METHOD OF SUTURELESS INTRASCLERAL HAPTIC-HOOK LENS IMPLANTATION

Abstract

A method of sutureless intrascleral haptic-hook lens implantation which improves the fixation process of the lens haptics, allowing the lens haptics to be bent and folded back into the vitreous cavity to generate a better stability, avoiding the complication of intrascleral fixation haptic slippage, meanwhile forming a sclera lamellar groove between two adjacent scleral incisions to bury the lens haptics. The method may be adapted to patients in need of intraocular lens implantation without sufficient capsular support, such as aphakia, intraocular lens, lens dislocation, etc. This method enhances the stability and centrality of the lens, the surgical procedures are simple and easy to master, which reduces the operation time.

Claims

1. A method of sutureless intrascleral haptic-hook lens implantation in an eye, comprising the following steps: (1) placing a lateral corneal incision a perfusion tube at the anterior chamber, cutting two opposing conjunctival incisions of 3.0 mm, symmetrical at 180, on the conjunctiva outside a margin of the cornea; (2) making two puncture openings at 1.5-2.0 mm outside the margin of the cornea, forming two puncture channels, the spacing distance between the two puncture openings being 1 mm, the puncture openings being parallel to the margin of the cornea, puncture directions of the two puncture openings being opposite, and cutting a lamellar sclera incision between the two puncture openings, thereby forming a groove; (3) repeating step (2) at the 180 symmetrical sides of the opposing corneas at the two puncture openings of step (2), forming two puncture openings at the other side and the groove between them, the puncture openings at the two places and the grooves between them being symmetrically at 180; (4) making a main corneal incision of 3.0 mm over the cornea, through which pushing the intraocular lens through the main corneal incision and into the anterior chamber, leaving one haptic outside the main corneal incision, introducing a membrane forceps into the eye from the puncture opening on one side, grasping one haptic of the intraocular lens and pulling said haptic out of the eye through one puncture opening, grasping the other haptic of the intraocular lens from the puncture opening on the other side and pulling out of the eye through the puncture opening on this side; (5) bending the haptic fixed outside the eye and then folding the bent haptic back into the vitreous cavity through the adjacent puncture opening, just leaving the haptic of the intraocular lens exposed outside the sclera embedded in the groove formed by the lamellar sclera incision between two adjacent puncture openings, adjusting the haptic to cause the intraocular lens to be centered; (6) removing the perfusion tube and closing the conjunctival incisions to complete the implantation and fixation of the intraocular lens.

2. The method of sutureless intrascleral haptic-hook lens implantation according to claim 1, wherein the two pairs of puncture openings set symmetrically opposing at 180 are set at the positions of 4 o'clock and 10 o'clock on the clock dial, respectively.

3. The method of sutureless intrascleral haptic-hook lens implantation according to claim 1, wherein the conjunctival incisions set symmetrically opposing at 180 are set at the positions of 4 o'clock and 10 o'clock on the clock dial, respectively.

4. The method of sutureless intrascleral haptic-hook lens implantation according to claim 1, wherein the intraocular lens is a 3-pieces posterior chamber intraocular lens, the haptic of which employed polyvinylidene fluoride (PVDF) provides support, and the haptic is in a C shape, forming an angle of 5 with the lens body.

5. The method of sutureless intrascleral haptic-hook lens implantation according to claim 1, wherein the closed conjunctival incisions in step (6) is closed by electrocoagulation or sewing.

6. The method of sutureless intrascleral haptic-hook lens implantation according to claim 1, wherein the puncture openings in step (2) form an angle of 30 with the surface of the sclera, the puncture channels being profiled in a splayed pattern.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0018] FIG. 1 is the graphical representation of surgical procedures of the present invention.

[0019] FIG. 2 is the graphical representation of surgical procedures of the present invention.

[0020] FIG. 3 is the graphical representation of surgical procedures of the present invention.

[0021] FIG. 4 is the graphical representation of surgical procedures of the present invention.

[0022] FIG. 5 is the graphical representation of surgical procedures of the present invention.

[0023] FIG. 6 is the graphical representation of surgical procedures of the present invention.

