US20230310800A1 - Devices for assisting with advancement of catheters and related systems and methods - Google Patents
Devices for assisting with advancement of catheters and related systems and methods Download PDFInfo
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- US20230310800A1 US20230310800A1 US18/332,290 US202318332290A US2023310800A1 US 20230310800 A1 US20230310800 A1 US 20230310800A1 US 202318332290 A US202318332290 A US 202318332290A US 2023310800 A1 US2023310800 A1 US 2023310800A1
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Images
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/0067—Catheters; Hollow probes characterised by the distal end, e.g. tips
- A61M25/0074—Dynamic characteristics of the catheter tip, e.g. openable, closable, expandable or deformable
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/0067—Catheters; Hollow probes characterised by the distal end, e.g. tips
- A61M25/0068—Static characteristics of the catheter tip, e.g. shape, atraumatic tip, curved tip or tip structure
- A61M25/0069—Tip not integral with tube
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/0067—Catheters; Hollow probes characterised by the distal end, e.g. tips
- A61M25/0074—Dynamic characteristics of the catheter tip, e.g. openable, closable, expandable or deformable
- A61M25/0075—Valve means
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- A—HUMAN NECESSITIES
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- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/0067—Catheters; Hollow probes characterised by the distal end, e.g. tips
- A61M25/008—Strength or flexibility characteristics of the catheter tip
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- A—HUMAN NECESSITIES
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- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/0102—Insertion or introduction using an inner stiffening member, e.g. stylet or push-rod
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/09—Guide wires
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/0067—Catheters; Hollow probes characterised by the distal end, e.g. tips
- A61M25/0074—Dynamic characteristics of the catheter tip, e.g. openable, closable, expandable or deformable
- A61M2025/0079—Separate user-activated means, e.g. guidewires, guide tubes, balloon catheters or sheaths, for sealing off an orifice, e.g. a lumen or side holes, of a catheter
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/0067—Catheters; Hollow probes characterised by the distal end, e.g. tips
- A61M25/008—Strength or flexibility characteristics of the catheter tip
- A61M2025/0081—Soft tip
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- A—HUMAN NECESSITIES
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- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M25/00—Catheters; Hollow probes
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/0105—Steering means as part of the catheter or advancing means; Markers for positioning
- A61M25/0108—Steering means as part of the catheter or advancing means; Markers for positioning using radio-opaque or ultrasound markers
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- A—HUMAN NECESSITIES
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- A61M31/00—Devices for introducing or retaining media, e.g. remedies, in cavities of the body
- A61M31/005—Devices for introducing or retaining media, e.g. remedies, in cavities of the body for contrast media
Definitions
- the various embodiments herein relate to advancement devices for assisting with advancement of a catheter through a blood vessel, including a tortuous or narrow blood vessel, while reducing the risk of damaging the inner wall of the blood vessel with the distal end of the catheter.
- a guiding catheter is a standard catheter that is generally a long tube with a pre-determined shape. It is typically used to gain access to the vasculature—such as a coronary artery—by advancing the catheter through the access point during an interventional procedure.
- the pre-determined, typically curved shape of the catheter facilitates accessing a specific branch or other portion of the vasculature that requires such a curvature in the catheter.
- a pre-shaped, curved distal end of a catheter including, but not limited to, a guiding catheter or sheath
- the advancement of the catheter can be impeded by the distal end contacting and damaging the inner wall of the vessel through which the catheter is being advanced.
- the pre-shaped distal end 12 of the guiding catheter 10 can potentially contact the inner wall 16 of the blood vessel 14 (at the area A as shown) as the catheter 10 is advanced distally through the vessel 14 (typically over a guidewire such as the guidewire depicted in FIGS.
- the balloon catheter 20 can be advanced through the inner lumen 24 of the guiding catheter 10 (or other type of catheter or sheath), positioned such that the balloon 22 is protruding from the distal end of the catheter 10 such that a portion of the balloon 22 is positioned within the distal end of the catheter 10 and a portion extends out of the distal end of the catheter 10 , and then the balloon 22 is inflated.
- the guiding catheter 10 can be advanced through the blood vessel 14 with the balloon 22 positioned to prevent direct contact between the distal end of the catheter 10 and the inner wall 16 of the vessel 14 , thereby preventing the “razor effect.”
- the balloon 22 is deflated and the balloon catheter 20 is withdrawn from the guiding catheter 10 so that the guiding catheter 10 is ready for use.
- any balloon catheter discussed herein can be any known balloon catheter, including, for example, a percutaneous transluminal coronary angioplasty (“PTCA”) balloon catheter.
- PTCA percutaneous transluminal coronary angioplasty
- balloon catheters are expensive.
- Another disadvantage is that the positioning of a balloon catheter at the distal end of the guiding catheter makes it difficult to inject any contrast or other fluid through the guiding catheter and past the inflated balloon of the balloon catheter. That is, the balloon must be deflated in order to allow for injection and then re-inflated.
- An additional disadvantage is that most known balloon catheters (including most PTCA balloon catheters) require the exchange of guidewires in the middle of the procedure.
- Another disadvantage relates to the use of a advancement device and the tension during introduction of the guide catheter between the need to attach the attachment device to the guide catheter and the need to be able to move the catheter in relation to the guidewire. That is, in use as best shown in FIG. 10 , the guiding catheter 10 is typically positioned within the blood vessel of the patient by first introducing a guidewire 18 and then advancing the catheter 10 over the stationary guidewire 18 . To accomplish this, the proximal valve 26 of the catheter 10 has an open configuration such that the guidewire 18 can pass through the valve 26 while allowing the passage of as little fluid as possible (in contrast to its closed configuration in which the valve 26 is fixedly coupled to the guidewire 18 and creates a fluidic seal therebetween).
- catheter insertion or advancement devices for use in assisting with advancement of a catheter through a blood vessel while reducing damage to the inner wall of the blood vessel.
- a catheter advancement assistance device comprises an elongate shaft, a capsule fixedly attached to a distal end of the elongate shaft, and an attachment tube associated with a proximal portion of the elongate shaft.
- the capsule comprises a guidewire lumen defined through the capsule, and an outer diameter substantially similar to an inner diameter of a catheter such that the capsule is sized to be positionable through the catheter.
- Example 2 relates to the device according to Example 1, wherein the attachment tube further comprises a tube body, a lumen defined within the tube body, a distal opening defined in a distal end of the tube body, wherein the distal opening is in fluidic communication with the lumen, and a proximal opening defined in a proximal end of the tube body, wherein the proximal opening is in fluidic communication with the lumen.
- Example 3 relates to the device according to Example 1, wherein the attachment tube is a compressible attachment tube.
- Example 4 relates to the device according to Example 3, wherein the compressible attachment tube comprises an elongate opening defined along a length of the compressible attachment tube.
- Example 5 relates to the device according to Example 1, wherein the capsule further comprises a distal portion, and a neck extending proximally from the distal portion, wherein the neck has a smaller diameter than the distal portion.
- Example 6 relates to the device according to Example 1, wherein the guidewire lumen has an inner diameter that is larger than an outer diameter of a standard guidewire.
- Example 7 relates to the device according to Example 1, wherein the guidewire lumen is sized to allow fluid to flow through the lumen when a standard guidewire is positioned therein.
- Example 9 relates to the device according to Example 1, wherein the capsule further comprises a lip formed around at least a portion of an outer circumference of the capsule.
- Example 10 relates to the device according to Example 9, wherein the lip comprises at least two lip segments formed around the outer circumference of the capsule.
- Example 11 relates to the device according to Example 1, wherein the capsule further comprises an expanded distal section, wherein the expanded distal segment is substantially elastic, a non-expanded proximal section having a smaller diameter than the expanded distal section, and a lip formed at a juncture between the expanded distal section and the non-expanded proximal section, wherein the lip is formed around at least a portion of a circumference of the capsule.
- Example 12 relates to the device according to Example 1, wherein the capsule further comprises a substantially elastic ridge formed around at least a portion of an outer circumference of the capsule.
- Example 13 relates to the device according to Example 12, wherein the substantially elastic ridge comprises at least two substantially elastic rig segments formed around the outer circumference of the capsule.
- Example 14 relates to the device according to Example 1, wherein the capsule further comprises a slot defined in a distal end of the capsule, whereby the distal end of the capsule is compressible.
- Example 15 relates to the device according to Example 1, wherein the capsule further comprises a void defined in a portion of the capsule, whereby an area of the capsule near the void is compressible.
- a catheter advancement assistance device comprises a push rod, a body fixedly attached to a distal end of the push rod, and a compressible attachment tube associated with a proximal portion of the push rod.
- the body comprises a distal plug portion, a proximal neck portion, wherein the proximal neck portion has a smaller diameter than the distal plug portion, and a guidewire lumen defined through the body.
- Example 18 relates to the device according to Example 16, wherein the body further comprises a channel defined longitudinally along an outer surface of the body.
- Example 19 relates to the device according to Example 16, wherein the body further comprises a seating component formed around at least a portion of an outer circumference of the capsule.
- Example 20 relates to the device according to Example 19, wherein the seating component comprises a lip or a ridge.
- a method of assisting advancement of a catheter through a blood vessel comprises inserting an advancement assistance device into a lumen of the catheter, the advancement assistance device comprising an elongate shaft, a body fixedly attached to a distal end of the elongate shaft, and an attachment tube associated with a proximal portion of the elongate shaft.
- the body comprises a distal plug portion, a proximal neck portion, wherein the proximal neck portion has a smaller diameter than the distal plug portion, and a guidewire lumen defined through the body.
- the method further comprises urging the advancement assistance device distally into the lumen of the catheter until a distal portion of the distal plug portion extends out of a distal opening in the catheter, a proximal portion of the distal plug portion is positioned within the lumen of the catheter, and the attachment tube is disposed within a proximal valve of the catheter, attaching the proximal valve to the attachment tube, urging the catheter distally into the blood vessel to a target site over a guidewire, and retracting the advancement assistance device from the catheter.
- Example 23 relates to the method according to Example 22, further comprising urging the advancement assistance device distally until the distal plug portion extends out of the distal opening, whereby space is provided between the body and the distal opening, urging contrast solution distally through the catheter and through the space between the body and the distal opening and into the blood vessel, and urging the advancement assistance device proximally until the distal portion of the distal plug portion extends out of the distal opening in the catheter and the proximal portion of the distal plug portion is positioned within the lumen of the catheter.
- the method further comprises urging the advancement assistance device distally into the lumen of the catheter until a distal portion of the body extends out of a distal opening in the catheter, a proximal portion of the body is positioned within the lumen of the catheter, and the attachment tube is disposed within a proximal valve of the catheter, attaching the proximal valve to the attachment tube, urging the catheter distally into the blood vessel to a target site over a guidewire, and retracting the advancement assistance device from the catheter.
- Example 25 relates to the method according to Example 24, further comprising urging contrast solution distally through the catheter and through the guidewire lumen and into the blood vessel.
- Example 26 relates to the method according to Example 24, wherein the body further comprises a channel defined longitudinally along an outer surface of the body.
- Example 27 relates to the method according to Example 26, further comprising urging contrast solution distally through the catheter and through the channel and into the blood vessel.
