INTERNAL CAROTID ARTERY THROMBECTOMY DEVICES AND METHODS
20210346039 · 2021-11-11
Inventors
- David Kallmes (Rochester, MN, US)
- Waleed Brinjikji (Rochester, MN, US)
- Brady Hatcher (Rogers, MN, US)
- Randy Beyreis (Rogers, MN, US)
Cpc classification
A61M2025/0039
HUMAN NECESSITIES
A61B17/22
HUMAN NECESSITIES
A61M25/005
HUMAN NECESSITIES
A61M2025/1063
HUMAN NECESSITIES
A61M2025/004
HUMAN NECESSITIES
A61B2017/3445
HUMAN NECESSITIES
A61M25/0023
HUMAN NECESSITIES
A61M2025/1061
HUMAN NECESSITIES
A61M2025/1052
HUMAN NECESSITIES
A61M2025/1077
HUMAN NECESSITIES
International classification
A61B17/22
HUMAN NECESSITIES
Abstract
The disclosure includes a balloon guiding sheath that includes an elongated sheath having a proximal end, a distal end opposite the proximal end, an inner tube extending between the proximal end and the distal end, an outer tube surrounding the inner tube and extending between the proximal end and the distal end, an access port located adjacent in the proximal end, a distal port located adjacent the distal end, and a working lumen extending through the elongated sheath between the access port and the distal port. The balloon guiding sheath also includes an inflatable balloon located on an outer surface of the elongated sheath adjacent the distal end, the inflatable balloon being fluidly coupled to an inflation lumen extending between the inflatable balloon and an inflation port located adjacent the proximal end.
Claims
1. A balloon guiding sheath, comprising: an elongated sheath having a proximal end, a distal end opposite the proximal end, an inner tube extending between the proximal end and the distal end, an outer tube surrounding the inner tube and extending between the proximal end and the distal end, an access port located adjacent the proximal end, a distal port located adjacent the distal end, and a working lumen extending through the elongated sheath between the access port and the distal port; and an inflatable balloon located on an outer surface of the elongated sheath adjacent the distal end, the inflatable balloon being fluidly coupled to an inflation lumen extending between the inflatable balloon and an inflation port located adjacent the proximal end, wherein the elongated sheath is sized and configured to enable direct insertion into a patient's vasculature through an arteriotomy in at least one of the patient's carotid artery and vertebral artery to position the balloon at a target site.
2. The balloon guiding sheath of claim 1, further comprising a reinforcement layer located between the inner tube and the outer tube, the reinforcement layer arranged and configured to enable flow of at least one of fluid and media through the inflation lumen.
3. The balloon guiding sheath of claim 1, wherein the elongated sheath defines a working length comprising a proximal portion, a distal tip, and a distal portion located between the proximal portion and the distal tip.
4. The balloon guiding sheath of claim 3, wherein the elongated sheath defines a generally constant outer diameter from the proximal portion to the distal portion.
5. The balloon guiding sheath of claim 4, wherein the generally constant outer diameter is equal to 0.123 inches.
6. The balloon guiding sheath of claim 4, wherein the generally constant outer diameter is equal to 0.110 inches.
7. The balloon guiding sheath of claim 4, wherein the generally constant outer diameter is equal to 0.102 inches.
8. The balloon guiding sheath of claim 3, wherein the elongated sheath defines a generally constant inner diameter from the proximal portion to the distal portion.
9. The balloon guiding sheath of claim 8, wherein the generally constant inner diameter is equal to 0.103 inches.
10. The balloon guiding sheath of claim 8, wherein the generally constant inner diameter is equal to 0.088 inches.
11. The balloon guiding sheath of claim 8, wherein the generally constant inner diameter is equal to 0.087 inches.
12. The balloon guiding sheath of claim 3, wherein the elongated sheath defines an outer diameter that tapers downward from the proximal portion to the distal portion.
13. The balloon guiding sheath of claim 1, wherein the inflatable balloon is located in a non-recessed portion of the outer surface.
