Abstract
Many clinical conditions exist in which standard penetrating keratoplasties are at high risk of failure. These situations require alternative interventions including keratoprostheses. The most challenging of this subset of patients to treat are those with corneal blindness due to autoimmune diseases. Studies have suggested that these patients respond poorly to transplantation due to alterations in corneal tissue at the level of the cellular, microbiological, and immunological microenvironments due to the inflammatory nature of autoimmune-related conjunctivitides. A variety of interventions exist for visual rehabilitation in this patient population depending on the severity of the condition. These options range from artificial keratoprostheses, such as the Boston keratoprosthesis type 1 in patients with a lubricated ocular surface, to the biologic keratoprostheses like the modified osteo-odonto keratoprosthesis (MOOKP) in the most severe autoimmune patients. The current literature suggests that in the setting of autoimmune dysfunction, biological keratoprostheses are far superior to their artificial keratoprosthesis alternatives.
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References
Ament JD, Todani A, Pineda R, et al. Global corneal blindness and the Boston keratoprosthesis type I. Am J Ophthalmol. 2010;149:537–9.
Harr T, French LE. Toxic epidermal necrolysis and Stevens-Johnson syndrome. Orphanet J Rare Dis. 2010;5:39.
Dietrich A, et al. Low N-acetylating capacity in patients with Stevens-Johnson syndrome and toxic epidermal necrolysis. Exp Dermatol. 1995;4(5):313–6.
Oliveira A, et al. O Espectro Clinico Sindrome De Stevens-Johnson E Necrolise Epidermica Toxica. Acta Med Port. 2011;24:995–1002.
Fernando SL, et al. Prevention of severe cutaneous adverse drug reactions: the emerging value of pharmacogenetic screening. CMAJ. 2010;182(5):476–80.
Yip LW, Thong BY, Lim J, Tan AW, Wong HB, Handa S, Heng WJ. Ocular manifestations and complications of Stevens-Johnson syndrome and toxic epidermal necrolysis: an Asian series. Allergy. 2007;62:527–31.
Zillikens D, et al. Incidence of autoimmune subepidermal blistering dermatoses in a region of central Germany. Arch Dermatol. 1995;131(8):957–8.
Foster CS. Cicatricial pemphigoid. Trans Am Ophthalmol Soc. 1986;84:527–663.
Bruch-Gerharz D, et al. Mucous membrane pemphigoid: clinical aspects, immunopathological features and therapy. Eur J Dermatol. 2007;17(3):191–200.
Chan CC, et al. The modified Cincinnati procedure: combined conjunctival limbal autografts and keratolimbal allografts for severe unilateral ocular surface failure. Cornea. 2012;31:1264–72.
Messmer EM, et al. Ocular cicatricial pemphigoid. Retrospective analysis of risk factors and complications. Ophthalmologe. 2000;97(2):113–20.
Saito T, Nishida K, Sugiyama H, et al. Abnormal keratocytes and stromal inflammation in chronic phase of severe ocular surface diseases with stem cell deficiency. Br J Ophthalmol. 2008;92:404e10.
Dudenhoefer EJ, Nouri M, Gipson IK, et al. Histopathology of explanted collar button keratoprostheses: a clinicopathologic correlation. Cornea. 2003;22:424–8.
Ciralsky J, et al. Keratoprosthesis in autoimmune disease. Ocul Immunol Inflamm. 2010;18(4):275–80.
Miri A, Al-Deiri B, Dua HS. Long-term outcomes of autolimbal and allolimbal transplants. Ophthalmology. 2010;117:1207–13.
Sant’ Anna AE, Hazarbassanov RM, de Freitas D, Gomes JA. Minor salivary glands and labial mucous membrane graft in the treatment of severe symblepharon and dry eye in patients with Stevens-Johnson syndrome. Br J Ophthalmol. 2012;96:234–9.
Biber JM, Skeens HM, Neff KD, et al. The Cincinnati procedure: technique and outcomes of combined living-related conjunctival limbal allografts and keratolimbal allografts in severe ocular surface failure. Cornea. 2011;30:765–71.
