阅读说明：本技术 用于腔内装置的锚固机构和系统 (Anchoring mechanisms and systems for endoluminal devices ) 是由 D·H·迪拉德 T·J·约翰逊 B·J·舒曼 J-M·巴亚尔容 L·劳尔 于 2015-03-30 设计创作，主要内容包括：公开了用于在至少一个方向上闭塞气道的装置和方法,在一些情况下,所述装置包括锚固机构,所述锚固机构被配置成将该装置的一个操作部分(例如,阀)沿着其内部署有该装置的内腔的长度保持就位。所述锚固机构可以包括锚固件,所述锚固件被配置成安放到内腔壁内,伴有很少的或不伴有该装置的该操作部分的轴向移动。在一些实施方案中,所述锚固机构包括第二组锚固件,所述第二组锚固件被配置成当主要锚固件安放到该内腔的壁内时与该内腔壁接合,以减小、抑制或防止该装置的该操作部分的轴向移动。(Devices and methods for occluding an airway in at least one direction are disclosed, in some cases, the devices include an anchoring mechanism configured to hold an operative portion of the device (e.g., a valve) in place along the length of a lumen in which the device is deployed. The anchoring mechanism may include an anchor configured to seat within the lumen wall with little or no axial movement of the operative portion of the device. In some embodiments, the anchoring mechanism includes a second set of anchors configured to engage the lumen wall when the primary anchor is seated within the lumen wall to reduce, inhibit, or prevent axial movement of the operative portion of the device.)

1. A mechanism for anchoring an endoluminal device to an inner lumen, the mechanism comprising:

a hub member configured to be located at a predetermined position inside the inner cavity; and

a plurality of anchor struts, the plurality of anchor struts comprising:

a spring portion attached to the hub member and configured to extend or contract during expansion and contraction of the lumen; and

an anchor portion connecting the spring portion to the inner cavity,

the anchoring portion is configured to penetrate a portion of the lumen;

wherein the hub member is positioned on a plane with the anchoring portions of the plurality of anchoring legs, and

each of the spring portions of the plurality of anchor struts includes a helically coiled spring.

2. The mechanism of claim 1, wherein the anchor portion comprises a bi-directional anchor tip comprising a first tip pointing in a first direction and a second tip pointing in a second direction, the second direction being at an angle to the first direction, wherein at least a portion of the first tip penetrates the lumen in a direction transverse to the lumen.

3. The mechanism of claim 1, wherein each of the plurality of anchor struts comprises the same length.

4. The mechanism of claim 1, wherein each of the spring portions of the plurality of anchor struts extends radially outward from the hub member.

5. The mechanism of claim 1, wherein the hub member includes a first hub and a second hub collinear with and connected to the first hub, wherein the plurality of anchor struts are connected to the first hub.

6. A mechanism for anchoring an endoluminal device to an inner lumen, the mechanism comprising:

a hub member configured to be located at a predetermined position inside the inner cavity; and

a plurality of anchor struts, the plurality of anchor struts comprising:

a spring portion attached to the hub member and configured to extend or contract during expansion and contraction of the lumen; and

an anchor portion connecting the spring portion to the inner cavity,

the anchoring portion is configured to penetrate a portion of the lumen;

wherein the hub member is positioned on a plane with the anchoring portions of the plurality of anchoring legs, and

wherein each of the spring portions of the plurality of anchor struts comprises a curved strut member configured to straighten during expansion of the lumen and bend during contraction of the lumen, and the curved strut member comprises a vortex shape when viewed along a longitudinal axis of the lumen.

7. The mechanism of claim 6, wherein the curved strut members comprise one or more thin portions and one or more thick portions, the thick portions being thicker than the thin portions.

8. A mechanism for anchoring an endoluminal device to an inner lumen, the mechanism comprising:

a hub member configured to be located at a predetermined position inside the inner cavity; and

a plurality of anchor struts, the plurality of anchor struts comprising:

a spring portion attached to the hub member and configured to extend or contract during expansion and contraction of the lumen; and

an anchor portion connecting the spring portion to the inner cavity,

the anchoring portion is configured to penetrate a portion of the lumen;

wherein the hub member is positioned on a plane with the anchoring portions of the plurality of anchoring legs, and

wherein each of the spring portions of the plurality of anchor struts comprises a curved strut member configured to straighten during extension of the lumen and bend during contraction of the lumen, and the curved strut member comprises a helical shape when viewed along a longitudinal axis of the lumen.

9. The mechanism of claim 8, wherein the curved strut members comprise one or more thin portions and one or more thick portions, the thick portions being thicker than the thin portions.

10. An endoluminal device comprising:

an operative portion configured to obstruct fluid flow inside the lumen;

a hub member connected to the operative portion and including a hub and a central rod; and

a plurality of anchor struts, the plurality of anchor struts comprising:

a strut portion attached to the hub member and configured to expand and contract in response to expansion and contraction of the lumen; and

an anchor portion connecting the deflectable portion to the lumen;

wherein the hub member remains substantially on or near the axis of the lumen during movement of the lumen.

11. The apparatus according to claim 10, wherein the strut portion is connected to a sliding hub configured to slide along the length of the center rod.

12. The device of claim 10, wherein the plurality of anchor struts comprises a plurality of quadrilateral members.

13. The device of claim 12, wherein each of the quadrilateral members lies in a separate plane parallel to the longitudinal axis of the device.

14. A mechanism for anchoring an endoluminal device to an inner lumen, the mechanism comprising:

a hub member;

a plurality of distal anchor struts connected to and extending radially and distally from the hub member and curving in a proximal direction, each of the plurality of distal anchor struts comprising an anchor tip; and

a plurality of opposing anchor struts connected to and extending proximally and radially from the hub member and curving in a distal direction, each of the plurality of opposing anchor struts including opposing anchor tips;

wherein the distal anchor strut and the opposing anchor strut are configured to compress a portion of the lumen.

15. A mechanism for anchoring an endoluminal device to an inner lumen, the mechanism comprising:

a hub member; and

a plurality of anchor struts extending radially outward and distally from the hub member, each of the plurality of anchor struts configured to transition from a straightened configuration to an arcuate configuration when deployed within the lumen, each of the plurality of anchor struts having a length when in the straightened configuration;

wherein in the straightened configuration, the length of one or more of the plurality of anchor struts is at least 1.5 times the fully extended diameter of the lumen.

16. A mechanism for anchoring an endoluminal device to an inner lumen, the mechanism comprising:

an operating portion including a plurality of frame struts, each frame strut including a frame strut tip;

a hub member connected to a distal end of the operative portion; and

a plurality of distal anchor struts extending radially from the hub member and curving in a proximal direction, each distal anchor strut including an anchor tip positioned between the hub member and the frame strut tip;

wherein the frame strut tip and the anchor tip are interposed when viewed in a lateral direction.

Technical Field

The present disclosure relates to an anchoring mechanism for a device used inside a lung airway.

Background

Struts with anchors (struts) are commonly used as anchoring devices for use inside the airways to the lungs. However, provided herein are devices and methods that may facilitate anchoring devices used inside the airway to the lung (e.g., using springs).

Disclosure of Invention

The present technology relates to anchoring mechanisms and systems for endoluminal devices (endoluminal devices).

A mechanism for anchoring an endoluminal device to an inner lumen can include a hub (hub) member that can be configured to be positioned at a predetermined location inside the inner lumen. The mechanism may include a plurality of anchor struts. The plurality of anchor struts includes a spring portion. The spring portion may be attached to the hub member. The spring portion may be configured to extend or contract during expansion and contraction of the lumen. The mechanism may include an anchoring portion. The anchor portion may connect the spring portion to the lumen. The anchor portion may be configured to penetrate a portion of the lumen. The hub member may be positioned on a plane with the anchor portions of the plurality of anchor struts.

The anchoring portion may include a bi-directional anchoring tip (tip). The bi-directional anchoring tip may include a first tip pointing in a first direction. The bi-directional anchoring tip may include a second tip pointing in a second direction, the second direction being at an angle to the first direction. At least a portion of the first tip may penetrate the lumen in a transverse direction of the lumen. The plurality of anchor struts may comprise the same length.

Each of the spring portions of the plurality of anchor struts may extend radially outward from the hub member. Each of the spring portions of the plurality of anchor struts may comprise a helically coiled spring. Each of the spring portions of the plurality of anchor struts may include a curved strut member configured to straighten during extension of the lumen and bend during contraction of the lumen.

The curved strut member may comprise a volute shape when viewed along the longitudinal axis of the lumen. The curved strut member may comprise a helical shape when viewed along the longitudinal axis of the lumen. Each of the curved strut members may comprise an undulating strut member having a substantially straight shape when viewed in a lateral direction.

The curved strut members may include one or more thin portions and one or more thick portions, the thick portions being thicker than the thin portions. The hub member may include a first hub and a second hub collinear with and connected to the first hub. The plurality of anchor struts may be connected to the first hub.

