Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods
  • A61B17/04—Surgical instruments, devices or methods for suturing wounds; Holders or packages for needles or suture materials
  • A61B17/06—Needles ; Sutures; Needle-suture combinations; Holders or packages for needles or suture materials
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods
  • A61B17/04—Surgical instruments, devices or methods for suturing wounds; Holders or packages for needles or suture materials
  • A61B17/06—Needles ; Sutures; Needle-suture combinations; Holders or packages for needles or suture materials
  • A61B17/06066—Needles, e.g. needle tip configurations
  • A61B17/06109—Big needles, either gripped by hand or connectable to a handle
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
  • A61F2/0004—Closure means for urethra or rectum, i.e. anti-incontinence devices or support slings against pelvic prolapse
  • A61F2/0031—Closure means for urethra or rectum, i.e. anti-incontinence devices or support slings against pelvic prolapse for constricting the lumen; Support slings for the urethra
  • A61F2/0036—Closure means for urethra or rectum, i.e. anti-incontinence devices or support slings against pelvic prolapse for constricting the lumen; Support slings for the urethra implantable
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
  • A61F2/0004—Closure means for urethra or rectum, i.e. anti-incontinence devices or support slings against pelvic prolapse
  • A61F2/0031—Closure means for urethra or rectum, i.e. anti-incontinence devices or support slings against pelvic prolapse for constricting the lumen; Support slings for the urethra
  • A61F2/0036—Closure means for urethra or rectum, i.e. anti-incontinence devices or support slings against pelvic prolapse for constricting the lumen; Support slings for the urethra implantable
  • A61F2/0045—Support slings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods
  • A61B17/34—Trocars; Puncturing needles
  • A61B17/3415—Trocars; Puncturing needles for introducing tubes or catheters, e.g. gastrostomy tubes, drain catheters
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods
  • A61B17/34—Trocars; Puncturing needles
  • A61B17/3468—Trocars; Puncturing needles for implanting or removing devices, e.g. prostheses, implants, seeds, wires
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods
  • A61B2017/00743—Type of operation; Specification of treatment sites
  • A61B2017/00805—Treatment of female stress urinary incontinence
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods
  • A61B17/04—Surgical instruments, devices or methods for suturing wounds; Holders or packages for needles or suture materials
  • A61B17/06—Needles ; Sutures; Needle-suture combinations; Holders or packages for needles or suture materials
  • A61B17/06004—Means for attaching suture to needle
  • A61B2017/06042—Means for attaching suture to needle located close to needle tip
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods
  • A61B17/04—Surgical instruments, devices or methods for suturing wounds; Holders or packages for needles or suture materials
  • A61B17/06—Needles ; Sutures; Needle-suture combinations; Holders or packages for needles or suture materials
  • A61B17/06066—Needles, e.g. needle tip configurations
  • A61B2017/06076—Needles, e.g. needle tip configurations helically or spirally coiled
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
  • A61B17/00—Surgical instruments, devices or methods
  • A61B17/04—Surgical instruments, devices or methods for suturing wounds; Holders or packages for needles or suture materials
  • A61B17/06—Needles ; Sutures; Needle-suture combinations; Holders or packages for needles or suture materials
  • A61B17/06066—Needles, e.g. needle tip configurations
  • A61B2017/06085—Needles, e.g. needle tip configurations having a blunt tip

Definitions

• the present invention relates to the technical field of treatment of rectal prolapse, in particular in elderly women.
• Prolapse phenomena generally result from a loosening of the suspension tissues of the genital or rectal organs, leading to disorders which require surgical intervention.
• a patent application FR 2 785 521 has proposed implementing an implant comprising a support body, from which extend two suspension cords, provided, at their ends, with parts anchoring intended to be sutured on areas known to be anatomically stable. This implant is then placed laparoscopically to lighten the surgical procedure
• the invention relates to an implant for the treatment of rectocele, having a thin and flexible structure and comprising a support body from which extend at least two upper suspension stabilizers arranged on one side and on the other side of a sagittal plane of the body of support and two lower suspension stabilizers also arranged on either side of the sagittal plane.
