OCCLUSIVE CUFF AND IMPLANTABLE OCCLUSIVE SYSTEM COMPRISING SUCH A CUFF

Abstract

The invention relates to an occlusive cuff (1) for selectively occluding an anatomical duct (2), comprising: a band (10) suited to surrounding said anatomical duct (2), provided with a closing device suited to maintaining the band wound upon itself over a determined length (L.sub.10), and an inflatable reservoir (11) arranged on an inner face of the band (10), said cuff being characterised in that the inflatable reservoir (11) extends over only a part (L.sub.11) of the length (L.sub.10) of the band (10), another part (L.sub.13) of said length (L.sub.10) defining a free inner surface (13) of the band configured to form a bearing zone for the anatomical duct, such that when the band (10) is maintained wound upon itself by the closing device, the inflatable reservoir (11) is opposite said free inner surface (13) of the band.

Claims

1. A method for selectively occluding an anatomical duct, comprising: providing a band comprising a closing device and an inflatable reservoir on an inner face of the band, said inflatable reservoir extending over only a first part of a length of the band, a second part of said length defining a free inner surface of the band; winding the band around the anatomical duct so that a first portion of the anatomical duct is supported by the free inner surface of the band, and a second portion of the anatomical duct opposite to the first portion is in contact with the inflatable reservoir; locking the closing device to maintain the band wound upon itself; and inflating the reservoir so as to compress the anatomical duct between the inflated reservoir and the free inner surface of the band.

2. The method of claim 1, wherein the anatomical duct is in direct contact with the free inner surface of the band.

3. The method of claim 1, wherein the first part of the length of the band is less than or equal to 75% of a length of the band in wound position.

4. The method of claim 3, wherein the first part of the length of the band is less than or equal to 60% of the length of the band in wound position.

5. The method of claim 4, wherein the first part of the determined length of the band is less than or equal to 50% of the length of the band in wound position.

6. The method of claim 1, wherein a length of the band in wound position is comprised between 30 and 110 mm.

7. The method of claim 1, wherein the band is formed of a textile coated with a biocompatible elastomer.

8. The method of claim 1, wherein the reservoir is made of a biocompatible elastomer.

9. The method of claim 8, wherein said biocompatible elastomer is silicone.

10. The method or claim 1, further comprising arranging a connector at a first end of the band to ensure a fluid connection between the reservoir and a tubing.

11. The method of claim 10, wherein the locking step comprises engaging an opening formed at a second end of the band opposite to the first end around the connector.

12. The method of claim 1, wherein the locking step comprises inserting an end of the band provided with teeth on a surface into a slot provided on the attachment device, hereby blocking the teeth against extraction force of said end.

13. The method of claim 12, wherein the teeth are arranged on an outer face of the band.

14. The method of claim 1, wherein the anatomical duct is a urethra or a bladder neck.

15. A method for minimizing local mechanical stresses applied on tissue surrounding an anatomical duct during selective occlusion thereof, comprising: providing a band comprising a closing device and an inflatable reservoir arranged on only a part of an inner face of the band; winding the band around the anatomical duct so that a first portion of the anatomical duct is in contact with the inflatable reservoir and a second portion of the anatomical duct is in contact with a free inner surface of the band; locking the closing device to maintain the band wound upon itself; and inflating the reservoir so as to compress the anatomical duct between the inflated reservoir and the free inner surface of the band, wherein a length of the inflatable reservoir and a length of the free inner surface of the band are chosen so as to avoid pinching the anatomical duct with the inflated reservoir.

Description

DESCRIPTION OF THE FIGURES

[0040] Other characteristics and advantages of the invention will become clear from the detailed description that follows, with reference to the appended drawings among which:

[0041] FIG. 1A is a schematic view of an occlusive cuff of known type, such as supplied to the surgeon with a view to implantation;

[0042] FIG. 1B is a schematic view of the cuff of FIG. 1A, after implantation around the anatomical duct (represented as not exerting any compression on said duct);

[0043] FIG. 2A is a schematic view of an occlusive cuff according to an embodiment of the invention, such as supplied to the surgeon with a view to implantation;

[0044] FIG. 2B a schematic view of the cuff of FIG. 2A, after implantation around the anatomical duct (represented as not exerting any compression on said duct);

