The invention relates to method and apparatus for secure vasectomy; more particularly, it relates to a vasectomy tool and a method of using same.
Current state of the art in vasectomy procedure is to transect (with optional disposal of a small section) the vas differens (“vas”) and then burn cauterize the body end of the vas to seal it. The problem (resulting in an estimated 8% failure rate for this procedure, where the vas rejoins and at least partial fertility is restored) is that the burned end is subject to necrosis, physical separation and reabsorption into the body, leaving the highly regenerative vas ends free to come into contact with each other and rejoin. What is needed is a procedure and device or kit for transecting the vas and scarring cut vas ends permanently so that nothing short of a surgical stent will ever restore fertility.
Vasectomy is the most effective form of birth control and the only permanent method of male birth control. No-scalpel vasectomy technique has provided a safer and easier method for approaching the vas during vasectomy and has increased its popularity. Yet the actual interruption of the vas is accomplished by numerous techniques, most of which have not been well studied in terms of efficacy. Vasectomy failure occurs in up to 9% of cases studied, and typically results from sperm leakage from the transected ends of the vas. Sperm then create an inflammatory reaction in the tissue and “find” the other end of the vas. A transient or permanent restructuring of the vas may then occur, allowing sperm to get into the semen. A number of ways have been used in an attempt to prevent sperm from successfully jumping the gap and causing the vasectomy to fail.
In particular, the method consisting of just taking out a piece of the vas and creating a gap is often unsuccessful and accounts for the largest number of vasectomy failures. Tying the cut ends with suture, after removing a piece of the vas, is the most common method worldwide. It is not technically challenging, and can be taught to ancillary medical personnel. Unfortunately, if the suture is tied too tightly, the end of the vas loses its blood supply, necroses, and falls off, as discussed above. This opens the way to recanalization, and in one study, 12% of such cases did recanalize.
In a ‘facial interposition’ method, a piece of the vas is removed, the ends are tied, and the body end of the vas is fixed in a separate tissue plane. It has the same shortcomings discussed above, however if sperm leak out they have a more difficult journey to the body end of the vas. This is not only a more difficult procedure, requiring extensive training, but the failure rate is still around 5%.
The most apparently effective method currently being used, apart from what is disclosed herein, is intravasal electro-cautery of mucosa, with a piece of the vas removed. An electro cautery unit with a hot wire is placed into the cut ends of the vas, destroying the mucosa or inner lining by heat. Scarring takes place inside the vas while the outside muscular layer remains viable. The scarring causes an effective sealing of the vas ends. The procedure requires expensive and specialized equipment, such as a disposable electro cautery unit—prohibitively expensive in many parts of the world. If a unipolar unit is used, the vas may be too extensively scarred and make later reversal impossible. Also the length of time the electro cautery is applied and the intensity of heat must be precisely controlled, for too much heat will destroy the entire end, lead to necrosis and the kind of leakage discussed above; too little results in ineffective scarring and no sperm seal.
There are no known devices that eliminate the inner mucosal surface of the vas without electrical means. What is needed is a device and method that only affects the mucosa of the vas, and optimally, a small amount of the muscle layer, so that there is greatly reduced chance of necrosis. What is needed is a method and tool that can be used worldwide that is simple with minimal tissue dissection, and can be used in areas where finances and or power supply irregularities do not permit electro cautery. What is needed is a device that can be either disposable, single use, or resterilizable, with readily available pre-sterilized kits.
What is here presented is such a device and method that only affects the epithelial layer of the vas, the mucosa of the vas, and optimally, a small amount of the muscle layer, so that there is greatly reduced chance of necrosis. It is a method and tool that can be used worldwide that is simple with minimal tissue dissection, and can be used in areas where finances and or power supply irregularities do not permit electro cautery. It is a device that can be either disposable, single use, or resterilizable, with readily available pre-sterilized kits.
A vasectomy tool with a reamer operatively engaged upon a pull rod is disclosed. The pull rod is extendable into a releasably locked position against spring tension and the reamer has a series of cutting disks on a shaft, the shaft having a blunt conical tip. The tool also has a handle, and the extendable pull rod and reamer are disposed within the handle. The handle has a catch release button interengageable with a spring catch release on the pull rod, and also desirably has an integral vas-clamping forceps mechanism disposed on an outside of the handle.
In general what is further disclosed is a probe-like reamer that has a series of cutting disks, or an array of concentric conical cutters, on a shaft, and the shaft has a radiused or blunt conical tip. The cutting disks have generally circumferential cutting edges. Preferred cutting disks have a generally frustoconical leading surface and either a generally back-cut back surface, or a generally straight or planar back surface, with the frusto conical leading surface and the back surface defining at least in part the circumferential cutting edge. The conical tip advantageously dilates the highly compliant vas tissue about twice its normal inner diameter, so that the cutters or cutting disks slide into place within the lumen of a partially transected vas, and the cutting edges readily engage the vas tissue.