An endoluminal device can include an operative portion. The operative portion may be configured to obstruct fluid flow within the lumen. The endoluminal device can include a hub member. The hub member may be connected to the operating portion. The hub member may include a hub and a central rod. The endoluminal device can include a plurality of anchor struts. The plurality of anchor struts may comprise a strut portion. The strut portion may be attached to the hub member. The strut portion may be configured to expand and contract in response to expansion and contraction of the lumen. The anchor portion may connect the deflectable portion to the lumen. The hub member may remain substantially on or near the axis of the lumen during movement of the lumen.

The strut portion may be connected to a sliding hub configured to slide along the length of the center rod. The plurality of anchor struts may comprise a plurality of quadrilateral members. Each of the quadrilateral members may lie in a discrete plane parallel to the longitudinal axis of the device.

A mechanism for anchoring an endoluminal device to an inner lumen can include a hub member. A plurality of distal anchor struts may be connected to the hub member. The plurality of distal anchor struts may extend radially and distally from the hub member and curve in a proximal direction. Each of the plurality of distal anchor struts may include an anchor tip. The mechanism for anchoring the endoluminal device may include a plurality of opposing anchor struts. The plurality of opposing anchor struts may be connected to the hub member. The plurality of opposing anchor struts may extend proximally and radially from the hub member and curve in a distal direction. Each of the plurality of opposing anchor struts may include opposing anchor tips. The distal anchor strut and the opposing anchor strut may be configured to compress a portion of the lumen.

A mechanism for anchoring an endoluminal device to an inner lumen can include a hub member. A plurality of anchor struts may extend radially outward and distally from the hub member. Each of the plurality of anchor struts may be configured to transition from a straightened configuration to an arcuate configuration when deployed within the lumen. Each of the plurality of anchor struts may have a length when in the straightened configuration. In the straightened configuration, the length of one or more of the plurality of anchor struts may be at least 1.5 times the fully extended diameter of the lumen.

A mechanism for anchoring an endoluminal device to an inner lumen can include an operative portion. The operative portion may include a plurality of frame struts. Each frame strut may include a frame strut tip. A hub member may be connected to a distal end of the operative portion. A plurality of distal anchor struts may extend radially from the hub member and curve in a proximal direction. Each distal anchor post may include an anchor tip. The anchor tip may be positioned between the hub member and the frame strut tip. The frame strut tip and the anchoring tip may be interjected when viewed in a lateral direction.

Drawings

The following drawings and associated description are provided to illustrate the present disclosure and not to limit the scope of the claims.

FIG. 1 shows a schematic view of one embodiment of a spring-type anchoring mechanism.

Fig. 2 shows a schematic view of an embodiment of a screw-type anchoring mechanism.

Fig. 3A and 3B illustrate perspective views of one embodiment of a scroll-type anchoring mechanism.

Fig. 4A and 4B show a schematic view of one embodiment of a wave-type anchoring mechanism.

Fig. 5A and 5B show a schematic view of one embodiment of a wave-type anchoring mechanism with a bend near the hub.

FIG. 6 illustrates a perspective view of one embodiment of a wave-type anchoring mechanism having a proximal strut.

Fig. 7A and 7B show schematic views of an embodiment of an anchoring mechanism with diamond-shaped anchoring struts.

Fig. 8A and 8B illustrate a schematic view of one example anchoring mechanism having a bow-tie shaped anchoring strut.

Fig. 9A and 9B illustrate perspective views of one embodiment of a compression-type anchoring mechanism.

Figure 10 shows a schematic view of one embodiment of an elongated anchor strut mechanism.

Fig. 11 shows a schematic view of one example shape of a compression-type anchoring mechanism with an elongated distal anchor.

Fig. 12A-12C illustrate an embodiment of a compression-type anchoring mechanism having an elongated distal anchor along with an operative portion.

Fig. 13A-13C illustrate different views of one embodiment of a bi-directional anchoring tip.

Fig. 14A-14C illustrate one embodiment of an anchoring mechanism with an intervening anchor.

Fig. 15A and 15B illustrate one embodiment of an elastic connecting portion.

Fig. 16A and 16B illustrate one embodiment of an elastic connection used in a branch lumen.

These and other features will now be described with reference to the drawings summarized above. The drawings and associated descriptions are provided to illustrate embodiments and not to limit the scope of any claims. Throughout the drawings, reference numerals may be reused to indicate correspondence between the labeled elements.

Detailed Description

Some anchoring mechanisms for devices used inside an airway leading to the lung may have anchoring struts that can apply an outward force to the lumen (e.g., lung airway). Such an anchoring mechanism may allow the device to be securely positioned during expansion and contraction of the lumen. The anchoring mechanism may enter the lumen in a compressed state when the device with the valve is inserted into the lumen. The outward force of the anchoring mechanism may allow the anchoring mechanism to reach its fully extended state during operation within the lumen. The outward force may maintain a slight outward pressure on the lumen during exhalation.

In some cases, the outward force of the anchor can deform the lumen wall. For example, the outward force may urge the lumen wall radially outward from a central axis of the lumen. Expansion of the anchor and/or deformation of the lumen wall can cause an operative portion (e.g., a valve portion) of the device to be pulled toward the anchor (e.g., in a distal direction) as the anchor moves outward and away from the axis of the lumen. Such "setting" of the anchor and the operative portion of the device may occur gradually or rapidly, depending on the geometry, elasticity, and/or other characteristics of the lumen in which the device is implanted.

Pulling the operating portion during extension of the lumen may cause the operating portion to move longitudinally from its initial placement position. Prior to placement of the device within the lumen, the device may be sized to cause such movement. Such calibration may be accomplished, for example, by adjusting the placement of the operative portion (e.g., by placing the operative portion proximal to the intended final location), although precise adjustment to cause the movement may be difficult. In some cases, movement of the device occurs over a period of time beyond which the physician can reasonably view using a visualization device (such as a bronchoscope). In some cases, it may be difficult for a physician to estimate the final placement location of the device. Displacement of the device due to body movement can lead to undesired side branch ventilation due to movement of the sealing portion from its initial position, which can compromise the efficacy of such a device. In some cases, the valve of the device may become over-compressed when moved (e.g., in a distal direction). In some cases, the valve of the device may be moved to a larger portion of the lumen than the valve, thereby reducing or eliminating the efficacy of the valve.

Some mechanisms use a stent anchoring design that can press the lumen wall and press it against approximately the full diameter of the device. Such a mechanism may be immediately attached to the final placement location within the lumen when the device is placed inside the lumen. However, such mechanisms can be problematic over time, as those mechanisms may not properly adjust with the expansion and contraction of the airway to the lungs caused by breathing. The tissue of the lumen may be reconfigured (remodel) to accommodate the diameter of the device, possibly resulting in the device being loosened and/or expectorated.

Disclosed herein are anchoring mechanisms that can track movement of a lumen wall (e.g., during exhalation and/or coughing) and can allow a sealing portion of a valve to remain in a substantially consistent position within an airway as the anchoring mechanism transitions to a final seated position. In some cases, the anchoring mechanism applies an outward force to the lumen wall with little or no axial component of the vortex expansion. In some cases, as the lumen lengthens (e.g., during re-extension of a contracted lung), the anchoring mechanism applies a force having an axial vector in the proximal direction to push the device in the proximal direction.

Spring type anchoring mechanism

An anchoring mechanism that can accommodate changes in lumen size can be used to place the medical device into the lumen. The medical device may be an intraluminal medical device. Intraluminal medical devices for use with the anchoring mechanism may include, for example, stents, sensors, valves, and the like. The lumen may include, for example, veins, airways, alimentary tracts, and the like. Fig. 1 shows a schematic transverse cross-sectional view of one example shape of a spring-type anchoring mechanism used inside a lumen. The spring-type anchoring mechanism 100 may include a hub 120 and a plurality of spring-type anchoring struts 130. The spring-type anchor post 130 may include an anchor tip 140.

The hub 120 may be a collet (collet) configured to bundle a plurality of spring-type anchor struts 130. Hub 120 may include a center rod and a forcep knob (not shown). The spring-type anchor struts 130 may be radially disposed from the hub 120. The spring-type anchor struts 130 may include coiled springs, bent springs, or other extendable geometries and configurations. The anchor strut 130 used in the spring-type anchor mechanism 100 may include a resilient structure configured to expand or contract in response to movement of the lumen. For example, the plurality of anchor struts 130 may include an extension spring, such as the spring-type anchor mechanism schematically illustrated in fig. 1. In some embodiments, the anchor strut 130 is formed as a compression spring.

The anchor tip 140 may be configured to be removably attached to the inner lumen 110. In some embodiments, the anchor tip 140 can be configured to penetrate a portion of the lumen 110. For example, anchor tip 140 may include a tapered shape. The anchor tip 140 may include a first piercing mechanism. The first piercing mechanism may comprise a handle (shank). The anchor tip 140 may include an anchor projection 150. The anchor tab 150 may include a second piercing mechanism that forms an angle with the spring-type anchor post 130. For example, as schematically shown in fig. 1, the anchor tab 150 may form an angle of approximately 90 degrees with the radius of the inner cavity 110. The anchoring protrusion 150 may form an angle with the radius of the lumen of less than 90 degrees, for example, about 75 degrees. The anchoring protrusion 150 may comprise a tack (tack). The anchor tab 150 may be configured to allow the anchor tip to penetrate a portion of the lumen 110. For example, the anchoring protrusion 150 may have a length equal to or less than about 2 times the diameter of the anchoring post.

