974 describes a device and method for applying sutures to a vascular puncture. US2004/0093027A1 describes barbed suture-like material that apposes the puncture site. US 2005/0121042 A1 describes a device and method for applying suture to a vascular puncture. Difficulties with these methods include the large number of steps necessary to deploy the needles, capture the suture, withdraw the suture, tie the knot, and cut the suture. In addition, the hole in the blood vessel is often widened by insertion of the instrument, and the suture remains intravascularly on the endothelial surface, and thus can be a nidus for thrombus or intravascular mural hyperplasia with later spontaneous and catastrophic closure of the vessel.
Extravascular plugs have also been proposed for closure of vascular punctures. U.S. Pat. No. 5,254,105 and U.S. Pat. No. 5,330,445 describe an extravascular plug which is slid down the external surface of the catheter or introducer and is placed into the puncture site in this manner. U.S. Pat. No. 5,643,318 relates to a similar device that has its own vessel locator device. US22022822A1 and US2004/0158287A1 describe an extravascular plug that is delivered with a specialized system. US24215232A1 describes an extravascular plug with an intravascular anchor set with a sheath with a detection port. US2005/0085855A1 describes an extravascular collagen plug, held in place with an intravascular anchor, and a device that locks over a piece of suture. U.S. Pat. No. 5,906,631 describes a plug made of hydrophilic material. U.S. Pat. No. 6,126,675 describes an intravascular anchor and a bioabsorble extravascular plug. U.S. Pat. No. 6,623,509 describes a bioabsorbable plug. U.S. Pat. No. 6,296,657 and U.S. Pat. No. 6,743,195 describe an inflatable balloon that puts pressure on the puncture site. U.S. Pat. No. 6,569,185 describes an injectable vascular plug. U.S. Pat. No. 6,663,655 describes a plug that screws in the puncture tract. US2004/0143290 A1 describes a combination of an intraluminal balloon and injectable sealant. Disadvantages to these methods are related to the high likelihood of thrombosis associated with the intravascular plug or anchor, and the presence of collagen or other bioabsorble materials which cause inflammation, activate the clotting cascade, and increase the likelihood of thrombosis, which, in an arterial system, is catastrophic.
Vascular patches have also been used for repairing blood vessels, but usually only for large areas of damage. U.S. Pat. No. 5,100,422 describes a vascular patch that is sutured to the external surface of the damaged blood vessel. U.S. Pat. No. 5,100,422 describes a vascular patch achieved by instilled adhesives and the device for doing such. These are generally impractical for catheter-based methods. U.S. Pat. No. 6,248,124 and U.S. Pat. No. 5,507,744 describe devices and methods that use electrocautery for sealing vascular punctures. This also requires a complicated device, and perforation and thrombosis are very real possibilities.
Vascular clips or staples delivered through a catheter device have also been proposed. These devices have penetrating members that bring the edges of the tissue together. U.S. Pat. No. 6,695,867 describes a clip or staple that is delivered by a specialized device. U.S. Pat. No. 6,749,622 describes a number of different clips with sharpened barbs or ends that include both intra- and extravascular portions, made of metal with memory characteristics. U.S. Pat. No. 5,861,005 describes an arterial staple that is delivered with a specialized device. U.S. Pat. No. 5,919,207 describes a stapling system based on long hooked wires that appose the surfaces, with a small staple gun to close the lesion. U.S. Pat. No. 6,022,372 describes a similar staple gun. U.S. Pat. No. 6,296,657, U.S. Pat. No. 6,663,655, and U.S. Pat. No. 6,749,621 describe a clip that is external to the vessel, but clips the two sides of the puncture together, and a device for achieving such. U.S. Pat. No. 5,782,861 and U.S. Pat. No. 5,964,782 describe clip devices composed of two or more prongs or hooks that, depending on the direction of the prongs, can clip together the puncture site from the intra- or extravascular position, through the use of a collar which forces the prongs together or other mechanisms. These clip devices are composed of thick semi-rigid material, and can be placed only with a specialized instruments, and because of the rigidity have great potential to injure or cut the blood vessel. Disadvantages of these clip devices in general include difficulty in retrieving the device if misplaced, excessive manipulation required, the thickness of the clip material which tends to cut or shear the blood vessel, the large forces that must be used to curve the staples and fix the clips, the increased possibility of tearing the blood vessel, and the general lack of control of the forces being applied to the blood vessel.
Accordingly, there is a need for methods and apparatuses that are suitable for closure of vascular punctures or other openings, and that do not suffer from the drawbacks of conventional approaches.SUMMARY OF THE INVENTION
The present invention provides methods and apparatuses that are suitable for closure of vascular punctures or other openings, and that do not suffer from the drawbacks of conventional approaches.