• the longitudinal axes of the upper stabilizers form, between them, an angle greater than 45 ° and, preferably but not strictly necessary, an angle between 100 ° and 180 ° and, preferably, between 115 ° and
• the sagittal plane constitutes an axis of symmetry of the implant and therefore bisector of the angle.
• upper suspension stabilizers having such a relative orientation makes it possible to place them judiciously in the trans-sacrosciatic region to ensure a good distribution of the forces undergone by the support body on the anatomical anchoring points of the stabilizers, while by ensuring the best spatial orientation of the body of the support implanted in the patient.
• the upper and / or lower suspension stabilizers have a length greater than 100 mm and, preferably, greater than or equal to 120 mm. Such a length allows a good extension of the suspension stabilizers in their respective insertion zones and takes advantage of the friction between the arms or suspension stabilizers and the tissues crossed to ensure the maintenance of the implant.
• the longitudinal axes of the lower stabilizers preferably, but not necessarily, form a non-zero angle ⁇ between them.
• the angle ⁇ . is greater than 10 ° to be preferably between 10 ° and 75 ° or, alternatively, between 100 ° and 180 °, depending on the pathology to be treated.
• the support body has a generally substantially rectangular shape.
• the support body then has a length between 60 mm and 90 mm and a width between 40 mm and 60 mm.
• the upper stabilizers extend substantially from the upper corners of the support body and the lower stabilizers extend from the lower corners of the support body.
• the upper stabilizers extend substantially from the upper corners of the support body, while the lower stabilizers extend from the two long sides of the support body.
• Each of the lower stabilizers then extends, preferably but not necessarily, at a distance from the upper edge of the support body being between 60% and 87% of the length of the support body.
• the lower stabilizers have an enlarged area at their connection with the support body of the implant.
• the invention also relates to an operating technique for the treatment of the rectocele.
• this technique consists in implementing an implant which comprises a support body from which extend at least two upper suspension stabilizers, arranged on either side of a sagittal plane, and at least two lower suspension stabilizers, also arranged on either side of the sagittal plane.
• the technique consists in placing, on the one hand, the upper suspension stabilizers, either in the corresponding transgluteal region, or in the corresponding sacrosciatic region and, on the other hand, the lower stabilizers in the transpuborectal region.
• this technique is implemented in the context of a surgery, known as minimally invasive, using the first approaches close to the organs to be treated as reduced as possible, so as to ensure a reduction in operating times and blood loss this reduces the risk of vaginal erosion by the prosthesis because the prosthesis is not strictly opposite the incision. It is thus possible to obtain short operating suites, with minimal discomfort for the patient.
• the simplicity of this technique allows its easy reproduction and minimizes the learning necessary for surgeons to master it.
• the implant also comprises pairs of suspension stabilizers upper and lower a pair of medium suspension stabilizers which are each located between an upper suspension stabilizer and a lower suspension stabilizer.
• the rectocele treatment technique using such an implant with six suspension stabilizers then provides for placing the implant in the body of the patient to be treated by placing: a the upper suspension stabilizers through the sacrosciatic region, ⁇ the medium suspension stabilizers across the puborectal region, "the lower suspension stabilizers across the perineal region," and the support body at the uterosacral region.
• the invention also relates to an introduction device which can be used, without this being absolutely necessary within the meaning of the invention, for the placement of an implant, as described above.
• this introduction device comprises an introducer which has a flexible structure and a shape similar to that of the implant and which comprises:
• a hollow body defining a cavity for receiving the support body of the implant
• tabular stabilizers extending from the hollow body and each defining a cavity for receiving an implant suspension stabilizer, • traction means extending from the end of each of the stabilizers of the implant introducer,
• the traction means comprise, for each tubular strap, a semi-rigid needle.
• the cutting means can be made in any suitable way, such as, for example, in the form of a line of least resistance capable of tearing when a pull is made at two opposite tabular stabilizers of the introducer.
• the cutting means comprise at least one opening for the passage of a cutting tool.
• the body of the introducer comprises a series of openings situated, on the one hand, near a line corresponding to the sagittal plane of the implant and, on the other hand, between the tabular stabilizers.
• the introduction device comprises an implant according to the invention, arranged in the cavity of the hollow body and of the tabular stabilizers of the introducer.
• the implant is free inside the introducer.
