Keratoplasty á Chaud, Limbal Autotransplantation and Transplantation of Amniotic Membrane in the Management of Severe Chemical Burns of the Eye

Trbolová, A. , I . Kozák, L. Kolodzieyski , T. Juhás, V. Ledeck ̆: Keratoplasty á Chaud, Limbal Autotransplantation and Transplantation of Amniotic Membrane in the Management of Severe Chemical Burns of the Eye. Acta Vet. Brno 2003, 72: 571-576. The purpose of this study was to assess the efficacy and safety of the management of severe chemical eye injuries using early keratoplasty combined with limbal autotransplantation and amniotic membrane transplantation. Ten New Zealand white male rabbits were used in the experiment. All procedures followed the rules of ARVO Statement for the Use of animals in Ophthalmic Research. Under general anaesthesia, injury was induced using a solution of 1.5 N NaOH. Surgery was done within 3 days of injury. Clinical examination was performed at 2 weeks, 4 weeks, 3 months, and 6 months post-operatively. This included evaluation for corneal oedema, opacification, vascularization, erosion, limbal ischaemia, tear film stability and postoperative uveitis. Histopathologic studies were also performed. Early post-operative oedema and uveitis cleared at 4 weeks after treatment. The grafts were transparent during the two months period of cyclosporin treatment after which opacification and vascularization occurred. Tear film was stable at the end of follow-up and no erosions were noted. Histologic sections of the corneal grafts showed rejection reaction and some areas of limbal autografts showed slight tissue oedema with lymphocytes and lymphoblast-like cells. Early keratoplasty with limbal autotransplantation and amniotic membrane transplantation promotes healing of damaged ocular surface after severe alkali burn. Clarity of corneal allografts is maintained during immunosuppressive therapy after which it is lost and graft reaction occurs. A controlled study to compare early versus late keratoplasty combined with limbal autotransplantation is needed to assess the proper timing of treatment. Chemical eye injury, limbal autotransplantation, early keratoplasty, amniotic membrane, ocular surface healing Chemical injuries of the eye may produce extensive damage to the ocular surface. Such injuries result in immediate damage to corneal and conjunctival epithelium, corneal stroma and limbus. The latter is a carrier of corneal stem cells and is indispensable for the maintenance of a healthy corneal epithelial surface. These limbal stem cells act as a proliferative source for the regeneration of the corneal epithelial cells (Schermer et al. 1986). Severe chemical burns may cause persistent epithelial defects, vascularization, scarring and keratinization (Kenyon and Tseng 1989). Thus, one important strategy of managing ocular burns in the acute stage is to promote epithelization, reduce inflammation, and prevent progressive tissue melting (Wagoner 1997). Limbal stem cells transplantation, preferably from the contralateral eye, is a currently available technique to re-estabilish a normal phenotype of corneal epithelium after severe chemical injuries. Amniotic membrane transplantation in the acute stage is an additional procedure used to promote epithelial healing and to reduce inflammation, vascularization and scarring after alkali burns (Meller et al. 2000). Even these two procedures done simultaneously may not prevent late corneal opacification. Such injuries may require ACTA VET. BRNO 2003, 72: 571–576 Address for correspondence: MVDr. Alexandra Trbolová, PhD Department of Surgery and Ophthalmology University of Veterinary Medicine Komenského 73, 04011 Ko‰ice, Slovak Republic Phone: +421 556 339 040 Fax: +421 556 337 832 E-mail: [email protected] http://www.vfu.cz/acta-vet/actavet.htm penetrating keratoplasty a few months after the original injury to restore corneal transparency in tectonically stable eyes. Immediate keratoplasty, combined with limbal autograft transplantation (LAT) and amniotic membrane transplantation, was investigated as a treatment for alkali chemical eye surface injury in rabbits. Using clinical and histopathological parameters, we evaluated the course of healing and the final clinical status of the treated eyes. Early treatment of severe chemical injuries is of paramount importance for the ultimate prognosis. Acute changes caused by chemicals usually have chronic sequelae in spite of currently available aggressive treatment. In this study we observed the therapeutic effectiveness of immediate keratoplasty combined with