- Example 28 relates to the method according to Example 24, wherein the body further comprises a seating component formed around at least a portion of an outer circumference of the body.
- Example 29 relates to the method according to Example 28, wherein the seating component comprises a lip or a ridge.
- Example 30 relates to the method according to Example 28, further comprising urging the advancement assistance device distally through the lumen of the catheter until the seating component is urged out of the distal opening in the catheter, and urging the advancement assistance device proximally until the seating component contacts the distal end of the catheter.
- Example 31 relates to the method according to Example 24, wherein the attachment tube is a compressible attachment tube, wherein the attaching the proximal valve to the attachment tube causes the compression of the compressible attachment tube.
- FIG. 1 A is a cross-sectional view of a known catheter being advanced through a blood vessel.
- FIG. 1 B is a cross-sectional view of a known balloon catheter positioned within a known catheter.
- FIG. 10 is a cross-sectional view of a known catheter with a proximal valve.
- FIG. 2 is a cross-sectional side view of a catheter advancement device positioned within a catheter, according to one embodiment.
- FIG. 3 A is a cross-sectional side view of a distal portion of a plug of a catheter advancement device, according to one embodiment.
- FIG. 3 B is a cross-sectional side view of a distal portion of a plug of a catheter advancement device, according to another embodiment.
- FIG. 4 is a cross-sectional side view of a catheter advancement device having visualization markers and positioned within a catheter, according to one embodiment.
- FIG. 5 is a cross-sectional side view of a catheter advancement device extending out of a distal end of a catheter, according to one embodiment.
- FIG. 6 is a cross-sectional side view of a catheter advancement device positioned within a catheter, according to another embodiment.
- FIG. 7 A is a cross-sectional side view of a catheter advancement device positioned within a catheter, according to a further embodiment.
- FIG. 7 B is a cross-sectional front view of the catheter advancement device of FIG. 7 A .
- FIG. 8 is a cross-sectional side view of a catheter advancement device positioned within a catheter, according to yet another embodiment.
- FIG. 9 is a cross-sectional side view of a catheter advancement device positioned within a catheter, according to an alternative embodiment.
- FIG. 10 A is a cross-sectional side view of a plug, according to another alternative embodiment.
- FIG. 10 B is a cross-sectional front view of the plug of FIG. 10 A .
- FIG. 11 A is a cross-sectional side view of a plug, according to another alternative embodiment.
- FIG. 11 B is a further cross-section side view of the plug of FIG. 11 A .
- FIG. 12 is a cross-sectional side view of a method of making a catheter advancement device, according to one embodiment.
- FIG. 13 A is a cross-sectional side view of a catheter advancement device having an attachment tube, according to one embodiment.
- FIG. 13 B is a cross-sectional side view of the catheter advancement device of FIG. 13 A disposed within a guiding catheter, according to one embodiment.
- FIG. 14 is an expanded side view of an attachment tube on a catheter advancement device, according to one embodiment.
- FIG. 15 A is an expanded side view of another attachment tube on a catheter advancement device, according to a further embodiment.
- FIG. 15 B is a cross-sectional view along the longitudinal axis of the attachment tube of FIG. 15 A , according to one embodiment.
- FIG. 16 is a cross-sectional side view of another catheter advancement device having an attachment tube disposed within a guiding catheter, according to another embodiment.
- the various embodiments disclosed or contemplated herein relate to catheter assertion or advancement devices and related methods for assisting in the advancement of a cardiovascular catheter through a blood vessel, including, for example, a cardiovascular guiding catheter or sheath with a curved shape, while reducing or eliminating the risk of damage to the blood vessel inner wall.
- the various embodiments include a distal capsule and a push rod attached thereto.
- Alternative embodiments include an attachment tube disposed at a proximal end of the push rod.
- FIG. 2 depicts, according to one embodiment, a catheter advancement device 30 (also referred to as an “insertion device,” a “catheter insertion device,” or an “advancement device”) for assisting with or use in advancing a catheter, such as, for example, a guiding catheter.
- the device 30 has a capsule (also referred to herein as a “body” or “insertion body”) 32 with a partially rounded distal end 33 and a push rod (also referred to herein as an “elongate component”) 34 coupled thereto.
- the capsule 32 has a lumen 36 defined therethrough that is configured to allow for passage of a guidewire 38 therethrough as shown.
- the push rod 34 is embedded in or otherwise fixedly coupled to the capsule 32 such that appropriate forces can be applied at the proximal end of the push rod 34 by a user (such as a surgeon or medical professional) to urge the capsule 32 distally or proximally during use.
- the distal end of the capsule insertion device 30 can be advanced through the inner lumen 42 of a guiding catheter 40 (by a user holding the proximal end of the rod 34 ) and positioned such that the capsule 32 is protruding from the distal end of the catheter 40 .
- a portion of the capsule 32 is positioned within the distal end of the catheter 40 and a portion extends out of the distal end of the catheter 40 .
- the user locks the device 30 into position in relation to the catheter 40 . That is, according to one embodiment, the user attaches the proximal end of the rod 34 to the catheter 40 in any known fashion.
- a known locking mechanism at the proximal end of the catheter 40 (such as a Tuohy-Borst adapter, for example) is used to lock the device 30 to the catheter 40 .
- the locking mechanism can be a proximal valve similar to the proximal valve 26 discussed above in the Background. As such, the advancement device 30 is locked or otherwise attached to the catheter 40 such that the device cannot move translationally in relation to the catheter 40 .
- the guiding catheter 40 can be advanced through a blood vessel with the capsule 32 positioned to prevent direct contact between the distal end of the catheter 40 and the inner wall of the vessel, thereby preventing the “razor effect.”
- the capsule catheter 30 is withdrawn from the guiding catheter 40 by a user pulling the push rod 34 in the proximal direction so that the guiding catheter 40 is ready for use.
- the capsule body 32 can be a solid body with a lumen 36 defined therethrough as shown.
- the capsule (such as capsule 32 ) can be any component or body that can be inserted through a guiding catheter and positioned to reduce or eliminate the razor effect.
- the capsule is non-inflatable.
- the capsule has a substantially cylindrical shape.
- the capsule can have any known shape that allows it to be advanced through a catheter and positioned out of the distal end thereof as described herein.
- the outer diameter of the body 32 can vary or have specific features as described herein depending on the desired functionality of the body 32 .
- the capsule 32 has a larger distal portion (also referred to herein as a “plug,” “distal plug,” or “distal body”) 44 and a smaller proximal portion (also referred to as a “neck,” or “tail”) 46 .
- the distal body 44 has a larger diameter than the neck 46 .
- the capsule 32 is a single integral body 32 having the larger distal portion 44 and the smaller proximal portion 46 as shown.
- the capsule 32 can have two separate portions coupled together: the first larger distal portion 44 and the second smaller proximal portion 46 attached thereto.
- the capsule 32 has an outer diameter ranging from about 0.05 inches to about 0.3 inches. Alternatively, the outer diameter ranges from about 0.065 inches to about 0.105 inches. In a further implementation, the capsule 32 has an outer diameter that fits snugly within (makes contact with the inner wall of) any cardiovascular guiding catheter, such as, for example, the Medtronic LauncherTM or Cordis VistaBriteTM 5 French to 8 French guiding catheters. Further, the capsule 32 can be sized to fit snugly within any guiding catheter having any size ranging from about 4 French to about 22 French.
- the “snug” fitting in this embodiment and in any other capsule embodiment disclosed or contemplated herein is a fitting of the capsule (such as capsule 32 ) within the catheter such that the outer surface of the capsule makes sufficient contact with the inner wall of the catheter to prevent passage of fluid therebetween.
- any capsule embodiment disclosed or contemplated herein is made of a polymeric material.
- the capsule can be made of polyethylene, Pebax, Nylon, polyester, or any other polymeric material or combination thereof.
- the capsule can also be made of metal or any other known material that can be used for medical devices.
- the capsule (such as capsule 32 ) can be made of two or more materials. More specifically, in certain embodiments, the capsule can be made of two or more materials having differing stiffness and/or flexibility such that one portion of the capsule (such as the distal end, for example) is stiffer, more rigid, and/or less flexible than another portion. In other words, the two or more materials can be used to create a capsule that has stiffness, rigidity, or flexibility that varies along the length of the capsule.
- any capsule embodiment disclosed or contemplated herein can also have a coating disposed on the outer surface of the capsule to increase the lubricity of the capsule.
- the coating can be hydrophilic or hydrophobic.
- the push rod (such as push rod 34 ) can be made of metal.
- the push rod can be made of any known material that can be used to make an elongate component with sufficient column strength such that the component can be used to advance a capsule through the lumen of a guiding catheter while also having some flexibility.
- the push rod also referred to as a “proximal elongate member” or “control rod” or “manipulation rod” in any embodiment herein can be any elongate component that is coupled to the proximal end of the capsule and can withstand the forces necessary for a user to urge the rod distally or proximally to move the capsule through a guiding catheter as described herein.
- the push rod can be integral with the capsule.
- various embodiments include a push rod and capsule formed together of the same materials such that the push rod is integral with the capsule.
- the capsule (such as capsule 32 ) can take a variety of shapes, so long as the capsule can be positioned out of the distal end of a guiding catheter as described herein and help with advancement thereof through a blood vessel.
- capsule 50 as best shown in FIG. 3 A according to one embodiment has a tapered distal end 52
- capsule 54 as best shown in FIG. 3 B in accordance with another implementation has a rounded distal end 56 .
- the capsule can have a distal end with an angled shape, a spherical shape, or any other known shape that helps to advance the guiding catheter when the capsule is positioned out of the distal end of the guiding catheter.
- any advancement device disclosed or contemplated herein can have at least one visualization marker disposed on the device.
- the capsule insertion device 60 has two visualization markers 64 A, 64 B.
- the first visualization marker 64 A is disposed at or near the distal end of the distal plug 62 A of the capsule 62
- the second marker 64 B is disposed on the neck 62 B of the capsule 62 .
- any device embodiment can have one marker or three or more markers. It is understood that the markers 64 A, 64 B (and any markers incorporated into any capsule insertion device embodiment as disclosed or contemplated herein) can be radiopaque markers.
- the markers can be made of any known material for a visualization marker.
- the catheter advancement device 80 has a capsule 82 with a distal body 82 A and a neck 82 B similar or identical to the capsule 32 described above.
- the capsule device 80 is urged distally (by a user urging the proximal end of the push rod 90 distally) such that the body 82 A of the capsule 82 is urged distally out of the lumen 86 of the guiding catheter 84 as shown in FIG. 5 .
- the capsule 82 is urged distally until the body 82 A is urged out of the lumen 86 such that space is created between the opening 88 of the guiding catheter 84 and the body 82 A, thereby making it possible for contrast to exit from the opening 88 as represented by arrows A.
- the capsule 82 need not be urged distally so far that the neck 82 B also exits the lumen 86 . Instead, the smaller diameter of the neck 82 B allows for sufficient space between the neck 82 B and the opening 88 to allow for contrast to exit the lumen 86 .
- the capsule 102 need not be advanced distally out of the lumen 110 of the guiding catheter 108 .