[0045] FIG. 2C is a schematic view of the cuff of FIG. 2A, after implantation around the anatomical duct, in configuration of obturation of said duct;

[0046] FIG. 3 illustrates an alternative of the system for closing the occlusive cuff;

[0047] FIG. 4A illustrates a simulation by finite elements of the compressive stress generated in a bladder neck by the compression exerted by a cuff such as illustrated in FIG. 1A;

[0048] FIG. 4B illustrates a simulation by finite elements of the compressive stress generated in the bladder neck by the compression exerted by a cuff according to an embodiment of the invention;

[0049] FIG. 5 illustrates an implantable occlusive system comprising a cuff according to an embodiment of the invention.

[0050] Identical reference signs from one figure to the other designate elements that are identical or at least fulfil the same function.

DETAILED DESCRIPTION OF EMBODIMENTS OF THE INVENTION

[0051] Compared to known occlusive cuffs, the invention proposes reducing the length of the inflatable reservoir.

[0052] FIGS. 2A-2C schematically illustrate a cuff 1 according to an embodiment of the invention, respectively in the free state, in the closed state without exerting compression on the duct and in a configuration of occlusion of said duct.

[0053] The inflatable reservoir 11 extends over less than 75% of the length L.sub.10 of the band, preferably less than 60% of the length of the band, and in an even more preferred manner less than 50% of the length of the band. The length of the inflatable reservoir is noted LU.

[0054] Thus, for example, for a cuff 10 cm long, the length of the inflatable reservoir is 4.5 cm.

[0055] In other words, the inner face of the band 10 is broken down into a region of length L.sub.11 on which is arranged the reservoir 11, and a region of length L.sub.13 which forms a free surface, that is to say devoid of reservoir, and which constitutes a bearing zone for the anatomical duct.

[0056] When the cuff is in closed position, the wall of the reservoir 11 thus lies facing the free surface 13 of the band (the anatomical duct 2 being interposed between these two surfaces, as shown in FIG. 2B).

[0057] To the contrary, in a cuff of known type such as represented in FIGS. 1A and 1B, the two ends of the reservoir are flush when the cuff is closed. Even if a slight play may subsist between these two ends, notably to take account of the variation in volume of the reservoir when it is inflated, the corresponding zone of the band does not constitute a bearing zone for the anatomical duct.

[0058] Returning to the invention, when the reservoir 11 is inflated, it pushes the anatomical duct against the free surface 13 of the band, thus progressively occluding the duct (cf. FIG. 2C). Thus, the anatomical duct is compressed between, on the one hand, the reservoir 11 and, on the other hand, the free surface 13.

[0059] Advantageously, a panoply of cuffs of different lengths is made available to the surgeon, from which the surgeon will chose the most suitable for the patient and for the location planned for the implantation. In this panoply, the length of the band is generally comprised between 3 and 11 cm.

[0060] For cuffs of small length (that is to say typically less than 7 cm), the inflatable reservoir may be arranged over the entire length of the cuff.

[0061] From a certain length of cuff (for example 7 cm), the length of the inflatable reservoir may be fixed (for example of the order of 4.5 cm). Thus, it is possible to use the same pump for all cuff dimensions, which avoids multiplying the housing references.

[0062] Such a cuff may be manufactured in the following manner.

[0063] On the one hand, the band is formed of a textile coated with a biocompatible elastomer. Advantageously, the textile is a biocompatible polyester fabric, known notably by the name of DACRON™ and the elastomer is silicone. The band may be cut, for example by water jet, from a sheet of large dimensions. The band thus formed has the advantage of being smooth, of not setting into the anatomical tissues (thus allowing potential explanation of the cuff) and of not being stretchable.

[0064] On the other hand, the reservoir is made of a biocompatible elastomer, for example silicone, preferably by dipping so as to ensure a perfectly smooth surface state in order to ensure a flexible contact with the anatomical duct.

[0065] The reservoir is bonded onto the band.

[0066] The connector is for its part moulded and bonded onto the face of the band opposite to the reservoir while passing through said band to ensure a fluid connection between the reservoir and the tubing which is sleeved on the connector.

[0067] According to an embodiment, illustrated in FIG. 2A, the closing device of the cuff 1 comprises an oblong opening 14 intended to engage on the connector 12.

