WO2018050201A1 - Système de cathéter - Google Patents
Système de cathéter Download PDFInfo
- Publication number
- WO2018050201A1 WO2018050201A1 PCT/EP2016/001563 EP2016001563W WO2018050201A1 WO 2018050201 A1 WO2018050201 A1 WO 2018050201A1 EP 2016001563 W EP2016001563 W EP 2016001563W WO 2018050201 A1 WO2018050201 A1 WO 2018050201A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- catheter
- sheath
- elongation
- distal end
- proximal end
- Prior art date
Links
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
- A61M25/01—Introducing, guiding, advancing, emplacing or holding catheters
- A61M25/0105—Steering means as part of the catheter or advancing means; Markers for positioning
- A61M25/0133—Tip steering devices
-
- 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
- A61M25/06—Body-piercing guide needles or the like
- A61M25/0662—Guide tubes
- A61M2025/0681—Systems with catheter and outer tubing, e.g. sheath, sleeve or guide tube
-
- 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
- A61M25/0054—Catheters; Hollow probes characterised by structural features with regions for increasing flexibility
Definitions
- the invention relates to a catheter system comprising a steerable and/or deflectable catheter having a distal end and a proximal end, the proximal end furthermore comprising a manipulator for bending the distal end area of the catheter.
- Steerable or deflectable catheters are well known in the state of the art and are typically used to reach into body areas or lumens of a patient that are difficult to access.
- a typical field of application that is preferably addresses in this specification is heart surgery in which it is intended to place an implant into the heart that at least reduces or preferably eliminates a heart valve insufficiency, i.e. regurgitation.
- the steerability of a catheter refer to the ability to turn or rotate the distal end of the catheter with like-for-like movement of the proximal end of the catheter to which typically a manipulator, preferably a handle is attached.
- Such catheters may provide strong torque transfer along the length of the catheter.
- Deflection refers to the ability to move the catheter tip or preferably a distal end area of the catheter independent of the remaining part of the catheter. In order to provide such function, it is known to transfer a movement at a manipulator situated at the proximal end of the catheter by means of at least one transfer means into a
- Such transfer means may be formed of pull wires or pull fibers that extend along the catheter length and are fixed at the distal end area of the catheter.
- This invention refers to both types of catheters and preferably to the ones providing deflection.
- the necessary implant comprises a closure element and at least one anchoring element, being connected to each other.
- the anchoring element is only connected to the atrial side of the closure element and serves to fix the position of the closure element with the mitral valve annulus.
- the anchoring element is in such a case preferably formed of an
- the expandable cage and the exterior surface of the expanded cage is intended to contact the internal surface of the atrial myocard, preferably without puncturing the myocard.
- the cross section of the expanded cage is typically bigger that the cross section of the atrium of the heart and the cage is resilient and provides at least in a radial direction a force against the myocard that provides fixation of the implant.
- the closure element is also expandable and typically self-expanding or expanded by inflating a balloon of the closure element.
- the exterior surface of the expanded closure element is intended to get in contact with the closing leaflets of the mitral valve and to close a remaining gap between the leaflets.
- Such an implant particularly if it is self-expanding, needs to be carefully positioned in the heart prior to expansion in order to avoid to harm the leaflets or the myocard.
- the anchoring element needs to be placed in the atrium and must not expand prior to be correctly placed.
- a catheter system comprising a steerable / deflectable catheter having a distal end and a proximal end, the proximal end furthermore comprising a manipulator for bending the distal end area of the catheter and comprising an elongation sheath coaxially surrounding the steerable / deflectable catheter at least in its distal end area, the elongation sheath being slidingly movable on the exterior surface of the catheter and along the extension of at least the distal end area of the catheter into a position in which the distal tip of the elongation sheath is projecting beyond the distal tip of the catheter.
- the elongation sheath may be movable between two positions, in the first position the distal tip of the sheath being positioned on the proximal side of the distal catheter tip and in the second position the distal tip of the sheath being positioned on the distal side of the distal catheter tip. Accordingly, in the first position there is no elongation of the catheter at all even though the sheath is positioned around the catheter near the tip. In the second position the catheter is elongated as mentioned before.
- the proximal end of the elongation sheath may comprise an operating means, particularly a handle, preferably near the manipulator of the catheter, the operating means being adapted to be moved by a surgeon in order to move the distal end of the sheath.
- the operating means and the sheath are directly connected.
- the elongation sheath may have a length so that during surgery the proximal end of the sheath or the operating means at the proximal end of the sheath is positioned outside a treated patient. This preferably means that the distance of the proximal end of the sheath to the proximal end of the catheter is smaller than the distance of the proximal end of the sheath to the distal end of the catheter.
