Various aspects of the present disclosure relate generally to surgical devices and methods. More specifically, the present disclosure relates to tissue suturing devices and related methods for minimally invasive surgery.
Laparoscopic suturing is challenging and may take years for a surgeon to master. For example, suturing the vaginal cuff during a total laparoscopic hysterectomy (TLH) is often the rate limiting step due to the dexterity and coordination required for suturing. In the United States alone, there are approximately 300,000 laparoscopic or robotic hysterectomies performed annually. In such procedures, the cervix is severed from the vagina and removed with the uterus, leaving behind the opening in the vaginal wall that must be closed. However, the geometry of this opening can make it difficult to suture effectively. Consequently, vaginal cuff dehiscence is a potentially catastrophic event where the vaginal cuff opens such that the bowel may herniate through the vagina. Bowel herniation through the vagina may require immediate surgery. The incidence of vaginal cuff dehiscence after a TLH has been found to be approximately 0.5-4%. A modifiable risk factor for vaginal cuff dehiscence is surgical technique, which has significant inter-operator variability. The present disclosure provides solutions for these problems.
The present disclosure is directed to devices and related methods for consistently and quickly suturing tissue, such as the vaginal cuff that results from separation of the cervix from the vagina. Disclosed devices are configured and adapted for introduction into the patient via the vagina, wherein a distal suturing head portion of the disclosed devices are sized and shaped to be introduced into the vaginal cuff by way of the vagina to effectuate fast, safe and effective suturing of the vaginal cuff.
Aspects of the present disclosure relate to, among other things, tissue extraction devices and related methods. Each of the aspects disclosed herein may include one or more of the features described in connection with any of the other disclosed aspects.
It may be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the features claimed.
As used herein, the terms “comprises,” “comprising,” or any other variation thereof, are intended to cover a non-exclusive inclusion such that a process, method, article, or apparatus that comprises a list of elements does not necessarily include only those elements, but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. The term “exemplary” is used in the sense of “example,” rather than “ideal.”
An illustrative apparatus for suturing tissue comprises a body having a proximate end and a distal end, a suturing head coupled to the distal end of the body, and an actuator coupled to the body. The suturing head including a first set of curved needles disposed therein, a second set of curved needles disposed therein, and a plurality of sutures disposed therein. A first end of a respective one of the plurality of sutures is coupled to a respective one of the curved needles of the first set. A second end of the respective one of the plurality of sutures is coupled to a respective one of the curved needles of the second set. The curved needles of the first set are oppositely oriented to the curved needles of the second set. The suturing head is configured and arranged to be positioned between two substantially parallel sections of tissue (e.g., the vaginal cuff). The actuator is configured and arranged to deploy the first and second sets of curved needles through the tissue to suture the two sections of tissue together in a single operation.
The apparatus further comprises a first anchor slidably coupled to a respective one of the sutures and a respective one of the curved needles of the first set and a second anchor fixedly coupled proximate an end of the suture and a respective one of the curved needles of the second set. A portion of the suture includes an end of the suture is free floating on one side of the first anchor.
The first and second anchors can be configured and arranged to pass through from a first surface of one of the sections of tissue to a second surface of one of the sections of tissue while coupled to the curved needle and separate from the curved needle and remain on the second surface subsequent to actuation of the suturing head.
Each of the curved needles can include at least one aperture on a surface of the curved needle. The first anchor can be initially positioned within the aperture of the curved needles of the first set. The second anchor can be initially positioned within the aperture of the curved needles of the second set. Each of the curved needles can includes another aperture on the surface of the curved needle. The suture can pass through the aperture and the other aperture.
Each of the curved needles can include a first, relatively proximal region having a first diameter and a second, relatively distal region having a second diameter. The distal region includes a distal tip of the curved needle. The second diameter is smaller than the first diameter. The first and second anchors are coupled to the curved needles in the distal region.
The first anchor can be configured and arranged to traverse the suture towards the second anchor to suture the two substantially parallel sections of tissue together. Each of the sutures can include a plurality of bumps along the suture that inhibit the traversal of the first anchor along the suture.