In some embodiments, the anchor tab 150 is configured to limit the extent of penetration of the anchor tip 140. For example, the anchoring protrusion 150 may include an additional pad portion that points in a vertical (e.g., circumferential) direction relative to the hub 120. The anchor protrusions 150 may be positioned against the inner surface of the lumen 110 to inhibit or prevent the anchor tips 140 from penetrating beyond a predetermined distance.

The dimensional changes of the inner cavity 110 may include longitudinal dimensional changes and radial dimensional changes. The lumen 110 may include a maximum fully expanded diameter and a minimum fully contracted diameter. A plurality of spring-type anchor struts 130 may extend radially from the hub 120 to contact the inner cavity 110. Each of the struts 130 may have an extended length (e.g., a length to which the struts 130 extend if unobstructed). In some embodiments, the struts extend for a length greater than the radius of extension of the lumen 110 within which the struts 130 are deployed. In some embodiments, struts 130 extend greater than 1.1 times, 1.25 times, 1.4 times, 2 times, and/or 4 times the radius of extension of lumen 100. Many variations are possible.

The length of the plurality of spring-type anchor struts 130 can include a coiled length (e.g., a minimum length that the struts 130 can assume when the struts 130 are compressed). In some embodiments, the coiled length of the struts 130 is less than the radius of the inner lumen 110 at the smallest fully contracted diameter of the inner lumen 110. For example, the coiled length of the struts 130 may be less than about 0.9 times, about 0.75 times, 0.6 times, and/or about 0.5 times the collapsed diameter of the lumen 100. Many variations are possible.

The spring-type anchoring mechanism 100 may include an even number of spring anchor struts 130. For example, as shown in fig. 1, the spring-type anchoring mechanism 100 may include 6 spring-type anchoring struts 130. An even number of spring-type anchor struts 130 may be used, for example, to counteract the extension and/or contraction force of opposing spring-type anchor struts 130. In some embodiments, the anchoring mechanism 100 includes an odd number of anchor struts 130.

The spring-type anchor struts 130 may comprise varying lengths. For example, two or more spring-type anchor struts 130 can have equal lengths and a third spring-type anchor strut 130 can have a length greater than or equal to the other two. In some cases, each of the struts 130 has a different length.

When the anchoring mechanism 100 is deployed, the hub 120 may be disposed on or near the longitudinal axis of the inner lumen 110. The spring-type anchor struts 130 may at least partially expand and maintain contact with the inner lumen 110 during expansion of the inner lumen 110. The spring-type anchor struts 130 may coil during contraction of the inner lumen 110 and apply a radially outward force to the inner lumen 110.

The struts 130 may be configured to maintain the hub 120 in a relatively stable position along the length of the lumen 110 in which the anchoring mechanism 100 is located before and/or after placement of the anchoring mechanism 100 (e.g., due to stretching of the airway by the outward force of the struts 130). During and/or prior to deployment, longitudinal movement of the hub 120 (e.g., movement along the length of the lumen 110) may be limited to within about 1 mm. During and/or prior to deployment, movement of the hub 120 may be limited to within about 2mm, within about 0.5mm, within about 0.3mm, and/or within about 0.2 mm.

The user may deploy the anchoring mechanism 100 by using a delivery device, such as an endoscope. The spring-type anchoring mechanism 100 can be folded and transported within a catheter used with an endoscope. The spring-type anchoring mechanism 100 may be deployed by pushing it out of the catheter. In some embodiments, the anchoring mechanism 100 may be deployed at the deployment site by withdrawing the catheter from the anchoring mechanism 100. Once the spring-type anchor struts 130 are placed outside the catheter, the spring-type anchor struts 130 may expand radially outward to contact the inner lumen 110. The spring-type anchor struts 130 may exert a radially outward force on the inner cavity 110 wall. This radially outward force may allow each of the anchor tips 140 to penetrate the lumen 110.

Upon deployment, the hub 120 and anchor tip 140 may be on the same or substantially the same transverse plane. In some embodiments, the anchoring mechanism 100 may include two or more anchoring struts 130. The spring-type anchor struts 130 may include a combination of resilient anchor struts and static anchor struts. For example, the spring-type anchor struts 130 may include two spring-shaped elastic anchor struts and one rigid static anchor strut. The hub 120 may include an axial bearing. The hub 120 may be positioned off-center. For example, the hub 120 may be positioned adjacent to a wall of the inner cavity 110. The hub 120 can comprise a variety of different shapes. For example, the hub may have a circular, polygonal, elliptical, or other shaped cross-section in a plane perpendicular to the longitudinal axis of the lumen 110. The anchor tip 140 may include a blunt tip such that no portion of the anchor tip penetrates the lumen 110. The anchor tip 140, which has a blunt tip, may include a traction surface. For example, the traction surface may include a plurality of cleats (cleats).

Screw type anchoring mechanism

The anchor strut may comprise a helical shape or a torsion spring shape. The helical shape may be used, for example, to apply a torsional force during expansion and contraction of the lumen. Fig. 2 shows a schematic transverse cross-sectional view of one example shape of a screw-type anchoring mechanism 200. The screw-type anchoring mechanism 200 may include a hub 220, a plurality of anchoring struts 230, and an anchoring tip 240. The plurality of anchor struts 230 can include an elongated (e.g., substantially straight) portion 232 and a helical portion 233. The anchor tip 240 may be configured to penetrate the lumen 210.

The hub 220 may be positioned on or near the longitudinal axis of the lumen 210. The hub 220 of the screw-type anchoring mechanism 200 may remain substantially at the same axial position regardless of the movement of the lumen. The hub 120 may rotate as the helix extends. For example, the hub 120 can rotate independently of the operative portion of the medical device during lumen extension or retraction. In some embodiments, the hub 120 is rotatably locked with and connected to the operative portion. The operative portion may be, for example, a lung airway valve.

During expansion and contraction of the inner lumen 110, the screw-type anchoring mechanism 200 may inhibit, reduce, or prevent displacement of the medical device while allowing the hub 220 to remain substantially at its initial position. For example, during expansion of the lumen, the helical portion 233 of the anchor strut 230 may straighten. The hub 220 may remain suspended from the lumen wall and remain substantially at its initial position. In some embodiments, the anchoring mechanism 200 is configured to maintain the hub 200 (e.g., and thus the operative portion) in a relatively constant position along the length of the lumen 210 within which the mechanism 200 is deployed.

The plurality of anchor struts 230 may be made of a shape memory material, such as nitinol. In some embodiments, the struts 230 are constructed of additional resilient and/or flexible materials. The plurality of anchor struts 230 may comprise a coiled length. The coiled length may include the shortest length between the end of the anchor tip 240 and the hub 220 when the struts 230 are radially compressed. In some embodiments, the coiled length of the struts 230 is less than about 0.9 times, about 0.75 times, about 0.6 times, about 0.4 times, and/or about 0.25 times the radius of the lumen 210. The plurality of anchor struts 230 may include a deployed length that is greater than a radius of the lumen 210. For example, the straight length of the anchor strut 230 may be more than 2 times, more than 1.5 times, and/or more than 1.1 times greater than the radius of the lumen 210.

The helical-shaped anchoring mechanism 200 may be transported through a catheter by being folded into the catheter prior to deployment. The anchor struts 230 may be further coiled to be transported through the catheter. When the helical-shaped anchoring mechanism 200 is pushed out of the catheter, it may be deployed to its pre-formed helical shape. In some embodiments, the anchoring mechanism 200 is deployed when the catheter is withdrawn from the strut 230 at one deployment site within the lumen 210. Once deployed, the anchor tip 240 may contact the lumen 210 and apply an outward force from the hub 220 to the lumen 210. The anchor tip 240 may penetrate the meat of the lumen 210 by applying an outward force. In some embodiments, the anchoring tip 240 includes a pad or other mechanism configured to limit the depth of penetration of the tip 240 into the lumen wall.

The anchor struts 230 may be straightened for transport through a catheter prior to deployment. The hub 220 may be a dual hub configured to allow the hub 220 to rotate without rotating an attachment portion (e.g., an operative portion) of the medical device. The helical-shaped anchoring mechanism 200 may include three or more anchoring struts 230. The anchor strut 230 may include a combination of different spring shapes. For example, the anchor struts 230 may include a plurality of helical anchor struts 130 (e.g., shown in fig. 1) that are helically coiled and form a helix around the hub 220.

Vortex type anchoring mechanism

The anchoring mechanism may comprise a plurality of flexible struts curved in the same circumferential direction to form a vortex shape when viewed in transverse cross-section. The flexible scroll struts may bend or straighten, further bending during contraction of the lumen and straightening as the lumen extends. Fig. 3A and 3B show perspective views of one example shape of the scroll-type anchoring mechanism. The scroll-type anchoring mechanism 300 may include a hub 320, flexible anchor struts 332, proximal struts 336, a center rod 360, and/or a toggle 362. Hub 320 may include a dual hub configuration having a distal hub 322 and a proximal hub 324. The flexible anchor strut 332 may include an anchor tip 340. The proximal strut 336 may include a curved contact surface 338. The proximal strut 336 may include a frame strut of the operative portion 1135 (e.g., shown in fig. 12A-12C).