- a capsule device 100 has a capsule 102 with a lumen 104 defined therein that has a larger inner diameter than is necessary to accommodate solely a guide wire 106 .
- the lumen 104 has a sufficient inner diameter to provide space for the guide wire 106 while also having sufficient additional space to allow for contrast solution to flow distally out of the guiding catheter 108 through the capsule lumen 104 and into the vasculature as represented by arrows B.
- the inner diameter of the lumen 104 ranges from about 0.01 inches to about 0.05 inches.
- the inner diameter ranges from about 0.02 inches to about 0.04 inches.
- the inner diameter of the lumen 104 is sufficiently large to receive a guidewire of any size ranging from 0.01 inches to 0.04 inches and still has at least a 0.004 inch diameter of space between the guidewire and the inner wall of the lumen 104 .
- the capsule 102 need not be moved in order to inject the contrast solution. Instead, the capsule 102 can remain in place while the contrast solution flows distally through the lumen 110 of the guiding catheter 108 and through the lumen 104 of the capsule 102 and out into the vasculature.
- the capsule device 120 has a capsule 122 with a channel (also referred to as a “slot” or “trough”) 126 defined longitudinally along the outer surface 124 of the capsule 122 (as best shown in FIG. 7 B ).
- the channel 126 defines a space between the capsule 122 and the inner surface of the lumen 130 of the guiding catheter 128 through which contrast solution can flow distally out into the vasculature as represented by arrows C.
- the channel 126 has an inner diameter ranging from about 0.002 inches to about 0.02 inches.
- the inner diameter ranges from about 0.004 inches to about 0.008 inches.
- the capsule 122 need not be moved in order to inject the contrast solution. Instead, the capsule 122 can remain in place while the contrast solution flows distally through the lumen 130 of the guiding catheter 128 and through the channel 126 of the capsule 122 and out into the vasculature.
- the channel 126 can be any feature or configuration on the capsule 122 or the outer surface 124 thereof that allows fluid flow between the capsule 122 and the inner wall of the lumen 130 .
- Both the larger lumen 104 of the capsule device 100 embodiment and the channel 126 of the capsule device 120 implementation make it easy for a user to inject contrast solution, as discussed above.
- these two embodiments can also assist with limiting contrast fluid use. Injection of excess contrast fluid into the vasculature of a patient during an interventional procedure can cause health issues for the patient, including contrast-induced nephropathy.
- the lumen 104 of a predetermined diameter in the device 100 embodiment or the channel 126 of a predetermined depth or diameter in the device 120 embodiment both provide mechanisms for injecting solution in known, more limited amounts than those injected when using a balloon catheter as described above.
- another capsule for use with any of the capsule device embodiments disclosed or contemplated herein—that has a seating component defined or disposed around an outer surface of the capsule that can assist with positioning the capsule in relation to the guiding catheter during use and further can create a smoother or more streamlined transition from the outer surface of the capsule to the outer surface of the guiding catheter in which the capsule is positioned.
- any of the seating components disclosed or contemplated herein can be defined or disposed around the entire 360 degree circumference of the capsule.
- any such components can be defined or disposed around only a portion of the circumference of the capsule.
- any such seating component can be defined or disposed intermittently around the circumference of the capsule such that there are two or more seating components disposed or defined thereon such that they are positioned at different locations along and around the circumference thereof.
- FIG. 8 shows one embodiment of a capsule 140 having a seating component (or “seating feature”) 144 .
- the seating component 144 is a lip 144 created by the capsule 140 having an expanded section 142 (which is a portion of the capsule 140 that has an increased diameter in comparison to the rest of the capsule 140 ). That is, the lip 144 is formed at the juncture of the expanded section 142 and the non-expanded section of the capsule 140 .
- the lip 144 can extend around the entire circumference, can extend around a portion of the circumference, or can constitute two or more lips 144 that are disposed or defined intermittently around the circumference.
- the expanded section 142 is a portion of the body 148 of the capsule 140 .
- the expanded section 142 can be the body itself (not shown), and the transition from the body (not shown) to the neck (not shown) constitutes the seating component.
- the expanded section 142 has an outer diameter that is substantially similar to or the same as the outer diameter of the guiding catheter 146 .
- the expanded section 142 or the entire capsule 140 has sufficient elasticity to allow for deformation of the expanded section 142 such that the capsule 140 can be advanced through the guiding catheter 146 despite the expanded section 142 having an outer diameter that is larger than the inner diameter of the guiding catheter 146 lumen.
- the capsule 140 has at least a portion of its outer surface that fits snugly within the catheter as described elsewhere herein such that no fluid can pass between the outer surface of the capsule 140 and the inner surface of the catheter.
- the capsule 140 is advanced distally through the guiding catheter 146 and positioned out of the distal opening 150 of the guiding catheter 146 according the same procedure used for all the capsule device embodiments herein.
- the capsule 140 has an expanded section 142 that has elastic characteristics that allow for the section 142 to deform sufficiently as the capsule 140 is advanced through the guiding catheter to allow for passage of the capsule 140 despite the expanded section 142 having a greater diameter than the inner diameter of the lumen of the guiding catheter 146 .
- the expanded section 142 of the capsule 140 is urged out of the opening 150 at the distal end of the guiding catheter 146 , the expanded section 142 expands back to its natural diameter, thereby causing formation of the lip 114 .
- the user can then urge the capsule 140 back in a proximal direction—via the push rod (not shown)—until the lip 114 is in contact with the guiding catheter 146 , thereby confirming for the user via increased resistance that the capsule 140 is in the desired position in relation to the guiding catheter 146 . It is understood that the user must be aware that she or he cannot use so much force that the expanded section 142 deforms and the capsule 140 is urged proximally past the desired capsule 140 position. Once the capsule 140 is positioned as desired, it can be seen in FIG.
- the expanded section 142 has a diameter that is substantially similar to the outer diameter of the guiding catheter 146 , thereby reducing the risk of the distal end of the guiding catheter 146 making contact with an inner wall of a blood vessel wall during advancement of the guiding catheter 146 .
- FIG. 9 shows a capsule 160 having a seating component 162 .
- the seating component 162 is a ridge 162 formed or disposed on the outer surface of the capsule 160 .
- the ridge 162 can extend around the entire circumference, can extend around a portion of the circumference, or can constitute two or more ridges 162 that are disposed or defined intermittently around the circumference.
- the ridge 162 has an outer diameter that is substantially similar to or the same as the outer diameter of the guiding catheter 164 .
- the ridge 162 or the entire capsule 160 has sufficient elasticity to allow for deformation of the ridge 162 such that the capsule 160 can be advanced through the guiding catheter 164 despite the ridge 162 having an outer diameter that is larger than the inner diameter of the guiding catheter 164 lumen.
- the capsule 160 has at least a portion of its outer surface that fits snugly within the catheter as described elsewhere herein such that no fluid can pass between the outer surface of the capsule 160 and the inner surface of the catheter.
- the capsule 160 is advanced distally through the guiding catheter 164 and positioned out of the distal opening 166 of the guiding catheter 164 according the same procedure used for all the capsule device embodiments herein.
- the ridge 162 on the capsule 160 has elastic characteristics that allow for the ridge 162 to deform sufficiently as the capsule 160 is advanced through the guiding catheter 164 to allow for passage of the capsule 160 despite the ridge 162 having a greater diameter than the inner diameter of the lumen of the guiding catheter 164 .
- the ridge 162 of the capsule 160 is urged out of the opening 166 at the distal end of the guiding catheter 164 , the ridge 162 expands back to its natural diameter.
- the user can then urge the capsule 160 back in a proximal direction until the ridge 162 is in contact with the guiding catheter 164 , thereby confirming that the capsule 160 is in the desired position in relation to the guiding catheter 164 . It is understood that the user must be aware that the user cannot use so much force that the ridge 162 deforms and the capsule 160 is urged proximally past the desired capsule 160 position.
- the ridge 162 has a diameter that is substantially similar to the outer diameter of the guiding catheter 164 , thereby reducing the risk of the distal end of the guiding catheter 164 making contact with an inner wall of a blood vessel wall during advancement of the guiding catheter 164 .
- a capsule 180 is provided that is a deformable or collapsible capsule 180 . That is, the capsule 180 has a slot 182 defined in the distal end of the capsule 180 along the length of the capsule 180 that also has a seating component 184 (similar to one of the seating components 144 , 162 described above). In use, the slot 182 allows for the capsule 180 to be deformed or have a smaller diameter as it is advanced through a guiding catheter, similar to the use of the capsules 140 , 160 discussed above.
- a capsule 190 is provided that is collapsible or deformable as a result of an opening 192 defined at a distal portion of the capsule along the length of the capsule 190 that also has a seating component 194 .
- the opening 192 allows for the capsule 190 to be deformed or have a smaller diameter as it is advanced through a guiding catheter, similar to the use of the capsules 140 , 160 discussed above.
- the seating components 184 , 194 described above with respect to FIGS. 10 A- 11 B can extend around the entire circumference, can extend around a portion of the circumference, or can constitute two or more such components that are disposed or defined intermittently around the circumference.
- a capsule 200 can be formed using an injection molding process.
- the starting point is an inner tube 202 , with the capsule 200 being injection molded over the inner tube 202 .
- the marker bands 204 A, 204 B are disposed over the inner tube 202 before the capsule 200 is injected molded thereon such that the material for the capsule 200 is injection molded onto the marker bands 204 A, 204 B, thereby resulting in the marker bands 204 A, 204 B being embedded in the capsule 200 .
- the push rod 206 can be embedded in the capsule 200 in a similar fashion. That is, the push rod 206 can be positioned along the inner tube 202 such that injection molding of the capsule 200 results in the push rod 206 being embedded therein.
- advancement device implementations include an attachment tube disposed at a proximal end of the push rod to allow for attaching the advancement device to the guiding catheter while the catheter can be advanced over a guidewire.
- FIG. 13 A depicts, according to one embodiment, another catheter advancement device 220 for assisting with or use in advancing a catheter, such as, for example, a cardiovascular guiding catheter.
- the device 220 has a capsule 222 and a push rod (also referred to herein as an “elongate component”) 224 coupled thereto.
- the capsule 222 can have a lumen 226 defined therethrough that is configured to allow for passage of a guidewire (not shown) therethrough.
- the various components of the device 220 are substantially similar to the various components described in the other device embodiments above and can incorporate any of the various alternative components and/or features thereof.
- the push rod 224 in this implementation has an attachment tube (also referred to as a “coupling tube”) 228 attached at a proximal end of the push rod 224 as shown such that a catheter valve (including any known valve on any known catheter as discussed elsewhere herein) can attach to the attachment tube 228 as desired and a guidewire can be moveably disposed therethrough. That is, the attachment tube 228 defines a lumen 230 disposed through the tube 228 as shown that is sized to slidably receive a guidewire.
- the lumen 274 in the tube 270 (or any lumen of any attachment tube disclosed or contemplated herein) has an inner diameter ranging from about 0.008 inches to about 0.040 inches. Alternatively, the inner diameter ranges from about 0.014 inches to about 0.030 inches. In a further alternative, the tube 270 is sized such that the lumen 274 can receive any known cardiovascular guidewire ranging in size from about 0.01 inches to about 0.04 inches.