14. The balloon guiding sheath of claim 3, wherein the working length is about 95 centimeters.
15. The balloon guiding sheath of claim 1, wherein the elongated sheath defines a working length long enough to enable the distal port to reach at least a cervical portion of a patient's internal carotid artery from the carotid artery.
16. The balloon guiding sheath of claim 15, wherein the working length is long enough to enable the distal port to reach a cavernous portion of the patient's internal carotid artery from the carotid artery.
17. The balloon guiding sheath of claim 1, wherein the elongated sheath is arranged and configured to have sufficient stiffness and tip flexibility to enable insertion of the working length of the sheath into a patient's vasculature through an arteriotomy in the patient's carotid artery to position the distal port at a target site in at least one of a petrous portion of a patient's internal carotid artery, a cavernous portion of the patient's internal carotid artery, and a cerebral portion of the patient's internal carotid artery.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0062] These and other features, aspects, and advantages are described below with reference to the drawings, which are intended to illustrate, but not to limit, the invention. In the drawings, like reference characters denote corresponding features consistently throughout similar embodiments.
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DETAILED DESCRIPTION
[0088] Although certain embodiments and examples are disclosed below, inventive subject matter extends beyond the specifically disclosed embodiments to other alternative embodiments and/or uses, and to modifications and equivalents thereof. Thus, the scope of the claims appended hereto is not limited by any of the particular embodiments described below. For example, in any method or process disclosed herein, the acts or operations of the method or process may be performed in any suitable sequence and are not necessarily limited to any particular disclosed sequence. Various operations may be described as multiple discrete operations in turn, in a manner that may be helpful in understanding certain embodiments; however, the order of description should not be construed to imply that these operations are order dependent. Additionally, the structures, systems, and/or devices described herein may be embodied as integrated components or as separate components.
[0089] For purposes of comparing various embodiments, certain aspects and advantages of these embodiments are described. Not necessarily all such aspects or advantages are achieved by any particular embodiment. Thus, for example, various embodiments may be carried out in a manner that achieves or optimizes one advantage or group of advantages as taught herein without necessarily achieving other aspects or advantages as may also be taught or suggested herein.
[0090] Additionally, reference is made to the accompanying drawings that form a part hereof, and in which the specific embodiments that may be practiced is shown by way of illustration. These embodiments are described in sufficient detail to enable those skilled in the art to practice the embodiments and it is to be understood that the logical, mechanical and other changes may be made without departing from the scope of the embodiments. The following detailed description is therefore not to be taken in a limiting sense.
LIST OF REFERENCE NUMERALS
[0091] 10—Balloon guiding sheath [0092] 12—Elongated sheath [0093] 13a, c—Inner tube [0094] 13b, d—Outer tube [0095] 14—Access port [0096] 16—Inflation port [0097] 18—Inflatable balloon [0098] 20—Distal port [0099] 21—Distal inflation port [0100] 22—Working lumen [0101] 30—First inflation lumen [0102] 31—Reinforcement layer [0103] 32—Second inflation lumen [0104] 34—Outer diameter [0105] 36—Inner diameter [0106] 38—Working length [0107] 39—Generally constant outer diameter [0108] 50—Internal carotid artery [0109] 52—Cervical portion [0110] 54—Petrous portion [0111] 56—Cavernous portion [0112] 58—Cerebral portion [0113] 59—Distal tip [0114] 60—Central axis [0115] 70—First portion [0116] 72—First inner diameter [0117] 74—Second portion [0118] 76—Second inner diameter [0119] 80—First inflation hole [0120] 82—Second inflation hole [0121] 84—Guide wire [0122] 90—Proximal portion [0123] 92—First outer diameter [0124] 94—Distal portion [0125] 96—Second outer diameter [0126] 98—Middle portion [0127] 110—Proximal inflation lumen [0128] 112—First inner diameter [0129] 114—Distal inflation lumen [0130] 116—Second inner diameter
[0131] Baby BOSS Multiple Tube Embodiments
[0132] A balloon guiding sheath 10a in accordance with embodiments of the invention can be described generally with reference to
[0133] The components of the balloon guiding sheath 10 may be formed from a polymer (e.g. polytetrafluoroethylene, nylon, and the like). In some embodiments, the components may comprise Pellethane 63D or higher. Generally, the material selection may be focused on enhancing pushability in the balloon guiding sheath 10 as opposed to flexibility. However, it should be appreciated that in some embodiments the material selection may be focused on either or both pushability and/or flexibility.
