AI Article Synopsis
- The study aimed to assess changes in scleral thickness in patients with Vogt-Koyanagi-Harada (VKH) disease during treatment.
- It involved 34 eyes from 17 patients, measuring scleral thickness at various time points before and after starting corticosteroid treatment.
- Results showed that scleral thickness decreased significantly in eyes with ciliochoroidal effusion within a week of treatment, indicating inflammation impacts both the choroid and sclera in VKH disease.
Article Abstract
Purpose: To evaluate changes in scleral thickness in Vogt-Koyanagi-Harada (VKH) disease.
Methods: This study included 34 eyes of 17 treatment-naïve patients with acute-phase VKH disease. Scleral thickness and the presence of ciliochoroidal effusion were examined using anterior segment optical coherence tomography at baseline and 1 week, 2 weeks, and 12 weeks after the start of corticosteroid treatment. Scleral thickness was measured 6 mm posterior to the scleral spur in four directions.
Results: Twenty-eight eyes (82.4%) initially had ciliochoroidal effusion, but this rapidly decreased to nine eyes (26.5%) after 1 week. The sclera with ciliochoroidal effusion became thinner from baseline to 1 week at the superior (400.2 ± 46.9-353.5 ± 47.9 µm), temporal (428.4 ± 53.6-387.8 ± 56.1 µm), inferior (451.5 ± 71.0-400.5 ± 50.5 µm), and nasal (452.4 ± 78.0-407.6 ± 62.9 µm) points (P < 0.01 for all), and no further changes were observed. The sclera without ciliochoroidal effusion remained unchanged.
Conclusion: In VKH disease, eyes with ciliochoroidal effusion exhibited the maximum scleral thickness during the acute phase. This thickening responded rapidly to treatment and became thinner within 1 week. Inflammation in VKH disease may affect not only the choroid but also the sclera.
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| http://dx.doi.org/10.1097/IAE.0000000000004129 | DOI Listing |
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