- the advancement device 220 can be disposed in a catheter 232 .
- the known catheter 232 has a known proximal valve 234 , which is a Toughy-borst valve or any known sealable valve. It is understood that the catheter 232 can be any known cardiovascular catheter as discussed elsewhere herein.
- the attachment tube 228 is disposed along the length of the push rod 224 such that when the device 220 is disposed within the catheter 232 as shown with the capsule 222 extending partially out of the distal end of the catheter 232 , the attachment tube 228 is disposed through the valve 234 of the catheter 232 (similar to valve 26 discussed above).
- the attachment tube 228 can receive a guidewire 236 in the lumen 230 of the attachment tube 228 when the catheter 232 and advancement device 220 are disposed over the guidewire 236 as shown.
- the valve 234 of the catheter 232 can be removably coupled to the attachment tube 228 (via any known mechanism that such a valve 234 is attached to a device disposed therethrough) such that the advancement device 220 is attached to the catheter 232 and thus both are advanced together (such that the advancement device 220 does not move axially in relation to the catheter 232 ) while the guidewire 236 can be slidably disposed through the lumen 230 of the tube 228 such that the catheter 232 and device 220 can be moved in relation to the guidewire 236 .
- the attachment tube 228 makes it possible for the advancement device 220 to be attached to the catheter 232 via the coupling of the catheter valve 234 to the tube 228 while the valve 234 is not attached to the guidewire 236 (because the guidewire 236 is slidably disposed through the tube 228 ).
- FIG. 14 One specific embodiment of an attachment tube 250 that can be incorporated into any advancement device as disclosed or contemplated herein is depicted in FIG. 14 , in accordance with one implementation.
- the tube 250 is coupled to a proximal end of a push rod 256 and has an elongate tubular body 252 that defines a lumen 254 as shown.
- the tubular body 252 has a distal opening 258 and a proximal opening 260 , both of which are in fluidic communication with the lumen 254 .
- the tubular body 252 is a substantially unitary body 252 having no substantial openings along the length of the body 252 .
- the tubular body 252 is configured to be disposed through a catheter valve (such as valve 234 discussed above) such that the valve can be attached to the body 252 .
- a catheter valve such as valve 234 discussed above
- FIGS. 15 A and 15 B Another embodiment of an attachment tube 270 that can be incorporated into any advancement device as disclosed or contemplated herein is depicted in FIGS. 15 A and 15 B .
- the tube 270 is coupled to a push rod 276 and has substantially the same features and characteristics as the tube 250 discussed above, and thus the description of the similar components and features above apply equally to this tube 270 embodiment as well, except as described herein.
- the tube 270 is a compressible tube 270 .
- the specific compressible tube 270 embodiment as shown has an elongate opening 282 defined along at least a portion of the length of the body 272 . More specifically, in the specific embodiment depicted in FIGS.
- the elongate opening 282 is a slot 282 that extends along the entire length of the body 272 from the distal opening 278 to the proximal opening 280 .
- the tubular body 272 and slot 282 are configured such that the body 272 can be disposed through a catheter valve (such as valve 234 discussed above) such that when the valve is clamped down on the tubular body 272 , the body 272 is compressed as a result of the slot 282 being collapsed by the valve such that the two opposing sides of the body 272 that define the slot 282 are urged toward each other.
- a catheter valve such as valve 234 discussed above
- the slot 282 has a width that ranges from about 0.004 inches to about 0.03 inches. Alternatively, the slot 282 has a width ranging from about 0.01 inches to about 0.02 inches. In a further embodiment, the slot 282 is gap in the circumference of the body 272 such that the gap constitutes a percentage of the total circumference of the body 272 ranging from about 4 percent to about 25 percent. Regardless of the size of the slot 282 , it is understood that the terms “attachment tube” and “tube” are intended herein to encompass any tubular structure having any sized slot, gap, slit, or opening defined therein, including a tubular structure having a gap that constitutes as much as 25 percent of the circumference of the structure.
- the slot 282 can extend along a portion of the length of the body 272 .
- the opening 282 can be any opening of any shape or configuration that allows for compression of the tubular body 272 when the valve (such as valve 234 , for example) is clamped down thereon.
- any opening 282 extending along the entire length of the body 272 can not only provide compressive qualities to the body 272 , but can also assist with positioning a guidewire (such as guidewire 284 as discussed below) into the lumen 274 of the tube 270 via the opening 282 . That is, rather than having to thread a guidewire into one of the openings 278 , 280 and thereby through the entire length of the lumen 274 , a user can insert the guidewire into the lumen 274 through the opening 282 .
- the body 272 of the compressible tube 270 has some degree of compliance that allows for the body 272 to be compressed such that the lumen 274 defined therein is reduced in size (or inner diameter) as a result of the compression.
- the lumen 274 in the uncompressed state has sufficient size such that there is space between the inner wall of the lumen 274 and the guidewire 284 .
- the body 272 can be compressed by some amount such that the inner diameter of the lumen 274 is reduced while still providing sufficient space between the inner wall of the lumen 274 and the guidewire 284 such that the guidewire 284 can still move axially in relation to the body 272 while minimizing the amount of blood loss through the lumen 274 by minimizing the space between the inner wall of the lumen 274 and the guidewire 284 .
- the tube 270 and any other compressible tube embodiment as disclosed or contemplated herein can have any structure or feature that provides or allows for compression of the tube 270 .
- the advancement device 300 has an attachment tube 302 with a blocking protrusion 304 extending from a proximal end thereof.
- the blocking protrusion 304 is a disk 304 disposed at or near the proximal end of the tube 302 .
- the blocking protrusion 304 can be a lip, a rim, or any other known structural feature or component that forms a radial protrusion or extension that is disposed at a proximal end of the attachment tube 302 and has an outer diameter or dimension that is greater than the inner diameter of the valve 308 of the catheter 306 , thereby preventing the blocking protrusion 304 from passing into or through the valve 308 .
- the blocking protrusion 304 can be incorporated into the attachment tube 302 such that the advancement device 300 cannot be inadvertently advanced distally so far that the attachment tube 302 passes through the valve 308 .
- attachment tube embodiments disclosed or contemplated herein can be incorporated into any of the advancement devices disclosed or contemplated herein.
- the various methods and devices disclosed or contemplated herein can be used to assist in the advancement of any type of catheter, pre-shaped or otherwise. It is understood that while many of the exemplary embodiments disclosed herein discuss cardiovascular guiding catheters, the various device implementations disclosed or contemplated herein can be used with any guiding, delivery, or other type of catheter or sheath.
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Abstract
Disclosed herein is a catheter advancement device having an elongate shaft and a capsule attached to or integral with the shaft, and related methods for assisting with advancement of catheters such as cardiovascular guiding catheters while reducing damage to the inner wall of the blood vessel. Some capsules have a distal plug portion and a neck portion having a smaller diameter than the plug. Other capsules have a channel defined along the outer surface of the capsule. Some elongate shafts have an attachment tube disposed at or near the proximal end thereof.
Description
- This application claims priority as a continuation application to U.S. application Ser. No. 16/672,708, filed Nov. 4, 2019, and entitled “Devices for Assisting with Advancement of Catheters and Related Systems and Methods,” which claims the benefit under 35 U.S.C. § 119(e) to U.S.
Provisional Application 62/756,184, filed Nov. 6, 2018 and entitled “Improved Catheter Advancement Device,” and further claims priority as a continuation-in-part application to U.S. application Ser. No. 15/499,194, filed Apr. 27, 2017 and entitled “Devices for Assisting with Advancement of Catheters and Related Systems and Methods,” which claims the benefit under 35 U.S.C. § 119(e) to U.S.Provisional Application 62/328,239, filed Apr. 27, 2016 and entitled “Devices for Assisting with Advancement of Guiding Catheters and Related Systems and Methods,” all of which are hereby incorporated herein by reference in their entireties. - The various embodiments herein relate to advancement devices for assisting with advancement of a catheter through a blood vessel, including a tortuous or narrow blood vessel, while reducing the risk of damaging the inner wall of the blood vessel with the distal end of the catheter.
- A guiding catheter (or “sheath”) is a standard catheter that is generally a long tube with a pre-determined shape. It is typically used to gain access to the vasculature—such as a coronary artery—by advancing the catheter through the access point during an interventional procedure. The pre-determined, typically curved shape of the catheter facilitates accessing a specific branch or other portion of the vasculature that requires such a curvature in the catheter.
- One disadvantage of a pre-shaped, curved distal end of a catheter (including, but not limited to, a guiding catheter or sheath) is that the advancement of the catheter can be impeded by the distal end contacting and damaging the inner wall of the vessel through which the catheter is being advanced. For example, as depicted in
FIG. 1A , the pre-shapeddistal end 12 of the guidingcatheter 10 can potentially contact theinner wall 16 of the blood vessel 14 (at the area A as shown) as thecatheter 10 is advanced distally through the vessel 14 (typically over a guidewire such as the guidewire depicted inFIGS. 1B and 1C , which can be, for example, a 0.035″ or 0.038″ guidewire), thereby scraping or otherwise causing damage to theinner wall 16. This scraping (or other damage) of the inner wall of the blood vessel by the catheterdistal end 12 is sometimes called a “razor effect.” - As best shown in
FIG. 1B , one standard, known technique for overcoming the “razor effect” has been the use of a balloon catheter, such as theballoon catheter 20 as shown in the figure. For example, in use, theballoon catheter 20 can be advanced through theinner lumen 24 of the guiding catheter 10 (or other type of catheter or sheath), positioned such that theballoon 22 is protruding from the distal end of thecatheter 10 such that a portion of theballoon 22 is positioned within the distal end of thecatheter 10 and a portion extends out of the distal end of thecatheter 10, and then theballoon 22 is inflated. Once theballoon 22 is inflated, the guidingcatheter 10 can be advanced through theblood vessel 14 with theballoon 22 positioned to prevent direct contact between the distal end of thecatheter 10 and theinner wall 16 of thevessel 14, thereby preventing the “razor effect.” Once thecatheter 10 is advanced to the desired position, theballoon 22 is deflated and theballoon catheter 20 is withdrawn from theguiding catheter 10 so that theguiding catheter 10 is ready for use. It is understood that any balloon catheter discussed herein can be any known balloon catheter, including, for example, a percutaneous transluminal coronary angioplasty (“PTCA”) balloon catheter. - One disadvantage of using a balloon catheter (such as
catheter 20 discussed above) to prevent the razor effect is the cost: balloon catheters are expensive. Another disadvantage is that the positioning of a balloon catheter at the distal end of the guiding catheter makes it difficult to inject any contrast or other fluid through the guiding catheter and past the inflated balloon of the balloon catheter. That is, the balloon must be deflated in order to allow for injection and then re-inflated. An additional disadvantage is that most known balloon catheters (including most PTCA balloon catheters) require the exchange of guidewires in the middle of the procedure. That is, most known balloon catheters in the required size range are only compatible with 0.014″ guidewires and thus, during the procedure described above, the surgeon is required to remove the 0.035″ or 0.038″ guidewire used to insert the pre-shaped catheter and replace it with an 0.014″ guidewire in order to be able to introduce the known balloon catheter. - Another disadvantage relates to the use of a advancement device and the tension during introduction of the guide catheter between the need to attach the attachment device to the guide catheter and the need to be able to move the catheter in relation to the guidewire. That is, in use as best shown in
FIG. 10 , the guidingcatheter 10 is typically positioned within the blood vessel of the patient by first introducing aguidewire 18 and then advancing thecatheter 10 over thestationary guidewire 18. To accomplish this, theproximal valve 26 of thecatheter 10 has an open configuration such that theguidewire 18 can pass through thevalve 26 while allowing the passage of as little fluid as possible (in contrast to its closed configuration in which thevalve 26 is fixedly coupled to theguidewire 18 and creates a fluidic seal therebetween). However, it is desirable to attach an advancement device (not shown) to thecatheter 10 during advancement by closing thevalve 26 to attach it to the advancement device such that the advancement device cannot move in relation to thecatheter 10 during advancement. Thus, the need to have thecatheter 10 attached to an advancement device combined with the need to have thecatheter 10 not attached to theguidewire 18 creates a complication. - Thus, there is a need in the art for an improved method and device for advancing a guiding catheter.