[0134] As shown in
[0135] The guiding sheath 10a may also include an inflation lumen 30a that extends between the inflation port 16a and the balloon 18a. In the embodiment disclosed in
[0136] Now with reference to
[0137] With reference to
[0138] The elongated sheath 12a may be sized and configured to enable direct insertion into a patient's vasculature through an arteriotomy in the patient's carotid artery and/or vertebral artery. During use, the guiding sheath 10a may be positioned at a target site, whereby the balloon 18a is inflated to occlude blood flow through the patient's artery. The working lumen 22a, via the access port 14a, shall be arranged and configured to receive various instrumentation, such as a guide wire, tool(s), and the like. The instrumentation is then advanced through the working lumen 22a to the target site to treat and remove the embolus.
[0139] Now with reference to
[0140] To further elaborate on the various outer and inner diameter 34, 36 sizes, in some embodiments, the inner diameter 36a is greater than 0.088 inches. For example, the inner diameter 36a may be substantially equal to 0.091 inches. In some embodiments, the inner diameter 36a is substantially equal to 0.103 inches. In some embodiments, the inner diameter 36a is substantially equal to 0.110 inches. In some embodiments, the inner diameter 36a is substantially equal to 0.120 inches. Generally, it should be appreciated that the inner diameter 36a may define any size diameter configured to perform thrombectomy or embolectomy in the internal carotid artery and other vessels of a patient.
[0141] Furthermore, in some embodiments, the outer diameter 34 is greater than or equal to 0.105 inches. More specifically, in some embodiments, the outer diameter 34 is substantially equal to 0.115 inches such that the elongated sheath fits through a 9 Fr Pinnacle sheath sold by Terumo Interventional Systems (www.terumois.com). Additionally, the outer diameter 34 may fit through a customized 8 Fr sheath whereby the sheath includes a coiled inner sheath that is laminated. The customized sheath may also include a braided outer layer for added stiffness, which is further described in this disclosure in various locations.
[0142] As shown in
[0143] Generally, the guiding sheath 10 disclosed herein is intended to maximize the inner diameter 36a, while maintaining a relatively thin outer diameter 34a. This may result in overall less inflation area within the inflation lumen 30 to inflate the balloon 18. Because inflation time is directly related to inflation area and length of the inflation lumen 30, the working length 38 shall be less than or equal to 30 centimeters. However, in some embodiments, the working length 38 is greater than or equal to 30 centimeters.
[0144] To effectively reach various portions of the patient's internal carotid artery, the elongated sheath 12 may be arranged and configured to have sufficient stiffness and tip flexibility to enable insertion of the working length 38 of the elongated sheath 12 into a patient's vasculature through an arteriotomy in the patient's carotid artery. As such, the distal port 20a may be positioned at a target site in the petrous portion 54, cavernous portion 56, and the cerebral portion 58 of the patient's internal carotid artery 50.
[0145] In order to safely remove the embolus from the target site, the balloon 18 may define various shapes and sizes. For example, as shown in
[0146] Generally, the guiding sheath 10 disclosed herein may be implemented with any size, shape, and location of balloon 18. For example, in some embodiments, the balloon 18 does not extend beyond the distal tip 59 of the working lumen 22.
