INTRAVENOUS MAGNESIUM-SULFATE AS AN ADJUNCT IN THE TREATMENT OF ACUTE ASTHMA

被引:118
|
作者
BLOCH, H [1 ]
SILVERMAN, R [1 ]
MANCHERJE, N [1 ]
GRANT, S [1 ]
JAGMINAS, L [1 ]
SCHARF, SM [1 ]
机构
[1] LONG ISL JEWISH MED CTR, ALBERT EINSTEIN COLL MED, DIV PULM & CRIT CARE, NEW HYDE PK, NY 11042 USA
关键词
ASTHMA; EMERGENCY DEPARTMENT; MAGNESIUM; TREATMENT;
D O I
10.1378/chest.107.6.1576
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
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 FEV(1) 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). FEV(1) 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 FEV(1) <25% predicted on presentation) or ''moderate'' (baseline FEV(1), 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 FEV(1) in the moderate group for magnesium-treated patients. However, in the severe group, there was a significant improvement in FEV(1) at 120 min and 240 min (p=0.014 and 0.026, respectively). Conclusion: Intravenous MgSO4 decreased admission rate and improved FEV(1) in patients with acute severe asthma but did not cause significant improvement in patients with moderate asthma.
引用
收藏
页码:1576 / 1581
页数:6
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