Multiple joint implant delivery systems for sequentially-controlled implant deployment

• US 20040193178A1
• Filed: 12/24/2003
• Published: 09/30/2004
• Est. Priority Date: 03/26/2003
• Status: Abandoned Application

• Current Assignee: Biosensors International Group, Ltd.
• Original Assignee: CardioMind, Inc. (Biosensors International Group, Ltd.)
• Inventors: Nikolchev, Julian
• Application Number:
  US10/746,452
• Publication Number:
  US 20040193178A1
• Time in Patent Office: Days
• US Class Current: 606/108
• 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 17/12109 in a blood vessel
• CPC Class Codes: A61B 17/12136 Balloons
• CPC Class Codes: A61B 17/1214 Coils or wires
• CPC Class Codes: A61B 2017/00867 shape memory effect for prostheses A61F2210/0014
• CPC Class Codes: A61B 2017/1205 Introduction devices
• CPC Class Codes: A61B 2017/12063 electrolytically detachable
• CPC Class Codes: A61B 90/39 Markers, e.g. radio-opaque or breast lesions markers
• CPC Class Codes: A61F 2/95 Instruments specially adapted for placement or removal of stents or stent-grafts
• CPC Class Codes: A61F 2002/9505 having retaining means other than an outer sleeve, e.g. male-female connector between stent and instrument
• CPC Class Codes: A61F 2002/9511 the retaining means being filaments or wires

Abstract

The invention provides an atraumatic, low profile device for the delivery of one or more implants into tubular organs or open regions of the body. The implant delivery device may simultaneously or independently release portions of the implant, e.g., the proximal and distal ends of the implant. This independent release feature allows better implant positioning at the target site. Upon deployment, the implants may be placed at the target site without a sheath.

Claims

1-21. -21. (Cancelled, without prejudice)

24. A implant delivery system comprising:

an elongate delivery guide member having a proximal end and a distal end, the delivery guide member configured to direct at least one implant having an exterior and interior surface to an anatomical treatment site by manipulation by a user,

the at least one implant having a delivery diameter prior to release of the at least one implant and located proximally of the distal end of the delivery guide member prior to release, and

a plurality of releasable joints, each joint configured to maintain a section of the at least one implant at the delivery diameter until release of the releasable joints, wherein the system is adapted for sequential release of the releasable joints.

22. The system of claim 24 wherein the implant exterior surface is smooth after deployment.

23. The system of claim 24 wherein the implant interior surface is smooth after deployment.

25. The system of claim 24 wherein the delivery guide member is closed at its distal end.

26. The system of claim 24 wherein the delivery guide member has a diameter distally and proximally of the at least one implant that is substantially equal to the at least one implant delivery diameter, whereby a substantially atraumatic implant delivery system is provided.

27. The system of claim 24 wherein the delivery guide member has no passageway from its proximal to its distal end.

28. The system of claim 24 further comprising an actuator for releasing the releasable joints, and wherein the delivery guide member has only a single passageway from its proximal to its distal end, that passageway contains the actuator, and that actuator does not extend beyond the distal end of the delivery guide member.

29. The system of claim 28 wherein the actuator for releasing the releasable joints is affixed to the distal end of the delivery guide member.

30. The system of claim 24 wherein the at least one implant comprises exactly one implant.

31. The system of claim 24 wherein the at least one implant comprises more than one implant.

32. The system of claim 24 wherein the delivery guide member comprises a distal guide section and a proximal guide section and a gap between the distal guide section and the proximal guide section and the at least one implant is located between the distal guide section and the proximal guide section.

34. The system of claim 24 wherein the delivery guide member is tubular in form, having a lumen therein.

35. The system of claim 34 further comprising an actuator slidably located at least partially within the delivery guide member lumen and configured to release at least one releasable joint upon axial movement within the delivery guide member.

38. The system of claim 34 further comprising an actuator slidably located at least partially within the delivery guide member lumen and configured to release at least one releasable joint upon rotational movement within the delivery guide member.

39. The system of claim 34 wherein at least one releasable joint is configured to release upon application of fluid pressure in the delivery guide member lumen and further comprising a fluid director slidably located at least partially within the delivery guide member lumen and configured to direct fluid to and to release that selected at least one releasable joint.

