초록 ▼

An implantable medical electrical lead particularly for stimulation of the sacral nerves comprises a lead body extending between a distal end and a proximal end, and the distal end having at least one electrode of an electrode array extending longitudinally from the distal end toward the proximal en

An implantable medical electrical lead particularly for stimulation of the sacral nerves comprises a lead body extending between a distal end and a proximal end, and the distal end having at least one electrode of an electrode array extending longitudinally from the distal end toward the proximal end. The lead body at its proximal end may be coupled to a pulse generator, additional intermediate wiring, or other stimulation device. A fixation mechanism is formed on or integrally with the lead body proximal to the electrode array that is adapted to be implanted in and engage subcutaneous tissue, particularly muscle tissue, to inhibit axial movement of the lead body and dislodgement of the stimulation electrodes. The fixation mechanism comprises a M tine elements arrayed in a tine element array along a segment of the lead proximal to the stimulation electrode array. Each tine element comprises at least N flexible, pliant, tines, each tine having a tine width and thickness and extending through a tine length from an attached tine end to a free tine end. The attached tine end is attached to the lead body from a tine attachment site and supports the tine extending outwardly of the lead body and proximally toward the lead proximal end. The M��N tines are adapted to be folded inward against the lead body when fitted into and constrained by the lumen of an introducer such that the tine free ends of more distal tines of more distal tine elements are urged toward or alongside the attached tine ends of the adjacent more proximal tines of more proximal tine elements, and the folded tines do not overlap one another.

대표청구항 ▼

We claim: 1. A method of providing electrical stimulation of body tissue at a stimulation site employing an implantable pulse generator comprising: providing an implantable medical lead comprising: a lead body extending between lead proximal and distal ends; P proximal connector elements formed in

We claim: 1. A method of providing electrical stimulation of body tissue at a stimulation site employing an implantable pulse generator comprising: providing an implantable medical lead comprising: a lead body extending between lead proximal and distal ends; P proximal connector elements formed in a connector ray in a proximal segment of the lead body; P stimulation electrodes arranged in an electrode array extending proximally from the lead distal end through a distal segment of the lead body; P lead conductors extending between the P connector elements and the P stimulation electrodes; and a plurality of M tine elements formed of a flexible biocompatible plastic, formed in a tine element array extending through a segment of the lead proximal to the electrode array, each tine element comprising N flexible, pliant, tines, each tine having a tine width and thickness and extending through a tine length from an attached tine end to a free tine end, the attached tine end attached to the lead body from a tine attachment site and supporting the tine extending outwardly of the lead body and proximally toward the lead proximal end, the M��N tines adapted to be folded inward and proximally against the lead body; percutaneously introducing an introducer having an introducer lumen extending between an introducer lumen proximal end opening and an introducer lumen distal end opening through body tissue to locate the introducer lumen distal end opening adjacent to the stimulation site; disposing the implantable medical lead within the introducer lumen with the M��N tines folded inward against the lead body by constraint imposed by the introducer lumen without overlapping one another; withdrawing the introducer proximally relative to the implantable medical lead to expose at least one stimulation electrode of the P stimulation electrodes but not so far as to release a tine of the tine element array, and then testing to determine whether positioning is complete; after the step of testing to determine whether positioning is complete, withdrawing the introducer proximally from the tine element array to successively release the N tines of each tine element array to deploy outward and proximally to engage body tissue and inhibit axial dislodgement of the P stimulation electrodes; and coupling the P proximal connector elements with the implantable pulse generator. 2. The method of claim 1, wherein the step of withdrawing the introducer proximally relative to the implantable medical lead to expose at least one stimulation electrode of the P stimulation electrodes but not so far as to release a tine of the tine element array includes; advancing the implantable medical lead from the introducer lumen distal end opening to dispose the P electrodes in operative relation to body tissue to be stimulated prior to withdrawing the introducer proximally. 3. The method of claim 2, wherein the step of disposing the implantable medical lead within the introducer lumen precedes the step of percutaneously introducing the introducer. 4. The method of claim 1, wherein the step of disposing the implantable medical lead within the introducer lumen precedes the step of percutaneously introducing the introducer. 5. The method of claim 1, wherein the flexible bio-compatible plastic is selected from the group consisting of medical grade polyurethane compounds and silicone rubber compounds. 6. The method of claim 1, wherein the tine attachment sites of the M tine elements are separated longitudinally along the lead body in the tine element array by a distance that is substantially equal to or exceeds the tine length when folded proximally against the lead body so that the tines are not overlapping one another. 7. The method of claim 1, wherein the tine attachment sites of each of the M tine elements are disposed in a common circumference of the lead body, and the tine attachment sites of adjoining tine elements along the lead body are radially offset from one another around the common circumference such that the tine free ends of the tines of each adjacent tine element engage against body tissue at radially and axially separated points along the tine element array, wherein the step of withdrawing the introducer proximally from the tine element array to successively release the N tines of each tine element array to deploy outward and proximally to engage body tissue and inhibit axial dislodgement of the P stimulation electrodes includes: engaging the tine free ends of the tines of each adjacent tine element against body tissue at radially and axially separated points along the tine element array. 8. The method of claim 7, wherein tine lengths and tine widths are selected to enable the more distal N tines of more distal tine elements of the tine element array to be folded proximally alongside and interleaved with the adjacent more proximal tines of more proximal tine elements, the step of disposing the implantable medical lead within the introducer lumen with the M-N tines folded inward against the lead body by constraint imposed by the introducer lumen without overlapping one another including: folding the tines of the more distal tine elements proximally alongside and interleaved with the adjacent more proximal tines of more proximal tine elements. 9. The method of claim 8, wherein N tines of the M tine elements are equal in number. 10. The method of claim 1, wherein N tines of the M tine elements are equal in number. 11. The method of claim 1, wherein P =1. 12. The method of claim 1 wherein the step of testing to determine whether positioning is complete includes: electrically testing to establish that positioning is completed. 13. The method of claim 12 wherein the step of withdrawing the introducer proximally relative to the implantable medical lead to expose at least one stimulation electrode of the P stimulation electrodes but not so far as to release a tine of the tine element array includes: viewing a marker adjacent the tine element array and the introducer to determine when the tines are about to deploy. 14. The method of claim 13 wherein the marker and introducer include fluoroscopically viewable material, the step of viewing a marker adjacent the tine element array and the introducer to determine when the tines are about to deploy includes: fluoroscopically viewing the marker and the introducer.