Methods and devices for maintaining patency of surgically created channels in tissue

• US 20040073155A1
• Filed: 06/09/2003
• Published: 04/15/2004
• Est. Priority Date: 01/14/2000
• Status: Abandoned Application

• Current Assignee: Bronucs Technologies, Inc.
• Original Assignee: Broncus Technologies, Inc
• Inventors: Estridge, Trudy, Laufer, Michael D., Reich, Cary J., Loomas, Bryan, Kaplan, Gary, Cole, Cary, Roschak, Ed
• Application Number:
  US10/458,085
• Publication Number:
  US 20040073155A1
• Time in Patent Office: Days
• US Class Current: 604/8
• CPC Class Codes: A61B 17/064 Surgical staples, i.e. penetrating the tissue
• CPC Class Codes: A61B 17/0644 penetrating the tissue, deformable to closed position
• CPC Class Codes: A61B 17/068 Surgical staplers , e.g. containing multiple staples or clampsstaplers containing only one staple A61B17/10; magazines or containers for staples A61B17/105; for performing anastomosis A61B17/115; staplers in general B25C5/00
• CPC Class Codes: A61B 17/08 Wound clamps or clips, i.e. not or only partly penetrating the tissue suture bridges A61B17/0466; Devices for bringing together the edges of a wound
• CPC Class Codes: A61B 17/11 for performing anastomosis; Buttons for anastomosis
• CPC Class Codes: A61B 17/12022 Occluding by internal devices, e.g. balloons or releasable wires plugging an opening in the wall of an organ A61B17/0057; occluders for the cervical canal A61F6/146; vas deferens occluders A61F6/20
• CPC Class Codes: A61B 17/12104 in an air passage
• CPC Class Codes: A61B 17/22 Implements for squeezing-off ulcers or the like on the inside of inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; Calculus removers; Calculus smashing apparatus; Apparatus for removing obstructions in blood vessels, not otherwise provided for dilators A61M29/00
• CPC Class Codes: A61B 18/1477 Needle-like probes
• CPC Class Codes: A61B 18/1485 having a short rigid shaft for accessing the inner body through natural openings
• CPC Class Codes: A61B 18/1492 having a flexible, catheter-like structure, e.g. for heart ablation A61B18/1477 takes precedence
• CPC Class Codes: A61B 18/1815 using microwaves
• CPC Class Codes: A61B 2017/00106 ultrasonic
• CPC Class Codes: A61B 2017/00252 for by-pass connections, i.e. connections from heart chamber to blood vessel or from blood vessel to blood vessel
• CPC Class Codes: A61B 2017/0046 with a releasable handle; with handle and operating part separable for prosthetic joint-implanting tools A61F2/4603
• CPC Class Codes: A61B 2017/00477 Coupling A61B2017/0046 takes precedence
• CPC Class Codes: A61B 2017/00575 for closure at remote site, e.g. closing atrial septum defects
• CPC Class Codes: A61B 2017/00601 Implements entirely comprised between the two sides of the opening
• CPC Class Codes: A61B 2017/1135 End-to-side connections, e.g. T- or Y-connections Y-shaped blood vessel prostheses A61F2002/065
• CPC Class Codes: A61B 2017/1139 Side-to-side connections, e.g. shunt or X-connections
• CPC Class Codes: A61B 2017/22051 : with an inflatable part, e.g. balloon, for positioning, blocking, or immobilisation A61B2017/22048, A61B2017/3486 take precedence
• CPC Class Codes: A61B 2017/22067 : Blocking; Occlusion A61B2017/22054 takes precedence
• CPC Class Codes: A61B 2017/22077 : with a part piercing the tissue A61B2017/22044 takes precedence
• CPC Class Codes: A61B 2018/00005 : Cooling or heating of the probe or tissue immediately surrounding the probe
• CPC Class Codes: A61B 2018/00029 : open
• CPC Class Codes: A61B 2018/00214 : Expandable means emitting energy, e.g. by elements carried thereon
• CPC Class Codes: A61B 2018/00273 : Anchoring means for temporary attachment of a device to tissue
• CPC Class Codes: A61B 2018/00285 : Balloons
• CPC Class Codes: A61B 2018/00541 : Lung or bronchi
• CPC Class Codes: A61B 2018/00738 : Depth, e.g. depth of ablation
• CPC Class Codes: A61B 2018/1417 : Ball
• CPC Class Codes: A61B 2018/1425 : Needle
• CPC Class Codes: A61B 2018/1437 : whereby the windings of the spiral touch each other such as to create a continuous surface
• CPC Class Codes: A61B 2018/1472 : for use with liquid electrolyte, e.g. virtual electrodes
• CPC Class Codes: A61B 2018/1475 : Electrodes retractable in or deployable from a housing
• CPC Class Codes: A61B 2090/08021 : of the patient or his organs
• CPC Class Codes: A61B 2090/3782 : transmitter or receiver in catheter or minimal invasive instrument
• CPC Class Codes: A61B 2090/395 : with marking agent for marking skin or other tissue
• CPC Class Codes: A61B 2218/002 : Irrigation
• CPC Class Codes: A61B 5/489 : Blood vessels
• CPC Class Codes: A61B 8/06 : Measuring blood flow measuring volume flow in general G01F, e.g. G01F1/66, G01F1/72; measuring speed of fluids in general G01P5/00
• CPC Class Codes: A61B 8/12 : in body cavities or body tracts, e.g. by using catheters catheters per se A61M25/00
• CPC Class Codes: A61B 90/36 : Image-producing devices or illumination devices not otherwise provided for
• CPC Class Codes: A61F 2/02 : Prostheses implantable into the body closure means for urethra or rectum or for artificial body openings therefor A61F2/0004
• CPC Class Codes: A61F 2/07 : Stent-grafts
• CPC Class Codes: A61F 2/20 : Epiglottis; Larynxes; Tracheae combined with larynxes or for use therewith tracheae, bronchi per se A61F2/04 ; tracheostomy tubes A61M16/0465
• CPC Class Codes: A61F 2/2412 : with soft flexible valve members, e.g. tissue valves shaped like natural valves check valves with flexible valve members in general F16K15/14
• CPC Class Codes: A61F 2/2418 : Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2/90 : characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2/91 : made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
• CPC Class Codes: A61F 2/92 : Stents in the form of a rolled-up sheet expanding after insertion into the vessel , e.g. with a spiral shape in cross-section
• CPC Class Codes: A61F 2002/043 : Bronchi
• CPC Class Codes: A61F 2002/061 : provided with means for allowing access to secondary lumens
• CPC Class Codes: A61F 2002/068 : Modifying the blood flow model, e.g. by diffuser or deflector
• CPC Class Codes: A61F 2002/8483 : Barbs
• CPC Class Codes: A61F 2220/0008 : Fixation appliances for connecting prostheses to the body
• CPC Class Codes: A61F 2220/005 : using adhesives
• CPC Class Codes: A61F 2220/0058 : soldered or brazed or welded
• CPC Class Codes: A61F 2220/0075 : sutured, ligatured or stitched, retained or tied with a rope, string, thread, wire or cable
• CPC Class Codes: A61F 2230/0008 : elliptical or oval
• CPC Class Codes: A61F 2230/0019 : rectangular
• CPC Class Codes: A61F 2230/005 : Rosette-shaped, e.g. star-shaped
• CPC Class Codes: A61F 2230/0078 : hyperboloidal
• CPC Class Codes: A61N 2007/0078 : with multiple treatment transducers

