This invention relates generally to the field of microsurgery and, more particularly, to ophthalmic microsurgery.
Current vitreoretinal techniques in which surgical instruments are inserted into the eye require the dissection of the conjunctiva and the creation of pars plana scleral incisions through the sclera. The dissection of the conjunctiva typically involves pulling back the conjunctiva about the eye so as to expose large areas of the sclera and the clipping or securing of the conjunctiva in that pulled back state. Following the creation of the incisions, surgical instruments are passed through these incisions and the inserted instruments are observed through the pupil using a microscope and corrective optics. These instruments are used to manipulate and/or dissect retinal tissues within the eye as is well as to implement the specific retinal treatment technique (e.g., photocoagulation). Prior art scleral incisions created for vitreoretinal surgery are made large enough to accommodate the required instruments, the inserted portions being typically 19 or 20 gauge (approximately 1 mm) in diameter. After completing the specific treatment procedure, the inserted instruments are removed from the incisions in the sclera. Because the incisions through the sclera are large enough to pass 19 or 20 gauge instruments, the incisions are typically too large to self-seal. Thus, the incisions must be sutured shut. Following the suturing of the scleral incisions, the surgical personnel reposition the conjunctiva in its normal position and reattach the free end(s) of the conjunctiva to the eye using sutures. While such methods and techniques have proven to be effective in the treatment of vitreoretinal disease, there is a strong motivation to move away from procedures requiring sutures and instead look to greatly simplified sutureless procedures. Therefore, recently surgical instruments have been miniaturized so that the cannulae or shafts of the instruments are on the order of 23 or 25 gauge. Such thin shafts are bent easily, particularly as they are manipulated within very tight wounds.
Therefore, a need continues to exist for a thin gauge probe that more easily resists bending during use.
The present invention improves upon the prior art by providing a thin gauge surgical probe having a retractable reinforcing sleeve. When the probe is inserted into the eye, through the trocar cannula, the trocar cannula becomes removably attached to the distal end of the sleeve is a trocar cannula, and acts as a stiffening device.
Accordingly, one objective of the present invention is to provide a thin gauge surgical probe.
Another objective of the present invention is to provide a thin gauge surgical probe that resists bending.
Yet another objective of the present invention is to provide a thin gauge surgical probe having a retractable reinforcing sleeve with a removably attached trocar cannula.
Another objective of the present invention is to provide a thin gauge surgical probe having a retractable reinforcing sleeve.
These and other advantages and objectives of the present invention will become apparent from the detailed description and claims that follow.
As best seen in
Cannula 14 generally is made of thin walled stainless steel or titanium tubing with an outside diameter of 20, 23 or 25 gauge or smaller. Cannula 14 movably extends through distal end 21 of body 12 and retained within body 12 by sleeve 22. Sleeve 22 reciprocates within interior cavity 16 and is urged toward distal end 21 of body 12 by spring 24.
Attached to distal end 26 of cannula 14 opposite spring 24 is trocar cannula 28. Trocar cannula 28 generally consists of cannula 30 that is attached to or integrally formed with hub 32. Trocar cannula 28 may be made from any suitable thermoplastic or metal, such as titanium or stainless steel. Hub 32 is sized to engage, frictionally and removably, or form the closure for and be removable from, distal end 26 of cannula 14.
As seen in
In addition, as trocar cannula is releasable from cannula 14, probe 10 may be disengaged from trocar cannula 28 and tool 20 removed from the surgical site so that another toll (not shown) may be inserted into the incision through trocar cannula 28.
This description is given for purposes of illustration and explanation. It will be apparent to those skilled in the relevant art that changes and modifications may be made to the invention described above without departing from its scope or spirit.