Device for controlling extra-vascular haemorrhage

• US 20030004462A1
• Filed: 06/24/2002
• Published: 01/02/2003
• Est. Priority Date: 12/23/1999
• Status: Abandoned Application

• Current Assignee: Richard Michael Bestall Halpin
• Original Assignee: Richard Michael Bestall Halpin
• Inventors: Halpin, Richard Michael Bestall
• Application Number:
  US10/168,912
• Publication Number:
  US 20030004462A1
• Time in Patent Office: Days
• US Class Current: 604/99.04
• CPC Class Codes: A61B 17/0057 Implements for plugging an opening in the wall of a hollow or tubular organ, e.g. for sealing a vessel puncture or closing a cardiac septal defect sutures A61B17/04; closing rectum or urethra near body surface A61F2/0009
• CPC Class Codes: A61B 2017/00557 inflatable A61B2017/22051 takes precedence
• CPC Class Codes: A61B 2017/00641 for closing fistulae, e.g. anorectal fistulae
• CPC Class Codes: A61F 2/82 Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents stent-grafts for tubular structures of the body other than blood vessels A61F2/04; stent-grafts for blood vessels A61F2/07; instruments specially adapted for placement or removal of stents or stent-grafts A61F2/95; for closing wounds, or holding wounds closed A61B17/04 - A61B17/115; dilators A61M29/00
• CPC Class Codes: A61M 25/1002 characterised by balloon shape A61M25/1006, A61M25/1009 take precedence

Abstract

The present invention provides an inflatable device 1 for insertion in a substantially deflated state, into a blood or other biological fluid carrying vessel 4 for controlling extra-vascular hemorrhage from a damaged portion 6 of the vessel 4 when the device 1 is in an inflated state. The device 1 defines in its inflated state an elongate open-ended tube having a passage 8 extending therethrough, through which blood or another biological fluid flows while allowing repair of the damaged portion 6 of the vessel 4.

Claims

1. An inflatable device for inserting, in a substantially deflated state, into a blood or other biological fluid carrying vessel of a human or animal, the device having an inflated state in which it defines an elongate open-ended tube means having an inlet end and an outlet end, said tube having a first outer wall formed and arranged to provide, in said inflated state, a close fit around the whole of the intima of the vessel in use of the device, and a second inner wall closely spaced apart from said first outer wall in said inflated state, said second inner wall defining a substantially uninterrupted passage means through the device through which blood or other biological fluid may flow, in use of the device, said first outer wall and said second inner wall defining an inflatable volume, which inflatable volume is in fluid communication with an inflation channel disposed inwardly of the inner wall, whereby in use of the device in an inflated state, blood or other biological fluid may pass through the device without leaking past or around the outside of the device, and without the flow thereof therethrough being substantially interrupted.

2. A device as claimed in claim 1 wherein the elongate tube means defined by the inflated device comprises at least one passage, defined between said inlet end and said outlet end, through the longitudinal length of the device.

3. A device as claimed in claim 1 or claim 2 wherein the diameter of said first inner wall is greater than 50% of the second outer wall of the inflated device.

4. A device as claimed in claims 1 or 2 wherein the diameter of said first inner wall is in the range of 90 to 95% of the second outer wall of the inflated device.

5. A device as claimed in any one of claims 1 to 4 wherein the device comprises one or more substantially collapsible walls defining said enclosed inflatable volume which can be inflated by injecting saline or another physiologically acceptable fluid, or combination of fluids, into the enclosed inflatable volume.

6. A device as claimed in any one of claims 1 to 5 wherein the device has a cross-section which is generally circular or elliptical when inflated.

7. A device as claimed in any one of claims 1 to 6 wherein the device has an irregular cross-section when inflated, according to the particular shape or configuration of the damaged blood or biological fluid carrying vessel in which the device is to be used.

8. A device as claimed in any one of claims 1 to 7 wherein in use of the device in a vessel having an injury area, the device has a length which extends to at least the same length as said injury area in a said vessel.

9. A device as claimed in any one of claims 1 to 8 wherein the device has a working channel or conduit extending at least part-way through the device wherein the working channel or conduit is formed and arranged for receiving therein at least one of the group comprising:

a fluid, a device and a guide-wire.

10. A device as claimed in claim 9 wherein the working channel or conduit is the hollow interior of an elongate conduit centrally positioned within the passage means.

11. A device as claimed in claim 10 wherein the elongate conduit is integrally formed with the inflatable device.

12. A device as claimed in claims 10 or 11 wherein the elongate conduit is fixed to the device at at least one point therealong, with opposite end portions of the elongate conduit protruding from respective opposite ends of the tube means defined by the inflated device.

13. A device as claimed in claim 12 wherein a first one of said protruding end portions is relatively long while the second end portion protrudes only a very short length beyond the tube means forming the inflated device.

14. A device as claimed in claim 13 wherein said first protruding end portion is provided with a first self-sealing entry port to allow the admission of fluids materials or devices, into the working channel, for delivery into a patient'"'"'s bloodstream.

15. A device as claimed in any one of claims 1 to 14 wherein the device is formed and arranged to slide over a guide wire to assist in the insertion and positioning of the device.