The flexible anchor struts 332 may extend radially outward from the distal hub 322. The proximal hub 324 may be coupled to the distal hub 322 and/or formed as an integral part with the distal hub 322. The proximal struts 336 may extend radially and proximally from the proximal hub 324. The proximal strut 336 may form a basket (basket). The proximal hub 324 may be a collet. The central rod 362 may be connected to the proximal hub 324 and extend proximally therefrom. The center rod 362 may connect the hub 320 and the tweezer 362. The clamp button 362 may be shaped and sized to be grasped by one of the clamps. The plurality of flexible anchor struts 332 may be configured to radially expand and exert an outward force on the lumen. The curved surfaces 338 of the plurality of proximal struts 336 may include portions of the proximal struts that curve at an angle from the remainder of each proximal strut member 336 toward the longitudinal axis or central rod 360. The curved contact surface 338 may be used, for example, to inhibit or prevent trauma to the lumen wall by the proximal strut 336.

The distal hub 322 and the proximal hub 324 may comprise collinear cylindrical structures. The distal hub 322 and the proximal hub 324 may comprise cylindrical structures having different diameters. For example, the diameter of the distal hub 322 may be smaller than the diameter of the proximal hub 324. The smaller diameter distal hub 322 may be shaped and sized, for example, to allow the plurality of distal struts to coil and fit inside a delivery catheter. Each of the plurality of proximal struts 322 can have a straightened length. The straightened length may include the length of the proximal strut member when in a fully straightened state without bending. The straightened length may be less than 1.5 times the length of the central rod 362. The straightened length may be equal to or less than the length of the central rod 362. In some cases, the straightened length may be greater than 1.5 times the length of the center rod 362.

The stiffness of the flexible anchor struts 332 may be adjusted to counteract forces (e.g., tension and compression) that occur during extension of the struts 332. For example, some portions of the struts 332 may be stiffer than other portions. The area near the hub 320 and near the anchor tip 340 may be relatively rigid, whereas the area near the middle of the strut may be made more flexible to allow bending. The stiffness may be adjusted by changing the size and/or shape of portions of the anchor strut 332. For example, the plurality of anchor struts 332 may include curved portions, thin portions, thick portions, and/or helical portions.

The vortex-shaped anchoring mechanism 300 can be folded and transported through a delivery catheter. The flexible anchor struts 332 may be coiled in a curved direction to fold and fit inside the catheter. For example, the flexible anchor post 332 shown in fig. 3A-3B may be coiled by rotating the hub 320 in a counterclockwise direction relative to the anchor tip 340. The proximal strut 336 may be straightened to fold and fit inside the catheter. The proximal strut 336 may be straightened along the length of the central rod 362.

The flexible anchor struts 332 in the fully coiled state may have a cross-sectional diameter equal to or less than 1.5 times the diameter of the proximal hub. The flexible anchor struts 332 in the fully coiled state may have a cross-sectional diameter equal to or less than the diameter of the proximal hub. The plurality of proximal struts 336 in the fully straightened state may have a cross-sectional diameter equal to or less than 1.5 times the diameter of the proximal hub. The plurality of proximal struts 336 in the fully straightened state may have a cross-sectional diameter equal to or less than the diameter of the proximal hub.

The scroll strut anchoring mechanism 300 may counteract the movement of the inner cavity. For example, the vortex strut anchoring mechanism 300 may be adjusted to expand during lumen extension and contract during lumen contraction. The anchor tip 340 may remain in a substantially same transverse plane (e.g., perpendicular to the centerline of the lumen) during expansion and contraction of the lumen. For example, the flexible anchor strut 330 may be further bent to have a smaller diameter such that the anchor tip 340 and the hub 320 may remain in a substantially constant transverse plane. The arc of curvature of the anchor strut 332 may straighten out to a greater extent as the lumen extends while the point of contact and the hub remain in substantially the same plane. The stiffness of the anchor strut may be adjusted to counteract the distal and proximal forces applied when the anchor strut 330 is extended. In some embodiments, the struts 332 are configured to remain in substantially the same transverse plane during placement of the device 300 and/or after placement of the device 300.

The plurality of proximal struts 336 may include two or more curved surfaces 338. For example, the proximal strut 336 may have two connected curved surfaces that form two angles with the proximal strut 336. Two or more curved surfaces 338 may be used, for example, to allow different atraumatic contact surfaces to contact the lumen during extension and retraction. For example, curved surface 338 may include a first surface configured to contact the lumen in the extended state and a second surface configured to contact the lumen in the collapsed state.

The plurality of flexible anchor struts 332 may include anchor tips 340. For example, the plurality of flexible anchor struts 332 may include a plurality of anchor structures that point in different directions. For example, the anchor tip 340 may include a bi-directional anchor tip 640 (shown in fig. 6). In some embodiments, the anchor tip 340 includes an atraumatic tip and/or a high friction tip configured to engage a wall of the lumen.

The plurality of flexible anchor struts 332 may comprise a helical shape, such as the helical anchor strut 230 shown and described above with reference to fig. 2. The proximal strut 336 may be used to counteract movement of an attached medical device in a proximal direction.

The positions of the proximal struts 336 and the flexible anchor struts 330 may be reversed. For example, the proximal struts 336 may be positioned distally relative to the flexible anchor struts 330. The proximal struts 336 may extend in opposite directions such that the curved contact surface 338 may be positioned distally relative to the hub 320. The vortex strut anchoring mechanism 300 may include a different number of flexible anchor struts 330 than the number of proximal struts 336. The scroll strut anchoring mechanism 300 may include the same number of flexible anchor struts 330 as the number of proximal struts 336. For example, where the vortex strut anchoring mechanism 300 has three flexible anchoring struts 330, the mechanism 300 may include three proximal struts 336. In some embodiments, each of the proximal struts 336 and each of the flexible anchor struts 330 may be connected and may form part of a single strut member. For example, a plurality of unitary strut structures may be bundled together by a collet between the two ends of each strut structure.

Wave type anchoring mechanism

In some embodiments, the anchoring mechanism 400 may include struts having a wave-like shape when viewed from a longitudinal cross-sectional view of the lumen. Fig. 4A and 4B illustrate a schematic of one example shape of a wave-type anchoring mechanism 400. The wave anchor mechanism 400 may include a hub 420, a center rod 460, and a plurality of undulating anchor struts 430. Undulating anchor post 430 may include one or more thick portions 433A, one or more thin portions 433B, and anchor tips 440. The undulating anchor post 430 may comprise a substantially straight shape when viewed in the lateral direction. The wave-type anchoring mechanism 400 may limit the displacement of the hub 420 when the lumen 410 transitions between the retracted state (fig. 4A) and the extended state (fig. 4B). In some cases, the anchoring mechanism 400 limits displacement of the hub 420 (e.g., and thus the operative portion connected to the hub 400) when the anchoring mechanism 400 is seated within the membrane 450.

Hub 420 may connect a plurality of undulating anchor struts 430 to central rod 460. For example, the wave anchor mechanism 400 may include two undulating anchor struts 430 connected to a central rod 460 via a hub 420. In some embodiments, the anchoring mechanism 400 includes three or more anchoring struts 430 emanating from the hub 420. The undulating anchor post 430 may include one or more inflection points and undulation points. For example, as shown in fig. 4A and 4B, the undulating anchoring mechanism 400 may have at least one undulation point on each strut 433.

When the anchor strut 430 is in the first less extended configuration, the anchor tip 440 may be located a distance D1 from the proximal end of the location of the hub 420. For example, within the lumen in the fully contracted state (fig. 4A), the distance between the anchor tip 440 and the hub 420 may constitute a first distance D1. Within the lumen (fig. 4B) in the fully extended state, the distance between the anchor tip 440 and the hub 420 may constitute a second distance D2. The displacement of the hub 420 may be limited such that a difference between the first distance D1 and the second distance D2 may be less than 0.5 mm. The difference between the first distance D1 and the second distance D2 may be less than 0.1 mm. The difference between the first distance D1 and the second distance D2 may be less than 0.05 mm. In some cases, the difference between the first distance D1 and the second distance D2 may be less than 0.02 mm.

The anchor struts 430 may have a non-uniform thickness between the hub 420 and the anchor tip 440. For example, the anchor strut 430 may include a thick portion 433A that may be more rigid than a thinner portion (e.g., having a greater degree of freedom). For example, thick portion 433A may retain its curved shape while undergoing deflection during extension of lumen 410 and/or during placement of anchoring mechanism 400. Anchoring mechanism 400 may include a thin portion 433B that may deflect to a greater extent during expansion of lumen 410 than thick portion 433A. Thick portion 433A and thin portion 433B may include portions of undulating anchor struts 430 having different configurations and sizes. For example, thick portion 433A may include a portion of strut member 430 having a greater thickness in a direction transverse to the longitudinal direction of lumen 410, while thin portion 433B includes a strut portion having a greater thickness in the longitudinal direction of lumen 410. Such a configuration may be used to allow thick portion 433A to withstand the stresses of repeated extension and retraction movements from lumen 410.