[0147] Baby BOSS Tip-Occluding Embodiments
[0148] Another balloon guiding sheath 10b in accordance with embodiments of the invention is now described with reference to
[0149] Similar to embodiment 10a, the guiding sheath 10b may also include a working lumen 22b extending through the elongated sheath 12b between the access port 14b and the distal port 20b. The guiding sheath 10b may include an inflation lumen 30b extending through the elongated sheath 12b between the inflation port 16b and the balloon 18b. Unlike embodiment 10a, guiding sheath 10b may be arranged and configured such that the working lumen 22b transitions between being in fluid communication with the inflation lumen 30b and then not being in fluid communication with the inflation lumen 30b. In this regard, prior to advancing the guide wire 84 through the working lumen 22b, the working lumen 22b and the inflation lumen 30b are in fluid communication with each other. However, once the guide wire 84 is advanced through the working lumen 22b and beyond the distal tip 59 of the elongated sheath 12b, the guide wire 84 thereby occludes the distal tip 59 which cuts off the fluid communication between the working lumen 22b and the inflation lumen 30b thereby allowing fluid and/or media to flow through the inflation lumen 30b and into the balloon 18b to inflate the balloon 18b.
[0150] Stated differently, the working lumen 22b may not be in fluid communication with the inflation lumen 30b when the balloon 18b is inflated. Additionally, the working lumen 22b may be in fluid communication with the inflation lumen 30b when the balloon 18b is at least partially deflated. However, either scenario may apply if the balloon 18b is in the midst of inflating or deflating. In other words, it can be said that the working lumen 22b is not in fluid communication with the inflation lumen 30b when the balloon 18b is inflated or at least partially inflated. Likewise, the working lumen 22b is in fluid communication with the inflation lumen 30b when the balloon 18b is deflated or at least partially deflated. Such tip-occluding embodiments may be beneficial because they maximize the inner diameter of the working lumen 22b while minimizing the outer diameter of the elongated sheath 12b.
[0151] To further describe the relationship between the working lumen 22b and the inflation lumen 30b we now refer to
[0152] With continued reference to
[0153] Similar to the embodiment described above, the elongated sheath 12b also has a generally constant outer diameter 39 along its working length 38b. Additionally, the elongated sheath 12b may also define a working length 38b long enough to enable the distal end to reach at least a cervical portion 52, petrous portion 54, cavernous portion 56, and a cerebral portion 58 of the patient's internal carotid artery 50 from the carotid artery.
[0154] Furthermore, the balloon 18b may extend around and beyond a distal tip 59 of the elongated sheath 12b and define a funnel-shaped opening into the distal port 20b when the balloon 18b is in an inflated state. Moreover, the elongated sheath 12b may also be arranged and configured to have sufficient stiffness and tip flexibility to enable insertion of the working length 38b of the elongated sheath 12b into a patient's vasculature through an arteriotomy in the patient's carotid artery to position the distal port 20b at a target site in at least one of the petrous portion 54, cavernous portion 56, and the cerebral portion 58 of the patient's internal carotid artery 50.
[0155] Now with reference to
[0156] As shown in
[0157] Furthermore, the guiding sheath 10b may include a second inflation hole 82 extending from the working lumen 22b through the sidewall of the elongated sheath 12b. Again, once the guide wire 84 creates a seal with the distal port 20b, this enables flow of fluid and/or media through the inflation lumen 30b into the second inflation hole 82 and into the balloon 18b to thereby inflate the balloon 18b. As shown in
[0158] Furthermore, while not shown, the working lumen 22 may define more than two portions having more two ore more different diameters. In this manner, the guide wire 84 may occlude various portions of the working lumen 22 thereby allowing one or more balloons 18 to inflate at specific intervals. Such configurations may be beneficial in treating and removing different types and sizes of emboli.
[0159] Now with reference to
[0160] The balloon guiding sheath 10c may also include one or more inflation hole(s) 80, 82 extending from the inflation lumen 30c through a sidewall of the elongated sheath 12c. As such, when a guide wire 84 is inserted into the inflation lumen 30c and out through the distal inflation port 21, the distal inflation port 21 may thereby create a seal against the guide wire 84. Once the seal is created, the inflation lumen 30c may enable flow of at least one of fluid and media through the inflation lumen 30c into the one or more inflation hole(s) 80, 82 and into the balloon 18c to thereby inflate the balloon 18c, as shown in
[0161]
[0162] As shown in
[0163] Additionally, in some embodiments, the entire elongated sheath 12 is foldable, or self-expanding. This may allow the elongated sheath 12, while in it's folded state, to be moved to the target site and then expanded to thereby provide antegrade blood flow cessation.
