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Dried Human Amniotic Membrane Does Not Alleviate Inflammation and Fibrosis in Experimental Strabismus Surgery

DOI: 10.1155/2013/369126

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Abstract:

Purpose. The purpose of this study was to evaluate the efficacy of dried human amniotic membrane (AM) in reducing the postoperative inflammatory response and scarring after strabismus surgery. Methods. The inflammatory response at the extraocular muscle reattachment site was analyzed after superior rectus (SR) resection in 12 rabbits. Dried human AM (Ambiodry2) was applied between the resected SR muscle plane and Tenon’s capsule of the left eyes of rabbits. As a control, the right eyes of rabbits underwent SR resection only. The surgeon randomly ordered which eye gets operated first during the experiment. Two weeks later, enucleation was performed. Six sagittal sections were made for each eye at the insertion of the SR muscle. The grade of postoperative inflammation and the presence of fibrosis were evaluated in histological examinations. Results. There was no statistically significant difference in the intensity of inflammation and fibrous proliferation between the eyes treated with dried human AM after SR resection and those treated with SR resection only. Conclusions. The use of dried human AM was not effective in controlling the postoperative inflammation and scarring in rabbit eyes after extraocular muscle surgery. However, this may be due to the devitalized dry preparation of human AM (Ambiodry2), which may have lost the expected anti-inflammatory and anti-scarring properties, and further studies on humans may be necessary. 1. Introduction Postoperative adhesion is one of the major complications of strabismus surgery that can cause motility problems that affect the surgical outcomes [1, 2]. Due to the fact that the suppression of inflammation is a key element in the prevention of further fibrovascular proliferation and scar formation in the conjunctiva [3], various approaches have been used to reduce postoperative inflammation and scarring following strabismus surgery. Among these are mechanical barrier devices that isolate the muscle from the sclera and the Tenon’s capsule, steroids, antiproliferative agents and viscoelastic substances [1–9]. However, none of these techniques has been widely accepted because of associated complications and inconsistent results. The use of the amniotic membrane (AM) in other applications of ophthalmology such as ocular surface reconstruction, filtration surgery, and the treatment of pterygium has increased [3, 10–12]. The AM can promote epithelialization of the cornea and the conjunctiva and reduce inflammation, scarring, and neovascularization in anterior segment surgeries [13, 14]. AM exhibits several

