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Title:
INTERNAL CAROTID ARTERY THROMBECTOMY DEVICES AND METHODS
Document Type and Number:
WIPO Patent Application WO/2020/018653
Kind Code:
A1
Abstract:
The disclosure includes a balloon guiding sheath that includes an elongated sheath having a proximal end and a distal end. The elongated sheath may include an inner tube and an outer tube. The guiding sheath may include an access port located on the proximal end, a distal port located on the distal end, a working lumen extending between the access port and the distal port, an inflation port on the proximal end, an inflatable balloon coupled to the distal end, an inflation lumen located between the inner tube and the outer tube, and a reinforcement layer located between the inner tube and the outer tube. The elongated sheath may be sized and configured to enable direct insertion into a patient's vasculature through an arteriotomy in the patient's carotid artery or vertebral artery to position the balloon at a target site.

Inventors:
KALLMES DAVID (US)
BRINJIKJI WALEED (US)
HATCHER BRADY (US)
BEYREIS RANDY (US)
Application Number:
PCT/US2019/042181
Publication Date:
January 23, 2020
Filing Date:
July 17, 2019
Export Citation:
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Assignee:
MARBLEHEAD MEDICAL LLC (US)
International Classes:
A61M25/10; A61M25/12; A61M25/14
Foreign References:
US20100204712A12010-08-12
US5195962A1993-03-23
US20060041228A12006-02-23
US6039721A2000-03-21
US7445642B22008-11-04
US6719718B22004-04-13
US20080188793A12008-08-07
Attorney, Agent or Firm:
SCHWIE, Wesley, Edward (US)
Download PDF:
Claims:
THE FOLLOWING IS CLAIMED:

1. A balloon guiding sheath, comprising:

an elongated sheath having a proximal end and a distal end, the elongated sheath comprising an inner tube and an outer tube that surrounds the inner tube;

an access port located on the proximal end;

a distal port located on the distal end;

a working lumen extending through the elongated sheath between the access port and the distal port;

an inflation port on the proximal end;

an inflatable balloon coupled to the distal end;

an inflation lumen located between the inner tube and the outer tube, the inflation lumen extending between the inflation port and the balloon; and

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,

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, 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.

3. The balloon guiding sheath of claim 1, wherein the elongated sheath defines an outer diameter less than or equal to 0.104 inches such that the elongated sheath fits through an 8 Fr opening, wherein the working lumen defines an inner diameter less than or equal to 0.090 inches and greater than or equal to 0.087 inches,

wherein the elongated sheath has a generally constant outer diameter along its working length, and

wherein the elongated sheath defines a working length that is long enough to enable the distal end to reach at least a cervical portion of a patient’s internal carotid artery from the carotid artery.

4. The balloon guiding sheath of claim 3, wherein the working length is long enough to enable the distal end to reach a cavernous portion of the patient’s internal carotid artery from the carotid artery.

5. The balloon guiding sheath of claim 1, wherein the balloon extends around and beyond a distal tip of the elongated sheath and defines a funnel-shaped opening into the distal port when the balloon is in an inflated state such that the balloon does not occlude the working lumen of the distal port.

6. A balloon guiding sheath, comprising:

an elongated sheath having a proximal end and a distal end;

an access port located on the proximal end;

a distal port located on the distal end;

a working lumen extending through the elongated sheath between the access port and the distal port;

an inflation port on the proximal end;

an inflatable balloon coupled to the distal end;

an inflation lumen extending through the elongated sheath between the inflation port and the balloon; and

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.

7. The balloon guiding sheath of claim 6, wherein the working lumen is not in fluid communication with the inflation lumen when the balloon is inflated.

8. The balloon guiding sheath of claim 6, wherein the working lumen is in fluid communication with the inflation lumen when the balloon is at least partially deflated.

9. The balloon guiding sheath of Claim 8, wherein an inner portion of the elongated sheath comprises a first portion defining a first inner diameter and a second portion defining a second inner diameter, wherein the second portion is located proximal to the first portion, and wherein the second inner diameter is greater than the first inner diameter.

10. The balloon guiding sheath of Claim 9, further comprising:

a first inflation hole extending from the working lumen through a sidewall of the elongated sheath, wherein when a guide wire is inserted into the working lumen and out through the distal port, the distal port thereby creates a seal against the guide wire, and wherein the inner portion of the elongated sheath is arranged and configured to enable flow of at least one of fluid and media through the inflation lumen into the first inflation hole and into the balloon to thereby inflate the balloon; and

a second inflation hole extending from the working lumen through the sidewall of the elongated sheath, wherein the inner portion of the elongated sheath is arranged and configured to enable flow of at least one of fluid and media through the inflation lumen into the second inflation hole and into the balloon to thereby inflate the balloon.

11. The balloon guiding sheath of claim 8, wherein the elongated sheath defines a central axis extending from the proximal end to the distal end, wherein at least a portion of the working lumen overlaps the central axis of the elongated sheath, and wherein the inflation lumen does not overlap the central axis of the elongated sheath.

