Closure devices, related delivery methods and tools, and related methods of use
A device for sealing a patent foramen ovale (PFO) in the heart is provided. The device includes a left atrial anchor adapted to be placed in a left atrium of the heart, a right atrial anchor adapted to be placed in a right atrium of the heart, and an elongate member adapted to extend through the passageway and connect the left and right atrial anchors. The right atrial anchor preferably includes a plurality of arms and a cover attached to the arms. The left atrial anchor also includes a plurality of arms and preferably does not include a cover. Preferably, the elongate member has a first end of fixedly connected to the left atrial anchor and a portion, proximal to the first end, releasably connected to the right atrial anchor.
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This invention relates to devices for closing a passageway in a body, for example a patent foramen ovale in a heart, related methods and devices for delivering such closure devices, and related methods of using such closure devices for sealing the passageway.
BACKGROUND OF THE INVENTION
Where anatomical closure of the foramen ovale does not occur, a patent foramen ovale (PFO) is created. A patent foramen ovale is a persistent, usually flap-like opening between the atrial septum primum (SP) and septum secundum (SS) of a heart. A patent foramen ovale results when either partial or no fusion of the septum primum (SP) to the septum secundum (SS) occurs. In the case of partial fusion, a persistent passageway exists between the superior portion of the septum primum (SP) and septum secundum (SS). It is also possible that more than one passageway may exist between the septum primum (SP) and the septum secundum (SS).
Studies have shown that a relatively large percentage of adults have a patent foramen ovale (PFO). It is believed that embolism via a PFO may be a cause of a significant number of ischemic strokes, particularly in relatively young patients. It has been estimated that in 50% of cryptogenic strokes, a PFO is present. Patients suffering a cryptogenic stroke or a transient ischemic attack (TIA) in the presence of a PFO often are considered for medical therapy to reduce the risk of a recurrent embolic event.
Pharmacological therapy often includes oral anticoagulants or antiplatelet agents. These therapies may lead to certain side effects, including hemorrhaging. If pharmacologic therapy is unsuitable, open heart surgery may be employed to close a PFO with stitches, for example. Like other open surgical treatments, this surgery is highly invasive, risky, requires general anesthesia, and may result in lengthy recuperation.
Nonsurgical closure of PFOs is possible with umbrella-like devices developed for percutaneous closure of atrial septal defects (ASD) (a condition where there is not a septum primum (SP)). Many of these conventional devices used for ASDs, however, are technically complex, bulky, and difficult to deploy in a precise location. In addition, such devices may be difficult or impossible to retrieve and/or reposition should initial positioning not be satisfactory. Moreover, these devices are specially designed for ASDs and therefore may not be suitable to close and seal a PFO, particularly because the septum primum (SP) overlaps the septum secundum (SS).
SUMMARY OF THE INVENTIONIn accordance with the invention, methods, tools, and devices for closing a passageway in a body, and more specifically closing a patent foramen ovale (PFO), are provided.
According to one aspect of the invention, a device for sealing a passageway in a human body is provided. The device comprises a first anchor adapted to be placed proximate a first end of the passageway, a second anchor adapted to be placed proximate a second end of the passageway, and an elongate member adapted to extend through the passageway and connect the first and second anchors, the elongate member having a first end fixedly connected to the first anchor and a second end that releasably connects to the second anchor.
According to another aspect of the invention, a device for sealing a passageway in a human body comprises a first anchor adapted to be placed proximate a first end of the passageway, a second anchor adapted to be placed proximate a second end of the passageway, and a flexible elongate member adapted to extend through the passageway and connect the first and second anchors, the elongate member capable of moving through the second anchor to vary a length of the elongate member between the first and second anchors.
According to another aspect of the invention, a device for sealing a passageway in a heart is provided. The device comprises a first anchor adapted to be placed proximate a first end of the passageway, a second anchor adapted to be placed proximate a second end of the passageway, and a flexible elongate member adapted to extend through the passageway and connect the first and second anchors, wherein the first anchor pivots relative to the elongate member and the second anchor pivots relative to the elongate member.
According to yet another aspect of the invention, a device for sealing a passageway in a heart comprises a first anchor adapted to be placed proximate a first end of the passageway, a second anchor adapted to be placed proximate a second end of the passageway, and a flexible elongate member adapted to extend through the passageway and connect the first and second anchors, wherein each of the first and second anchors is collapsible from a deployed state to a collapsed delivery state.
