van de Beek D, de Gans J, McIntyre P, Prasad K
Academic Medical Center University of Amsterdam, Department of Neurology, Center for Infection and Immunity Amsterdam (CINIMA), P.O. Box 22700, 1100 DE, Amsterdam, Netherlands.
Cochrane Database Syst Rev. 2007 Jan 24(1):CD004405. doi: 10.1002/14651858.CD004405.pub2.
In experimental studies, the clinical outcome of acute bacterial meningitis has been related to the severity of the inflammatory process in the subarachnoidal space. Treatment with corticosteroids can reduce this inflammatory response and thereby may improve outcome. We conducted a meta-analysis of randomised controlled trials (RCTs) of adjuvant corticosteroids in the treatment of acute bacterial meningitis.
We conducted a systematic review examining the efficacy and safety of adjuvant corticosteroid therapy in acute bacterial meningitis.
In this updated review, we searched the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library Issue 2, 2006); MEDLINE (1966 to July 2006); EMBASE (1974 to June 2006); Current Contents (2001 to June 2006); and reference lists of all articles. We also contacted manufacturers and researchers in the field.
Eligible published and non-published RCTs on corticosteroids as adjuvant therapy in acute bacterial meningitis. Patients of any age and in any clinical condition, treated with antibacterial agents and randomised to corticosteroid therapy (or placebo) of any type, could be included. At least case fatality rate or hearing loss had to be recorded for inclusion.
Two review authors independently assessed trial quality and extracted data. Adverse effects were collected from the trials. Additional analyses were performed for children and adults, causative organisms, and low-income and developed countries.
Eighteen studies involving 2750 people were included. Overall, adjuvant corticosteroids were associated with lower case fatality (relative risk (RR) 0.83, 95% CI 0.71 to 0.99), lower rates of severe hearing loss (RR 0.65, 95% CI 0.47 to 0.91) and long-term neurological sequelae (RR 0.67, 95% CI 0.45 to 1.00). In children, corticosteroids reduced severe hearing loss (RR 0.61, 95% CI 0.44 to 0.86). In adults, corticosteroids gave significant protection against death (RR 0.57, 95% CI 0.40 to 0.81) and short-term neurological sequelae (RR 0.42, 95% CI 0.22 to 0.87). Subgroup analysis for causative organisms showed that corticosteroids reduced mortality in patients with meningitis due to Streptococcus pneumoniae (RR 0.59, 95% CI 0.45 to 0.77) and reduced severe hearing loss in children with meningitis due to Haemophilus influenzae (RR 0.37, 95% CI 0.20 to 0.68); subgroup analysis for patients with meningococcal showed a nonsignificant favourable trend in mortality (RR 0.71, 95% CI 0.31 to 1.62). Sub analyses for high-income and low-income countries of the effect of corticosteroids on mortality showed RRs of 0.83 (95% CI 0.52 to 1.05) and 0.87 (95% CI 0.72 to 1.05), respectively. Corticosteroids were protective against short-term neurological sequelae in patients with bacterial meningitis high-income countries (RR 0.56, 95% CI 0.3 to 0.84); in low-income countries this RR was 1.09 (95% CI 0.83 to 1.45). For children with bacterial meningitis admitted in high-income countries, corticosteroids showed a protective effect of on severe hearing loss (RR 0.61, 95% CI 0.41 to 0.90) and favourable point estimates for severe hearing loss associated with non-Haemophilus influenzae meningitis (RR 0.51, 95% CI 0.23 to 1.13) and short-term neurological sequelae (RR 0.72, 95% CI 0.39 to 1.33). For children in low-income countries, the use of corticosteroids was neither associated with benefit nor with harmful effects. Overall, adverse events were not increased significantly with the use of corticosteroids.
AUTHORS' CONCLUSIONS: Overall, corticosteroids significantly reduced rates of mortality, severe hearing loss and neurological sequelae. In adults with community-acquired bacterial meningitis, corticosteroid therapy should be administered in conjunction with the first antibiotic dose. In children, data support the use of adjunctive corticosteroids in children in high-income countries. We found no beneficial effect of corticosteroids for children in low-income countries.