12. The balloon guiding sheath of claim 8, wherein the elongated sheath defines an outer diameter less than or equal to 0.104 inches such that the elongated sheath fits through an 8 Fr opening, wherein the working lumen defines an inner diameter less than or equal to 0.090 inches and greater than or equal to 0.087 inches,

wherein the elongated sheath defines a working length long enough to enable the distal end to reach a cavernous portion of a patient’s internal carotid artery from the carotid artery, and

wherein the elongated sheath defines a generally constant outer diameter along the working length.

13. The balloon guiding sheath of claim 8, wherein the balloon extends around and beyond a distal tip of the elongated sheath and defines a funnel-shaped opening into the distal port when the balloon is in an inflated state such that the balloon does not occlude the working lumen of the distal port.

14. The balloon guiding sheath of claim 8, 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.

15. A balloon guiding sheath, comprising:

an elongated sheath having a proximal end and a distal end;

an access port located on the proximal end;

a distal port located on the distal end;

a working lumen extending through the elongated sheath between the access port and the distal port;

an inflation port on the proximal end;

an inflatable balloon coupled to the distal end;

an inflation lumen extending through the elongated sheath between the inflation port and the balloon, the inflation lumen comprising a distal inflation port extending through an endwall of the elongated sheath, wherein the inflation lumen is not in fluid communication with the working lumen between the access port and the distal port; and 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.

16. The balloon guiding sheath of Claim 15, further comprising a first inflation hole extending from the inflation lumen through a sidewall of the elongated sheath, wherein when a guide wire is inserted into the inflation lumen and out through the distal inflation port, the distal inflation port thereby creates a seal against the guide wire, and wherein the inflation lumen is arranged and configured to enable flow of at least one of fluid and media through the inflation lumen into the first inflation hole and into the balloon to thereby inflate the balloon.

17. The balloon guiding sheath of Claim 16, wherein the inflation lumen is a first inflation lumen, the balloon guiding sheath further comprising:

a second inflation lumen extending through the elongated sheath between the inflation port and the balloon, the second inflation lumen comprising a second distal inflation port extending through the endwall of the elongated sheath, wherein the second inflation lumen is not in fluid communication with the working lumen between the access port and the distal port; and

a second inflation hole extending from the second inflation lumen through the sidewall of the elongated sheath, wherein when a second guide wire is inserted into the second inflation lumen and out through the second distal inflation port, the second distal inflation port thereby creates a seal against the second guide wire, and wherein the second inflation lumen is arranged and configured to enable flow of at least one of fluid and media through the second inflation lumen into the second inflation hole and into the balloon to thereby inflate the balloon.

18. The balloon guiding sheath of claim 15, wherein the elongated sheath defines a central axis extending from the proximal end to the distal end, wherein at least a portion of the working lumen overlaps the central axis of the elongated sheath, and wherein the inflation lumen does not overlap the central axis of the elongated sheath.

19. The balloon guiding sheath of claim 15, wherein the working length is long enough to enable the distal end to reach a cavernous portion of the patient’s internal carotid artery from the carotid artery.

20. The balloon guiding sheath of claim 15, 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:
INTERNAL CAROTID ARTERY THROMBECTOMY DEVICES AND

METHODS

CROSS REFERENCE TO RELATED APPLICATION

This application claims the benefit of ET.S. Provisional Patent Application No. 62/700,173; filed July 18, 2018; and entitled INTERNAL CAROTID ARTERY THROMBECTOMY DEVICES AND METHODS; the entire contents of which are incorporated herein by reference.

The entire contents of the following application are incorporated by reference herein: International Patent Application PCT US2017/031311; having an international filing date of May 5, 2017 and a priority date of May 6, 2016; and entitled INTERNAL CAROTID ARTERY THROMBECTOMY DEVICES AND METHODS.

BACKGROUND

Field of Invention

The invention relates generally to medical devices and methods of use. Embodiments of the invention include devices for performing thrombectomy or embolectomy in the internal carotid artery and other vessels of a patient.

Description of Related Art

Acute Ischemic Stroke (AIS) can be caused by thrombus, embolus or other occlusions in regions of the internal carotid artery (ICA) such as the Petrous part, Cavernous part or Cerebral part. Approaches for performing thrombectomy or embolectomy to treat AIS include positioning a balloon guiding catheter in the carotid artery at a location upstream from the occlusion, typically at a proximal location in the artery such as the cervical part. After the balloon is inflated to provide antegrade blood flow cessation, suction can be applied to the catheter to retrieve the embolus. Thrombectomy tools such as stent retrievers can also be delivered directly to the embolus through the guiding catheter to break up the embolus and enhance the retrieval process. These thrombectomy procedures may involve placing a sheath through an arteriotomy in the patient’s common femoral artery, and delivering the guiding catheter to the ICA through the sheath. For example, an 8-9 French (Fr) inner diameter (ID) (0.015- 0.118 inches) sheath having a length on the order of twenty-five centimeters can be used to provide the access to the arterial tree through the arteriotomy. A balloon guiding catheter having a 7-8 Fr outer diameter (OD) (0.092-0.105 inches), commonly about ninety centimeters in length, can then be delivered to the ICA through the sheath. A 10-11 Fr (0.131-0.144 inch) arteriotomy may be required for the sheath during procedures of these types. Unfortunately these relatively large arteriotomies can enhance the risk of bleeding, especially since patient’s undergoing these procedures may be receiving thrombolytics that may increase the risks of hemorrhagic complications.