• the introduction device also comprises at least one ancillary which includes an elongated perforator guide or trocar, one end of which is intended to be introduced into the body of the patient. and the other end of which is provided with a handle.
• at least one ancillary which includes an elongated perforator guide or trocar, one end of which is intended to be introduced into the body of the patient. and the other end of which is provided with a handle.
• the perforator guide has an arcuate shape in a plane.
• the arcuate part of the perforator extends over an angular sector greater than 140 ° and, preferably but not necessarily, less than 180 ° and, preferably, between 150 ° and 170 °.
• the arcuate part of the perforating guide then has a radius of curvature between 30 mm and 60 mm and, preferably, for the part of the perforating guide extending between the handle and the end intended to be introduced into the patient's body, between 40 mm and 50 mm, the end part of the perforator then having a variable radius of curvature.
• the perforating guide has, at its end opposite the handle or distal, a helical shape.
• the perforating guide then has the shape of a portion of helical coil extending over an angle between 180 ° and 360 ° and, preferably, between 255 ° and 270 °.
• the turn of the perforating guide has a radius of curvature between 20 mm and 40 mm, with a pitch between 15 mm and 25 mm.
• the device introduction in order to reduce the trauma suffered by the patient's body during the introduction of the implant, includes, in addition, a tabular jacket of complementary shape to that of the perforator guide.
• This tabular folder is then intended to be engaged on the perforator guide and to remain in the patient's body after removal of the perforator guide to define a tunnel for the passage of the means of traction of the introducer.
• the tabular jacket is then removed, after passage of the traction means during the withdrawal of the introducer.
• the tabular folder can be made of any flexible biocompatible material, such as, for example but not exclusively, PNC.
• the fig. 1 is an elevation, in flat view, of an implant according to the invention intended for the treatment of rectocele.
• the fig. 2 is an elevation, partially cut away, of a perforating guide which can be used for the positioning of the implant according to the invention and having an arcuate shape.
• the fig. 3 is an elevation of another embodiment of a perforator guide according to the invention, having an insertion end of helical shape.
• Fig. 4 is a view from the left of the perforator guide according to FIG. 3.
• Fig. 5 is a bottom view of the perforator illustrated in FIG. 3.
• Fig. 6 is a view of an introducer according to the invention, allowing the implant illustrated in FIG. 1. - . .
• Fig. 7 is a view, similar to FIG. 1, showing an alternative embodiment of the implant according to the invention.
• Fig. 8 is a view, similar to FIG. 6, showing an introducer for the establishment of the implant illustrated in FIG. 7.
• Figs. 9 to 12 are views, similar to FIGS. 2 to 3, showing alternative embodiments of perforator guides for the installation of an implant according to the invention.
• FIG. 13 and 14 are views, similar to FIG. 1, showing alternative embodiments of an implant according to the invention.
• Fig. 15 is an anatomical view showing an example of implantation in a woman of an implant according to FIG. 14.
• the invention proposes an implant more particularly designed for the treatment of the rectocele and designated as a whole by the reference 1 in FIG. 1.
• This implant 1 has a thin and flexible structure and is made from a suitable biocompatible material, such as, for example, a synthetic material, woven or not, or, again, knitted, based on polypropylene or polyester fibers. . Such a synthetic material may then be coated or not with products promoting cell growth.
• the implant according to the invention could be made of natural materials, such as "fascia latta" or, again, any biological or synthetic absorbable material.
• the implant 1 comprises a support body 2 from which extend two upper suspension stabilizers 3, arranged on either side of a sagittal plane S.
• the implant also comprises, two lower suspension stabilizers 4, also arranged on either side of the sagittal plane S. These stabilizers act by the constriction produced by the muscular masses
• the support body 2 has a substantially rectangular shape, without such a shape being able to be considered strictly necessary within the meaning of the invention, and the upper suspension stabilizers 3 each extend from 'an upper corner of the body 2.
• the lower suspension stabilizers 4 extend, in turn, each from one side of the support body 2 of rectangular shape.
• the lower suspension stabilizers 4 originate on one side of the support body 2, at a distance d from the upper edge 30 of the support body 2, preferably, but not strictly necessary, being between 60% and 87% of the length L 2 of the support body.
• the support body 2 is chosen to have a length L 2 of between 60 mm and 90 mm and a width of between 40 mm and 60 mm.
