Classifications

• • 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
  • A61M25/0043—Catheters; Hollow probes characterised by structural features
  • A61M25/0045—Catheters; Hollow probes characterised by structural features multi-layered, e.g. coated
• • 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
• • 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
  • A61M25/0009—Making of catheters or other medical or surgical tubes
• • 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
  • A61M25/0021—Catheters; Hollow probes characterised by the form of the tubing
• • 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
  • A61M25/0043—Catheters; Hollow probes characterised by structural features
• • 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
  • A61M25/0021—Catheters; Hollow probes characterised by the form of the tubing
  • A61M25/0023—Catheters; Hollow probes characterised by the form of the tubing by the form of the lumen, e.g. cross-section, variable diameter
  • A61M25/0026—Multi-lumen catheters with stationary elements
  • A61M2025/0034—Multi-lumen catheters with stationary elements characterized by elements which are assembled, connected or fused, e.g. splittable tubes, outer sheaths creating lumina or separate cores
• • 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
  • A61M25/0021—Catheters; Hollow probes characterised by the form of the tubing
  • A61M25/0023—Catheters; Hollow probes characterised by the form of the tubing by the form of the lumen, e.g. cross-section, variable diameter
• • 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
  • A61M25/0021—Catheters; Hollow probes characterised by the form of the tubing
  • A61M25/0023—Catheters; Hollow probes characterised by the form of the tubing by the form of the lumen, e.g. cross-section, variable diameter
  • A61M25/0026—Multi-lumen catheters with stationary elements
  • A61M25/0029—Multi-lumen catheters with stationary elements characterized by features relating to least one lumen located at the middle part of the catheter, e.g. slots, flaps, valves, cuffs, apertures, notches, grooves or rapid exchange ports
• • 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
  • A61M25/0021—Catheters; Hollow probes characterised by the form of the tubing
  • A61M25/0023—Catheters; Hollow probes characterised by the form of the tubing by the form of the lumen, e.g. cross-section, variable diameter
  • A61M25/0026—Multi-lumen catheters with stationary elements
  • A61M25/0032—Multi-lumen catheters with stationary elements characterized by at least one unconventionally shaped lumen, e.g. polygons, ellipsoids, wedges or shapes comprising concave and convex parts

Definitions

• This invention relates to medical catheters, and more particularly, to catheters formed from one or more modular elements.
• Medical catheters serve various functions.
• the catheters may be employed in a number of procedures ranging from interventional stroke treatment, angioplasty procedures, aneurysm treatment procedures, and many other operations.
• Catheters may be used in conjunction with one or more wire guides that facilitate introduction of the catheter to a desired site.
• the catheters may infuse or aspirate fluid, deliver instruments, perform imaging operations, and/or may be used for other purposes during a procedure.
• Medical catheters may be adapted for insertion into numerous bodily regions, such as vessels or ducts. Such catheters may be relatively rigid or flexible, and may be substantially uniform or vary along their lengths, depending on the needs of the procedure, the vessels or ducts involved, and other variables associated with an operation.
• a typical catheter extrusion process may have various limitations. For example, it may be difficult to vary the profile, properties or characteristics along the longitudinal axis of the catheter using a single extrusion. Also, if thermal techniques are employed to secure two catheter materials together, limitations may arise when dealing with processing temperatures used to form an adhesive bond. If an adhesive is used to affix multiple catheter elements, further steps associated with the adhesion process are required.
• a catheter comprises a core element having proximal and distal regions, an exterior surface and a longitudinal axis. At least one channel is formed in the exterior surface of the core element. The channel extends along at least a portion of the longitudinal axis of the catheter and is at least partially surrounded by a jacket member, thereby forming at least one side lumen in the catheter.
• the side lumen may be relatively small and may be disposed near an exterior surface of the catheter. Such a lumen may be difficult to achieve using previously-known manufacturing techniques.
• a modular catheter comprising a first core element having proximal and distal regions and a longitudinal axis, a second core element having proximal and distal regions and a longitudinal axis, and a jacket member disposed at least partially around the first core element and the second core element.
• the catheter is adapted for insertion into a selected body cavity.
• the first core element may be longitudinally movable with respect to the second core element.
• first core element and/or second core elements may comprise an indentation formed in a lateral surface thereof, wherein the indentations may house a third core element, or alternatively, may form a void region suitable for use as a catheter lumen.
• first .core element may comprise a longitudinal bore formed therein, and the second core element may comprise a substantially circular shape that is adapted for insertion into the longitudinal bore. The second core element may extend distal to the first core element, thereby allowing the catheter to comprise a distal region of reduced cross-section relative to a proximal region of the catheter.
