Pulse Methylprednisolone with Oral Prednisolone versus Adrenocorticotropic Hormone in Children with West Syndrome: a Randomized Controlled Trial.

Journal of epilepsy research Pub Date : 2021-12-31 eCollection Date: 2021-12-01 DOI:10.14581/jer.21020
Kanij Fatema, Mizanur Rahman, Mohammad Monir Hossain, Shaheen Akhter, Dewan Afsana Shomee, Sohela Akhter, Mazharul Mannan
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Abstract

Background and purpose: West syndrome is an epileptic encephalopathy of infancy. According to guidelines, adrenocorticotrophic hormone (ACTH) is probably effective for the short-term management of infantile spasm, but there is little uniformity in treatment due to variable response. This study has been done to evaluate the efficacy of pulse methylprednisolone as compared to ACTH in children with West syndrome.

Methods: Children between 3 months to 24 months with the diagnosis of West syndrome were included and ACTH and pulse methyl prednisolone followed by oral prednisolone were given after randomization. Total duration of treatment was 6 weeks in both groups.

Results: Total 87 children were enrolled; 12 patients lost in follow up. Finally, 43 received ACTH and 32 received pulse methylprednisolone. In pulse methylprednisolone group, 28.13% showed 50-80% response, 28.13% showed 80-99% response and 21.87% patients showed 100% response. In ACTH group, 41.86% showed 50-80% response, 25.58% showed 80-99% response and only 3 (6.97%) patients showed 100% response. Methylprednisolone treatment regimen did not cause significant or persistent adverse effects.

Conclusions: Pulse methylprednisolone followed by oral prednisolone for 6 weeks is as effective as ACTH. Thus, methylprednisolone therapy can be an important alternative to ACTH.

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脉冲甲泼尼龙与口服泼尼松龙对比促肾上腺皮质激素治疗韦斯特综合征患儿:随机对照试验。
背景和目的:韦斯特综合征是一种婴儿期癫痫性脑病。根据指南,肾上腺皮质激素(ACTH)可能对婴儿痉挛症的短期治疗有效,但由于反应不一,治疗方法几乎没有统一性。本研究旨在评估脉冲甲基强的松龙与促肾上腺皮质激素相比对韦斯特综合征患儿的疗效:方法:纳入 3 个月至 24 个月的诊断为韦斯特综合征的儿童,在随机分配后给予促肾上腺皮质激素和脉冲甲基强的松龙,然后口服强的松龙。两组的总治疗时间均为 6 周:结果:共有 87 名儿童入组;12 名患者失去了随访机会。最后,43 名儿童接受了促肾上腺皮质激素治疗,32 名儿童接受了脉冲甲基强的松龙治疗。在脉冲甲基强的松龙组中,28.13%的患者有50%-80%的反应,28.13%的患者有80%-99%的反应,21.87%的患者有100%的反应。在促肾上腺皮质激素组中,41.86%的患者有 50-80% 的反应,25.58% 的患者有 80-99% 的反应,只有 3 名(6.97%)患者有 100% 的反应。甲基强的松龙治疗方案没有引起明显或持续的不良反应:脉冲甲基强的松龙后口服强的松龙 6 周的疗效与促肾上腺皮质激素相同。因此,甲基强的松龙疗法可以作为促肾上腺皮质激素的重要替代疗法。
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