- the mechanical properties, particularly the stiffness in axial and/or radial direction of the sheath may vary along the longitudinal extension of the sheath. Accordingly, in a proximal part the sheath may have a bigger axial stiffness compared to the distal part in order to provide like-for-like movement in axial direction if the surgeon moves the operations means in order to advance the elongation sheath.
- the sheath may have a smaller axial stiffness but a bigger radial stiffness in order to withstand the radial forces of self-expanding implant.
- the elongation sheath may comprises an exterior wall and an interior wall, having coiled or braided wires/fibers being
- the proximal end of the catheter, particularly the manipulator of the catheter may comprise an operating means for moving the elongation sheath, the operating means and the elongation sheath being separate, spaced and connected along the distance of separation by at least one transfer means, the transfer means extending between the operating means and the sheath, preferably the transfer means being guided through the catheter, particularly through a hollow catheter wall.
- an operating means for moving the elongation sheath the operating means and the elongation sheath being separate, spaced and connected along the distance of separation by at least one transfer means, the transfer means extending between the operating means and the sheath, preferably the transfer means being guided through the catheter, particularly through a hollow catheter wall.
- the elongation sheath of the catheter system may be totally positioned inside a patient if he is treated.
- the distance of the proximal end of the sheath to the proximal end of the catheter is in this case preferably bigger than the distance of the proximal end of the sheath to the distal end of the catheter. Furthermore, the distance between the proximal end of the sheath and the proximal end of the catheter, particularly the length of the at least one transfer means is bigger than the length of the sheath in its longitudinal direction.
- a catheter system of one of the aforementioned embodiments and even of non- mentioned but comprised embodiments may provide a novel technique of treatment, particularly of placing an implant into the heart.
- Figure 1A, B, C, D illustrate the different stages of the method to place and implant into the heart using a first embodiment of the catheter system
- FIG. 2 illustrates this first embodiment of the system
- FIG. 3 illustrates a second embodiment of the catheter system Detailed description of the invention
- the system is used to forward the distal end area 1 of a steerable / deflectable catheter 2, particularly through the aortic valve 3, into the ventricle 4 below the mitral valve 5.
- the catheter tip 6 may be positioned to have the frontal area of the catheter tip 6 facing the opening in the mitral valve annulus, particularly the distal end of the catheter 1 aiming through the mitral valve annulus.
- the distal end area 1 of the catheter 2 may have a straight end portion 1a ending in the catheter tip 6, the imaginary middle axis 7 of this portion being positioned in the vale annulus and surrounded by it.
- the elongation sheath 8 that is coaxially surrounding at least the distal end area 1 of the catheter 2 may now be advanced, i.e. moved towards the atrium 9 into a position projecting beyond the distal tip 6 of the catheter 1 , particularly starting from a position not projecting beyond the distal tip of the catheter. If the distal end 1 of the catheter 2 has a straight portion 1a the elongation sheath 8 will follow the extension of this portion along the axis / line 7.
- the implant 11 may now be moved out of the steerable / deflectable catheter 1 into the elongation sheath 8 and through the elongation sheath 8.
- the implant 11 will be released from the elongation sheath 8, particularly at least the anchoring element 11a, preferably the self-expanding anchoring element 11a of the implant 11 into the atrium of the heart, as shown in Figure 1 C.
- the sheath 8 protects to valve annulus from the expanding anchoring cage and accordingly placing the implant is totally atraumatic.
- the elongation sleeve does not at all restrict the diameter of the implant. Since the inner diameter of the sheath 8 is bigger than the outer diameter of the catheter 1 and the diameter of the implant 11 is smaller than the inner diameter of the catheter. Any implant that may be fed through the catheter will automatically also pass through the elongation sheath 8.
- Figure 1C shows that the anchoring cage 11a of the implant is expanded and fixes the position of the implant by contacting the myocard in the atrium.
- the elongation sheath that still surrounds the closure element 11 b of the implant 11 may be retracted, particularly by doing so the closure element 11 b of the implant 11 is released from the elongation sheath 8 into the mitral valve annulus and may be now expanded for example by inflating with a fluid if it is not self-expanding. This is shown in Figure 1 D.
- the catheter 1 may now be retracted together with the surrounding sheath 8.
- the catheter system may be also used explanting an implant situated in the heart at least in part.
- the method just comprises the steps shown in Figure 1C and 1 D in opposite direction.
- the method comprises forwarding the distal end area of the steerable / deflectable catheter, particularly through the aortic valve, into the ventricle below the mitral valve, steering / deflecting the distal end area of the catheter to have the frontal area of the catheter tip facing the mitral valve annulus, particularly the distal end of the catheter aiming through the mitral valve annulus and advancing an elongation sheath that is coaxially surrounding at least the distal end area of the catheter into a position projecting beyond the distal tip of the catheter, particularly starting from a position not projecting, furthermore collapsing an expanded closure element of the expanded implant, particularly by releasing a fluid out of the inflated closure element and moving the distal tip or distal end area of the elongation sheath over the collapsed / deflated closure element and through the mitral valve annulus by furthermore advancing the elongation sheath, furthermore comprising pulling the closure element of the implant into the elongation sheath and the catheter after separating the closure
- a retracted separated closure element may now be replaced by a new closure element that gets connected to the remaining anchoring element.