The actuator can includes a trigger coupled to the body configured and arranged to deploy the first and second sets of curved needles. The trigger is coupled to a proximate end of an elongated member coupled to the suturing head. The suturing head and the elongated member cooperate to form a plurality of racks and pinions formed by racks of a distal end of the elongated member and pinions of the suturing head. The curved needles are coupled to the pinions such that rotation of a respective one of the pinions in a first direction causes rotation of the curved needles away from the suturing head in a second direction opposite to the first direction.
The actuator can include a knob coupled to the body configured and arranged to deploy the first and second sets of curved needles. The curved needles of the first set are coupled to a first axle and the curved needles of the second set are coupled to a second axle (2232). The knob is coupled to a belt coupled to a gear of the first axle and a gear of the second axle.
The curved needles of the first and second sets can be arcuate needles.
The two substantially parallel sections of tissue can be an anterior section and a posterior section of a separated vaginal cuff. The suturing head can fit within the separated vaginal cuff.
The suturing head can include at least one alignment marking to position the suturing head between the two substantially parallel sections of tissue.
The suturing head can be removably coupled to the distal end of the body.
A method of suturing tissue comprises positioning a first set of curved needles and a second set of curved needles between two substantially parallel sections of tissue. The curved needles of the first set are oppositely oriented to the curved needles of the second set. The method can include simultaneously (or serially, if desired) deploying the sets of curved needles such that the curved needles of the first set pass through a first section of tissue and the curved needles of the second set pass through a second section of tissue and positioning a pair of anchors, coupled to a suture, proximate a surface of the first section of tissue and a surface of the second section tissue. A first anchor of the pair is coupled to one of the curved needles of the first set and a second anchor of the pair is coupled to one of the curved needles of the second set. The method includes removing the sets of curved needles from between the sections of tissue. The method includes ratcheting a first anchor of the pair along the suture and towards a second anchor of the pair to suture the first section of tissue to the second section of tissue.
Deploying the sets of curved needles can include serially or simultaneously rotating the curved needles of the first set in a first direction about a center point of the curved needles of the first set and rotating the curved needles of the second set in a second direction, opposite to the first direction, about the center point of the curved needles of the second set. Removing the sets of curved needles can include serially or simultaneously rotating the curved needles of the first set in the second direction about the center point of the curved needles of the first set and rotating the curved needles of the second set in the first direction about the center point of the curved needles of the second set.
Deploying the sets of curved needles can include serially, or simultaneously, rotating the curved needles of the first set in a first direction about a first axle coupled to the curved needles of the first set and rotating the curved needles of the second set in a second direction, opposite to the first direction, about a second axle coupled to the curved needles of the second set. Removing the sets of curved needles can include serially, or simultaneously, rotating the curved needles of the first set in the second direction about the first axle and rotating the curved needles of the second set in the first direction about the second axle.
Positioning the pair of anchors can include separating the first anchor from the curved needle of the first set and the second anchor from the curved needle of the second set.
The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate exemplary aspects of the present disclosure and together with the description, serve to explain the principles of the disclosure.
The present disclosure is drawn to laparoscopic tissue devices and related methods. Reference now will be made in detail to aspects of the present disclosure, examples of which are illustrated in the accompanying drawings. Wherever possible, the same reference numbers will be used throughout the drawings to refer to the same or like parts. The term “distal” refers to a portion farthest away from a user when introducing a device into a subject. By contrast, the term “proximal” refers to a portion closest to the user when placing the device into the subject. The term “approximately,” when used to describe a numerical value, may be anywhere in a range of ±5% from the numerical value.
The suturing head 106 includes a plurality of slits 212-1, 212-2, 212-3, 212-4, 212-5, and 212-6 (collectively referred to as the slits 212). A suture is removed from the suturing head 106 through each of the slits 212 subsequent to deployment and retraction of curved needles.
In at least one embodiment, the second set 216 includes curved needles that are mirror images of the curved needle 214-1. That is, the positioning of the first aperture 218 and the second aperture 219 are switched. In at least one embodiment, the curved needles of the first set 214 and the second set 216 are arcuate needles. For example, each of the curved needles can be a quarter arc. The radius of the arc can be nine mm.