在实验研究中,急性细菌性脑膜炎的临床结局与蛛网膜下腔炎症过程的严重程度相关。使用皮质类固醇进行治疗可减轻这种炎症反应,从而可能改善结局。我们对辅助性皮质类固醇治疗急性细菌性脑膜炎的随机对照试验(RCT)进行了一项荟萃分析。
我们进行了一项系统评价,以检验辅助性皮质类固醇治疗急性细菌性脑膜炎的疗效和安全性。
在本次更新的评价中,我们检索了Cochrane对照试验中心注册库(CENTRAL)(2006年第2期《Cochrane图书馆》);MEDLINE(1966年至2006年7月);EMBASE(1974年至2006年6月);《现刊目次》(2001年至2006年6月);以及所有文章的参考文献列表。我们还联系了该领域的制造商和研究人员。
关于皮质类固醇作为急性细菌性脑膜炎辅助治疗的合格已发表和未发表的RCT。任何年龄、处于任何临床状况、接受抗菌药物治疗并随机接受任何类型皮质类固醇治疗(或安慰剂)的患者均可纳入。纳入研究至少需记录病死率或听力损失情况。
两名评价作者独立评估试验质量并提取数据。从试验中收集不良反应。对儿童和成人、致病微生物以及低收入和发达国家进行了额外分析。
纳入了18项研究,涉及2750人。总体而言,辅助性皮质类固醇与较低的病死率(相对危险度(RR)0.83,95%可信区间0.71至0.99)、较低的严重听力损失发生率(RR 0.65,95%可信区间0.47至0.91)和长期神经后遗症发生率(RR 0.67,95%可信区间0.45至1.00)相关。在儿童中,皮质类固醇降低了严重听力损失(RR 0.61,95%可信区间0.44至0.86)。在成人中,皮质类固醇对死亡(RR 0.57,95%可信区间0.40至0.81)和短期神经后遗症(RR 0.42,95%可信区间0.22至0.87)有显著保护作用。对致病微生物的亚组分析表明,皮质类固醇降低了肺炎链球菌所致脑膜炎患者的死亡率(RR 0.59,95%可信区间0.45至0.77),并降低了流感嗜血杆菌所致脑膜炎儿童的严重听力损失(RR 0.37,95%可信区间0.20至0.68);对脑膜炎球菌患者的亚组分析显示死亡率有不显著的有利趋势(RR 0.71,95%可信区间0.31至1.62)。对高收入和低收入国家皮质类固醇对死亡率影响的亚组分析显示RR分别为0.83(95%可信区间0.52至1.05)和0.87(95%可信区间0.72至1.05)。皮质类固醇对高收入国家细菌性脑膜炎患者的短期神经后遗症有保护作用(RR 0.56,95%可信区间0.3至0.84);在低收入国家,该RR为1.09(95%可信区间0.83至1.45)。对于高收入国家入院的细菌性脑膜炎儿童,皮质类固醇对严重听力损失有保护作用(RR 0.61,95%可信区间0.41至0.90),对于与非流感嗜血杆菌脑膜炎相关的严重听力损失和短期神经后遗症有有利的点估计值(RR 0.51,95%可信区间0.23至1.13)和(RR 0.72,95%可信区间0.39至1.33)。对于低收入国家的儿童,使用皮质类固醇既未显示有益也未显示有害作用。总体而言,使用皮质类固醇未显著增加不良事件。
总体而言,皮质类固醇显著降低了死亡率、严重听力损失和神经后遗症的发生率。对于社区获得性细菌性脑膜炎成人患者,应在给予首剂抗生素时同时给予皮质类固醇治疗。对于儿童,数据支持在高收入国家儿童中使用辅助性皮质类固醇。我们发现皮质类固醇对低收入国家儿童无有益作用。