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Volume 108, Issue 4, Pages 765-772 (April 2001)


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Intravitreal triamcinolone for uveitic cystoid macular edema: an optical coherence tomography study

Historical image

Richard J Antcliff (FRCOphth)aCorresponding Author Information, David J Spalton (FRCS, FRCP)b, Miles R Stanford, MDa, Elizabeth M Graham (FRCP, FRCOphth)b, Timothy J ffytche (FRCS, FRCOphth)b, John Marshall, PhDa

Received 28 March 2000; accepted 28 November 2000.

Abstract 

Purpose

To investigate the use of intravitreal injection of triamcinolone acetonide (TA) for the treatment of refractory uveitic cystoid macular edema (CME).

Design

Prospective, nonrandomized, self-controlled comparative trial.

Participants

Six patients with chronic CME resistant to treatment with systemic steroids, orbital floor steroids, and cyclosporine A. Three patients were followed for more than 1 year, and the other three for between 3 and 9 months.

Intervention

Injection of 2 mg of TA into the vitreous cavity.

Testing

Optical coherence tomography scanning of the fovea before and after injection and logarithmic minimal angle of resolution visual acuity.

Main outcome measures

Visual acuity, retinal thickness, cystoid space height, and intraocular pressure.

Results

There was complete anatomic resolution of CME in five of the six cases within 1 week after injection. Cystoid spaces began to return between 6 weeks and 3 months after injection. Two patients with longer term follow-up responded to further orbital floor steroid injection and had no CME 1 year later. One patient had raised intraocular pressure develop, requiring a trabeculectomy. Mean improvement in visual acuity after 12 months was 0.27 (range, 0.14–0.42).

Conclusions

Complete anatomic and, to some extent, functional recovery can be induced by intravitreal TA despite long-term refractory inflammatory CME. Optical coherence tomography aids in the management of these cases.

Manuscript no. 200172.

a GKT Department of Ophthalmology, Rayne Institute, St Thomas’ Hospital, London, England, UK

b Department of Ophthalmology, St Thomas’ Hospital, London, England, UK

Corresponding Author InformationReprint requests to Richard J. Antcliff, FRCOphth, GKT Department of Ophthalmology, Rayne Institute, St Thomas’ Hospital, Lambeth Palace Road, London SE1 7EH. England

 Supported by the Allerton Fund, London, England, and the Iris Fund for the Prevention of Blindness, London, England.

PII: S0161-6420(00)00658-8


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