According to a further aspect of the invention, a device for sealing a patent foramen ovale in a heart is provided. The device includes a first anchor including a first plurality of arms adapted to be placed proximate a first end of the patent foramen ovale, a second anchor including a second plurality of arms adapted to be placed proximate a second end of the patent foramen ovale, and a flexible elongate member adapted to extend through the patent foramen ovale and connect the first and second anchors, the elongate member having a first end fixedly connected to the first anchor and a second end that releasably connects to the second anchor, and wherein each of the first and second plurality of arms are collapsible from a deployed state to a delivery state.
According to another aspect of the invention, an assembly for sealing a passageway in a heart is provided. The assembly comprises a positioning catheter capable of extending to the passageway, and a closure device capable of sealing the passageway, the closure device including a first anchor adapted to be placed proximate a first end of the passageway, a second anchor adapted to be placed proximate a second end of the passageway, and a flexible elongate member adapted to extend through the passageway and connect the first and second anchors, wherein the closure device is positionable within the positioning catheter in a first collapsed state and extendable from the positioning catheter in a second deployed state.
According to yet another aspect of the invention, an assembly for sealing a patent foramen ovale in a heart is provided. The assembly comprises a guide catheter capable of extending to the patent foramen ovale, a positioning catheter capable of extending through the guide catheter to a position near the patent foramen ovale, and a closure device capable of sealing the patent foramen ovale, the closure device including a first anchor having a first plurality of arms adapted to be placed proximate a first end of the patent foramen ovale, a second anchor having a second plurality of arms adapted to be placed proximate a second end of the patent foramen ovale, a flexible elongate member adapted to extend through the patent foramen ovale and connect the first and second anchors, and a releasable fixation mechanism that selectively engages a distal portion of the positioning catheter to releasably connect the second end of the elongate member to the second anchor, wherein the closure device is positionable within the positioning catheter in a first state wherein each of the first and second plurality of arms are collapsed and extendable from the positioning catheter in a second deployed state wherein each of the first and second plurality of arms are extended.
According to another aspect of the invention, a method of sealing a passageway in a heart is provided. The method comprises placing a first anchor proximate a first end of the passageway, placing a second anchor proximate a second end of the passageway, and moving the second anchor relative to the first anchor along a flexible elongate member disposed between the first and second anchors within the passageway.
According to another aspect of the invention, a method of placing a closure device to seal a passageway in a heart comprises advancing a catheter into a first end of the passageway and out a second end of the passageway, advancing a first anchor of a closure device out of a distal end of the catheter, withdrawing the catheter through the passageway, positioning the first anchor adjacent the second end of the passageway, advancing a second anchor of the closure device out of the distal end of the catheter, and positioning the second anchor of the closure device adjacent the first end of the passageway.
According to a further aspect of the invention, a method of delivering a closure device to a patent foramen ovale in a heart is provided. The method includes advancing a catheter into the right atrium of the heart, advancing the catheter through the patent foramen ovale into the left atrium of the heart, deploying a first anchor of the closure device in the left atrium, withdrawing the catheter into the right atrium of the heart, and deploying a second anchor of the closure device in the right atrium.
According to another aspect of the invention, a closure device for sealing a passageway in a heart comprises a left atrial anchor configured to close a first end of the passageway, a right atrial anchor configured to close a second end of the passageway, and a flexible elongate member connecting the left and right atrial anchors, wherein the elongate member has a first end fixedly connected to the left atrial anchor and wherein the right atrial anchor is movable with respect to the elongate member and is configured to releasably attach to the elongate member at any one of a plurality of points along a length of the elongate member.
According to another aspect of the invention, an assembly for sealing a passageway in a heart includes a guide catheter configured to extend from a point of entry into a body to the passageway, and a closure device capable of sealing the passageway, the closure device including a first anchor adapted to be placed proximate a first end of the passageway, a second anchor adapted to be placed proximate a second end of the passageway, and a flexible elongate member connecting the first and second anchors, wherein a first end of the elongate member is connected to the first anchor and wherein the elongate member extends through the second anchor and through the catheter to the point of entry into the body.