Abstract

Devices and methods are directed to altering gaseous flow within a lung to improve the expiration cycle of, for instance, an individual having chronic obstructive pulmonary disease. More particularly, methods and devices are disclosed that inhibit closure of channels surgically created through an airway wall such that air is able to pass directly out of the lung tissue to facilitate both the exchange of oxygen ultimately into the blood and/or to decompress hyper-inflated lungs. Devices, instruments, medicine, bioactive agents, or combinations thereof serve to maintain the patency of the surgically created channels. In one embodiment of the present invention, a conduit includes a bioactive coating that inhibits tissue overgrowth when the conduit is deployed in a surgically created channel. Still other methods and devices are described that serve to maintain surgically created channels.

Claims

1. A conduit for maintaining the patency of a channel created in tissue, said conduit having a low-profile delivery state when the conduit is being delivered to said channel and an expanded deployed state when the conduit is deployed in said channel, said conduit comprising:

a radially expandable center section having a first end and a second end and a passageway extending between said first and second ends, said passageway having an axis;

at least one extension member extending from each of said first end and said second end of said center section, each of said extension members having a fixed end connected to one of said first and second ends of the center section and a movable end such that each of said extension members is capable of being deflected about said fixed end to form an angle with said axis when said conduit is in said deployed state; and

a bioactive substance disposed on at least a portion of a surface of said conduit.

2. The conduit of claim 1, wherein said center section comprises a mesh formed from a plurality of ribs and said center-control segment connects at least one rib to an adjacent rib.

3. The conduit of claim 1, further comprising a tissue barrier coaxially covering said passageway, said tissue barrier forming said exterior surface.

4. The conduit of claim 3, wherein said tissue barrier further covers at least a portion of said extension members.

5. The conduit of claim 4, further comprising at least one visualization feature disposed on a portion of said tissue barrier.

6. The conduit of claim 5, wherein said visualization feature is a stripe circumferentially disposed about at least a portion of said center section.

