Prior art involves many methods of laparoscopic wound closure. For many years a small suture guide device having at least two guide channels, but not limited to two guide channels, originating from a large proximal end, and exiting at an angle on a tapered shaft. Said device was inserted into the surgical wound created by a trocar. When the trocar is removed the wound will need to be closed with suture. Said small device has a tapered shaft compatible for the size of the trocar used. Said device is inserted into the wound until said large proximal end is in contact with the abdomin which sets the correct depth of said device. The surgeon will use a small grasper having a means to hold suture and a sharp distal end to pierce the patient tissue. Said grasper will hold suture as it is inserted into a first guide channel. Said guide channel aides in placing suture at the correct position to properly pierce the peritoneum. After properly piercing said peritoneum and placing said suture the surgeon will release the suture and withdraw said grasper. Using a second guide channel said grasper is inserted and the grasper is oriented to capture the dangling suture inside the body cavity previously placed. Upon capture of said suture said surgeon will pull said suture back through said second guide channel and withdraw said grasper. Said suture is of sufficient length to have suture ends exposed and available for said surgeon to tie said suture and close the wound. Said suture guide had a single purpose of guiding suture placement, made as a single component usually of plastic or stainless steel. There were no moving parts or additional functions in this prior art.
This embodiment will be concerned with devices that have at least two or more combined functions used for wound closure. For those skilled in the art, it is well understood that single function devices known as guides are used in cooperation with a separate and non-integral suture grasper having a sharp distal end for piercing tissue and grasping suture.
A popular prior art wound closure device is comprised of two distinct components: an elongated body in the shape of a shaft having internal acute angled guide channels with a distal end having an anchoring means involving pivoting members that contract and expand when the proximal end is operated from a natural first position to a second position and back again. Said proximal end is usually spring loaded to return said proximal end back to a first natural position. The purpose of said pivoting members prevent removal of said wound closure device from within the body cavity by the geometry change of said anchoring means usually forming a triangular shape when expanded and a cylindrical shape matching said elongated body when contracted.
An external and separate suture grasping device has a piercing distal end commonly constructed to have a suture grasping means. Said piercing distal end can be constructed in a means such as a distal end jaw configuration that opens and closes to hold or release suture. Another prior art suture grasper has a distal piercing point similar to a hypodermic needle having stored inside a dual end flexible metal wire to facilitate retracting or extending from said distal piercing point. Said internal metal wire may have different end configurations designed to capture and release suture. Said suture grasping device is external of said wound closure device and enters the body through said acute angled guide channels.
An additional prior art method involves the above configuration but having two curved needles integral to said anchoring means attached at the distal end of the elongated shaft. Said curved needles have suture affixed to them. Said curved needles are held in place at said anchoring means and the excess suture length between said needles is placed in a groove retaining the loop of suture along said elongated body. Said anchoring means is slimmed to allow insertion into the patient wound. Said curved needles are sized so the arc of the needle is confined within the diameter of said elongated shaft and penetrate the peritoneum upward from the distal end of said wound closure device through the peritoneum. As the curved needles complete their circular travel they are stored within said elongated body for removal.
The embodiment of this novel integrated wound closure invention combining multiple functions into a single elongated device with a proximal selective means to operate said multiple functions. The details of which will be clearly itemized in the drawing descriptions.
A novel invention for a laparoscopic wound closure device comprising: a means to stage suture in a pre-determined target location, an operable means to sequentially engage functions necessary to close a surgical wound and maintain surgical position for inserting integrated sharp needles through the peritoneum and up to the target location, extending a grasper from said sharp needles to capture and retract targeted suture within said sharp needles. Upon wound withdrawal of said wound closure device suture ends are exposed so the surgeon may tie a knot and close the wound.
The following drawings will depict and illustrate one means of construction for this novel integrated closure device but those skilled in the art can readily understand that the construction shown is used to portray the functional details of this embodiment and not necessarily reflect the actual shape and assembly of production components.
Said novel invention called an integrated closure device 100 combines five distinct systems, 300, 400, 500, 600, 700 into said device 100 which are operable by the surgeon during wound closure. Each system will be described in detail after the overall description of said device 100. Said device 100 facilitates suture loading by a sterile field technician using off the shelf suture and staging said suture onto said device 100. The proximal end has a selective system 300 for a first downward movement which extends and closes the distal anchoring system 400, and a suture management system 500 for routing and holding suture. After loading suture, the sterile field technician will then hand-off said device 100 to a surgeon to insert said device 100 into the wound. The second downward movement of the selective system 300 opens the anchoring system 400 to allow contact with the peritoneum setting the correct surgical depth. The beginning portion of the third downward movement of the selective system 300 extends the piercing system 600 out the guide channels 120 through the peritoneum until reaching a stop, the remaining portion of the third downward movement extends the grasper system 700 beyond said piercing system 600 to capture the suture at the target location. Upon release of said proximal end selective system 300 a spring returns said grasper system 700 into said piercing system 600. A grasper hook 712 is drawn inside the sharp distal end 626 until finally the sharp distal end 626 returns to the stowed position in the distal channel 120. The fourth downward movement of the proximal selective system 300 closes the anchoring system 400 and the device 100 is withdrawn from the bringing the suture ends out of the wound. Said suture ends slip out of the retaining ring 510 as said device 100 is moved away from the wound. Said, free suture ends are then tied by the surgeon to close the wound.