[0068] According to another embodiment, illustrated in FIG. 3, the band has at a first end a plurality of teeth 15 and at its other end, preferably at the level of the connector 12, an attachment device 16 comprising a slot suited to enabling the insertion of the first end and provided with a retaining system only allowing a displacement of the band 10 in the direction of the insertion (the teeth opposing a traction movement aiming to make the band come out of the slot). Advantageously, the teeth 15 lie on the outer face of the band 10, in order not to risk eroding the compressed part of the duct. The teeth may form an integral part of the band or be manufactured by moulding then bonded onto the band.

[0069] Naturally, those skilled in the art could choose any other closing device without however going beyond the scope of the present invention.

[0070] The reduction in the length of the inflatable reservoir has three main advantageous effects.

[0071] A first effect is a decrease in the bulkiness of the cuff, which facilitates its implantation in zones where the available space is limited. In the deflated state prior to implantation, the cuff is in the form of a band having a small thickness, which can thus be inserted relatively easily into the zone dissected around the bladder neck, unlike the cuff described in the document WO 2013/165563, which uses the cooperation of an anvil integral with the inner surface of the band and a hammer integral with the reservoir to compress the anatomical duct. The anvil and hammer being relatively rigid, they have a non-negligible bulkiness in the implantation zone. Conversely, in the present invention, as is clearly shown in FIGS. 2B and 2C, when the cuff is implanted around the anatomical duct, said duct is in direct contact with the reservoir 11 and with the free surface 13 of the band which are flexible parts, which makes it possible to minimise the thickness of the cuff and reduce the risk of erosion of body tissues.

[0072] A second advantageous effect of the invention is a reduction in the volume of fluid necessary to swell the reservoir in order to occlude the anatomical duct.

[0073] Consequently, the volume of the recipient of variable volume contained in the housing remains limited, and the autonomy of the energy source is not penalised.

[0074] A third effect is a modification of the mode of action of the cuff on the anatomical duct.

[0075] FIG. 4A shows the result of a simulation by finite elements of the compressive stresses applied to the bladder neck by a cuff according to the prior art, such as illustrated in FIG. 1A, for a fluid pressure in the cuff of 120 cm H.sub.2O. It may be observed that the curvature of the cuff combined with a swelling of the reservoir has the effect of dividing the reservoir 11′ into four pockets which each extend over around one quarter of the inner circumference of the cuff. Yet, the bladder neck is pinched between two adjacent pockets, and is subjected, in these pinch zones P, to local mechanical stresses well above the stresses to which the remainder of the neck is subjected. These localised stresses are liable to damage the bladder neck, for example atrophying it.

[0076] In FIGS. 4A and 4B, the stress levels represented by dark colours correspond to high stresses on the colour scale shown on the right of each simulation.

[0077] FIG. 4B shows the result of a simulation by finite elements of the compressive stresses applied to the bladder neck by a cuff according to an embodiment of the invention, such as illustrated in FIG. 2A, for a fluid pressure in the cuff of 120 cm H.sub.2O. It may be observed that the reduction in the length of the inflatable reservoir 11 has the effect of eliminating the pinch zones of the bladder neck, and consequently eliminating the excess stresses undergone locally by the bladder neck. The bladder neck is thus less likely to be damaged.

[0078] FIG. 5 illustrates an implantable occlusive system comprising an implantable housing comprising a pump, and an occlusive cuff such as described above, in fluid connection with the pump. The pump is advantageously one of the devices described in the document WO 2016/083428.

[0079] The housing 4 contains the recipient of variable volume, the actuator as well as said electronic module(s) and, if need be, the energy source. The housing contains a gas, for example air. Said housing must be leak tight to avoid any transfer of fluid or gas from or to the intracorporal medium. The housing is made of a biocompatible material and may for example be made of implantable titanium and sealed by laser welding. A control of the leak tightness may notably be carried out with helium (for example, leakage rate less than 10.sup.−9 mbar.Math.l/s of helium) to ensure the total leak tightness of the housing for the period for which the system is implanted.

[0080] The recipient of variable volume is connected to the cuff 1 by the tubing 3.

[0081] Advantageously, the housing comprises, in a wall delimiting the recipient of variable volume, a puncture port 5 perforable by a needle and able to close in a leak tight manner after removal of the needle, making it possible to inject or to remove fluid from the recipient.