Systems and methods for removing undesirable material within a circulatory system utilizing a balloon catheter

Patent metadata

Field	Value
Publication number	US-2024215996-A1
Application number	US-202418602646-A
Country	US
Kind code	A1
Filing date	Mar 12, 2024
Priority date	Dec 20, 2007
Publication date	Jul 4, 2024
Grant date	—

Abstract

A system is provided which includes a cannula and a secondary device. The cannula includes an expandable member, a cannula lumen, and a cannula proximal end. The expandable member includes a proximal most end, a distal most end, at least two movable sections, with the space between the at least two moveable sections, and an impermeable membrane extending across the space between each of the at least two moveable sections. In addition, the impermeable membrane extends from the expandable member distal most end to the expandable member proximal most end. The secondary device is configured to be coaxially placed through the cannula lumen. The cannula proximal end is configured to operatively couple to a vacuum source configured to create a negative pressure to pull an undesirable material into the cannula lumen.

First claim

What is claimed is:

1 . A system comprising:
a cannula comprising an expandable member, a cannula lumen, and a cannula proximal end; the expandable member comprising a proximal most end, a distal most end, at least two moveable sections, with a space between the at least two moveable sections, and an impermeable membrane extending across the space between each of the at least two moveable sections and extending from the expandable member distal most end to the expandable member proximal most end; a secondary device configured to be coaxially placed through the cannula lumen; and the cannula proximal end is configured to operatively couple to a vacuum source configured to create a negative pressure to pull an undesirable material into the cannula lumen.

2 . The system of claim 1 , wherein the secondary device is configured to macerate or dislodge the undesirable material.

3 . The system of claim 2 , wherein the cannula proximal end further comprises a port configured to introduce the secondary device into the cannula lumen.

4 . The system of claim 3 , wherein the at least two moveable sections together with the impermeable membrane define a shape of a funnel.

5 . The system of claim 4 , wherein the undesirable material comprises either a pulmonary embolism, en bloc clots, a thrombi, an emboli, a thromboemboli, a deep vein thrombosis, or an infected vegetation.

6 . The system of claim 1 , wherein the impermeable membrane is a continuous membrane configured to circumferentially surround the expandable member.

7 . The system of claim 1 , wherein the vacuum source is manually operated.

8 . The system of claim 1 , wherein the secondary device comprises a fragmentation thrombectomy device configured to macerate the undesirable material.

9 . The system of claim 1 , wherein the expandable member further comprises an actuation mechanism configured to expand the at least two moveable sections.

10 . The system of claim 1 , wherein the cannula further comprises a radiopaque member configured to aid in visualization of the cannula.

11 . A system comprising:
a cannula comprising a cannula lumen, a cannula proximal end, a cannula distal end, and an expandable funnel coupled to the cannula distal end, the expandable funnel defined by multiple moveable members, with a space between each of the multiple moveable members, and an impermeable membrane extending across the space between each of the multiple moveable members and extending from a distal most end of the expandable funnel to a proximal most end of the expandable funnel; the cannula proximal end configured to operatively couple to a vacuum source configured to create a negative pressure to pull an undesirable material into the cannula lumen; and a macerator configured to be coaxially placed through the cannula lumen; wherein the macerator is configured to macerate the undesirable material and aid in the removal of the undesirable material.

12 . The system of claim 11 , wherein the expandable funnel is configured to transition between an unexpanded state and an expanded state.

13 . The system of claim 11 , wherein proximal ends of the multiple moveable members are configured to be coupled to the cannula distal end.

14 . The system of claim 11 , wherein the expandable funnel comprises a collapsed position in which the multiple moveable members are substantially adjacent to one another and an expanded position in which the multiple moveable members are flared open into a substantially funnel shape.

15 . The system of claim 11 , wherein the impermeable membrane extends along an inner surface of the multiple moveable members.

16 . A system comprising:
a cannula comprising a cannula lumen, a cannula proximal end, a cannula distal end, a radiopaque member configured to aid in visualization of the cannula, and an expandable funnel coupled to the cannula distal end, the expandable funnel defined by an actuating unit comprising a plurality of actuating members and an impermeable membrane, the impermeable membrane extending across a space between each of adjacent actuating members of the plurality of actuating members and surrounding an entirety of the actuating unit; the cannula proximal end configured to operatively coupled to a vacuum source configured to create a negative pressure to pull an undesirable material into the cannula lumen; and a fragmentation thrombectomy device configured to be coaxially placed through the cannula lumen; wherein the fragmentation thrombectomy device is configured to disrupt or dislodge the undesirable material and aid in the removal of the undesirable material.

17 . The system of claim 16 , further comprising a reservoir in fluid communication with the cannula and configured to collect blood and undesirable material aspirated by the vacuum source.

18 . The system of claim 15 , further comprising a sheath configured to be coaxially and independently moveable relative to the cannula.

19 . The system of claim 18 , wherein the sheath is configured to be coaxially moved toward the cannula distal end and collapse the expandable funnel, and wherein the sheath is configured to be coaxially moved away from the cannula distal end, thereby exposing and causing expansion of the expandable funnel.

20 . The system of claim 15 , wherein the negative pressure generated by the vacuum source and movement of the fragmentation thrombectomy device together macerate and aspirate the undesirable material from a treatment site.

Assignees

• Angiodynamics Inc

Inventors

• Aklog Lishan
• Glennon Michael

Classifications

• A61M1/804

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• A61M1/77

  Suction-irrigation systems (aspiration tips supplying fluids A61M1/85; specific for negative pressure wound therapy A61M1/92; combined with tracheal tubes A61M16/0463) · CPC title

• A61M1/84

  Drainage tubes; Aspiration tips (for negative pressure wound therapy A61M1/90; for surgical cutting instruments A61B17/32) · CPC title

• A61M1/79

  Filters for solid matter (specially adapted for dental use A61C17/065) · CPC title

• A61M1/3621

  Extra-corporeal blood circuits (single-needle circuits A61M1/30) · CPC title