• the first core element may be disposed proximal to the second core element, such that a distal region of the first core element abuts a proximal region of the second core element.
• the first core element and the second core element may be formed of materials having different properties to enable the catheter to achieve differing flexibilities along a longitudinal axis.
• a catheter having proximal and distal regions comprises a core element having first and second ends, and further having constrained and expanded states.
• a jacket member is configured to encircle the core element in the constrained state, wherein the core element is held in the constrained state by the jacket member such that the first and second ends form a substantially circular shape that conforms to an interior surface of the jacket member.
• the core element may be provided with a working lumen formed when constrained in the substantially circular shape. The core element may then be deployed to an expanded state to serve a variety of medical purposes.
• FIGS. IA- IB are, respectively, a perspective view of a catheter provided in accordance with a first embodiment of the present invention, and a cross-sectional view of the catheter along line A— A.
• FIG. 2 illustrates a cross-sectional view of a catheter provided in accordance with an alternative embodiment of the present invention.
• FIG. 3 illustrates a cross-sectional view of a catheter provided in accordance with a further alternative embodiment of the present invention.
• FIGS. 4A-4B illustrate cross-sectional views of catheters provided in accordance with further alternative embodiments of the present invention.
• FIGS. 5A-5E illustrate, respectively, a side view of a catheter provided in accordance with an alternative embodiment of the present invention, cross-sectional views of the catheter of FIG. 5A along line B--B in constrained and unconstrained states, a side-sectional view of an alternative embodiment of the catheter of FIGS. 5A-5C, and a cross-sectional view of a further alternative embodiment of FIGS. 5A-5C.
• FIGS. 6A-6B are, respectively, a side view of a catheter provided in accordance with an alternative embodiment of the present invention, and a cross-sectional view of the catheter of FIG. 6A along line C-C.
• FIGS. 7A-7B illustrates, respectively, a side sectional view and side view of a catheter provided in accordance with a further alternative embodiment of the present invention, and a side sectional view of an alternative embodiment of the catheter of FIG. 7 A.
• the present invention is directed to medical catheters that may be modularly constructed to facilitate manufacture and/or provide properties that may be difficult to achieve with a catheter formed from a single extrusion.
• the term "modular" relates generally to a device having more than one component.
• catheter 20 may be constructed of one or more core elements that may be partially or completely surrounded by a jacket member in a variety of configurations.
• proximal refers to a direction that is generally towards a physician during a medical procedure
• distal refers to a direction that is generally towards a target site within a patent's anatomy during a medical procedure.
• catheter 20 comprises core element 30, which has proximal and distal regions and a longitudinal axis.
• catheter 20 further comprises jacket member 22, which may be disposed circumferentially around core element 30 along at least a portion of its longitudinal axis.
• core element 30 of catheter 20 comprises a substantially circular main body having an exterior surface 31.
• catheters provided in accordance with the present invention may comprise multiple core elements, each having various configurations.
• core element 30 of FIGS. 1A-1B preferably spans an entire longitudinal length of catheter 20, multiple core elements may be provided along the length of a modular catheter in overlapping or abutting fashion, for example, as described with respect to FIGS. 7A-7B hereinbelow.
• channels 23 and 25 may be formed in exterior surface 31 of core element 30. The channels may serve a variety of functions.
• catheter 20 permits the formation of side lumens that are substantially close to an exterior surface of catheter 20. Typically, for catheters having a single core extrusion, it may be difficult to form a lumen that is in close
• one or more core elements 30 may comprise different properties than jacket member 22.
• the component used for core element 30 may comprise a strong yet flexible material, for example, a thermoplastic elastomer such as polyurethane, polyester copolymers or an elastomeric alloy. Alternatively, silicone rubber may be used. Further materials suitable for core element 30 will be apparent to one skilled in the art.
• the materials used for jacket member 22 may encompass different properties than the materials used for core element 30.
• jacket 22 may comprise a biocompatible, lubricious material.
• One exemplary material is polytetrafluoroethylene (PTFE). Therefore, by employing a modular construct in accordance with the present invention, a relatively strong and flexible core element may be used in conjunction with a lubricious jacket member.
• an exterior surface of jacket member 22 may be selectively provided with a desired coating, such as a hydrophilic coating, depending on the needs of the surgical procedure.
• jacket member 22 may comprise a material having translucent or transparent properties. Such construction may facilitate viewing of objects within catheter 20. For example, a physician may endoscopically view movement of wire guide 40 within side lumen 24 because jacket member 22 is translucent or transparent. This enhanced visualization may not be achievable if catheter 20 had been fabricated of one material, such as an opaque thermoplastic polymer having a wire guide lumen formed therein.
