The teachings herein are directed generally to medical devices and methods, including devices and methods for performing atherectomies.
An atherectomy is a minimally invasive procedure for removing atherosclerosis from blood vessels within the body and is an alternative to angioplasty in the treatment of narrowing arteries. Common applications include peripheral arterial disease and coronary artery disease. Unlike angioplasty and stents, which push plaque into the vessel wall, the atherectomy procedure cuts plaque away from the wall of a blood vessel. While atherectomies are usually used to remove plaque from arteries, they can also be used in veins and vascular bypass grafts, for example.
Atherectomies can offer improvements over balloon dilatation and stent placement, which are considered traditional interventional surgical methods of treating atherosclerosis. In balloon dilatation, a collapsed balloon is inserted into a blood vessel and inflated to push plaque against the vessel wall, and the stent can be placed to hold the plaque as a scaffolding in order to try and maintain the integrity of the lumen of the vessel. However, such traditional treatments can stretch the artery and induce scar tissue formation, while the placement of a stent may also cut arterial tissue and induce scar tissue formation. The scar tissue formation can lead to restenosis of the artery. Moreover, the dilatation with the balloon can also rip the vessel wall. Because atherectomies enlarge the lumen by removing plaque rather than stretching the vessel, risk of suffering vessel injuries, such as dissections that can lead to increased restenosis, is reduced.
Unfortunately, the art suffers performance limitations in state-of-the-art atherectomy devices. For example, current devices with rotating cutters cannot handle the variety of soft, fibrous and calcific plaque effectively, either not cutting all types of plaque or breaking up the plaque into large pieces that remain in the arterial bed as emboli that can clog blood vessels downstream. As plaque is a tissue made of fat, cholesterol, calcium, fibrous connective tissue and other substances found in the body, it can be highly variable and classified mainly into four different types of tissue: calcified and hard, necrotic and soft, fibrotic, and a combination thereof. Calcified plaque can be hard as a bone; fatty plaque is typically soft; and fibrotic plaque is typically viscoelastic, stretchy yet firm, and thus difficult to cut. Some state-of-the-art devices have burrs that can grind-away hard plaque but can't cut soft or viscoelastic plaque. Worse yet, they can loosen debris that can become dangerous emboli. Some state-of-the-art devices have a sharp cutter that can be deflected against one side of the vessel to do eccentric cutting, which is desirable, but the amount of deflection can't be effectively controlled. And, some state-of-the-art devices have a “nose cone” that prevents the cutter from cutting through lesion that doesn't allow enough progression of the device to reach the cutter blades.
Most importantly, however, is that patients having “tight” or “tough” lesions are currently unable to receive treatments with balloons, stents, or atherectomy devices. Such lesions are occlusions that leave only a very small luminal opening, or no opening, making it difficult-to-impossible to achieve passage of a guidewire, much less passage of a balloon or stent on the guidewire. For example, a luminal opening that is only 0.5 mm may allow passage of a guidewire, perhaps, but the smallest stents may be 1.0 mm, and the smallest balloon may be 0.75 mm, neither of which can pass through a tough, small lesion for the treatment. And, as noted above, current atherectomy devices have a difficult time cutting away the plaque, even if the guidewire might be able to pass through the luminal opening. In situations having a total occlusion, the problem is exacerbated.
As such, one of skill will appreciate an atherectomy device that (i) can effectively cut and remove the 4 different types of plaque tissue, namely calcified and hard, necrotic and soft, fibrotic, and a combination thereof; (ii) can render a concentric vessel lumen with minimal plaque burden; (iii) can safely self-collect and remove plaque particles to avoid release of emboli; and, (iv) can effectively treat a blood vessel with a reduced risk of suffering vessel injuries that can lead to increased restenosis. In addition, the skilled artisan will certainly appreciate having an atherectomy device that (v) can handle these tight or tough lesions.
Atherectomy devices, and methods of using them are provided, namely devices and methods that (i) can effectively cut and remove the 4 different types of plaque tissue, namely calcified and hard, necrotic and soft, fibrotic, and a combination thereof; (ii) can render a concentric vessel lumen with minimal plaque burden; (iii) can safely self-collect and remove plaque particles to avoid release of emboli; (iv) can effectively treat a blood vessel with a reduced risk of suffering vessel injuries that can lead to increased restenosis; and, importantly, (v) can also handle tight or tough lesions having little to no luminal opening in the lesion. The atherectomy devices taught herein can be telescoping, self-driving, lateral pushing, or a combination thereof.
In some embodiments, the atherectomy device is a telescoping atherectomy device. In these embodiments, the device can have a distal end, a proximal end, a long axis, and a guidewire lumen passing through the device in the direction of the long axis. The device can include a flexible sheath having an outer diameter and a sheath lumen; a cutter having a proximal end, a distal end, and a body with a plurality of helical flutes, a point at the distal end having a plurality of cutting lips, a cutter lumen, and a cleared diameter; and, a drive assembly. The drive assembly can have a flexible driveshaft including an axis, a proximal end, a distal end, an outer surface, and a driveshaft lumen, the distal end of the flexible drive shaft having a fixed connection with the cutter, wherein the flexible drive shaft is rotatably translational with the lumen of the flexible sheath. The drive assembly can also have a positive displacement pump that begins pumping at the distal end of the drive shaft and adjacent to the helical flutes at the proximal end of the cutter. And, in these embodiments, the cleared diameter of the cutter can be greater than the outer diameter of the flexible drive shaft; the flexible drive shaft can be longer than the flexible sheath to enable a reversible telescoping of the drive assembly from the lumen of the flexible sheath at the distal end of the flexible sheath; and, the guidewire lumen can include the cutter lumen and the driveshaft lumen.
In some embodiments, the cleared diameter of the cutter can be greater than the outer diameter of the flexible sheath. And, in some embodiments, the positive displacement pump can be a screw pump attached to the outer surface of the drive shaft, the distal end of the screw pump being adjacent to the helical flutes at the proximal end of the cutter.
In some embodiments, the telescoping atherectomy device can be self-driving. For example, the screw pump can extend beyond the flexible sheath and can be exposed for contact with a vascular lumen during use of the atherectomy device within the vascular lumen. In some embodiments, the screw pump can be a right hand screw when the cutter is rotated in the right-hand direction; and, in some embodiments, the screw pump can be a left hand screw when the cutter is rotated in the left-hand direction.
In some embodiments, the telescoping atherectomy device can further comprise a reversibly-expandable, lateral pushing member at the distal end of the flexible sheath. In some embodiments, the telescoping atherectomy device can further comprise a reversibly-expandable, lateral pushing member at the distal end of the flexible sheath, the lateral pushing member having a proximal end, a distal end, a collapsed state, and an expanded state, the proximal end having an operable connection with the flexible sheath, and the distal end having an operable connection with the cutter. The operable connection with the flexible sheath and the operable connection with the cutter can each be configured to receive an axial force (i) applied along the axis of the flexible drive shaft from the cutter to the flexible sheath and (ii) transferred through the lateral pushing member during the collapse and the expansion of the lateral pushing member with the reversible telescoping of the flexible drive shaft from the flexible sheath. Moreover, the operable connection with the cutter can be configured as a rotatably translatable connection to facilitate a rotation of the cutter and the flexible drive shaft without rotating the lateral pushing member during operation of the atherectomy device.
In some embodiments, the atherectomy device is a self-driving atherectomy device. In these embodiments, the device can have a distal end, a proximal end, a long axis, and a guidewire lumen passing through the device in the direction of the long axis. The device can include a flexible sheath having an outer diameter and a sheath lumen; a cutter having a proximal end, a distal end, and a body with a plurality of helical flutes, a point at the distal end having a plurality of cutting lips, a cutter lumen, and a cleared diameter; and, a drive assembly. The drive assembly can have a flexible driveshaft including an axis, a proximal end, a distal end, an outer surface, and a driveshaft lumen, the distal end of the flexible drive shaft having a fixed connection with the cutter, wherein the flexible drive shaft is rotatably translational with the lumen of the flexible sheath. The drive assembly can also have a screw pump attached to the outer surface of the drive shaft and adjacent to the helical flutes at the proximal end of the cutter, the screw pump including a drive screw portion. In some embodiments, the drive screw portion can extend beyond the flexible sheath and can be exposed for contact with a vascular lumen during use of the atherectomy device within the vascular lumen. In some embodiments, the drive screw portion can be a right hand screw when the cutter is rotated in the right-hand direction; and, in some embodiments, the drive screw portion can be a left hand screw when the cutter is rotated in the left-hand direction. And, in these embodiments, the cleared diameter of the cutter can be greater than the outer diameter of the flexible drive shaft; and, the guidewire lumen can include the cutter lumen and the driveshaft lumen.
In some embodiments, the cleared diameter of the cutter of the self-driving atherectomy device can be greater than the outer diameter of the flexible sheath. And, in some embodiments, the drive screw portion can be the distal portion of the screw pump.
In some embodiments, the flexible drive shaft of the self-driving atherectomy device can be longer than the flexible sheath to enable a reversible telescoping of the drive assembly from the lumen of the flexible sheath at the distal end of the flexible sheath.
In some embodiments, the self-driving atherectomy device can further comprise a reversibly-expandable, lateral pushing member at the distal end of the flexible sheath. In some embodiments, the lateral pushing member can have a proximal end, a distal end, a collapsed state, and an expanded state, the proximal end having an operable connection with the flexible sheath, and the distal end having an operable connection with the cutter. The operable connection with the flexible sheath and the operable connection with the cutter can each be configured to receive an axial force (i) applied along the axis of the flexible drive shaft from the cutter to the flexible sheath and (ii) transferred through the lateral pushing member during the collapse and the expansion of the lateral pushing member with the reversible telescoping of the flexible drive shaft from the flexible sheath. Moreover, in some embodiments, the operable connection with the cutter can be configured as a rotatably translatable connection to facilitate a rotation of the cutter and the flexible drive shaft without rotating the lateral pushing member during operation of the atherectomy device.