Relatively small diameter distal access aspiration catheters (e.g., up to about 0.087 inch OD) are sometimes used during thrombectomy in the ICA. Such distal aspiration catheters include the ACE 68 from Penumbra, Inc. and the Sophia Plus from Microvention, Inc. For example, during these procedures the distal aspiration catheter can inserted with the end positioned at the distal middle cerebral artery. Other thrombecotomy tools such as stent retrievers are sometimes delivered to the intracranial vasculature through distal access catheters used in this manner. However, balloon guiding catheters have IDs that are too small to accommodate these distal aspiration catheters. Other known balloon guide catheters include the MO.MA Ultra and Cello devices from Medtronic, Inc., and the Flowgate2 device from Stryker Neurovascular. The relatively long period of time required to place a sheath and then a balloon guide catheter can detract from the benefits of this treatment.

Stents and other endovascular tools are sometimes placed in the ICA or other vasculature using guiding sheaths that do not have balloons. Guiding sheaths are typically about ninety centimeters in length. These devices act as a combination of access sheath and guiding catheter. The need for a separate sheath is obviated by the use of these guiding sheaths since they are sufficiently long to provide access to the target vessel. Although guiding sheaths do not provide arterial occlusion, they can be rapidly placed.

There is a continuing need for improved devices and methods for performing mechanical revascularization such as thrombectomy and embolectomy in the ICA and other vasculature. In particular, there is a need for such devices and methods that provide enhanced efficacy. Devices and methods of these types that can improve the efficiency of health care delivery would be especially desirable.

SUMMARY

The present disclosure describes a balloon guiding sheath that includes an elongated sheath having a proximal end and a distal end. The elongated sheath may include an inner tube and an outer tube that surrounds the inner tube. The guiding sheath may also include an access port located on the proximal end, a distal port located on the distal end, a working lumen extending through the elongated sheath between the access port and the distal port, an inflation port on the proximal end, an inflatable balloon coupled to the distal end, an inflation lumen located between the inner tube and the outer tube. The inflation lumen may extend between the inflation port and the balloon. The guiding sheath may also include a reinforcement layer located between the inner tube and the outer tube. The reinforcement layer may be arranged and configured to enable flow of at least one of fluid and media through the inflation lumen. The elongated sheath may be 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.

The elongated sheath may define an outer diameter less than or equal to 0.104 inches such that the elongated sheath fits through an 8 Fr opening. The working lumen may define an inner diameter less than or equal to 0.090 inches. In some embodiments, the inner diameter of the working lumen is greater than or equal to 0.087 inches.

In many embodiments, the elongated sheath has a generally constant outer diameter along its working length. Furthermore, the elongated sheath may define a working length that is long enough to enable the distal end to reach at least a cervical portion of a patient’s internal carotid artery from the carotid artery. In some embodiments, the working length is long enough to enable the distal end to reach a cavernous portion of the patient’s internal carotid artery from the carotid artery.

In some embodiments, the balloon extends around and beyond a distal tip of the elongated sheath. When the balloon is inflated, the balloon may thereby define a funnel- shaped opening into the distal port such that the balloon does not occlude the working lumen of the distal port.

The elongated sheath may be 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.

The disclosure also includes a balloon guiding sheath that includes an elongated sheath having a proximal end and a distal end, an access port located on the proximal end, a distal port located on the distal end, a working lumen extending through the elongated sheath between the access port and the distal port, an inflation port on the proximal end, an inflatable balloon coupled to the distal end, and an inflation lumen extending through the elongated sheath between the inflation port and the balloon. The elongated sheath may be 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.

In some embodiments, the working lumen is not in fluid communication with the inflation lumen when the balloon is inflated. Likewise, in some embodiments, the working lumen is in fluid communication with the inflation lumen when the balloon is at least partially deflated.

The elongated sheath may define a central axis extending from the proximal end to the distal end. In some embodiments, at least a portion of the working lumen overlaps the central axis of the elongated sheath. Additionally, in some embodiments, the inflation lumen does not overlap the central axis of the elongated sheath.

An inner portion of the elongated sheath may comprise a first portion defining a first inner diameter and a second portion defining a second inner diameter. The second portion may be located proximal to the first portion, and the second inner diameter may be greater than the first inner diameter.

The balloon guiding sheath may include a first inflation hole extending from the working lumen through a sidewall of the elongated sheath. When a guide wire is inserted into the working lumen and out through the distal port, the distal port may thereby create a seal against the guide wire. An inner portion of the elongated sheath may be arranged and configured to enable flow of at least one of fluid and media through the inflation lumen into the first inflation hole and into the balloon to thereby inflate the balloon.