• an external access port may be provided.
• a section of jacket member 22 that was covering channel 23 may be removed to form access port 42, as shown in FIG. IA.
• access port 42 may be adapted for use in short wire or intraductal exchange procedures. More specifically, wire guide 40 is inserted into a patient's body cavity and guided to a target location. Catheter 20 is then advanced over wire guide 40 via side lumen 24. Wire guide 40 may exit side lumen 24 at access port 42, i.e., in a region where jacket member 22 does not cover channel 23, as shown in FIG. IA. Using this technique, the length of wire guide 40 may be significantly reduced to facilitate a surgical procedure since only a portion of catheter 20 is coupled to wire guide 40. [0035] Alternatively, a full-length wire guide may be employed in conjunction with catheter 20.
• the full-length wire guide may be inserted into a patient's body cavity and guided to a target location.
• the distal end of catheter 20 is then inserted over a proximal end of the wire guide, for example, using side lumen 24 or 26, or alternatively, internal lumen 28.
• a variety of procedures may be performed, such as an imaging procedure and/or an interventional procedure.
• jacket member 22 may be manufactured using a splittable material to allow a wire guide to be removed from one of the channels. While most thin polymer jacket members may be split with sufficient lateral force applied against it, it is preferred that the polymeric materials produce a clean, straight split when the wire guide is removed.
• jacket member 22 may comprise one or more perforations (not shown).
• the perforations may be formed in a distal region of jacket member 22 that overlays channel 25. Fluid may be infused via side lumen 26 and may exit the catheter at a target location via the perforations disposed in the jacket member.
• Modular catheter 20 also may be used in conjunction with an imaging system that is integral to, or separate from, catheter 20.
• an imaging system that is integral to, or separate from, catheter 20.
• endoscopic visualization may be performed through lumen 28 by employing fiber optic lines coupled to an external viewing device.
• IVUS intravascular ultrasound
• catheter 20 may be used in conjunction with catheter 20.
• One or more balloons may be provided on an exterior surface of jacket member 22.
• the balloons may be provided on a distal region of catheter 20, in fluid communication with one or more lumens 24, 26 and 28. Fluid communication may be achieved by forming a side port (not shown) in a lateral surface of jacket member 22, such that the side port is disposed within the confines of the balloon and coupled to a corresponding lumen.
• the balloon may be selectively inflated for a variety of purposes, e.g., during a balloon angioplasty procedure, dilation and/or stone extraction.
• catheter 20 may be used to deploy a self-expanding member, such as a shape-memory stent (not shown).
• a stent may be provided in a collapsed delivery configuration around an exterior surface of jacket member 22, and an exterior sheath (not shown) may cover jacket member 22 to restrain the stent in the delivery configuration.
• an exterior sheath (not shown) may cover jacket member 22 to restrain the stent in the delivery configuration.
• the outer sheath may be retracted proximally with respect to jacket member 22 to expose the stent and permit its expansion within a body cavity.
• multiple jacket members may be employed along a longitudinal and/or circumferential length of catheter 20.
• the jacket members may have similar or different characteristics, depending on the needs of a procedure.
• a first jacket member may be disposed over the entire circumference of catheter 20 along its proximal region, while a second jacket member may be disposed over the circumference of a distal region of catheter 20.
• a first jacket member may be partially disposed about a circumferential region of catheter 20, e.g., covering channel 23, while a second jacket member may be disposed over another circumferential region, e.g., covering channel 25, and so forth.
• catheter 20' is similar to catheter 20 of FIGS. 1 A-IB, with a main exception that jacket member 22' comprises a shrinkable material.
• shrinkable material suitable for use with the present invention is heat-shrinkable polytetrafluoroethylene (PTFE) 5 although other materials may be employed.
• PTFE heat-shrinkable polytetrafluoroethylene
• catheter 120 comprises multiple core elements coupled together by at least one jacket member 122.
• jacket member 122 comprises a shrinkable material, such as heat-shrinkable PTFE, that permits the core elements to be held together to form the overall catheter structure.
• Catheter 120 comprises first core element 124 having lumens 128 and 129 formed therein, second core element 130 having lumen 132 formed therein, and third core element 136. While the core elements of FIG. 3 show two substantially semi-circular core elements having a rectangular core element disposed therebetween, any number of core element configurations may be provided. For example, the core elements may be square-shaped, circular, oval-shaped, pie- shaped, and so forth.