A preferred tool has the reamer removably engaged upon the pull rod. In one embodiment, the pull rod terminates in a collet, and the reamer terminates, at an end opposite the conical tip, in a chuck end sized to releasably engage the collet.
In one embodiment of the vasectomy tool, a reamer is operatively engaged upon a pull rod, the pull rod is extendable into a releasably locked position against spring tension from a spring. The tool advantageously has a handle like that of a retractable pen, and the extendable pull rod and reamer are disposed within the handle. The handle advantageously has a catch release button interengageable with a spring catch release on the pull rod. Optionally, the handle has an integral forceps mechanism disposed on an outside of the handle, and cooperates with the handle to grip the vas while the inserted reamer is removed quickly under spring tension. In general it is believed that the inertia of the vas, even when not firmly gripped by forceps or fingers, and the sudden accelerated motion of the reamer withdrawing from the vas, causes the cutting edges to engage the wall of the vas lumen and cut, either relatively cleanly with a back-cut kind of blade, or bluntly with tearing with a blade that has a straight or planar back. The uniform, and selectably variable (with optional selection of different spring rate springs for any particular tool) extraction force eliminates technique variables and allows all operators to achieve repeatable and optimal results.
Preferred embodiments of the tool have most if not all of the cutting disks spaced from one another along the shaft at a distance approximately the same as a diameter of the cutting disks which in preferred embodiments have uniformly sized diameters. The cutting disks may advantageously be spaced from one another along the shaft at a distance between 60% and 110% of a diameter of a disk, with around 90% of a diameter of a disk (+/−3 to 5%) being a particularly well adapted spacing. One tool disclosed has cutting disks that are approximately 1.1 millimeters in diameter and spaced from one another by approximately 1 millimeter. In an alternate injection molded plastic embodiment, the cutting disks are spaced from one another along the shaft at a distance approximately ⅔ of a diameter of a disk.
The optional forceps preferably terminate in a pair of generally hemi-cylindrical jaws, the jaws extending past a body of the handle so that they are disposed to grip and overlap a vas section around the reamer when it is an extended and locked position. The forceps jaws advantageously each have notches that are complimentary and overlapping with respect of one jaw to the other.
The reamer cuts or tears off its relatively precise volume of tissue, including lining mucosa and a thin layer of muscle, and pulls it inwardly toward the central reamer shaft and carries it out as the reamer is extracted. Spacing of cutting disks can be optimized for tissue removing effectiveness of the cutter array. In general if they are too closely spaced, the epithelium can not be squeezed in between the cutting disks to engage the cutting edges, and the area between disks is too small to remove sufficient tissue to induce the scarring response to the tissue injury. If they are too far apart, the inter-disk spaces become clogged with too much tissue and the cutting action can be halted or interfered with before all the epithelium between each pair of disks is effectively removed. In general optimal spacing is as disclosed herein.
A preferred kit would comprise such a tool or a set of them, if disposable, and a set of reamers if reusable with a double ended carrier/installation tool, along with the usual cutting blade, clamps, and surgical accessories appropriate to the procedure.
Also disclosed is a vasectomy method, with the steps of 1) sliding into a vas opening a multi-bladed reamer; 2) holding the vas against the inserted reamer; 3) quickly pulling the reamer out of the vas to remove at least a portion of vas mucosal layer and some of the vas muscle layer tissue; whereby scarification of the vas is induced, and the vas is sealed by resultant scarring. The reamer is optimally sized to dilate the vas into which it is inserted, and preferred cutting edges of the cutting disks are adapted for tearing rather than cutting tissue as the reamer is removed quickly. In preferred methods, the reamer has the spring-loaded pull bar feature, and the pull bar and attached reamer are pulled out of the vas under selectable spring tension. Preferably, the reamer and pull bar are disposed within a spring-loaded handle that includes a vas-gripping forceps mechanism, and the step of holding the vas is accomplished with the forceps, and the step of quickly pulling out the reamer is accomplished with the release of the spring-loaded pull bar. The reamer is preferably removably attachable to the pull bar, and before and after the steps of sliding in the reamer and quickly removing the reamer, a removable reamer is respectively attached to the pull bar, and removed from the pull bar, with the steps of attaching and removing the removable reamer being effected with a holder tool, preferably double ended, for inserting and removing the reamer into and out of the pull bar.
