The present invention relates generally to the field of neurovascular surgery, and more specifically, to a stent delivery system for delivering intracranial stents for a neuro-interventional procedure.
Atherosclerosis diseases. The devices used to treat this disease include guidewire, balloon catheter, a stent and its delivery stem. There isn't a consistent way of treating this disease, varying from patient to patient and from doctors' discretion. But the current clinical practice most widely utilized would be to dilate the disease lesion with a balloon prior to deploying a stent at the target lesion/artery location. Then use the balloon subsequent to stent placement within the stent and vessel wall again to ensure the stent apposition against the vessel wall. This procedure is time consuming because it requires the balloon catheter and stent delivery system to be exchange in and out of the body. Further challenges are due to tortuosity and vessel size and recrossing the stented area and not entangling the guidewire or balloon catheter.
Accordingly, there is a need for an improved system and method of delivering and detaching an implant to a target site or location within the neurovascular space/body of patient. The present invention is directed toward systems and methods for stent delivery system
This invention presents a way to deliver the stent to the patient with the shortest procedural times, least opportunity for wire entanglement, and ensure accurate and fully dilated stent and diseased artery. The new method also includes guidewires, balloon catheter and stent all in one system with the low crossing profile while eliminating the need for catheter exchanges.
The present invention presents method of integrating a balloon catheter as the delivery system for the self-expanding stent with guidewire support into one system for delivering intracranial stents for neuro-interventional procedure like intracranial atherosclerosis.
Embodiments of the present invention are directed to a stent delivery system comprising a balloon catheter having a catheter shaft with a balloon mounted on a distal end with a self-expanding stent positioned on the catheter shaft proximal to the balloon (tandemly) with a delivery sheath covering the self-expanding stent. In use, the stent delivery system is advanced on the guidewire to the target lesion and the balloon is inflated to dilate the lesion. The balloon is deflated and advanced distally past the lesion until the self-expanding stent positioned proximate the lesion. The sheath is withdrawn, releasing the self-expanding stent to expand and contact the lesion. Once the self-expanding stent has expanded, the balloon can move back to post dilate the stent vessel for better wall apposition, then the stent delivery system (the balloon and sheath) and guidewire are withdrawn from the lesion.
The present invention describes systems and methods using a stent delivery system having a balloon and self-expanding stent mounted tandemly on the proximal end of a balloon catheter. A delivery sheath covers the self-expanding stent during delivery to a desired location.
The stent delivery system disclosed herein will minimize the risk to the patient by eliminating a balloon catheter/stent delivery catheter exchange and provide constant access to the lesion. This procedure would furthermore reduce the likelihood of vasospasm occurring during the procedure and also shortening the amount of time during the procedure.
In use, the stent delivery system is advance on a guidewire to a target lesion. The balloon is inflated to dilate the target lesion. The balloon is then deflated. At this point in a normal procedure, the doctor would withdraw the balloon catheter and exchange to a normal stent delivery system. The present invention does not require this time consuming exchange because the doctor advances the stent delivery system so the balloon is distal to the target lesion and the self-expanding stent is positioned at the dilated target lesion. The sheath is withdrawn, releasing the self-expanding stent to expand against the dilated lesion to hold it open. Optionally, the balloon can move back to post dilate the stent vessel for better wall apposition, the stent delivery system is then withdrawn leaving the stent in place.
The catheter shaft 102 includes a guidewire lumen and a balloon inflation lumen in fluid communication with the inflatable balloon 108. The connector housing 110 includes a first connector 116 coupled to the guidewire lumen and a second connector 118 coupled to the inflation lumen. The distal end of the shaft 102 includes a flexible tip 120.
The inflatable balloon 108 is then deflated and the stent delivery system 100 is withdrawn 113 proximally. In some cases, the self-expanding stent 312 does dilate the lesion 202a and the inflatable balloon 308 is not needed. The stent delivery system 300 is withdrawn 313 from lesion 202a leaving the self-expanding stent 112a to keep the lesion dilated
In some embodiments, the stent delivery system 100 is advanced to a second lesion to use the inflatable balloon 108 to dilate the second lesion.
In one embodiment, the stent delivery system is pre-assembled with the balloon and self-expanding stent positioned tandemly on the catheter shaft.
In another embodiment, the self-expanding stent and delivery sheath are combined with a balloon catheter, with that the self-expanding stent mounted on the catheter shaft proximal to the balloon catheter (tandemly) with the delivery sheath to cover the stent, as a “System”. The doctor can advance the “System” on a guidewire to a target lesion as currently preformed, then using the balloon to dilate the lesion. At this point, the doctor doesn't need to withdraw the balloon and exchange to the stent delivery system (as normal procedure), but instead the doctor would advance the system further to deploy the stent as one while the balloon and guidewire stay beyond the distal lesion and stent placement. At this point the doctor may choose to post dilate the stent/lesion again to ensure the stent wall apposition to the vessel.
The stent delivery system 300 includes a catheter shaft 302 with a proximal end 304 and a distal end 306. An inflatable balloon 308 is coupled to the catheter shaft adjacent the distal end 306 and a self-expanding stent 312 is positioned on the inflatable balloon 308 with a delivery sheath 314 covering the self-expanding stent 312 and the inflatable balloon 308.
The catheter shaft 302 includes a guidewire lumen and a balloon inflation lumen in fluid communication with the inflatable balloon 308. The connector housing 310 includes a first connector 316 coupled to the guidewire lumen and a second connector 318 coupled to the inflation lumen. The distal end 304 of the shaft 302 includes a flexible tip 320.
If the self-expanding stent 312 does not dilate the lesion 202, the inflatable balloon 308 can inflate to dilate and expand the self-expanding stent 312 in the vessel for better wall apposition and dilate the lesion 202 at the same time. The inflatable balloon is then deflated and the stent delivery system 300 is withdrawn 313 proximally. In some cases, the self-expanding stent 312 does dilate the lesion 202a and the inflatable balloon 308 is not needed. The stent delivery system 300 is withdrawn 313 from lesion 202a leaving the self-expanding stent 112a to keep the lesion dilated and advanced to a different lesion 204 to use the inflatable balloon 308 to dilate the second lesion 204a.
Example embodiments of the methods and systems of the present invention have been described herein. As noted elsewhere, these example embodiments have been described for illustrative purposes only and are not limiting. Other embodiments are possible and are covered by the invention. Such embodiments will be apparent to persons skilled in the relevant art(s) based on the teachings contained herein. Thus, the breadth and scope of the present invention should not be limited by any of the above-described exemplary embodiments but should be defined only in accordance with the following claims and their equivalents.
This application claims the benefit of U.S. Provisional Application No. 63/416,467 filed Oct. 14, 2022, which is incorporated herein by reference.
Number | Date | Country | |
---|---|---|---|
63416467 | Oct 2022 | US |