[0164] All of the illustrated embodiments have shown the inflation holes 80, 82 to be disposed closer to the distal port 20 then the access port 14; however, many embodiments may be configured whereby the inflation holes 80, 82 are disposed closer to the access port 14 then the distal port 20. Such embodiments may result in shorter time to inflate and deflate the balloon 18.
[0165] Additionally, because of the need to minimize air in the balloon 18 during use, the guiding sheath 10 may be arranged and configured to include a vent hole(s) at the proximal end of the balloon 18. The vent hole(s) may be formed by bonding a wire between the balloon 18 and the elongated sheath 12, and then removing the wire prior to use. Thereby when the balloon 18 is inflated, the vent hole may allow air to escape through the vent hole, but not let fluid and/or media leak out. In this regard, the vent hole is large enough to allow air through, but small enough to prevent liquid and media from passing through.
[0166] Baby BOSS Method Embodiments
[0167] With reference to
[0168] As shown in
[0169] Furthermore, methods may include applying relatively low pressure to the access port 14a, 14b to suction an embolus (at step 1506). Methods may thereby include deflating the balloon 18a, 18b (at step 1508) and thereby withdrawing the guiding sheath 10a, 10b through the arteriotomy in the carotid artery (at step 1510).
[0170] Now with reference to
[0171] As shown in
[0172] In order to begin the balloon inflation process, the user may insert a guide wire 84 into the working lumen 22b and out through the distal port 20b (at step 1704) to thereby seal an inner surface of the distal port 20b against the guide wire 84 (at step 1706). Once the distal port 20b has been sealed, methods may include flowing fluid and/or media through a space around the inflation lumen 30b into the first inflation hole 80 and/or second inflation hole 82 and into the balloon 18b to inflate the balloon 18b (at step 1708). As the fluid and/or media flows into the balloon 18b via the inflation lumen 30b, the balloon 18b may become inflated (at step 1710) to occlude the artery.
[0173] Once the balloon 18b has been inflated, the user may perform none or any combination of steps 1600, 1602, 1604, and/or 1606 in order to remove the embolus. Upon completion of such steps, the user may remove the guide wire 84 from the working lumen 22b (at step 1712). As such, the working lumen 22b and the inflation lumen 30b may once again be in fluid communication, which means that the inflation lumen 30b is not able to adequately flow liquid and/or media into the balloon 18b to keep the balloon inflated. As such, in response to removing the guide wire 84 from the working lumen 22b, the balloon 18b may deflate (at step 1714).
[0174] As illustrated in
[0175] Once the guiding sheath 10c has been positioned in its desired location within the patient's carotid artery, methods may include inserting a guide wire 84 into the inflation lumen 30c and out through the distal inflation port 21 (at step 1804) and sealing an inner surface of the distal inflation port 21 against the guide wire 84 (at step 1806). Once the seal has been created, the method may include flowing at least one of fluid and media through the inflation lumen 30c into the first inflation hole 80 and into the balloon 18c to thereby inflate the balloon 18c (at step 1808) and thereby inflating the balloon 18c via the inflation lumen 30c (at step 1810).
[0176] In order to deflate the balloon 18c, methods may include removing the guide wire 84 from the inflation lumen 30c (at step 1812). In response to removing the guide wire 84 from the inflation lumen 30c, methods may include the step of deflating the balloon 18c (at step 1814).
[0177] BOSS Max and BOSS Slender Multiple Tube Embodiments
[0178] A balloon guiding sheath 10d in accordance with embodiments of the invention can be described generally with reference to
[0179] Similar to other embodiments described throughout this disclosure, the components of the balloon guiding sheath 10d may be formed from a polymer (e.g. polytetrafluoroethylene, nylon, and the like). In some embodiments, the components may comprise Pellethane 65D or higher. Generally, the material selection may be focused on enhancing pushability in the balloon guiding sheath 10d as opposed to flexibility. However, it should be appreciated that in some embodiments the material selection may be focused on either or both pushability and/or flexibility. Generally, in many embodiments, the elongated sheath 12d is arranged and configured to have sufficient stiffness and tip flexibility to enable insertion of the working length 38d of the elongated sheath 12d into a patient's vasculature through an arteriotomy in the patient's femoral artery to position the distal port 20 at a target site in at least one of a petrous portion 54 of a patient's internal carotid artery 50, a cavernous portion 56 of a patient's internal carotid artery 50, and a cerebral portion 58 of a patient's internal carotid artery 50.