- Figure 2 shows the embodiment of the system used in connection with figures 1.
- the system comprises the steerable or deflectable catheter 1 surrounded by the elongation sheath 8.
- First the sheath 8 has a position POS.1 in which the distal tip of the sheath does not project beyond the tip 6 of the catheter 1.
- the manipulator 12 at the proximal end of the catheter 1 is used to steer / deflect the catheter in the desired way and the operation means 13 at the proximal end of the sheath 8 is used to move the sheath along the catheter 1.
- the tip 10 of the sheath 8 may be advance into position POS.2, in which the tip 10 is moved beyond the catheter tip 6.
- the sheath has a length so that the proximal end of the sheath 8 is situated outside the patient and the sheath is fed through the skin of the patient.
- the body boundary of the patient is depicted by 14.
- Figure 3 depicts the same situation with a slightly different embodiment of the system.
- the sheath 8 is situated totally within the body of the patient and separated from the operation means 13 that may be integrated into the manipulator 12 of the catheter.
- the distance between the proximal end of the sheath 8 and the operation means 13 is bridged by a transfer means 15. Any movement of the operations means 13 will be transferred by the transfer means to the sheath 8.
Abstract
L'invention concerne un système de cathéter comprenant un cathéter orientable/déformable ayant une extrémité distale et une extrémité proximale, l'extrémité proximale comprenant en outre un manipulateur pour courber la zone d'extrémité distale du cathéter et une gaine d'allongement entourant coaxialement le cathéter orientable/déformable au moins dans sa zone d'extrémité distale. La gaine d'allongement est mobile de manière coulissante sur la surface extérieure du cathéter et le long de l'extension d'au moins la zone d'extrémité distale du cathéter dans une position dans laquelle la pointe distale de la gaine d'allongement est en saillie au-delà de la pointe distale du cathéter. L'invention concerne en outre une méthode de traitement de l'insuffisance de la valve mitrale cardiaque d'une valve cardiaque malade ayant un espace restant entre des feuillets de valve fermée, par implantation d'un implant dans le cœur.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/EP2016/001563 WO2018050201A1 (fr) | 2016-09-16 | 2016-09-16 | Système de cathéter |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/EP2016/001563 WO2018050201A1 (fr) | 2016-09-16 | 2016-09-16 | Système de cathéter |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2018050201A1 true WO2018050201A1 (fr) | 2018-03-22 |
Family
ID=57123949
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2016/001563 WO2018050201A1 (fr) | 2016-09-16 | 2016-09-16 | Système de cathéter |
Country Status (1)
Country | Link |
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WO (1) | WO2018050201A1 (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113784665A (zh) * | 2019-05-03 | 2021-12-10 | 皇家飞利浦有限公司 | 心脏图像的共配准 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1988001885A1 (fr) * | 1986-09-19 | 1988-03-24 | Versaflex Delivery Systems Inc. | Systeme de catheters echangeables de l'exterieur |
WO2003090835A1 (fr) * | 2002-04-25 | 2003-11-06 | Medtronic, Inc. | Systeme et procede ameliores pour l'installation de dispositifs medicaux implantables dans les veines coronaires |
WO2010088374A1 (fr) * | 2009-01-29 | 2010-08-05 | Boston Scientific Scimed, Inc. | Emploi d'une gaine secondaire avec un cathéter d'ablation |
US20160096001A1 (en) * | 2014-10-07 | 2016-04-07 | Pacesetter, Inc. | Delivery catheter systems and methods |
-
2016
- 2016-09-16 WO PCT/EP2016/001563 patent/WO2018050201A1/fr active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1988001885A1 (fr) * | 1986-09-19 | 1988-03-24 | Versaflex Delivery Systems Inc. | Systeme de catheters echangeables de l'exterieur |
WO2003090835A1 (fr) * | 2002-04-25 | 2003-11-06 | Medtronic, Inc. | Systeme et procede ameliores pour l'installation de dispositifs medicaux implantables dans les veines coronaires |
WO2010088374A1 (fr) * | 2009-01-29 | 2010-08-05 | Boston Scientific Scimed, Inc. | Emploi d'une gaine secondaire avec un cathéter d'ablation |
US20160096001A1 (en) * | 2014-10-07 | 2016-04-07 | Pacesetter, Inc. | Delivery catheter systems and methods |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113784665A (zh) * | 2019-05-03 | 2021-12-10 | 皇家飞利浦有限公司 | 心脏图像的共配准 |
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