As shown in fig. 4A and 4B, the wave-type anchoring mechanism 400 may include an anchoring tip 440. The anchor tip 440 may be curved and point in a distal direction. The wave anchor mechanism 400 may be placed proximal or distal to an operative portion of the medical device, such as a valve.

The undulating anchor struts 430 may include struts having different lengths, shapes, inflection/relief points, stiffness, and the like. For example, fig. 5A and 5B illustrate one example shape of a wave-type anchoring mechanism having an arcuate bend near hub 520. The wave anchoring mechanism 500 having a relatively sharp bend near the hub 520 may include a center rod 560, a hub 520, and a plurality of anchoring struts 530. The plurality of anchor struts 530 may include a thick portion 533A, a thin portion 533B, an arcuate bend 533C, and anchor tips 540. Arcuate bend 533B may comprise a different configuration than the remainder of anchor strut 530. For example, arcuate bend 533B may include a curved shape in the transverse direction.

The anchor point 440 may lie in the same transverse plane as the hub 420. The anchor tip 440 may point in a proximal direction or a distal direction. In some embodiments, the anchor tip 440 includes a pad portion configured to limit the depth to which the anchor tip 440 penetrates the lumen 410. The wave anchor struts 430 may extend radially from the hub 420. For example, fig. 6 illustrates a perspective view of one example shape of an undulating anchoring mechanism 600 including undulating struts 632. The anchoring mechanism 600 may share many or most of the features and characteristics of the anchoring mechanism 300 described above, wherein the distal anchor 632 comprises undulating struts rather than the vertical struts 332 described above, and wherein like parts comprise like numerals (e.g., proximal strut 336 versus proximal strut 636). The hub 620 may include a proximal hub 622 and a distal hub 624. The plurality of swirling struts 632 may include a thick portion 633A, a thin portion 633B, and a bi-directional anchoring tip 640. The bi-directional anchoring tip 640 may include a first anchoring tip 640A and a second anchoring tip 640B. The second anchor tip 640B may be configured to limit the extent of the first anchor tip 640A.

As shown in fig. 6, the undulating anchoring mechanism 600 including undulating struts may include three or more undulating struts 632. The bi-directional tip 640 may include bi-directional tips 1335A, 1335B shown and described with reference to fig. 13A-13C of the present application.

Diamond anchoring mechanism

Fig. 7A and 7B schematically illustrate an embodiment of a diamond-shaped anchoring mechanism. The diamond-shaped anchoring mechanism 700 may include a tweezer button 762, a center rod 760 extending distally from the tweezer button 762, a first hub 720 coupled to the center rod 760 from the distal end of the tweezer button 762, a second hub 722 coupled to the center rod 760 at the distal end of the first hub 720, and/or a plurality of diamond-shaped anchoring struts 730. The plurality of diamond-shaped anchor struts 730 may include a proximal portion 734, a distal portion 732, a distal point 795, and anchor tips 740. In some embodiments, the operating portion 750 is coupled to the center rod 760 between the first hub 720 and the tweezer 762.

Center rod 760 may connect clamp button 762 and distal point 795. For example, a distal point of the strut 730 may be connected to the second hub 722. The proximal portion 734 and the distal portion 732 may include two sides of a diamond shape. The proximal portion 734 and the distal portion 732 may comprise a single strut member, wherein the proximal portion 734 is coupled to the first hub 720.

The proximal portion 734 and the distal portion 732 may form an included angle. For example, in a first state (e.g., prior to deployment of the device 700 and/or prior to deployment of the lumen 710), the proximal portion 734 and the distal portion 732 may form an angle of less than about 150 degrees. In the initial state, the proximal portion 734 and the distal portion 732 may form an angle of less than about 80 degrees. In the initial state, the proximal portion 734 and the distal portion 732 may form an angle of less than about 60 degrees. In the initial state, the proximal portion 734 and the distal portion 732 may form an angle of less than about 45 degrees.

The anchor tip 740 may include an anchor structure. For example, the anchor tip may include a barb, high friction pad, or other structure configured to penetrate the lumen 710 and/or frictionally engage the lumen 710. The anchor point 740 may comprise a bi-directional anchor point. For example, the anchor tip 740 may include a bi-directional tip as shown and described with reference to fig. 13A-13C of the present application. In some embodiments, the anchor tip 740 may include a wedge, a stud (stud), a rail, or the like.

As shown in fig. 7A-7B, the diamond-shaped anchoring struts 730 may comprise one diamond shape or two mirror image triangles when viewed in longitudinal cross-section. The proximal end of the triangle may be connected to the first hub 720. In some embodiments, the distal end of the triangle is connected to the second hub 722. The struts 730 may be configured to expand and/or contract in a radial direction in response to expansion and contraction of the lumen 710 (e.g., due to respiration, placement device 700, or other conditions).

The struts 730 may be configured to expand/contract in a radial direction with limited or no movement of the central shaft 760 along the length of the inner lumen 710. For example, the first hub 720 can be a sliding hub (fig. 7A). Hub 720 may include an annular shape with a hollow center shaped and sized to slide along center rod 760. The hub 720 (e.g., and the proximal end of the strut 730) may be configured to slide in a distal direction when the strut 730 is extended. Mechanism 700 may include a proximal stop 743 configured to limit proximal movement of first hub 720 along hub 760.

In some embodiments, the second hub 722 is configured to slide along the central rod 760 (fig. 7B). In some cases, second hub 722 is slidable and first hub 720 is fixed on center rod 760. The second hub 722 (e.g., and the distal end of the strut 730) can be configured to slide in a proximal direction when the strut 730 is extended. In some embodiments, mechanism 700 includes a distal stop 745 configured to limit distal movement of second hub 722 when second hub 722 is a sliding hub (fig. 7B).

In some cases, sliding of the first hub 720 or the second hub 722 may permit radial extension and retraction of the struts 730 (e.g., in response to inhalation/exhalation and/or placement of the mechanism 700) with little or no movement of the central rod 760 along the length of the inner lumen 710. Limiting or preventing movement of the center rod 760 along the length of the inner lumen 710 may facilitate constant or semi-constant positioning of the operative portion 750.

The proximal portion 734 and the distal portion 732 may have approximately equal lengths. In some embodiments, the proximal portion 734 and the distal portion 732 comprise different lengths. The diamond anchoring mechanism 700 may include a telescoping slide rod. For example, a sliding rod may slidably couple the central rod 760 to the distal point 795. Center rod 760 may include a hollow core shaped and sized to receive the sliding rod.

Bowknot-shaped anchoring mechanism

Fig. 8A and 8B illustrate one example shape of an anchoring mechanism having a bow-tie shaped anchoring post 834 for use with the operative portion 825. The bow-tie anchoring mechanism 800 may include a knob 862 and a central rod 860 coupled to the knob 862 and extending distally from the knob 862. An operating portion 825 (e.g., a valve) may be connected to the central rod 860 from the distal end of the knob 862. Mechanism 800 may include a hub 820 coupled to a central rod 860 at a distal end of operative portion 825.

As illustrated, the mechanism 800 may include a plurality of bowtie-shaped anchoring struts 830. The struts 830 may be connected to the hub 820 and extend radially from the hub 820. The bow-tie shaped anchor strut 830 may comprise a plurality of quadrilateral members. Each of struts 830 can include a proximal portion 834, a distal portion 832, and an anchor tip 850. The proximal portion 834 can include a proximal end point 835A. Distal portion 832 may include a distal point 835B. Proximal end point 835A and distal end point 835B may comprise bendable or hinged joints. The bow-tie shaped anchor strut 800 may be used with an operative portion 825, such as a valve used in a lung airway valve.

The shape of the bow-tie anchor strut 830 may change during movement of the lumen 815 (e.g., during inspiration/expiration and/or during placement of the mechanism 800). For example, the distance between the axis of the lumen 815 and the anchor tip 850 may become greater during extension of the lumen wall. The proximal end point 835A and the distal end point 835B may move away from each other during contraction of the inner lumen 810. Proximal end point 835A and distal end point 835B may move closer together during extension of lumen 810.

In some embodiments, the points 835A, 835B of each strut 830 lie on a plane that is substantially parallel to the longitudinal axis of the lumen 815. In some cases, the points 835A, 835B of each strut 830 lie on a plane that is substantially perpendicular to the longitudinal axis of the inner lumen 815. In some embodiments, the points 835A, 835B of each strut 830 lie on a plane that is neither perpendicular to the longitudinal axis of the lumen 815 nor parallel to the longitudinal axis of the lumen 815. Many variations are possible.

The struts 830 can be configured to expand and/or contract with little or no movement of the hub 820 (e.g., and thus the operative portion 825) along the length of the inner lumen 815. For example, radial movement of the anchor portion 850 of the strut 830 may occur in a substantially constant plane perpendicular to the length of the lumen 815.

Opposed anchor strut mechanisms

In some cases, the anchoring mechanism can include one or more anchors configured to engage with the lumen wall to inhibit or prevent movement of the operative portion of the device in the distal direction. For example, two or more anchor struts may be used to crush a portion of the lumen.

