ATRAUMATIC TENACULUM FOR FACILITATION OF TRANSCERVICAL PROCEDURES

Abstract

A medical device used for grasping a body tissue has a main body having a first arm rotatably connected to a second arm at a pivot point. The main body has a proximal end and a distal end. A handle portion and a locking portion are disposed at the proximal end of the main body. A gripping portion including at least one flexible member is disposed at a distal end of the main body. The at least one flexible member is one of a flexible silicone band and a first gel-filled silicone pad and a second gel-filled silicone pad.

Claims

1. A medical device, comprising: a main body having a first arm rotatably connected to a second arm at a pivot point, the main body having a proximal end and a distal end; a handle portion disposed at the proximal end of the main body; a locking mechanism disposed at the proximal end of the main body; and a gripping portion including at least one flexible member disposed at the distal end of the main body, wherein the gripping portion includes a first projection extending vertically upward from a distal end of the first arm, a second projection extending vertically upward from a distal end of the second arm, a first c-shaped connector extending outwardly from the first projection, and a second c-shaped connector extending outwardly from the second projection.

2. The medical device of claim 1, wherein the medical device is made a biosafe material, the biosafe material being at least one of stainless steel, medical grade plastic, and medical grade silicone.

3. The medical device of claim 1, wherein the first arm of the medical device is rotatably connected to the second arm using one of a screw, a rivet, and a hinge.

4. The medical device of claim 1, wherein the main body has length between twenty-five centimeters and forty centimeters.

5. The medical device of claim 1, wherein the first projection is connected to an intermediate point of the first c-shaped connector and the second projection is connected to an intermediate point of the second c-shaped connector.

6. The medical device of claim 1, wherein the first projection extends vertically upward from the distal end of the first arm, and wherein the second projection extends vertically upward from the distal end of the second arm, thereby forming a parallel line with the first projection.

7. The medical device of claim 1, wherein a first flexible member is disposed on an inner surface of the first c-shaped connector and a second flexible member is disposed on an inner surface of the second c-shaped connector.

8. The medical device of claim 6, wherein each of the first flexible member and the second flexible member has a textured surface configured to maximize contact with and stabilize a body tissue.

9. The medical device of claim 6, wherein each of the first flexible member and the second flexible member is a gel-filled silicone pad.

10. The medical device of claim 8, wherein each gel-filled silicone pad on the first flexible member and the second flexible member has a textured surface.

11. The medical device of claim 2, wherein the first flexible member is affixed to the first c-shaped connector and the second flexible member is affixed to the second c-shaped connector using a medical grade adhesive.

12. The medical device of claim 1, wherein the locking mechanism includes a ratchet mechanism configured to lock the first arm and the second arm in place in operation.

13. The medical device of claim 1, wherein the locking mechanism is a friction lock including a slit and a screw configured to lock the first arm and the second arm in place in operation.

14. The medical device of claim 1, wherein the first C-shaped connector and second C-shaped connector have a radius of curvature measuring between one centimeter and ten centimeters.

15. The medical device of claim 1, wherein the distal end of each arm has two substantially straight portions that form an obtuse angle therebetween.

16. The medical device of claim 15, wherein the obtuse angle of the first arm faces the obtuse angle of the second arm.

17. The medical device of claim 1, wherein the handle portion includes two finger grips.

18. The medical device of claim 1, wherein the two finger grips are circular.

19. A medical device, comprising: a main body having a first arm rotatably connected to a second arm at a pivot point, the main body having a proximal end and a distal end; a handle portion disposed at the proximal end of the main body; a locking mechanism disposed at the proximal end of the main body, the locking mechanism including one of a ratchet mechanism and a slit and screw mechanism configured to lock the first arm and the second arm in place in operation; a gripping portion including a first connecting means disposed at a distal end of the first arm, a second connecting means disposed at a distal end of the second arm; and at least one flexible member wherein the at least one flexible member is a first gel-filled silicone pillow and a second gel-filled silicone pillow. cm 20. A method of stabilizing a body tissue using a medical device on a patient, the method comprising the steps of: providing a medical device comprising: a main body having a first arm rotatably connected to a second arm at a pivot point, the main body and each of the first arm and the second arm having a proximal end and a distal end; a handle portion disposed at the proximal end of the main body; a locking mechanism disposed at the proximal end of the main body; and a gripping portion including at least one flexible member disposed at the distal end of the main body, the at least one flexible member including a first gel-filled silicone pillow and a second gel-filled silicone pillow; gripping the handle portion of the medical device; manipulating the handle portion at the proximal end of the medical device to create an opening at the distal end; positioning the at least one flexible member adjacent a body tissue; manipulating the handle portion of the medical device to secure the at least one flexible member to the body tissue; engaging the locking mechanism of the medical device; performing a medical procedure; disengaging the locking mechanism; manipulating the handle portion at the proximal end of the medical device to create an opening at the distal end; releasing the body tissue from the at least one flexible member; and removing the medical device from the patient.