Additionally, the balloon guiding sheath may include a second inflation hole extending from the working lumen through the sidewall of the elongated sheath. The inner portion of the elongated sheath may thereby be arranged and configured to enable flow of at least one of fluid and media through the inflation lumen into the second inflation hole and into the balloon to thereby inflate the balloon.

The disclosure also includes a balloon guiding sheath that includes an elongated sheath having a proximal end and a distal end, an access port located on the proximal end, a distal port located on the distal end, a working lumen extending through the elongated sheath between the access port and the distal port, an inflation port on the proximal end, an inflatable balloon coupled to the distal end, an inflation lumen extending through the elongated sheath between the inflation port and the balloon. The inflation lumen may include a distal inflation port extending through an endwall of the elongated sheath. In some embodiments, the inflation lumen is not in fluid communication with the working lumen between the access port and the distal port. The elongated sheath may be 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.

In some embodiments, the balloon guiding sheath includes a first inflation hole extending from the inflation lumen through a sidewall of the elongated sheath. In this regard, when a guide wire is inserted into the inflation lumen and out through the distal inflation port, the distal inflation port thereby may create a seal against the guide wire. When this occurs, the inflation lumen may be arranged and configured to enable flow of at least one of fluid and media through the inflation lumen into the first inflation hole and into the balloon to thereby inflate the balloon.

The inflation lumen may be referred to as a first inflation lumen. In such embodiments, the balloon guiding sheath may further include a second inflation lumen extending through the elongated sheath between the inflation port and the balloon. The second inflation lumen may comprise a second distal inflation port extending through the endwall of the elongated sheath. The second inflation lumen may not be in fluid communication with the working lumen between the access port and the distal port. The balloon guiding sheath may also include a second inflation hole extending from the second inflation lumen through the sidewall of the elongated sheath. As such, when a second guide wire is inserted into the second inflation lumen and out through the second distal inflation port. The second distal inflation port may thereby create a seal against the second guide wire. Accordingly, the second inflation lumen may thereby be arranged and configured to enable flow of at least one of fluid and media through the second inflation lumen into the second inflation hole and into the balloon to thereby inflate the balloon.

The elongated sheath may thereby define a central axis extending from the proximal end to the distal end whereby at least a portion of the working lumen overlaps the central axis of the elongated sheath and the inflation lumen does not overlap the central axis of the elongated sheath. In some embodiments, the elongated sheath has a generally constant outer diameter along its working length.

In some embodiments, the elongated sheath defines a working length that is long enough to enable the distal end to reach at least a cervical portion of a patient’s internal carotid artery from the carotid artery. The working length may be long enough to enable the distal end to reach a cavernous portion of the patient’s internal carotid artery from the carotid artery. Furthermore, the elongated sheath may be 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.

The disclosure also includes methods for using a balloon guiding sheath comprising an elongated sheath having a proximal end, a distal end, an inner tube, and an outer tube that surrounds the inner tube, the guiding sheath including an access port located on the proximal end, a distal port located on the distal end, a working lumen extending through the elongated sheath between the access port and the distal port, an inflation port on the proximal end, an inflatable balloon coupled to the distal end, an inflation lumen located between the inner tube and the outer tube and extending between the inflation port and the balloon, and 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. Methods may include inserting the guiding sheath directly into a patient’s vasculature through an arteriotomy in a patient’s carotid artery, advancing the guiding sheath through the patient’s vasculature and positioning the distal end in a target site of a patient’s internal carotid artery, and inflating the balloon via the inflation lumen.

In some embodiments, the target site is at least a cervical portion of the internal carotid artery. As well, in some embodiments, the target site is at least a cavernous portion of the internal carotid artery.

Methods may include applying relatively low pressure to the access port to suction an embolus, deflating the balloon, and withdrawing the guiding sheath through the arteriotomy in the carotid artery. Even still, methods may include inserting a tool into the guiding sheath through the access port after positioning the distal end at the target site, advancing the tool through the guiding sheath, actuating the tool to retrieve an embolus, withdrawing the tool from the guiding sheath, deflating the balloon, and withdrawing the guiding sheath through the arteriotomy in the carotid artery.

The disclosure may also include methods for using a balloon guiding sheath comprising an elongated sheath having a proximal end and a distal end, the guiding sheath including an access port located on the proximal end, a distal port located on the distal end, a working lumen extending through the elongated sheath between the access port and the distal port, an inflation port on the proximal end, an inflatable balloon coupled to the distal end, an inflation lumen extending through the elongated sheath between the inflation port and the balloon. Methods may include inserting the guiding sheath directly into a patient’s vasculature through an arteriotomy in a patient’s carotid artery, advancing the guiding sheath through the patient’s vasculature and positioning the distal end in a target site of a patient’s internal carotid artery, and inflating the balloon via the inflation lumen.