Fig. 9A and 9B illustrate perspective views of one example shape of a compression-type anchoring mechanism 900. Mechanism 900 may include a hub 920 and a plurality of distal struts 934 extending distally and/or radially outward from hub 920. Mechanism 900 may include a plurality of opposing struts 933 extending radially outward from hub 920 proximal of distal struts 934. The plurality of distal struts 934 may include distal anchor tips 940A. The opposing struts may include opposing anchor tips 940B. The distal anchor tip 940A and the opposing anchor tip 940B may comprise bi-directional anchor tips (shown in fig. 13A-13C).

In some embodiments, mechanism 900 includes a plurality of proximal struts 935 extending proximally from hub 920. The plurality of proximal struts 935 may include frame struts (shown in fig. 12A to 12C) of the operation portion 1235.

The plurality of distal struts 934 may comprise a strut member comprising one or more bends. For example, as shown in fig. 9A and 9B, the plurality of distal struts 934 may include two bends, each bend curving each distal strut member 934 in a proximal direction. The opposing strut 933 may comprise strut members that mirror strut 934 relative to a plane perpendicular to the longitudinal axis of central rod 960. For example, the opposing struts 933 can include strut members that extend radially outward from the hub 920 and initially extend in a proximal direction and curve in a distal direction, as shown in fig. 9A and 9B. The opposing strut 933 can include opposing anchor tips 940B. The anchor tips 940A, 940B may include a second tip 954. The second tip 954 of the anchor tips 940A, 940B may be configured to limit the depth to which the anchor tips 940A, 940B (e.g., or the piercing portions 952 thereof) penetrate the lumen wall. For example, the second tip 954 of the proximal anchor tip 940A may be pointed in a proximal direction while the second tip 954 of the opposite anchor tip 940B may be pointed in a distal direction. In some embodiments, the second tips 954 of the anchor tips 940A, 940B point in the same direction.

The hub 920 may include a dual hub configuration, as described above with reference to fig. 3A and 3B. The hub may include a distal hub 922 and a proximal hub 924. As shown in fig. 9A and 9B, a distal strut 934 may extend radially from the distal hub 922. An opposing strut 933 can extend radially from the proximal hub 924.

The opposing strut 933 can be configured to counteract forces caused by movement of the compression-type anchoring mechanism 900 in a distal direction (e.g., due to placement of the mechanism 900). The distal strut 934 and the opposing strut 933 can be configured for use inside the lumen while minimizing crushing of the lumen. Such a configuration may be used, for example, to minimize trauma to the lumen.

The compression of the distal strut 934 and the opposing strut 933 can cause the walls of the lumen to become wrinkled (see, e.g., fig. 12A-12C). Crimping of the lumen wall may be used to allow point loads to be applied to the wall while permitting the use of proximal struts 933 having reduced radial stiffness as compared to distal struts 934. For example, the crimping of the lumen wall may permit the proximal struts 933 to contact and/or penetrate the lumen wall at a lesser angle relative to the longitudinal axis of the mechanism 900 than if no crimping were present. The crimping of the lumen wall and the minimal opposing forces can be used to inhibit or reduce the likelihood of compression necrosis that may be caused by directly opposing forces through opposing struts. The opposing strut 933 can be shorter than the distal strut 934. Distal strut 934 may include the elongate anchoring mechanism shown and described with reference to fig. 10.

The compression-type anchoring mechanism 900 may be configured to fit inside a delivery catheter. For example, as illustrated in fig. 9A and 9B, the distal strut 934 may be straightened in a distal direction and the opposing strut 933 may be straightened in a proximal direction to fit inside the catheter. The user may place the compression-type anchoring mechanism 900 at a desired location inside the lumen and push the compression-type anchoring mechanism 900 distally. In some cases, the mechanism 900 is dispatched to an installation site using a catheter, and the catheter is withdrawn from the mechanism 900 to deploy the mechanism at the installation site. Once the distal strut 934 has been released, portions of the distal anchor tip 940A may connect the compression-type anchor mechanism 900 to and penetrate the lumen. The user may pull the catheter to further release the compression-type anchoring mechanism 900 so that the opposing strut 933 may be released. The opposing strut 933 can transition shape from a straightened state inside the catheter and return to its original fully arcuate shape. The opposing struts 933 can form a relatively straight shape within the catheter, and can transform shape to arc in the distal direction when deployed from the catheter. The opposing anchor tips 940B of the opposing struts 933 can be embedded within the lumen. The deflection force applied to the lumen as the distal strut 934 and the opposing strut 933 return to their respective original shapes can compress the lumen, forming a pleat. In some cases, the change in shape of the compression-type anchoring mechanism 900 may be triggered or actuated by a change in temperature, by passing a current to a strut member, physical manipulation, or the like.

The distal strut 934 and the opposing strut 933 can comprise struts having different lengths, shapes, inflection/relief points, stiffnesses, and the like. For example, the distal strut 934 and the opposing strut 933 can comprise strut members having an arcuate shape without bends.

Elongate distal anchor

An anchoring mechanism having an elongated strut member may be used to reduce movement of the medical device caused by body movement and/or placement of the anchoring mechanism. The degree of movement of the medical device may be less with anchoring mechanisms that use longer strut members than with mechanisms that use shorter strut members. The longer strut members may extend in a large arc, thereby reducing axial movement of the endoluminal device due to the strut members extending to an equilibrium position (e.g., emplacement). Figure 10 schematically illustrates one example shape of an elongate strut anchoring mechanism. The elongate strut anchor mechanism 1000 may include a plurality of elongate anchor struts 1034 and a hub 1020.

The elongated anchor struts 1034 may be configured to reduce or limit the amount of longitudinal movement of a device connected to the hub 1020. A plurality of elongated anchor struts 1034 may include anchor tips 1040. The anchor tip 1040 may be in the first position P1 within the fully collapsed lumen. The anchor tip 1040 may be in the second position P2 in the fully extended state. The anchor tip 1040 may travel a longitudinal travel distance D3 between P1 and P2. The longitudinal travel distance D3 may be reduced by having elongated anchor struts 1040. For example, the longitudinal travel distance D3 may be less than 0.1 mm. The longitudinal travel distance D3 may be less than 0.05 mm. The longitudinal travel distance D3 may be less than 0.02 mm. In some cases, the longitudinal travel distance D3 may be less than 0.01 mm. Many variations are possible.

The elongated anchor strut 1034 may include an arcuate strut member, as schematically illustrated in fig. 10. The elongated anchor strut 1034 may include a straight length that corresponds to the length of the strut member as it straightens. The straight length may be longer than the diameter of the elongated lumen. For example, elongate anchor strut 1034 may have a straight length that is at least about 1.5 times the diameter of the extended lumen. The elongate anchor strut 1034 may have a straight length that is at least about twice the diameter of the extended lumen. The elongate anchor strut 1034 may have a straight length that is at least about three times the diameter of the extended lumen. The elongate anchor strut 1034 may have a straight length that is at least about four times the diameter of the extended lumen. In some embodiments, struts 1034 have a straight length that is between about one to four times the diameter of the extended lumen. Many variations are possible.

The user may select the shape and size of the elongate strut anchoring mechanism 1000 based on the lumen 1010. The straight length and curvature of the elongated anchor struts 1034 may be adjusted to correspond to the lumen size changes. For example, for lumens that show little change in size between fully extended and fully contracted states, strut members having a greater degree of curvature and/or having a shorter straightened length may be used. The user may also calibrate the distance traveled by the hub 1020 by adjusting the length and/or curvature of the straight. The user may limit the amount of longitudinal distance traveled by the hub 1020 to less than 0.02mm, for example, by selecting a strut 1040 having a particular length.

The elongated anchor struts 1034 may include strut members of different lengths and configurations. Fig. 11 illustrates one example shape of a squeeze-type anchoring mechanism having a plurality of elongate distal anchor struts 1134. The compression-type anchoring mechanism 1100 may include a hub 1175. The mechanism 1100 may include a plurality of elongate distal anchor struts 1134 connected to the hub 1175 and extending in a distal direction from the hub 1175. The mechanism 1100 may include a plurality of opposing struts 1133 connected to a hub 1175 and positioned to the proximal end of a distal strut 1134. The elongate distal anchor strut 1134 may include a distal anchor tip 1136. The distal anchor tip 1136 may include a first anchor tip 1136A and a second anchor tip 1136B. The plurality of opposing anchors can include opposing anchor tips 1190.

As illustrated in fig. 11, opposing struts 1133 may extend radially outward from hub 1175 and in a distal direction. Opposing anchor tips 1190 may extend at an angle from opposing struts 1133. The opposing anchor tips 1190 may form an angle of between about 90 and 170 with the opposing struts 1133. The first anchor tip 1136A of the elongate distal anchor strut 1134 may extend in the same direction as the elongate distal anchor strut 1134. Second anchor tip 1136B may point in a proximal direction and form an angle with first anchor 1136A. The angle may be about 30 degrees to about 170 degrees. The angle may be about 45 degrees to about 150 degrees. The angle may be about 60 degrees to about 120 degrees. The angle may be about 80 degrees to about 100 degrees. The angle may be about 90 degrees. In some embodiments, the second anchor tip 1136B is configured to interact with the wall of the lumen and limit the depth to which the first anchor tip 1136A penetrates the lumen wall.