The present invention comprises a tissue closure device, comprising a plurality of tissue engagement elements, mounted with each other such that in a first compressed configuration the tissue engagement elements can pass through a tissue opening to be closed, and such that in a second compressed configuration the tissue engagement elements bring the edges of the opening into apposition, and such that in an expanded configuration the tissue engagement elements span the opening, wherein the tissue engagement elements engage the tissue in the compressed configuration and in the expanded configuration.
The present invention also comprises methods for closing tissue openings, comprising passing a device while in the first compressed condition through a sheath that penetrates the proximal surface of the tissue; expelling the device from the sheath into space beyond the proximal surface of the tissue such that the device assumes the expanded configuration; c) manipulating the device such that the tissue engagement elements engage the tissue; d) causing the device to assume the second compressed configuration, bringing the edges of the opening into apposition.
The present invention can provide a catheter-delivered umbrella-like device comprising fine, strong, flexible material that after delivery expands in a blood vessel so that the individual members extend beyond the catheter edges and/or puncture dimensions. The device can be viewed as analagous in structure and design as contemporary expandable vascular filters and closure umbrellas, although its purpose and function is completely different. As the catheter is withdrawn, the device is pulled against the interior of the blood vessel and the hooks or grasping devices on the ends of the members seize the interior of the vessel wall. Because of the very fine and flexible nature of the members and their multiplicity, there is minimal shear force applied to the blood vessel. While pulling on the retaining suture to keep the device against the blood vessel, a retaining lock is then advanced distally starting at the proximal portion of the members, which causes the members to first angle the device into a conical shape and then force the individual members together in a linear parallel direction, which because the members are engaged with the vessel wall, brings the edges of the punctured tissue together into apposition. The retainer lock is then locked onto the parallel members and can keep tension on the wound externally, and can prevent intravascular migration of the device. If there is no blood leakage through the closure and the device is properly positioned and stable, then the guidewire can be removed and the retaining suture or string loop cut, resulting is complete and rapid closure, which can then heal.
Since this device brings the puncture edges together, there is true blood vessel healing with little endothelial disruption, reducing the chances of thrombosis or intimal hyperplasia. The device can be supplied in different diameters (e.g., french) to accommodate different sizes of catheters and different sizes of puncture holes.
The present invention can comprise a device with umbrella-like structure, which can be viewed as analogous to the various designs of intravascular filters and aperture seals, which are delivered in a folded or compressed form, and then expanded to their filter shapes. U.S. Pat. No. 4,969,891 describes a self-expanding removable filter device that is placed with a sheath. U.S. Pat. No. 5,634,942 and U.S. Pat. No. 5,634,942 describe a similar device but with two sets of arms which protrude in opposite directions. U.S. Pat. No. 6,241,746 B1 is a similar version that can be converted to a vascular stent. U.S. Pat. No. 6,361,546 is a version with a central guidewire lumen. U.S. Pat. No. 6,428,559 describes a variable-diameter vascular filter system. U.S. Pat. No. 6,485,501 B1 also describes a filter with a guidewire. US 2003/0208227 describes different construction configurations of a filter. US 2004/0087999 A1 reveals various types of structures to retain the filter in the vessel. U.S. Pat. No. 5,709,707 describes a typical umbrella-type closure device used to close apertures. Each of the preceding patents and applications are incorporated herein by reference. The present device, analogous to many of the vascular filters and umbrella closure devices noted above, is both expandable like an umbrella and retrievable if it had to be retrieved because of misplacement. Unlike previous umbrella closure devices, the present device engages the tissue in both the expanded and compressed configurations, and functions by bringing tissue edges into apposition rather than by providing a patch that covers the opening. In addition, although the embodiments shown here generally have linear members, these members, like the structure of the intravascular filters and umbrella-type devices, need not be strictly linear, but can assume a number of complex geometrical shapes and structural patterns.
The present device, like some contemporary vascular filters, can utilize an expanding material, preferably with memory characteristics, that opens up spontaneously within the blood vessel. The device also, like some contemporary filters, can have tissue hooks or penetrators, in order to seize the vessel wall and stabilize the device. However, unlike an umbrella-style vascular filter, the device uses this opening-closing quality to seize the edges of the puncture site, and close them, resulting in a complete vascular closure. Although the device can be viewed as analogous to some contemporary self-expanding and retractable vascular filters, it is unlike them in that in certain embodiments it has a retaining lock to force the umbrella to reassume its folded state.DESCRIPTION OF THE FIGURES
The invention is explained by using embodiment examples and corresponding drawings, which are incorporated into and form part of the specification.