In some embodiments, the atherectomy device is a lateral pushing atherectomy device. In these embodiments, the device can have a distal end, a proximal end, a long axis, and a guidewire lumen passing through the device in the direction of the long axis. The device can include a flexible sheath having an outer diameter and a sheath lumen. a cutter having a proximal end, a distal end, and a body with a plurality of helical flutes, a point at the distal end having a plurality of cutting lips, a cutter lumen, and a cleared diameter; and, a drive assembly. The drive assembly can have a flexible driveshaft including an axis, a proximal end, a distal end, an outer surface, and a driveshaft lumen, the distal end of the flexible drive shaft having a fixed connection with the cutter, wherein the flexible drive shaft is rotatably translational with the lumen of the flexible sheath. The drive assembly can also have a positive displacement pump that begins pumping at the distal end of the drive shaft and adjacent to the helical flutes at the proximal end of the cutter. And, the lateral pushing atherectomy device can also have a reversibly-expandable, lateral pushing member at the distal end of the flexible sheath. In these embodiments, the cleared diameter of the cutter can be greater than the outer diameter of the flexible drive shaft; and, the guidewire lumen can include the cutter lumen and the driveshaft lumen.
In some embodiments, the cleared diameter of the cutter can be greater than the outer diameter of the flexible sheath.
In some embodiments, the lateral pushing member can have a proximal end, a distal end, a collapsed state, and an expanded state, the proximal end having an operable connection with the flexible sheath, and the distal end having an operable connection with the cutter. In some embodiments, the operable connection with the flexible sheath and the operable connection with the cutter can each be configured to receive an axial force (i) applied along the axis of the flexible drive shaft from the cutter to the flexible sheath and (ii) transferred through the lateral pushing member during the collapse and the expansion of the lateral pushing member with the reversible telescoping of the flexible drive shaft from the flexible sheath. And, in some embodiments, the operable connection with the cutter can be configured as a rotatably translatable connection to facilitate a rotation of the cutter and the flexible drive shaft without rotating the lateral pushing member during operation of the atherectomy device.
In some embodiments, the flexible drive shaft of the laterally pushing atherectomy device can be longer than the flexible sheath to enable a reversible telescoping of the drive assembly from the lumen of the flexible sheath at the distal end of the flexible sheath. And, in some embodiments, the laterally pushing atherectomy device can comprise a drive screw attached to the outer surface of the distal end of the drive shaft and adjacent to the screw pump at the distal end of the screw pump. The drive screw can extend beyond the flexible sheath and can be exposed for contact with a vascular lumen during use of the atherectomy device within the vascular lumen. In some embodiments, the drive screw can be a right hand screw when the cutter is rotated in the right-hand direction; and, in some embodiments, the drive screw can be a left hand screw when the cutter is rotated in the left-hand direction.
Systems are also provided. In some embodiments, any of the atherectomy devices taught herein can be a system comprising the atherectomy device and a guidewire.
Methods of performing an atherectomy in a subject using any of the atherectomy devices taught herein are provided. In some embodiments, the methods can include creating a point of entry in a vascular lumen of the subject; inserting the atherectomy device into the vascular lumen; telescoping the flexible drive shaft; cutting a plaque from the vascular lumen with the cutter of the atherectomy device; discharging the cut plaque from the vascular lumen with the positive displacement pump; and, removing the atherectomy device from the vascular lumen of the subject.
In some embodiments, the methods can include creating a point of entry in a vascular lumen of the subject; inserting the atherectomy device into the vascular lumen; driving the atherectomy device through the vascular lumen with the exposed drive screw; cutting a plaque from the vascular lumen with the cutter of the atherectomy device; discharging the cut plaque from the vascular lumen with the positive displacement pump; and, removing the atherectomy device from the vascular lumen of the subject.
Likewise, in some embodiments, the methods can include creating a point of entry in a vascular lumen of the subject; inserting the atherectomy device into the vascular lumen; pushing the distal portion of the atherectomy device laterally in the vascular lumen, the pushing including expanding the lateral pushing member; cutting a plaque from the vascular lumen with the cutter of the atherectomy device; discharging the cut plaque from the vascular lumen with the positive displacement pump; and, removing the atherectomy device from the vascular lumen of the subject.
Atherectomy devices, and methods of using them are provided, namely devices and methods that (i) can effectively cut and remove the 4 different types of plaque tissue, namely calcified and hard, necrotic and soft, fibrotic, and a combination thereof, including fibrocalcific tissue; (ii) can render a concentric vessel lumen with minimal plaque burden; (iii) can safely self-collect and remove plaque particles to avoid release of emboli; (iv) can effectively treat a blood vessel with a reduced risk of suffering vessel injuries that can lead to increased restenosis. And, importantly, one of skill will certainly appreciate an atherectomy device that, surprisingly, (v) can also handle tight or tough lesions having little to no luminal opening in the lesion. The atherectomy devices taught herein can be telescoping, self-driving, lateral pushing, or a combination thereof. The devices provided herein can, for example, render a concentric lumen with minimal plaque burden (<30% vessel diameter) while avoiding damage to vessel wall and minimizing embolization.
Those of skill understand that guidewires can be used to locate a diseased region, or target region, in a blood vessel. Also, a guidewire can be used to direct the atherectomy devices taught herein, namely the cutter, over the target region. In some embodiments, the guidewire lumen can include the cutter lumen and the driveshaft lumen. In some embodiments, the guidewire lumen diameter can range in size from 0.01 to 0.20 inches, from 0.01 to 0.18 inches, from 0.01 to 0.15 inches, from 0.01 to 0.10 inches, or any range therein in some embodiments. In some embodiments, the guidewire lumen diameter can range from 0.01 to 0.14 inches. In some embodiments, the guidewire lumen diameter is 0.01 inches (0.254 mm), 0.02 inches (0.508 mm), 0.04 inches (1.016 mm), 0.06 inches (1.524 mm), 0.08 inches (2.032 mm), 0.10 inches (2.540 mm), 0.12 inches (3.048 mm), 0.14 inches (3.556 mm), 0.16 inches (4.064 mm), 0.18 inches (4.572 mm), 0.20 inches (5.080 mm), or any diameter therein in increments of 0.01 inches (0,254 mm).
Generally speaking the atherectomy devices can include a cutter, or cutting head, that is attached to a drive shaft that rotates the cutter, and the drive shaft rotates within a sheath. The sheath can be interchangeably called a “flexible tube”, in some embodiments; and, the drive shaft can be referred to as a “torque shaft”, in some embodiments. In some embodiments, the cutter can be designed to telescope from the sheath and, in some embodiments, reversibly telescope from the sheath. In some embodiments, the cutter can extend out, or telescope, from the sheath as far as desired. For example, the cutter can telescope from, perhaps, 10 mm to 500 mm from the end of the sheath on the drive shaft in some embodiments. The telescoping allows the cutter and the distal portion of the drive shaft to advance ahead of the sheath during which an improved engagement between the cutter and the plaque tissue can be achieved. In addition, leaving the sheath static while moving the cutter in advance of the sheath allows the sheath to resist drill through. In some methods, the telescoping can be the sole step in the removal of plaque from a vessel. In some embodiments, the telescoping can provide an initial cutting path to facilitate a subsequent and more target-specific eccentric cutting.
The drive shaft can be made using any construct known to one of skill that meets the axial stiffness, flexural stiffness, torsional stiffness, and the like. In some embodiments, for example, the drive shaft includes a distal end and a proximal end, in which the distal end connects to or affixed to the cutter, and the proximal end connected to a rotatable element such as a gear attached to a motor or attached to motor itself. The drive shaft may be, in turn, driven by the motor in the handle. The drive shaft can be made using a metal braid and/or one or more metal coils, and one or more portions of the drive shaft embedded in a polymer. In some embodiments, the polymer can include PEBAX, polyurethane, polyethylene, fluoropolymers, parylene, polyimide, PEEK, PET, or a combination thereof. In some variations, the drive shaft can include a rigid material such as plastic, rendered flexible by incorporation of a spiral relief or groove. During a procedure, the motor drives the gear to rotate drive shaft and cutter to cut the tissue in a target lesion.
One of skill will appreciate that the “cleared diameter” of a vessel can be used to describe the diameter of the lumen of the blood vessel after passage of the cutter portion of the atherectomy device through the lumen of the vessel. Since the vessel is often elastic, the cleared diameter 260 of the lumen of a blood vessel may or may not be equal to the diameter of the cutter 230. The cleared diameter 260 of the cutter 230 can be greater than the outer diameter of the flexible drive shaft 250. In some embodiments, the cleared diameter of the cutter can be greater than the outer diameter of the flexible sheath. And, in some embodiments, the cleared diameter 260 of the lumen is less than the diameter of the body of the cutter 230.
Table 1 lists example arterial lumen diameters in mm, beginning at the aorta and descending down a human leg, for example. Peripheral vascular disease in the legs is an example of a condition that can be treated using the atherectomy devices taught herein.
the superior femoral artery, located about mid-femur, generally has a diameter of about 5 to 7 mm, or about 0.2 to 0.25 inch. As the artery descends below the knee, the popliteal artery generally has a diameter of about 4 to 4.5 mm (0.157 inch to 0.177 inch), and then reduces to about 3.5 mm (0.137 inch) as you move in the direct of the subject's foot. The popliteal artery branches again into the anterior tibial artery and the tibioperoneal trunk, reducing further in diameter to about 3.0 mm and then about 2.5 mm or about 0.118 inch to 0.098 inch. The tibioperoneal trunk further subdivides into the posterior tibial and peroneal arteries, further reducing in diameter to about 2.0 mm (0.078 inch). Generally speaking, the diameters of the peripheral arteries of the leg can vary, typically, from about 2 mm to about 7 mm. Any blood vessel can contain plaque and be a prospective target area for the atherectomy devices taught herein. For example, coronary arteries are about 3 mm in size, varies from 2.5-4.5 in diameter, and coronary arteries are prospective target areas for the atherectomy devices taught herein.
Although it seems reasonable to simply increase the diameter of the cutter for larger blood vessels, the skilled artisan will realize that the diameter of the cutter can also be limited by physical complications of the patient's anatomy. For example, there can be complications that occur during surgery due to bleeding at the arterial puncture access, tortuous vessels, vessel size variations, and the like. The diameter of the cutter can range from about 0.70 mm to about 2.20 mm in some embodiments, 1.00 mm to 2.20 mm in some embodiments, 1.20 mm to 2.20 mm in some embodiments, 1.40 mm to 2.20 mm in some embodiments, 1.50 to 2.20 mm in some embodiments, or any range therein in increments of 0.10 mm. In some embodiments, the diameter of the cutter can be about 0.90 mm, 1.00 mm, 1.10 mm, 1.20 mm, 1.30 mm, 1.40 mm, 1.50 mm, 1.60 mm, 1.70 mm 1.80 mm, 1.90 mm, 2.00 mm, 2.10 mm, 2.20 mm, 2.30 mm, or any diameter therein, or range therein, in increments of 0.05 mm. This is significant, as blood vessel lumen diameters can be very small or quite large, and vessels having diameters of 1.00 mm are quite tight for cutters, and vessels having diameters over about 2.30 mm are becoming larger than a cutter can be made, in some embodiments. The skilled artisan will recognize that eccentric cutting allows for cutting a larger region than the diameter of the cutter assembly without adding or exchanging the cutter for other larger tools for removal. The cutter can be biased off-center within the larger blood vessels to clear a lumen that is larger than the diameter of the cutter.