• catheter 120 may comprise fewer or greater than three core elements, and each core element may have one or more lumens, or no lumen whatsoever, as generally depicted in FIG. 3. Further, catheter 120 may comprise side lumens formed from channels, as described with respect to FIGS. 1 -2 above. If lumens are provided within the core elements, they may be used for any number of purposes ranging from serving as a wire guide lumen, fluid aspiration or infusion conduit, device delivery lumen, imaging channel, and so forth.
• void spaces may be formed between core elements.
• catheter 120' of FIG. 4A is similar to catheter 120 of FIG. 3, with the exception that third core element 136 has been removed.
• void region 1 75 is formed in a central region of catheter 120'.
• the void region may be formed by providing indentation 161 on semi-circular first core element 124, and further providing opposing indentation 163 on semi-circular second core element 130.
• void region 175 may be formed by providing an indentation within only one of the core elements. Void region 175 may be used as a conduit to deliver fluids, instruments, and perform other functions.
• the void region may be provided along any region about the cross-section of catheter 120', for example, it may be formed in a central region as shown in FIG. 4A, or alternatively, near an exterior region such that jacket member 122 fully or partially encloses the void region. If desired, void region 175 may span the entire longitudinal length of catheter 120', or may only span a portion of its length. [0048] In addition, the core elements may securely interlock, as generally depicted in FIG. 4B.
• first core element 124' comprises indentation 185 disposed therein
• second core element 130' comprises protrusion 184, which is configured to securely interlock with indentation 185. While nested triangular protrusions and indentations are depicted in FIG. 4B, any number of interlocking shapes may be provided. It should also be noted that any of the embodiments described above may employ the interlocking components of FIG. 4B, and may further employ any combination of side lumens, void regions and other components depicted herein.
• FIGS. 3-4 have several advantages over previously-known catheters that are manufactured by a single extrusion, or formed by co- extrusion of two or more materials into a single profile.
• the latter method is relatively complex, and may not be feasible when the processing temperatures of different materials are disparate.
• core elements 124 and 130, and optionally core element 136 may be held together, even if they have different material properties.
• third core element 136 may comprise a substantially rigid metal strip having a compliance that is different than core elements 124 and/or 130.
• the core elements of FIGS. 3-4 which need not be thermally fused together, may be movable relative to one another.
• FIG. 3 may be slidable longitudinally with respect to first and second core elements 124 and 130, respectively. Such movement may occur when the catheter is inserted through tortuous vasculature, i.e., the design permits the core elements to move with respect to one another to help the catheter conform to the anatomy. Alternatively, movement of the core elements may occur by manual manipulation by a physician, e.g., by proximally retracting or distally advancing proximal ends of the individual core elements, or mechanisms operably coupled to thereto. By permitting core elements to slide with respect to one another, catheter 120 may change its fundamental shape and/or physical properties. Further, distal advancement of one or more core elements 124, 130 and 136 beyond the distal end of catheter 120 may have functional purposes, either in combination with, or in lieu of, advancing other instruments through their associated working lumens.
• Catheter 220 has proximal region 221 and distal region 223, as shown in FIG. 5 A.
• the catheter comprises at least one core element 224 having first end 225 and second end 226, and further comprises jacket member 222, as shown in FIG. 5B.
• Core element 224 preferably is flexible and may move from a constrained state, depicted in FIG. 5B, to a relaxed, expanded state, as shown in FIG. 5C.
• core element 224 is provided along at least a portion of distal region 223, and more preferably, at the distal most end of catheter 220.
• another core element may be disposed within jacket member 222 at a location proximal to core element 224.
• a non-expandable circular core element having a lumen therein (not shown) is disposed proximal to, and abutting, core element 224.
• core element 224 is held in the constrained configuration by jacket member 222, as shown in FIG. 5B.
• Jacket member 222 may shrink about the constrained core element, e.g., by employing heat-shrink tubing.
• Core element 224 is held in the constrained state by jacket member 222 such that first and second ends 225 and 226 form a substantially circular shape that conforms to an interior surface of jacket member 222.
• first end 225 does not touch second end 226, thereby forming gap 237 therebetween.
• lumen 231 may be formed therein, as shown in FIG. 5B.
• Catheter 220 may be delivered into a patient's body cavity with core element 224 being in the constrained state.
• Lumen 231 may be employed as a wire guide lumen to guide catheter 220 to a target location. Additionally, infusion or aspiration may be provided through lumen 231, or medical instruments may be delivered therethrough. If a circular core element having a lumen therein is disposed proximal to core element 230, as discussed above, its lumen preferably is in fluid communication with lumen 231.