- Discussed herein are various catheter insertion or advancement devices for use in assisting with advancement of a catheter through a blood vessel while reducing damage to the inner wall of the blood vessel.
- In Example 1, a catheter advancement assistance device comprises an elongate shaft, a capsule fixedly attached to a distal end of the elongate shaft, and an attachment tube associated with a proximal portion of the elongate shaft. The capsule comprises a guidewire lumen defined through the capsule, and an outer diameter substantially similar to an inner diameter of a catheter such that the capsule is sized to be positionable through the catheter.
- Example 2 relates to the device according to Example 1, wherein the attachment tube further comprises a tube body, a lumen defined within the tube body, a distal opening defined in a distal end of the tube body, wherein the distal opening is in fluidic communication with the lumen, and a proximal opening defined in a proximal end of the tube body, wherein the proximal opening is in fluidic communication with the lumen.
- Example 3 relates to the device according to Example 1, wherein the attachment tube is a compressible attachment tube.
- Example 4 relates to the device according to Example 3, wherein the compressible attachment tube comprises an elongate opening defined along a length of the compressible attachment tube.
- Example 5 relates to the device according to Example 1, wherein the capsule further comprises a distal portion, and a neck extending proximally from the distal portion, wherein the neck has a smaller diameter than the distal portion.
- Example 6 relates to the device according to Example 1, wherein the guidewire lumen has an inner diameter that is larger than an outer diameter of a standard guidewire.
- Example 7 relates to the device according to Example 1, wherein the guidewire lumen is sized to allow fluid to flow through the lumen when a standard guidewire is positioned therein.
- Example 8 relates to the device according to Example 1, wherein the capsule further comprises a channel defined longitudinally along an outer surface of the capsule.
- Example 9 relates to the device according to Example 1, wherein the capsule further comprises a lip formed around at least a portion of an outer circumference of the capsule.
- Example 10 relates to the device according to Example 9, wherein the lip comprises at least two lip segments formed around the outer circumference of the capsule.
- Example 11 relates to the device according to Example 1, wherein the capsule further comprises an expanded distal section, wherein the expanded distal segment is substantially elastic, a non-expanded proximal section having a smaller diameter than the expanded distal section, and a lip formed at a juncture between the expanded distal section and the non-expanded proximal section, wherein the lip is formed around at least a portion of a circumference of the capsule.
- Example 12 relates to the device according to Example 1, wherein the capsule further comprises a substantially elastic ridge formed around at least a portion of an outer circumference of the capsule.
- Example 13 relates to the device according to Example 12, wherein the substantially elastic ridge comprises at least two substantially elastic rig segments formed around the outer circumference of the capsule.
- Example 14 relates to the device according to Example 1, wherein the capsule further comprises a slot defined in a distal end of the capsule, whereby the distal end of the capsule is compressible.
- Example 15 relates to the device according to Example 1, wherein the capsule further comprises a void defined in a portion of the capsule, whereby an area of the capsule near the void is compressible.
- In Example 16, a catheter advancement assistance device comprises a push rod, a body fixedly attached to a distal end of the push rod, and a compressible attachment tube associated with a proximal portion of the push rod. The body comprises a distal plug portion, a proximal neck portion, wherein the proximal neck portion has a smaller diameter than the distal plug portion, and a guidewire lumen defined through the body.
- Example 17 relates to the device according to Example 16, wherein the guidewire lumen is sized to allow fluid to flow through the lumen when a standard guidewire is positioned therein.
- Example 18 relates to the device according to Example 16, wherein the body further comprises a channel defined longitudinally along an outer surface of the body.
- Example 19 relates to the device according to Example 16, wherein the body further comprises a seating component formed around at least a portion of an outer circumference of the capsule.
- Example 20 relates to the device according to Example 19, wherein the seating component comprises a lip or a ridge.
- Example 21 relates to the device according to Example 16, wherein the compressible attachment tube comprises an elongate opening defined along a length of the compressible attachment tube.
- In Example 22, a method of assisting advancement of a catheter through a blood vessel comprises inserting an advancement assistance device into a lumen of the catheter, the advancement assistance device comprising an elongate shaft, a body fixedly attached to a distal end of the elongate shaft, and an attachment tube associated with a proximal portion of the elongate shaft. The body comprises a distal plug portion, a proximal neck portion, wherein the proximal neck portion has a smaller diameter than the distal plug portion, and a guidewire lumen defined through the body. The method further comprises urging the advancement assistance device distally into the lumen of the catheter until a distal portion of the distal plug portion extends out of a distal opening in the catheter, a proximal portion of the distal plug portion is positioned within the lumen of the catheter, and the attachment tube is disposed within a proximal valve of the catheter, attaching the proximal valve to the attachment tube, urging the catheter distally into the blood vessel to a target site over a guidewire, and retracting the advancement assistance device from the catheter.
- Example 23 relates to the method according to Example 22, further comprising urging the advancement assistance device distally until the distal plug portion extends out of the distal opening, whereby space is provided between the body and the distal opening, urging contrast solution distally through the catheter and through the space between the body and the distal opening and into the blood vessel, and urging the advancement assistance device proximally until the distal portion of the distal plug portion extends out of the distal opening in the catheter and the proximal portion of the distal plug portion is positioned within the lumen of the catheter.
- In Example 24, a method of assisting advancement of a catheter through a blood vessel comprises inserting an advancement assistance device into a lumen of the catheter, the advancement assistance device comprising an elongate shaft, a body fixedly attached to a distal end of the elongate shaft, the body comprising a guidewire lumen defined through the body, and an attachment tube associated with a proximal portion of the elongate shaft. The method further comprises urging the advancement assistance device distally into the lumen of the catheter until a distal portion of the body extends out of a distal opening in the catheter, a proximal portion of the body is positioned within the lumen of the catheter, and the attachment tube is disposed within a proximal valve of the catheter, attaching the proximal valve to the attachment tube, urging the catheter distally into the blood vessel to a target site over a guidewire, and retracting the advancement assistance device from the catheter.
- Example 25 relates to the method according to Example 24, further comprising urging contrast solution distally through the catheter and through the guidewire lumen and into the blood vessel.
- Example 26 relates to the method according to Example 24, wherein the body further comprises a channel defined longitudinally along an outer surface of the body.
- Example 27 relates to the method according to Example 26, further comprising urging contrast solution distally through the catheter and through the channel and into the blood vessel.
- Example 28 relates to the method according to Example 24, wherein the body further comprises a seating component formed around at least a portion of an outer circumference of the body.
- Example 29 relates to the method according to Example 28, wherein the seating component comprises a lip or a ridge.
- Example 30 relates to the method according to Example 28, further comprising urging the advancement assistance device distally through the lumen of the catheter until the seating component is urged out of the distal opening in the catheter, and urging the advancement assistance device proximally until the seating component contacts the distal end of the catheter.
- Example 31 relates to the method according to Example 24, wherein the attachment tube is a compressible attachment tube, wherein the attaching the proximal valve to the attachment tube causes the compression of the compressible attachment tube.
- While multiple embodiments are disclosed, still other embodiments of the present invention will become apparent to those skilled in the art from the following detailed description, which shows and describes illustrative embodiments of the invention. As will be realized, the invention is capable of modifications in various obvious aspects, all without departing from the spirit and scope of the present invention. Accordingly, the drawings and detailed description are to be regarded as illustrative in nature and not restrictive.
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FIG. 1A is a cross-sectional view of a known catheter being advanced through a blood vessel. -
FIG. 1B is a cross-sectional view of a known balloon catheter positioned within a known catheter. -
FIG. 10 is a cross-sectional view of a known catheter with a proximal valve. -
FIG. 2 is a cross-sectional side view of a catheter advancement device positioned within a catheter, according to one embodiment. -
FIG. 3A is a cross-sectional side view of a distal portion of a plug of a catheter advancement device, according to one embodiment. -
FIG. 3B is a cross-sectional side view of a distal portion of a plug of a catheter advancement device, according to another embodiment. -
FIG. 4 is a cross-sectional side view of a catheter advancement device having visualization markers and positioned within a catheter, according to one embodiment. -
FIG. 5 is a cross-sectional side view of a catheter advancement device extending out of a distal end of a catheter, according to one embodiment. -
FIG. 6 is a cross-sectional side view of a catheter advancement device positioned within a catheter, according to another embodiment. -
FIG. 7A is a cross-sectional side view of a catheter advancement device positioned within a catheter, according to a further embodiment. -
FIG. 7B is a cross-sectional front view of the catheter advancement device ofFIG. 7A . -
FIG. 8 is a cross-sectional side view of a catheter advancement device positioned within a catheter, according to yet another embodiment. -
FIG. 9 is a cross-sectional side view of a catheter advancement device positioned within a catheter, according to an alternative embodiment. -
FIG. 10A is a cross-sectional side view of a plug, according to another alternative embodiment. -
FIG. 10B is a cross-sectional front view of the plug ofFIG. 10A . -
FIG. 11A is a cross-sectional side view of a plug, according to another alternative embodiment. -
FIG. 11B is a further cross-section side view of the plug ofFIG. 11A . -
FIG. 12 is a cross-sectional side view of a method of making a catheter advancement device, according to one embodiment. -
FIG. 13A is a cross-sectional side view of a catheter advancement device having an attachment tube, according to one embodiment. -
FIG. 13B is a cross-sectional side view of the catheter advancement device ofFIG. 13A disposed within a guiding catheter, according to one embodiment. -
FIG. 14 is an expanded side view of an attachment tube on a catheter advancement device, according to one embodiment. -
FIG. 15A is an expanded side view of another attachment tube on a catheter advancement device, according to a further embodiment. -
FIG. 15B is a cross-sectional view along the longitudinal axis of the attachment tube ofFIG. 15A , according to one embodiment. -
FIG. 16 is a cross-sectional side view of another catheter advancement device having an attachment tube disposed within a guiding catheter, according to another embodiment. - The various embodiments disclosed or contemplated herein relate to catheter assertion or advancement devices and related methods for assisting in the advancement of a cardiovascular catheter through a blood vessel, including, for example, a cardiovascular guiding catheter or sheath with a curved shape, while reducing or eliminating the risk of damage to the blood vessel inner wall. The various embodiments include a distal capsule and a push rod attached thereto. Alternative embodiments include an attachment tube disposed at a proximal end of the push rod.