According to yet another aspect of the invention, a device for sealing a passageway in a human body comprises a first anchor adapted to be placed proximate a first end of the passageway, a second anchor adapted to be placed proximate a second end of the passageway, and a flexible elongate member adapted to extend through the passageway and connect the first and second anchors, the elongate member capable of moving through the second anchor to vary a tension of the elongate member.
According to another aspect of the invention, a device for closing a passageway in a human body comprises a first anchor adapted to be placed proximate a first end of the passageway, a second anchor adapted to be placed proximate a second end of the passageway, and a flexible elongate member adapted to extend through the passageway and connect the first and second anchors, the elongate member having a first end releasably connected to the first anchor and a second end releasably connected to the second anchor.
According to another aspect of the invention, a device for closing a passageway in a heart comprises a left atrial anchor adapted to be placed in a left atrium of the heart and including a plurality of uncovered arms, a right atrial anchor adapted to be placed in a right atrium of the heart and including a plurality of arms and a cover attached to the plurality of arms, and a flexible elongate member adapted to extend through the passageway and connect the left and right atrial anchors, the elongate member having a first end fixedly connected to the left atrial anchor and a second end releasably connected to the right atrial anchor.
According to another aspect of the invention, a device for sealing a passageway in a heart comprises a first anchor adapted to be placed proximate a first end of the passageway, the first anchor comprising a plurality of uncovered arms, a second anchor adapted to be placed proximate a second end of the passageway, the second anchor comprising a plurality of uncovered arms, and a flexible elongate member adapted to extend through the passageway and connect the first and second anchors, the elongate member having a first end fixedly connected to the first anchor and a second end that releasably connects to the second anchor.
Additional advantages of the invention will be set forth in part in the description which follows, and in part will be obvious from the description, or may be learned by practice of the invention. The objects and advantages of the invention will be realized and attained by means of the elements and combinations particularly pointed out in the appended claims.
The foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the invention, as claimed.
BRIEF DESCRIPTION OF THE DRAWINGSThe accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate several embodiments of the invention and together with the description, serve to explain the principles of the invention.
Reference will now be made in detail to embodiments of the invention, examples of which are illustrated in the accompanying drawings. Wherever possible, the same reference numbers will be used throughout the drawings to refer to the same or like parts.
The various Figures show embodiments of patent foramen ovale (PFO) closure devices, tools, devices and methods for delivery of the PFO closure devices, and methods of using the device to close a PFO. The devices and related methods are described herein in connection with use in sealing a PFO. These devices, however, also are suitable for closing other openings or passageways, including other such openings in the heart, for example atrial septal defects, ventricular septal defects, and patent ductus arterioses, and openings or passageways in other portions of a body such as an arteriovenous fistula. The invention therefore is not limited to use of the inventive closure devices to close PFOs.
As embodied herein and shown in
In one embodiment, tether 16 is formed of a multifilar braided polymeric material. Suitable materials include, but are not limited to, multifilament yarns of ultra-high molecular weight polyethylene (UHMWPE) such as SPECTRA or DYNEEMA. Other suitable materials include liquid crystal polymer (LCP) such as VECTRAN, polyester, or other high strength fibers. Other suitable materials of sufficient strength and flexibility may be used for tether 16.
Releasable fixation mechanism 30 is preferably spring-loaded and is shown in
Piercing pin 32 has a sharpened end and is oriented generally orthogonal to tether 16. Spring portion 32a is connected to housing 31 such that the natural, unbiased position of spring portion 32a forces piercing pin 32 through tether 16. Piercing pins 32 are illustrated as passing completely through tether 16, but it is contemplated that pins 32 may pass only partially into tether 16.
Piercing pins 32 cooperate with a piercing collar 34 that is attached to housing 31. Collar 34 has an internal passage which is somewhat larger than tether 16. In the embodiment shown, collar 34 also has two passageways, one for each piercing pin 32, through which piercing pins 32 pass. Once piercing pins 32 have passed into (and potentially through) tether 16, piercing pins 32 securely lock tether 16 relative to fixation mechanism 30 and thus to right atrial anchor 14. Piercing collar 34 also holds tether 16 in place if piercing pins 32 are desired to be extracted from tether 16, as will be described later.