7. The conduit of claim 2, wherein said bioactive substance is selected from the group consisting of antimetabolites, antithrobotics, anticoagulants, antiplatelet agents, thorombolytics, antiproliferatives, antinflammatories, agents that inhibit hyperplasia, agents that inhibit restenosis, smooth muscle cell inhibitors, growth factors, growth factor inhibitors, cell adhesion inhibitors, cell adhesion promoters, drugs that enhance the formation of healthy neointimal tissue, analgesics, anticonvulsives, antiinfectives, antineoplastics, Histamine 2 antagonists, steroids, non-steroidal antiinflammatories, hormones, immunomodulators, mast cell stabilizers, nucleoside analogues, respiratory agents, antihypertensives, antihistamines, ACE inhibitors, cell growth factors, nerve growth factors, anti-angiogenic agents, angiogenesis inhibitors, tissue irritants, poisons, cytotoxic agents, metals, silver, arsenic, pyrolitic carbon, titanium-nitride-oxide, taxanes, paclitaxel, fibrinogen, collagen, thrombin, phosphorylcholine, heparin, rapamycin, radioactive 188Re and 32P, silver nitrate, dactinomycin, sirolimus, everolimus, Abt-578, tacrolimus, camtophecin, etoposide, vincristine, mitomycin, fluorouracil, and cell adhesion peptide.

8. The conduit of claim 2, further comprising a binding agent disposed on the exterior surface of the conduit such that the bioactive substance adheres to the conduit, at least in part, via the binding agent.

9. The conduit of claim 1, further comprising at least one center-control segment configured to restrict radial expansion of said passageway to a maximum profile.

10. The conduit of claim 1, wherein said conduit is constructed to automatically assume its deployed state.

11. The conduit of claim 1, wherein when said conduit is radially expanded said conduit has an overall length and an inner diameter such that a ratio of the overall length to the inner diameter ranges from 1/6 to 2/1 12. The conduit of claim 11, wherein said ratio ranges from 1/4 and 1/1.

12. The conduit of claim 11, wherein said ratio ranges from 1/4 and 1/1.

13. The conduit of claim 12, wherein said ratio ranges from 1/4 to 1/2.

14. The conduit of claim 11, wherein said exterior surface is a tissue barrier coating coaxially disposed over at least the center section of the conduit.

15. The conduit of claim 14, wherein said tissue barrier coating is a polymeric coating.

16. The conduit of claim 11, wherein said bioactive substance is contained in a polymeric matrix that is configured to gradually release said substance from said matrix.

17. The conduit of claim 1, where the bioactive agent is contained in a polymer matrix, where the polymer matrix is loaded onto the conduit such that the polymer matrix readily detaches from the conduit.

18. A method for improving pulmonary function in an individual comprising:

forming a channel through an airway wall tissue; and

treating the airway tissue such that the channel remains open to allow airflow through the channel into the airway.

19. The method of claim 18, wherein treating the airway tissue comprises inhibiting healing of the airway wall tissue.

20. The method of claim 19, wherein inhibiting comprises delivering a medicine to the channel.

21. The method of claim 19, wherein inhibiting comprises delivering a medical device to the channel that at least physically prevents the channel from closing.

22. The method of claim 21, comprising delivering a substance that does not induce tissue encapsulation of the medical device.

23. The method of any of claims 19, comprising delivering energy to the channel to inhibit healing of the airway.

24. The method of claim 18, where treating the airway tissue comprises preventing ingrowth of tissue into the channel.

25. The method of claim 24, wherein treating the airway tissue comprises impeding the wound healing process of lung tissue such that the lung tissue cannot heal and the channel remains patent.

26. The method of claim 24, wherein treating the airway tissue comprises accelerating the wound healing process such that the channel remains patent.

27. The method of claim 26, wherein the step of accelerating the wound healing process comprises increasing the growth of epithelial cells.

28. The method of claim 24, treating the airway tissue comprises inserting a conduit in said channel.

29. The method of claim 28, further comprising treating the lung tissue with a bioactive substance.

30. The method of claim 29, wherein said treating the lung tissue is performed by supplying said bioactive substance on a surface of said conduit.

31. The method of claim 30, wherein said conduit includes a tissue barrier coaxially surrounding at least a center section of said conduit and said bioactive substance is disposed on said tissue barrier.

32. The method of claim 31, wherein said bioactive substance is selected from the group consisting of antimetabolites, antithrobotics, anticoagulants, antiplatelet agents, thorombolytics, antiproliferatives, antinflammatories, agents that inhibit hyperplasia, agents that inhibit restenosis, smooth muscle cell inhibitors, growth factors, growth factor inhibitors, cell adhesion inhibitors, cell adhesion promoters, drugs that enhance the formation of healthy neointimal tissue, analgesics, anticonvulsives, antiinfectives, antineoplastics, Histamine 2 antagonists, steroids, non-steroidal antiinflammatories, hormones, immunomodulators, mast cell stabilizers, nucleoside analogues, respiratory agents, antihypertensives, antihistamines, ACE inhibitors, cell growth factors, nerve growth factors, anti-angiogenic agents, angiogenesis inhibitors, tissue irritants, poisons, cytotoxic agents, metals, silver, arsenic, pyrolitic carbon, titanium-nitride-oxide, taxanes paclitaxel, fibrinogen, collagen, thrombin, phosphorylcholine, heparin, rapamycin, radioactive 188Re and 32P, silver nitrate, dactinomycin, sirolimus, everolimus, Abt-578, tacrolimus, camtophecin, etoposide, vincristine, mitomycin, fluorouracil, and cell adhesion peptide.