16. A device as claimed in any one of claims 10 to 15 wherein a wall forming the elongate conduit contains, in the thickness thereof, said inflation channel for said fluid communication with the inflatable volume of the device, and through which a biologically compatible fluid is injected into the device in order to inflate the device.

17. A device as claimed in claim 16 wherein an input end of the inflation terminates in and is connected to a second self-sealing entry port provided in the same end portion of the elongate conduit as the first entry port.

18. A device as claimed in claims 16 or 17 wherein one or more walls forming said central elongate conduit contain one or more further channels in fluid communication with further separate entry ports provided on the same protruding end of the central elongate conduit, for separately carrying one or more of a biologically compatible fluid, contrast imaging fluids and other fluids or devices therealong, to, from or through the device.

19. A device as claimed in any one of claims 1 to 18 wherein the device has at least one inflatable support strut within the passage means, said inflatable support strut being in fluid communication with said inflatable volume.

20. A device as claimed in claim 19 wherein the at least one strut spans the inner diameter of the device.

21. A device as claimed in claim 19 or 20 wherein two, three, four or more support struts are provided.

22. A device as claimed in claim 19 or 20 when dependant on any one of claims 10 to 18 wherein the at least one support strut is formed and arranged such that, in the inflated state of the device, the strut extends radially outwardly from the central elongate conduit to the annular outer portion of the inflated device, defined between said first inner wall and said second outer wall.

23. A device as claimed in any one of claims 19 to 22 when dependant on any one of claims 10 to 18 wherein the at least one support strut is in fluid communication with the inner channel formed in the wall of the central elongate conduit.

24. A device as claimed in any one of claims 1 to 23 wherein the inflated device is non-uniform in outer diameter along the longitudinal length thereof.

25. A device as claimed in any one of claims 1 to 24 wherein the inflated device presents a generally hour-glass shaped side profile, having a relatively narrow waist portion and relatively wide end portions.

26. A device as claimed in claim 25 wherein the device in its inflated condition, provides a leak-proof fit with the intima of the blood/biological fluid conveying vessel and the waist portion defines a working space between the outer surface of the device and the intima of the blood/biological fluid conveying vessel.

27. A device as claimed in either of claims 25 and 26 wherein the waist portion is separately inflatable from the rest of the inflatable volume of the device.

28. A device as claimed in any one of claims 1 to 27 wherein the device is provided with one or more openings through the side walls of said tube and which are formed and arranged to allow perfusion of blood therethrough from the passage means in a flow direction generally perpendicular to the axis of the device when said openings are located at branching points within a branched vessel.

29. A device as claimed in claim 28 wherein the device has a non-uniform diameter along its length, having a relatively narrow first end portion provided with said openings, and a relatively wide second portion.

30. A device as claimed in claims 24 to 29 wherein the device has a waist portion disposed between first and second ends of the device, wherein the waist portion has a reduced outer diameter portion extending at least part-way around the outer circumference of the device and defines a working area between the intima of a said vessel and the inflated device.

31. A device as claimed in claim 30 wherein the reduced outer diameter portion has a longitudinal extent at least as great as its extent about the circumference of the device.

32. A device as claimed in any one of claims 19 to 31 where the tube forming the device is formed from at least two inflatable semi-circular wall portions, each wall portion having two major longitudinally extending edges which extend substantially parallel to a corresponding edge of an adjacent wall portion;

said at least two wall portions are in fluid communication with a said support strut, wherein said support strut is formed and arranged to align the respective major edges of the at least two wall portions such that the major edges of adjacent wall portions abut against one another to form a more or less fluid tight seal therebetween and along the extent thereof when the device is in an inflated condition.

33. A device as claimed in any one of claims 1 to 32 wherein the device is fabricated from one or more physiologically acceptable materials selected from the group including rubber, synthetic rubber, and plastics materials, polyurethane, polyethylene, Pluronic (RTM), and/or block, and/or co-polymers thereof.

34. A kit of parts comprising an inflatable device as claimed in any one of claims 1 to 33 for inserting into a blood or other fluid carrying vessel, and insertion means for facilitating access to the inside of said vessel.

35. A kit-of-parts as claimed in claim 34 which includes deployment means for deploying the device to its inflated condition.

36. A method of controlling extra-vascular haemorrhage comprising the steps of:

inserting an inflatable device of claim 1, in its deflated condition, into a damaged blood vessel;

locating the device adjacent to a damaged portion of the blood vessel; and

inflating the device so as to substantially occlude the damaged portion so as to minimise leakage of blood from said damaged portion and thereby permit the substantially uninterrupted passage of blood through the device.

37. A method of inserting and deploying a stent in a blood vessel comprising the steps of:

locating an expandable generally tubular stent, in a collapsed state thereof, of the device of claim 1 so that the stent is coaxial with and circumferentially surrounds the inflatable device;

inserting the inflatable device, in its deflated condition, and with the stent located thereon, into a blood vessel to be stented and locating the device in the desired portion thereof; and

inflating the device so as to deploy the stent to an expanded condition in which it supports the wall of the blood vessel.