Piercing pins 32 are preferably formed of an elastic metal with spring characteristics. Suitable materials include but are not limited to stainless steel, nickel-titanium, ELGILOY, or MP35N. Housing 31 is preferably a thin walled tube formed of a biocompatible metal or polymer. The releasable fixation mechanism 30 illustrated in
Balloon 24 is shown in
RPC 22 described and illustrated with respect to
Although arms 40 preferably pass through hub 42, in an alternative arrangement arms 40 may not actually pass though hub 42, i.e., they may extend radially from hub 42. Additionally, it is possible that instead of arms 40, the anchors 12, 14 may comprise spiral structures, flat braided structures, or webs. Any structure of sufficient size and shape to hold the septum primum (SP) in contact with the septum secondum (SS) to close the PFO may be used.
Arms 40 are preferably fabricated of metallic wire, such as stainless steel, nickel-titanium, ELGILOY, or MP35N. In the case of nickel-titanium, the wires may be used in either a super-elastic mode, whereby the wires deploy due to the super-elastic properties of this alloy, or they may be used in a thermal-transforming mode. In the thermal-transforming mode, the wires may be chilled prior to deployment, for example by the introduction of chilled saline in the delivery assembly, and subsequently warmed by exposure to the blood, once guide catheter 20 (or a delivery sheath) is withdrawn.
As shown in
To minimize frictional forces between a guide catheter 20 (or delivery sheath) and the undeployed anchors, as well as minimizing tissue trauma during deployment, the ends of arms 40 are preferably rounded (as shown by the right-hand arm in
Right atrial anchor 14 preferably includes a fabric or other membrane covering that span between arms 50. This covering, represented in
In another embodiment according to the present invention, the closure device 10 need not incorporate a releasable fixation mechanism such as those described above. Instead, other structures may be used to fix right anchor 14 to tether 16. In such an embodiment, as illustrated in
Locking element 70 is preferably tubular and includes a number of projecting grips 72. These grips 72 may be oriented in a ratchet-like manner (not shown) such that locking element 70 can be advanced distally along tether 16, but will resist proximal movement. Alternately, locking element 70 can be positioned in the desired location on tether 16, and swaged down to bite into the surface of tether 16. As a further alternative, locking element 70 may have an outer surface 74 which is tapered to engage with a tapered inner surface 36a of anchor attachment hub 36 in a wedge-like manner, as shown in
While not shown, locking element 70 could also be used in conjunction with the embodiments above which utilize a releasable fixation mechanism. As such, locking element 70 would provide extra security in the fixation of right atrial anchor 14 to tether 16.
As described earlier, RPC 22 includes balloon 24 for engaging right atrial anchor 14. Therefore RPC 22 is provided with a manifold 90 at a proximal end which includes a port 92 in fluid communication with balloon 24. Manifold 90 may further include a touhy borst seal 94, through which tether 16 extends.
As mentioned,
When it is desired to deploy left atrial anchor 12, right atrial positioning catheter 22 is advanced relative to guide catheter 20, or guide catheter 20 is withdrawn relative to the RPC 22, or both. Since RPC 22 is engaged with right atrial anchor 12, the forces required for advancement of left atrial anchor 14 can be compressively transferred to abutting left atrial anchor 12.
As embodied herein and shown in
Then, as shown in
While guide catheter 20 and delivery components are within the left atrium, only left atrial anchor 12 is deployed from guide catheter 20.
In the next step of an embodiment of the delivery method, left atrial anchor 12 is pulled against the opening of the PFO, as shown in
As shown in
Once left atrial anchor 12 is positioned, right atrial anchor 14 may be deployed. As shown in
Right atrial anchor 14 is temporarily connected to a right atrial anchor positioning catheter (RPC) 22, as shown in
In the next step of this embodiment of a closure device delivery method, right atrial anchor 14 is advanced into contact with the right atrial septal wall, as shown in
In the next step of an embodiment of the delivery method, right atrial anchor 14 is fixed to tether 16.
At this point, closure device 10 is in its final position, with the exception that flexible tether 16 extends between closure device 10 and guide catheter 20. Closure device 10, however, is essentially uninfluenced by guide catheter 20 or the extension of tether 16 to and through guide catheter 20. The effectiveness of the closure and sealing of the PFO can be tested by conventional techniques, such as contrast visualization, or a Valsalva maneuver combined with injection of bubbles, visualized with (TEE) or intracardiac ultrasound.