In some embodiments, distal anchor tip 1136 may comprise a bi-directional anchor tip (e.g., as shown in fig. 13A-13C). The distal anchor tip 1136 and the opposing anchor tip 1190 may be configured to press against the lumen wall. For example, the elongate distal anchor strut 1136 and opposing strut 1133 may be configured to oppose each other to compress the lumen wall. In some embodiments, opposing struts 1133 are configured to inhibit, limit, or prevent distal movement of an operative portion (e.g., a valve) connected to hub 1175 when distal anchor 1134 is seated within the lumen wall.

Fig. 12A-12C illustrate one example shape of a compression-type anchoring mechanism having a plurality of elongate distal anchor struts for use with a medical device within a lumen. As shown in fig. 12A, a compression-type anchoring mechanism having a plurality of elongate distal anchoring struts 1100 may include the compression-type anchoring mechanism 1100 and an operative portion 1135. The operation portion 1135 may include a lung airway valve. A hub 1175 can connect the compression-type anchoring mechanism 1100 to the operative portion 1135.

As seen in fig. 12A-12C, the elongate distal anchor struts 1134 may transition from a straightened configuration and gradually return to an arcuate configuration. As seen in fig. 12A-12C, the lumen 1110 may form a lumen wall pleat 1115 as the elongate distal anchor struts 1134 change shape. Lumen wall pleats 1115 may be formed between the elongate distal anchor struts 1134 and the opposing struts 1133. In some embodiments, the opposing strut 1133 comprises a bifurcated tip comprising a pad configured to limit the extent to which the opposing strut 1133 pierces the lumen 1100.

The elongate distal anchor struts 1134 may comprise a shape memory material. The elongate distal anchor strut 1134 may change shape in response to electronic actuation, temperature changes, physical manipulation, dimensional changes due to release of the device from the catheter, and the like. For example, the elongate distal anchor struts 1134 in the straightened form as shown in fig. 12A can be activated by passing an electrical current. When activated, the elongate distal anchor struts 1134 may form an arcuate shape, as shown in fig. 12C. The elongate distal anchor strut 1134 in the form of an arc in fig. 12C may be activated to straighten. For example, activating the elongate distal anchor struts 1134 in fig. 12C can straighten the elongate distal anchor struts 1134 to form the straightened shape in fig. 12A. In some embodiments, struts 1133, 1134 are biased to their respective deployed configurations and are mechanically straightened (e.g., via a catheter and/or forceps) to fit within the working channel of a catheter or endoscope.

Anchor tip

Body movement (e.g., inhalation and/or exhalation, coughing, etc.) may cause medical devices used inside the lumen to move in different directions. Anchoring points pointing in different directions may anchor the device to counteract such movement of the device. Fig. 13A-13C illustrate different views of one example shape of the bi-directional anchoring tip 1340. The bi-directional anchor tip 1340 may be connected to the strut member 1330. The strut member 1330 may include preformed bends 1392A, 1392B. Strut member 1330 can be connected to anchor hub 1375. In some embodiments, anchor hub 1375 is connected to an operative portion (e.g., a valve) of a medical device. The bi-directional anchoring tip 1340 can include a first anchoring tip 1335A and a second anchoring tip 1335B. In some embodiments, the first anchor tip 1335A and/or the second anchor tip 1335B extend from the forked body 1337.

First 1335A and second 1335B anchor tips may extend from the forked body 1337. The forked body 1337 may connect the first anchor tip 1335A and the second anchor tip 1335B to the strut member 1330. In some embodiments, the anchor tips 1335A, 1335B are formed by introducing a slit into the distal end of the strut member 1330 to split the distal end of the strut member 1330 into two discrete portions (e.g., a first tip 1335A and a second tip 1335B). The first anchor tip 1335A may extend generally in the same direction as the strut member 1330. For example, the first anchor tip 1335A may extend in a radial direction from the hub 1375. Second anchor tip 1335B may include a bend. Second anchor tip 1335B may form an angle with first anchor tip 1335A. For example, the second anchor tip 1335B may be bent from the forked body 1337 at an angle of about 10 degrees to about 170 degrees. The first anchor tip 1335A and the second anchor tip 1335B may comprise different tip configurations. For example, the first anchor tip 1335A may include a pointed tip structure, such as the tip structures used for the first anchor tip 1335A shown in fig. 13A-13C. Second anchor tip 1335B may include a blunt tip configuration as shown in fig. 13A-13C.

The first anchor tip 1335A may be configured to penetrate the lumen. The second anchor tip 1335B may be configured to limit the depth of penetration of the second anchor tip 1335A. The second anchor tip 1335B may be directed proximally, as shown in fig. 13A. The second anchor tip 1335B may be configured to apply a radially outward force to the lumen wall. For example, the second anchor tip 1335B may be configured to inhibit or limit movement of the device in the longitudinal direction. The proximal direction of the second anchor tip 1335B may be used to block movement of a medical device used with the bi-directional anchor tip 1300 in the proximal direction inside the lumen.

The second anchor tip 1335B may be positioned on the strut member 1330 distal from the first anchor tip 1335A. Second anchor tip 1335B may include a sharp bend. The first anchor tip 1335A may form an angle with the forked body 1337.

Membrane frame strut

Endoluminal devices having a shorter overall axial length may be useful. For example, endoluminal devices having shorter axial lengths may be used in short lumens. In cases where the anchoring portion needs to be close to the operative portion, for example to avoid anchoring the device to a scratch patch (abrased patch) of the lumen wall, a device having a shorter axial length may be used. In some cases, it may be beneficial to use shorter devices when the devices are implanted adjacent to the intersection of multiple branches of the airway or other body lumen.

Figures 14A-14C illustrate perspective views of one example endoluminal device 1400 with strut members interposed therebetween. The apparatus 1400 may include a hub 1420. In some embodiments, the device 1400 includes an anchoring portion 1432 coupled to the hub and an operating portion 1435 coupled to the hub 1475. The anchor portion 1432 can include a plurality of anchor struts 1432. The plurality of anchor struts 1432 may include anchor tips 1440. The anchor tip may include bidirectional tips 1335A, 1335B (shown in fig. 13A and 13B). The operating portion 1425 may include a membrane post 1435 and a membrane 1463 attached to the membrane post 1435. The handling portion 1425 (e.g., membrane strut 1435) can be connected to the hub 1475 and extend proximally from the hub 1475. The device 1400 may include a central rod 1460 that is connected to the hub 1475 and is positioned between the membrane strut 1435 and the crimp button 1462 on a proximal end of the central rod 1460.

The anchoring strut 1432 can include a curved shape having an anchoring tip 1440 pointing in a radially outward direction, as shown in fig. 14A-14C. In some embodiments, the anchoring post 1432 includes a pad or other structure adjacent the tip 1440 to limit the extent to which the tip 1440 penetrates the airway wall. As shown in fig. 14B, frame struts 1435 can be interposed between the anchor struts 1432 around the circumference of the device 1400 such that frame strut tips 1436 can be interposed between the anchor tips 1440 when viewed in a lateral direction. In some cases, the number of anchor tips 1440 and anchor struts 1432 matches the number of struts 1435. The intervention of the struts 1435, 1432 may be used, for example, to minimize the overall diameter of the endoluminal device 1400 when the endoluminal device 1400 is compressed within a delivery catheter.

The anchor struts 1432 may extend outward from the hub 1475 and bend in a proximal direction, as shown in fig. 14A-14C. In some embodiments, the anchor struts 1432 are configured to exert a radially outward force on the lumen within which the device 1400 is deployed. When placed inside the lumen, the handling portion 1435 may be disposed proximal to the anchoring portion 1432. When placed inside the lumen, the frame strut tip 1436 and the anchor tip 1440 of the operative portion 1435 can be placed a distance D4 apart. The distance D4 between the anchor tip 1440 and the frame post tip 1436 of the operative portion 1425 can be large enough to reduce the risk of contact between the tip 1440 and the membrane 1463. The distance D4 may be about 0.02mm to about 5 mm. The distance D4 may be about 0.05mm to about 4 mm. The distance D4 may be about 0.1mm to about 3 mm. The distance D4 may be about 0.15mm to about 2 mm. The distance D4 may be about 0.2mm to about 1 mm.

Positioning the anchor tip 1440 near the frame post tip 1436 can reduce movement of the operative portion 1425 when the anchor tip 1440 is seated within the wall of the lumen in which the device 1400 is deployed. For example, the anchor strut 1432 can be configured to limit movement of the operative portion 1435 to less than about 0.2 mm. The anchor strut 1432 can be configured to limit movement of the operative portion 1435 to less than about 0.15 mm. The anchor strut 1432 can be configured to limit movement of the operative portion 1435 to less than about 0.05 mm. The anchor strut 1432 can be configured to limit movement of the operative portion 1435 to less than about 0.02 mm. The anchor strut 1432 can be configured to limit movement of the operative portion 1435 to less than about 0.01 mm.