Description

DRAWINGS

[0018] The above, as well as other advantages of the present disclosure, will become readily apparent to those skilled in the art from the following detailed description, particularly when considered in the light of the drawings described hereafter.

[0019] FIG. 1 is a rear perspective view of a tenaculum according to one embodiment of the present disclosure, the tenaculum shown in an open, unlocked position;

[0020] FIG. 2 is a front perspective view of a tenaculum according to another embodiment of the present disclosure, the tenaculum shown in a closed, locked position;

[0021] FIG. 3 is a bottom elevational view of the tenaculum shown in FIG. 2;

[0022] FIG. 4 is an enlarged fragmentary front perspective view of the gripping mechanism of the tenaculum shown in FIG. 2, the gripping mechanism in a partially open position;

[0023] FIG. 5 is an enlarged fragmentary front perspective view of the locking mechanism of the tenaculum shown in FIG. 2, the locking mechanism in a locked position;

[0024] FIG. 6 is a side elevational view of the tenaculum of FIG. 2 in use in a patient, the tenaculum grasping and stabilizing the patient's cervix;

[0025] FIG. 7 is an enlarged front elevational view of the tenaculum taken at callout A in FIG. 6, the tenaculum grasping and stabilizing the patient's cervix;

[0026] FIG. 8 is a side elevational view of the tenaculum of FIG. 1 in use in a patient, the tenaculum grasping and stabilizing the patient's cervix;

[0027] FIG. 9 is an enlarged front elevational view of the tenaculum taken at callout B in FIG. 8, the tenaculum grasping and stabilizing the patient's cervix; and

[0028] FIG. 10 is a diagram illustrating a method for using the tenaculum of FIGS. 1-9.

DETAILED DESCRIPTION

[0029] The following detailed description and appended drawings describe and illustrate various embodiments of the invention. The description and drawings serve to enable one skilled in the art to make and use the invention and are not intended to limit the scope of the invention in any manner.

[0030] A medical device 2 used to stabilize a cervix 4 (shown in FIGS. 6-9) according to various embodiments of the present disclosure is shown in FIGS. 1-9. The medical device 2 includes a main body 6, a handle portion 8, a locking mechanism 10, and a gripping mechanism 12. The medical device 2 is made from any biosafe material or combination of biosafe materials suitable for placement in a human body such as stainless steel, biosafe plastic, and biosafe silicone, as non-limiting examples. Other suitable materials may also be selected by one skilled in the art within the scope of the present disclosure.

[0031] The main body 6 has a proximal end 14 and a distal end 16. In certain embodiments, the main body 6 has a substantially scissor-like shape including a first arm 18 having a proximal end 20 and a distal end 22 and a second arm 24 having a proximal end 26 and a distal end 28. The first arm 18 and the second arm 24 are substantially symmetrical with the proximal ends 20, 26 being substantially straight and the distal ends 22, 28 having a curvilinear or bow shape. In preferred embodiments, the main body 6 measures between twenty-five centimeters (25 cm) and forty centimeters (40 cm). One of ordinary skill in the art may select any other suitable size and shape, including dimensions, for the main body 6 including the first arm 18 and the second arm 24, as desired.

[0032] The first arm 18 intersects with the second arm 24 at a crossing section 29. The first arm 18 is rotatably connected to the second arm 24 at a pivot point 30 of the crossing section 29 using any suitable attachment mechanism 32 such as a screw, rivet, or hinge, as non-limiting examples. The pivot point 30 is located centrally in the crossing section 29. The first arm 18 and the second arm 24 rotate freely about the pivot point 30.

[0033] The handle portion 8 is integral with and disposed adjacent to the proximal end 14 of the main body 6, as shown in FIGS. 1-3, and is configured to provide a comfortable, easy-to-use grip for a user. The user manipulates the handle portion 8 to open and close the gripping mechanism 12, and in some cases to activate and release the locking mechanism 10, in operation.

[0034] In certain embodiments, the handle portion includes two finger grips 34, with one disposed adjacent the proximal end 30 of the first arm 18 and the other disposed adjacent the proximal end 26 of the second arm 24. Each finger grip 34 is generally circular or ring-like in shape, in certain embodiments. It should be appreciated that the handle portion 8 is not limited to any particular shape, size, or configuration, and one of ordinary skill in the art may select other suitable configurations having various shapes and sizes for the handle portion 8, as desired.