40. The system of claim 39 wherein the fluid director is configured to sequentially release the plurality of releasable joints upon application of fluid pressure in the delivery guide member lumen.

41. The system of claim 34 wherein the releasable joints are configured to release upon application of a suitable DC current to the releasable joints, the system further comprising an electrical conductor located at least partially within the delivery guide member lumen to supply the suitable DC current to and to thereby release at the releasable joints.

44. The system of claim 24 wherein the implant is a stent.

45. The system of claim 44 wherein the stent is unsheathed.

46. The system of claim 24 wherein the implant is an occlusive coil.

47. The system of claim 24 wherein the implant further comprises a therapeutic agent.

48. The system of claim 47 wherein the therapeutic agent is selected from the group consisting of antibiotics, anticoagulants, antifungal agents, anti-inflammatory agents, antineoplastic agents, antithrombotic agents, endothelialization promoting agents, free radical scavengers, immunosuppressive agents, thrombolytic agents, and combinations thereof.

49. The system of claim 24 wherein the delivery guide member further comprises a radioopaque marker.

50. The system of claim 24 having flexibility and remote directability, wherein the remote directability is such that a user may direct the distal end of the delivery guide member into and introduce the at least one implant into a coronary artery solely by manipulation of the delivery guide member from its proximal end.

76. A system for treating a target site in a tubular organ comprising:

the implant delivery system of any one of claims 22-32, 34, 35, 38-41 or 44-50; and

a balloon catheter.

77. The system of claim 76 further comprising an embolic filter.

78. The system of claim 77 wherein the embolic filter is attached to the proximal end of the delivery guide member.

79. The system of claim 76 wherein the implant is a stent.

80. The system of claim 76 wherein the implant is an occlusive coil.

95. The method of claim 81 wherein the stent implant delivery system is selected from those described in any one of claims 22-32, 34, 35, 38-41, 44-50 or 76-80.

97. The system of claim 25, wherein an atraumatic tip provides the end closure

98. The system of claim 24 wherein the delivery guide member has a distal diameter between about 0.010 and about 0.020 inches, whereby a low-profile delivery system is provided.

99. The system of claim 24 wherein the delivery guide member is noninflatable.

100. The system of claim 24 wherein the system is guidewireless.

101. The system of claim 25, wherein an atraumatic tip provides the end closure

33. (Cancelled, without prejudice)

36. , 37. (Cancelled, without prejudice).

42. , 43. (Cancelled, without prejudice)

51-75. -75. (Cancelled, without prejudice)

81. A method for delivering an implant in a subject comprising:

accessing a body region;

advancing an implant delivery guide to a target site in the body region; and

releasing the implant at the target site by releasing one portion of the implant after another in a sequential fashion.

82. The method of claim 81 further comprising deploying at least one embolic filter.

83. The method of claim 81 wherein the releasing comprises releasing a distal end of the implant from the delivery guide before releasing a proximal end of the implant from the delivery guide.

84. The method of claim 81 wherein the releasing comprises a mechanical detachment process.

85. The method of claim 81 wherein the releasing comprises a hydraulic detachment process.

86. The method of claim 81 wherein the releasing comprises an electrolytic detachment process.

87. The method of claim 81 wherein the body region is a tubular or hollow organ.

88. The method of claim 87 wherein the tubular or hollow organ is selected from the group consisting of blood vessels, arteriovenous malformations, aneurysms, arteriovenous fistulas, cardiac chambers, bile ducts, mammary ducts, fallopian tubes, ureters, large and small airways, stomach, intestines, and bladder.

89. The method of claim 81 wherein the body region is a blood vessel.

90. The method of claim 81 wherein the implant is a stent.

91. The method of claim 81 wherein the implant is an occlusive coil.

92. The method of claim 81 wherein the target site comprises an aneurysm.

93. The method of claim 81 wherein the subject is human.

94. The method of claim 81 wherein the accessing is performed percutaneously.

96. The method of claim 81 further comprising:

advancing a balloon catheter to the target site;

performing angioplasty with the balloon catheter prior to the releasing of the implant.