Said invention has a first system means called a selector system 300 which selectively operates all three functions 400, 600, 700, in an orderly manner by rotating 60 degrees on each full stroke down and up. Said second system means called an anchoring system 400 prevents the removal of said device 100 from the patient peritoneum. Said third system means called a piercing system 600 has sharp distal ends 626 for piercing the peritoneum and retracting from said peritoneum. Said fourth system means called a grasping system 700 is a flexible wire hook 712 which extends beyond said sharp distal ends 612 to reach over said suture 530 to retrieve said suture 530 at the target location span 424 and retracting said suture 530 into said sharp distal end 612.
Said device 100 is first operated by said sterile technician. To begin, said device 100 is removed from a sterile pouch. Said device is in a normal state with said anchoring system 400 open. The first operation is to depress the selective system 300 plunger button 310 which rotates a shaft 330 in 60-degree increments for each downward movement. As said plunger button 310 is depressed the plunger 330 having a ramp 334 causes rotation by 30 degrees upon contact with a distal ramp 354. Upon release of the plunger button 310 the plunger ramp 336 strikes a lead surface 347 or 348 to cause an additional 30-degree rotation, placing said plunger ramp 336 against a fence 346 to hold the anchoring system 400 closed. The sterile technician will acquire some suture from a storage cabinet and remove it from the holder and if equipped will detach a needle. Said sterile technician holding the suture ends in one hand whereby two vertical strands forming a loop when draped. Said device 100 having a trough 434 on said distal nose 430 is placed against the suture loop allowing said suture to nest in said trough 434 of distal nose 430. Said sterile technician routes one suture strand into the lower wing 420 grooves 422 straddling an open window span 424, around and upward into the upper wing 410 grooves 412 straddling an open window span 414, then under the distal nose 112, feeding one strand into the suture track 114 and suture guide 118 to be finally pulled into a pinch gap 515 for suture end retention. The suture 530 follows said grooves 412, 422 as they trace a staging path near the pivot points 232, 412, 426, 428, 432 to maintain a near zero length change when the anchoring system 400 is open or closed. The alternate suture strand is staged in an identical fashion albeit on the opposite lower wing 421, upper wing 411, tab 113, suture track 115, and finally pulled into a pinch gap 515. With the anchoring system 400 retained in the closed condition and suture secured by the pinch gap 515, said device 100 with staged suture 530 is handed to the surgeon.
During a laparoscopic surgical procedure said device 100 is used to close surgical wounds created by laparoscopic trocar devices. If the trocar is an 8 mm trocar it will leave a wound slightly larger than 8 mm; therefore, said integrated closure device 100 will be sized to correspond to the wound diameter whether 8 mm by this example or some other size. The surgeon usually removes the trocar from the wound and then inserts the integrated closure device 100 to begin the process of closing a wound. Said integrated closure device can be reloaded and reused multiple times per patient.
Since suture 530 used in this novel invention 100 is pre-loaded in the staged position by a sterile field technician the surgeon carefully plunges said device 100 into the patient wound until reaching the desired depth. The surgeon depresses the plunger button 310 causing selector tabs 332 to abut proximal driver ends 452 protruding through a slot 382 in said collar 380 downward as the shaft 330 rotates 30 degrees at the end of stroke. Upon release of the plunger button 310 a spring 450 returns said anchoring system 400 to a triangular shape whereby the wings 410 are pulled into contact with the peritoneum. Said anchoring system 400 is held in the normally open position by the spring 450.
After said anchoring system 400 was opened said piercing system 600 is ready to pierce said peritoneum. Depressing said selector plunger button 310 allows the plunger fins 332 to push a shelf 384 on the non-rotatable selector collar 380 downward. The piercing system 600 includes said pusher 640 having proximally attached needle shafts 622, flex joint 624, and sharp distal end 626. Said sharp distal end 626 is retained in said distal guide channels 120, 220 having a bend 122, 222 and straight run 124, 224. Said sharp distal end 626 is stored within the distal guide channels 120, 220. Said sharp distal end 626 has a hypodermic style pierce point 612 being parallel to the elongated body axis 116 so as not to expose the sharp distal end 626 when retracted. Said selector collar 380 having two 60 degrees of collar slot 382 for operating said anchoring system 400, and two 120 degrees of collar shelf 384 for operating piercing system 600 and grasper system 700. The first 60 degrees of said 120 degrees of collar shelf 384 activates the piercing and grasping systems 600, 700 respectively. When the selector fins 332 contact the collar shelf 384 said beginning stroke drives the collar 380 and subsequently drives the needles 626 through the peritoneum passed the open window span 414 of the upper wing 410 and said collar 380 hits a beginning stroke stop 132. Depressing the selector button 310 after the stroke stop 132 compresses the needle spring 650 extending the grasper system 700 hook 712. Said grasper system 700 having a distal hook 712 on an angular leg 714 allows said hook 712 to pass over said staged suture 530 spanning said open window 422 until said suture touches said angular leg 714. Upon reversing said ending stroke said hook 712 captures said suture 530 and retracts said suture 530 into said sharp distal end 626. For suture to retract into said sharp distal end 612 of said novel invention 100 the additional suture length is drawn from the suture ends slipping through the pinching gap 512 as tension is created by a pinch ring 510 and pinch spring 520.
The lower view shows the suture 530 in relation to the novel invention 100 from the distal end cap 430 trough 432, passing from the lower wing 420, 421 groove 422 across the target location span 424 into the upper wing 410, 411 groove 412 across the span 414, under the distal tab 112, through the suture track 114 into the suture guide 118 and under the suture ring 510 pinching the suture tails 530 by the pinch gap 515.