In some methods, an inner portion of the elongated sheath comprises a first portion defining a first inner diameter and a second portion defining a second inner diameter. The second portion may be located proximal to the first portion. The second inner diameter may be greater than the first inner diameter. The elongated sheath comprises a first inflation hole extending from the working lumen through a sidewall of the elongated sheath. Methods may thereby include inserting a guide wire into the working lumen and out through the distal port, sealing an inner surface of the distal port against the guide wire, and flowing at least one of fluid and media through the inflation lumen into the first inflation hole and into the balloon to thereby inflate the balloon.

The elongated sheath may comprise a second inflation hole extending from the working lumen through a sidewall of the elongated sheath. Methods may further include flowing at least one of fluid and media through the inflation lumen into the second inflation hole and into the balloon to thereby inflate the balloon. As well, methods may include removing the guide wire from the working lumen, and in response to removing the guide wire from the working lumen, deflating the balloon.

The disclosure also includes a method for using a balloon guiding sheath comprising an elongated sheath having a proximal end and a distal end, the guiding sheath including an access port located on the proximal end, a distal port located on the distal end, a working lumen extending through the elongated sheath between the access port and the distal port, an inflation port on the proximal end, an inflatable balloon coupled to the distal end, an inflation lumen extending through the elongated sheath between the inflation port and the balloon, the inflation lumen comprising a distal inflation port extending through an endwall of the elongated sheath. In such embodiments, the inflation lumen is not in fluid communication with the working lumen between the access port and the distal port.

Methods may include inserting the guiding sheath directly into a patient’s vasculature through an arteriotomy in a patient’s carotid artery and advancing the guiding sheath through the patient’s vasculature and positioning the distal end in a target site of a patient’s internal carotid artery. Methods may also include inflating the balloon via the inflation lumen.

The balloon guiding sheath may further include a first inflation hole extending from the inflation lumen through a sidewall of the elongated sheath. In such embodiments, the method further includes inserting a guide wire into the inflation lumen and out through the distal inflation port and thereby sealing an inner surface of the distal inflation port against the guide wire. Once the seal has been achieved methods may include flowing at least one of fluid and media through the inflation lumen into the first inflation hole and into the balloon to thereby inflate the balloon.

In some embodiments, the inflation lumen may be referred to as a first inflation lumen. In these embodiments, the balloon guiding sheath may further include a second inflation lumen extending through the elongated sheath between the inflation port and the balloon. The second inflation lumen may include a second distal inflation port extending through the endwall of the elongated sheath, and a second inflation hole extending from the second inflation lumen through the sidewall of the elongated sheath. Accordingly, methods may include inserting a second guide wire into the second inflation lumen and out through the second distal inflation port and sealing an inner surface of the second distal inflation port against the second guide wire. In response, methods may thereby include the step of flowing at least one of fluid and media through the second inflation lumen into the second inflation hole and into the balloon to thereby inflate the balloon.

Methods may also include removing the guide wire from the working lumen. In response to removing the guide wire from the working lumen, methods may include the step of deflating the balloon.

Other objects and advantages of the embodiments herein will become readily apparent from the following detailed description taken in conjunction with the accompanying drawings. The embodiments described above include many optional features and aspects. Features and aspects of the embodiments can be combined.

BRIEF DESCRIPTION OF THE DRAWINGS

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.

Figure 1 A illustrates a balloon guiding sheath, according to some embodiments.

Figures 1B and 1C illustrate a cross-sectional view of section 1-1 of the balloon guiding sheath, with the balloon in a deflated state and an inflated state, respectively according to some embodiments.

Figure 2 illustrates a cross-sectional view of section 2-2 of the balloon guiding sheath, according to some embodiments.

Figure 3 illustrates a cross-sectional view of section 3-3 of the balloon guiding sheath, according to some embodiments.

Figure 4 illustrates a cross-sectional view of section 2-2 of the balloon guiding sheath, according to some embodiments.

Figure 5 illustrates a working length and generally constant outer diameter of the elongated sheath, according to some embodiments.

Figure 6 illustrates an anatomy of an internal carotid artery, according to some embodiments.

Figures 7A and 7B illustrate cross-sectional views of section 7-7 of the balloon guiding sheath with the balloon in a deflated state and an inflated state, respectively, according to some embodiments.

Figure 8 illustrates another balloon guiding sheath, according to some embodiments.

Figure 9 illustrates a cross-sectional view of section 9-9 of the balloon guiding sheath, according to some embodiments.

Figure 10 illustrates a cross-sectional view of section 10-10 of the balloon guiding sheath, according to some embodiments.

Figures 11 A and 11B illustrate cross-sectional views of section 11-11 of the balloon guiding sheath with the balloon in a deflated state and an inflated state, respectively, according to some embodiments.

Figures 12A and 12B illustrate cross-sectional views of section 12-12 of the balloon guiding sheath with the balloon in a deflated state and an inflated state, respectively, according to some embodiments.

Figures 13A, 13B, and 13C illustrate cross-sectional views of section 13-13 of the balloon guiding sheath, according to some embodiments.

Figure 14A illustrates another balloon guiding sheath, according to some embodiments.

