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加巴喷丁作为异动型脑性瘫痪儿童三己芬迪附加疗法的随机对照试验

Gabapentin as Add-on Therapy to Trihexyphenidyl in Children with Dyskinetic Cerebral Palsy: A Randomized, Controlled Trial.

作者信息

Kumar Sonu, Shankar Kaushik Jaya, Verma Savita, Dabla Surekha

机构信息

Department of Pediatrics, SGT University, Gurugram, Haryana, India.

Department of Pediatrics, Pt. B. D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, Haryana, 124001, India.

出版信息

Indian J Pediatr. 2023 Sep;90(9):873-879. doi: 10.1007/s12098-022-04265-2. Epub 2022 Jul 22.

DOI:10.1007/s12098-022-04265-2
PMID:35867274
Abstract

OBJECTIVE

To compare the efficacy of gabapentin as add-on therapy to trihexyphenidyl in the treatment of children with dyskinetic cerebral palsy (CP).

METHODS

An open-labelled, randomized, controlled trial was conducted among children aged 3-9 y with dyskinetic CP [Gross Motor Functional Classification System (GMFCS) 4-5]. Participants were assigned into two groups: gabapentin with trihexyphenidyl (n = 30) and trihexyphenidyl alone (n = 30). Dyskinesia Impairment Scale (DIS), Dystonia Severity Assessment Plan (DSAP), and International Classification of Functioning, Disability, and Health-Children and Youth Version (ICF-CY) were measured at baseline, 4 and 12 wk.

RESULTS

There was significant reduction in baseline dystonia in both the groups (DIS: p < 0.001; DSAP: p = 0.007; ICF-CY: p < 0.001) but when data were compared between the groups, there was no significant difference in the severity of dystonia at 4 wk and at 12 wk (DIS: p = 0.09; DSAP: p = 0.49; ICF-CY: p = 0.25). Constipation was the commonest side effect observed in both the groups [3 (11.5%) vs. 4 (14.3%)].

CONCLUSION

Trihexyphenidyl alone is as effective as combination of gabapentin with trihexyphenidyl in decreasing the severity of dystonia at 12 wk. Hence, there is no added benefit of gabapentin as add-on therapy for dystonia among children with dyskinetic CP.

TRIAL REGISTRATION

CTRI/2019/04/018603.

摘要

目的

比较加巴喷丁作为苯海索附加疗法治疗运动障碍型脑性瘫痪(CP)患儿的疗效。

方法

对年龄在3至9岁的运动障碍型CP患儿[粗大运动功能分类系统(GMFCS)4 - 5级]进行了一项开放标签、随机对照试验。参与者被分为两组:加巴喷丁联合苯海索组(n = 30)和单独使用苯海索组(n = 30)。在基线、4周和12周时测量运动障碍损害量表(DIS)、肌张力障碍严重程度评估计划(DSAP)以及国际功能、残疾和健康分类-儿童和青少年版(ICF-CY)。

结果

两组的基线肌张力障碍均有显著降低(DIS:p < 0.001;DSAP:p = 0.007;ICF-CY:p < 0.001),但在组间比较数据时,4周和12周时肌张力障碍的严重程度无显著差异(DIS:p = 0.09;DSAP:p = 0.49;ICF-CY:p = 0.25)。便秘是两组中最常见的副作用[3例(11.5%)对4例(14.3%)]。

结论

单独使用苯海索在12周时降低肌张力障碍严重程度方面与加巴喷丁联合苯海索的效果相同。因此,对于运动障碍型CP患儿,加巴喷丁作为肌张力障碍的附加疗法并无额外益处。

试验注册号

CTRI/2019/04/018603。

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