• the longitudinal axes A 3 of the upper stabilizers 3 form an angle oc greater than 45 °, preferably between 100 ° and 180 ° being, more particularly preferably, between 115 ° and 170 °.
• the axes A of the lower suspension stabilizers 4 form between them a non-zero angle ⁇ , preferably greater than 10 ° and, according to this exemplary embodiment, an angle ⁇ of between 100 ° and 180 °.
• the sagittal plane S corresponds to a plane of symmetry of the implant 1 and is therefore bisector of the angles ⁇ and ⁇ .
• the upper 3 and lower 4 suspension stabilizers In order to allow easy installation of the suspension stabilizers in their corresponding insertion zone, while providing an optimal surface for friction with the tissues passed through, the upper 3 and lower 4 suspension stabilizers have a length respectively L 3 , L measured between the distal end of each suspension stabilizer and the support body 2, preferably but not necessarily, greater than 100 mm and, more particularly preferably, greater than 120 mm.
• the suspension stabilizers also have a width, preferably, but not exclusively, between 5 mm and 15 mm and worth, for example, ten millimeters.
• the implant 1, as described above, is intended to be placed at the level of the recto vaginal septum of a patient. To this end, in order to minimize the dissection of this region and the trauma resulting therefrom, the invention proposes to the surgeon carrying out the treatment to use one or more elongated perforator guides 10, such as those more particularly illustrated in FIGS. 2 and 3 to 5.
• such a perforating guide 10 comprises an elongated body or mandrel 11, one end 12 of which is intended to be introduced into the body of the subject to be treated and the other end 13 of which is provided with a handle 14.
• the introduction end 12 is preferably constituted by a foam tip, that is to say a atraumatic tip which is not likely to injure or cut the tissues into which it must be introduced.
• the perforator guide 10 has an arcuate shape in a plane. This arcuate shape in a plane is more particularly suitable for the installation of suspension stabilizers in the transperineal and transgluteal areas.
• the arcuate part of the perforating guide then has a radius of curvature R of between 30 mm and 60 mm and, preferably, for the part 15 of the perforating guide 10 extending between the handle 14 and the end 12, between 40 mm and 50 mm, the end part 16 of the perforator guide 10 then having a variable radius of curvature.
• the elongated body 11 of the guide 10 has an end 17 of helical shape, also suitable for the installation of suspension stabilizers in the upper or lower zones of the closed holes.
• the distal end 17 of the perforating guide then has the form of a portion of helical coil extending over an angle ⁇ between 180 ° and 360 ° and, preferably, between 255 ° and 270 °.
• the turn 17 of the perforating guide has a radius of curvature between 20 mm and 40 mm, with a pitch between 15 mm and 25 mm.
• the implant 1 according to the invention is preferably arranged so as to present no residual tension after its installation for at least some of its suspension stabilizers.
• the invention proposes, in an intervention variant, using an introducer, more particularly illustrated in FIG. 6 and designated as a whole by the reference 20.
• the introducer 20 has a flexible structure similar in shape to that of the implant.
• the introducer 20 is preferably made of a biocompatible polymeric material, from the family of plastics with a low coefficient of friction, such as, for example, polyethylene.
• the introducer 20 then comprises a hollow body 21 defining a cavity for receiving the body 2 of the implant 1.
• the introducer 20 also includes tabular stabilizers 22 which extend from the hollow body 21 and which each define a cavity for receiving a suspension stabilizer 3, 4 and 5 of the implant 1.
• Each tabular strap 22 then has traction means 23 extending from the free end of the corresponding strap 22.
• the traction means 23 can be produced in any suitable manner such as, for example, by systems for hooking the ends of the stabilizers 22 onto a perforating guide 10.
• the traction means 23 include, for each strap 22, a flexible or semi-rigid needle with an atraumatic or foam end.
• a needle can be made from the same material as the material constituting the introducer 20 or, more generally, from a material chosen from synthetic polymers preferably having a low coefficient of friction.
• the introducer 20 finally comprises cutting means 24, the function of which will appear subsequently, of the hollow body 21 at least of the introducer 20.
