Prevention of kinks in catheter irrigation tubes
09757189 · 2017-09-12
Assignee
Inventors
Cpc classification
A61M25/0009
HUMAN NECESSITIES
A61M25/005
HUMAN NECESSITIES
Y10T29/49826
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
A61B18/1492
HUMAN NECESSITIES
A61M2025/0063
HUMAN NECESSITIES
International classification
Abstract
A medical device includes an insertion tube, having a distal end for insertion into a body of a subject and an opening at the distal end. A lumen, which includes a flexible tube which passes longitudinally through the insertion tube so as to communicate with the opening at the distal end of the insertion tube, is secured under tension inside the insertion tube.
Claims
1. A method for producing a medical device, comprising: providing an insertion tube configured for insertion into a body of a subject, the insertion tube having a distal end with an opening at the distal end, and an inner wall; inserting a flexible tube longitudinally through the insertion tube so as to communicate with the opening at the distal end of the insertion tube; bending the insertion tube to form a curve; fastening the flexible tube under tension directly to the inner wall of the insertion tube while the insertion tube is bent, the flexible tube being secured under tension to the insertion tube, the flexible tube being secured under tension in any position of the insertion tube including when the insertion tube is substantially straight; and locating an adhesive on the flexible tube and the inner wall of the insertion tube at two or more locations in spaced relation to each other for securing the flexible tube to the inner wall of the insertion tube.
2. The method according to claim 1, wherein fastening the flexible tube comprises fixing the flexible tube within the insertion tube along the inner wall of the curve.
3. A method for providing a flexible tube under tension within an insertion tube, comprising: providing an insertion tube having a distal end for insertion into a body of a subject and an opening at the distal end; inserting a flexible tube longitudinally through the insertion tube such that the flexible tube communicates with the opening at the distal end of the insertion tube; bending the insertion tube to form a curve; fastening the flexible tube under tension directly to an inner wall of the insertion tube while the insertion tube is in a curved shape such that the flexible tube is secured under tension, the flexible tube being secured under tension in any position of the insertion tube including the insertion tube being substantially straightened; and locating an adhesive on the flexible tube and the inner wall of the insertion tube at two or more locations in spaced relation to each other for securing the flexible tube to the inner wall of the insertion tube.
4. The method of claim 3, further comprising: Maintaining the tension of the flexible tube secured to the inner wall of the insertion tube when the insertion tube is in a plurality of positions including a substantially straight position.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1)
(2)
(3)
DETAILED DESCRIPTION OF THE INVENTION
(4)
(5) An operator 26 of system 20 inserts a catheter 28 through a blood vessel into a chamber of a heart 24 of a subject 22, and manipulates the catheter so that a distal end 32 of the catheter contacts the endocardium in an area that is to be treated. The distal tip of the catheter has one or more openings to enable irrigation of the treatment area and a tensioned lumen for conveying irrigation fluid to the distal tip, as shown and described hereinbelow. In other respects, however, system 20 resembles systems for cardiac ablation treatment that are known in the art, such as the above-mentioned Biosense Webster system, and the components of such systems may be adapted for use in system 20.
(6) After positioning distal end 32 at an ablation site, and ensuring that the tip is in contact with the endocardium at the site, operator 26 actuates a radio frequency (RF) energy generator 44 in a control console 42 to supply RF energy via a cable 38 to distal end 32. Meanwhile, an irrigation pump 48 supplies a cooling fluid, such as saline solution, via a tube 40 and the lumen in catheter 28 to the distal end. Operation of the RF energy generator and the irrigation pump may be coordinated in order to give the appropriate volume of irrigation during ablation, so as to cool the tip of the catheter and the tissue without overloading the heart with irrigation fluid. A temperature sensor (not shown in the figures) in distal end 32 may provide feedback to console 42 for use in controlling the RF energy dosage and/or irrigation volume.
(7)
(8) The outer surface of distal tip 50 is penetrated by several openings 54. A lumen, in the form of a flexible irrigation tube 56 running longitudinally through insertion tube 60, conveys irrigation fluid from pump 48 and tube 50 to openings 54 in order to irrigate the tissue in the vicinity of the site that is being ablated. Although for the sake of simplicity, only a few openings 54 are shown in
(9) Typically, in cardiac applications, insertion tube 60 has a diameter no greater than 3 mm. Irrigation tube 56 typically comprises a flexible plastic material, such as Polyimide. To fit inside insertion tube 60, and still leave room for cabling and other elements, the diameter of tube 56 is generally less than 1 mm (roughly 800 μm is typical), and its wall thickness is typically no more than about 60 μm. As a result, tube 56 is liable to kink and close off when the catheter bends, thus interrupting the flow of irrigation fluid, with potentially dire consequences.
(10) In order to improve resistance to kinking of this sort, irrigation tube 56 is held under tension within insertion tube 60. This tension causes the wall of tube 56 to deform more evenly over its length when bent, relative to a flaccid tube, and therefore causes the tube to resist kinking unless catheter 28 is very sharply bent. The mechanical performance and safety of the fluid delivery lumen in catheter 28 are therefore enhanced.
(11)
(12) Although the technique illustrated in
(13) It will thus be appreciated that the embodiments described above are cited by way of example, and that the present invention is not limited to what has been particularly shown and described hereinabove. Rather, the scope of the present invention includes both combinations and subcombinations of the various features described hereinabove, as well as variations and modifications thereof which would occur to persons skilled in the art upon reading the foregoing description and which are not disclosed in the prior art.