Placement of chronic micro-catheter device and method

• US 7,588,581 B2
• Filed: 03/26/2002
• Issued: 09/15/2009
• Est. Priority Date: 03/26/2002
• Status: Active Grant

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: Parmer, Kari, Solar, Matthew S., Lee, David, Murdock, Frank
• Primary Examiner(s): Lucchesi; Nicholas D
• Assistant Examiner(s): Stigell; Theodore J
• Application Number:
  US10/106,773
• Publication Number:
  US 20030187459A1
• Time in Patent Office: 2,730 Days
• Field of Search: 606/108, 606/129, 60416401-17003, 604/264, 604/543, 604/541, 604/506, 604/272, 604/93.01, 600/434, 600/129, 600/114, 600128-130
• US Class Current: 606/129
• CPC Class Codes: A61M 2025/0042 Microcatheters, cannula or the like having outside diameters around 1 mm or less
• CPC Class Codes: A61M 25/0668 splittable, tear apart

Abstract

A device and method of placement of a chronic micro-catheter is shown that allows effective guiding of micro-catheters through a host catheter that is later removable while leaving the micro-catheter implanted in place within the patient. The novel configuration allows the micro-catheter to be completely radially enclosed during insertion, and still allows the host catheter to be removed, leaving the micro-catheter behind. Additionally, the configuration allows several micro-catheters to be placed at any number of depths and orientations while still using a minimally invasive host catheter.

Claims

1. A guide device, having a guide axis, comprising:

a sheath that defines a radially enclosed longitudinal cavity in a first state, and has a longitudinal weakened portion to allow the sheath to be split substantially along a longitudinal wall and radially removed from the guide axis in a second state;

a mandrel, having an axial portion and a plurality of dividing members extending radially from the axial portion, the mandrel, when inserted into the sheath in its first state, defines a plurality of substantially continuous longitudinal guide regions, each guide region bounded by a longitudinal portion of the mandrel, and by a longitudinal portion of the sheath; and

a shield portion on the mandrel, wherein when the mandrel is fully inserted in the sheath, the shield portion substantially shields a distal opening in the sheath in its first state.

2. The guide device of claim 1, wherein the axial portion is coaxial with the mandrel and the sheath when the mandrel is inserted in the sheath in its first state.

3. The guide device of claim 1, wherein the shield portion includes a dynamic shape changing portion.

4. The guide device of claim 1, wherein the shield portion includes a curved end portion.

5. The guide device of claim 1, further including a ramp located at a distal end of the guide region the ramp directing the distal end of the guide region at least partially radially outward from the guide axis.

6. The guide device of claim 5, further comprising:

a primary medical device capable of insertion through the guide region.

7. The guide device of claim 5, wherein the shield portion is located at a distal end of the mandrel and substantially covers the distal opening of the sheath in the first state when the mandrel is fully inserted in the sheath.

8. The guide device of claim 1, wherein the mandrel is fully inserted into the sheath as the distal opening in the sheath is inserted into a patient.

9. The guide device of claim 1, wherein the shield portion is formed at a distal end of the axial portion.

10. A method of insertion of a medical device comprising:

inserting a guide device into a patient to a target location, the guide device including a mandrel, a sheath, and a blunt tipped shield portion near an end of the mandrel to protect a distal opening of the guide device while inserting the guide device;

wherein inserting the guide device includes;

inserting the mandrel with the blunt tipped shield portion near the end of the mandrel into the sheath;

positioning the blunt tipped shield portion near a distal opening of the sheath; and

inserting the sheath and mandrel with the blunt tipped shield portion into the patient.

inserting a primary medical device into the guide device to the target location;

removing the guide device from the patient without moving the primary medical device from the target location;

wherein the guide device is radially removed from the primary medical device.

11. The method of claim 10, wherein the blunt tip tipped shield portion is solid.

12. The method of claim 10, wherein inserting the primary medical device into the guide device includes inserting the primary medical device into a continuous longitudinal guide region defined on a first longitudinal portion by the mandrel, and on a second longitudinal portion by the sheath.

13. The method of claim 12, wherein removing the guide device from the patient includes:

removing the mandrel from the sheath wherein the first longitudinal portion of the longitudinal guide region is radially removed from a side of the primary medical device as it exits the patient; and

removing the sheath from the patient by peeling the sheath apart radially from the side portion of the primary medical device as the sheath exits the patient.

14. The method of claim 12, wherein inserting the primary medical device into the substantially continuous longitudinal guide region includes inserting the primary medical device into one of a plurality of continuous longitudinal guide regions, each of the plurality of continuous guide regions being defined on a first longitudinal portion by the mandrel, and on a second longitudinal portion by the sheath.

15. The method of claim 12, wherein inserting the guide device includes;

moving the primary medical device along the longitudinal guide region;

engaging a ramp with the primary medical device; and

directing the primary medical device radially from the mandrel with the ramp.

16. The method of claim 10, wherein inserting a guide device into a patient includes inserting the blunt tipped shield portion in a first shape during insertion of the guide device, and changing the blunt tipped shield portion to a second shape during removal of the guide device.

17. The method of claim 16, wherein changing the blunt tipped shield portion to a second shape during removal of the guide device includes deflating an inflatable chamber of the blunt tipped shield portion.

18. The method of claim 10, further comprising:

positioning the blunt tipped shield portion defined by the mandrel near a distal tip of the sheath by adjusting a knob at a proximal end of the mandrel to engage a proximal end of the sheath;

after inserting the sheath and mandrel into the patient, moving the knob away from the sheath to allow access to a longitudinal guide region defined between the mandrel and the sheath;

wherein inserting a primary medical device includes inserting the primary medical device into the longitudinal guide region defined between the mandrel and the sheath and accessed only by moving the knob away from the proximal end of the sheath.

19. An insertion system comprising:

a guide device, having a guide axis, comprising;

a sheath that defines a radially enclosed longitudinal cavity in a first state, and is adapted to be split substantially along a longitudinal wall and radially removed from the guide axis in a second state;

a mandrel that, when inserted into the sheath in its first state, defines a substantially continuous longitudinal guide region bounded on a first longitudinal portion by the mandrel, and on a second longitudinal portion by the sheath;

a primary medical device capable of insertion through the guide region;

a shield portion, such that when the mandrel is fully inserted in the sheath, the shield portion substantially shields a distal opening in the sheath in its first state; and

a ramp located near a distal end of the guide region between a proximal end of the mandrel and the shield portion, the ramp directing the distal end of the guide region at least partially radially outward from the guide axis.

20. The insertion system of claim 19, wherein the primary medical device includes an electrode.

21. The insertion system of claim 19, wherein the primary device includes a drug delivery device.