For optimizing results with an optimal amount of tissue repeatably removed from the vas lumen during each procedure, irrespective of size variations which might cause a reamer to fit more or less tightly, a clamping forceps is advantageously provided. The forceps compresses the vas generally circumferentially, urging the mucosa into the spaces between the cutters on the reamer before the reamer withdrawal spring is released to extract the reamer. A tissue stop is now also desirably provided which prevents the rearward motion, or elongation, of the vas as the reamer pulls it back during extraction.
After insertion of the reamer, the operator squeezes the forceps sufficiently to just close the clamp around the vas, and then continues to squeeze further to further compress or bow the arms of the forceps to push against the button on the tool handle, whereby the spring catch protruding from the casing of the pull rod is pressed and the spring is released to pull the reamer back.
The optional notches on the rim of the jaws can capture a larger diameter vas and compress it against the reamer before the surfaces of the opposing jaws come into contact. The notches of the two jaws overlap as they come together and the width of the opposing arches gets smaller; thus the tissue of smaller diameter vasi is also compressed circumferentially until the jaws come into full contact. The gentle spring pressure of the long forceps arms applies uniform clamping force on all size vasi and this assures uniform success.
A low-cost disposable version of the reamer can be produced by plastic injection molding if the profile of the cutting disks is modified to eliminate undercuts inherent in the alternate lathe-turned steel design. The resulting chisel edges chop into the vas lumen mucosa as the applicator's clamping forceps squeeze the vas. The multiple segments are thus held firmly between the disks as the spring snaps the reamer back. It is believed this action causes the captive mucosa to delaminate from the soft smooth muscle which makes up the body of the vas and be carried out by the reamer. This configuration desirably produces a rougher surface on the inside of the vas. This, in combination with the bruising effect of the clamping forceps, facilitates the formation of a robust occlusive scar.
Optimal separation between the cutting flutes in this configuration is approximately equal to two-thirds of the diameter of the reamer. This allows enough space between the cutters for the mucosa to drape over the edges and at the same time produces the smallest possible sections, which enables easy delamination and tissue removal.
The optional double-ended cylindrical changing tool that is illustrated allows the operator to change reamers easily without handling the reamers directly, preventing contamination and fumbling any of the tiny reamer tools.
a is a side elevation of a reamer holder/installation tool.
b is a schematic partial side elevation of a vasectomy tool, before the reamer is installed.
Turning now to the drawings, the invention will be described in preferred embodiments by reference to the numerals of the drawing figures wherein like numbers indicate like parts.
Reamer 50 illustrated in
The spring motivated extractor embodiment of vasectomy tool 10 in
The reusable embodiment of vas tool 10 uses a kind of flat two jaw collet 42 to hold reamer 50. This design facilitates side installation and removal of the reamer, which in turns facilitates easy removal of a tissue filled reamer, after extraction from the vas, and replacement of it with a fresh reamer for each successive vas segment to be reamed. Other reamer attachment methods may be employed, such as screw threads or clamps. A low cost, single-use, injection molded embodiment of the tool (not shown) functions roughly as described above, with the reamer and pull rod being a single unit, either by conventionally fusing or snap fitting a plastic reamer to a pull rod, or molding the reamer and pull rod as a unit. Such a single use embodiment would thus require 4 units per typical patient.
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Scarification of the distal and proximal ends of the partially transected vas is believed to be effective because the regenerative epithelial basement membrane of the vas is completely removed at the reamed site without harming vasal blood supply. Surgical dissection, tissue trauma and discomfort are reduced, as well as the chance of complications such as bleeding or formation of a sperm granuloma.
With regard to systems and components above referred to, but not otherwise specified or described in detail herein, the workings and specifications of such systems and components and the manner in which they may be made or assembled or used, both cooperatively with each other and with the other elements of the invention described herein to effect the purposes herein disclosed, are all believed to be well within the knowledge of those skilled in the art. No concerted attempt to repeat here what is generally known to the artisan has therefore been made.
What is presented is a method and tool that can be used worldwide that is simple with minimal tissue dissection, and can be used in areas where finances and or power supply irregularities do not permit electro cautery. It is a device that can be either disposable, single use, or resterilizable, with readily available pre-sterilized kits.
In compliance with the statute, the invention has been described in language more or less specific as to structural features. It is to be understood, however, that the invention is not limited to the specific features shown, since the means and construction shown comprise preferred forms of putting the invention into effect. The invention is, therefore, claimed in any of its forms or modifications within the legitimate and valid scope of the appended claims, appropriately interpreted in accordance with the doctrine of equivalents.
This application claims priority to U.S. Provisional Application 60/621,405 filed Oct. 22, 2004 and 60/647,377 filed Jan. 26, 2005.
Number | Date | Country | |
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60621405 | Oct 2004 | US | |
60647377 | Jan 2005 | US |