The skilled artisan will also realize that the length of the cutter has to be limited to have the maneuverability needed. One of skill will realize that the size of the cutter can be any size known to be suitable in the art for the particular treatment. In some embodiments, the length of the cutter can range from about 0.50 mm to about 3.00 mm, from about 0.60 mm to about 2.80 mm, from about 0.80 mm to about 2.60 mm, from about 1.00 mm to about 2.40 mm, from about 1.00 mm to about 2.20 mm, from about 1.00 mm to about 2.00 mm, from about 1.20 mm to about 1.80 mm, or any range therein in increments of 0.10 mm.
The atherectomy device 200 further includes a drive assembly to drive the cutter 230. The drive assembly can have a flexible driveshaft 250 including a long axis having a central axis that can be coincident with the central axis 205 of the atherectomy device 200. The flexible driveshaft 250 can further have a proximal portion with a proximal end (not shown), a distal portion with a distal end 252, an outer surface 254, and a driveshaft lumen 256, the distal end 252 of the flexible drive shaft 250 having a fixed connection with the cutter 230. The flexible drive shaft 250 can be rotatably translational with the lumen 221 of the flexible sheath 215. The drive shaft 250 can extend to reach a driving engine located outside the subject receiving the atherectomy, the driving engine powered by an electric engine, in some embodiments, or powered by an air compressor in some embodiments, and the drive shaft 250 can be operably connected to a handle (not shown) at the proximal end of the atherectomy device for control by a user. The drive assembly can also have a positive displacement pump that pumps from the distal portion of the drive shaft 250 and adjacent to the helical flutes 238 at the proximal end of the cutter 230. In some embodiments, the positive displacement pump extends from the distal portion of the drive shaft 250 to the proximal portion of the driveshaft 250 to pump cut pieces of arterial plaque from a blood vessel.
One of skill will appreciate that the subject is a patient that is receiving the atherectomy. The term “subject” and “patient” can be used interchangeably and refer to an animal such as a mammal including, but not limited to, non-primates such as, for example, a cow, pig, horse, cat, dog, rabbit, rat and mouse; and primates such as, for example, a monkey or a human. The subject can also be a cadaver, in some embodiments, or a portion of a cadaver.
The flexible drive shaft 250 can be longer than the flexible sheath 215 to enable a reversible telescoping 270 of the drive assembly from the lumen 221 of the flexible sheath 215 at the distal end 252 of the flexible sheath 215. The guidewire lumen can include the cutter lumen 242 and the driveshaft lumen 256. Although the flexural stiffness of the drive shaft 250 remains the same between the collapsed and expanded states of the device, the flexural movement 290 increases upon the telescoping 270 of the drive shaft from the flexible sheath 215. As such, the amount of flexural movement 290 available is greater in
In some embodiments, the cutter can be operably attached to the drive shaft using a friction fitting, so that the drive shaft is allowed slip on the base of the cutter when engaged with plaque and meeting a maximum torque limit. And, in some embodiments, the positive displacement pump can be a screw pump 280, also referred to as an Archimedes screw in some embodiments. The positive displacement pump can be attached to the outer surface 254 of the drive shaft 250, the distal end of the screw pump being adjacent to the helical flutes 238 at the proximal end 232 of the cutter 230 to transport pieces of cut plaque from the cutter in a distal to proximal direction to the proximal end of the atherectomy device for removal of the cut plaque from the subject.
The self-driving feature of the atherectomy devices taught herein can reduce the pressure required from a surgeon performing the procedure. In some embodiments, the pressure required from the surgeon performing the atherectomy can be reduced by 100%, 95%, 90%, 85%, 80%, 75%, 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 30%, 25%, 20%, 15%, 10%, 5%, or any amount or range therein in increments of 1%. In some embodiments, the pressure required from the surgeon performing the atherectomy can be reduced in an amount ranging from about 25% to about 100%, from about 30% to about 100%, from about 35% to about 100%, from about 40% to about 100%, from about 45% to about 100%, from about 50% to about 100%, from about 60% to about 100%, from about 65% to about 100%, from about 70% to about 100%, from about 75% to about 100%, from about 80% to about 100%, from about 85% to about 100%, from about 90% to about 100%, from about 95% to about 100%, or any range therein in increments of 1%. Likewise, in some embodiments, the pressure required from the surgeon performing the atherectomy can be reduced in an amount ranging from about 25% to about 95%, from about 30% to about 90%, from about 35% to about 85%, from about 40% to about 80%, from about 45% to about 75%, from about 50% to about 70%, from about 60% to about 100%, from about 65% to about 100%, from about 70% to about 100%, from about 75% to about 100%, from about 80% to about 100%, from about 85% to about 100%, from about 90% to about 100%, from about 95% to about 100%, or any range therein in increments of 1%. Likewise, in some embodiments, the pressure required from the surgeon performing the atherectomy can be reduced in an amount ranging from about 25% to about 50%, from about 50% to about 100%, or any range therein in increments of 1%. Likewise, in some embodiments, the pressure required from the surgeon performing the atherectomy can be reduced by at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, or at least any range therein in increments of at 1%.
In some embodiments, a surgeon may need to apply a negative pressure, for example holding or pulling and not pushing, at times to aid control in the cutting of a lesion. It should be appreciated that the negative pressure can be a negative 1%, 5%, 10%, 15%, 20%, or 25%, or any amount therein in increments of 1%, in some embodiments. Such a negative pressure can result in slowing the forward movement of the cutting, stopping the cutting, or moving the cutting in a direction that opposes the self-driving direction of the cutter.
Those of skill in the art will appreciate that the atherectomy devices will offer a needed versatility and maneuverability in the art for tortuous blood vessels. When plaque is located in tortuous vessels or occluded eccentric to the passage of the vessel, eccentric cutting of the tissues can be useful to maneuver the cutting head to remove plaque. There have been atherectomy devices that offer a mechanism in the device that can create a curvature in the distal end of the device by pulling a “tendon” that pulls the end laterally. These devices suffer in that they create a “snapback” or “whip” motion of the device due to an imbalance of stresses being placed along the long axis of the atherectomy device. The devices provided herein provide eccentric cutting without the “snapback” or “whip” created by these earlier known mechanisms.
The lateral pushing member can be made of any material known to be suitable by those of skill. For example, the lateral pushing member can be made of a flexible metal, a flexible metal that is biocompatible, such as titanium alloy such as Nickel Titanium. In some embodiments, the lateral pushing member can be made of a polymer such as PEEK, Polyimid or Nylon. The length of the trusses, or ribbon, can be designed to provide any desired protuberance. For example, the length of the trusses may vary from 1 mm-100 mm in some embodiments, 10 mm-30 mm in some embodiments, 10 mm to 40 mm in some embodiments, 10 mm to 50 mm in some embodiments, 20 mm to 60 mm in some embodiments, 20 mm to 80 mm in some embodiments, or any range therein. In some embodiments, the length of the trusses can be 1 mm, 2 mm, 4 mm, 6 mm, 8 mm, 10 mm, 12 mm, 14 mm, 16 mm, 18 mm, 20 mm, 30 mm, 40 mm, 50 mm, 60 mm, 70 mm, 80 mm, 100 mm, or any length therein in increments of 1 mm.
The reversibly-expandable portion has trusses 488 that expand and collapse the reversibly-expandable lateral pushing member 444 through the application of axial forces on the lateral pushing member 444. The trusses can be referred to as “ribbons”, in some embodiments. The proximal end of the lateral pushing member 444 has an operable connection with the flexible sheath 415, and the distal end of the lateral pushing member 444 has an operable connection with the cutter 430. The operable connection with the flexible sheath 415 and the operable connection with the cutter 430 can each be configured to receive an axial force (i) applied along the axis of the flexible drive shaft 450 from the cutter 430 to the flexible sheath 415 and (ii) transferred through the lateral pushing member 444 to expand the lateral pushing member 444 when applying a distal to proximal axial force, and the collapse the lateral pushing member 444 when applying a proximal to distal axial force, the axial forces applied in the desired direction with the reversible telescoping action of the flexible drive shaft 450 within the flexible sheath 415. The lateral pushing member 444 has an effective radius upon collapse 445c and upon expansion 445e.
In some embodiments, proximal-to-distal and distal-to-proximal forces are received by the lateral pushing member 444 at a proximal collar 455 on the proximal portion of the lateral pushing member 444 and at a distal collar 466 on the distal portion of the lateral pushing member 444. Moreover, the operable connection between the lateral pushing member 444 and the cutter 430 can be configured as a rotatably translatable connection to facilitate a rotation of the cutter 430 and the flexible drive shaft 450 without rotating, or undesirably torquing, the distal end of the lateral pushing member 444 during operation of the atherectomy device 400.
The axial forces can be applied using any structure, a centralized member, for example a tendon, that applies the force along the central axis of the drive shaft to avoid inducing a load on the atherectomy device resulting in release of the snapback or whip forces along the long axis of the device. In some embodiments, the structure providing the axial force can be the drive shaft that is already located central to the device, for example, concentric within the sheath. As such, in some embodiments, the method of expanding the lateral pushing member includes applying a distal-to-proximal force to the distal portion of the lateral pushing member, the force applied along the central axis of the atherectomy device, the central axis of the drive shaft, or the central axis of the sheath.
The contact of the lateral pushing member 444 on the vessel wall laterally pushes the cutter 430 away from the central axis of the vessel lumen opposite direction of expansion of the trusses 488. The magnitude of the diversion of the cutter 430 is adjustable and controllable.