Additionally, at this stage of delivery of closure device 10, hemodynamic parameters such as oxygen saturation and pulmonary wedge pressure can be measured. In some rare instances, closure of a PFO may excessively increase pulmonary arterial pressure, in which case the closure device 10 can be removed, as described below. It may be necessary to leave the closure device in place for several hours or even days to fully assess the impact on hemodynamic parameters. If this is desired, the excess tether is simply left to extend from the closure device to the introduction site. At such time that the device is desired for permanent implanation, the excess tether is cut, or if the device is desired for removal, it is removed as described below.
At this point in the delivery method, or at any other earlier point in the procedure, closure device 10 can be completely removed from the patient. This may be necessary if, for example, device 10 is not creating a complete seal due to any of a number of causes, including, for example, the selected device being too small. To remove closure device 10, RPC 22 is re-engaged with right atrial anchor 14 to reverse the fixation mechanism that secures right atrial anchor 14 to tether 16. This allows right atrial anchor 14 to slide relative to tether 16. Right atrial anchor 14 may then be collapsed by retracting RPC 22 and right atrial anchor 14 within the delivery
assembly 18, and specifically into guide catheter 20. Guide catheter 20 then may be re-advanced through the PFO track, while at the same time tension is maintained on tether 16. Continued advancement of guide catheter 20 will advance catheter 20 over left atrial anchor 12 to collapse anchor 12 within catheter 20 as shown in
If closure device 10, as shown in
As mentioned above, closure device 10, according to one aspect of the invention, can be re-captured at any time prior and up to the state of closure device 10 depicted in
The various described embodiments of closure devices and methods and tools for their delivery are suitable for closure of a wide variety of PFOs. For example, PFOs with a relatively long overlap between the septum primum (SP) and septum secundum (SS) may be suitably closed, as shown in
Other embodiments of the invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. The specification and examples are exemplary, with a true scope and spirit of the invention being indicated by the following claims.
Claims
1-102. (canceled)
103. A device for sealing a passageway in a human heart, the device comprising:
- a first anchor adapted to be placed proximate a first end of the passageway, the first anchor including a plurality of arms made of a first material, wherein the first anchor does not include a structure spanning between the plurality of arms;
- a second anchor adapted to be placed proximate a second end of the passageway, the second anchor including a plurality of arms and a cover spanning between the plurality of arms; and
- an elongate member adapted to extend through the passageway and connect the first and second anchors, the elongate member being made of a second material different from the first material.
104. The device of claim 103, wherein the passageway is a patent foramen ovale.
105. The device of claim 103, wherein the elongate member is flexible.
106. The device of claim 103, wherein the plurality of arms of the first anchor extend from a central hub of the first anchor.
107. The device of claim 103, wherein the plurality of arms of the first anchor can assume a collapsed state and a deployed state.
108. The device of claim 103, wherein the plurality of arms of the second anchor extend from a central hub of the second anchor.
109. The device of claim 103, wherein the plurality of arms of the second anchor can assume a collapsed state and a deployed state.
110. The device of claim 103, wherein the first anchor pivots relative to the elongate member.
111. The device of claim 103, wherein the second anchor pivots relative to the elongate member.
112. The device of claim 103, wherein the device is a closure device for sealing a patent foramen ovale in a heart, the first anchor is configured to engage a left atrial opening of the passageway, and the second anchor is configured to engage a right atrial opening of the passageway.
113. The device of claim 103, wherein the elongate member has a first end fixedly connected to the first anchor.
114. The device of claim 103, wherein the elongate member is capable of moving through the second anchor to vary a length of the elongate member between the first and second anchors.
115. The device of claim 103, wherein the second anchor is movable with respect to the elongate member.
116. The device of claim 115, wherein the elongate member includes a fixing portion configured to receive a fixing element for fixing a position of the second anchor relative to the elongate member, and wherein the fixing element may be positioned at any point along a length of the fixing portion of the elongate member.
117. The device of claim 103, wherein the elongate member is configured to permanently connect the first and second anchors when implanted in the body.
118. The device of claim 103, wherein the elongate member is configured to move through the second anchor to vary a tension of the elongate member.
119. The device of claim 103, wherein the device includes a fixing element positioned on and movable relative to the elongate member to fix the location of the second anchor with respect to the elongate member.
120. The device of claim 119, wherein the elongate member includes a fixing portion configured to receive the fixing element, and wherein the fixing element may be positioned at any point along a length of the fixing portion of the elongate member.
