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静脉注射硫酸镁作为治疗急性哮喘的辅助药物。

Intravenous magnesium sulfate as an adjunct in the treatment of acute asthma.

作者信息

Bloch H, Silverman R, Mancherje N, Grant S, Jagminas L, Scharf S M

机构信息

Department of Emergency Medicine, Long Island Jewish Medical Center, Albert Einstein College of Medicine, New Hyde Park, NY 12042, USA.

出版信息

Chest. 1995 Jun;107(6):1576-81. doi: 10.1378/chest.107.6.1576.

Abstract

STUDY OBJECTIVE

This study was conducted to determine whether intravenous magnesium sulfate (MgSO4), when used as part of a standardized treatment protocol, can improve pulmonary function and decrease admission rate in patients presenting to the emergency department with exacerbations of asthma.

DESIGN

In this randomized double-blind placebo-controlled study, patients with acute asthma were treated with inhaled beta-agonists at regular intervals and intravenous (IV) steroids. At 30 min after entry, patients received either 2 g IV MgSO4 or IV placebo. Patients were monitored for up to 4 h with regular measurements of pulmonary function. Patients who were discharged from the emergency department were contacted at 1 day and 7 days for follow-up.

SETTING

Emergency departments of a university-affiliated, voluntary hospital and municipal hospital.

PARTICIPANTS

Asthmatics aged 18 to 65 years during acute exacerbation with FEV1 less than 75% predicted both before and after a single albuterol treatment.

INTERVENTIONS

Patients were given 2 g of MgSO4 or placebo as an adjunct to standardized emergency department procedure for acute asthma.

MEASUREMENTS AND RESULTS

One hundred thirty-five patients were studied. Hospital admission rates were 35.3% for placebo-treated group and 25.4% for the magnesium-treated group (p = 0.21). FEV1 measured at 120 min was 56% predicted for the placebo-treated group and 55% predicted for the magnesium-treated group. (p = 0.92) For subgroup analysis, patients were divided into "severe" (baseline FEV1 < 25% predicted on presentation) or "moderate" (baseline FEV1, 25 to 75% predicted on presentation). For the severe group, admission rates were 78.6% (11/14) for the placebo-treated group and 33.3% (7/21) for the magnesium-treated group (p = 0.009). For the moderate patients, admission rates were 22.4% (11/49) for the placebo-treated group and 22.2% (10/25) for the magnesium-treated group (p = 0.98). There was no significant improvement in FEV1 in the moderate group for magnesium-treated patients. However, in the severe group, there was a significant improvement in FEV1 at 120 min and 240 min (p = 0.014 and 0.026, respectively).

CONCLUSION

Intravenous MgSO4 decreased admission rate and improved FEV1 in patients with acute severe asthma but did not cause significant improvement in patients with moderate asthma.

摘要

研究目的

本研究旨在确定静脉注射硫酸镁(MgSO4)作为标准化治疗方案的一部分,能否改善急诊科因哮喘急性加重就诊患者的肺功能并降低入院率。

设计

在这项随机双盲安慰剂对照研究中,急性哮喘患者定期接受吸入β-受体激动剂和静脉注射(IV)类固醇治疗。入院30分钟后,患者接受2g静脉注射硫酸镁或静脉注射安慰剂。对患者进行长达4小时的监测,并定期测量肺功能。从急诊科出院的患者在第1天和第7天接受随访。

地点

一家大学附属医院和市立医院的急诊科。

参与者

年龄在18至65岁之间的哮喘患者,在单次使用沙丁胺醇治疗前后,预测第一秒用力呼气容积(FEV1)均低于75%。

干预措施

患者接受2g硫酸镁或安慰剂,作为急性哮喘标准化急诊科治疗程序的辅助治疗。

测量与结果

共研究了135名患者。安慰剂治疗组的住院率为35.3%,硫酸镁治疗组为25.4%(p = 0.21)。安慰剂治疗组在120分钟时测量的FEV1为预测值的56%,硫酸镁治疗组为预测值的55%。(p = 0.92)进行亚组分析时,患者被分为“重度”(就诊时基线FEV1 < 预测值的25%)或“中度”(就诊时基线FEV1为预测值的25%至75%)。对于重度组,安慰剂治疗组的住院率为78.6%(11/14),硫酸镁治疗组为33.3%(7/21)(p = 0.009)。对于中度患者,安慰剂治疗组的住院率为22.4%(11/49),硫酸镁治疗组为22.2%(10/25)(p = 0.98)。硫酸镁治疗的中度组患者的FEV1没有显著改善。然而,在重度组中,120分钟和240分钟时FEV1有显著改善(分别为p = 0.014和0.026)。

结论

静脉注射硫酸镁可降低急性重度哮喘患者的入院率并改善FEV1,但对中度哮喘患者没有显著改善。

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