As shown in
One or more expandable trusses can be used. In some embodiments, there is a single truss. In some embodiments, there are 2 trusses. In some embodiments, there are 3 trusses. In some embodiments, there are 4 trusses. In some embodiments, there are at least 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 trusses. The trusses can be pre-shaped to create a biased curve or angle to protrude outwardly from the central axis of the device. That is, in some embodiments, the trusses have a shape memory that allows the trusses to remain in the collapsed state, and the expanded state is obtained by applying a force to the trusses, for example, by pulling on the central tendon, or drive shaft. In some embodiments, the trusses have a shape memory that allows the trusses to remain in the expanded state, and the collapsed state is maintained by holding the trusses in the collapsed state, and the expanded state is obtained by releasing that holding force and allowing the shape memory to return to the trusses. The trusses can be any shape and, in some embodiments, can be a single truss or a plurality of trusses. In some embodiments, the trusses can for a basket shape. In some embodiments, a balloon can be inflated to bias the cutter, rather than use a truss or trusses. For example, the trusses can be arched or angled ribbons, for example, that help to stabilize the flexible drive shaft.
The eccentric cutting of the devices provided herein can offer safe and clean cutting in tortuous and non-tortuous vessels, as well as eccentric lesions. The lateral pushing member 444 increases safety because, without such lateral protrusion, the cutter assembly is biased to move towards the outer side of the vessel curvature, which may accidently cut the vessel wall instead of the targeted plaque at the inner side of the vessel. The lateral pushing member 444 addresses that problem by correcting the bias by bulging the trusses 488 towards the outer side of the vessel curvature to laterally push the cutter to the opposite side of the blood vessel to achieve more controlled, effective, and safe cutting than conventional cutters. When debulking an eccentric lesion, for example, the adjustable lateral pushing enables the cutter assembly to target specifically towards the side of the vessel having the greater amount of the stenotic material to achieve eccentric cutting.
In some embodiments, the effective cutting diameter may be approximately half the diameter of the cutter plus the lateral extent of the protrusion from central axis of cutter. For example, if the cutter is 2.2 mm in diameter, and the protrusion is extended 3.0 mm from cutter axis, the effective cutting diameter is 4.1 mm. As can be seen, the eccentric cutting leads to a cutting area that is much larger than the diameter of the cutter.
The magnitude of the protrusion (from slightly protruded to maximally protruded) is adjustable, in some embodiments. For example, the distance between the two ends or collar of the lateral pushing member can be adjusted. That is, the distance between the two ends or collars of the lateral pushing member can be set as desired. In some embodiments, the distance between the collars is increased to reduce the expansion of the trusses and, thus, reduce the deflection of the cutter. Likewise, the distance between the collars can be decreased to increase the expansion of the trusses and, thus increase the deflection of the cutter. One of skill will appreciate that a dial, knob, button, or other actuator on the device can provide the user of the device with a measure of the distance between the collars of the lateral pushing member 444. In some embodiments, an increase in the distance that the drive shaft has moved relative to the sheath increases the expansion of the trusses 488. Likewise, in some embodiments, a decrease in the distance that the drive shaft has moved relative to the sheath decreases the expansion of the trusses 488.
In some embodiments, the proximal portion or proximal end of the lateral pushing member 444 will have a fixed contact with the distal portion or distal end of the sheath, and the distal portion or distal end of the drive shaft will have a rotatably translational connection with the cutter; with a component proximal to the cutter, the component including a race and a step to allow for rotation of the cutter despite the presence of the drive shaft. The race can be referred to as a “bearing surface” in some embodiments. The component can be, for example, a fixed race or bearing; and the like, such that the drive shaft freely rotates at the distal portion or distal end of the laterally pushing member while the laterally pushing member does not rotate.
Interestingly, it was discovered that the relative flexural stiffness of the drive shaft 450 as compared to the trusses 488 can also help control which portion of the cutter 430 makes contact with, and cuts, plaque on the vascular lumen wall 499. For example, if the flexural stiffness of the drive shaft 450 is greater than the flexural stiffness of the trusses 488, then the expansion of the trusses 488 will likely not cause a deformation 490 of the drive shaft 450, and the contact between the cutter 430 and the vascular lumen wall 499 will occur moreso on the side of the body of the cutter 430. However, if the flexural stiffness of the drive shaft 450 is less than the flexural stiffness of the trusses 488, the drive shaft 450 is expected to deform, and the contact between the cutter 430 and the vascular lumen wall 499 will begin to occur moreso toward the distal end of the cutter 430.
In some embodiments, the flexural stiffness of the distal portion of the flexible atherectomy device, FD, is less than or equal to the flexural stiffness of the lateral pushing member, FLPM. In some embodiments, the flexural stiffness of the distal portion of the flexible atherectomy device, FD, is greater than or equal to the flexural stiffness of the lateral pushing member, FLPM. In some embodiments, the flexural stiffness of the distal portion of the flexible atherectomy device, FD, is greater than the flexural stiffness of the lateral pushing member, FLPM.
FD can be reduced relative to FLPM by 75%, 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 30%, 25%, 20%, 15%, 10%, 5%, or any amount or range therein in increments of 1%. In some embodiments, FD can be reduced relative to FLPM in an amount ranging from about 25% to about 80%, from about 30% to about 75%, from about 35% to about 75%, from about 40% to about 75%, from about 45% to about 75%, from about 50% to about 75%, from about 60% to about 75%, from about 65% to about 75%, from about 70% to about 75%, or any range therein in increments of 1%. Likewise, in some embodiments, FD can be reduced relative to FLPM in an amount ranging from about 25% to about 50%, from about 30% to about 50%, from about 35% to about 50%, from about 40% to about 50%, from about 45% to about 50%, or any range therein in increments of 1%. Likewise, in some embodiments, FD can be reduced relative to FLPM in an amount ranging from about can be reduced by at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, or at least any range or amount therein in increments of at 1%.
Given this information, one of skill will appreciate that the amount of deformation can be selected by selecting the relative ratios of flexural stiffness of the drive shaft 450 and the trusses 488, which will allow additional control of the cutter to the user of the atherectomy device. As such, in some embodiments, the atherectomy device 400 can be designed such that the flexural stiffness of the trusses 488 is greater than the flexural stiffness of the drive shaft 450 to obtain a desired amount of deflection of the drive shaft to direct a desired surface of the cutter 430 to the vascular lumen wall 499. In some embodiments, the flexural stiffness of the drive shaft can be equal to or greater than the flexural stiffness of the trusses 488 to avoid a deflection of the drive shaft. One of skill will appreciate that there are methods to vary the flexural stiffness of the drive shaft. The stiffness or flexibility of the drive shaft may be adjusted, for example, by varying the orientation or association of the filaments that compose the drive shaft. In some embodiments, to increase flexural stiffness, the filaments on the shaft can be bound together with stiffer material, or the flexural stiffness can be increased (or reduced) by increasing (or decreasing) the filament size.
The lateral pushing member can be designed to expand to a curved protuberance. In some embodiments, the lateral pushing member can collapse to have an effective radius 445c that is less than or equal to the radius of the sheath. In some embodiments, the lateral pushing member can collapse to have an effective radius 445c that is less than or equal to the radius of the cutter. In some embodiments, the lateral pushing member collapses to have an effective radius 445c that is less than or equal to the radius of the cleared diameter of the cutter to help facilitate movement of the device in the blood vessel.
Torsional stress on the lateral pushing member 444 is a design consideration. In order to reduce the concerns about the torsional stress induced on the lateral pushing member 444, the torsional stress on the distal end of the lateral pushing member can be reduced, the torsional stiffness of the lateral pushing member can be increased, or both of these design modifications can be implemented.
It should be appreciated that each of the telescoping feature, the self-driving feature, and the lateral pushing feature are distinct technical advantages. As such, the atherectomy device can be a self-driving atherectomy device only, meaning the device doesn't require telescoping or lateral pushing. In these embodiments, the components of which can be labeled the same or similar to the other embodiments taught herein, the device can have a distal portion with a distal end, a proximal portion with a proximal end, a long axis with a central axis, and a guidewire lumen passing through the device in the direction of the long axis. The device can include a flexible sheath having an outer diameter and a sheath lumen; a cutter having a proximal end, a distal end, and a body with a plurality of helical flutes. There can also be a point at the distal end of the cutter having a plurality of cutting lips, as well as a cutter lumen, and a cleared diameter. These devices also include a drive assembly. The drive assembly can have a flexible driveshaft including an axis, a proximal end, a distal end, an outer surface, and a driveshaft lumen, the distal end of the flexible drive shaft having a fixed connection with the cutter, wherein the flexible drive shaft is rotatably translational with the lumen of the flexible sheath. The drive assembly can also have a screw pump attached to the outer surface of the drive shaft and adjacent to the helical flutes at the proximal end of the cutter. The screw pump can include a drive screw portion. In some embodiments, the drive screw portion can be the distal portion of the screw pump.
To be self-driving, for example, the drive screw portion can extend beyond the flexible sheath and can be exposed for contact with a vascular lumen during use of the atherectomy device. To effectively assist in driving the device through the vascular lumen, the drive screw should turn in the same direction as the cutter. For example, if the flutes of the cutter spiral in the right hand direction the drive screw should spiral in the right hand direction. Likewise, if the flutes of the cutter spiral in the left hand direction the drive screw should spiral in the left hand direction. As such, in some embodiments, the drive screw portion can be a right hand screw when the cutter is rotated in the right-hand direction; and, in some embodiments, the drive screw portion can be a left hand screw when the cutter is rotated in the left-hand direction.
The relative size of the lumen, the cutter, and the drive screw can be designed to optimize the self-driving feature. In these embodiments, the cleared diameter of the cutter can be greater than the outer diameter of the flexible drive shaft; and, in some embodiments, the cleared diameter of the cutter can be greater than the outer diameter of the flexible sheath.
Of course, any of the self-driving devices can also include a telescoping feature, the components of which can be labeled the same or similar to the other embodiments taught herein. For example, the flexible drive shaft of the self-driving atherectomy device can be longer than the flexible sheath to enable a reversible telescoping of the drive assembly from the lumen of the flexible sheath at the distal end of the flexible sheath.
Moreover, any of the self-driving devices can also include a reversibly-expandable, lateral pushing member, the components of which can be labeled the same or similar to the other embodiments taught herein. In some embodiments, the lateral pushing member can have a proximal end, a distal end, a collapsed state, and an expanded state, the proximal end having an operable connection with the flexible sheath, and the distal end having an operable connection with the cutter. The operable connection with the flexible sheath and the operable connection with the cutter can each be configured to receive an axial force (i) applied along the axis of the flexible drive shaft from the cutter to the flexible sheath and (ii) transferred through the lateral pushing member during the collapse and the expansion of the lateral pushing member with the reversible telescoping of the flexible drive shaft from the flexible sheath. Moreover, in some embodiments, the operable connection with the cutter can be configured as a rotatably translatable connection to facilitate a rotation of the cutter and the flexible drive shaft without rotating the lateral pushing member, particularly the distal portion of the lateral pushing member, during operation of the atherectomy device.
