Parlak Ismet, Erdur Bulent, Parlak Mine, Ergin Ahmet, Turkcuer Ibrahim, Tomruk Onder, Ayrik Cuneyt, Ergin Nesrin
Mersin University, School of Medicine, Department of Emergency Medicine, Mersin, Turkey.
Postgrad Med J. 2007 Oct;83(984):664-8. doi: 10.1136/pgmj.2007.057570.
To determine the therapeutic effect (alleviation of vascular type headache) and side effects of a slow intravenous metoclopramide infusion over 15 min compared with those effects of a bolus intravenous metoclopramide infusion over 2 min in the treatment of patients with recent onset vascular type headache.
All adults treated with metoclopramide for vascular type headache were eligible for entry into this clinical randomised double blinded trial. This study compared the effects of two different rates of intravenous infusion of metoclopramide over a period of 13 months at a university hospital emergency department. During the trial, side effects and headache scores were recorded at baseline (0 min), and then at 5, 15, 30 and 60 min. Repeated measures analysis of variance was used to compare the medication's efficacy and side effects.
A total of 120 patients presenting to the emergency department met the inclusion criteria. Of these, 62 patients (51.7%) were given 10 mg metoclopramide as a slow intravenous infusion over 15 min (SIG group) and 58 patients (48.3%) were given 10 mg metoclopramide intravenous bolus infusion over 2 min (BIG group). 17 of the 58 patients in the BIG group (29.3%) and 4 of the 62 patients (6.5%) in the SIG group had akathisia (p = 0.001). There were no significant differences between the BIG and SIG groups in terms of mean headache scores (p = 0.34) and no adverse reactions in the study period. Metoclopramide successfully relieved the headache symptom(s) of patients in both the BIG and SIG groups.
Slowing the infusion rate of metoclopramide is an effective strategy for the improvement of headache and reducing the incidence of akathisia in patients with vascular type headache.
确定在治疗近期发作的血管性头痛患者时,静脉缓慢输注甲氧氯普胺15分钟的治疗效果(缓解血管性头痛)及副作用,并与静脉推注甲氧氯普胺2分钟的效果进行比较。
所有接受甲氧氯普胺治疗血管性头痛的成年人都有资格进入这项临床随机双盲试验。本研究在一家大学医院急诊科比较了13个月期间两种不同静脉输注速率的甲氧氯普胺的效果。试验期间,在基线(0分钟)以及5、15、30和60分钟时记录副作用和头痛评分。采用重复测量方差分析来比较药物的疗效和副作用。
共有120名到急诊科就诊的患者符合纳入标准。其中,62名患者(51.7%)接受了10毫克甲氧氯普胺15分钟的缓慢静脉输注(SIG组),58名患者(48.3%)接受了10毫克甲氧氯普胺2分钟的静脉推注(BIG组)。BIG组的58名患者中有17名(29.3%)出现静坐不能,SIG组的62名患者中有4名(6.5%)出现静坐不能(p = 0.001)。BIG组和SIG组在平均头痛评分方面无显著差异(p = 0.34),且在研究期间无不良反应。甲氧氯普胺成功缓解了BIG组和SIG组患者的头痛症状。
减慢甲氧氯普胺的输注速率是改善血管性头痛患者头痛症状并降低静坐不能发生率的有效策略。