Surgical device for conjunctival sac stenosis repair
By using a device with shovel needle, suture and anti-adhesion components in conjunctiva stenosis repair, the problem of suture cutting conjunctiva and conjunctiva adhesion is solved, achieving a more stable fixation effect and better repair effect.
Patent Information
- Application Number
- CN202421659553.3
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-07-15
- Publication Date
- 2025-06-03
- Estimated Expiration
- 2034-07-15
AI Technical Summary
In the repair of conjunctiva stenosis, direct fixation of sutures with sutures can easily lead to the conjunctiva being cut and ruptured by sutures, and adhesions may occur between the two layers of conjunctiva, affecting the repair effect.
A surgical device including a spatula, suture and anti-adhesion assembly was designed. The anti-adhesion assembly includes a lower fornix barrier and a skin surface barrier. By placing soft silicone material between the conjunctiva, suture, and skin, it reduces iatrogenic damage and prevents conjunctiva adhesion.
This device effectively prevents the conjunctiva from being cut by sutures, maintains the stability of the fixed structure, predictively improves the repair effect, and avoids adhesions on both sides of the conjunctiva during the repair process.
Smart Images

Figure CN222929915U_ABST
Abstract
Description
Technical Field
[0001] The utility model belongs to the technical field of medical surgery, and particularly relates to a surgical device for conjunctival sac stenosis repair, especially a spacer device for preventing adhesion of the conjunctival sac. Background Art
[0002] The conjunctiva is a thin, semi-transparent mucous membrane that is soft, smooth, and elastic. It covers the back of the eyelids (palpebral conjunctiva, firmly adhered to the tarsal plate and cannot be pushed. Under normal circumstances, small blood vessels can be seen running and some meibomian gland ducts can be seen through), the surface of the anterior part of the sclera of the eyeball (bulbar conjunctiva, covering the surface of the anterior part of the sclera of the eyeball, ending at the corneal limbus, which is the thinnest and most transparent part of the conjunctiva, can be pushed, and there is a loose connection between the bulbar conjunctiva and the sclera by the fascia bulbi. It fuses with the fascia bulbi and the sclera within 3 mm near the corneal limbus), and the reflected part from the eyelid part to the bulbar part (forniceal conjunctiva, the conjunctival tissue is loose and has many folds to facilitate eye movement. The superior fornix has the attachment of the levator palpebrae superioris fibers, and the inferior fornix has the fibers of the inferior rectus muscle sheath incorporated). These three parts of the conjunctiva form a sac-like space with the palpebral fissure as the opening, called the conjunctival sac.
[0003] Conjunctival sac stenosis refers to the situation where after the eyeball is removed due to trauma, inflammation, or other eye diseases, the conjunctival sac shrinks or even contracts, causing the conjunctival sac to become shallower and smaller, resulting in the inability to insert an artificial eye (false eye) of an appropriate size and shape, or the spontaneous prolapse of the artificial eye piece, causing appearance defects and seriously affecting the appearance and self-confidence. In response to this situation, free grafting of the lower lip or (and) buccal mucosa is required to perform conjunctival sac plasty for these patients to deepen the fornix. However, to ensure the long-term and stable deepening effect, the deepened forniceal conjunctiva needs to be temporarily fixed to the periosteum of the lower orbital margin. The specific operation is to insert a double-needle suture from the corresponding conjunctiva in the lower fornix, pass through the periosteum of the lower orbital margin and then exit from the skin surface, and tie it on the skin surface. However, clinically, directly fixing and suturing with sutures often causes the conjunctiva to be cut by the sutures and rupture, weakening the fixation effect. Summary of the Invention
[0004] To solve the above technical problems, it can be considered to solve the problem of being cut by the suture through padding. Currently, there is no ready-made fixing material in clinical practice that can pad between the suture and the conjunctiva and between the suture and the skin. Therefore, the utility model provides a spacer device for preventing adhesion of the conjunctival sac. By padding between the conjunctiva, the suture, and the skin, it is used to reduce iatrogenic injury and avoid adhesion between the two layers of the conjunctiva (the two surfaces of the conjunctival sac) during tissue repair.