Likewise, the atherectomy device can be a lateral pushing atherectomy device only, a device doesn't require self-driving, the components of which can be labeled the same or similar to the other embodiments taught herein. It does require telescoping, however, at least to the extent needed for an expanding and a collapsing of the lateral pushing member. In these embodiments, the device can have a distal end, a proximal end, a long axis, and a guidewire lumen passing through the device in the direction of the long axis. The device can include a flexible sheath having an outer diameter and a sheath lumen. The device can have a cutter having a proximal end, a distal end, and a body with a plurality of helical flutes, a point at the distal end having a plurality of cutting lips, a cutter lumen, and a cleared diameter; and, a drive assembly. The drive assembly can have a flexible driveshaft including an axis, a proximal end, a distal end, an outer surface, and a driveshaft lumen, the distal end of the flexible drive shaft having a fixed connection with the cutter, wherein the flexible drive shaft is rotatably translational with the lumen of the flexible sheath. The drive assembly can also have a positive displacement pump that begins pumping at the distal end of the drive shaft and adjacent to the helical flutes at the proximal end of the cutter. And, the lateral pushing atherectomy device can also have a reversibly-expandable, lateral pushing member at the distal end of the flexible sheath.
The relative size of the lumen and the cutter can be designed to optimize movement of the atherectomy device through the lumen. For example, the cleared diameter of the cutter can be greater than the outer diameter of the flexible drive shaft. In some embodiments, the cleared diameter of the cutter can be greater than the outer diameter of the flexible sheath. The size of the cutter lumen and the drive shaft lumen can be configured for passage of a guidewire of a desired gauge and, accordingly, the guidewire lumen can include the cutter lumen and the driveshaft lumen.
In some embodiments, the lateral pushing member can have a proximal portion with a proximal end, a distal portion with a distal end, a collapsed state, and an expanded state, the proximal end having an operable connection with the flexible sheath, and the distal end having an operable connection with the cutter. In some embodiments, the operable connection with the flexible sheath and the operable connection with the cutter can each be configured to receive an axial force (i) applied along the axis of the flexible drive shaft from the cutter to the flexible sheath and (ii) transferred through the lateral pushing member during the collapse and the expansion of the lateral pushing member with the reversible telescoping of the flexible drive shaft from the flexible sheath. And, in some embodiments, the operable connection with the cutter can be configured as a rotatably translatable connection to facilitate a rotation of the cutter and the flexible drive shaft without rotating the lateral pushing member during operation of the atherectomy device.
In some embodiments, atherectomy device can also be telescoping, the components of which can be labeled the same or similar to the other embodiments taught herein. That is, the flexible drive shaft of the laterally pushing atherectomy device can be longer than necessary for the expansion of the lateral pushing member. The flexible drive shaft of the laterally pushing atherectomy device can be longer than flexible sheath to enable a reversible telescoping of the drive assembly from the lumen of the flexible sheath at the distal end of the flexible sheath.
And, in some embodiments, the lateral pushing atherectomy device can also be self-driving, the components of which can be labeled the same or similar to the other embodiments taught herein. That is, the lateral pushing atherectomy device can comprise a drive screw attached to the outer surface of the distal end of the drive shaft and adjacent to the screw pump at the distal end of the screw pump. The drive screw can be a part of the screw pump, and it can extend beyond the flexible sheath and be exposed for contact with a vascular lumen during use. In some embodiments, the drive screw can be a right hand screw when the cutter is rotated in the right-hand direction; and, in some embodiments, the drive screw can be a left hand screw when the cutter is rotated in the left-hand direction.
We found that the ratios of (i) dimensions and (ii) stiffness of an atherectomy device taught herein each contribute to the performance and behavior of the device, the ease of advancement of the cutter, the ability to rotate the atherectomy device, the ability to steer the device, the relative amount of plaque removed, and the like. Table 2 provides example dimensions of the components of the atherectomy device, and Table 3 provides example ratios of the dimensions of the components of the atherectomy device.
It was found that the relative sizes of the device component had a significant impact on the movement of the device within a vessel lumen. In some embodiments, the cutter diameter should be at least 30% greater than the drive shaft diameter. The ratio of cutter diameter to drive shaft diameter can range from 1.3 to 2.0 in some embodiments, 1.3 to 1.8 in some embodiments, 1.3 to 1.7 in some embodiments, 1.3 to 1.6 in some embodiments, 1.3 to 1.5 in some embodiments, 1.3 to 1.4 in some embodiments, or any range therein. In some embodiments, the ratio of cutter diameter to drive shaft diameter can be 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.1, 2.2, 2.3, 2.4, or 2.5, or any ratio therein in increments of 0.05, in some embodiments. In some embodiments, however, the cutter diameter is 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, 26%, 27%, 28%, 29%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, or any percent therein in increments of 0.5%, greater than the drive shaft diameter.
In some embodiments, the cutter diameter should be at least 20% greater than the sheath. The ratio of cutter diameter to sheath diameter can range from 1.2 to 2.0 in some embodiments, 1.2 to 1.8 in some embodiments, 1.2 to 1.7 in some embodiments, 1.2 to 1.6 in some embodiments, 1.2 to 1.5 in some embodiments, 1.2 to 1.4 in some embodiments, 1.2 to 2.0 in some embodiments, or any range therein. In some embodiments, the ratio of cutter diameter to drive shaft diameter can be 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.1, 2.2, 2.3, 2.4, or 2.5, or any ratio therein in increments of 0.05, in some embodiments. In some embodiments, however, the cutter diameter is 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23%, 24%, 25%, 26%, 27%, 28%, 29%, 30%, 31%, 32%, 33%, 34%, 35%, 36%, 37%, 38%, 39%, 40%, or any percent therein in increments of 0.5%, greater than the sheath diameter.
The skilled artisan will appreciate that, given the teachings herein, the drive shaft, sheath and, in some embodiments, the lateral pushing member can be designed to have mechanical and physical properties that are desirable for the atherectomy procedure. In some embodiments, the mechanical and physical properties of the device provide adequate strength to push the cutter forward during the procedure yet flexible enough to maneuver and align the cutter with the guidewire in tortuous vessels.
One of skill will appreciate that the technology provided herein can include flexural stiffness design selections for components to facilitate enhanced performance, maneuverability, and reliability of the atherectomy devices. Flexural stiffness is a measure of deformability expressed in units of N/mm. For example, flexural stiffness may be described as the ability of the component to bend in response to an applied bending force without breaking or deforming the component. For example, one of skill may choose a flexural stiffness of the drive shaft, sheath, or both, in some embodiments, for maneuverability of the atherectomy device to follow a guide wire around tortuous vessels.
One of skill will also appreciate that the technology provided herein can include torsional stiffness design selections for components to facilitate enhanced performance through torsional strength. Torsional stiffness is resistance to twist from torsional loading, allowing the component to transmit a rotational load (torque) without untwisting, over-twisting. and/or deforming, and is in units of N*mm/rad. For example, one of skill may choose a torsional stiffness of the drive shaft, lateral pushing member or both, in some embodiments, to help ensure that the cutter can cut against resistance from the plaque without failure of the drive shaft, and the lateral pushing member doesn't rotate, or at least rotates only a limited amount, to avoid failure of the lateral pushing member device during the atherectomy procedure.
One of skill will also appreciate that the technology provided herein can include axial tensile stiffness design selections for components to facilitate enhanced performance through better response of the atherectomy devices to push and pull. Axial tensile stiffness is the resistance to stretch or contraction of along the length of the component under axial loading and is in units of N/mm. Key components that should include an axial tensile stiffness design selection include the drive shaft, the sheath, and the lateral pushing member.
Tables 4 and 5 provide examples of flexural stiffness, torsional stiffness, and axial stiffness of components of the atherectomy devices taught herein, as well as ratios of the relative stiffnesses of the components.
The flexural stiffness of the sheath should be at least 3× greater than the drive shaft, in some embodiments. The ratio of flexural stiffness of the drive shaft to the flexural stiffness of the sheath can range from 0.03 to 0.40 in some embodiments, 0.05 to 0.30 in some embodiments, 0.05 to 0.25 in some embodiments, 0.06 to 0.30 in some embodiments, or any range therein. In some embodiments, the ratio of flexural stiffness of the drive shaft to the flexural stiffness of the sheath can be 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.10, 0.11, 0.12, 0.13, 0.14, 0.15, 0.16, 0.17, 0.18, 0.19, 0.20, 0.21, 0.22, 0.23, 0.24, 0.25, 0.26, 0.27, 0.28, 0.29, 0.30, 0.31, 0.32, 0.33, 0.34, 0.35, 0.36, 0.37, 0.38, 0.39, 0.40 or any ratio or range therein in increments of 0.005, in some embodiments. In some embodiments, however, the flexural stiffness of the sheath is 3×, 4×, 5×, 6×, 7×, 8×, 9×, 10×, or any range therein, greater than the flexural stiffness of the drive shaft.
The compressible sleeve 500 can be placed outside of the flexible drive shaft and in-between the proximal and distal ends of the lateral pushing member, such that the flexible drive shaft 550 spins inside of the compressible sleeve. As shown herein, there can be a collar at each end of the laterally pushing member, a proximal collar and a distal collar, and the proximal portion 505 of the compressible sleeve 500 is operably attached to the proximal collar of the lateral pushing member, and the distal portion 510 of the compressible sleeve 500 is operably attached to the distal collar of the lateral pushing member. Due to the design of the compressible portion 515, the compressible sleeve 500 may be bent and compressed when the ribbons of the lateral pushing member protrude outwardly from a flat state while providing an added torsional stiffness between the proximal collar and the distal collar of the lateral pushing member to address torsion stresses on the lateral pushing member. In some embodiments, the distal and proximal collars of the lateral pushing member do not twist relative to each other, or any torsional movement is at least reduced. The compressible sleeve 500 also serves to cover the positive displacement pump, referred to as an Archimedes screw in some embodiments. As such, the compressible sleeve 500 can act as a safety shield during aspiration of the cut plaque particles with the Archimedes screw. And, it should be appreciated that having the cover over the positive displacement pump mechanism can assist the pump in the removal of particles by helping to retain the particles in a fixed space. For example, in the case of the screw pump, the compressible sleeve is in close proximity to the screw mechanism to retain plaque particles in the lumen of the compressible sleeve 500, helping the screw mechanism 580 move the particles out of the treated blood vessel with more efficiency. Moreover, the expanded trusses 588 of the lateral pushing member require the proximal and distal collars of the lateral pushing member to move closer together when compressing the compressible sleeve 500, the compressing occurring in the gaps between the spirals of the compressible sleeve 500 to allow the shortening to occur.