121. The device of claim 119, wherein the fixing element is a locking element movable in only one direction along the elongate member.
122. The device of claim 119, wherein the fixing element is a releasable fixation element.
123. The device of claim 122, wherein the releasable fixation element forms a central portion of the second anchor.
124. The device of claim 103, wherein the cover spanning between the plurality of arms of the second anchor is formed from a single sheet of material.
125. The device of claim 103, wherein the cover spanning between the plurality of arms of the second anchor is made from one of a woven polyester, a knit polyester, and ePTFE.
126. The device of claim 103, wherein the cover spanning between the plurality of arms of the second anchor comprises a porous material having a porosity sufficient to encourage ingrowth of tissue.
127. The device of claim 103, wherein the cover spanning between the plurality of arms of the second anchor includes a non-thrombogenic coating.
128. The device of claim 127, wherein the non-thrombogenic coating is heparin.
129. The device of claim 103, wherein the cover is attached to the plurality of arms of the second anchor by sutures.
130. The device of claim 103, wherein the second material is a polymeric material.
131. The device of claim 130, characterized in that the second material is one of ultra-high molecular weight polyethylene, liquid crystal polymer, and polyester.
132. The device of claim 131, wherein the second material is an ultra-high molecular weight polyethylene and wherein the second material is one of SPECTRA and DYNEEMA.
133. The device of claim 131, wherein the second material is the liquid crystal polymer VECTRAN.
134. The device of claim 103, wherein the elongate member has sufficient flexibility to conform to a shape of the passageway.
135. The device of claim 103, wherein the plurality of arms of the second anchor are made of the first material.
136. The device of claim 103, wherein the first material is metallic.
137. The device of claim 136, wherein the first material is a metallic wire.
138. The device of claim 136, wherein the first material is one of stainless steel, nickel-titanium, ELGILOY, or MP35N.
139. The device of claim 103, wherein the elongate member is a braided structure.
140. The device of claim 103, wherein the elongate member is a multifilar structure.
141. A device for sealing a passageway in a human heart, the device comprising:
- a first anchor adapted to be placed proximate a first end of the passageway, the first anchor including a plurality of arms, wherein the first anchor does not include a structure spanning between the plurality of arms;
- a second anchor adapted to be placed proximate a second end of the passageway, the second anchor including a plurality of arms and a cover spanning between the plurality of arms; and
- an elongate member adapted to extend through the passageway and connect the first and second anchors, the elongate member having sufficient flexibility to conform to a shape of the passageway.
142. The device of claim 141, wherein the passageway is a patent foramen ovale.
143. The device of claim 141, wherein the elongate member is flexible.
144. The device of claim 141, wherein the plurality of arms of the first anchor can assume a collapsed state and a deployed state.
145. The device of claim 141, wherein the plurality of arms of the second anchor can assume a collapsed state and a deployed state.
146. The device of claim 141, wherein the first anchor pivots relative to the elongate member.
147. The device of claim 141, wherein the second anchor pivots relative to the elongate member.
148. The device of claim 141, wherein the device is a closure device for sealing a patent foramen ovale in a heart, the first anchor is configured to engage a left atrial opening of the passageway, and the second anchor is configured to engage a right atrial opening of the passageway.
149. The device of claim 141, wherein the second anchor is movable with respect to the elongate member.
150. The device of claim 149, wherein the elongate member includes a fixing portion configured to receive a fixing element for fixing a position of the second anchor relative to the elongate member, and wherein the fixing element may be positioned at any point along a length of the fixing portion of the elongate member.
151. The device of claim 141, wherein the device includes a fixing element positioned on and movable relative to the elongate member to fix the location of the second anchor with respect to the elongate member.
152. The device of claim 151, wherein the elongate member includes a fixing portion configured to receive the fixing element, and wherein the fixing element may be positioned at any point along a length of the fixing portion of the elongate member.
153. The device of claim 151, wherein the fixing element is a locking element movable in only one direction along the elongate member.
154. The device of claim 141, wherein the cover spanning between the plurality of arms of the second anchor is formed from a single sheet of material.
155. The device of claim 141, wherein the cover spanning between the plurality of arms of the second anchor is made from one of a woven polyester, a knit polyester, and ePTFE.
156. The device of claim 141, wherein the cover spanning between the plurality of arms of the second anchor comprises a porous material having a porosity sufficient to encourage ingrowth of tissue.