[0035] With renewed reference to FIGS. 1-3, the locking mechanism 10 is disposed at the proximal end 14 of the main body 6. In certain embodiments, the locking mechanism 10 includes a ratchet mechanism 36, as shown in FIG. 1. The rachet mechanism 36 includes a plurality of teeth 37 disposed on the proximal end 20 of the first arm 18 and the proximal end 26 of the second arm 24. The teeth 37 disposed on the first arm 18 are configured to lockingly engage with the teeth 37 disposed on the second arm 24 such that the user may lock the medical device 2 in a variety of desired positions using the handle portion 8.

[0036] In an alternative embodiment, as shown in FIGS. 2, 3, and 5, the locking mechanism 10 includes a channel or slit 38 disposed in the proximal ends 20, 26 of one of the first arm 18 and the second arm 24. As shown in FIG. 5, a screw 40 fastened to a nut 41 may be slidingly disposed in the slit 38, thereby selectively forming a friction lock upon a tightening of the nut 41 on the screw. The nut 41 may include a wing nut (not shown), for example, or any other suitable shape that permits for ease in manual tightening or untightening of the nut 41 by the user in operation. In such case the screw 40 may be permanently affixed to an opposite one of the first arm 18 and the second arm 24 and laterally slidably disposed within the slit 38 where the nut 41 is not sufficiently tightened. This arrangement advantageously permits for a selective locking of the device 2 in a particular position in operation.

[0037] In an alternative embodiment, the screw 40 and the slit 38 form a friction lock when the screw 40 is wedged into a narrowed portion of the slit 38 (not shown). It should be appreciated that any other suitable locking mechanism 10 configured to lock the first arm 18 and the second arm 24 in place, thereby preventing rotation about the pivot point 30, may also be employed within the scope of the present disclosure. It should be understood that the locking mechanism 10 in preferred embodiments includes a mechanism (not shown) for rapid release.

[0038] As shown in FIG. 1, the gripping mechanism 12 may be integral with and disposed adjacent the distal end 16 of the main body 6. In a particular embodiment, the gripping mechanism 12 includes a first projection 42 extending vertically upward from the distal end 22 of the first arm 18 and a second projection 44 extending vertically upward from the distal end 28 of the second arm 24. In certain embodiments, each of the first and second projections 42, 44 extends vertically upward from the distal ends 22, 28 at an approximately 90-degree angle, respectively. One of ordinary skill in the art may determine that the first and second projections 42, 44 should extend vertically upward from the distal ends 22, 28 at other various angles, as desired, and in certain embodiments each of the first and second projections 42, 44 may further be adjustable with respect to the distal ends 22, 28.

[0039] A first connector 46 extends outwardly from the first projection 42 and a second connector 48 extends outwardly from the second projection 44. In certain embodiments, the first and second connectors 46, 48 extend outwardly on a plane that is parallel to a plane on which the first and second arms 18, 24 are located. It should be understood that placement of the first and second projections 42, 44 relative to the first and second arms 18, 24 and placement of the first and second connectors 46, 48 relative to the first and second projections 42, 44 and the first and second arms 18, 24 may vary according to different embodiments and as determined by one of ordinary skill in the art. In certain embodiments, each of the first and second connectors 46, 48 may be adjustable with respect to the first and second projections 42, 44.

[0040] As shown in FIGS. 1 and 8-9, a first C-shaped member 50 is integral with and extends outwardly from the first connector 46. Likewise, a second C-shaped member 51 is integral with and extends outwardly from the second connector 48. In certain embodiments, the first and second C-shaped members 50, 51 may be adjustable with respect to the first and second connectors 46, 48, respectively.

[0041] In preferred embodiments, a first flexible member 52 is permanently bonded to the first C-shaped member 50 and a second flexible member 53 is permanently bonded to the second C-shaped member 51. The first and second flexible members 52, 53 may be permanently bonded to the first and second C-shaped members 50, 51 using biosafe adhesive as a non-limiting example. One of ordinary skill in the art may select suitable biosafe adhesives as desired.

[0042] A textured inner surface 54 of the first flexible member 52 and a textured inner surface of the second flexible member 53 are adapted to maximize the atraumatic contact with the cervix 4.

[0043] In a most particular embodiment, the first and second flexible members 52, 53 are soft, compressible, biosafe gel-filled silicone pads or pillows. It should be understood that any biosafe, soft, compressible material capable of transmitting a pressure exerted by the gripping mechanism 12 onto a maximized area of the cervix 4 without pinching or puncturing the cervix 4 may be used for the first and second flexible members 52, 53.

[0044] The first and second C-shaped members 50, 51 may each have a radius of curvature that is suitable for the typical cervix 4. More specifically, the first and second C-shaped members 50, 51 have a radius of curvature that is suitable for the cervix 4 measuring between one centimeter (1 cm) and ten centimeters (10 cm), and, most specifically, for the cervix 4 measuring between two centimeters (2 cm) and five centimeters (5 cm). Likewise, an opening 56 between the first and second flexible members 52, 53 has a length that is suitable for the typical cervix 4.