Magalhães FP, et al. Boston type I keratoprosthesis. Review. Arq Bras Oftalmol. 2012;75(3):218–22.
Khan BF, Harissi-Dagher M, Khan DM, Dohlman CH. Advances in Boston keratoprosthesis: enhancing retention and prevention of infection. Int Ophthalmol Clin. 2007;47:61–71.
Sejpal K, Yu F, Aldave AJ. The Boston keratoprosthesis in the management of corneal limbal stem cell deficiency. Cornea. 2011;30(11):1187–94.
Pujari S, Siddique SS, Dohlman CH, Chodosh J. The Boston keratoprosthesis type II: The Massachusetts Eye and Ear Infirmary experience. Cornea. 2011;30(12):1298–303.
Yaghouti F, Nouri M, Abad JC, et al. Keratoprosthesis: preoperative prognostic categories. Cornea. 2001;20:19–23.
Sayegh RR, Ang LP, Foster CS, Dohlman CH. The Boston keratoprosthesis in Stevens-Johnson syndrome. Am J Ophthalmol. 2008;145:438–44.
Jiiraskova N, et al. AlphaCor artificial cornea: clinical outcome. Eye (Lond). 2011;25:1138–46.
Huang Y, Dong Y, Wang L, et al. Long-term outcomes of MICOF keratoprosthesis in the end stage of autoimmune dry eyes: an experience in China. Br J Ophthalmol. 2012;96:28–33.
Falcinelli G, Falsini B, Taloni M, Colliardo P, Falcinelli G. Modified osteo-odonto-keratoprosthesis for treatment of corneal blindness: long term anatomical and functional outcomes in 181 cases. Arch Ophthalmol. 2005;123:1319–51329.
Tan A, et al. Osteo-odonto keratoprosthesis: systematic review of surgical outcomes and complication rates. Ocul Surf. 2012;10(1):15–25.
Michael R, Charoenrook V, de la Paz MF, Hitzl W, Temprano J, Barraquer RI. Long-term functional and anatomical results of osteo- and osteodonto-keratoprosthesis. Graefes Arch Clin Exp Ophthalmol. 2008;246(8):1133–7.
Mockenhaupt M. The current understanding of Stevens–Johnson syndrome and toxic epidermal necrolysis. Expert Rev Clin Immunol. 2011;7(6):803–15.
Chan LS. Ocular and oral mucous membrane pemphigoid (cicatricial pemphigoid). Clin Dermatol. 2012;30:34–7.
Dohlman JG, Foster CS, Dohlman CH. Boston keratoprosthesis in Stevens-Johnson syndrome: a case of using infliximab to prevent tissue necrosis. Digit J Ophthalmol. 2009;15:1–5.
Foster CS, Ahmed AR. Intravenous immunoglobulin therapy for ocular cicatricial pemphigoid: a preliminary study. Ophthalmology. 1999;106:2136–43.
Araki Y, Sotozono C, Inatomi T. Successful treatment of Stevens–Johnson syndrome with steroid pulse therapy at disease onset. Am J Ophthalmol. 2009;147(6):1004–11, 1011.e1.
Valeyrie-Allanore L, Wolkenstein P, Brochard L, et al. Open trial of ciclosporin treatment for Stevens–Johnson syndrome and toxic epidermal necrolysis. Br J Dermatol. 2010;163(4):847–53.
Chan LS, Ahmed AR, Anhalt GJ, et al. The first international consensus on mucous membrane pemphigoid: definition, diagnostic criteria, pathogenic factors, medical treatment, and prognostic indicators. Arch Dermatol. 2002;138:370–9.
Traish AS, Chodosh J. Expanding application of the Boston type I keratoprosthesis due to advances in design and improved postoperative therapeutic strategies. Semin Ophthalmol. 2010;25:239–43.
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Weiss, M.J., Perez, V.L. (2015). Keratoprostheses in the Setting of Autoimmune Disorders. In: Cortina, M., de la Cruz, J. (eds) Keratoprostheses and Artificial Corneas. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-55179-6_16
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DOI: https://doi.org/10.1007/978-3-642-55179-6_16
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