The present disclosure relates generally to catheter assemblies having a balloon threadably coupled to the catheter body, and to methods for assembling the same.
Balloon catheters are employed in a wide variety of medical procedures, including dilation of narrowed blood vessels, placement of stents and other implantable devices, temporary or permanent occlusion of blood vessels, drug delivery, thrombectomy, embolectomy, atherectomy, angioplasty, other endovascular procedures, and other procedures within the lumen of a mammalian body such as a human body. In a typical application, a balloon catheter can be advanced to the desired location in the vascular system or other lumen in the body. The balloon is then pressure-expanded in accordance with a medical procedure. Thereafter, the pressure is released from the balloon, allowing the balloon to contract and permitting removal of the balloon catheter.
Balloon catheters are typically formed by coupling an inflatable balloon to a catheter body. The catheter body is typically made of a non-compliant material. In contrast, the inflatable balloon can be made of various materials, depending on whether it will be compliant or non-compliant. The inflatable balloon section can be coupled to the catheter body using adhesives, laser welding, thermal bonding, crimps, shrink tubes, olives, or various other means.
However, commonly used means for coupling the balloon to the catheter body can require increased manufacturing cost and complexity, or can limit the materials used. For example, due to chemical differences, adhesives do not always form strong bonds between compliant materials, such as silicone, and typical catheter-body materials, such as polyurethane. When a compliant balloon is inflated repeatedly, or to high pressures, the balloon can peel away from the catheter body, causing the bond to fail.
Thus, technology that simplifies the process of coupling a balloon to a catheter body is desirable because it can potentially increase production efficiency and balloon catheter quality. Additionally, technology that improves the means of coupling a balloon to a catheter body is desirable because it can potentially improve balloon catheter performance and increase the available materials for manufacture.
In general, the present disclosure provides systems and methods for balloon catheter assemblies wherein the balloon is threadably coupled to the catheter body. For example, in various embodiments, a device is provided comprising a tube member having a first end and a second end with a lumen extending therebetween, and a balloon, wherein the balloon is in fluid communication with the lumen and is threadably coupled to the tube member. In further embodiments, methods of assembling or disassembling a balloon catheter are provided.
The accompanying drawings are included to provide a further understanding of the present disclosure and are incorporated in, and constitute a part of, this specification, illustrate various embodiments, and together with the description, serve to explain the principles of the disclosure.
a illustrates a perspective view of the disassembled components of a catheter assembly.
b illustrates a perspective view of an assembled catheter assembly.
c illustrates a perspective view of an assembled and inflated catheter assembly.
d illustrates a cross-sectional view of an assembled and inflated catheter assembly.
a illustrates a side view of a catheter assembly, wherein the balloon is viewed cross-sectionally.
b illustrates a side view of a catheter assembly, wherein the balloon is viewed cross-sectionally.
Persons skilled in the art will readily appreciate that various aspects of the present disclosure may be realized by any number of methods and apparatuses configured to perform the intended functions. Stated differently, other methods and apparatuses may be incorporated herein to perform the intended functions. It should also be noted that the accompanying drawing figures referred to herein are not all drawn to scale, but may be exaggerated to illustrate various aspects of the present disclosure, and in that regard, the drawing figures should not be construed as limiting. Finally, although the present disclosure may be described in connection with various principles and beliefs, the present disclosure should not be bound by theory.
As used herein, the term “proximal,” refers to a portion of the catheter assembly closer to the entity assembling, operating, or otherwise using the catheter assembly than a second reference point; the term “distal,” as used herein, refers to a portion of the catheter assembly farther from the practitioner assembling, operating, or otherwise using the catheter assembly than a second reference point. With further regard to the terms proximal and distal, and because the present disclosure is not limited to peripheral and/or central approaches, this disclosure should not be narrowly construed with respect to these terms. Rather, the assemblies described herein can be altered and/or adjusted relative to the anatomy of a patient.
Additionally, catheter bodies used in medical procedures are generally tubes or otherwise cylindrical structures. However, although the terms “catheter body” and “tube member” are used interchangeably herein, other non-cylindrical shapes which incorporate the present disclosure's elements may likewise be used.
Additionally, as used herein, balloon catheters generally refer to medical devices wherein a tube can be inserted into a body cavity, duct, or vessel, and an attached balloon can be inflated hydraulically or pneumatically to, alone or in conjunction with one or more endoluminal devices, enlarge an opening or passage in the body. Accordingly, as used herein, the term “catheter assembly” refers to a device that can be inserted into a body and inflated to enlarge an opening or passage in that body. Briefly, other passage-enlarging devices may likewise benefit from the present disclosure, and use of the term “catheter assembly” herein is not intended to limit the scope, applicability, or configuration of the disclosure in any way.
