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Published Online First: 29 May 2008. doi:10.1136/bjo.2007.130567
British Journal of Ophthalmology 2008;92:1211-1217
Copyright © 2008 by the BMJ Publishing Group Ltd.

ORIGINAL ARTICLES

Visual rehabilitation in end-stage inflammatory ocular surface disease with the osteo-odonto-keratoprosthesis: results from the UK

C Liu1,2, S Okera1, R Tandon3, J Herold4, C Hull5 and S Thorp6

1 The Sussex Eye Hospital, Eastern Road, Brighton, UK
2 Tongdean Eye Clinic, 4 Tongdean Road, Hove, UK
3 Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences (AIIMS), New Delhi, India
4 Department of Maxillo-Facial Surgery, Royal Sussex County Hospital, Brighton, UK
5 Henry Wellcome Laboratory for Visual Sciences, Department of Optometry & Visual Science, City University, London, UK
6 Department of Anaesthesia, Royal Sussex County Hospital, Brighton, UK

Correspondence to:
Mr C S C Liu, Sussex Eye Hospital, Brighton BN2 5BF, UK; cscliu{at}aol.com

Aims: To report the long-term results of osteo-odonto-keratoprosthesis (OOKP) surgery in the visual rehabilitation of patients with corneal blindness from end-stage inflammatory ocular surface disease.

Methods: A non-comparative retrospective case series of 36 consecutive patients treated at the National OOKP referral centre in Brighton, UK, between November 1996 and March 2006.

Results: A total of 36 patients, with age ranging from 19 to 87 years (mean 51 (SD 19) years), were included in the analysis. The main preoperative diagnoses were Stevens–Johnson syndrome (n = 16, or 44%), severe thermal or chemical burns (n = 6, or 17%), and mucous membrane pemphigoid (n = 5, or 14%). The remainder of the cases comprised miscellaneous causes of dry eye (n = 9, or 25%), which included one each of graft versus host disease, ectodermal dysplasia, ionising radiation damage, cicatrising conjunctivitis from topical medication, trachoma, congenital trigeminal nerve hypoplasia, linear IgA disease, Sjögren syndrome and nutritional deficiency. Follow-up ranged from 6 months to 9 years (mean 3.9 (SD 2.5) years). Anatomical retention during the entirety of the follow-up period was seen in 72% of patients. The main factor resulting in anatomical failure was resorption of the OOKP lamina, which occurred in seven cases (or 19%). Predicted resorption in three cases resulted in successful planned exchange of the lamina, but two cases underwent emergency removal of the OOKP, and two cases developed endophthalmitis. Human leucocyte antigen-matched allografts suffered a higher rate of laminar resorption. Out of the entire cohort, 30 patients (or 83%) had some improvement in vision, 28 (or 78%) achieved vision of 6/60 or better, and 19 (or 53%) achieved 6/12 or better. The best-achieved vision was retained throughout the follow-up period in 61% of cases. Survival analysis suggested that the probability of retaining vision >6/60 5 years after surgery was 53 (10)%. Vision-threatening complications occurred in nine cases (or 25%) and included endophthalmitis, retinal detachment and glaucoma. De novo glaucoma occurred in six patients (or 24%) but was seen overall in 17 patients (or 47%), 10 of whom required surgical treatment.

Conclusion: OOKP surgery can restore useful and lasting vision in patients suffering from end-stage ocular surface disease, for whom conventional corneal surgery is not possible. The main problems seen in this study were laminar resorption, particularly in allografts, and glaucoma.

SO and RT contributed equally.

Competing interests: None.

Patient consent: Obtained.


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