低剂量环孢素(100mg每日一次)治疗慢性Vogt-Koyanagi-Harada病的效果。

Nippon Ganka Gakkai zasshi Pub Date : 2017-06-01
Mami Haruta, Maiko Yoshioka, Akira Fukutomi, Takamasa Minami, Hisashi Mashimo, Hiroshi Shimojo, Nobuyuki Ohguro
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引用次数: 0

摘要

目的:探讨低剂量环孢素(CyA)治疗慢性Vogt-Koyanagi-Harada (VKH)病患者对全身皮质类固醇治疗抵抗的影响。方法:回顾性评估2013年3月至2016年3月在日本社区卫生保健组织(JCHO)大阪医院诊断为慢性VKH病的患者对全身皮质类固醇治疗的耐受性。我们对这些患者进行了全身低剂量CyA (100mg,每日一次)治疗。将患者分为眼前炎症组和眼后炎症组。回顾了人口统计数据,包括年龄,性别,初次就诊时和CyA治疗后三个月是否存在炎症,以及副作用。结果:本研究纳入13例慢性VKH病患者23只眼(女性11例,男性2例;平均年龄(54.6±11.9岁)。眼前炎症9例,眼后炎症7例(包括重叠病例)。CyA治疗后3个月,眼前炎症组13只眼消退,眼后炎症组10只眼消退。我们不得不停止治疗的一个病人,因为血清甘油三酯严重增加。结论:低剂量CyA治疗对全身皮质类固醇治疗的慢性VKH耐药患者有效。我们的结果表明,这种治疗在眼前炎症组比眼后炎症组更有效;然而,需要更多的患者和更长的观察期来证实这些结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effect of Low-dose Cyclosporine (100 mg Once Daily) for Chronic Vogt-Koyanagi-Harada Disease.

Purpose: To determine the effect of low-dose cyclosporine (CyA) treatment for patients with chronic Vogt-Koyanagi-Harada (VKH) disease resistance to systemic corticosteroid treatment. Methods: We retrospectively evaluated patients diagnosed with chronic VKH disease resistance to systemic corticosteroid treatment at Japan Community Health Care Organization (JCHO) Osaka Hospital between March 2013 and March 2016. We followed the observation with systemic low-dose CyA (100 mg once daily) treatment of these patients. The patients were divided into two groups, anterior ocular inflammation group and posterior ocular inflammation group. Demographic data were reviewed, including age, gender, the existence of inflammation at the initial visit and three months after CyA treatment, and side effect. Results: Twenty-three eyes of thirteen patients with chronic VKH disease were included in this study (11 women, 2 men; mean age, 54.6±11.9 years). Nine cases showed anterior ocular inflammation and seven cases showed posterior ocular inflammation (includes overlapping cases). Thirteen of fourteen eyes in the anterior ocular inflammation group subsided at three months after CyA treatment, and ten of thirteen eyes in the posterior ocular inflammation group subsided at three months after treatment. We had to stop the treatment in one patient because of severe increase of serum triglyceride. Conclusions: Low-dose CyA treatment was effective in patients with chronic VKH resistance to systemic corticosteroid treatment. Our results suggest that this treatment was more effective in the anterior ocular inflammation group than in the posterior ocular inflammation group; however, a larger number of patients and longer observation periods are needed to confirm these results.

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