-
FIG. 2 depicts, according to one embodiment, a catheter advancement device 30 (also referred to as an “insertion device,” a “catheter insertion device,” or an “advancement device”) for assisting with or use in advancing a catheter, such as, for example, a guiding catheter. Thedevice 30 has a capsule (also referred to herein as a “body” or “insertion body”) 32 with a partially roundeddistal end 33 and a push rod (also referred to herein as an “elongate component”) 34 coupled thereto. Thecapsule 32 has alumen 36 defined therethrough that is configured to allow for passage of a guidewire 38 therethrough as shown. Thepush rod 34 is embedded in or otherwise fixedly coupled to thecapsule 32 such that appropriate forces can be applied at the proximal end of thepush rod 34 by a user (such as a surgeon or medical professional) to urge thecapsule 32 distally or proximally during use. - In use as shown in the figure, the distal end of the
capsule insertion device 30 can be advanced through theinner lumen 42 of a guiding catheter 40 (by a user holding the proximal end of the rod 34) and positioned such that thecapsule 32 is protruding from the distal end of thecatheter 40. In this position, a portion of thecapsule 32 is positioned within the distal end of thecatheter 40 and a portion extends out of the distal end of thecatheter 40. At this point, the user locks thedevice 30 into position in relation to thecatheter 40. That is, according to one embodiment, the user attaches the proximal end of therod 34 to thecatheter 40 in any known fashion. For example, in one specific implementation, a known locking mechanism at the proximal end of the catheter 40 (such as a Tuohy-Borst adapter, for example) is used to lock thedevice 30 to thecatheter 40. Alternatively, the locking mechanism can be a proximal valve similar to theproximal valve 26 discussed above in the Background. As such, theadvancement device 30 is locked or otherwise attached to thecatheter 40 such that the device cannot move translationally in relation to thecatheter 40. Once thecapsule 32 is positioned as shown (and, in some cases, thedevice 30 is locked in place), the guidingcatheter 40 can be advanced through a blood vessel with thecapsule 32 positioned to prevent direct contact between the distal end of thecatheter 40 and the inner wall of the vessel, thereby preventing the “razor effect.” Once thecatheter 40 is advanced to the desired position, thecapsule catheter 30 is withdrawn from the guidingcatheter 40 by a user pulling thepush rod 34 in the proximal direction so that the guidingcatheter 40 is ready for use. - The
capsule body 32 can be a solid body with alumen 36 defined therethrough as shown. Alternatively, in the various embodiments disclosed or contemplated herein, the capsule (such as capsule 32) can be any component or body that can be inserted through a guiding catheter and positioned to reduce or eliminate the razor effect. According to some embodiments, the capsule is non-inflatable. In certain implementations, the capsule has a substantially cylindrical shape. Alternatively, the capsule can have any known shape that allows it to be advanced through a catheter and positioned out of the distal end thereof as described herein. - In certain embodiments, the outer diameter of the
body 32 can vary or have specific features as described herein depending on the desired functionality of thebody 32. In this specific implementation, thecapsule 32 has a larger distal portion (also referred to herein as a “plug,” “distal plug,” or “distal body”) 44 and a smaller proximal portion (also referred to as a “neck,” or “tail”) 46. Thedistal body 44 has a larger diameter than theneck 46. In the embodiment as shown, thecapsule 32 is a singleintegral body 32 having the largerdistal portion 44 and the smallerproximal portion 46 as shown. Alternatively, thecapsule 32 can have two separate portions coupled together: the first largerdistal portion 44 and the second smallerproximal portion 46 attached thereto. - In one embodiment, the
capsule 32 has an outer diameter ranging from about 0.05 inches to about 0.3 inches. Alternatively, the outer diameter ranges from about 0.065 inches to about 0.105 inches. In a further implementation, thecapsule 32 has an outer diameter that fits snugly within (makes contact with the inner wall of) any cardiovascular guiding catheter, such as, for example, the Medtronic Launcher™ or Cordis VistaBrite™ 5 French to 8 French guiding catheters. Further, thecapsule 32 can be sized to fit snugly within any guiding catheter having any size ranging from about 4 French to about 22 French. It is understood that the “snug” fitting in this embodiment and in any other capsule embodiment disclosed or contemplated herein is a fitting of the capsule (such as capsule 32) within the catheter such that the outer surface of the capsule makes sufficient contact with the inner wall of the catheter to prevent passage of fluid therebetween. - In one embodiment, any capsule embodiment disclosed or contemplated herein (such as capsule 32) is made of a polymeric material. For example, the capsule can be made of polyethylene, Pebax, Nylon, polyester, or any other polymeric material or combination thereof. Alternatively, the capsule can also be made of metal or any other known material that can be used for medical devices. In a further implementation, the capsule (such as capsule 32) can be made of two or more materials. More specifically, in certain embodiments, the capsule can be made of two or more materials having differing stiffness and/or flexibility such that one portion of the capsule (such as the distal end, for example) is stiffer, more rigid, and/or less flexible than another portion. In other words, the two or more materials can be used to create a capsule that has stiffness, rigidity, or flexibility that varies along the length of the capsule.
- Further, any capsule embodiment disclosed or contemplated herein (such as capsule 32) can also have a coating disposed on the outer surface of the capsule to increase the lubricity of the capsule. In certain implementations, the coating can be hydrophilic or hydrophobic.
- According to any embodiment disclosed or contemplated herein, the push rod (such as push rod 34) can be made of metal. Alternatively, the push rod can be made of any known material that can be used to make an elongate component with sufficient column strength such that the component can be used to advance a capsule through the lumen of a guiding catheter while also having some flexibility. It is understood that the push rod (also referred to as a “proximal elongate member” or “control rod” or “manipulation rod”) in any embodiment herein can be any elongate component that is coupled to the proximal end of the capsule and can withstand the forces necessary for a user to urge the rod distally or proximally to move the capsule through a guiding catheter as described herein. In certain alternative implementations, the push rod can be integral with the capsule. Further, various embodiments include a push rod and capsule formed together of the same materials such that the push rod is integral with the capsule.
- It is understood that the capsule (such as capsule 32) can take a variety of shapes, so long as the capsule can be positioned out of the distal end of a guiding catheter as described herein and help with advancement thereof through a blood vessel. For example,
capsule 50 as best shown inFIG. 3A according to one embodiment has a tapereddistal end 52, whilecapsule 54 as best shown inFIG. 3B in accordance with another implementation has a roundeddistal end 56. According to further alternatives, the capsule can have a distal end with an angled shape, a spherical shape, or any other known shape that helps to advance the guiding catheter when the capsule is positioned out of the distal end of the guiding catheter. - In certain implementations, any advancement device disclosed or contemplated herein can have at least one visualization marker disposed on the device. One exemplary embodiment is depicted in
FIG. 4 , in which thecapsule insertion device 60 has twovisualization markers first visualization marker 64A is disposed at or near the distal end of thedistal plug 62A of thecapsule 62, while thesecond marker 64B is disposed on theneck 62B of thecapsule 62. Alternatively, any device embodiment can have one marker or three or more markers. It is understood that themarkers markers markers capsule insertion device 60. - In use, it is often necessary or helpful to inject contrast solution through the lumen of a guiding catheter and into the vasculature of the patient to assist with placement of the guiding catheter. As discussed above, if a known balloon catheter is being used to assist with advancement of the guiding catheter, the process for injecting the contrast solution is complicated by the presence of the balloon, which must be deflated in order to inject the solution. However, as best shown in
FIGS. 5-7B , various embodiments of the capsule device disclosed or contemplated herein eliminate those complications. - For example, in one implementation as shown in
FIG. 5 , thecatheter advancement device 80 has acapsule 82 with adistal body 82A and aneck 82B similar or identical to thecapsule 32 described above. To inject contrast solution after thecapsule 82 has been positioned at the distal end of the guiding catheter 84 (for advancing thecatheter 84 through the vasculature as described above), thecapsule device 80 is urged distally (by a user urging the proximal end of thepush rod 90 distally) such that thebody 82A of thecapsule 82 is urged distally out of thelumen 86 of the guidingcatheter 84 as shown inFIG. 5 . More specifically, thecapsule 82 is urged distally until thebody 82A is urged out of thelumen 86 such that space is created between the opening 88 of the guidingcatheter 84 and thebody 82A, thereby making it possible for contrast to exit from theopening 88 as represented by arrows A. In certain implementations such as that shown inFIG. 5 , thecapsule 82 need not be urged distally so far that theneck 82B also exits thelumen 86. Instead, the smaller diameter of theneck 82B allows for sufficient space between theneck 82B and theopening 88 to allow for contrast to exit thelumen 86. - In an alternative embodiment, as shown in
FIG. 6 , thecapsule 102 need not be advanced distally out of thelumen 110 of the guidingcatheter 108. More specifically, one implementation of acapsule device 100 has acapsule 102 with alumen 104 defined therein that has a larger inner diameter than is necessary to accommodate solely aguide wire 106. As such, thelumen 104 has a sufficient inner diameter to provide space for theguide wire 106 while also having sufficient additional space to allow for contrast solution to flow distally out of the guidingcatheter 108 through thecapsule lumen 104 and into the vasculature as represented by arrows B. In one embodiment, the inner diameter of thelumen 104 ranges from about 0.01 inches to about 0.05 inches. Alternatively, the inner diameter ranges from about 0.02 inches to about 0.04 inches. In a further implementation, the inner diameter of thelumen 104 is sufficiently large to receive a guidewire of any size ranging from 0.01 inches to 0.04 inches and still has at least a 0.004 inch diameter of space between the guidewire and the inner wall of thelumen 104. - In use, once the
capsule device 100 is positioned at the distal end of the guidingcatheter 108 such that thecapsule 102 is positioned as desired for advancing thecatheter 108, thecapsule 102 need not be moved in order to inject the contrast solution. Instead, thecapsule 102 can remain in place while the contrast solution flows distally through thelumen 110 of the guidingcatheter 108 and through thelumen 104 of thecapsule 102 and out into the vasculature. - Another configuration as depicted in
FIGS. 7A and 7B also allows for contrast solution injection without moving the capsule device. In this implementation, thecapsule device 120 has acapsule 122 with a channel (also referred to as a “slot” or “trough”) 126 defined longitudinally along theouter surface 124 of the capsule 122 (as best shown inFIG. 7B ). As such, thechannel 126 defines a space between thecapsule 122 and the inner surface of thelumen 130 of the guidingcatheter 128 through which contrast solution can flow distally out into the vasculature as represented by arrows C. In one embodiment, thechannel 126 has an inner diameter ranging from about 0.002 inches to about 0.02 inches. Alternatively, the inner diameter ranges from about 0.004 inches to about 0.008 inches. In use, once thecapsule device 120 is positioned at the distal end of the guidingcatheter 128 such that thecapsule 122 is positioned as desired for advancing thecatheter 128, thecapsule 122 need not be moved in order to inject the contrast solution. Instead, thecapsule 122 can remain in place while the contrast solution flows distally through thelumen 130 of the guidingcatheter 128 and through thechannel 126 of thecapsule 122 and out into the vasculature. It is understood that, according to various alternatives, thechannel 126 can be any feature or configuration on thecapsule 122 or theouter surface 124 thereof that allows fluid flow between thecapsule 122 and the inner wall of thelumen 130. - Both the
larger lumen 104 of thecapsule device 100 embodiment and thechannel 126 of thecapsule device 120 implementation make it easy for a user to inject contrast solution, as discussed above. In addition, these two embodiments can also assist with limiting contrast fluid use. Injection of excess contrast fluid into the vasculature of a patient during an interventional procedure can cause health issues for the patient, including contrast-induced nephropathy. Thelumen 104 of a predetermined diameter in thedevice 100 embodiment or thechannel 126 of a predetermined depth or diameter in thedevice 120 embodiment both provide mechanisms for injecting solution in known, more limited amounts than those injected when using a balloon catheter as described above. - In certain alternative implementations, another capsule is provided—for use with any of the capsule device embodiments disclosed or contemplated herein—that has a seating component defined or disposed around an outer surface of the capsule that can assist with positioning the capsule in relation to the guiding catheter during use and further can create a smoother or more streamlined transition from the outer surface of the capsule to the outer surface of the guiding catheter in which the capsule is positioned. It is understood that any of the seating components disclosed or contemplated herein can be defined or disposed around the entire 360 degree circumference of the capsule. Alternatively, any such components can be defined or disposed around only a portion of the circumference of the capsule. In a further embodiment, any such seating component can be defined or disposed intermittently around the circumference of the capsule such that there are two or more seating components disposed or defined thereon such that they are positioned at different locations along and around the circumference thereof.
