This document relates to treating occlusions within body vessels, for example fully occluded body vessels.
Many people suffer from lack of vascular supply, for example to the lower extremities. In fact, in some cases people may have total occlusions of a body vessel, for example in the peripheral arterial system for patients suffering from peripheral arterial disease. Total occlusions may consist of different kinds of substances causing the occlusion within the artery. For example, certain portions of the arterial system may be occluded with soft material or with atheroma. Other areas may have hardened calcific plaque which is not easy to penetrate.
Various devices are known for treating body vessels containing soft material and hardened calcific plaque. Such devices include rotational atherectomy devices that include a rotational burr element that is able to break up or free hardened plaque formed on a vessel wall. Devices such as guidewires have also been used to push through softer materials contained within the vessel and thereby create a more open passageway within the vessel. Treating vascular occlusions is made challenging when there is variability in the plaque morphology, and when occlusions are located at or near a curvature in a vessel. In some cases, it is possible through imaging techniques for a medical practitioner to visualize the passage that is to be traversed; in other cases the path cannot be visualized clearly.
This document describes, in one aspect, systems and methods for treating occlusions within body vessels. Generally, such a system includes a lumen-forming device, for example a rotational atherectomy device, having an elongate shaft and a distal plaque-treating portion, for example a burr element, adapted to dislodge hardened plaque from within a body vessel. The system also includes a multi-balloon positioning catheter with a lumen into and through which lumen the plaque-threating device may be extended. The positioning catheter has at least three inflatable balloons positioned circumferentially about the lumen to controllably position the lumen and its distal opening at a desired location and trajectory within the body vessel. As such, the positioning catheter controls the location and trajectory of the plaque-treating device when extended from the distal end of the positioning catheter's lumen.
In another aspect, this document describes a method for treating deposits from a body vessel. The method includes introducing a positioning catheter into a body lumen. In this method, the positioning includes a lumen into and through which lumen a deposit-treating device is extendable. The positioning catheter further includes at least three inflatable balloons positioned circumferentially about the positioning catheter lumen. The method also includes controlling an inflation level of each of the at least three circumferentially positioned inflatable balloons to position the lumen and its distal end at the desired location and trajectory within the body vessel, introducing the deposit-treating device into the lumen until its deposit-treating distal portion extends distal of a distal opening of the positioning catheter, and treating deposits from within the vessel using the deposit-treating device.
The details of one or more embodiments of the invention are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the invention will be apparent from the description and drawings, and from the claims.
The systems and devices described in this document and shown in the accompanying figures are designed to traverse and treat total occlusions, for example in the peripheral arterial system for patients suffering with peripheral arterial disease. One example patient population that may be served by the systems and devices are people suffering from a lack of vascular supply to the lower extremities. In this example, total occlusions in this patient population may consist of different kinds of substances causing the occlusion within the artery. For example, certain portions of the arterial system may be occluded with soft material such as atheroma. Other areas may contain hardened calcific plaque which is not easy to penetrate. In some embodiments, the systems and devices allow crossing of these peripheral occlusive segments of the arterial system so that recanalization can be performed to allow vascular supply to the lower extremity. Other embodiments of the systems and devices may be applied to other arterial circulations within the body, for example recanalization of occluded arteries in the heart.
In some implementations, the device 100 includes a control device adapted to control inflation of the circumferentially positioned inflatable balloons to position the lumen at the desired location within the cross-section of the body vessel. For example, using the control device, a medical practitioner can inflate the balloons 102, e.g., using the pumps 116 that are included with or connected to the control device. In some implementations, the control device is adapted to provide lubricant 120 into the positioning catheter lumen 122 for supply of the lubricant 120 to the distal plaque-treating portion 114.
In one embodiment applicable at least to treat occlusions of peripheral arteries, a positioning catheter 104 will be of a smaller caliber, for example #4 French to #5 French in size. In addition, the outside of the positioning catheter 104 may be coated with lubricant 120 (e.g., lubricious “glide” coating) to allow easy passage through the occluded segment. The lubricant 120 may be supplied through the lumen 122 in the positioning catheter 104.