References

[1]  J. S. Mora, D. T. Sprunger, E. M. Helveston, and A. P. Evan, “Intraoperative sponge 5-fluorouracil to reduce postoperative scarring in strabismus surgery,” Journal of AAPOS, vol. 1, no. 2, pp. 92–97, 1997.
[2]  S. B. ?zkan, E. Kir, N. Culhaci, and V. Dayanir, “The effect of seprafilm on adhesions in strabismus surgery—an experimental,” Journal of AAPOS, vol. 8, no. 1, pp. 46–49, 2004.
[3]  A. Solomon, E. M. Espana, and S. C. G. Tseng, “Amniotic membrane transplantation for reconstruction of the conjunctival fornices,” Ophthalmology, vol. 110, no. 1, pp. 93–100, 2003.
[4]  N. Sondhi, F. D. Ellis, L. M. Hamed, and E. M. Helveston, “Evaluation of an absorbable muscle sleeve to limit postoperative adhesions in strabismus surgery,” Ophthalmic Surgery, vol. 18, no. 6, pp. 441–443, 1987.
[5]  F. J. Elsas, D. C. Gowda, and D. W. Urry, “Synthetic polypeptide sleeve for strabismus surgery,” Journal of Pediatric Ophthalmology and Strabismus, vol. 29, no. 5, pp. 284–286, 1992.
[6]  V. Fulga, R. Koren, N. Ezov, R. Gal, A. Nimrod, and H. Savir, “Sodium hyaluronate as a tool in strabismus surgery in rabbits,” Ophthalmic Surgery and Lasers, vol. 27, no. 3, pp. 228–233, 1996.
[7]  L. E. M. R. de Carvalho, M. R. Alves, M. A. L. G. da Silva, and M. F. G. Vadas, “Experimental strabismus surgery using triamcinolone: outcomes and effects on inflammatory response,” Arquivos Brasileiros de Oftalmologia, vol. 70, no. 2, pp. 209–215, 2007.
[8]  O. A. Cruz, “Evaluation of mitomycin to limit postoperative adhesions in strabismus surgery,” Journal of Pediatric Ophthalmology and Strabismus, vol. 33, no. 2, pp. 89–92, 1996.
[9]  A. E?me, C. Yildirim, S. Tatlipinar, E. Düzcan, V. Yaylali, and S. ?zden, “Effects of intraoperative sponge mitomycin C and 5-fluorouracil on scar formation following strabismus surgery in rabbits,” Strabismus, vol. 12, no. 3, pp. 141–148, 2004.
[10]  A. Solomon, R. T. F. Pires, and S. C. G. Tseng, “Amniotic membrane transplantation after extensive removal of primary and recurrent pterygia,” Ophthalmology, vol. 108, no. 3, pp. 449–460, 2001.
[11]  H. Fujishima, J. Shimazaki, N. Shinozaki, and K. Tsubota, “Trabeculectomy with the use of amniotic membrane for uncontrollable glaucoma,” Ophthalmic Surgery and Lasers, vol. 29, no. 5, pp. 428–431, 1998.
[12]  D. H.-K. Ma, L.-C. See, S.-B. Liau, and R. J.-F. Tsai, “Amniotic membrane graft for primary pterygium: comparison with conjunctival autograft and topical mitomycin C treatment,” British Journal of Ophthalmology, vol. 84, no. 9, pp. 973–978, 2000.
[13]  S. C. G. Tseng, P. Prabhasawat, and S.-H. Lee, “Amniotic membrane transplantation for conjunctival surface reconstruction,” American Journal of Ophthalmology, vol. 124, no. 6, pp. 765–774, 1997.
[14]  H. Sheha, V. Casas, and Y. Hayashida, “The use of amniotic membrane in reducing adhesions after strabismus surgery,” Journal of AAPOS, vol. 13, no. 1, pp. 99–101, 2009.
[15]  S. C. Tseng, D. Q. Li, and X. Ma, “Suppression of transforming growth factor-beta isoforms, TGF-β receptor type II, and myofibroblast differentiation in cultured human corneal and limbal fibroblasts by amniotic membrane matrix,” Journal of Cellular Physiology, vol. 179, pp. 325–335, 1999.
[16]  G. R. Kandavel and R. S. Chuck, “Staining properties of deepithelialized human amniotic membrane,” Cornea, vol. 24, no. 7, pp. 853–856, 2005.
[17]  C. Y. Park, S. Kohanim, L. Zhu, P. L. Gehlbach, and R. S. Chuck, “Immunosuppressive property of dried human amniotic membrane,” Ophthalmic Research, vol. 41, no. 2, pp. 112–113, 2009.
[18]  N. Minguini, K. M. Monteiro de Carvalho, P. M. S. Akaishi, and I. M. S. De Luca, “Histologic effect of mitomycin C on strabismus surgery in the rabbit,” Investigative Ophthalmology and Visual Science, vol. 41, no. 11, pp. 3399–3401, 2000.
[19]  R. Von Hertwig, M. P. Rigueiro, P. D. Rodrigues, F. A. N. Torres, and M. Nishi, “Immunosuppresive effect of intramuscular cyclosporine used at differenet post-operative period on a penetrating keratoplasty model in the rat,” Arquivos Brasileiros De Oftalmologia, vol. 62, no. 6, pp. 717–725, 1999.
[20]  K. Tsubota, Y. Satake, M. Ohyama et al., “Surgical reconstruction of the ocular surface in advanced ocular cicatricial pemphigoid and Stevens-Johnson syndrome,” American Journal of Ophthalmology, vol. 122, no. 1, pp. 38–52, 1996.
[21]  A. Solomon, M. Rosenblatt, D. Monroy, Z. Ji, S. C. Pflugfelder, and S. C. G. Tseng, “Suppression of interleukin 1 α and interleukin 1 β in human limbal epithelial cells cultured on the amniotic membrane stromal matrix,” British Journal of Ophthalmology, vol. 85, no. 4, pp. 444–449, 2001.
[22]  M. X. Wang, T. B. Gray, W. C. Park et al., “Reduction in corneal haze and apoptosis by amniotic membrane matrix in excimer laser photoablation in rabbits,” Journal of Cataract and Refractive Surgery, vol. 27, no. 2, pp. 310–319, 2001.
[23]  W. C. Park and S. C. G. Tseng, “Modulation of acute inflammation and keratocyte death by suturing, blood, and amniotic membrane in PRK,” Investigative Ophthalmology and Visual Science, vol. 41, no. 10, pp. 2906–2914, 2000.
[24]  G. T. Williams and W. J. Williams, “Granulomatous inflammation: a review,” Journal of Clinical Pathology, vol. 36, no. 7, pp. 723–733, 1983.
[25]  J. P. Kersey and A. J. Vivian, “Mitomycin and amniotic membrane: a new method of reducing adhesions and fibrosis in strabismus surgery,” Strabismus, vol. 16, no. 3, pp. 116–118, 2008.
[26]  K. Barton, D. L. Budenz, P. T. Khaw, and S. C. G. Tseng, “Glaucoma filtration surgery using amniotic membrane transplantation,” Investigative Ophthalmology and Visual Science, vol. 42, no. 8, pp. 1762–1768, 2001.
[27]  H. Thomasen, M. Pauklin, K.-P. Steuhl, and D. Meller, “Comparison of cryopreserved and air-dried human amniotic membrane for ophthalmologic applications,” Graefe's Archive for Clinical and Experimental Ophthalmology, vol. 247, no. 12, pp. 1691–1700, 2009.
[28]  R. M. Ingram, “Tissue repair after the operations of recession and resection,” The British Journal of Ophthalmology, vol. 49, pp. 18–28, 1965.

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