[0005] The specific structure is as follows:
[0006] A surgical device for the repair of conjunctival sac stenosis, the device comprising a spatula needle and a suture, the spatula needle being a double-headed suture needle, and the needle tails of the two suture needles being connected by a suture; further comprising an anti-adhesion component, the anti-adhesion component including a lower fornix barrier component and a skin surface barrier;
[0007] The lower fornix barrier is rod-shaped, with a wire hole running through it along the long axis direction, and side holes are provided at both ends; the suture passes through the wire hole and exits through the side hole;
[0008] The skin surface barrier is a gasket provided with two needle exit holes, and the needle exit holes are provided at both ends of the gasket (3) along the thickness direction of the gasket.
[0009] Further, the lower fornix barrier is a rod-shaped body with a diameter of 3 mm and a length of 8 mm.
[0010] Further, the diameter of the wire hole is 1.5 mm.
[0011] Further, there are two side holes, and the two side holes are arranged in a straight line on any side of the lower fornix barrier.
[0012] Further, the distance between the two side holes is 4 mm.
[0013] Further, the gasket is 8 mm long, 4 mm wide, and 2 mm thick.
[0014] Further, the needle exit hole includes a needle inlet and a needle outlet, and is an "eight"-shaped inclined hole with the needle outlet facing inwards.
[0015] Further, the hole distance between the needle inlets of the two needle exit holes is 4 mm.
[0016] Further, the needle exit holes are provided 2 mm from both ends.
[0017] Introduction to the working principle of the present utility model:
[0018] 1) Insert one needle of the non-absorbable thread of the double-headed stainless steel spatula needle 1 (2-0 or 1-0) into the first side hole 421 of the silicone rod, and then pass through and exit from the first side hole 421;
[0019] 2) Insert the two needles into the lower fornix palpebral conjunctiva surface, pass through the suborbital margin periosteum and exit from the skin surface, and place the lower fornix barrier 4 at the bottom of the lower fornix (between the bulbar conjunctiva and the palpebral conjunctiva);
[0020] 3) Then pass the two needles through the needle exit holes 51 of the 8 mm long skin surface barrier 5 to obtain the silicone sheet;
[0021] 4) Tie a knot outside the silicone sheet with the suture 2;
[0022] 5) According to the condition of the conjunctival sac, place 2-3 groups of the above devices to complete the operation.
[0023] Compared with the prior art, the beneficial effects of the present utility model are as follows:
[0024] (1) While the soft silicone protects the conjunctiva and skin by elastic pad application, it is not easily cut by the suture, which can ensure the structural stability during fixation and make the fixation effect more predictable.
[0025] (2) The silicone rod is placed at the bottom of the lower fornix. While maintaining the depth of the fornix, it can also keep the width of the lower fornix, especially avoiding the adhesion of the conjunctiva on both sides of the silicone rod (two surfaces of the conjunctival sac) during the tissue repair process. BRIEF DESCRIPTION OF THE DRAWINGS
[0026] Figure 1 is a schematic structural diagram of the present utility model;
[0027] Figure 2 is a schematic structural diagram of the needle outlet hole of the skin surface barrier member of the present utility model;
[0028] Figure 3 is a sectional view of the use state of the present utility model;
[0029] Figure 4 is a schematic diagram of the use part of the present utility model;
[0030] Figure 5 is a sectional view of the superposed use state of the present utility model;
[0031] In the figures, 1 - spatula needle; 2 - suture; 3 - anti - adhesion component; 4 - lower fornix barrier member; 41 - wire hole; 42 - side hole; 421 - first side hole; 422 - second side hole; 43 - end; 5 - skin surface barrier member; 51 - needle outlet hole; 511 - needle inlet; 512 - needle outlet; 6 - eye; 61 - superior fornix conjunctiva; 62 - bulbar conjunctiva; 63 - palpebral conjunctiva; 64 - inferior fornix conjunctiva. DETAILED DESCRIPTION OF THE EMBODIMENTS
[0032] To make the purpose, technical solutions and advantages of the present utility model clearer, the present utility model will be further described in detail below in conjunction with the specific embodiments and with reference to the accompanying drawings. It should be understood that these descriptions are exemplary and are not intended to limit the scope of the present utility model. In addition, in the following description, the descriptions of well - known structures and technologies are omitted to avoid unnecessarily confusing the concepts of the present utility model.
