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苯巴比妥治疗轻度胃肠炎伴良性惊厥的疗效:一项随机、安慰剂对照试验。

Efficacy of phenobarbital for benign convulsions with mild gastroenteritis: A randomized, placebo-controlled trial.

作者信息

Takami Yuichi, Nakagawa Taku

机构信息

Department of Pediatrics, Japanese Red Cross Society Himeji Hospital, Hyogo, Japan.

Department of Pediatrics, Japanese Red Cross Society Himeji Hospital, Hyogo, Japan.

出版信息

Brain Dev. 2019 Aug;41(7):600-603. doi: 10.1016/j.braindev.2019.03.014. Epub 2019 Apr 3.

DOI:10.1016/j.braindev.2019.03.014
PMID:30954360
Abstract

OBJECTIVE

This study was performed to evaluate the efficacy and safety of intravenous phenobarbital (PB) for benign convulsions with mild gastroenteritis (CwG).

METHODS

A randomized, single-blind, placebo-controlled trial involving patients with CwG was conducted at the Japanese Red Cross Society Himeji Hospital. Patients with CwG who had experienced two or more seizures were eligible. Patients were excluded if any anticonvulsant was used before enrollment. Patients who were allocated to the PB group were administered 10 mg/kg of PB intravenously. Patients who were allocated to the placebo group were administered 20 ml of normal saline.

RESULTS

From April 2016 to October 2018, 13 of 24 patients with CwG were randomized (PB group, n = 7; placebo group, n = 6; age, 1-3 years). Five of six patients in the placebo group had seizures after administration of placebo. However, patients in the PB group had no seizures after administration of PB, with a significant difference in efficacy between the two groups (P = 0.005). Five patients who had seizures after administration of normal saline were administered 10 mg/kg of PB, and no patients had a seizure thereafter. No significant differences were found in heart rate, blood pressure, or saturation of percutaneous oxygen between the two groups.

CONCLUSION

This is the first randomized controlled trial to evaluate the efficacy of an anticonvulsant for CwG. Intravenous PB at 10 mg/kg is effective and well tolerated for CwG.

摘要

目的

本研究旨在评估静脉注射苯巴比妥(PB)治疗轻度胃肠炎伴良性惊厥(CwG)的疗效和安全性。

方法

在日本红十字会姬路医院对CwG患者进行了一项随机、单盲、安慰剂对照试验。有两次或更多次惊厥发作的CwG患者符合入选标准。如果在入组前使用过任何抗惊厥药物,则将患者排除。分配到PB组的患者静脉注射10mg/kg的PB。分配到安慰剂组的患者静脉注射20ml生理盐水。

结果

2016年4月至2018年10月,24例CwG患者中有13例被随机分组(PB组,n = 7;安慰剂组,n = 6;年龄1至3岁)。安慰剂组6例患者中有5例在注射安慰剂后出现惊厥。然而,PB组患者在注射PB后未出现惊厥,两组疗效差异有统计学意义(P = 0.005)。5例在注射生理盐水后出现惊厥的患者注射了10mg/kg的PB,此后无患者再出现惊厥。两组在心率、血压或经皮血氧饱和度方面未发现显著差异。

结论

这是第一项评估抗惊厥药物治疗CwG疗效的随机对照试验。静脉注射10mg/kg的PB对CwG有效且耐受性良好。

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