Abstract
BACKGROUND - The occurrence of antimalarial retinopathy is reducing all over the world, but are few brazilian studies. OBJECTIVES - Analysis of the occurrence of adverse effects, triggered by use of 250mg/d of chloroquine diphosphate in 350 patients with for lupus erythematosus. METHODS - Review of clinical records and analysis between adverse effects and the daily dose per kg, age and the differents types of lupus erythematosus; and the periodicity of ophthalmologic screening. RESULTS - 35,7% of adverse effects, ocular toxicity (17,4%): retinal pigmentation suggestive of antimalarial retinopathy (12%), corneal deposits (3,1%) and acute visual symptoms(2,3%); gastrointestinal (10%), cutaneous (3,4%), headache (2,9%), neuromuscular (1,7%) and psychiatric (0,3%). Antimalarial retinopathy confirmed in 2,6%. No statistically significant association between occurrence of adverse effects and retinotoxicity with the daily dose per kg and the type of lupus erythematosus. Retinotoxicity was statistically significant (p=0,004) in patients over 50 years. Ophthalmologic screening was conducted on average after 10,5 months. CONCLUSIONS - Antimalarial retinopathy occurred in 2,6% of the patients. Ophthalmologic screening had to be more careful in patients over 50 years because the difficulty to differentiate between initial antimalarial retinopathy and senile macular degeneration. ©2005 by Anais Brasileiros de Dermatologia.
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Ponchet, M. R. N. C., Vilela, M. A. C., Suni Sinahara, K. K., & De Freitas Dotto, P. (2005). Evaluation of adverse events triggered by the use of chloroquine diphosphate, emphasis on retina toxicity, in 350 patients with lupus erythematosus. In Anais Brasileiros de Dermatologia (Vol. 80). Sociedade Brasileira de Dermatologia. https://doi.org/10.1590/s0365-05962005001000003
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