[0180] As shown in
[0181] Furthermore, the guiding sheath 10d may include an inflation lumen 30d that extends between the inflation port 16d and the balloon 18d. In the embodiment disclosed with respect to
[0182] With reference back to
[0183] Now with reference to
[0184] In many embodiments, the elongated sheath 12d is sized and configured to enable direct insertion into a patient's vasculature through an arteriotomy in the patient's femoral artery to position the balloon 18d at a target site. As shown in
[0185] With regard to specific dimensions, in some embodiments, the first outer diameter 92a is approximately equal to 0.123 inches. Even still, in some embodiments, the first outer diameter 92a is approximately equal to 0.137 inches. The second outer diameter 96a may be approximately equal to 0.104 inches such that the elongated sheath 12d fits through an 8 French (Fr) opening. In some embodiments, the second outer diameter 96a is approximately equal to 0.124 inches such that the elongated sheath 12d fits through a 10 French (Fr) opening. Generally, it should be appreciated that the first outer diameter 92a, second outer diameter 96a, and any other dimension recited in this disclosure may be equal to any value based on medical application and patient anatomy.
[0186] With continued reference to
[0187] Again, in regards to various commercial embodiments, the proximal and distal portions 90a, 94a may define a variety of different dimensions arranged and configured to meet the needs of specific applications and patient anatomies. For example, the working lumen 22d may define an inner diameter having a substantially constant diameter from the distal end to the proximal end. Specifically, in some embodiments, the inner diameter is approximately equal to 0.088 inches.
[0188] However, in many embodiments, the working lumen 22d does not define a constant inner diameter from the distal end to the proximal end. In some embodiments, the proximal portion 90a of the working lumen 22d defines a first inner diameter 112a approximately equal to 0.090 inches, while the distal portion 94a of the working lumen 22d defines a second inner diameter 116a greater than or equal to 0.086 inches and less than or equal to 0.090 inches. Even still, in some embodiments, the first inner diameter 112a is greater than or equal to 0.101 inches and less than or equal to 0.113 inches, and the second inner diameter 116a is greater than or equal to 0.101 inches and less than or equal to 0.113 inches. With even more specificity, in some embodiments, the first inner diameter 112a is approximately equal to 0.113 inches and the second inner diameter 116a is approximately equal to 0.101 inches.
[0189] The elongated sheath 12d may define a variety of working lengths sized and configured to accommodate treatment locations in different target sites. In some embodiments, the working length 38d is long enough to enable the distal end to reach at least a cervical portion 52 of a patient's internal carotid artery 50 from the femoral artery. The working length 38d may be long enough to enable the distal end to reach at least a petrous portion 54 of the patient's internal carotid artery 50 from the femoral artery. Even still, the working length 38d may be long enough to enable the distal end to reach at least a cavernous portion 56 of the patient's internal carotid artery 50 from the femoral artery. In some embodiments, the working length 38d is approximately equal to 95 centimeters. However, it should be appreciated that the working length 38d may be any length less than or greater than 95 centimeters. In some embodiments, the proximal portion 90a of the working lumen 22d equals approximately 85 centimeters in length, while the distal portion 94a of the working lumen 22d equals approximately 10 centimeters in length. However, the lengths of the proximal portion 90a and the distal portion 94a may define any length such that they equal the overall working length 38d.
