Stent delivery system

• US 6,027,510 A
• Filed: 12/08/1997
• Issued: 02/22/2000
• Est. Priority Date: 12/08/1997
• Status: Expired due to Term

• Current Assignee: Boston Scientific Scimed, Inc. (Boston Scientific Corporation)
• Original Assignee: InFlow Dynamics, Inc. (Boston Scientific Corporation)
• Inventors: Alt, Eckhard
• Primary Examiner(s): Buiz, Michael
• Assistant Examiner(s): TRUONG, KEVIN THAO
• Application Number:
  US08/999,737
• Time in Patent Office: 806 Days
• Field of Search: 606/108, 606/192, 606/194, 606/198, 606/191, 606/195
• US Class Current: 606/108
• CPC Class Codes: A61F 2/958 Inflatable balloons for placing stents or stent-grafts
• CPC Class Codes: A61F 2002/9583 Means for holding the stent on the balloon, e.g. using protrusions, adhesives or an outer sleeve
• CPC Class Codes: A61M 25/10 Balloon catheters A61M25/0125 takes precedence; embolectomy A61B17/22032; retractors A61B17/02; inflatable balloons for placing stents or stent-grafts A61F2/958 ; stomach balloons for treatment of obesity A61F5/0003; oesophagal tubes A61J15/00

Abstract

A stent delivery system includes a catheter having a balloon mounted at its distal end for advancement into and withdrawal from a patient'"'"'s vascular system by manipulation of the catheter from a point external to the patient'"'"'s body, a lumen extending through the catheter into the balloon to allow the balloon to be selectively inflated and deflated from a pressurizing medium external to the patient'"'"'s body, and spaced-apart radiopaque projections on the catheter adjacent the proximal and distal ends of the balloon to receive and retain a stent therebetween in overlying relation to the balloon and to provide x-ray markers thereof. The stent is deployed at a designated target site by selectively inflating the balloon to radially expand the diameter of the stent against the vascular wall. The projections are shaped (i) to protect the stent from being dislodged during travel through the vessel, but not to interfere with radial expansion of the stent during balloon inflation and (ii) to avoid injury to tissue of the vascular wall during movement of the catheter through the vessel. A method of fabricating such a stent delivery system includes providing a catheter with an elongate flexible body of size and shape suitable for traversing the vascular system and with a selectively inflatable balloon located distally on the catheter; and employing spaced-apart projections on the catheter at the ends of the balloon to retain a stent which, after the catheter is inserted through the stent, is tightly crimped onto the balloon between the projections, in readiness for radial expansion when delivered to the target site and the balloon inflated. The catheter diameter may be greater between than outside the projections, for tight crimping of the stent on the balloon, and the projections are integral with the catheter including its region of greater diameter.

Claims

1. A stent delivery system for implanting a stent at a predetermined target site in a vessel in a patient'"'"'s body to maintain the lumen of the vessel open at said site, comprising a catheter having an elongate flexible cylindrical body, a selectively inflatable balloon located distally on said body of the catheter and having distal and proximal ends, a pair of spaced-apart retainers composed of the same flexible material as, and projecting radially from, said body of the catheter, said retainers located at respective ones of said distal and proximal ends of the balloon and each of said retainers having an inner surface located directly adjacent its respective end of said balloon of smooth contour and substantially perpendicular to the longitudinal axis of said body of the catheter and an outer surface opposite from said inner surface also of smooth contour but of substantially more gradual slope than said inner surface, a tubular metal stent crimped onto said balloon between said retainers, said retainers projecting radially beyond the diameter of said tubular crimped stent whereby to retain said crimped stent captive therebetween protected against being dislodged from its captive position and prevented from scraping the wall of said vessel during travel of the stent delivery system through the vessel, each of said retainers including a radiopaque marker for fluoroscopic designation of said ends of the balloon and, thereby, the location of said crimped stent during said travel.

2. The stent delivery system of claim 1, wherein the respective inner surfaces of said spaced apart retainers are shaped to secure said crimped stent therebetween without interference with expansion of the diameter of the stent when the balloon is inflated.

3. The stent delivery system of claim 2, wherein the respective outer surfaces of said spaced apart retainers are shaped to allow said delivery system to traverse the vessel without injury to the wall thereof during said travel.

4. The stent delivery system of claim 1, wherein each of said retainers completely encircles the surface of said cylindrical body of the catheter in a band perpendicular to the longitudinal axis of said bode of the catheter at said distal and proximal ends of the balloon.

5. The stent delivery system of claim 1, wherein said body of the catheter has a diameter between said retainers which exceeds the diameter of the catheter proximal and distal of said spaced apart retainers, to enable a tighter fit of the stent when crimped onto the balloon.

6. A device for delivering a stent to a target site in a duct within a patient, comprising a lead composed of flexible biocompatible material and having distal and proximal ends, for traversing the duct by manipulation from outside the patient, a stent, a mounting balloon for said stent, said balloon being attached adjacent said distal end of the lead and inflatable via a lumen within the lead to enable deployment of said stent mounted thereon at said target site, and asymmetrically shaped, longitudinally spaced apart protective radiopaque projections composed of the flexible material of said lead and positioned on the lead at opposite ends of the balloon for captivity retaining said mounted stent on said lead without binding thereon and for protecting the wall of said duct from injury during travel of said device through the duct with said stent mounted on said balloon between said projections, said lead having a diameter between said spaced apart projections greater than its diameter outside said spaced apart projections to enhance crimping said stent on said balloon.

7. The device of claim 6, wherein each of the projections has a diameter which is predetermined to exceed the diameter of said stent when tightly crimped on the balloon, by at least about 0.05 millimeter.

8. The device of claim 6, wherein said stent is tightly crimped on the balloon between the spaced apart projections.

9. The device of claim 6, wherein the space between the projections exceeds the length of the stent by only an amount sufficient for a snug fit between the projections when the stent is crimped on the balloon, the radiopacity of the projections serving to designate the extremities of the stent under fluoroscopy when the lead is being manipulated to deliver the stent to the target site within the duct internally of the patient'"'"'s body, whereby to enable improved positioning of the stent during deployment thereof at the target site.

10. The device of claim 6, wherein the spaced apart projections are integral with the lead.

11. A stent delivery system for implanting a stent at a predetermined target site in a vessel in a patient'"'"'s body to maintain the lumen of the vessel open at said site, comprising a catheter with an elongate flexible body and a selectively inflatable balloon located distally on the catheter;

and retention means integral with the catheter at each end of the balloon for mounting a stent over the balloon and for protecting the stent against being dislodged from its mounted position during travel of the delivery system through the vessel, said retention means including spaced apart projections on the catheter at distal and proximal ends of the balloon, and said catheter having a diameter between said projections which exceeds the diameter of the catheter proximal and distal of the spaced apart projections, to enable a tighter fit of the stent when crimped onto the balloon.

12. A device for delivering a stent to a target site in a duct within a patient, comprising a flexible lead having distal and proximal ends, for traversing said duct by manipulation from outside the patient, a mounting balloon for a stent, said balloon being attached adjacent said distal end of the lead and inflatable via a lumen within the lead to enable deployment of said stent at the target site, and longitudinally spaced apart protective radiopaque projections positioned on the lead at opposite ends of said balloon for protectively retaining the stent on the lead during travel through said duct when said stent is crimped onto the balloon between said projections, said lead having a diameter between said projections which exceeds the diameter of the lead outside said spaced apart projections, to enable tight crimping of said stent on the balloon between said projections.