• the cutting means 24 can then be produced in any suitable manner and, depending on the example illustrated, include a series of six openings 24 made at the periphery of the hollow body 21, between each of the tabular stabilizers 22, to allow the passage of a cutting tool to ensure a cutting of the hollow body 21 along lines 25 materialized by mixed lines in fig. 6.
• the implant 1 is located inside the hollow body 21 and the tabular stabilizers 22 while being preferably free inside the latter, so that the forces exerted on the introducer 20 are not not passed to implant 1 itself.
• the patient to be treated is first of all undergoing anesthesia which may be general or regional or, alternatively; local, according to the surgeon's preferences and the patient's state of health.
• the operating position of the patient on the operating table will be that of usual vaginal surgery, i.e. the patient's buttocks slightly outside the operating table and the thighs moderately bent on the abdomen.
• a rectal wick is put in place and an ischemic injection is performed.
• a traction is exerted on the cervix, in order to expose the posterior vaginal sac.
• a vaginal incision is made on the posterior part of the cervix, transversely on the cervical side of the vaginal cul de sac well exposed by traction. This incision can be described as a horizontal retrocervical.
• the slice of lower vaginal section thus produced is fully grasped by means, for example, of three Alis forceps which are pulled downwards exposing the rectovaginal plane.
• a rectovaginal detachment is conducted gradually by releasing the posterior vaginal wall. This detachment is stopped at the bottom and in the middle above the anal cap. The detachment is continued laterally according to the dissection plane and in contact with the levator muscle by traversing, from bottom to top, the pubococcygeal bundle, then the ilio-coccygeal bundle to reach the level of the coccygeal muscle and the sacrosciatic ligament. This dissection is carried out cautiously by pushing back the peri-rectal fat and the rectum inside. It should be noted that there is then no structure to be cut and that it suffices to repress inside the peri-rectal fat while remaining in contact with the muscular floor.
• an arcuate perforator guide 10 of the surgeon's choice, as described above in relation to FIGS. 2 and 3 to 5, can be used.
• the perforator guide 10 is then led through the patient's buttock by a puctiferous incision situated approximately 15 mm behind the midpoint of the line extending from the anus to the ischium.
• a finger slipped into the lateral detachment in contact with the sacroiliac ligament previously executed will then receive the tip of the perforator guide, so as to lead it into the lower vaginal incision.
• the towed strap then passes through the sacrosciatic ligament. It should be noted that in the absence of an introducer 20, the distal end of the upper suspension stabilizer is directly fixed to the perforator guide 10 in order to be towed.
• the same gesture is made for the installation of the second upper strap 3.
• the upper stabilizers 3 thus passed to ensure a transgluteal suspension are then put on hold on clamps.
• the lower suspension stabilizers 4 are then passed through the puborectal muscle on either side of the anal canal and exteriorized by the same gluteal opening as the upper stabilizers 3.
• the introducer 20 is cut so as to release the implant 1.
• the withdrawal of the various constituent elements of the introducer 20 by pulls exerted two by two on the tabular stabilizers 22 opposite thus allows the implant 1 to be deposited, without any constraint, on the latter, so that it is in a state which could be qualified as relaxed.
• the support body 2 of the implant 1 is then fixed on the uterosacral ligaments and the apron 9 on the underside of the cervix, by one or more and, preferably, three points of absorbable wire.
• the posterior vaginal incision is then sutured with absorbable wire, then traction is exerted on the upper suspension stabilizers 3 crossing the sacrosciatic region in order to raise the vaginal dome in the right position. Any excess of the upper 3 and lower 4 suspension stabilizers can then be sectioned and the gluteal orifices closed by means of points made of absorbable suture.
• vaginal wick is placed, as well as a bladder catheter which will be removed 48 hours after the intervention.
• the post-voiding residues are then measured by sampling, in order to ensure that the bladder emptying is satisfactory, so as to authorize an exit of the patient.
• the intervention for the treatment of rectocele will last approximately one hour and an average hospital stay of four days should be adopted.
• the technique proposed previously thus makes it possible to treat only the pathology, namely the imbalance of the pelvic statics and therefore to restore an anatomy as normal as possible while preserving the body diagram of the individual.
• This technique advantageously makes it possible to keep the organs healthy or that do not adversely influence pelvic statics. Indeed, the cancer pathology will have been ruled out by the preoperative assessment and it will be possible to ensure after the surgical intervention a reliable gynecological monitoring.
