Somatostatin analogues as a treatment option for cystoid maculopathy in retinitis pigmentosa

Author:

Heutinck Pam A T,van den Born L Ingeborgh,van Laar Jan A M,van Hagen P Martin,Smailhodzic Dzenita,Meester-Smoor Magda A,Klaver Caroline C W,Verhoeven Virginie J M,Thiadens Alberta A H JORCID

Abstract

AimsThis study aimed to evaluate the effectiveness of somatostatin analogues (SA) for cystoid maculopathy (CM) in retinitis pigmentosa (RP) patients.Materials and methodsIn this retrospective case series, clinical and imaging characteristics of 28 RP patients with CM, unresponsive to carbonic anhydrase inhibitors, were collected from medical charts. All patients received SA treatment as an alternative (octreotide long-acting release at 20 mg/month or 30 mg/month, or lanreotide at 90 mg/month or 120 mg/month). Outcome measures were mean reduction in foveal thickness (FT) and foveal volume (FV) and mean increase in best-corrected visual acuity at 3, 6 and 12 months of treatment initiation. Linear mixed models were used to calculate the effectiveness over time.Results52 eyes of 28 RP patients were included; 39% were male. The median age at the start of treatment was 39 years (IQR 30–53). Median follow-up was 12 months (range 6–12). From baseline to 12 months, the mean FT decreased from 409±136 µm to 334±119 µm and the mean FV decreased from 0.31±0.10 mm3to 0.25±0.04 mm3. Linear mixed model analyses showed a significant decrease in log FT and log FV at 3, 6 and 12 months after the start of treatment compared with baseline measurements (p<0.001, p<0.001, p<0.001). Mean best-corrected visual acuity did not increase significantly (0.46±0.35 logMAR to 0.45±0.38 logMAR after 12 months).DiscussionSA may be an effective alternative treatment to reduce CM in RP patients.

Funder

Stichting Steunfonds Uitzicht

Algemene Nederlandse Vereniging ter voorkoming van Blindheid

Landelijke Stichting voor Blinden en Slechtzienden

Erasmus MC fellowship to V.J.M. Verhoeven

Prof. dr. Henkes stichting

Publisher

BMJ

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