- One example of such a capsule is depicted in
FIG. 8 , which shows one embodiment of acapsule 140 having a seating component (or “seating feature”) 144. In this specific example, theseating component 144 is alip 144 created by thecapsule 140 having an expanded section 142 (which is a portion of thecapsule 140 that has an increased diameter in comparison to the rest of the capsule 140). That is, thelip 144 is formed at the juncture of the expandedsection 142 and the non-expanded section of thecapsule 140. As discussed above, thelip 144 can extend around the entire circumference, can extend around a portion of the circumference, or can constitute two ormore lips 144 that are disposed or defined intermittently around the circumference. In one embodiment, the expandedsection 142 is a portion of thebody 148 of thecapsule 140. Alternatively, the expandedsection 142 can be the body itself (not shown), and the transition from the body (not shown) to the neck (not shown) constitutes the seating component. The expandedsection 142 has an outer diameter that is substantially similar to or the same as the outer diameter of the guidingcatheter 146. In certain embodiments, the expandedsection 142 or theentire capsule 140 has sufficient elasticity to allow for deformation of the expandedsection 142 such that thecapsule 140 can be advanced through the guidingcatheter 146 despite the expandedsection 142 having an outer diameter that is larger than the inner diameter of the guidingcatheter 146 lumen. Regardless of the specific embodiment of the capsule with the seating component (such as seating component 144), it is understood that thecapsule 140 has at least a portion of its outer surface that fits snugly within the catheter as described elsewhere herein such that no fluid can pass between the outer surface of thecapsule 140 and the inner surface of the catheter. - In use, the
capsule 140 is advanced distally through the guidingcatheter 146 and positioned out of thedistal opening 150 of the guidingcatheter 146 according the same procedure used for all the capsule device embodiments herein. As mentioned above, thecapsule 140 has an expandedsection 142 that has elastic characteristics that allow for thesection 142 to deform sufficiently as thecapsule 140 is advanced through the guiding catheter to allow for passage of thecapsule 140 despite the expandedsection 142 having a greater diameter than the inner diameter of the lumen of the guidingcatheter 146. As the expandedsection 142 of thecapsule 140 is urged out of theopening 150 at the distal end of the guidingcatheter 146, the expandedsection 142 expands back to its natural diameter, thereby causing formation of the lip 114. The user can then urge thecapsule 140 back in a proximal direction—via the push rod (not shown)—until the lip 114 is in contact with the guidingcatheter 146, thereby confirming for the user via increased resistance that thecapsule 140 is in the desired position in relation to the guidingcatheter 146. It is understood that the user must be aware that she or he cannot use so much force that the expandedsection 142 deforms and thecapsule 140 is urged proximally past the desiredcapsule 140 position. Once thecapsule 140 is positioned as desired, it can be seen inFIG. 8 that the expandedsection 142 has a diameter that is substantially similar to the outer diameter of the guidingcatheter 146, thereby reducing the risk of the distal end of the guidingcatheter 146 making contact with an inner wall of a blood vessel wall during advancement of the guidingcatheter 146. Once thecapsule 140 is positioned, the user then advances the guidingcatheter 146 via the push rod (not shown). - Another example of a capsule with a seating component is depicted in
FIG. 9 , which shows acapsule 160 having aseating component 162. In this specific example, theseating component 162 is aridge 162 formed or disposed on the outer surface of thecapsule 160. As discussed above, theridge 162 can extend around the entire circumference, can extend around a portion of the circumference, or can constitute two ormore ridges 162 that are disposed or defined intermittently around the circumference. Theridge 162 has an outer diameter that is substantially similar to or the same as the outer diameter of the guidingcatheter 164. In certain embodiments, theridge 162 or theentire capsule 160 has sufficient elasticity to allow for deformation of theridge 162 such that thecapsule 160 can be advanced through the guidingcatheter 164 despite theridge 162 having an outer diameter that is larger than the inner diameter of the guidingcatheter 164 lumen. As with all capsule implementations herein, regardless of the specific embodiment of the capsule with the seating component (such as seating component 162), it is understood that thecapsule 160 has at least a portion of its outer surface that fits snugly within the catheter as described elsewhere herein such that no fluid can pass between the outer surface of thecapsule 160 and the inner surface of the catheter. - In use, the
capsule 160 is advanced distally through the guidingcatheter 164 and positioned out of thedistal opening 166 of the guidingcatheter 164 according the same procedure used for all the capsule device embodiments herein. As mentioned above, theridge 162 on thecapsule 160 has elastic characteristics that allow for theridge 162 to deform sufficiently as thecapsule 160 is advanced through the guidingcatheter 164 to allow for passage of thecapsule 160 despite theridge 162 having a greater diameter than the inner diameter of the lumen of the guidingcatheter 164. As theridge 162 of thecapsule 160 is urged out of theopening 166 at the distal end of the guidingcatheter 164, theridge 162 expands back to its natural diameter. The user can then urge thecapsule 160 back in a proximal direction until theridge 162 is in contact with the guidingcatheter 164, thereby confirming that thecapsule 160 is in the desired position in relation to the guidingcatheter 164. It is understood that the user must be aware that the user cannot use so much force that theridge 162 deforms and thecapsule 160 is urged proximally past the desiredcapsule 160 position. Once thecapsule 160 is positioned as desired, it can be seen inFIG. 9 that theridge 162 has a diameter that is substantially similar to the outer diameter of the guidingcatheter 164, thereby reducing the risk of the distal end of the guidingcatheter 164 making contact with an inner wall of a blood vessel wall during advancement of the guidingcatheter 164. Once thecapsule 160 is positioned, the user then advances the guidingcatheter 164. - In certain implementations in which the capsule has a seating component (such as the
seating components FIGS. 10A and 10B , instead of the capsule having elasticity as described above, acapsule 180 is provided that is a deformable orcollapsible capsule 180. That is, thecapsule 180 has aslot 182 defined in the distal end of thecapsule 180 along the length of thecapsule 180 that also has a seating component 184 (similar to one of theseating components slot 182 allows for thecapsule 180 to be deformed or have a smaller diameter as it is advanced through a guiding catheter, similar to the use of thecapsules - In another embodiment, a
capsule 190 is provided that is collapsible or deformable as a result of anopening 192 defined at a distal portion of the capsule along the length of thecapsule 190 that also has aseating component 194. In use, theopening 192 allows for thecapsule 190 to be deformed or have a smaller diameter as it is advanced through a guiding catheter, similar to the use of thecapsules - As discussed above, it is understood that the
seating components FIGS. 10A-11B can extend around the entire circumference, can extend around a portion of the circumference, or can constitute two or more such components that are disposed or defined intermittently around the circumference. - The various catheter insertion device embodiments disclosed or contemplated herein can be made in any number of known ways. In one embodiment as shown in
FIG. 12 , acapsule 200 can be formed using an injection molding process. In this process, the starting point is aninner tube 202, with thecapsule 200 being injection molded over theinner tube 202. In certain implementations in which thecapsule 200 has twomarker bands marker bands inner tube 202 before thecapsule 200 is injected molded thereon such that the material for thecapsule 200 is injection molded onto themarker bands marker bands capsule 200. Further, thepush rod 206 can be embedded in thecapsule 200 in a similar fashion. That is, thepush rod 206 can be positioned along theinner tube 202 such that injection molding of thecapsule 200 results in thepush rod 206 being embedded therein. - Other advancement device implementations include an attachment tube disposed at a proximal end of the push rod to allow for attaching the advancement device to the guiding catheter while the catheter can be advanced over a guidewire.