The anchor strut 1432 may include a plurality of preformed bends. In some cases, the anchoring strut 1432 can have an arcuate shape without a recognizable bend. The anchor strut 1432 may have a uniform thickness along the length of the strut 1432. In some embodiments, some portion of the post 1432 is thicker than other portions of the post 1432. The thick portion may be configured to have a lower flexibility than the thinner portion. For example, the thinner portion may be configured to allow greater bending than the thicker portion.

The endoluminal device 1400 can be transported using a delivery catheter. For example, the intervening anchor struts 1432 can be folded together with the frame struts 1435 while intervening frame struts 1435 to fit inside the catheter. The endoluminal device 1400 can be deployed by pushing the endoluminal device 1400 out of the catheter. In some embodiments, the endoluminal device 1400 is deployed by withdrawing the catheter from the endoluminal device 1400 when the device 1400 is positioned at the deployed position. The endoluminal device 1400 can be advanced such that the hub 1475, anchor tip 1440, and membrane strut tip 1432 can then exit the catheter. Once the anchoring tip 1440 exits the catheter, the anchoring tip 1440 may latch onto the surface of the lumen 1410. Once the anchoring tip 1440 is latched onto the lumen 1410, the user can pull the catheter away from the frame post 1435.

In some embodiments, anchor posts 1432 having a preformed curved shape can be straightened to extend in a distal direction from hub 1475 to fit inside and be transported through a catheter. The anchor strut 1432 can include a different number of struts than the number of frame struts 1435A.

Connecting member

The anchor strut may be coupled to the operative portion by an extendable and/or flexible connecting member. Figures 15A and 15B illustrate one embodiment of an endoluminal device 1500 having extendable linkage members 1560. The endoluminal device 1500 can include an operative portion 1535, a connecting member 1560 coupled to the operative portion 1535, and an anchor portion 1530 coupled to the connecting member 1560. The anchor portion 1530 may include a distal hub 1575B, anchor struts 1532 connected to the distal hub 1575B and extending from the distal hub 1575B, and anchor tips 1540. Anchoring tip 1540 may include a first tip 1536A and a second tip 1536B. The second tip 1536B may be configured to limit the depth to which the first tip 1536A penetrates into the wall of the lumen in which the endoluminal device 1500 is mounted. The handling portion 1535 may include a proximal hub 1575A, a plurality of frame struts 1535 connected to the proximal hub 1575A and extending from the proximal hub 1575A, and a membrane 1535B connected to the frame struts 1535A.

The anchoring portion 1530 may be disposed at a distal end of the operating portion 1535. The anchor struts 1530 may extend radially and generally in a distal direction from the distal hub 1575B. Frame post 1535A may include a curved surface 938 (as shown in fig. 9). The curved surface 937 can be configured to minimize trauma to the lumen 1510. Frame struts 1535A may extend proximally from proximal hub 1575A. The connecting member 1560 may connect the distal hub 1575B and the proximal hub 1575A. The connecting member 1560 may connect the anchoring portion 1530 and the operating portion 1535. The connecting member 1560 may be extendable. For example, the connecting member 1560 may be a helical spring, as shown in fig. 15A and 15B.

In the first configuration shown in fig. 15A, the connecting member 1560 can be retracted to bring the operative portion 1535 and the anchor portion 1530 closer together. In a second configuration shown in fig. 15B, the connecting member 1560 may be extended, and the operative portion 1535 and the anchor portion 1530 may be spaced farther apart from one another. In the second configuration, the distance between the proximal hub 1575A and the distal hub 1575B is greater than in the first configuration.

The connecting member 1560 may expand and/or contract in response to a change in lumen size. The connecting member 1560 may be sufficiently resilient to allow axial movement of the anchor portion 1530 without displacing the operating portion 1535. In some embodiments, the anchor portion 1530 can move away from the handling portion 1535 as the anchor struts 1532 and the lumen wall 1515 expand outward. In some cases, movement of the anchor portion 1530 away from the handling portion 1535 may be achieved with little or no movement of the handling portion 1535 toward the anchor portion 1530.

Regardless of the change in the dimensions of the lumen 1510, the connecting member 1560 may include a tensile strength sufficient to hold the operative portion 1535 in place. For example, the connecting member 1560 may be configured to counteract the contraction of the lumen 1510, such that when the connecting mechanism 1560 initially expands during the contraction of the lumen, the strength of the connecting mechanism 1560 may spring back to its original length and re-expand the lumen 1510. The spring portion 1560 may include a resilient structure, such as an elastomer. For example, the spring portion 1560 may include synthetic rubber, silicone, or the like.

Connecting member in bifurcated lumen

The endoluminal device 1500 can be used within a bifurcated lumen (such as a bifurcated airway). The extendable link member 1560 may be used in airways having a small diameter. Figures 16A and 16B illustrate one embodiment of an endoluminal device 1500 having an extendable linkage member for use within a bifurcated lumen 1610. Bifurcated lumen 1610 may include a first lumen 1615A and a second lumen 1615B. The first lumen 1615A and the second lumen 1615B may comprise different sizes. For example, the first lumen 1615A may include a diameter that is smaller than a diameter of the second lumen 1615B. The first and second lumens 1615A, 1615B may extend or retract individually or together.

Figure 16A shows an endoluminal device 1500 primarily disposed within a first lumen 1615A. The anchoring portion 1530 may be disposed distal of the first lumen 1615A, and the operative portion 1535 may be disposed at or near the entrance to the first lumen 1615A. The manipulation portion 1535 can contact the first lumen 1615A at the stretched contact diameter 1590B. The contact diameter 1590B may include the diameter of the first lumen 1615A within which a portion of the outer surface of the operative portion is in contact with the lumen 1615A.

Fig. 16B shows the first lumen 1615A in a collapsed state. In the collapsed state, the first lumen 1615A may exert a force on the manipulation portion 1535, and portions of the manipulation portion 1535 may be disposed outside the first lumen 1615A. For example, the manipulation portion 1535 can contact the first lumen 1615A at the constricted contact diameter 1590A. The contracted contact diameter 1590A may be closer to the proximal hub 1575A than the expanded contact diameter 1590B. The contracted contact diameter 1590A may be less than the expanded contact diameter 1590B.

The connecting portion 1560 may be elastically extended to allow the operating portion 1535 to move proximally while the first lumen 1615A is contracted. The connecting portion 1560 may pull the operative portion distally as the first lumen 1615A is extended. The elastic extension and pulling of the connecting portion may exert sufficient counterforce to seat the endoluminal device 1500 inside the airway without causing removal of the anchoring mechanism from its position. The distance that the connection part 1560 may extend may be determined by the angle of the taper of the valve part and the diameter of the airway wall covered by the operation part 1535.

A post 1535A within the handling portion 1535 may rest against an opening of the first lumen 1615A and be positioned within the larger lumen 1605 to counteract pulling from the anchor portion 1530, as shown in fig. 16A and 16B. The anchor portion 1530 may remain in the same position within the first lumen 1615A during expansion and contraction. In some cases, during placement of the anchor portion 1530, the anchor portion 1530 moves distally within the first lumen 1615A. For example, within the expanded first lumen 1615A in fig. 16A, the connecting member 1560 may be at a first length D5. Within the collapsed first lumen 1615A shown in fig. 16B, the connecting portion 1560 may be at a second length D6. The first length D5 may be shorter than the second length D6. The manipulation portion 1535 may be moved further outward in the proximal direction to the larger lumen 1605 as the first lumen 1615A is retracted. During contraction of the inner lumen 1615A, the distance between the proximal hub 1575A and the distal hub 1575B may increase. During extension of the inner lumen 1615A, the distance between the proximal hub 1575A and the distal hub 1575B may decrease. The elastic force generated by the connection part 1560 may be adjusted to hold the operation part 1535 against the opening.

Although the operative portion 1535 is suitable for larger airways, it may also be used in smaller airways having an opening to the larger airway. As shown in fig. 16A and 16B, the handling portion 1535 may be nested within the proximal end of the first lumen 1615A. For example, the first lumen 1615A may include a contact diameter 1590A that is smaller than an outermost diameter of the operative portion 1535. The outermost diameter of the handling portion 1535 may be the largest diameter of the handling portion 1535. A portion of the manipulation portion 1535 may be located inside the first lumen 1615A, while the remainder of the manipulation portion 1535 may extend outside the entrance to the first lumen 1615A. The operative portion 1535 may be shaped and sized to ensure airflow through the second lumen 1615B.

Although these inventions have been disclosed in the context of certain preferred embodiments and examples, it will be understood by those skilled in the art that the scope of the present invention extends beyond the specifically disclosed embodiments to other alternative embodiments and/or uses of the invention and obvious modifications and equivalents thereof. In addition, while several variations of the invention have been shown and described in detail, other modifications, which are within the scope of these inventions, will be readily apparent to those of skill in the art based upon this disclosure. It is also contemplated that combinations and sub-combinations of the specific features and aspects of the embodiments may be made and still fall within the scope of the invention. It should be understood that various features and aspects of the disclosed embodiments can be combined with, or substituted for, one another in order to form varying modes of the disclosed inventions. Thus, the scope of at least some of the inventions disclosed herein should not be limited by the specific disclosed embodiments described above.