The present invention provides apparatuses and methods for closing a vascular puncture wound or any tissue aperture, for example those resulting from the insertion of a vascular catheter or surgical instrument, trauma or disease. The present invention embraces both apparatus and method aspects of devices for closing a vascular puncture, and the methods for delivering such a device. The present device can be closed in the delivery system (catheter or sheath) and when discharged, be open in the blood vessel. In some embodiments, at least a portion of the device can be formed of a memory metal or similar material, as is currently done in vascular filters. The stress free state corresponds to the state at which the apparatus has opened in a blood vessel, and the stressed state in the catheter and when a retaining lock is put into position. Example embodiments of tissue closure apposition devices according to the present invention are shown in
The vascular closure apposition umbrella of
In operation, the tissue closure apposition umbrella is closed within the catheter or sheath, corresponding to the illustration of
The radial members 201 in
The embodiment of
Delivery of the device can be done sequentially, or can be done with a dedicated device. For sequential delivery of the device, the following sequence of steps are suitable: 1) the guidewire and sheath are in place, 2) the device is pushed down the sheath, either next to the guidewire or with the guidewire in the lumen of the umbrella; 3) the umbrella is extruded, and then using the thread or suture, pulled tight against the lumen of the vessel; 4) the retaining lock is pushed down the thread and/or guidewire, and is pushed onto the umbrella while applying traction (the sheath can be removed partially at this stage); 5) after the retaining lock is seated, the sheath is observed for bleeding; 6) if there is no bleeding, then the sheath and guidewire are removed. For a dedicated device, there can be a sheath with the umbrella, a pushing device to push the umbrella out (another sheath), a sheath to push the retaining lock, and a thread/suture to oppose the other sheaths and to retrieve the umbrella if it is misplaced.
A closed loop of string or suture (not shown) can be joined to the device by ways of a lumen or loop.
Accordingly, the double action vascular closure apposition device of
Accordingly, the collarless double action vascular closure apposition device is first closed, then opens, and then closes again, with the second closure occurring spontaneously, by contraction of the opposite facing members which have dominant memory characteristics over the umbrella members. The central junction can be loose enough (e.g., made of a flexible polymer) to permit the forces from the contraction of the opposite facing members to be exerted on the umbrella members. In some embodiments each opposite facing member can be continuous with a corresponding umbrella member (i.e., a first portion of a single wire comprises an umbrella member, a second portion of the same wire comprising an opposite facing member). For simplicity, only two opposing members are shown in the figure; in embodiments where an umbrella member and a opposite facing member are formed from a single wire, the number of umbrella members can equal the number of opposite facing members, and each opposing member-umbrella member can be an integrated piece of memory material. After the device has been delivered and vascular closure is complete, then the guidewire can be removed.
In any of the embodiments described, the umbrella-like structure, members of this structure or components of the umbrella can be made from any number of suitable materials, including radiopaque materials and materials coated to be made radiopaque, including bioabsorbable polymers or compounds, non-absorbable alloys and compounds including stainless steel, MP35, Nitinol, Nickel-Titanium ally, Kevlar, nylon polyester acrylic, gold, platinum, tantalum, niobium, molybdenum, rhodium, palladium silver, hafnium, tungsten, iridium. Materials with memory would also be preferable to allow the umbrella to spontaneously open after placement by the sheath. These can be made in the form of wires, fibers, filaments, small beams, and other extruded, woven, or formed shapes. Piano wire, super elastic memory wire, chromium allows, alloys of titanium and nickel, and other elastic memory materials previously mentioned as well as others can be used as well The umbrella fabric can be made from a number of suitable materials, including flexible polymeric materials with elastomeric properties including polyurethane, polyethylene, polyestenurethane, polyimide, olyethreimide, polycarbonate, polysiloxane, polyvinyls, hydroxyethylmethacrylate, related polymers, co-polymers of these or other polymers, or drug-embedded or drug-eluting polymers to prevent coagulation or intimal hyperplasia (such as Taxol), also which can be made radiopaque by markers and addition of appropriate radiopaque materials.EXAMPLE EMBODIMENTS
The present invention can comprise a device to close puncture wounds caused by catheter procedures and especially angiography comprised of an expandable umbrella-like device that in the compressed state resides in a sheath, and after being expelled from the sheath assumes a planar or conical or other shape, engages vessel wall by means of tissue hooks or penetrators, is collapsed, analogous to umbrella tines, and brings the edges of the vessel wound or puncture into apposition. The device can have a retaining locking device that prevents the umbrella-like structure from reopening. This locking can be achieved by mechanical means including deformable enlargements on the members, dentates, male-female connectors, peg and hole, or other directional mating/locking devices on the members and retaining locking device. This locking device can have a washer like appearance, but can also take a number of different forms, including an inverted umbrella device made of metal, plastic, composites, or biodegradable material.