33. The method of claim 30, wherein said conduit includes a tissue barrier coaxially surrounding at least a center section of said conduit and said tissue barrier is at least partially formed of said bioactive substance.

34. The method of claim 33, wherein said bioactive substance is selected from the group consisting of antimetabolites, antithrobotics, anticoagulants, antiplatelet agents, thorombolytics, antiproliferatives, antinflammatories, agents that inhibit hyperplasia, agents that inhibit restenosis, smooth muscle cell inhibitors, growth factors, growth factor inhibitors, cell adhesion inhibitors, cell adhesion promoters, drugs that enhance the formation of healthy neointimal tissue, analgesics, anticonvulsives, antiinfectives, antineoplastics, Histamine 2 antagonists, steroids, non-steroidal antiinflammatories, hormones, immunomodulators, mast cell stabilizers, nucleoside analogues, respiratory agents, antihypertensives, antihistamines, ACE inhibitors, cell growth factors, nerve growth factors, anti-angiogenic agents, angiogenesis inhibitors, tissue irritants, poisons, cytotoxic agents, metals, silver, arsenic, pyrolitic carbon, titanium-nitride-oxide, taxanes, paclitaxel, fibrinogen, collagen, thrombin, phosphorylcholine, heparin, rapamycin, radioactive 188Re and 32P, silver nitrate, dactinomycin, sirolimus, everolimus, mitomycin, Abt-578, tacrolimus, camtophecin, etoposide, vincristine, fluorouracil, and cell adhesion peptide.

35. The method of claim 18, wherein treating airway tissue comprises inhibiting closure of the channel.

36. The method of claim 35, wherein treating the airway tissue comprises irradiating at least a portion of the channel.

37. The method of claim 35, wherein treating the airway tissue comprises deployment of a medical device into said channel.

38. The method of claim 37 further comprising delivering a bioactive substance into or around the channel.

39. The method of claim 38, where the bioactive substance is located within a polymer carrier.

40. The method of claim 38 wherein the bioactive substance is delivered locally.

41. The method of claim 38, wherein the bioactive substance is delivered systemically.

42. The method of claim 37, wherein the bioactive substance is disposed on an exterior surface of the device.

43. The method of claim 37, wherein the bioactive substance is contained in a reservoir of said medical device.

44. The method of claim 37, wherein bioactive substance is mixed with a biodegradable compound and disposed on an exterior surface of said medical device, said biodegradable compound different from said medical agent.

45. The method of claim 37, wherein bioactive substance is covered by an outer biodegradable substance.

46. The method of claim 37, wherein the medical device is a conduit.

47. The method of claim 38, wherein the bioactive substance is selected from the group consisting tissue growth inhibitors, tissue growth enhancers, anti-microbial agents, anti-inflammatory agents, biological reaction inhibitors, immune-response inhibitors, antimetabolites, steroids, metals, and anti-infection agents.

48. The method of claim 38, wherein the bioactive substance is selected from the group consisting of pyrolitic carbon, titanium-nitride-oxide, taxanes, paclitaxel, fibrinogen, collagen, thrombin, phosphorylcholine, heparin, rapamycin, radioactive 188Re and 32P, silver nitrate, dactinomycin, sirolimus, everolimus, mitomycin, fluorouracil, Abt-578, tacrolimus, camtophecin, etoposide, vincristine, or cell adhesion peptide.

49. The method of claim 35, comprising deploying a vessel graft in said channel, said vessel graft having a passageway for air to flow through.

50. The method of claim 37, wherein said medical device is a sponge.

51. The method of claim 50, further comprising removing said sponge.

52. The method of claim 50, wherein said sponge is biodegradable.

53. The method of claim 50, wherein the sponge comprises a medical agent.

54. The method of claim 35, wherein said inhibiting closure includes systemically delivering a medicine.

55. The method of claim 54, wherein said systemically delivering a medicine is performed via any one of the following ways of ingestion, inhalation, injection, and absorption.

56. The method of claim 55, wherein said channel remains device free.

57. The method of claim 35, wherein inhibiting closure includes applying thermal energy to at least a portion of the channel.

58. The method of claim 49, wherein said graft has been inverted prior to said deploying step.