• the lower suspension stabilizers 4 extend from the sides of the support body, however this is not strictly necessary for the production of an implant according to the invention.
• fig. 7 shows an implant 39 according to the invention, the four suspension stabilizers of which two upper 3 and two lower 4 extend from the four corners of the support body 2.
• the axes A 3 of the upper suspension stabilizers form an angle ⁇ having the same characteristics as those of the implant 1 described above, while the axes A of the lower suspension stabilizers 4 form an angle ⁇ understood, preferably but not exclusively, between 10 ° and 75 °.
• FIG. 8 illustrates an example of an introducer 20 more particularly adapted to the conformation of the implant 39.
• the operation for the treatment of the rectocele by means of the implant 39 is carried out as that described previously with regard to the dissection of the rectovaginal area receiving the support body 2 and fitting the upper 3 and lower 4 suspension stabilizers.
• the enlarged portions 40 of the lower suspension stabilizers 4 can be fixed by absorbable stitches to the lifting muscles in the puborectal region.
• the introduction device used comprises simple perforator guides 10.
• the introduction device used comprises simple perforator guides 10.
• the introduction device used comprises simple perforator guides 10.
• the shirt 50 is engaged on the perforator guide 10 which then has a stop or guard 51 on which the shirt 50 comes to bear when the perforator guide 10 is introduced into the body of the patient.
• the jacket 50 is left in place in the patient's body after removal of the perforator guide 10 and before the implant 1, 39 is put in place.
• the jacket used thus makes it possible to create a channel for the passage of a traction element.
• 23 of the introducer 20 and in which a tabular strap 23 and the associated stabilizer or suspension arm 3, 4 or a single stabilizer or suspension arm 3, 4 can be moved by sliding, so as to adjust the position of the implant 1, 39 without abrasion of the tissues crossed.
• a jacket 50 is then used for the positioning of each suspension stabilizer 3, 4, 5.
• the shirts 50 are then removed at the same time as the tabular straps 23 enveloping the suspension stabilizers of the implant or when the implant is placed naked - after adjusting the implant position.
• the implementation of shirts 50 avoids acute inflammatory phenomena and reduces tissue trauma, insofar as the implantation sites are composed of very specialized muscle tissues which have lost a large part of their capacity for regeneration and rapid healing.
• the upper suspension stabilizers 3 and 4 extend from the body of the implant in divergence and thus gives the implant a shape which could be qualified as a star.
• this star pattern is not strictly necessary for the production of an implant according to the invention and for certain pathologies, it may appear necessary to have an implant whose suspension stabilizers do not diverge but on the contrary whose free ends of the upper stabilizers 3 and lower stabilizers 4 are directed downwards.
• the longitudinal axes A 3 of the upper stabilizers then form an angle ⁇ greater than 180 ° and preferably greater than 200 °.
• Fig. 13 shows such an embodiment of an implant 51 according to the invention whose upper suspension stabilizers 3 extend from the sides of the body 52 of the implant at a distance from its upper edge while the two lower stabilizers 4 extend from the lower corners of the support body 52.
• This particular configuration then defines a sort of upper apron 53, provided with two orifices 54 for the passage of an added stabilization strip or for the passage of the posterior stabilizers of an anterior prosthesis used in association with the implant according to the invention, once the stabilizers of said anterior prosthesis have trans-fixed the uterosacral ligaments.
• the axes A 3 of the upper suspension stabilizers 3 form an angle ⁇ more particularly between 210 ° and 260 ° while the axes A 4 of the lower suspension stabilizers 4 form an angle ⁇ less than 45 ° and preferably zero.
• Fig. 14 illustrates yet another alternative embodiment of an implant 55 for the treatment of prolapse of the vaginal dome and of the rectocele, the suspension stabilizers of which are all oriented downwards.
• the body 56 of the implant has a rectangular shape.
• Both stabilizers "of upper 3 and the two lower suspension stabilizers suspension 4 then extend respectively from upper and lower corners of the support body 56.
• stabilizers upper suspensions 3 are arcuate and moyemies fibers A 3 which are the equivalent of the axes A 3 in the case of a straight arm or stabilizer form an angle ⁇ greater than 180 °
• the angle ⁇ is measured between two tangents of the average fibers of the upper suspension stabilizers. It should be noted that the concavity of the upper suspension stabilizers 3 is oriented downwards.
