Delivery system assemblies and associated methods for implantable medical devices

• US 9,808,629 B2
• Filed: 02/02/2015
• Issued: 11/07/2017
• Est. Priority Date: 10/24/2011
• Status: Active Grant

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: Steingisser, H. Allan, Tran, Don H., Berthiaume, William A., Locsin, Brent L.
• Primary Examiner(s): Woo, Julian W
• Application Number:
  US14/611,582
• Publication Number:
  US 20150148815A1
• Time in Patent Office: 1,009 Days
• Field of Search: 600139, 600146, 600149
• CPC Class Codes: A61N 1/3622 comprising two or more electrodes co-operating with different heart regions
• CPC Class Codes: A61N 1/37205 Microstimulators, e.g. implantable through a cannula
• CPC Class Codes: A61N 1/3756 Casings with electrodes thereon, e.g. leadless stimulators
• CPC Class Codes: A61N 2001/0578 having means for removal or extraction

Abstract

A delivery system assembly includes an outer tube, an inner member, extending within a lumen of the outer tube, and a deflectable shaft, extending within the outer tube lumen and around the inner member; the tube and inner member are longitudinally moveable with respect to the shaft, and a distal end of the inner member is located distal to the shaft within the tube lumen. A medical device can be loaded into the tube lumen, along a distal-most portion of the tube, and contained between the inner member and a distal opening of the tube lumen. Deflecting the shaft orients the distal-most portion for navigation of the assembly, and, when the distal end of the inner member is engaged within the tube lumen, distal movement of the tube, with respect to the shaft, causes similar distal movement of the inner member and the loaded medical device toward an implant site.

Claims

1. A method for deploying an implantable cardiac medical device, the method comprising:

loading an entirety of the implantable medical device into a distal-most portion of an outer tube of a delivery system assembly such that a proximal end of the medical device abuts a distal end of an inner member of the delivery system assembly, the inner member extending within a lumen formed by the outer tube;

advancing the delivery system assembly within a venous system of a patient to locate the distal-most portion of the outer tube, with the medical device loaded therein, within a right atrium of the patient;

orienting the located distal-most portion of the outer tube toward a tricuspid valve of the patient by deflecting a distal end of a shaft of the delivery system assembly independently of the outer tube and the inner member, the shaft extending within the lumen of the outer tube and around the inner member such that the distal end of the shaft is positioned proximal to the distal end of the inner member;

advancing, with respect to the deflected distal end of the shaft, the distal-most portion of the outer tube through the tricuspid valve and into a right ventricle of the patient to a target implant site, such that the distal-most portion of the outer tube abuts the implant site, the advancing carrying the distal end of the inner member and the loaded medical device along with the distal-most portion, by means of an engagement of the distal end of the inner member within the lumen of the outer tube; and

retracting the outer tube with respect to the distal end of the inner member and the shaft to expose a fixation member of the medical device for engagement of tissue at the implant site.

2. The method of claim 1, further comprising:

attaching a tether to the proximal end of the implantable medical device when loading the device into the distal-most portion of the delivery system assembly;

threading the tether through a lumen of the inner member such that terminal ends of the tether are accessible at a proximal end of the delivery system assembly;

withdrawing the inner member along the tether and away from the medical device, after retracting the outer tube; and

tugging on the tether to test engagement of the fixation member of the medical device, after withdrawing the inner member.

3. The method of claim 2, further comprising:

evaluating engagement of the fixation member of the device by tugging on the proximal portion of the tether; and

responsive to the evaluated engagement of the fixation member not being acceptable, re-loading the device into the distal-most portion of the outer tube of the delivery system assembly by;

advancing the inner member back toward the medical device so that the proximal end of the device abuts the distal end of the inner member while pulling on the proximal portion of the tether to remove any slack in the tether; and

advancing the outer tube over the shaft and the inner member until both the distal end of the inner member and an entirety of the medical device are contained within the distal-most portion of the outer tube; and

repositioning the delivery system assembly and the re-loaded medical device such that the distal-most portion of the outer tube abuts another target implant site.

4. The method of claim 3, wherein the repositioning comprises re-orienting the distal-most portion of the outer tube of the delivery system assembly by adjusting the deflection of the shaft of the delivery system assembly.

5. The method of claim 3, further comprising deflecting the inner member, in proximity to the distal end thereof, the deflecting of the inner member to further orient the distal-most portion of the outer tube prior to, or in conjunction with, advancing the distal-most portion to the target implant site or to the other target implant site.

6. The method of claim 3, further comprising rotating the outer tube to further orient the distal-most portion of the outer tube prior to, or in conjunction with, advancing the distal-most portion to the target implant site or to the other target implant site.

7. The method of claim 1, further comprising deflecting the inner member, in proximity to the distal end thereof, the deflecting of the inner member to further orient the distal-most portion of the outer tube prior to, or in conjunction with, advancing the distal-most portion to the target implant site.

8. The method of claim 1, further comprising rotating the outer tube to further orient the distal-most portion of the outer tube prior to, or in conjunction with, advancing the distal-most portion to the target implant site.

9. The method of claim 1, further comprising positioning an overlay of the delivery system to coincide with a valve of an introducer sheath through which the delivery system assembly is advanced, after advancing the delivery system assembly within the venous system and prior to advancing the distal-most portion of the outer tube through the tricuspid valve, the overlay being slideable over the outer tube and, when positioned, providing an enhanced interface between the valve of the introducer sheath and the delivery system assembly.