This document relates to catheters. More specifically, this document relates to catheters usable in medical procedures, and to perforation systems including catheters.
The following summary is intended to introduce the reader to various aspects of the detailed description, but not to define or delimit any invention.
Catheters are disclosed. According to some aspects, a catheter includes an elongate shaft extending longitudinally between a proximal portion defining a proximal end and a distal portion defining a distal end. A lumen extends through the shaft from the proximal end to the distal end. The shaft includes a heat-shielding layer and an outer layer adjacent the heat-shielding layer. The heat-shielding layer includes an inner liner layer adjacent the lumen, an intermediate layer adjacent the inner liner layer. In the distal portion, at least a section of the outer layer is radiopaque.
In some examples, the liner layer includes a first polymer. The first polymer can be or can include polytetrafluoroethylene (PTFE).
In some examples, the intermediate layer includes a second polymer. The second polymer can be melt processable and flexible. The second polymer can be or can include at least one of a polyether block amide (PEBA), an aliphatic polyether-based thermoplastic polyurethane (TPU), a nylon, a polyurethane, and a polyethylene. In some examples, the second polymer is polyether block amide.
In some examples, the outer layer includes a third polymer. The third polymer can be or can include at least one of a polyether block amide (PEBA), an aliphatic polyether-based thermoplastic polyurethane (TPU), a nylon, a polyurethane, and a polyethylene. In some examples, the third polymer is polyether block amide (PEBA).
In some examples, in the section that is radiopaque, the third polymer is filled with a radiopaque filler. The radiopaque filler can be or can include at least one of tungsten, barium sulphate, and bismuth. In some examples, the radiopaque filler includes tungsten.
In some examples, the section that is radiopaque extends along an entirety of the distal portion.
In some examples, the section that is radiopaque includes a radiopaque band in the distal portion. The radiopaque band can be at the distal end.
In some examples, the distal portion has a length of between about 1 mm and about 5 mm.
In some examples, the liner layer, intermediate layer, and outer layer are of a constant thickness between the proximal end and the distal end.
In some examples, the proximal portion includes at least a first tapered section adjacent the distal portion, and the outer layer tapers in thickness in the tapered section.
In some examples, the distal portion is tapered.
Perforation systems are also disclosed. According to some aspects, a perforation system includes a catheter, a perforation device, and a radiofrequency generator. The catheter includes an elongate shaft extending longitudinally between a proximal portion defining a proximal end and a distal portion defining a distal end, and a lumen extending through the shaft from the proximal end to the distal end. The shaft includes a heat-shielding layer and an outer layer adjacent the heat-shielding layer. The heat-shielding layer includes an inner liner layer adjacent the lumen, and an intermediate layer adjacent the inner liner layer. In the distal portion, at least a section of the outer layer is radiopaque. The perforation device includes a shaft receivable in the catheter and having a heat-generating radiofrequency electrode positionable proximate the distal end of the catheter. The radiofrequency generator is connectable to the perforation device to supply radiofrequency energy to the radiofrequency electrode.
The accompanying drawings are for illustrating examples of articles, methods, and apparatuses of the present disclosure and are not intended to be limiting. In the drawings:
Various apparatuses or processes or compositions will be described below to provide an example of an embodiment of the claimed subject matter. No example described below limits any claim and any claim may cover processes or apparatuses or compositions that differ from those described below. The claims are not limited to apparatuses or processes or compositions having all of the features of any one apparatus or process or composition described below or to features common to multiple or all of the apparatuses or processes or compositions described below. It is possible that an apparatus or process or composition described below is not an embodiment of any exclusive right granted by issuance of this patent application. Any subject matter described below and for which an exclusive right is not granted by issuance of this patent application may be the subject matter of another protective instrument, for example, a continuing patent application, and the applicants, inventors or owners do not intend to abandon, disclaim or dedicate to the public any such subject matter by its disclosure in this document.