The device can have single or multiple hooks and penetrating devices to engage and seize the vessel wall. Each hook can be a single or multiple hook. The device can have members (or tines) of the umbrella-like structure that are linear, curvilinear, spiral, leaf-like, diamond shaped, woven, or other complex shapes, but still function as an opening-closing structure that can accommodate a retaining lock. The device when expanded can have a planar or conical or reverse conical geometry, or other complex shape that can collapse into near-linear form with traction and locking of the retaining lock. The device can have a retrieval fitting, usually a loop, fitted with a closed loop thread, string, or suture in order to apply traction to the device. The device can have a lumen for a guidewire.
The device can have members that are coated or backed with a fabric or membrane, either completely or partially. The device can elute therapeutic material to prevent thrombogenesis, hemorrhage, inflammation, and intimal hyperplasia with vascular closure. The device can be used in angiography, angioplasty, vascular puncture, tissue biopsy, or trauma that cause a puncture wound that should be closed. The device can comprise materials with memory, so that the device spontaneously assumes it therapeutic shape when expelled from the sheath. The device can comprise at least 2 or more members; 3 or more members can be preferable in some applications. The device can have members with angled dentates or tissue penetrators to prevent movement or migration of the device into the lumen of the blood vessel. These can also be used to retain the retaining lock.
A tissue opening can be closed according to the present invention by a) introducing a guidewire and sheath, b) penetrating the proximal surface of the blood vessel by the sheath and the guidewire, c) placing a device in the closed form in the sheath, with the loop of string or suture, d) extruding the device from the sheath and expanding while in the tissue (e.g., while inside a blood vessel), e) pulling the device against the tissue wall (e.g., the blood vessel wall), seating the hooks in the tissue, f) partially removing the sheath is to seat the device while a retaining lock is advanced, g) advancing the retaining lock over the members of the device while applying traction with the string, forcing them in the closed position, h) bringing the edges of the puncture wound together; if no bleeding occurs, i) then removing the guidewire, j) cutting the loop of string, leaving the device safely seated and locked with the puncture repaired.
A tissue opening can be closed according to the present invention with sequential delivery of a device. For example, the following steps can be taken 1) first the guidewire and sheath are in place, 2) next the umbrella is pushed down the sheath, either next to the guidewire or with the guidewire in the lumen of the umbrella; 3) the umbrella is extruded, and then using the thread or suture, pulled tight against the lumen of the vessel; 4) next the retaining lock is pushed down the thread and/or guidewire, and is pushed onto the umbrella while applying traction (the sheath can be removed partially at this stage, 5) after the retaining lock is seated, the sheath is observed for bleeding, 6) if there is no bleeding, then the sheath and guidewire are removed.
A tissue opening can be closed according to the present invention employing a dedicated device consisting of a sheath containing a device, a pushing device to push the device out (e.g., another sheath), a sheath to push the retaining lock, and a thread/suture to oppose the movement of the other sheaths and to retrieve the umbrella if it is misplaced.
The particular sizes and equipment discussed above are cited merely to illustrate particular embodiments of the invention. It is contemplated that the use of the invention may involve components having different sizes and characteristics. It is intended that the scope of the invention be defined by the claims appended hereto.
1) A tissue closure device, comprising:
- a) A junction body;
- b) A plurality of tissue engagement elements, each having first and second ends, each mounted with the junction body near its first end in a manner that allows the tissue engagement elements to assume first and second configurations, and each comprising a portion spaced from the first end adapted to engage the tissue in both the first and second configurations, wherein: i) In the first configuration, the second ends of the tissue engagement elements are spaced from each other by at least a first distance; ii) In the second configuration, the second ends of the tissue engagement elements are spaced from each other by no more than a second distance, where the second distance is less than the first distance.
2) A tissue closure device, comprising a plurality of tissue engagement elements, mounted with each other such that in a first compressed configuration the tissue engagement elements can pass through a tissue opening to be closed, and such that in a second compressed configuration the tissue engagement elements bring the edges of the opening into apposition, and such that in an expanded configuration the tissue engagement elements span the opening, wherein the tissue engagement elements engage the tissue in both the compressed configuration and in the expanded configuration.
3) A device as in claim 2, wherein the tissue engagement elements comprise hooks.