As used herein, “threads” refer to generally helical or spiral ridges and valleys on one component that are configured to engage generally similar ridges and valleys on another component in order to facilitate securing the components to one another. As used herein, “threads” can be either “right-handed” or “left-handed.”
Numerous materials can be used to achieve each element of the apparatus disclosed herein. Typical materials used to construct the present disclosure can include commonly known materials such as Amorphous Commodity Thermoplastics that include Polymethyl Methacrylate (PMMA or Acrylic), Polystyrene (PS), Acrylonitrile Butadiene Styrene (ABS), Polyvinyl Chloride (PVC), Modified Polyethylene Terephthalate Glycol (PETG), Cellulose Acetate Butyrate (CAB); Semi-Crystalline Commodity Plastics that include Polyethylene (PE), High Density Polyethylene (HDPE), Low Density Polyethylene (LDPE or LLDPE), Polypropylene (PP), Polymethylpentene (PMP); Amorphous Engineering Thermoplastics that include Polycarbonate (PC), Polyphenylene Oxide (PPO), Modified Polyphenylene Oxide (Mod PPO), Polyphenylene Ether (PPE), Modified Polyphenylene Ether (Mod PPE), Thermoplastic Polyurethane (TPU); Semi-Crystalline Engineering Thermoplastics that include Polyamide (PA or Nylon), Polyoxymethylene (POM or Acetal), Polyethylene Terephthalate (PET, Thermoplastic Polyester), Polybutylene Terephthalate (PBT, Thermoplastic Polyester), Ultra High Molecular Weight Polyethylene (UHMW-PE); High Performance Thermoplastics that include Polyimide (PI, Imidized Plastic), Polyamide Imide (PAI, Imidized Plastic), Polybenzimidazole (PBI, Imidized Plastic); Amorphous High Performance Thermoplastics that include Polysulfone (PSU), Polyetherimide (PEI), Polyether Sulfone (PES), Polyaryl Sulfone (PAS); Semi-Crystalline High Performance Thermoplastics that include Polyphenylene Sulfide (PPS), Polyetheretherketone (PEEK); and Semi-Crystalline High Performance Thermoplastics, Fluoropolymers that include Fluorinated Ethylene Propylene (FEP), Ethylene Chlorotrifluroethylene (ECTFE), Ethylene, Ethylene Tetrafluoroethylene (ETFE), Polychlortrifluoroethylene (PCTFE), Polytetrafluoroethylene (PTFE), expanded Polytetrafluoroethylene (ePTFE), Polyvinylidene Fluoride (PVDF), Perfluoroalkoxy (PFA). Other commonly known medical grade materials include elastomeric organosilicon polymers, polyether block amide or thermoplastic copolyether (PEBAX) and metals such as stainless steel and nickel/titanium alloys. Additionally various materials can be combined to obtain the most attractive characteristics of existing (or as yet unknown) plastic, metal, or composite materials, and can be incorporated into the elements disclosed herein.
As noted above, in conventional balloon catheters, the balloon is coupled to the catheter body through various means including adhesives, laser welding, thermal bonding, crimps, olives, and the like. In accordance with the present disclosure, manufacturing efficiencies and quality improvements can be achieved through incorporation of a threaded balloon catheter seal.
For example, a balloon catheter can be improved by coupling the balloon to the catheter body with a threaded seal. Threads located on the catheter or balloon components can increase the pressure-bearing surface area which creates the seal between the catheter body and the balloon. As a result, the seal can be less likely to fail when the balloon is subjected to high pressures during inflation.
Additionally, use of a threaded seal can improve manufacturing efficiencies and ease of assembly. For example, by eliminating the need for additional components such as olives, crimps, and chemical sealants, as well as the need for manufacturing processes such as heat sealing and crimping, cost efficiencies can be achieved. Use of a threaded seal can also ease assembly, allowing users, rather than the manufacturer, to couple the balloon to the catheter and optionally detach the balloon from the catheter, and in some embodiments do so in vivo. As such, balloon catheter components can be manufactured or sold as modular components; and users can assemble different components based on a particular need, while still maintaining the functionality and quality of the balloon catheter seal.
Further, while threadably coupling the balloon to the catheter can create a seal sufficient to withstand high pressure associated with balloon inflation, other methods of creating a balloon catheter seal can be used in conjunction with the present disclosure. For example, a balloon can be threadably coupled to a catheter body and also generally coupled through various means including adhesives, laser welding, thermal bonding, crimps, olives, and the like.