As shown in the figures, the positioning catheter 104 includes the lumen 122 allowing passage through the positioning catheter 104 of the plaque-treating device, such as the rotational atherectomy device 108 or another device that delivers ultrasonic vibrations or laser energy to a distal portion of the plaque-removal device. The lumen 122 of the positioning catheter 104 may further be sized so that the positioning catheter 104 may allow passage of the rotational atherectomy device 108, as well as lubricant 120 to bathe the device beyond its distal tip 124. The lumen 122 of the positioning catheter 104 may also allow passage of the guidewire 110, for example a 0.035 guidewire. In addition or alternatively, the guidewire 110 may be introduced through a lumen 122 in the rotational atherectomy device 108.
The distal portion of the positioning catheter 104 has, in one embodiment, three inflatable balloons 102. The balloons 102 will serve as a mechanism to allow directional movement of a tip 126 of the rotational atherectomy device 108 within the cross-section of the body lumen 128, as well as providing a locking mechanism that allows stabilization of the catheter tip just above a total occlusion.
The three inflatable balloons 102 may be, as shown in the figures, of similar size to one another and positioned around the entire circumference of the lumen 122 of the positioning catheter 104. In other embodiments, there may be more than three balloons 102, and they may be sized differently from one another. Each of the positioning balloons 102 may be controlled independently. The balloons 102 will serve as a mechanism to allow directional movement of the tip within the cross-section of the body lumen 122, as well as providing a locking mechanism that allows stabilization of the catheter tip just above a total occlusion.
In use, the positioning catheter 104 may be passed down an arterial sheath that is placed above a total occlusion. Once the positioning catheter 104 is in position at the site of total occlusion, the guidewire 110 (for example, a 0.035 French guidewire) may be used to loosen soft deposits 142 (see
At a location where the presence of hardened plaque 140 is detected, for example by feel, the medical practitioner may advance the positioning catheter 104 to be near the site of the hardened plaque 140 (see
The rotational atherectomy device 108 can be positioned in a heavily calcified plaque and turned on allowing ablation of the calcific plaque and the creation of a small, for example 1 mm or less, orifice or hole through the calcified plaque. The rotational atherectomy device 108 may be moved forward in small increments using the distal portion of the positioning catheter 104 as well as a 0.035/0.014/0.018 wire that advances through and can operate to guide the rotational atherectomy device 108.
At the sites of total occlusion, the device 100 can be turned on without fear of perforation as the tip of the rotational atherectomy device 108 is stabilized by the catheter which is directly above it (the catheter is locked into position by inflating the balloons 102 which oppose the walls of the lumen of the artery 136).
As shown in
Referring now to
Control of the positioning catheter 104 may be achieved by use of a control unit that may be provided with the system. The control unit may provide a visual display to the operator through the procedure. The control unit may include actuation mechanisms (such as a joystick, buttons, etc.) that receive inputs from the operator to control the inflatable balloons 102 in a desired manner. The control unit may include a processing component that receives the user input, calculates an appropriate inflation level for each of the balloons 102, and provides an output signal to actuation mechanisms that inflate or deflate each of the balloons 102 to the appropriate calculated level.
The shaft of the rotational atherectomy device 108 may be strengthened so as not to buckle in its distal 2 cm. The rotational atherectomy device 108 may have a cutting tip estimated to be one-tenth of a millimeter in diameter. The forward half of the rotational atherectomy device 108 may be covered with industrial diamonds 130 that will allow ablation of calcific plaque. The rotational atherectomy device 108 may include a lumen to allow passage of said guidewire 110. All the above equipment may be radiopaque to allow visualization under fluoroscopic guidance.
A number of embodiments of the invention have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention. Accordingly, other embodiments are within the scope of the following claims.
This application claims the benefit of U.S. Provisional Application Ser. No. 61/606,655, filed Mar. 5, 2012. The disclosure of the prior application is considered part of (and is incorporated by reference in) the disclosure of this application.
Filing Document | Filing Date | Country | Kind |
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PCT/US13/29153 | 3/5/2013 | WO | 00 |
Number | Date | Country | |
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61606655 | Mar 2012 | US |