limbal autotransplantation (LAT) and transplantation of amniotic membrane (AM) in severe experimental alkali injury. Materials and Methods Ten white New Zealand male rabbits weighing 2.5-3.5 kg were used. All rabbits were handled in compliance with the Association for Research and Vision in Ophthalmology (ARVO) Statement for the Use of Animals in Ophthalmic Research. Prior to acceptance for use, all rabbits underwent a baseline ocular examination to rule out pre-existing anterior segment anbormalities. The chemical injuries and all surgical procedures were preceded by general anaesthesia. Premedication was intramuscular atropin 0.05 mg/kg (Atropin Spofa inj. 0.5 mg/ml). General anaesthesia was induced with xylazin hydrochloride (Rometar 2%, a.u.v.) 5 mg/kg and ketamin hydrochloride (Narkamon 5%, a.u.v.) 40 mg/kg. One eye of each rabbit received a drop of tetracaine for local anaesthesia after which 1.5 N NaOH solution was spread over the ocular surface with a cotton tipped applicator and left for 10 seconds. The injured area was then continually washed for 5 minutes by saline solution. Surgery in each rabbit was performed within 3 days after the chemical injury. Amniotic membrane with attached placenta was acquired during Caesarean delivery from clinically healthy cow. Under sterile conditions amniotic membrane/placenta complex was repeatedly washed in saline solution. Subsequent blunt preparation separated the amniotic membrane from chorion and other decidual tissue and amniotic membrane was cut to pieces 5 × 5 cm. The tissue was kept in solution containing 50 μg/ml penicillin, 50 μg/ml streptomycin and 100 μg/ml naomycin. The pieces of amniotic membrane were thus preserved in refrigerator at 2 oC and used the following day for surgery. Corneal grafts were collected from euthanised rabbits of the same breed and sex, aged 1-1.5 years and weighing 3-4 kg. The rabbits had been used previously in an orthopedic experiment. These donor corneas were kept in Optisol solution for 10 days at 4 oC. Limbal grafts of 2.5 3 mm width and from 11-2 o’clock position were acquired from each contralateral uninjured eye. The donor groove was covered by adjacent conjunctiva using non-resorbable suture (Ethilon 10.0 with microfilament polyamide fiber and atraumatic 6 mm “micro-point” needle with 3/8 curvature). The donor corneal button was prepared using 8.5 mm punch and placed in a Petri dish with saline solution. The central corneal portion of the injured eye was trephined using 8.0 mm Barron trephine; the presence of aqueous humour indicated penetration into the anterior chamber. The rest of the button was released by circumferentially cutting the edges by curved scissors. The recipient eye was washed with saline solution and a surgical iris coloboma was produced at 12.00 h. Bleeding from the iris was stopped by microcautery and blood was washed out of the surgical field. Viscoelastic material was applied to recipient’s eye anterior chamber and the donor cornea was placed in the recipient stromal bed. Four cardinal Ethilon 10.0 sutures fixed the donor button and eight additional interrupted sutures were applied to attach the button. Balanced saline solution was used to wash the anterior chamber and test the competency of the suturing. Next amniotic membrane was applied on top of the corneal transplant and the ocular surface using interrupted 8.0 Vicryl sutures. Its peripheral border was 5 mm from the limbus. In the post-operative period the treated eyes received Infectoflam® (gentamycin + fluorometholone, NOVARTIS) eyedrops 5 times a day for 1 month and 2% cyclosporine eyedrops two times a day for 2 months. Each rabbit was examined clinically at 2 weeks, 4 weeks, 3 months, and finally at 6 months after surgery. The extent of oedema, vascularization, blepharospasm, conjunctival hyperemia, limbal ischaemia and signs of uveitis was measured using biomicroscopy. Fluorescein was used to test for erosion and tear film stability. Each parameter was scored as follows: 0-absent, 1-mild, 2-moderate, 3-severe (see tables). Graft assessment was performed by slit lamp examination. Diagnosis of allograft rejection was based on oedema, lack of clarity, inflammation and, neovascularization of the graft. At the end of follow-up period the rabbits were euthanised and the treated eyes were taken for histopathologic examination. Microscopic sections stained with haematoxylin and eosin were studied under different magnification. The specimens were photographed using the Photo Microscop Nikon, Japan with digital camera COOLPIX 950. 572