The compressible sleeve 500 can be made of any suitable material known to one of skill, the choice of material dictating the required band width and thickness, for example. In some embodiments, the compressible sleeve may be made of stainless steel, Nitinol, other metal alloys, or polymers, PEEK, polycarbonate, nylon, or polyimide.
Example dimensions for the compressible sleeve 500 are listed in Table 6, at least for lower extremity vasculature,
The stiffness and ratio of the drive shaft and the compressible sleeve are listed below in Tables 8 and 9:
The flexural stiffness of the drive shaft should be at least 50% greater than the drive compressible sleeve, in some embodiments. The ratio of flexural stiffness of the drive shaft to the flexural stiffness of the compressible sleeve can range from 1.5 to 6.0 in some embodiments, 1.5 to 5.0 in some embodiments, 1.6 to 5.0 in some embodiments, 1.7 to 5.0 in some embodiments, or any range therein. In some embodiments, the ratio of flexural stiffness of the drive shaft to the flexural stiffness of the compressible sleeve can be 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.2, 2.4, 2.6, 2.8, 3.0, 3.2, 3.4, 3.6, 3.8, 4.0, 4.2, 4.4, 4.6, 4.8, 5.0, 5.2, 5.4, 5.6, 5.8, 6.0, or any ratio or range therein in increments of 0.1, in some embodiments. In some embodiments, however, the flexural stiffness of the drive shaft is 2×, 3×, 4×, 5×, 6×, or any amount in increments of 0.1×, or any range therein, greater than the flexural stiffness of the compressible sleeve.
Although the performance of cutters can vary, depending on factors that include tissue type, for example, any cutter known to one of skill may be used with the atherectomy devices taught herein.
The cutter in
The cutter in
Atherectomy systems can also be assembled to include the atherectomy devices taught herein. In some embodiments, any of the atherectomy devices taught herein can be a system comprising the atherectomy device and a guidewire.
The atherectomy devices also lend to several methods of performing an atherectomy in a subject. In some embodiments, the methods can include creating a point of entry in a vascular lumen of the subject; inserting the atherectomy device into the vascular lumen; telescoping the flexible drive shaft; cutting a plaque from the vascular lumen with the cutter of the atherectomy device; discharging the cut plaque from the vascular lumen with the positive displacement pump; and, removing the atherectomy device from the vascular lumen of the subject.
In some embodiments, the methods can include creating a point of entry in a vascular lumen of the subject; inserting the atherectomy device into the vascular lumen; driving the atherectomy device through the vascular lumen with the exposed drive screw; cutting a plaque from the vascular lumen with the cutter of the atherectomy device; discharging the cut plaque from the vascular lumen with the positive displacement pump; and, removing the atherectomy device from the vascular lumen of the subject.
Likewise, in some embodiments, the methods can include creating a point of entry in a vascular lumen of the subject; inserting the atherectomy device into the vascular lumen; pushing the distal portion of the atherectomy device laterally in the vascular lumen, the pushing including expanding the lateral pushing member; cutting a plaque from the vascular lumen with the cutter of the atherectomy device; discharging the cut plaque from the vascular lumen with the positive displacement pump; and, removing the atherectomy device from the vascular lumen of the subject.
Likewise, in some embodiments, the methods can include grinding the plaque with a burr like, for example, the burr portion 609 of
Likewise, in some embodiments, the methods can include hammering the plaque with a hammering cutting blade configuration like, for example, the cutting portion 612 of the cutter of
One of skill will appreciate that the steps set-forth above represent only example of a series of steps that may be used in an atherectomy. In a simple embodiment, for example, the method includes
It should be appreciated that the devices, systems and methods provided herein allow for enhanced functionality during an atherectomy procedure. In some embodiments, a method of steering a cutting head are provided, and these methods can include redirecting the distal end of the flexible atherectomy device. In some embodiments, the redirecting can include
The centralized “member” can be, for example, either the flexible drive shaft, or perhaps a centralized tendon that is also freely translatable in the axial direction, meaning translatable in the longitudinal axis direction, and perhaps even forming the guidewire lumen in some embodiments. A truly surprising and unexpected benefit was provided by the centralized pull on or near the central axis of the atherectomy device, central axis of the sheath, and or central axis of the drive shaft. To reiterate this surprising result, prior art Telescoping, self-driving, and laterally-pushing atherectomy devices are provided, each having a flexible sheath, a cutter with helical flutes, and a drive assembly. The drive assembly can have a flexible driveshaft that is rotatably translational with the lumen of the flexible sheath, a positive displacement pump that begins pumping at the distal end of the drive shaft adjacent to the helical flutes at the proximal end of the cutter, and the flexible drive shaft can be longer than the flexible sheath to enable a reversible telescoping of the drive assembly from the lumen of the flexible sheath. The positive displacement pump can be a screw pump having a drive screw portion extending beyond the flexible sheath, exposed for contact with a vascular lumen for the self-driving. And, the devices can have a reversibly-expandable, lateral pushing member at the distal end of the flexible sheath for the lateral pushing.
This is a continuation application of U.S. application Ser. No. 17/518,294, filed Nov. 3, 2021, which claims priority to U.S. Provisional Application Nos. 63/126,847, filed Dec. 17, 2020, and 63/197,970, filed Jun. 7, 2021, each of which is hereby incorporated herein by reference in its entirety.
Number | Name | Date | Kind |
---|---|---|---|
4167944 | Banko | Sep 1979 | A |
4306570 | Matthews | Dec 1981 | A |
4445509 | Auth | May 1984 | A |
4598710 | Kleinberg et al. | Jul 1986 | A |
4598716 | Hileman | Jul 1986 | A |
4631052 | Kensey | Dec 1986 | A |
4669469 | Gifford et al. | Jun 1987 | A |
4690140 | Mecca | Sep 1987 | A |
4696667 | Masch | Sep 1987 | A |
4732154 | Shiber | Mar 1988 | A |
4770652 | Mahurkar | Sep 1988 | A |
4781186 | Simpson et al. | Nov 1988 | A |
4790812 | Hawkins et al. | Dec 1988 | A |
4804364 | Dieras et al. | Feb 1989 | A |
4808153 | Parisi | Feb 1989 | A |
4844064 | Thimsen | Jul 1989 | A |
4857045 | Rydell | Aug 1989 | A |
4857046 | Stevens et al. | Aug 1989 | A |
4867157 | McGurk-Burleson | Sep 1989 | A |
4886490 | Shiber | Dec 1989 | A |
4887599 | Muller | Dec 1989 | A |
4894051 | Shiber | Jan 1990 | A |
4911148 | Sosnowski | Mar 1990 | A |
4950277 | Farr | Aug 1990 | A |
4994067 | Summers | Feb 1991 | A |
4994087 | Konrad et al. | Feb 1991 | A |
5074841 | Ademovic | Dec 1991 | A |
5100426 | Nixon | Mar 1992 | A |
5114399 | Kovalcheck | May 1992 | A |
5122134 | Borzone et al. | Jun 1992 | A |
5231989 | Middleman et al. | Aug 1993 | A |
5242461 | Kortenbach et al. | Sep 1993 | A |
5267955 | Hanson | Dec 1993 | A |
5282813 | Redha | Feb 1994 | A |
5282821 | Donahue | Feb 1994 | A |
5284128 | Hart | Feb 1994 | A |
5304189 | Goldberg et al. | Apr 1994 | A |
5312427 | Shturman | May 1994 | A |
5314438 | Shturman | May 1994 | A |
5320635 | Smith | Jun 1994 | A |
5332329 | Hill et al. | Jul 1994 | A |
5334211 | Shiber | Aug 1994 | A |