[0190] BOSS Max and BOSS Slender Tip-Occluding Embodiments
[0191] Yet another balloon guiding sheath 10e in accordance with embodiments of the invention is now described with reference to
[0192] With respect to
[0193] Similar to the embodiment described with respect to
[0194] In some embodiments, the elongated sheath 12e includes more than one inflation lumen. For example, the balloon guiding sheath 10e may thereby include a second inflation lumen 32e extending through the elongated sheath 12e between the inflation port 16e and the balloon 18e. The second inflation lumen 32e may include a second distal inflation port 21e extending through the endwall of the elongated sheath 12e. In such embodiments, the second inflation lumen 32e is not in fluid communication with the working lumen 22e between the access port 14e and the distal port 20e. The guiding sheath 10e may thereby include a second inflation hole 82e extending from the second inflation lumen 32e through the sidewall of the elongated sheath 12e. Similar to the inflation technique described above, when a second wire 84 is inserted into the second inflation lumen 32e and out through the second distal inflation port 21e, the second distal inflation port 21e may thereby create a seal against the second wire 84. Once this occurs, the flow of fluid and/or media through the second inflation lumen 32e into the second inflation hole 82e and into the balloon 18e thereby inflates the balloon 18e.
[0195] Regarding specific orientations of the working lumen 22e with respect to the inflation lumen 30e, the elongated sheath 12e may define a central axis extending from the proximal end to the distal end. As shown in
[0196] The elongated sheath 12e may be sized and configured to enable direct insertion into a patient's vasculature through an arteriotomy in the patient's femoral artery to position the balloon 18e at a target site. As shown in
[0197] With continued reference to
[0198] Generally, embodiments disclosed with respect to
[0199] BOSS Max and BOSS Slender Method Embodiments
[0200] With reference to
[0201] As shown in
[0202] As further shown, many methods include applying relatively low pressure to the access port 14d, 14e to suction an embolus (at step 2506). Once this is complete, methods may include deflating the balloon (at step 2508) and thereby withdrawing the guiding sheath 10d, 10e through the arteriotomy in the carotid artery (at step 2510).
[0203] However, clinicians may need to perform other treatments to the target site, which may require the use of additional equipment. Accordingly, methods may include the following intervening steps that may occur after step 2504. As shown in
[0204] As shown in
[0205] In some embodiments, methods may also include removing the wire 84 from the working lumen 22e (at step 2708) and in response to removing the wire 84 from the working lumen 22e, deflating the balloon 18e (at step 2710).
[0206]
[0207] Interpretation
[0208] As presented in this disclosure, the term “substantially” shall mean “for the most part.” As such, if we say that a first object is substantially horizontally aligned with a second object this means that at least half a surface area of the first object overlaps with at least half a surface area of the second object. Within a numerical context “substantially” shall mean±0.001 inches. For example, to say that an inner diameter of a working lumen is substantially equal to 0.091 inches, means that the inner diameter is 0.091±0.001 inches.
[0209] As presented in this disclosure, the term “generally” shall be interpreted numerically as ±0.003 inches. For example, to say that an elongated sheath defines a generally constant outer diameter shall mean that the outer diameter is generally constant but may vary by ±0.003 inches. For example, if the outer diameter is 0.123 inches and generally constant shall mean that the outer diameter may vary between 0.126 inches and 0.120 inches.
[0210] Furthermore, as presented in this disclosure, the term “about” shall mean approximately or roughly. Within a numerical context “about” shall mean±0.5 centimeters. For example, to say that the length of a guiding sheath is about 90 centimeters, means that the guiding sheath is 90±0.5 centimeters.
[0211] None of the steps described herein is essential or indispensable. Any of the steps can be adjusted or modified. Other or additional steps can be used. Any portion of any of the steps, processes, structures, and/or devices disclosed or illustrated in one embodiment, flowchart, or example in this specification can be combined or used with or instead of any other portion of any of the steps, processes, structures, and/or devices disclosed or illustrated in a different embodiment, flowchart, or example. The embodiments and examples provided herein are not intended to be discrete and separate from each other.
[0212] The section headings and subheadings provided herein are nonlimiting. The section headings and subheadings do not represent or limit the full scope of the embodiments described in the sections to which the headings and subheadings pertain. For example, a section titled “Topic 1” may include embodiments that do not pertain to Topic 1 and embodiments described in other sections may apply to and be combined with embodiments described within the “Topic 1” section.