As shown in
Pulling the trigger 104 causes the gear 1668 to push elongated member 1140 toward the suturing head 106, as indicated by the arrow 1672, via a gear track 1661. The elongated member 1140 includes a plurality of pins 1660 positioned in a slot 1662 of the body 102. The pins 1660 and slot 1662 cooperate to control the motion of the elongated member 1140.
Pulling the trigger 104 (not shown) causes the elongated member 1140 and the racks 626 to move distally as indicated by the arrow 1144. The motion of the racks 626 causes the axle 630 to rotate in a first direction (clockwise from the perspective of
The motion of the racks 626 as indicated by the arrow 1144 causes the axle 632 to rotate in the second direction (counterclockwise from the perspective of
Releasing the trigger 104 causes the elongated member 1140 and the racks 626 to move proximally, opposite to the direction indicated by the arrow 1144. The motion of the racks 626 causes the axles 630 and 632 to rotate in directions opposite to those indicated by the arrows 1146 and 1148. Because the curved needles 214-2 and 216-2 are in an interference fit with the axles 630 and 632, respectively, the rotation of the axles 630 and 632 in directions opposite to those indicated by the arrows 1146 and 1148 causes the curved needles 214-2 and 216-2 to rotate in directions opposite to that indicated by the arrows 1150 and 1152. Thus, the rotation of the axles 630 and 632 retract the curved needles of the first set 214 and the second set 216 back into the suturing head 106. Note that the axles 630 and 632 rotate simultaneously so that the curved needles of the first set 214 and the second set 216 retract simultaneously.
The gear 2240 is coupled to a gear 2242 of a second instance of the set of curved needles 2460. The second instance is the same as the first instance but the first instance is driven by the gear 2230 on the axle 2232 whereas the second instance is driven by the gear 2242 on the axle 2232.
Rotating the knob 1872 causes rotation of the gears 2110, 2112, 2116, 2220, 2224, 2226, 2230, 2238, 2240, and 2242. Rotating the knob 1872 in a first direction causes rotation of the gear 2230 driven by the gear 2226, which causes the curved needles 2234 of the first instance of the set 2460 to rotate about the axle 2232 (clockwise from the perspective of
Rotating the knob 1872 in a second direction, opposite to the first direction, causes rotation of the gear 2230 driven by the gear 2226, which causes the curved needles 2234 of the first instance of the set 2460 to rotate about the axle 2232 (counterclockwise from the perspective of
The suturing head 1870 includes a plurality of suture feeding tubes 2250-1, 2250-2, 2250-3, 2250-4, 2250-5, and 2250-6 (collectively referred to as the suture feeding tubes 2250). The suturing head 1870 is not removably coupled to the body 1871. Thus, the suturing head 1871 has to be loaded with sutures prior to each use. The sutures are fed through the suture feeding tubes 2250. After feeding the sutures, each of the sutures are coupled to an anchor (e.g. the anchor 2236-1) of the first instance of the set 2460 and an anchor (e.g. the anchor 2236-1) of the second instance of the set 2460.
The embodiments described with respect to
It will be apparent to those skilled in the art that various modifications and variations can be made in the disclosed devices and methods without departing from the scope of the disclosure. While a variety of devices and methods have been made and used for suturing tissue, it is believed that no one prior to Applicant has made or used the technology described herein. Other aspects of the disclosure will be apparent to those skilled in the art from consideration of the specification and practice of the features disclosed herein. It is intended that the specification and examples be considered as exemplary only.
The present patent application is a continuation of and claims the benefit of priority to U.S. patent application Ser. No. 16/368,495, filed Mar. 28, 2019, and issued Jan. 28, 2020 as U.S. Pat. No. 10,542,968, which in turn is a continuation of and claims the benefit of priority to International Application No. PCT/US2017/068342 filed Dec. 22, 2017, which in turn claims the benefit of priority to U.S. Provisional Patent Application Ser. No. 62/438,579, filed Dec. 23, 2016. Each of the aforementioned patent applications is incorporated herein by reference in its entirety for any purpose whatsoever.
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Number | Date | Country | |
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Parent | 16368495 | Mar 2019 | US |
Child | 16752712 | US | |
Parent | PCT/US2018/068342 | Dec 2017 | US |
Child | 16368495 | US |