• the implant 55 further comprises medium suspension stabilizers 57 arranged on either side of the sagittal plane S and between the upper 3 and lower stabilizers 4.
• the ends of the medium suspension stabilizers are oriented downwards and their axes As form an angle ⁇ preferably greater than 200 ° and more particularly preferably between 210 ° and 260 °.
• the ends of the upper 3 and middle stabilizers 57 located on the same side of the sagittal plane S converge towards a point or at least substantially in the same direction as shown in FIG. 14, this characteristic facilitating the procedure of implantation as shown in the following.
• the placement of the prosthesis as illustrated in fig. 14 and described above for the treatment of prolapse of the vaginal dome and rectocele includes after anesthesia of the patient a dissection phase. Muze forceps are then used which pull the cervix in order to expose the posterior vaginal pouch. A vaginal incision is made on the posterior side of the cervix transversely on the cervical side of the vaginal cul-de-sac well exposed by traction. The posterior vaginal section is gripped entirely by 3 Alis forceps which are pulled down exposing the rectovaginal plane. Rectovaginal detachment is carried out gradually by everting the posterior vaginal wall. This detachment is stopped at the bottom and in the middle above the anal cap.
• any dissection of the recto anal plane is perfectly useless, even harmful, because it is a non-anatomical plane but obviously created by surgery. It is advisable to dissect the dissection plane laterally and in contact with the levator muscle traveling from low to high the pubo-coccygeal bundle then the ilio-coccygeal bundle to reach the level of the coccygeal muscle and the sacrosciatic ligament. This dissection is carried out carefully, pushing back the peri-rectal fat and the rectum inside. There is no structure to cut; it suffices to push the peri-rectal fat inside while remaining in contact with the muscular floor. The most practical is to use the finger, the compress, and especially a set of two long and narrow vaginal valves; these gradually open up under visual control the space without excessive enlargement of the dissected space enough to slide a finger.
• a perforator guide 10 is led through the buttock by a punctate incision 60 located 15 mm behind the midpoint of the line extending from the anus to the ischium as shown in fig.15.
• the finger slid into the lateral detachment in contact with the sacroiliac ligament will receive the tip of the perforator guide 10 and lead it into the posterior vaginal incision one end of an upper stabilizer 3 of the implant is fixed on the guide perforator 10 and towed through the sacrosciatic ligament (sacrosciatic suspension), the same gesture is made on the other side for the other upper stabilizer of the implant 55.
• the upper edge of the implant is then sutured by 2 to 4 points on the posterior aspect of the isthmus and the uterosacral ligaments.
• the two free ends of the upper stabilizers 3 of the implant are then placed on hold on a clamp.
• the medium suspension stabilizers 57 called puborectal suspension, are passed through the puborectal muscles by a transperineal route using the same posterior entry orifice as for the upper suspension stabilizers but with an orientation inside to emerge at 1/3 the height of the colpocele across the puborectal muscle.
• the lower suspension stabilizers also called perineal, are passed on either side of the vulval fork thanks to a perforator guide 10 which it is more prudent to introduce from inside to outside (top towards the bottom) than from bottom to top, because in this direction, in its course, the instrument approaches the rectum and can threaten it.
• the posterior vaginal incision is sutured by an absorbable wire and a medium traction is exerted on the upper and middle suspension stabilizers in order to raise the vaginal dome in good position, and to position the pre hammock without excessive tension. rectal.

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• 2004
  • 2004-03-26 AU AU2004229194A patent/AU2004229194B2/en not_active Ceased
  • 2004-03-26 RU RU2005131716/14A patent/RU2005131716A/ru not_active Application Discontinuation
  • 2004-03-26 WO PCT/FR2004/000765 patent/WO2004091442A2/fr not_active Ceased
  • 2004-03-26 BR BRPI0408903-0A patent/BRPI0408903A/pt not_active Application Discontinuation
  • 2004-03-26 CA CA002520818A patent/CA2520818A1/fr not_active Abandoned
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  • 2004-03-29 US US10/811,158 patent/US7588598B2/en not_active Expired - Fee Related
• 2009
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