This disclosure relates to a surgical device and, more particularly, to a surgical device for forming a purse string suture using a plurality of retractable needles and a suture.
Purse string suture devices may include a pair of serrated tissue clamping jaws provided with teeth for clamping the tissue to be sutured therebetween. Such devices include needle passages which extend through the teeth on each jaw for receiving a needle attached to a suture to be threaded through the tissue. In use, the tissue to be sutured is clamped between the jaws and the needle is manually passed through the needle passages in both jaws to thread the suture through the tissue. Thereafter, the jaws are opened and the purse string suture is tightened and wrapped to draw the tissue together. With this type of device, a considerable amount of manual effort and dexterity is required to accomplish the purse string suturing technique. Also, in such devices, it is difficult to control the flow of tissue between the teeth because an insufficient amount of space is provided to gather the tissue clamped by the jaws.
In accordance with the disclosure, a suture device includes an outer sleeve defining a lumen therethrough, a needle driver, an inner shaft, and a needle assembly. The needle driver includes a stem extending through the lumen of the outer sleeve, and a wing extending radially outward from the stem. The inner shaft includes an elongate member and a support coupled to a distal end portion of the elongate member. The needle assembly includes a needle and a suture. The needle is rotatably supported on the support of the inner shaft such that the needle is transitionable between a retracted position, in which, the needle is disposed radially inward of a peripheral portion of the outer sleeve, and an extended position, in which, the needle extends radially outward from the peripheral portion of the outer sleeve.
In an embodiment, the outer sleeve may have a frusto-conical configuration.
In another embodiment, the needle may have an arcuate profile.
In yet another embodiment, the needle may have a first end having a tip configured to penetrate tissue, and a second end operatively supported on the support of the inner shaft to enable rotation thereof.
In still yet another embodiment, the second end of the needle may have a boss configured to be received in a groove defined in the support of the inner shaft.
In still yet another embodiment, the second end of the needle may define a bore dimensioned to receive the suture therethrough.
In an embodiment, the support may define the groove adjacent a peripheral portion of the support.
In another embodiment, the outer sleeve may define an aperture at a proximal end portion thereof. The aperture may be in communication with the lumen of the outer sleeve.
In yet another embodiment, the support of the inner shaft may include a guide protrusion configured to be received in a groove defined in the outer sleeve to facilitate axial displacement of the inner shaft relative to the outer sleeve.
In still yet another embodiment, the outer sleeve, the needle driver, and the inner shaft may be concentrically disposed.
In an embodiment, a proximal end portion of the needle driver may extend proximally from a proximal end portion of the outer sleeve, and a proximal end portion of the inner shaft may extend proximally from the proximal end portion of the needle driver.
In accordance with another embodiment, a suture device includes an outer sleeve defining a lumen therethrough, a needle driver, a suture assembly, and an inner shaft. The needle driver includes a stem and wings extending radially outward from the stem. The suture assembly includes needles and a suture. The inner shaft includes a support configured to support the needles thereon. The needles are separated by the wings of the needle driver and rotatably supported on the support of the inner shaft, such that rotation of the needle driver transitions the needles from a retracted position, in which, the needles are disposed flush with a peripheral portion of the outer sleeve or radially inward of the peripheral portion of the outer sleeve, and an extended position, in which, the needles extend radially outward from the peripheral portion of the outer sleeve to enable penetration through tissue.
In an embodiment, the outer sleeve may have a tapered configuration.
In accordance with yet another embodiment, a suture device includes a suture assembly, an outer sleeve, a needle driver, and an inner shaft. The suture assembly includes needles and a suture extending through needles. The needle driver includes a stem and wings configured for concomitant rotation with the stem. The inner shaft includes a support configured to support the needles of the suture assembly between the support and the outer sleeve. The needle driver is rotatable to transition the needles between a retracted position, in which, the needles are disposed radially inward of the support of the inner shaft and the outer sleeve, and an extended position, in which, the needles are disposed radially outward of the support of the inner shaft and the outer sleeve to engage tissue. The inner shaft is movable towards and away from the outer sleeve to receive the needles therebetween.
Various embodiments of the disclosure are described hereinbelow with reference to the drawings, wherein:
This disclosure will now be described in detail with reference to the drawings, in which like reference numerals designate identical or corresponding elements in each of the several views. As used herein, the term “distal,” as is conventional, will refer to that portion of the instrument, apparatus, device or component thereof which is farther from the user while, the term “proximal,” will refer to that portion of the instrument, apparatus, device or component thereof which is closer to the user. In the following description, well-known functions or constructions are not described in detail to avoid obscuring the disclosure in unnecessary detail.
Referring to
Through the use of the suture device 10, the formation of a purse string suture is simplified by, e.g., eliminating the need for maneuvering a needle inside an anal canal. In addition, uniform needle rotation, tissue penetration, and/or suture advancement may be obtained independent of the skill of the clinician. In this manner, injuries to tissue may be reduced.
The inner shaft 300 is configured to extend through the passage of the needle driver 200. In this manner, the outer sleeve 100, the needle driver 200, and the inner shaft 300 may be concentrically disposed. In particular, the inner shaft 300 includes an elongate member 310 and a support 320 coupled to a distal end portion 312 of the elongate member 310. The support 320 has a planar surface configured to support a plurality of needles 410 of the needle assembly 400 against a distal end portion 104 of the outer sleeve 100. In particular, the support 320 may include guide protrusions 322 configured to be received in respective grooves (not shown) defined in an annular wall of the distal end portion 104 of the outer sleeve 100. Axial mating of the guide protrusions 322 with the respective grooves in the annular wall of the distal end portion 104 facilitates axial displacement of the inner shaft 300 towards and away from the outer sleeve 100.
The plurality of needles 410 is operatively associated with the needle driver 200. The needles 410 are separated by the plurality of wings 220 of the needle driver 200. Under such a configuration, when the wings 220 are rotated about the elongate stem 210, the wings 220 rotate the needles 410 about the respective bosses 416. In this manner, the needles 410 may be transitioned from a retracted position (
The needles 410 may be made from semi-stiff implantable wire. Alternatively, the suture device 10 may include plastic or absorbable materials. Examples of materials that can be used in constructing the needles 410 may include titanium, titanium alloys, stainless steel, nickel, chrome alloys and any other biocompatible implantable metals. Alternatively, other options for materials are liquid crystal polymers, HDPE, polyglycolic acid, and polyglycolid hydroxyacetic acid. At least a portion of each of the needles 410 may be coated with a biocompatible lubricious material that provides for easier delivery of the needles 410 into tissue.
Although the illustrative embodiments of the disclosure have been described herein with reference to the accompanying drawings, the above description, disclosure, and figures should not be construed as limiting, but merely as exemplifications of particular embodiments. For example, it is also contemplated that the suture 420 may include barbs or a sharp point to enhance anchoring characteristics thereof. It is further contemplated that the suture device 10 may be adapted for use in robotic surgery.
It is also to be appreciated that the disclosure may be utilized in a number of applications including ligating tissue, hernia mesh repair, and in conjunction with implant drug delivery systems or procedures involving positioning of surgical or implantable devices in patients. It is to be understood, therefore, that the disclosure is not limited to those precise embodiments, and that various other changes and modifications may be effected therein by one skilled in the art without departing from the scope or spirit of the disclosure.
This application claims the benefit of and priority to U.S. Provisional Patent Application Ser. No. 62/832,304, filed Apr. 11, 2019, the entire disclosure of which is incorporated by reference herein.
Number | Date | Country | |
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62832304 | Apr 2019 | US |