玻璃体内皮质类固醇治疗糖尿病黄斑水肿:随机对照试验的网络荟萃分析。

Lu Gao, Xu Zhao, Lei Jiao, Luosheng Tang
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引用次数: 3

摘要

背景:评价不同玻璃体内皮质类固醇治疗糖尿病性黄斑水肿(DME)的疗效和安全性。方法:系统检索四个数据库,比较不同玻璃体内皮质类固醇治疗二甲醚的随机对照试验。主要终点是首次注射后6个月内最佳矫正视力(BCVA)的变化(短期BCVA)。次要结果是1年内BCVA的变化(长期BCVA)和首次注射后6个月内中央黄斑厚度(CMT)和眼压(IOP)的变化。进行网络荟萃分析以汇总来自各个研究的结果。结果:共纳入19项试验,涉及2839只眼。玻璃体内注射曲安奈德(TA)(≥8mg和4- 8mg)、氟西诺酮(FA)植入物(0.5µg/天)和地塞米松(DEX)植入物(700µg)改善了短期BCVA (logMAR的平均变化[95%置信区间]- 0.27 [- 0.40,- 0.15];- 0.12 [- 0.18, - 0.06];- 0.10 [- 0.21, - 0.01];- 0.06[- 0.11, - 0.01])。玻璃体内TA注射(4mg,多次)、FA植入物(0.5µg/天和0.2µg/天)和DEX植入物(350µg)改善了长期BCVA (logMAR的平均变化[95%置信区间]- 0.11 [- 0.21,- 0.02];- 0.09 [- 0.15, - 0.03];- 0.09 [- 0.14, - 0.02];- 0.04[- 0.07, - 0.01])。所有的玻璃体内皮质类固醇均能降低CMT,不同剂量的TA在增加IOP方面没有显着差异。结论:玻璃体内皮质类固醇可有效改善DME患者的BCVA,且剂量越大效果越好。TA并不亚于FA或DEX,可以被认为是DME患者的低成本替代选择。不同皮质类固醇的长期疗效和安全性值得进一步研究。前瞻性注册:PROSPERO, CRD42020219870。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Intravitreal corticosteroids for diabetic macular edema: a network meta-analysis of randomized controlled trials.

Intravitreal corticosteroids for diabetic macular edema: a network meta-analysis of randomized controlled trials.

Intravitreal corticosteroids for diabetic macular edema: a network meta-analysis of randomized controlled trials.

Intravitreal corticosteroids for diabetic macular edema: a network meta-analysis of randomized controlled trials.

Background: To evaluate the efficacy and safety of different intravitreal corticosteroids for treating diabetic macular edema (DME).

Methods: Four databases were systematically searched for randomized controlled trials comparing different intravitreal corticosteroids for treating DME. The primary outcome was the change in best-corrected visual acuity (BCVA) within 6 months after the first injection (short-term BCVA). Secondary outcomes were the change in BCVA over 1 year (long-term BCVA) and changes in central macular thickness (CMT) and intraocular pressure (IOP) within 6 months after the first injection. Network meta-analysis was performed to aggregate the results from the individual studies.

Results: Nineteen trials involving 2839 eyes were included. Intravitreal triamcinolone acetonide (TA) injections (≥ 8 mg and 4-8 mg), fluocinolone acetonide (FA) implants (0.5 µg/day) and dexamethasone (DEX) implants (700 µg) improved short-term BCVA (mean changes in logMAR [95% confidence interval] - 0.27 [- 0.40, - 0.15]; - 0.12 [- 0.18, - 0.06]; - 0.10 [- 0.21, - 0.01]; and - 0.06 [- 0.11, - 0.01]). Intravitreal TA injections (4 mg, multiple times), FA implants (0.5 µg/day and 0.2 µg/day), and DEX implants (350 µg) improved long-term BCVA (mean changes in logMAR [95% confidence interval] - 0.11 [- 0.21, - 0.02]; - 0.09 [- 0.15, - 0.03]; - 0.09 [- 0.14, - 0.02]; and - 0.04 [- 0.07, - 0.01]). All intravitreal corticosteroids reduced CMT, and different dosages of TA did not show significant differences in increasing IOP.

Conclusions: Intravitreal corticosteroids effectively improved BCVA in DME patients, with higher dosages showing greater efficacies. TA was not inferior to FA or DEX and may be considered a low-cost alternative choice for DME patients. The long-term efficacy and safety of different corticosteroids deserve further investigation. Trial registration Prospectively registered: PROSPERO, CRD42020219870.

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