Figure 14B illustrate cross-sectional views of section 14B-14B of the balloon guiding sheath, according to some embodiments.

Figures 15, 16, 17, and 18 illustrate methods of using a balloon guiding sheath, according to some embodiments.

DETAILED DESCRIPTION

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.

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.

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

10 - Balloon guiding sheath

12 - Elongated sheath 13a - Inner tube

13b - Outer tube

14 - Access port

16 - Inflation port

18 - Inflatable balloon

20 - Distal port

21 - Distal inflation port

22 - Working lumen

30 - Inflation lumen

31 - Reinforcement layer

34 - Outer diameter

36 - Inner diameter

38 - Working length

39 - Generally constant outer diameter

50 - Internal carotid artery

52 - Cervical portion

54 - Petrous portion

56 - Cavernous portion

58 - Cerebral portion

59 - Distal tip

60 - Central axis

70 - First portion

72 - First inner diameter

74 - Second portion

76 - Second inner diameter

80 - First inflation hole

82 - Second inflation hole

84 - Guide wire

Multiple Tube Embodiments

A balloon guiding sheath 10 in accordance with embodiments of the invention can be described generally with reference to Figs. 1 A-7. As shown in Fig. 1 A, a balloon guiding sheath lOa may comprise an elongated sheath l2a having a proximal end and a distal end. With reference to Fig. 2, the elongated sheath l2a may include an inner tube l3a and an outer tube l3b that surrounds the inner tube 13 a. It should be appreciated that many embodiments may also be implemented with one tube, as will be discussed later regarding Fig. 8. Other embodiments may include three or more tubes, also referred to as layers.

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.

As shown in Fig. 1 A, the guiding sheath lOa may include an access port l4a located on the proximal end and an inflation port l6a also located on the proximal end. The guiding sheath lOa may include an inflatable balloon l8a coupled to the distal end and a distal port 20a also located on the distal end. As shown in Figs. 2 and 3, the guiding sheath lOa may include a working lumen 22a extending through the elongated sheath 12 between the access port l4a and the distal port 20a.

The guiding sheath lOa may also include an inflation lumen 30a that extends between the inflation port l6a and the balloon l8a. In the embodiment disclosed in Figs. 1-7, the inflation lumen 30a is located between the inner tube l3a and the outer tube l3b. As illustrated, the inflation lumen 30a is not in fluid communication with the working lumen 22a. However, as will be discussed with regards to Figs. 8-11B, embodiments may be arranged and configured whereby the working lumen 22 is in fluid communication with the inflation lumen 30.

Now with reference to Figs. 1B and 1C, a cross-sectional side view of section 1-1 is illustrated. As shown, the balloon l8a may move between a deflated state (Fig. 1B) and an inflated state (Fig. 1C) in response to fluid and/or media traveling through the inflation lumen 30a and into the balloon l8a. In such embodiments, the inflation lumen 30a is not in fluid communication with working lumen 22a. In this regard, the balloon l8a may be arranged and configured to inflate and deflate irrespective of any interaction with the working lumen 22a.

With reference to Fig. 2, the guiding sheath lOa may include a reinforcement layer 31 located between the inner tube l3a and the outer tube l3b. The reinforcement layer 31 may be arranged and configured to enable flow of at least one of fluid and media through the inflation lumen 30a to thereby inflate the balloon l8a. The reinforcement layer 31 may be comprised of coiled and/or braided strands of material (e.g. stainless steel or polymer wire).

The elongated sheath l2a 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 lOa may be positioned at a target site, whereby the balloon l8a is inflated to occlude blood flow through the patient’s artery. The working lumen 22a, via the access port l4a, 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.

Now with reference to Fig. 4, the elongated sheath l2a may define an outer diameter 34a that is less than or equal to 0.104 inches. In this regard, the elongated sheath l2a may fit through an 8 Fr opening. It should be appreciated that the opening may be a puncture, cavity, and/or aperture whether in the patient’s vasculature or in any medical device used to treat the embolus. Moreover, the working lumen 22a may define an inner diameter 36a less than or equal to 0.090 inches. In some embodiments, the inner diameter 36a of the working lumen 30a is greater than or equal to 0.087 inches. However, it should be appreciated that the outer and inner diameters 34a, 36a may define any such dimension. For example, the outer diameter 34a may be greater than or equal to 0.104 inches. Additionally, in some embodiments, the inner diameter 36a may be less than or equal to 0.088 inches, or greater than or equal to 0.090 inches.

As shown in Fig. 5, the elongated sheath l2a may have a generally constant outer diameter along its working length 38a. However, some embodiments may have varying diameters along the working length 38. With additional reference to Fig. 6, the elongated sheath l2a may have a working length 38a that 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 carotid artery. Even still, in some embodiments, the working length 38a may be long enough to enable the distal end to reach a petrous portion 54, cavernous portion 56, and/or a cerebral portion 58 of a patient’s internal carotid artery 50 from the carotid artery. It should be appreciated that the location of the dashed boxes in Fig. 6 are not exact and merely intended to distinguish between the various portions of the patient’s internal carotid artery.