Generally disclosed herein are catheters and related systems. The catheters can be used in various medical procedures, such as (but not limited to) perforation procedures. As will be described in further detail below, the catheters disclosed herein have at least one radiopaque section in the distal portion thereof. For example, the entire length of the distal portion can be radiopaque, or the distal portion can include one or more radiopaque bands. During a medical procedure, the radiopaque section can be viewed under fluoroscopy, to facilitate proper positioning of the catheter. Furthermore, as will be described below, the distal portion is configured so that the radiopaque section is shielded from heat (e.g. heat generated by other medical devices). This can allow for the radiopaque section to be positioned at or proximate the distal end of the catheter, while preventing or inhibiting failure of the radiopaque section due to heat exposure.
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In the example shown, the system 100 includes a catheter 102, a radiofrequency (RF) perforation device 104, and an RF generator 106. The RF perforation device 104 includes an elongate body 108 and an RF electrode 110. The RF perforation device 104 is connectable to the RF generator 106, so that the RF generator 106 can supply RF energy to the RF electrode 110. Optionally, the system 100 can further include a dilator (not shown).
In one example of use, the catheter 102 can be advanced intravenously via the femoral vein towards the right atrium of the patient's heart. The RF perforation device 104 can be connected to the RF generator 106, which can in turn be connected to one or more grounding pads (not shown). The RF perforation device 104 can then be advanced through the catheter 102 (optionally via the dilator). When the catheter 102 is in the desired position in the patient's heart, for example adjacent the fossa ovalis, the RF perforation device 104 can be advanced to position the RF electrode 110 adjacent the fossa ovalis, and the RF generator 106 can be activated to deliver RF energy to the RF electrode 110, to perforate the fossa ovalis. Such procedures can be carried out, for example, as a medical treatment, or to gain access to the left atrium for a subsequent medical treatment.
As mentioned above and as will be described in further detail below, the catheter 102 can include at least one radiopaque section in the distal portion thereof. During the procedure, fluoroscopy can be used to visualize the radiopaque section and thereby confirm or determine or check the position of the catheter 102 within the patient's body. However, delivery of RF energy can cause significant heat to be generated by the RF electrode 110 (i.e. the RF electrode is heat generating), and heat can cause failure of radiopaque materials. The catheter 102 is thus configured such that the radiopaque section is shielded from heat generated by the RF electrode 110.
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In the example shown, the proximal portion 116 makes up a majority of the length of the shaft 112, while the distal portion 120 makes up a relatively small portion of the length. For example, the proximal portion 116 can be sufficiently long to extend between the femoral vein and the heart (e.g. approximately 250 cm), while the distal portion 120 can be only a few centimeters (e.g. between 1 cm and 5 cm, or about 3 cm).
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As will be described below, the shaft 112 includes a plurality of layers, at least one of which includes a radiopaque section, and at least another of which is configured as a heat-shielding layer to shield the radiopaque section from heat.
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In general, in the distal portion 120, at least a section (also referred to herein as a ‘radiopaque section’) of the outer layer 130 is radiopaque. Referring to
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In the example shown, the liner layer 126, intermediate layer 128, and outer layer 130 are of a constant thickness between the proximal end 118 and the distal end 122. In alternative examples, as will be described below, one or more of the layers may have a varying thickness. For example, one or more of the layers may be tapered.
In the example shown, the liner layer 126, intermediate layer 128, and outer layer 130 all extend to the distal end 122 of the shaft. In alternative examples, one or more of these layers may extend to a position that is slightly shy of the distal end of the shaft. For example, the inner liner layer may extend to and define the distal end of the shaft. The intermediate layer and outer layer may extend to a position that is slightly shy of the distal end of the shaft, i.e. so that the inner liner layer extends proud of the intermediate layer and outer layer. This can further shield the radiopaque section of the outer layer from heat.
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While the above description provides examples of one or more processes or apparatuses or compositions, it will be appreciated that other processes or apparatuses or compositions may be within the scope of the accompanying claims.
To the extent any amendments, characterizations, or other assertions previously made (in this or in any related patent applications or patents, including any parent, sibling, or child) with respect to any art, prior or otherwise, could be construed as a disclaimer of any subject matter supported by the present disclosure of this application, Applicant hereby rescinds and retracts such disclaimer. Applicant also respectfully submits that any prior art previously considered in any related patent applications or patents, including any parent, sibling, or child, may need to be re-visited.
Filing Document | Filing Date | Country | Kind |
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PCT/IB2021/052851 | 4/6/2021 | WO |
Number | Date | Country | |
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63007662 | Apr 2020 | US |