[0213] The various features and processes described above may be used independently of one another, or may be combined in various ways. All possible combinations and subcombinations are intended to fall within the scope of this disclosure. In addition, certain method, event, state, or process blocks may be omitted in some implementations. The methods, steps, and processes described herein are also not limited to any particular sequence, and the blocks, steps, or states relating thereto can be performed in other sequences that are appropriate. For example, described tasks or events may be performed in an order other than the order specifically disclosed. Multiple steps may be combined in a single block or state. The example tasks or events may be performed in serial, in parallel, or in some other manner. Tasks or events may be added to or removed from the disclosed example embodiments. The example systems and components described herein may be configured differently than described. For example, elements may be added to, removed from, or rearranged compared to the disclosed example embodiments.
[0214] Conditional language used herein, such as, among others, “can,” “could,” “might,” “may,” “e.g.,” and the like, unless specifically stated otherwise, or otherwise understood within the context as used, is generally intended to convey that certain embodiments include, while other embodiments do not include, certain features, elements and/or steps. Thus, such conditional language is not generally intended to imply that features, elements and/or steps are in any way required for one or more embodiments or that one or more embodiments necessarily include logic for deciding, with or without author input or prompting, whether these features, elements and/or steps are included or are to be performed in any particular embodiment. The terms “comprising,” “including,” “having,” and the like are synonymous and are used inclusively, in an open-ended fashion, and do not exclude additional elements, features, acts, operations and so forth. Also, the term “or” is used in its inclusive sense (and not in its exclusive sense) so that when used, for example, to connect a list of elements, the term “or” means one, some, or all of the elements in the list. Conjunctive language such as the phrase “at least one of X, Y, and Z,” unless specifically stated otherwise, is otherwise understood with the context as used in general to convey that an item, term, etc. may be either X, Y, or Z. Thus, such conjunctive language is not generally intended to imply that certain embodiments require at least one of X, at least one of Y, and at least one of Z to each be present.
[0215] The term “and/or” means that “and” applies to some embodiments and “or” applies to some embodiments. Thus, A, B, and/or C can be replaced with A, B, and C written in one sentence and A, B, or C written in another sentence. A, B, and/or C means that some embodiments can include A and B, some embodiments can include A and C, some embodiments can include B and C, some embodiments can only include A, some embodiments can include only B, some embodiments can include only C, and some embodiments include A, B, and C. The term “and/or” is used to avoid unnecessary redundancy.
[0216] Although the embodiments herein are described with various specific embodiments, it will be obvious for a person skilled in the art to practice the invention with modifications. However, all such modifications are deemed to be within the scope of the claims. While certain example embodiments have been described, these embodiments have been presented by way of example only, and are not intended to limit the scope of the inventions disclosed herein. Thus, nothing in the foregoing description is intended to imply that any particular feature, characteristic, step, module, or block is necessary or indispensable. Indeed, the novel methods and systems described herein may be embodied in a variety of other forms; furthermore, various omissions, substitutions, and changes in the form of the methods and systems described herein may be made without departing from the spirit of the inventions disclosed herein.
[0217] Furthermore, the foregoing description of the specific embodiments will so fully reveal the general nature of the embodiments herein that others can, by applying current knowledge, readily modify and/or adapt for various applications such specific embodiments without departing from the generic concept, and, therefore, such adaptations and modifications should and are intended to be comprehended within the meaning and range of equivalents of the disclosed embodiments. It is to be understood that the phraseology or terminology employed herein is for the purpose of description and not of limitation. Therefore, while the embodiments herein have been described in terms of preferred embodiments, those skilled in the art will recognize that the embodiments herein can be practiced with modification within the spirit and scope of the appended claims.
[0218] Implementation
[0219] The aforementioned embodiments can be implemented, for example, using a machine-readable medium or article which is able to store an instruction or a set of instructions that, if executed by a machine, can cause the machine to perform a method and/or operations described herein. Such machine can include, for example, any suitable processing platform, computing platform, computing device, processing device, electronic device, electronic system, computing system, processing system, computer, processor, or the like, and is able to be implemented using any suitable combination of hardware and/or software.