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.

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 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.

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 Figs. 7A and 7B, the balloon may be arranged and configured to extend around and beyond a distal tip 59 of the elongated sheath 12. With specific reference to Fig. 7B, the balloon 18 may define a funnel- shaped opening into the distal port 20 when the balloon 18 is in an inflated state. The funnel-shape may thereby ensure that the embolus and any harmful tissue is effectively directed and guided into the working lumen 22 for complete removal from the patient’s artery. Furthermore, the funnel-shape may safeguard the balloon 18 so that the balloon 18 does not occlude the working lumen 22 and any instrumentation or tissue that needs to travel through the working lumen 22.

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. Tip-Occluding Embodiments

Another balloon guiding sheath lOb in accordance with embodiments of the invention is now described with reference to Figures 8-13C. As shown in Fig. 8, the guiding sheath lOb includes an elongated sheath l2b having a proximal end and a distal end. The guiding sheath lOb may include an access port l4b located on the proximal end and an inflation port l6b on the proximal end. The guiding sheath lOb may include an inflatable balloon 18b coupled to the distal end and a distal port 20b located on the distal end. The elongated sheath l2b may be 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 18b at the target site of the embolus.

Similar to embodiment lOa, the guiding sheath lOb may also include a working lumen 22b extending through the elongated sheath l2b between the access port l4b and the distal port 20b. The guiding sheath lOb may include an inflation lumen 30b extending through the elongated sheath l2b between the inflation port l6b and the balloon l8b. Unlike embodiment lOa, guiding sheath lOb 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 l2b, 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.

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 l2b.

To further describe the relationship between the working lumen 22b and the inflation lumen 30b we now refer to Fig. 9. The elongated sheath l2b may define a central axis 60 extending from the proximal end to the distal end. As shown in Fig. 9, at least a portion of the working lumen 22b may overlap the central axis 60 of the elongated sheath l2b, while the inflation lumen 30b does not overlap the central axis 60 of the elongated sheath l2b.

With continued reference to Fig. 9, the elongated sheath l2b may define an outer diameter 34b less than or equal to 0.104 inches such that the elongated sheath l2b fits through an 8 Fr opening. Additionally, the working lumen 30b may define an inner diameter 36b less than or equal to 0.090 inches. In some embodiments, the inner diameter 36b of the working lumen 30b is greater than or equal to 0.087 inches. Similar to above, it should be appreciated that the outer and inner diameters 34b, 36b may define any such dimension. For example, the outer diameter 34b may be greater than or equal to 0.104 inches. Additionally, in some embodiments, the inner diameter 36b may be less than or equal to 0.087 inches, or greater than or equal to 0.090 inches.

Similar to the embodiment described above, the elongated sheath l2b also has a generally constant outer diameter along its working length 38b. Additionally, the elongated sheath l2b 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.

Furthermore, the balloon 18b may extend around and beyond a distal tip 59 of the elongated sheath l2b and define a funnel-shaped opening into the distal port 20b when the balloon 18b is in an inflated state. Moreover, the elongated sheath l2b may also be arranged and configured to have sufficient stiffness and tip flexibility to enable insertion of the working length 38b of the sheath l2b 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.

Now with reference to Fig. 10, the working lumen 22b may define various portions having different size diameters. As shown, the working lumen 22b may comprise a first portion 70 defining a first inner diameter 72 and a second portion 74 defining a second inner diameter 76. As shown, the second portion 74 is located proximal to the first portion 70. The second inner diameter 76 may be greater than the first inner diameter 72.

As shown in Figs. 11 A and 11B, the balloon guiding sheath lOb may include a first inflation hole 80 extending from the working lumen 22b through a sidewall of the elongated sheath l2b. In this regard, when a guide wire 84 is inserted into the working lumen 22b and out through the distal port 20b, the distal port 20b thereby creates a seal against the guide wire 84. 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 first inflation hole 80 and into the balloon 18b to thereby inflate the balloon 18b. While many of the figures show the balloon 18 disposed flush with the distal port 20, it should be appreciated that the balloon 18 may be offset by any distance, as shown in Figs. 11 A and 11B. In some embodiments, the balloon 18 is offset about 4 millimeters from the distal port 20.

Furthermore, the guiding sheath lOb may include a second inflation hole 82 extending from the working lumen 22b through the sidewall of the elongated sheath l2b. 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 Figs. 11A and 11B, the first and second inflation holes 80, 82 may be horizontally offset from each other. However, in some embodiments, the first and second inflation holes 80, 82 are substantially horizontally aligned with each other. The inflation holes may be staggered to thereby inflate various portions of the balloon at different times.

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.

Now with reference to Figs. 12A and 12B, the guiding sheath lOc may include one or more inflation lumen(s) 30c extending through the elongated sheath l2c between the inflation port l6c and the balloon l8c. As shown, the inflation lumen 30c may comprise a distal inflation port 21 extending through an endwall of the elongated sheath l2c. In this regard, the inflation lumen 30c is not in fluid communication with the working lumen between the access port l6c and the distal port 20c.