• core element 224 When catheter 220 is positioned at a desired location, core element 224 may be deployed by proximally retracting jacket member 222 with respect to core element 224. When core element 224 is no longer constrained by jacket 222, it may return to its relaxed, expanded state, as shown in FIG. 5C. In the expanded state, core element 224 may be used to apply a radially outward pressure within a body cavity. If used in a vessel, core element 224 may function like a stent by being configured to expand the vessel in a radially outward direction.
• core element 224 may be transferred from the constrained state to the expanded state by employing a cutting instrument (not shown).
• the cutting instrument may be delivered through lumen 231 , and may selectively cut through jacket member 222 via gap 237. Once the jacket member has been cut, it no longer constrains core element 224 and permits its expansion within a body cavity.
• FIG. 5D an alternative embodiment of catheter 220 is provided. Distal end 223' of catheter 220' houses multiple core elements 224a, 224b and 224c. As will be apparent to one skilled in the art, greater or fewer than three core elements may be provided, and they may be similar to core element 224 of FIGS. 5B-5C. Tn the embodiment of FIG.
• proximal retraction of jacket member 222 with respect to the constrained core elements will first deploy core element 224c. Further proximal retraction of the jacket member may deploy core elements 224b and 224a, respectively, at desired target sites.
• core element 255 of catheter 250 comprises a coil-shape in the constrained configuration when housed within jacket member 222, and may expand to a larger coil-shape or a circular shape when deployed.
• third core element 136 may be retained in a constrained state when disposed between first and second core elements 124 and 130, and further held in place by jacket member 122. However, if third core element 136 is advanced distally beyond catheter 120, such that it is no longer constrained by jacket member 122, it may assume an expanded shape. In such embodiments, a core element may return to a predetermined, expanded configuration due to its mechanical properties, or because the core element comprises a shape-memory material such as Nitinol.
• catheter 320 comprises proximal region 321 and. distal region 323.
• proximal region 321 comprises first core element 328 and second core element 338.
• Second core element 338 may be disposed substantially coaxially within a portion of first core element 328.
• first core element 328 may comprise longitudinal bore 335
• second core element 338 may be adapted to be seated within bore 335.
• Second core element 338 may be partially directly exposed to jacket member 322 at region 352, as shown in FIG. 6B.
• distal region 323 may only comprise second core element 338.
• catheter 320 by providing a modular catheter in accordance with catheter 320, it is possible to provide a catheter having a variable cross-section along its longitudinal axis. In particular, it may be desirable to construct the catheter having a smaller outer diameter along distal region 323, and a relatively larger diameter along proximal region 322, as generally depicted in FIG. 6A.
• first core element 328 may extend distal to second core element 338, i.e., in a manner that is opposite to the distal region 323 depicted in FIG. 6A.
• First core element 328 may comprise one or more lumens, e.g., auxiliary lumens 341 , 342 and 343, while second core element 338 may comprise working lumen 339.
• catheter 320 may be advanced over a wire guide via one of the lumens.
• first core element 328 and jacket member 322 may initially span the entire length of catheter 320, i.e., they may extend along distal region 323 such that the outer diameter along the length of catheter 320 is substantially uniform.
• a physician may proximally retract first core element 328 and jacket member 322 with respect to second core element 338, for example, to obtain the configuration depicted in FIG. 6A.
• the retraction may be achieved by pulling proximal ends of first core element 328 and jacket member 322, or any mechanisms that are operably coupled thereto.
• the entire catheter assembly may be further maneuvered as one unit, e.g., by advancing the assembly of FIG. 6A distally within a vessel.
• a physician may further retract first core element 328 and jacket member 332, or may retract the entire assembly.
• catheter 420 comprises proximal region 421 and distal region 423.
• Proximal region 421 comprises first core element 431
• distal region 423 comprises second core element 437.
• one jacket member 422 is disposed along the entire length of catheter 420, such that the jacket member circumferentially surrounds first core element 431 and second core element 437.
• First core element 431 may comprise a distal end that abuts a proximal end of second core element 437, as depicted in FIG. 7A, or alternatively, first core element 431 ' may partially overlap with second core element 437', as shown in FIG. 7B.
• first core element 431 ' may partially overlap with second core element 437', as shown in FIG. 7B.
• catheter 420 may have variable properties along its longitudinal axis. For example, proximal region
• first core element 431 comprises first lumen 441 and second lumen 442, while second core element 437 comprises lumen 447.

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• 2006
  • 2006-12-12 JP JP2008547315A patent/JP5137846B2/ja active Active
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