Bloch H, Silverman R, Mancherje N, Grant S, Jagminas L, Scharf S M
Department of Emergency Medicine, Long Island Jewish Medical Center, Albert Einstein College of Medicine, New Hyde Park, NY 12042, USA.
Chest. 1995 Jun;107(6):1576-81. doi: 10.1378/chest.107.6.1576.
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.
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.
Emergency departments of a university-affiliated, voluntary hospital and municipal hospital.
Asthmatics aged 18 to 65 years during acute exacerbation with FEV1 less than 75% predicted both before and after a single albuterol treatment.
Patients were given 2 g of MgSO4 or placebo as an adjunct to standardized emergency department procedure for acute asthma.
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).
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.
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。
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。
一家大学附属医院和市立医院的急诊科。
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%。
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。
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)。
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。