Kew Kayleigh M, Kirtchuk Liza, Michell Clare I
Population Health Research Institute, St George's, University of London, Cranmer Terrace, London, UK, SW17 0RE.
Cochrane Database Syst Rev. 2014 May 28;2014(5):CD010909. doi: 10.1002/14651858.CD010909.pub2.
Asthma is a chronic respiratory condition characterised by airways inflammation, constriction of airway smooth muscle and structural alteration of the airways that is at least partially reversible. Exacerbations of asthma can be life threatening and place a significant burden on healthcare services. Various guidelines have been published to inform management personnel in the acute setting; several include the use of a single bolus of intravenous magnesium sulfate (IV MgSO4) in cases that do not respond to first-line treatment. However, the effectiveness of this approach remains unclear, particularly in less severe cases.
To assess the safety and efficacy of IV MgSO4 in adults treated for acute asthma in the emergency department.
We identified trials from the Cochrane Airways Review Group Specialised Register (CAGR) up to 2 May 2014. We also searched www.ClinicalTrials.gov and reference lists of other reviews, and we contacted trial authors to ask for additional information.
We included randomised controlled trials (RCTs) of adults treated in the emergency department (ED) for exacerbations of asthma if they compared any dose of IV MgSO4 with placebo.
All review authors screened titles and abstracts for inclusion, and at least two review authors independently extracted study characteristics, risk of bias and numerical data. Disagreements were resolved by consensus, and we contacted trial investigators to obtain missing information.We analysed dichotomous data as odds ratios using study participants as the unit of analysis, and we analysed continuous data as mean differences or standardised mean differences using fixed-effect models. We rated all outcomes using GRADE and presented results in Summary of findings table 1.We carried out subgroup analyses on the primary outcome for baseline severity of exacerbations and whether or not ipratropium bromide was given as a co-medication. Unpublished data and studies at high risk of bias for blinding were removed from the main analysis in sensitivity analyses.
Fourteen studies met the inclusion criteria, randomly assigning 2313 people with acute asthma to the comparisons of interest in this review.Most studies were double-blinded trials comparing a single infusion of 1.2 g or 2 g IV MgSO4 over 15 to 30 minutes versus a matching placebo. Eleven were conducted at a single centre, and three were multi-centre trials. Participants in almost all of the studies had already been given at least oxygen, nebulised short-acting beta2-agonists and IV corticosteroids in the ED; in some studies, investigators also administered ipratropium bromide. Ten studies included only adults, and four included both adults and children; these were included because the mean age of participants was over 18 years.Intravenous MgSO4 reduced hospital admissions compared with placebo (odds ratio (OR) 0.75, 95% confidence interval (CI) 0.60 to 0.92; I(2) = 28%, P value 0.18; n = 972; high-quality evidence). In absolute terms, this odds ratio translates into a reduction of seven hospital admissions for every 100 adults treated with IV MgSO4 (95% CI two to 13 fewer). The test for subgroup differences revealed no statistical heterogeneity between the three severity subgroups (I(2) = 0%, P value 0.73) or between the four studies that administered nebulised ipratropium bromide as a co-medication and those that did not (I(2) = 0%, P value 0.82). Sensitivity analyses in which unpublished data and studies at high risk for blinding were removed from the primary analysis did not change conclusions.Within the secondary outcomes, high- and moderate-quality evidence across three spirometric indices suggests some improvement in lung function with IV MgSO4. No difference was found between IV MgSO4and placebo for most of the non-spirometric secondary outcomes, all of which were rated as low or moderate quality (intensive care admissions, ED treatment duration, length of hospital stay, readmission, respiration rate, systolic blood pressure).Adverse events were inconsistently reported and were not meta-analysed. The most commonly cited adverse events in the IV MgSO4 groups were flushing, fatigue, nausea and headache and hypotension (low blood pressure).
AUTHORS' CONCLUSIONS: This review provides evidence that a single infusion of 1.2 g or 2 g IV MgSO4 over 15 to 30 minutes reduces hospital admissions and improves lung function in adults with acute asthma who have not responded sufficiently to oxygen, nebulised short-acting beta2-agonists and IV corticosteroids. Differences in the ways the trials were conducted made it difficult for the review authors to assess whether severity of the exacerbation or additional co-medications altered the treatment effect of IV MgSO4. Limited evidence was found for other measures of benefit and safety.Studies conducted in these populations should clearly define baseline severity parameters and systematically record adverse events. Studies recruiting participants with exacerbations of varying severity should consider subgrouping results on the basis of accepted severity classifications.
