南亚婴儿癫痫痉挛综合征患儿的首选激素疗法:随机对照试验的网络荟萃分析。

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY Epilepsia Open Pub Date : 2024-11-08 DOI:10.1002/epi4.13086
Nagita Devi, Priyanka Madaan, Nidhun Kandoth, Parth Lal, Jitendra Kumar Sahu, Dipika Bansal
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引用次数: 0

摘要

考虑到南亚地区婴儿癫痫痉挛综合征(IESS)所面临的特殊挑战以及激素疗法使用上的巨大差异,我们比较了各种激素疗法对南亚地区婴儿癫痫痉挛综合征患儿的疗效和安全性。我们检索了从开始到 2024 年 4 月的 PubMed、Embase、Scopus 和 Web of Science 数据库。我们仅纳入了评估南亚地区激素疗法对 IESS 的疗效和安全性的随机临床试验 (RCT)。癫痫痉挛(ES)完全停止、电临床反应以及治疗 2 周或 6 周后无痉挛所需的时间是疗效结果,而不良事件的发生是安全性结果。疗效估计值以几率比(OR)或平均差(MD)的形式报告,带95%置信区间(CI),Cochrane偏倚风险2.0(ROB 2.0)用于每项研究的质量评估。累积排序曲线下表面值(SUCRA)用于对不同疗法进行排序,并以 0 至 1 的 p 值进行报告。在747篇引文中,共纳入了9项RCT研究,其中包括566名IESS患儿。经过两周治疗后,地塞米松(OR:6.72;95% CI:1.47,30.72)、促肾上腺皮质激素疗法(ACTH)高剂量(HD)(OR:5.30;95% CI:1.05,26.91)和泼尼松龙高剂量(OR:2.41;95% CI:1.07,5.46)与促肾上腺皮质激素疗法低剂量(LD)相比,对停止 ES 的疗效显著更高。同样,在电临床反应方面,地塞米松(OR:9.63;95% CI:1.99,46.70)和泼尼松龙 HD(OR:3.46;95% CI:1.38,8.68)与促肾上腺皮质激素低剂量相比具有更高的疗效。安全性结果显示,与促肾上腺皮质激素 HD 相比,促肾上腺皮质激素 LD 和泼尼松龙 HD 的高血压发生率明显较低。这项研究为南亚地区首选激素疗法治疗 IESS 提供了高质量的证据。促肾上腺皮质激素 HD、地塞米松和泼尼松龙 HD 是最有效的激素疗法,其疗效与剂量有关。白话摘要:这项研究深入探讨了在南亚地区治疗婴儿癫痫痉挛综合征(IESS)的各种疗法中选择一线激素疗法的问题。研究结果表明,这些疗法的有效性与剂量有关,高剂量的促肾上腺皮质激素、地塞米松和泼尼松龙对停止癫痫痉挛最有效。
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First-choice hormonal therapies for children with infantile epileptic spasms syndrome in South Asia: A network meta-analysis of randomized controlled trials

Considering the peculiar challenges with infantile epileptic spasms syndrome (IESS) in South Asia and a wide variation in the usage of hormonal therapies, we compared the efficacy and safety of various hormonal therapies for children with IESS in South Asia. We searched PubMed, Embase, Scopus, and Web of Science databases from the inception until April 2024. We included only randomized clinical trials (RCTs) evaluating the efficacy and safety of hormonal therapies for IESS in the South Asian region. Complete cessation of epileptic spasms (ES), electro-clinical response, and time taken to be spasm-free at 2 or 6 weeks of therapy were efficacy outcomes, while the occurrence of adverse events was the safety outcome. Effect estimates were reported as odds ratio (OR) or mean difference (MD) with 95% confidence intervals (CI) and Cochrane risk of bias 2.0 (ROB 2.0) used for quality assessment of each study. The surface under the cumulative ranking curve (SUCRA) was used to rank the different therapies and reported as a p-score ranging from 0 to 1. Of 747 citations, nine RCTs comprising 566 children with IESS were included. After 2-week treatment, dexamethasone (OR: 6.72; 95% CI: 1.47, 30.72), adrenocorticotropic hormone therapy (ACTH) high dose (HD) (OR: 5.30; 95% CI: 1.05, 26.91), and prednisolone HD (OR: 2.41; 95% CI:1.07, 5.46) had shown significantly greater efficacy for cessation of EScompared with ACTH low dose (LD). Similarly, for electroclinical response, dexamethasone (OR: 9.63; 95% CI: 1.99, 46.70) and prednisolone HD (OR: 3.46; 95% CI: 1.38, 8.68) had greater efficacy compared with ACTH LD. Safety outcomes revealed that hypertension was significantly less common with ACTH LD and prednisolone HD as compared with ACTH HD. This study provides quality evidence on preferred first-choice hormonal therapy for managing IESS in South Asia. ACTH HD, dexamethasone, and prednisolone HD are the most effective hormonal therapy options with dose-dependent therapeutic efficacy.

Plain Language Summary

This study provides insights into the selection of first-line hormonal therapies among the various treatments for managing infantile epileptic spasms syndrome (IESS) in South Asia. The study findings suggested that the effectiveness of these therapies is dose-dependent, with high doses of ACTH, dexamethasone, and prednisolone being the most effective for achieving cessation of epileptic spasms.

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来源期刊
Epilepsia Open
Epilepsia Open Medicine-Neurology (clinical)
CiteScore
4.40
自引率
6.70%
发文量
104
审稿时长
8 weeks
期刊最新文献
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