- For example,
FIG. 13A depicts, according to one embodiment, anothercatheter advancement device 220 for assisting with or use in advancing a catheter, such as, for example, a cardiovascular guiding catheter. As with the other advancement device embodiments disclosed herein, thedevice 220 has acapsule 222 and a push rod (also referred to herein as an “elongate component”) 224 coupled thereto. Thecapsule 222 can have alumen 226 defined therethrough that is configured to allow for passage of a guidewire (not shown) therethrough. The various components of thedevice 220 are substantially similar to the various components described in the other device embodiments above and can incorporate any of the various alternative components and/or features thereof. - In addition, the
push rod 224 in this implementation has an attachment tube (also referred to as a “coupling tube”) 228 attached at a proximal end of thepush rod 224 as shown such that a catheter valve (including any known valve on any known catheter as discussed elsewhere herein) can attach to theattachment tube 228 as desired and a guidewire can be moveably disposed therethrough. That is, theattachment tube 228 defines alumen 230 disposed through thetube 228 as shown that is sized to slidably receive a guidewire. - In one embodiment, the
lumen 274 in the tube 270 (or any lumen of any attachment tube disclosed or contemplated herein) has an inner diameter ranging from about 0.008 inches to about 0.040 inches. Alternatively, the inner diameter ranges from about 0.014 inches to about 0.030 inches. In a further alternative, thetube 270 is sized such that thelumen 274 can receive any known cardiovascular guidewire ranging in size from about 0.01 inches to about 0.04 inches. - In use, as best shown in
FIG. 13B , according to one implementation, theadvancement device 220 can be disposed in acatheter 232. The knowncatheter 232 has a knownproximal valve 234, which is a Toughy-borst valve or any known sealable valve. It is understood that thecatheter 232 can be any known cardiovascular catheter as discussed elsewhere herein. Theattachment tube 228 is disposed along the length of thepush rod 224 such that when thedevice 220 is disposed within thecatheter 232 as shown with thecapsule 222 extending partially out of the distal end of thecatheter 232, theattachment tube 228 is disposed through thevalve 234 of the catheter 232 (similar tovalve 26 discussed above). Further, theattachment tube 228 can receive aguidewire 236 in thelumen 230 of theattachment tube 228 when thecatheter 232 andadvancement device 220 are disposed over theguidewire 236 as shown. As a result, thevalve 234 of thecatheter 232 can be removably coupled to the attachment tube 228 (via any known mechanism that such avalve 234 is attached to a device disposed therethrough) such that theadvancement device 220 is attached to thecatheter 232 and thus both are advanced together (such that theadvancement device 220 does not move axially in relation to the catheter 232) while theguidewire 236 can be slidably disposed through thelumen 230 of thetube 228 such that thecatheter 232 anddevice 220 can be moved in relation to theguidewire 236. In other words, theattachment tube 228 makes it possible for theadvancement device 220 to be attached to thecatheter 232 via the coupling of thecatheter valve 234 to thetube 228 while thevalve 234 is not attached to the guidewire 236 (because theguidewire 236 is slidably disposed through the tube 228). - One specific embodiment of an
attachment tube 250 that can be incorporated into any advancement device as disclosed or contemplated herein is depicted inFIG. 14 , in accordance with one implementation. Thetube 250 is coupled to a proximal end of apush rod 256 and has an elongatetubular body 252 that defines alumen 254 as shown. Thetubular body 252 has adistal opening 258 and aproximal opening 260, both of which are in fluidic communication with thelumen 254. In this implementation, thetubular body 252 is a substantiallyunitary body 252 having no substantial openings along the length of thebody 252. As with the other attachment tube embodiments disclosed or contemplated herein, thetubular body 252 is configured to be disposed through a catheter valve (such asvalve 234 discussed above) such that the valve can be attached to thebody 252. - Another embodiment of an
attachment tube 270 that can be incorporated into any advancement device as disclosed or contemplated herein is depicted inFIGS. 15A and 15B . Thetube 270 is coupled to a push rod 276 and has substantially the same features and characteristics as thetube 250 discussed above, and thus the description of the similar components and features above apply equally to thistube 270 embodiment as well, except as described herein. Additionally, in this specific implementation, thetube 270 is acompressible tube 270. The specificcompressible tube 270 embodiment as shown has anelongate opening 282 defined along at least a portion of the length of thebody 272. More specifically, in the specific embodiment depicted inFIGS. 15A and 15B , theelongate opening 282 is aslot 282 that extends along the entire length of thebody 272 from thedistal opening 278 to theproximal opening 280. Thetubular body 272 and slot 282 are configured such that thebody 272 can be disposed through a catheter valve (such asvalve 234 discussed above) such that when the valve is clamped down on thetubular body 272, thebody 272 is compressed as a result of theslot 282 being collapsed by the valve such that the two opposing sides of thebody 272 that define theslot 282 are urged toward each other. - In one embodiment, the
slot 282 has a width that ranges from about 0.004 inches to about 0.03 inches. Alternatively, theslot 282 has a width ranging from about 0.01 inches to about 0.02 inches. In a further embodiment, theslot 282 is gap in the circumference of thebody 272 such that the gap constitutes a percentage of the total circumference of thebody 272 ranging from about 4 percent to about 25 percent. Regardless of the size of theslot 282, it is understood that the terms “attachment tube” and “tube” are intended herein to encompass any tubular structure having any sized slot, gap, slit, or opening defined therein, including a tubular structure having a gap that constitutes as much as 25 percent of the circumference of the structure. - Alternatively, instead of extending along the entire length of the
body 272, theslot 282 can extend along a portion of the length of thebody 272. In a further embodiment, theopening 282 can be any opening of any shape or configuration that allows for compression of thetubular body 272 when the valve (such asvalve 234, for example) is clamped down thereon. According to another implementation, anyopening 282 extending along the entire length of thebody 272 can not only provide compressive qualities to thebody 272, but can also assist with positioning a guidewire (such asguidewire 284 as discussed below) into thelumen 274 of thetube 270 via theopening 282. That is, rather than having to thread a guidewire into one of theopenings lumen 274, a user can insert the guidewire into thelumen 274 through theopening 282. - Regardless of the exact size, shape, and configuration of the
opening 282, thebody 272 of thecompressible tube 270 has some degree of compliance that allows for thebody 272 to be compressed such that thelumen 274 defined therein is reduced in size (or inner diameter) as a result of the compression. Thus, as best shown inFIG. 15B , thelumen 274 in the uncompressed state has sufficient size such that there is space between the inner wall of thelumen 274 and theguidewire 284. As such, thebody 272 can be compressed by some amount such that the inner diameter of thelumen 274 is reduced while still providing sufficient space between the inner wall of thelumen 274 and theguidewire 284 such that theguidewire 284 can still move axially in relation to thebody 272 while minimizing the amount of blood loss through thelumen 274 by minimizing the space between the inner wall of thelumen 274 and theguidewire 284. - In another alternative embodiment, the
tube 270 and any other compressible tube embodiment as disclosed or contemplated herein can have any structure or feature that provides or allows for compression of thetube 270. - In accordance with another embodiment as depicted in
FIG. 16 , theadvancement device 300 has anattachment tube 302 with a blockingprotrusion 304 extending from a proximal end thereof. In this implementation, the blockingprotrusion 304 is adisk 304 disposed at or near the proximal end of thetube 302. Alternatively, the blockingprotrusion 304 can be a lip, a rim, or any other known structural feature or component that forms a radial protrusion or extension that is disposed at a proximal end of theattachment tube 302 and has an outer diameter or dimension that is greater than the inner diameter of thevalve 308 of thecatheter 306, thereby preventing the blockingprotrusion 304 from passing into or through thevalve 308. As such, the blockingprotrusion 304 can be incorporated into theattachment tube 302 such that theadvancement device 300 cannot be inadvertently advanced distally so far that theattachment tube 302 passes through thevalve 308. - It is understood that any of the attachment tube embodiments disclosed or contemplated herein can be incorporated into any of the advancement devices disclosed or contemplated herein.
- Alternatively, the various methods and devices disclosed or contemplated herein can be used to assist in the advancement of any type of catheter, pre-shaped or otherwise. It is understood that while many of the exemplary embodiments disclosed herein discuss cardiovascular guiding catheters, the various device implementations disclosed or contemplated herein can be used with any guiding, delivery, or other type of catheter or sheath.
- Although the various implementations have been described with reference to preferred embodiments, persons skilled in the art will recognize that changes may be made in form and detail without departing from the spirit and scope thereof.
Claims (1)
1. A catheter advancement assistance device, the device comprising:
(a) an elongate shaft;
(b) a capsule fixedly attached to a distal end of the elongate shaft, the capsule comprising:
(i) a guidewire lumen defined through the capsule;
(ii) an outer diameter substantially similar to an inner diameter of a catheter such that the capsule is sized to be positionable through the catheter; and
(c) an attachment tube associated with a proximal portion of the elongate shaft.
Priority Applications (1)
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US18/332,290 US20230310800A1 (en) | 2016-04-27 | 2023-06-09 | Devices for assisting with advancement of catheters and related systems and methods |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
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US201662328239P | 2016-04-27 | 2016-04-27 | |
US15/499,194 US20170333681A1 (en) | 2016-04-27 | 2017-04-27 | Devices for Assisting with Advancement of Catheters and Related Systems and Methods |
US201862756184P | 2018-11-06 | 2018-11-06 | |
US16/672,708 US11712539B2 (en) | 2016-04-27 | 2019-11-04 | Devices for assisting with advancement of catheters and related systems and methods |
US18/332,290 US20230310800A1 (en) | 2016-04-27 | 2023-06-09 | Devices for assisting with advancement of catheters and related systems and methods |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US16/672,708 Continuation US11712539B2 (en) | 2016-04-27 | 2019-11-04 | Devices for assisting with advancement of catheters and related systems and methods |
Publications (1)
Publication Number | Publication Date |
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US20230310800A1 true US20230310800A1 (en) | 2023-10-05 |
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US5499975A (en) | 1989-01-31 | 1996-03-19 | Cook Incorporated | Smooth transitioned dilator-sheath assembly and method |
US5466222A (en) | 1994-03-30 | 1995-11-14 | Scimed Life Systems, Inc. | Longitudinally collapsible and exchangeable catheter |
JP3855243B2 (en) | 1996-02-21 | 2006-12-06 | 日本ゼオン株式会社 | Medical insertion aid |
JPH09253215A (en) | 1996-03-26 | 1997-09-30 | Nippon Sherwood Kk | Multiplex lumen catheter |
US20040260333A1 (en) | 1997-11-12 | 2004-12-23 | Dubrul William R. | Medical device and method |
US7655022B2 (en) | 2003-04-28 | 2010-02-02 | Cardiac Pacemakers, Inc. | Compliant guiding catheter sheath system |
WO2006044670A1 (en) | 2004-10-14 | 2006-04-27 | Crossman Arthur W | Vascular catheter device and related method of using the same |
JP4608462B2 (en) | 2006-06-14 | 2011-01-12 | テルモ株式会社 | Catheter assembly |
US8900214B2 (en) | 2007-03-30 | 2014-12-02 | Onset Medical Corporation | Expandable trans-septal sheath |
JP5455492B2 (en) | 2009-07-30 | 2014-03-26 | 日本コヴィディエン株式会社 | Stylet and catheter set |
CN109394216B (en) | 2012-03-18 | 2021-11-02 | 特洛玛泰克解决方案私人有限公司 | Device and method for vascular access and treatment |
JP2015525636A (en) | 2012-07-09 | 2015-09-07 | ボストン サイエンティフィック サイムド,インコーポレイテッドBoston Scientific Scimed,Inc. | Expandable guide extension catheter |
JP2015525638A (en) | 2012-07-13 | 2015-09-07 | ボストン サイエンティフィック サイムド,インコーポレイテッドBoston Scientific Scimed,Inc. | Guide extension catheter |
US11000676B2 (en) | 2012-09-04 | 2021-05-11 | Asher Holzer | Guide for intravascular device |
WO2014152191A1 (en) | 2013-03-15 | 2014-09-25 | Qxmedical, Llc | Boosting catheter and related systems and methods |
US10322260B2 (en) * | 2013-05-30 | 2019-06-18 | Terumo Kabushiki Kaisha | Treatment method for treating lower limbs using multi-member catheter assembly |
WO2017059186A1 (en) | 2015-10-01 | 2017-04-06 | QXMedical, LLC. | Catheter structure with improved support and related systems, methods and devices |
JP2019514523A (en) | 2016-04-27 | 2019-06-06 | キューエックスメディカル リミテッド ライアビリティ カンパニー | Device and related systems and methods for assisting catheter advancement |
EP3600492A1 (en) | 2017-03-22 | 2020-02-05 | QXMedical, LLC | Improved over-the-wire balloon catheter and related systems and methods |
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