[0024] Wherein, 1lateral corneal incision, 2puncture opening, 3groove, 4main corneal incision, 5haptic, 100perfusion tube, 101cornea, 102conjuctiva, 103conjunctival incision, 201puncture channel, 202lamellar sclera incision, 401anterior chamber, 402membrane forcep, 403intraocular lens, 501vitreous cavity.

[0025] FIG. 7 is the anterior segment photographs 6 months after the surgery of the present invention; wherein FIG. 7A is the image of the slit lamp microscopy showing the scleral wounds; FIG. 7B is the UBM image showing the centration of the lens; FIG. 7C is the UBM image showing the intraocular lens haptic in the sclera.

DETAILED DESCRIPTION

[0026] The present invention now will be further illustrated in combination with FIG. 1, FIG. 2, FIG. 3, FIG. 4, FIG. 5, FIG. 6, and FIG. 7.

[0027] After anesthetization, for patients not undergoing vitreous surgery, conventional vitrectomy or anterior vitrectomy was conducted in advance, a lateral corneal incision was made at the position of 2 o'clock and a perfusion tube 100 was placed at the anterior chamber 401, two conjunctival incisions 103 of 3.0 mm were cut on the conjunctiva 102 outside the margin of cornea 101, at the positions of 4 o'clock and 10 o'clock respectively; two puncture openings 2 were made at the position of 4 o'clock, in a distance of 1.5-2.0 mm outside the margin of cornea 101 with a 26G pinhead, forming two puncture channels 201, the spacing distance between the two puncture openings 2 was 1 mm, the puncture openings 2 were parallel to the margin of cornea 101 and formed an angle of 30 with the surface of the sclera, the puncture directions of the two puncture openings 2 were opposite, making the puncture channels 201 profiled in a splayed pattern, and a lamellar sclera incision 202 was cut in the distance of 1 mm between the two puncture openings 2, forming a groove 3; and then the same processes were conducted at the symmetrical position of 10 o'clock, as shown in FIG. 1.

[0028] A main corneal incision 4 of 3.0 mm was made over the cornea 101, through which the intraocular lens 403 was pushed into the anterior chamber 401, leaving one haptic 5 outside the main corneal incision 4, a 25G membrane forceps 402 went into the eye from the puncture opening 2 on one side, grasping one haptic 5 of the intraocular lens 403 and pulling it out of the eye through one puncture opening 2, similarly the other haptic 5 of the intraocular lens 403 was grasped from the puncture opening 2 on the other side at the position of 10 o'clock and pulled out of the eye through the puncture opening 2 on this side; as shown in FIG. 2.

[0029] The haptic 5 fixed outside the eye was bent and then folded back into the vitreous cavity 501 through the adjacent puncture opening 2, just leaving the haptic 5 of the intraocular lens 403 exposed outside the sclera embedded in the groove 3 formed by the lamellar sclera incision 202 between two adjacent puncture openings 2; as shown in FIG. 3.

[0030] The lens haptic 5 looks like a fishhook as shown in figures, with the tip in the vitreous cavity 501; as shown in FIG. 4.

[0031] The main corneal incision 4 was watertight, the conjunctival incisions 103 were sewed with absorbable suture to complete the implantation and fixation of the intraocular lens 403, as shown in FIG. 5.

[0032] The fact that the haptic 5 of the intraocular lens 403 could be bent smoothly and folded back into the vitreous cavity 501 was related to the use of Matrix AcrylicAurium 400 intraocular lens 403 in the operation, wherein the haptic 5 employed polyvinylidene fluoride (PVDF), which was in a revised C shape, and formed an angle of 5 with the lens body. Finally, the main corneal incision 4 was watertight, the conjunctival incisions 103 were sewed with 8-0 absorbable suture.

[0033] Our improved technique was conducted in 15 patients. This technique, in combination with vitrectomy, has removed the vitreous bodies of all patients partially or completely. The average preoperative BCVA is 0.82 logMAR units, and is 0.44 logMAR units in the follow-up visit after 6 months (Table 1). The follow-up visit after the patients come back shows good lens center and stable tactile fixation (FIG. 6). In the follow-up inspection after 6 months, there were no complications such as postoperative inflammation, hyphema, decentration, glaucoma, corneal edema, or wound leakage, etc. observed (Table 2). No eyes need the subsequent surgery.