5356418 | Shturman | Oct 1994 | A |
5358472 | Vance et al. | Oct 1994 | A |
5360432 | Shturman | Nov 1994 | A |
5370609 | Drasler et al. | Dec 1994 | A |
5372587 | Hammerslag et al. | Dec 1994 | A |
5409454 | Fischell et al. | Apr 1995 | A |
5417703 | Brown et al. | May 1995 | A |
5423799 | Shiu | Jun 1995 | A |
5429604 | Hammersmark et al. | Jul 1995 | A |
5429617 | Hammersmark et al. | Jul 1995 | A |
5431173 | Chin et al. | Jul 1995 | A |
5456680 | Taylor et al. | Oct 1995 | A |
5474532 | Steppe | Dec 1995 | A |
3358472 | Klipping et al. | Jan 1996 | A |
5489291 | Wiley | Feb 1996 | A |
5501653 | Chin | Mar 1996 | A |
5520609 | Moll et al. | May 1996 | A |
5529580 | Kusunoki et al. | Jun 1996 | A |
5540706 | Aust | Jul 1996 | A |
5554163 | Shturman | Sep 1996 | A |
5556408 | Farhat | Sep 1996 | A |
5569197 | Helmus | Oct 1996 | A |
5569275 | Kotula | Oct 1996 | A |
5584843 | Wulfman | Dec 1996 | A |
5618294 | Aust | Apr 1997 | A |
5626562 | Castro | May 1997 | A |
5632755 | Nordgren | May 1997 | A |
5634178 | Sugiura | May 1997 | A |
5634883 | Chin | Jun 1997 | A |
5643178 | Moll | Jul 1997 | A |
5643251 | Hillsman | Jul 1997 | A |
5643297 | Nordgren | Jul 1997 | A |
5643298 | Nordgren | Jul 1997 | A |
5649941 | Lary | Jul 1997 | A |
5656562 | Wu | Aug 1997 | A |
5665062 | Houser | Sep 1997 | A |
5665098 | Kelly | Sep 1997 | A |
5669926 | Aust | Sep 1997 | A |
5690634 | Muller | Nov 1997 | A |
5690643 | Wijay | Nov 1997 | A |
5695506 | Pike | Dec 1997 | A |
5716327 | Warner | Feb 1998 | A |
5725543 | Redha | Mar 1998 | A |
5728129 | Summers | Mar 1998 | A |
5733297 | Wang | Mar 1998 | A |
5743456 | Jones | Apr 1998 | A |
5746758 | Nordgren | May 1998 | A |
5749885 | Sjostrom | May 1998 | A |
5755731 | Grinberg | May 1998 | A |
5766196 | Griffiths | Jun 1998 | A |
5772329 | Bardon | Jun 1998 | A |
5779721 | Nash | Jul 1998 | A |
5782834 | Lucey | Jul 1998 | A |
5820592 | Hammerslag | Oct 1998 | A |
5826582 | Sheehan | Oct 1998 | A |
5828582 | Conklen | Oct 1998 | A |
5843103 | Wulfman | Dec 1998 | A |
5851208 | Trott | Dec 1998 | A |
5851212 | Zirps | Dec 1998 | A |
5865082 | Cote | Feb 1999 | A |
5865098 | Anelli | Feb 1999 | A |
5873882 | Straub | Feb 1999 | A |
5876414 | Straub | Mar 1999 | A |
5882329 | Patterson | Mar 1999 | A |
5882333 | Schaer | Mar 1999 | A |
5885098 | Witkowski | Mar 1999 | A |
5890643 | Razon | Apr 1999 | A |
5895399 | Barbut | Apr 1999 | A |
5895508 | Halow | Apr 1999 | A |
5897566 | Shturman | Apr 1999 | A |
5902263 | Patterson | May 1999 | A |
5902283 | Darouiche | May 1999 | A |
5902313 | Redha | May 1999 | A |
5910150 | Saadat | Jun 1999 | A |
5941869 | Patterson | Aug 1999 | A |
5941893 | Saadat | Aug 1999 | A |
6001112 | Taylor | Dec 1999 | A |
6015420 | Gordon | Jan 2000 | A |
6027450 | Brown | Feb 2000 | A |
6027514 | Stine | Feb 2000 | A |
6042593 | Storz | Mar 2000 | A |
6048339 | Zirps | Apr 2000 | A |
6053923 | Veca | Apr 2000 | A |
6066153 | Lev | May 2000 | A |
6080170 | Nash | Jun 2000 | A |
6086153 | Heidmann | Jul 2000 | A |
6090118 | McGuckin | Jul 2000 | A |
6113615 | Wulfman | Sep 2000 | A |
6132444 | Shturman | Oct 2000 | A |
6139557 | Passafaro | Oct 2000 | A |
6142955 | Farascioni | Nov 2000 | A |
6146395 | Kanz | Nov 2000 | A |
6152938 | Curry | Nov 2000 | A |
6156046 | Passafaro | Dec 2000 | A |
6165209 | Patterson | Dec 2000 | A |
6183487 | Barry | Feb 2001 | B1 |
6206898 | Honeycutt | Mar 2001 | B1 |
6237405 | Leslie | May 2001 | B1 |
6238405 | Findlay | May 2001 | B1 |
6241744 | Imran | Jun 2001 | B1 |
6258098 | Taylor | Jul 2001 | B1 |
6258109 | Barry | Jul 2001 | B1 |
6264630 | Mickley | Jul 2001 | B1 |
6284830 | Gottschalk | Sep 2001 | B1 |
6299622 | Snow | Oct 2001 | B1 |
6319242 | Patterson | Nov 2001 | B1 |
6355027 | Le | Mar 2002 | B1 |
6371928 | Mcfann | Apr 2002 | B1 |
6406422 | Landesberg | Jun 2002 | B1 |
6406442 | Mcfann | Jun 2002 | B1 |
6451036 | Heitzmann | Sep 2002 | B1 |
6454779 | Taylor | Sep 2002 | B1 |
6482215 | Shiber | Nov 2002 | B1 |
6482217 | Pintor | Nov 2002 | B1 |
6494890 | Shturman | Dec 2002 | B1 |
6497711 | Plaia | Dec 2002 | B1 |
6554846 | Hamilton | Apr 2003 | B2 |
6554848 | Boylan | Apr 2003 | B2 |
6562049 | Norlander | May 2003 | B1 |
6565195 | Blair | May 2003 | B2 |
6565588 | Clement | May 2003 | B1 |
6572630 | McGucin | Jun 2003 | B1 |
6578851 | Bryant | Jun 2003 | B1 |
6579298 | Wyzgala | Jun 2003 | B1 |
6579299 | McGuckin | Jun 2003 | B2 |
6596005 | Kanz | Jul 2003 | B1 |
6602264 | McGuckin | Aug 2003 | B1 |
6620148 | Tsugita | Sep 2003 | B1 |
6623495 | Findlay | Sep 2003 | B2 |
6629953 | Boyd | Oct 2003 | B1 |
6638233 | Corvi | Oct 2003 | B2 |
6638288 | Shturman | Oct 2003 | B1 |
RE38335 | Aust | Nov 2003 | E |
6656195 | Peters | Dec 2003 | B2 |
6658195 | Senshu | Dec 2003 | B1 |
6666854 | Lange | Dec 2003 | B1 |
6666874 | Heitzmann | Dec 2003 | B2 |
6682545 | Kester | Jan 2004 | B1 |
6702830 | Demarais | Mar 2004 | B1 |
6746422 | Noriega | Jun 2004 | B1 |
6758851 | Shiber | Jul 2004 | B2 |
6790215 | Findlay | Sep 2004 | B2 |
6800085 | Selmon | Oct 2004 | B2 |
6802284 | Hironaka | Oct 2004 | B2 |
6808531 | Lafontaine | Oct 2004 | B2 |
6818001 | Wulfman et al. | Nov 2004 | B2 |
6818002 | Shiber | Nov 2004 | B2 |
6830577 | Nash | Dec 2004 | B2 |
6843797 | Nash | Jan 2005 | B2 |
6860235 | Anderson | Mar 2005 | B2 |
6866854 | Chang | Mar 2005 | B1 |
6868854 | Kempe | Mar 2005 | B2 |
6876414 | Hara | Apr 2005 | B2 |
6936056 | Nash | Aug 2005 | B2 |
6991409 | Noland et al. | Jan 2006 | B2 |
6997934 | Snow | Feb 2006 | B2 |
7008375 | Weisel | Mar 2006 | B2 |
7025751 | Silva | Apr 2006 | B2 |
7033357 | Baxter | Apr 2006 | B2 |
7037316 | McGuckin | May 2006 | B2 |
RE39152 | Aust | Jun 2006 | E |
7172610 | Heitzmann | Feb 2007 | B2 |
7172810 | Hashimoto | Feb 2007 | B2 |
7235088 | Pintor | Jun 2007 | B2 |
7316697 | Shiber | Jan 2008 | B2 |
7344546 | Wulfman | Mar 2008 | B2 |
7344548 | Toyota | Mar 2008 | B2 |
7381198 | Noriega | Jun 2008 | B2 |
7399307 | Evans | Jul 2008 | B2 |
7479147 | Honeycutt | Jan 2009 | B2 |
7534249 | Nash | May 2009 | B2 |
7655016 | Demarais | Feb 2010 | B2 |
7666161 | Nash | Feb 2010 | B2 |
7734332 | Sher | Jun 2010 | B2 |
7771445 | Heitzmann | Aug 2010 | B2 |
7875018 | Tockman | Jan 2011 | B2 |
7879022 | Bonnette | Feb 2011 | B2 |
7892230 | Woloszko | Feb 2011 | B2 |
7981128 | To | Jul 2011 | B2 |
8007500 | Lin | Aug 2011 | B2 |
8007506 | To | Aug 2011 | B2 |
8015420 | Cherian | Sep 2011 | B2 |
8052704 | Olson | Nov 2011 | B2 |
8070762 | Escudero et al. | Dec 2011 | B2 |
8236016 | To et al. | Aug 2012 | B2 |
8337516 | Escudero | Dec 2012 | B2 |
8361094 | To et al. | Jan 2013 | B2 |
8469979 | Olson | Jun 2013 | B2 |
8517994 | Li | Aug 2013 | B2 |
8545447 | Demarais | Oct 2013 | B2 |
8568432 | Straub | Oct 2013 | B2 |
8572630 | Woundy | Oct 2013 | B2 |
8579926 | Pintor | Nov 2013 | B2 |
8585726 | Yoon | Nov 2013 | B2 |
8628549 | To et al. | Jan 2014 | B2 |
8632560 | Pal et al. | Jan 2014 | B2 |
8647355 | Escudero | Feb 2014 | B2 |
8747350 | Chin | Jun 2014 | B2 |
8795306 | Smith et al. | Aug 2014 | B2 |
8876414 | Taniguchi | Nov 2014 | B2 |
8881849 | Shen et al. | Nov 2014 | B2 |
8888801 | To et al. | Nov 2014 | B2 |
8932208 | Kendale et al. | Jan 2015 | B2 |
9050127 | Bonnette et al. | Jun 2015 | B2 |
9095371 | Escudero et al. | Aug 2015 | B2 |
9198679 | To et al. | Dec 2015 | B2 |
9220530 | Moberg | Dec 2015 | B2 |
9498247 | Patel et al. | Mar 2016 | B2 |
9308016 | Escudero et al. | Apr 2016 | B2 |
9314263 | Escudero et al. | Apr 2016 | B2 |
9345511 | Smith | May 2016 | B2 |
9498600 | Rosenthal et al. | Nov 2016 | B2 |
9604291 | Kountanya et al. | Mar 2017 | B2 |
9675376 | To et al. | Jun 2017 | B2 |
9717520 | Zeroni et al. | Aug 2017 | B2 |
9770258 | Smith et al. | Sep 2017 | B2 |
9883873 | Kulas et al. | Feb 2018 | B2 |
9968371 | Todd et al. | May 2018 | B2 |