157. The device of claim 141, wherein the cover spanning between the plurality of arms of the second anchor includes a non-thrombogenic coating.
158. The device of claim 157, wherein the non-thrombogenic coating is heparin.
159. The device of claim 141, wherein the cover is attached to the plurality of arms of the second anchor by sutures.
160. The device of claim 141, wherein the elongate member is a braided structure.
161. The device of claim 141, wherein the elongate member is a multifilar structure.
162. An improved occlusion device, comprising:
- a center post;
- first and second fixation devices connected to the center post, the first and second fixation devices comprising at least five arms;
- first and second sheets attached to the first and second fixation devices respectively.
163. The occlusion device of claim 162, wherein a length of the arms of the first fixation device is not equal to a length of the arms of the second fixation device.
164. The occlusion device of claim 163, wherein the arms of the first fixation device do not have equal lengths.
165. The occlusion device of claim 164, wherein the arms of the second fixation device do not have equal lengths.
166. The occlusion device of claim 162, wherein each arm is spaced at an equal angle from the adjacent arm.
167. The occlusion device of claim 162, wherein the number of sides of the first and second sheets is equal to the number of arms of the fixation devices.
168. The occlusion device of claim 162, wherein the first and second fixation devices comprise six arms.
169. The occlusion device of claim 168, wherein the six arms are formed by three wires extending through holes in the center post.
170. An occlusion device with improved seating ability, the occlusion device comprising:
- a center post;
- first and second fixation devices emanating from the center post, wherein the first and second fixation devices comprise at least six arms; and
- first and second sails attached to the first and second fixation devices, respectively.
171. The occlusion device of claim 170, wherein a length of the arms of the first fixation device is not equal to a length of the arms of the second fixation device.
172. The occlusion device of claim 170, wherein the arms do not have equal lengths.
173. The occlusion device of claim 170, further comprising holes in the center post through which the first fixation device extends.
174. The occlusion device of claim 170, wherein the first and second fixation devices comprise eight arms.
175. The occlusion device of claim 170, wherein the first and second fixation devices comprise ten arms.
176. The occlusion device of claim 170, wherein the number of sides of the first and second sails is equal to the number of arms of the fixation devices.
177. An occlusion device for occluding a septal defect, the occlusion device comprising:
- a first fixation device configured to be placed on a first side of a septal defect, the first fixation device comprising at least five arms; and
- a second fixation device configured to be positioned on a second side of a defect, the second fixation device comprising at least five arms.
178. The occlusion device of claim 177, wherein a length of the arms of the first fixation device is not equal to a length of the arms of the second fixation device.
179. The occlusion device of claim 178, wherein the arms of the first fixation device do not have equal lengths.
180. The occlusion device of claim 179, wherein the arms of the second fixation device do not have equal lengths.
181. The occlusion device of claim 177, wherein each arm is spaced at an equal angle from the adjacent arm.
182. The occlusion device of claim 177, further comprising first and second sails attached to the first and second fixation devices.
183. The occlusion device of claim 177, wherein the first and second fixation devices comprise six arms.
184. The occlusion device of claim 177, further comprising a center post to which the first and second fixation devices are attached.
185. The occlusion device of claim 177, wherein the arms of the first and second fixation devices are formed to have a stiffness that ensures proper occlusion of the defect and provides the desired tension, yet does not decrease fatigue life of the fixation devices.
186. An occlusion device for occluding a septal defect, the occlusion device comprising:
- a first fixation device configured to be placed on a first side of a septal defect, the first fixation device comprising a plurality of arms which do not have equal lengths; and
- a second fixation device configured to be positioned on a second side of a septal defect, the second fixation device comprising a plurality of arms which do not have equal lengths.
187. The occlusion device of claim 186, wherein the length of the arms of the first fixation device is not equal to the length of the arms of the second fixation device.
188. The occlusion device of claim 186, wherein the plurality of arms comprises five arms.
189. The occlusion device of claim 186, wherein the plurality of arms comprises six arms.
Type: Application
Filed: Jul 21, 2005
Publication Date: Dec 1, 2005
Applicant:
Inventors: Dennis Wahr (Ann Arbor, MI), David Blaeser (Champlin, MN), Peter Keith (St. Paul, MN), Thomas Ressemann (St. Cloud, MN)
Application Number: 11/185,951