The above being noted, in accordance with an embodiment of the present disclosure, a catheter assembly comprises a tube member having a first end and a second end with a lumen extending therebetween, and a balloon, wherein the balloon is in fluid communication with the lumen and is threadably coupled to the tube member. Briefly, these features of the present disclosure are provided in order that the detailed description herein will be better understood and appreciated; however, the present disclosure can also comprise additional features, which will be subsequently described.
For example, with reference to
In various embodiments, the tube member 101 can be made with materials such as those previously described herein. However, one skilled in the relevant art will recognize that the tube member can be made of any number of plastics or composite materials. Further, the tube member's physical characteristics, such as flexibility, diameter, wall thickness, and weight can be varied in any way necessary to accomplish the desired performance characteristics, while still falling within the scope of the present disclosure.
The tube member 101 can be generally cylindrical in shape. However, the tube member can take any number of shapes potentially varying in length, wall-thickness, diameter, or cross-sectional profile. In accordance with the present disclosure, variations in tube member diameter can allow the balloon to slide over portions of the tube member without threadably coupling to it. For example and with reference to
Additionally, in accordance with the present disclosure and with reference to
For example, and with reference to
The tube member 101 can additionally comprise an aperture 106. The aperture 106 can be adapted to allow fluid communication (pneumatic or hydraulic) between the lumen 104 and the interior of the balloon 107. Fluid communication can facilitate balloon inflation when the catheter assembly 100 is fully assembled. The aperture 106 generally can be located between the tube ends 102, 103.
That being said, the aperture can be located on any portion of the tube member such that it facilitates balloon inflation. Further, the aperture can vary in size and shape. One skilled in the relevant art will recognize that the aperture can take any number of shapes and sizes depending on the particular requirements of the catheter assembly, and the embodiments described herein are not intended to limit the scope of the present disclosure.
In accordance with an embodiment, the catheter assembly further comprises a balloon 107. In various embodiments, the balloon 107 generally can be made of compliant or non-compliant materials, such as those previous described herein, depending on the particular requirements of the catheter assembly. That being said, catheter balloons can be made of numerous materials. Although an exhaustive list is not included herein, one skilled in the art will appreciate that various plastics, metals, composites, and various combinations thereof can be used, all of which fall within the scope of the present disclosure.
In an assembled catheter assembly, the balloon can at least partially surround the tube member. With reference to
Additionally and with reference to
The balloon can further comprise at least one balloon end. For example, and with reference to
In accordance with the present disclosure, the balloon 107 can further comprise balloon threads 110. Balloon threads 110 can be located on the interior surface of the balloon 107. Further, the balloon threads 110 can extend axially for a distance along at least one balloon end. For example, with reference to
In accordance with the present disclosure, the balloon can take any of numerous shapes. In general, the shape of the balloon can be complimentary with the shape of the tube member to which it is coupled and/or an endoluminal device used with the balloon. Complimentary shapes can facilitate creation of a seal between the balloon and the tube member or endoluminal device. For example, with reference to
For example, the shape of the balloon, as well as the location, number, and configuration of balloon ends and balloon threads can vary depending on the configuration of the tube member, tube ends, and tube threads. In like manner, the number of balloons can vary. For example, a catheter assembly can comprise a plurality of any combination of the tube member and balloon assemblies described herein.
With reference to
Alternatively and with reference to
Alternatively and with reference to
That being said, the described embodiments are merely illustrations of how the balloon shape and tube member shape can be adapted in various embodiments of the present disclosure. Described embodiments are not intended to limit the scope of the present disclosure in any way. Those skilled in the art will recognize that the embodiments herein are merely examples, and the balloon and tube member can take various shapes and configurations, all while falling within the scope of the present disclosure.
With reference to
Alternatively and with reference to
Alternatively and with reference to
Numerous characteristics and advantages have been set forth in the preceding description, including various alternatives together with details of the structure and function of the devices and/or methods. The disclosure is intended as illustrative only and as such is not intended to be exhaustive. It will be evident to those skilled in the art that various modifications may be made, especially in matters of structure, materials, elements, components, shape, size, and arrangement of parts including combinations within the principles of the invention, to the full extent indicated by the broad, general meaning of the terms in which the appended claims are expressed. To the extent that these various modifications do not depart from the spirit and scope of the appended claims, they are intended to be encompassed therein.
Number | Date | Country | |
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61739578 | Dec 2012 | US |