9976356 | Burhan et al. | May 2018 | B2 |
10022145 | Simpson et al. | Jul 2018 | B2 |
10028767 | Germain et al. | Jul 2018 | B2 |
10154854 | To et al. | Dec 2018 | B2 |
10251667 | Cohen et al. | Apr 2019 | B2 |
10349974 | Patel et al. | Jul 2019 | B2 |
10441311 | Smith et al. | Oct 2019 | B2 |
10507036 | Schuman et al. | Dec 2019 | B2 |
10524824 | Rottenberg et al. | Jan 2020 | B2 |
10555753 | Moberg et al. | Feb 2020 | B2 |
10568655 | Simpson et al. | Feb 2020 | B2 |
10774596 | Zhang et al. | Sep 2020 | B2 |
11304723 | To et al. | Apr 2022 | B1 |
11317940 | Smith et al. | May 2022 | B2 |
20010005909 | Findlay | Jan 2001 | A |
20010004700 | Honeycutt | Jun 2001 | A1 |
20020004680 | Plaia | Jan 2002 | A1 |
20020007190 | Wulfman | Jan 2002 | A1 |
20020198550 | Nash | Jan 2002 | A1 |
20020029057 | McGuckin | Mar 2002 | A1 |
20020169487 | Graindorge | Mar 2002 | A1 |
20020077642 | Patel | Jun 2002 | A1 |
20020077842 | Charisius | Jun 2002 | A1 |
20020168467 | Puech | Jul 2002 | A1 |
20020107479 | Bates | Aug 2002 | A1 |
20020151918 | Lafontaine | Oct 2002 | A1 |
20020169467 | Heitzmann | Nov 2002 | A1 |
20030018346 | Follmer | Jan 2003 | A1 |
20030078606 | Lafontaine | Apr 2003 | A1 |
20030100911 | Nash | May 2003 | A1 |
20030114869 | Nash | Jun 2003 | A1 |
20030125758 | Simpson | Jul 2003 | A1 |
20030139751 | Evans | Jul 2003 | A1 |
20030139802 | Wulfman | Jul 2003 | A1 |
20040006358 | Wulfman | Jan 2004 | A1 |
20040181249 | Torrance | Jan 2004 | A1 |
20040199051 | Weisel | Mar 2004 | A1 |
20040220519 | Wulfman | Mar 2004 | A1 |
20040230212 | Wulfman | Mar 2004 | A1 |
20040230213 | Wulfman | Mar 2004 | A1 |
20040235611 | Nistal | Mar 2004 | A1 |
20040236312 | Nistal | Mar 2004 | A1 |
20040238312 | Sudau | Mar 2004 | A1 |
20040243162 | Wulfman | Mar 2004 | A1 |
20040202772 | Matsuda | Apr 2004 | A1 |
20040087988 | Heitzmann | May 2004 | A1 |
20040097995 | Nash | May 2004 | A1 |
20040102772 | Baxter | May 2004 | A1 |
20040103516 | Bolduc | Jun 2004 | A1 |
20040147934 | Kiester | Jul 2004 | A1 |
20040167533 | Wilson | Aug 2004 | A1 |
20040167553 | Simpson | Aug 2004 | A1 |
20040167554 | Simpson | Aug 2004 | A1 |
20050004585 | Hall | Jan 2005 | A1 |
20050020327 | Chung | Jan 2005 | A1 |
20050020974 | Noriega | Jan 2005 | A1 |
20050059990 | Ayala | Mar 2005 | A1 |
20050149084 | Kanz | Mar 2005 | A1 |
20050222519 | Simpson | Apr 2005 | A1 |
20050113853 | Noriega | May 2005 | A1 |
20050177068 | Simpson | Aug 2005 | A1 |
20050197661 | Carrison et al. | Sep 2005 | A1 |
20050197861 | Omori | Sep 2005 | A1 |
20050240146 | Nash | Oct 2005 | A1 |
20060020327 | Lashinski | Jan 2006 | A1 |
20060239982 | Simpson | Jan 2006 | A1 |
20060074442 | Noriega | Apr 2006 | A1 |
20060241564 | Corcoran | Apr 2006 | A1 |
20060229646 | Sparks | Oct 2006 | A1 |
20070225739 | Pintor | May 2007 | A1 |
20070282303 | Nash | May 2007 | A1 |
20070135733 | Soukup | Jun 2007 | A1 |
20070282350 | Hernest | Jun 2007 | A1 |
20070250000 | Magnin | Oct 2007 | A1 |
20070282358 | Remiszewski | Dec 2007 | A1 |
20080004643 | To | Jan 2008 | A1 |
20080004644 | To | Jan 2008 | A1 |
20080004645 | To | Jan 2008 | A1 |
20080004647 | To | Jan 2008 | A1 |
20080045986 | To | Feb 2008 | A1 |
20080234715 | Pesce | Mar 2008 | A1 |
20080249364 | Korner | Apr 2008 | A1 |
20080103516 | Wulfman | May 2008 | A1 |
20080140101 | Carley | Jun 2008 | A1 |
20080004646 | To | Oct 2008 | A1 |
20090018565 | To et al. | Jan 2009 | A1 |
20090018566 | Escudero | Jan 2009 | A1 |
20090018567 | Escudero | Jan 2009 | A1 |
20090024085 | To | Jan 2009 | A1 |
20090234378 | Escudero | Sep 2009 | A1 |
20100010492 | Lockard | Jan 2010 | A1 |
20100049225 | To | Feb 2010 | A1 |
20100324567 | Root | Jun 2010 | A1 |
20100174302 | Heitzmann | Jul 2010 | A1 |
20100324576 | Pintor | Aug 2010 | A1 |
20110040315 | To | Feb 2011 | A1 |
20110152906 | Escudero | Feb 2011 | A1 |
20110152907 | Escudero | Feb 2011 | A1 |
20110112563 | To | May 2011 | A1 |
20110270289 | To | Jul 2011 | A1 |
20110301626 | To | Aug 2011 | A1 |
20120083810 | Escudero | Apr 2012 | A1 |
20130158578 | Ghodke | Mar 2013 | A1 |
20130085515 | To | Apr 2013 | A1 |
20130090674 | Escudero | Apr 2013 | A1 |
20130096587 | Smith | Apr 2013 | A1 |
20130103062 | To | Apr 2013 | A1 |
20130103063 | Escudero | Apr 2013 | A1 |
20130296901 | Olson | Nov 2013 | A1 |
20140039532 | Vrba | Feb 2014 | A1 |
20140058423 | Smith | Feb 2014 | A1 |
20140107680 | Escudero | Apr 2014 | A1 |
20150224585 | Kuroda | Jan 2015 | A1 |
20160183966 | McGuckin, Jr. | Jun 2016 | A1 |
20170273698 | McGuckin et al. | Feb 2017 | A1 |
20180193056 | Colyer et al. | Jul 2018 | A1 |
20200029801 | Tachibana et al. | Jan 2020 | A1 |
20200029998 | Ogle et al. | Jan 2020 | A1 |
20200060718 | Patel et al. | Feb 2020 | A1 |
20200129202 | Schoenle et al. | Apr 2020 | A1 |
20200315654 | Patel et al. | Oct 2020 | A1 |
20200352552 | Rousso et al. | Nov 2020 | A1 |
20220387071 | To et al. | Jun 2022 | A1 |
Number | Date | Country |
---|---|---|
0254414 | Aug 1992 | EP |
0817594 | Mar 1996 | EP |
0817595 | Mar 1996 | EP |
0950456 | Oct 1999 | EP |
1158910 | Jan 2000 | EP |
1176915 | Feb 2002 | EP |
1178315 | Feb 2002 | EP |
1315460 | Jun 2003 | EP |
1603486 | Jun 2006 | EP |
1722694 | Nov 2006 | EP |
1870044 | Dec 2007 | EP |
1617893 | Aug 2008 | EP |
2579791 | Jun 2010 | EP |
2462881 | Jun 2012 | EP |
2617372 | Jul 2013 | EP |
2641551 | Sep 2013 | EP |
2424608 | Mar 2014 | EP |
2211732 | May 2018 | EP |
2164409 | Aug 2018 | EP |
3027126 | Oct 2019 | EP |
2931151 | Nov 2019 | EP |
2006511256 | Apr 2006 | JP |
2011136180 | Jul 2011 | JP |
2013531542 | Aug 2013 | JP |
6266108 | Jan 2018 | JP |
6356604 | Jul 2018 | JP |
WO 1992001423 | Feb 1992 | WO |
WO 1992014506 | Sep 1992 | WO |
WO 1994024946 | Nov 1994 | WO |
WO 1995021576 | Aug 1995 | WO |
WO 1996029941 | Oct 1996 | WO |
WO 1996029942 | Oct 1996 | WO |
WO 1999023958 | May 1999 | WO |
WO 1999035977 | Jul 1999 | WO |
WO 2000054659 | Sep 2000 | WO |
WO 2000054859 | Sep 2000 | WO |
WO 2001064115 | Sep 2001 | WO |
WO 2001074255 | Oct 2001 | WO |
WO 2001076680 | Oct 2001 | WO |
WO 2005084562 | Sep 2005 | WO |
WO 2005123169 | Dec 2005 | WO |
WO 2006028886 | Mar 2006 | WO |
WO 2007010389 | Jan 2007 | WO |
WO 2008005888 | Jan 2008 | WO |
WO 2008005891 | Jan 2008 | WO |
WO 2009005779 | Jan 2009 | WO |
WO 2009054968 | Apr 2009 | WO |
WO 2009126309 | Oct 2009 | WO |
WO 2010050391 | May 2010 | WO |
WO 2013056262 | Apr 2013 | WO |
WO 2013172970 | Nov 2013 | WO |
WO 2015017114 | Feb 2015 | WO |
WO 2020234203 | Nov 2020 | WO |
Entry |
---|
U.S. Appl. No. 63/126,847 (priority for U.S. Appl. No. 17/518,294, cited herein), To, et al.—owned by Applicant, filed Dec. 17, 2020. |
U.S. Appl. No. 63/197,970 (priority for U.S. Appl. No. 17/518,294, cited herein), To, et al.—owned by Applicant, filed Jun. 7, 2021. |
PCT/US22/32428 Published as WO 2022/261043, To—owned by Applicant, Jun. 7, 2022. |
Written opinion and search report for PCT/US22/32428, To—owned by Applicant, Jun. 7, 2022. |
Ikeno et al. Initial Experience with the Novel 6 F r-Compatible System for Debulking De Novo Coronary Arterial Lesions. Catheterization and Cardiovascular Interventions 62:308-17. (2004). |
Kanjwal et al. Peripheral Arterial Disease—A Silent Killer. JK-Practitioner 11(4):225-32 (2004). |
Nakamura et al. Efficacy and Feasibility of Helixcision for Debulking Neointimal Hyperplasia for In-Stent Restenosis. Catheterization and Cardiovascular Interventions 57:460-66 (2002). |
Number | Date | Country | |
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20220192698 A1 | Jun 2022 | US |
Number | Date | Country | |
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63197970 | Jun 2021 | US | |
63126847 | Dec 2020 | US |
Number | Date | Country | |
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Parent | 17518294 | Nov 2021 | US |
Child | 17692522 | US |