TABLE-US-00001 TABLE 1 Baseline characteristics and postoperative data of the patients Characteristics Data Number of eyes (Number of patients) 17 (15) Age, years 56.4 13.5 Male/female, n 7/8 Preoperative visual acuity 0.82 0.89 Postoperative visual acuity at 0.44 0.45 6 months.sup.a Preoperative intraocular 18.0 3.0 pressure, mmHg Postoperative intraocular 14.8 7.2 pressure at 1 week, mmHg.sup.a Postoperative intraocular 17.1 2.9 pressure at 6 months, mmHg.sup.a All values stands mean standard deviation BCVA = best corrected visual acuity; IOP = intraocular pressure. .sup.a compared by Fisher exact test; others compared by two-paired test.

TABLE-US-00002 TABLE 2 Clinical features and postoperative surgical outcome of each eyes Associated ocular Type of Preoperative Postoperative Gender/ Operated conditions from dislocation at logMAR logMAR BCVA Postoperative Cases Age Eye previous surgery presentation BCVA at 6 months complications 1 M/53 Right PCR and sulcus-fixated Out-of-the-bag 0.22 0.50 None IOL 2 M/46 Right PCR and sulcus-fixated In-the-bag 1.30 1.30 None IOL 3 M/24 Left PCR and sulcus-fixated Out-of-the-bag 0.22 0.22 None IOL 4 M/48 Right PCR and sulcus-fixated Out-of-the-bag 0.05 0 None IOL 5 M/48 Left Marchesani Syndrome, In-the-bag 0.10 0 None subluxated crystalline lens 6 M/75 Left Trauma, aphakic Absence of 2.60 1.30 None capsular bag 7 M/58 Left Trauma, aphakic Absence of 0.10 0.22 None capsular bag 8 F/53 Left Trauma, luxated Out-of-the-bag 0.40 0.52 None crystalline lens 9 F/59 Right PCR and sulcus-fixated Out-of-the-bag 2.30 0.40 None IOL 10 F/59 Left PCR and sulcus-fixated Out-of-the-bag 2.60 0.22 None IOL 11 F/69 Right PCR and sulcus-fixated Out-of-the-bag 0.70 0.70 None IOL 12 M/72 Left Subluxated crystalline In-the-bag 1.00 0.10 None lens 13 F/35 Right Subluxated crystalline In-the-bag 0.40 0.40 None lens 14 F/60 Right Luxated crystalline In-the-bag 0.10 0.15 None lens 15 F/68 Right Subluxated crystalline In-the-bag 1.00 0.52 None lens 16 F/60 Left Subluxated crystalline In-the-bag 0.00 0.00 None lens 17 F/71 Right Luxated crystalline In-the-bag 0.80 1.30 None lens BCVA = best corrected visual acuity; PCR = posterior capsule rupture.

[0034] The method of sutureless intrascleral haptic-hook lens implantation proposed in the present invention may be adapted to patients in need of intraocular lens 403 implantation while without sufficient capsular support, such as aphakia, intraocular lens 403 or lens dislocation, etc. This method enhances the stability and centrality of the lens, the surgical procedures are simple and easy to master, which reduces the operation time. In the cases implemented currently, we have not found the complications such as incision leakage, retinal detachment, endophthalmitis, tilt or dislocation of the intraocular lens 403, vitreous hemorrhage, and the like, and the postoperative visual acuities of patients have been significantly improved.

[0035] It should be understood to persons skilled in the relevant art that the present invention has been described following the above detailed description, while the inventive ideas of the present invention were not restricted to the present invention, and any variations employing the ideas of the present invention should be included in the protection scope of the claims.

[0036] The above descriptions were only the preferred embodiments of the present invention, the protection scope of which should not be limited by the above embodiments, and all technical schemes within the spirit of the present invention all belong to the protection scope of the present invention. It should be noted to persons of ordinary skills in the art that several improvements and modifications without departing from the principle of the present invention also should be deemed as the protection scope of the present invention.