[0045] As shown in FIGS. 2 and 4, a flexible member 62 may include a substantially ring-shaped band 68. It should be appreciated that the substantially ring-shaped band 68 is not entirely closed, so as to permit its opening and closing by the device 2 for interaction with the cervix 4. The ring-shaped band 68 may be disposed between the first and second ends 64, 66 that is configured to wrap around the cervix 4 in use. The flexible member 62 has a first end 64 that is one of integral with or permanently bonded to the first connector 58, and a second end 66 that is one of integral with or permanently bonded to the second connector 60.

[0046] In a particular embodiment, as shown in FIGS. 2-7, the substantially ring-shaped band 68 may be separately formed and then permanently bonded to the first and second ends 64, 66. For example, the distal end 22 of the first arm 18 may have a first connector 58 and the distal end 28 of the second arm 24 may have a second connector 60 disposed therein. In certain embodiments, the first and second connectors 58, 60 are slits formed in the distal ends 22, 28 of the first and second arms 18, 24, respectively, in which the first and second ends 64, 66 of the flexible member 62 are disposed. The first and second ends 64, 66 of the flexible member 62 may be permanently bonded within the slits, for example.

[0047] The flexible member 62 including the gel-filled silicone pads or pillows (shown in FIG. 1) or the substantially ring-shaped band (shown in FIG. 2) may further have a textured inner surface 70. The textured inner surface 70 of the flexible member 62 is adapted to maximize contact with the cervix 4. For example, the textured inner surface 70 may be a rubberized surface formed from a medical grade polymer such as silicone. The textured inner surface 70 may include grooves formed into the pillows or the band 68, or in other examples may include nodules or bumps formed into the pillows or the band 68.

[0048] It should be appreciated that the flexible member 62 has a suitable length adapted to circumscribe the cervix 4 and a suitable width adapted to grip the cervix 4 without slipping. In a most particular embodiment, the flexible member 62 is made from biosafe silicone or any other soft, biosafe material capable of grasping the cervix 4 atraumatically.

[0049] With reference to FIG. 10, a method 100 of using the medical device 2 according to various embodiments of the invention is described herein. In first step 102, the user selects the medical device 2. In a second step 104, the user grips the finger grips 34 of the handle portion 8 and inserts the medical device 2 into the patient. The user then manipulates the handle portion 8 at the proximal end 14 of the main body 6 in a third step 106 to move the distal ends 22, 28 of the first and second arms 18, 24 and create the opening 56 having a sufficient width to allow the gripping mechanism 12 to circumscribe the cervix 4. Next, according to one embodiment of the invention, the user positions in a fourth step 108 the flexible members 52, 53 adjacent the cervix 4 and manipulates in a fifth step 110 the handle portion 8 to atraumatically secure the flexible members 52, 53 to the cervix 4. Using an alternative embodiment, the user positions in an alternative fourth step 108 the flexible member 62 adjacent the cervix 4 and manipulates in the fifth step 110 the handle portion 8 to atraumatically circumscribe and secure the flexible member 62 to the cervix 4. Next, the user engages the locking mechanism in a sixth step 112 and performs a medical procedure in a seventh step 114. Upon completion, the user disengages the locking mechanism in an eight step 116 and manipulates the handle portion 8 at the proximal end 14 of the medical device 2 in a ninth step 118 to release the cervix 4 from the gripping mechanism 12 in a tenth step 120. Finally, the user removes the medical device 2 from the patient in an eleventh step 122 of the method 100.

[0050] It should be appreciated that the medical device 2 facilitates insertion of a surgical device 72, shown in FIGS. 6 and 8, such as an intrauterine device, an endometrial biopsy device, a hysteroscope, or a suction or sharp curette as non-limiting examples. The medical device 2 is capable of fitting through a speculum and can stabilize the cervix 4, for example, as shown in FIGS. 7 and 9, without closing the cervical os.

[0051] It should also be appreciated that the medical device 2, in preferred embodiments, has no separable parts and no sharp projections or angles that may cause harm to the cervix 4 or a surrounding area. The medical device 2 may be disposable or reusable and is sterilizable and inexpensive to manufacture.

[0052] Advantageously, the medical device 2 easily and atraumatically attaches to the cervix 4 and provides traction without causing damage and bleeding. The medical device 2 can easily be released from the cervix 4 and removed and reapplied by the user without injuring the cervix and without interfering with trans-cervical procedures. The medical device 2 is substantially flat and the flexible members 52, 53, 62 are positioned in such a manner so as not to interfere with visualizing the cervix 4.

[0053] While certain representative embodiments and details have been shown for purposes of illustrating the invention, it will be apparent to those skilled in the art that various changes may be made without departing from the scope of the disclosure, which is further described in the following appended claims.