4) A device as in claim 2, wherein the tissue engagement elements comprise wires each having a hook at a first end and slidably mounted with a lock device at a second end, wherein the wires assume the expanded configuration when not constrained by the lock device and assume the compressed configuration when constrained by the lock device.
5) A device as in claim 4, wherein the wires mount together at their second ends with a string receiving element adapted to engage a string such that tension on the string opposed to force on the lock device urges the wires through the lock device substantially along the direction of the tension on the string.
6) A tissue closure device, comprising:
- a) A junction element, having a string engagement portion;
- b) A plurality of members, where each member has a tissue engagement feature at a first end, and mounted with the junction element such that the members extend away from the junction element defining a truncated cone;
- c) A lock element comprising a collar defining an interior passage, wherein passage of the junction element through the interior passage manipulates the members such that the area of the base of the truncated cone defined by the members is reduced.
7) A device as in claim 6, wherein the members comprise wires each having a hook at its first end.
8) A device as in claim 6, wherein the members comprise wires each having a plurality of hooks at its first end.
9) A device as in claim 6, wherein the lock element comprises a tissue engagement portion adapted to engage tissue over an area more than three times the area of the interior passage.
10) A device as in claim 6, wherein the junction element comprises a collar defining an interior passage suitable for passage of a guidewire therethrough.
11) A device as in claim 6, wherein each member further comprises one or more secondary tissue engagement features mounted with the member not at the first end.
12) A device as in claim 6, wherein the secondary tissue engagement members comprise projections from the member oriented toward the first end.
13) A device as in claim 6, further comprising a covering extending between the members.
14) A device as in claim 6, wherein the covering comprises a therapeutic material eluted when the device is placed in tissue.
15) A device as in claim 6, wherein the members comprise elongated diamond shaped elements.
16) A device as in claim 6, wherein the members are connected to each other by intermember struts.
17) A tissue closure device, comprising:
- a) A junction element, having a string engagement portion;
- b) A plurality of members, where each member has a tissue engagement feature at a first end, and mounted with the junction element such that the members extend away from the junction element defining a truncated cone, and having one or more secondary tissue engagement features mounted with the member and oriented toward the first end.
18) A device to close openings in blood vessels comprising an expandable umbrella-like device that in the compressed state resides in a sheath; after being expelled from the sheath assumes a planar or conical shape; after being brought into contact with a vessel wall engages the vessel wall; and can be collapsed to bring the edges of the opening into apposition.
19) A method of closing an opening in tissue, comprising:
- a) passing a device, as in claim 2, while in the first compressed condition through a sheath that penetrates the proximal surface of the tissue;
- b) expelling the device from the sheath into space beyond the proximal surface of the tissue such that the device assumes the expanded configuration;
- c) manipulating the device such that the tissue engagement elements engage the tissue;
- d) causing the device to assume the second compressed configuration, bringing the edges of the opening into apposition.
20) A method as in claim 19, further comprising configuring the device such that it will remain in the second compressed configuration.
21) A method as in claim 19, wherein causing the device to assume the second compressed configuration comprises applying traction to the device.
22) A device as in claim 6, wherein the junction element defines a lumen suitable for passage of a guidewire therethrough.
23) A device as in claim 2, wherein the tissue engagement elements comprise a shape memory material such that the tissue engagement elements assume the expanded configuration unless forced to another configuration.
24) A method of as in claim 19, wherein:
- a) The device comprises a string attachment portion, to which a string is attached;
- b) Manipulating the device such that the tissue engagement elements engage the tissue comprises pulling the string to encourage the device towards the tissue;
- c) Causing the device to assume the second compressed configuration comprises passing the string through a central passageway of a locking element, passing the locking element down the string to the device, pulling the string such that a portion of the device engages the locking element, which engagement causes the device to assume the second compressed configuration.
25) A tissue closure device as in claim 2, wherein
- a) the tissue engagement elements comprise elongated members, where each elongated member defines a first portion and a second portion along the length of the member, and are mounted with each other near the boundaries of the first and second portions of the members;
- b) each tissue engagement element is shaped such that, absent external restraining force, the first portion and second portion of the member form an angle less than 180 degrees to each other, and the mounting of the tissue engagement elements is such that, when the first portions of the members are substantially parallel to each other, the second portions extend approximately radially outward from the mounting, defining the expanded configuration;
- c) each tissue engagement element comprises a resilient material, such that the members can be forced to a configuration where the first portions of the members and the second portions of the members can be contemporaneously contained within a sheath, defining the compressed configuration.
International Classification: A61M 5/178 (20060101);