哮喘是一种慢性呼吸道疾病,其特征为气道炎症、气道平滑肌收缩以及气道结构改变,且这种改变至少部分是可逆的。哮喘发作可能危及生命,并给医疗服务带来沉重负担。已发布了各种指南,为急性情况下的管理人员提供指导;其中一些指南建议在对一线治疗无反应的病例中使用单次静脉注射硫酸镁(IV MgSO4)。然而,这种方法的有效性仍不明确,尤其是在不太严重的病例中。
评估静脉注射硫酸镁(IV MgSO4)在急诊科治疗成人急性哮喘的安全性和有效性。
我们检索了截至2014年5月2日的Cochrane气道综述小组专业注册库(CAGR)中的试验。我们还检索了www.ClinicalTrials.gov以及其他综述的参考文献列表,并联系试验作者以获取更多信息。
如果将任何剂量的静脉注射硫酸镁(IV MgSO4)与安慰剂进行比较,我们纳入在急诊科(ED)治疗哮喘发作的成人随机对照试验(RCT)。
所有综述作者筛选标题和摘要以确定是否纳入,至少两名综述作者独立提取研究特征、偏倚风险和数值数据。通过协商解决分歧,我们联系试验研究者以获取缺失信息。我们将二分数据作为比值比进行分析,以研究参与者作为分析单位,将连续数据作为均值差或标准化均值差进行分析,采用固定效应模型。我们使用GRADE对所有结局进行评级,并在结果总结表1中呈现结果。我们对主要结局进行亚组分析,分析加重的基线严重程度以及是否联合使用异丙托溴铵。在敏感性分析中,将未发表的数据和存在高偏倚风险的盲法研究从主要分析中剔除。
14项研究符合纳入标准,将2313例急性哮喘患者随机分配至本综述感兴趣的比较组。大多数研究为双盲试验,比较在15至30分钟内单次静脉输注1.2 g或2 g IV MgSO4与匹配的安慰剂。11项研究在单一中心进行,3项为多中心试验。几乎所有研究中的参与者在急诊科已接受至少氧气、雾化吸入短效β2受体激动剂和静脉注射糖皮质激素治疗;在一些研究中,研究者还给予了异丙托溴铵。10项研究仅纳入成人,4项研究同时纳入成人和儿童;纳入这些研究是因为参与者的平均年龄超过18岁。与安慰剂相比,静脉注射硫酸镁(IV MgSO4)减少了住院率(比值比(OR)0.75,95%置信区间(CI)0.60至0.92;I² = 28%,P值0.18;n = 972;高质量证据)。从绝对值来看,该比值比意味着每100例接受IV MgSO4治疗的成人中,住院人数减少7例(95% CI减少2至13例)。亚组差异检验显示,三个严重程度亚组之间(I² = 0%,P值0.73)或四项联合使用雾化异丙托溴铵的研究与未使用的研究之间(I² = 0%,P值0.82)均无统计学异质性。在主要分析中剔除未发表的数据和存在高盲法偏倚风险的研究后进行的敏感性分析未改变结论。在次要结局方面,三项肺功能指标的高质量和中等质量证据表明,IV MgSO4可使肺功能有所改善。对于大多数非肺功能测量的次要结局,IV MgSO4与安慰剂之间未发现差异,所有这些结局均被评为低质量或中等质量(重症监护病房入院、急诊科治疗持续时间、住院时间、再入院、呼吸频率、收缩压)。不良事件报告不一致,未进行荟萃分析。IV MgSO4组最常提及的不良事件为潮红、疲劳、恶心、头痛和低血压(低血压)。
本综述提供的证据表明,在15至30分钟内单次静脉输注1.2 g或2 g IV MgSO4可减少对氧气、雾化吸入短效β2受体激动剂和静脉注射糖皮质激素反应不佳的成人急性哮喘患者的住院率,并改善其肺功能。试验实施方式的差异使综述作者难以评估加重的严重程度或额外的联合用药是否会改变IV MgSO4的治疗效果。关于其他益处和安全性指标的证据有限。在这些人群中进行的研究应明确界定基线严重程度参数,并系统记录不良事件。招募不同严重程度加重患者的研究应考虑根据公认的严重程度分类对结果进行亚组分析。