The balloon guiding sheath lOc may also include one or more inflation hole(s) 80, 82 extending from the inflation lumen 30c through a sidewall of the elongated sheath l2c. 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 l8c to thereby inflate the balloon l8c, as shown in Fig. 12B. As further shown in Figs. 12A and 12B, the elongated sheath l2c may have a generally constant outer diameter along its working length.

Figs. 13A, 13B, and 13C illustrate a variety of cross-sectional views of section 13- 13 of the elongated sheath l2c. As shown, the guiding sheath 10 may include one or more inflation lumen(s) 30c arranged in a variety of configurations. For example, as shown in Fig. 13A, the elongated sheath l2c may include six inflation lumens 30c arranged in any pattern around the working lumen 22c. As illustrated in Fig. 13B, the elongated sheath l2c may include two inflation lumens 30c arranged on opposite sides of the working lumen 22c. Even still, as shown in Fig. 13C, the elongated sheath l2c may include one inflation lumen 30c adjacent an oval-shaped working lumen 22c that is off-center with respect to the central axis. It should be appreciated that the working lumen 22c may define any such cross-sectional shape, such as circular, round, oblong, and even shapes such as triangular, rectangular, and any shape defining five or more sides.

As shown in Figs. 14A and 14B, the elongated sheath l2d may define another embodiment whereby the balloon 18d extends along the entire outer surface area, or at least more than half of the outer surface area, of the elongated sheath l2d. In such embodiments, the balloon 18d may extend all the way from the access port l4d to the distal port 20d. The balloon 18d material may be arranged and configured such that certain sections of the balloon may inflate/deflate at predetermined zones. Some embodiments, with respect to Fig. 14A and 14B, may be devoid of inflation holes 80, 82.

Additionally, in some embodiments, the entire elongated sheath 12 is foldable, or self-expanding. This may allow the 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.

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.

Additionally, because of the need to minimize air in the balloon 18 during use, the 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.

Method Embodiments

With reference to Figs. 15-18, the disclosure also includes methods for using the balloon guiding sheaths lOa, lOb as described above. Some methods may be implemented with either guiding sheath lOa or lOb. However, some methods may only be implemented with embodiment lOb. Each circumstance will be described in detail below.

As shown in Fig. 15, methods may include inserting the guiding sheath lOa, lOb directly into a patient’s vasculature through an arteriotomy in a patient’s carotid artery (at step 1500). Methods may also include advancing the guiding sheath lOa, lOb through the patient’s vasculature and positioning the distal end in a target site of a patient’s internal carotid artery 50 (at step 1502). Once the guide sheath lOa, lOb has been advanced, methods may include inflating the balloon l8a, 18b via the inflation lumen 30a, 30b (at step 1504). As previously disclosed, the target site may be at least a cervical portion 52, petrous portion 54, cavernous portion 56, and a cerebral portion 58 of the internal carotid artery 50.

Furthermore, methods may include applying relatively low pressure to the access port l4a, l4b to suction an embolus (at step 1506). Methods may thereby include deflating the balloon l8a, 18b (at step 1508) and thereby withdrawing the guiding sheath lOa, lOb through the arteriotomy in the carotid artery (at step 1510).

Now with reference to Fig. 16, after positioning the distal end at the target site, the user may insert a tool into the guiding sheath lOa, lOb through the access port l4a, l4b (at step 1600). The user may advance the tool through the guiding sheath lOa, lOb (at step 1602) and actuate the tool to retrieve the embolus (at step 1604). Once the embolus has been retrieved, the tool may be withdrawn from the guiding sheath lOa, lOb (at step 1606). In order to complete the embolus removal, the user may thereby deflate the balloon l8a, 18b (at step 1608) and withdraw the guiding sheath lOa, lOb through the arteriotomy in the carotid artery (at step 1610).

As shown in Fig. 17, the method may also include specific method steps to be performed only with balloon guiding sheath lOb. In some embodiments, methods include inserting the guiding sheath lOb directly into a patient’s vasculature through an arteriotomy in a patient’s carotid artery (at step 1700). The user may then advance the guiding sheath 10b through the patient’ s vasculature and position the distal end in a target site of a patient’ s internal carotid artery (at step 1702).

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.

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).

As illustrated in Fig. 18, methods may include steps for using a tip-occluding embodiment whereby the inflation lumen 30c is not in fluid communication with the working lumen 22c. Using such embodiments, methods may include inserting the guiding sheath lOc directly into a patient’s vasculature through an arteriotomy in a patient’s carotid artery (at step 1800). Methods may also include advancing the guiding sheath lOc through the patient’s vasculature and positioning the distal end at a target site of a patient’s internal carotid artery (at step 1802).

Once the guiding sheath lOc 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 l8c to thereby inflate the balloon l8c (at step 1808) and thereby inflating the balloon l8c via the inflation lumen 30c (at step 1810).

In order to deflate the balloon l8c, 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 l8c (at step 1814).

Interpretation

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.

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.

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.

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.

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.

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.

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.

Implementation

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.