[0033] Embodiment: A surgical device for conjunctival sac stenosis repair, the device comprising a spatula needle 1, a suture 2, and an anti-adhesion assembly 3. The spatula needle 1 is a double-headed suture needle, and the needle tails of the two-headed suture needles are connected by the suture 2. The anti-adhesion assembly 3 includes a lower fornix barrier assembly and a skin surface barrier 5; the lower fornix barrier 4 is a rod-shaped body made of soft silicone with a diameter of 3 mm and a length of 8 mm. A wire hole 41 is provided in the middle of the rod-shaped body along the long axis direction. The diameter of the wire hole 41 is 1.5 mm and the length is 4 mm. The two ends 43 of the lower fornix barrier assembly are hemispherical end caps, and side holes 42 are also provided near the end heads 43. The side holes 42 include a first side hole 421 and a second side hole 422. The first side hole 421 and the second side hole 422 are respectively located at both ends of the fornix barrier assembly and the distance therebetween is 4 mm. The first side hole 421 is 2 mm away from the left end head 43, and the second side hole 422 is 2 mm away from the right end head 43; the first side hole 421 and the second side hole 422 are perpendicular to the wire hole 41 and communicate with the wire hole 41. The skin surface barrier 5 is a soft silicone sheet with a length of 8 mm, a width of 4 mm, and a thickness of 2 mm and having double-sided inclined holes. The double-sided inclined holes on the silicone sheet are the needle outlet holes 51 of the present invention. The needle outlet holes 51 penetrate through both ends of the gasket along the thickness direction of the gasket, including a needle inlet 511 and a needle outlet 512, which are "eight"-shaped inclined holes with the needle outlet 512 facing inwards. The inward inclined hole design facilitates knotting of the suture 2. The hole spacing of the needle inlets 511 of the two inclined holes is 4 mm and they are respectively 2 mm away from both ends.
[0034] It should be understood that the above specific embodiments of the present invention are only used for exemplary illustration or explanation of the principle of the present invention, and do not constitute a limitation to the present invention. Therefore, any modifications, equivalent replacements, improvements, etc. made without departing from the spirit and scope of the present invention shall be included within the protection scope of the present invention. In addition, the appended claims of the present invention are intended to cover all variations and modifications that fall within the scope and boundary of the appended claims, or equivalent forms of such scope and boundary.
Claims
1. A surgical device for repairing conjunctival sac stenosis, the device comprising a shovel needle (1) and a suture (2), wherein the shovel needle (1) is a double-ended suture needle, and the needle tails of the two ends of the suture needle are connected by the suture (2); characterized in that: It also includes an anti-adhesion component (3), wherein the anti-adhesion component (3) includes a lower fornix barrier (4) and a skin surface barrier (5); The lower fornix barrier (4) is in the shape of a rod, with a thread hole (41) extending through the longitudinal direction thereof, and side holes (42) at both ends thereof; the suture (2) is passed through the thread hole (41) and exits from the side hole (42); The skin surface barrier (5) is a gasket provided with two needle outlet holes (51), and the needle outlet holes (51) are arranged at both ends of the gasket through the gasket thickness direction.
2. A surgical device for repairing conjunctival sac stenosis according to claim 1, characterized in that: The lower fornix barrier (4) is a rod-shaped body with a diameter of 3 mm and a length of 8 mm.
3. A surgical device for repairing conjunctival sac stenosis according to claim 1, characterized in that: The diameter of the wire hole (41) is 1.5 mm.
4. The surgical device for repairing conjunctival sac stenosis according to claim 1, characterized in that: The side holes (42) include two, and the two side holes (42) are arranged in a straight line on any side surface of the lower dome barrier (4).
5. A surgical device for repairing conjunctival sac stenosis according to claim 4, characterized in that: The distance between the two side holes (42) is 4 mm.
6. The surgical device for repairing conjunctival sac stenosis according to claim 1, characterized in that: The gasket is 8 mm long, 4 mm wide and 2 mm thick.
7. The surgical device for repairing conjunctival sac stenosis according to claim 1, characterized in that: The needle outlet hole (51) comprises a needle inlet (511) and a needle outlet (512), and is an "eight" shaped inclined hole with the needle outlet (512) facing inwards.
8. The surgical device for repairing conjunctival sac stenosis according to claim 7, characterized in that: The hole spacing between the needle inlet (511) and the two needle outlet holes (51) is 4 mm.
9. The surgical device for repairing conjunctival sac stenosis according to claim 1, characterized in that: The needle outlet hole (51) is arranged at a distance of 2 mm from both ends.