Prasad K, Singh M B
All India Institute of Medical Sciences, Department of Neurology, Ansarinagar, New Delhi, India 110029.
Cochrane Database Syst Rev. 2008 Jan 23(1):CD002244. doi: 10.1002/14651858.CD002244.pub3.
Tuberculous meningitis, a serious form of tuberculosis that affects the meninges covering the brain and spinal cord, is associated with high mortality and disability among survivors. Corticosteroids have been used as an adjunct to antituberculous drugs to improve the outcome, but their role is controversial.
To evaluate the effects of corticosteroids as an adjunct to antituberculous treatment on death and severe disability in people with tuberculous meningitis.
In September 2007, we searched the Cochrane Infectious Diseases Group Specialized Register, CENTRAL (The Cochrane Library 2007, Issue 3), MEDLINE, EMBASE, LILACS, and Current Controlled Trials. We also contacted researchers and organizations working in the field, and checked reference lists.
Randomized controlled trials comparing a corticosteroid plus antituberculous treatment with antituberculous treatment alone in people with clinically diagnosed tuberculosis meningitis and which include death and/or disability as outcome measures.
We independently assessed search results and methodological quality, and independently extracted data. We analysed the data using relative risks (RR) with 95% confidence intervals (CI) and the fixed-effect model. We also conducted complete-case and best-worst case analyses.
Seven trials involving 1140 participants (with 411 deaths) met the inclusion criteria. All used dexamethasone or prednisolone. Overall, corticosteroids reduced the risk of death (RR 0.78, 95% CI 0.67 to 0.91; 1140 participants, 7 trials). Data on disabling residual neurological deficit from three trials showed that corticosteroids reduce the risk of death or disabling residual neurological deficit (RR 0.82, 95% CI 0.70 to 0.97; 720 participants, 3 trials). Adverse events included gastrointestinal bleeding, bacterial and fungal infections and hyperglycaemia, but they were mild and treatable.
AUTHORS' CONCLUSIONS: Corticosteroids should be routinely used in HIV-negative people with tuberculous meningitis to reduce death and disabling residual neurological deficit amongst survivors. However, there is not enough evidence to support or refute a similar conclusion for those who are HIV positive.
结核性脑膜炎是一种严重的结核病形式,会影响覆盖大脑和脊髓的脑膜,幸存者中死亡率和致残率较高。皮质类固醇已被用作抗结核药物的辅助药物以改善治疗结果,但其作用存在争议。
评估皮质类固醇作为抗结核治疗的辅助药物对结核性脑膜炎患者死亡和严重残疾的影响。
2007年9月,我们检索了Cochrane传染病专业组注册库、CENTRAL(Cochrane图书馆2007年第3期)、MEDLINE、EMBASE、LILACS和当前对照试验。我们还联系了该领域的研究人员和组织,并查阅了参考文献列表。
随机对照试验,比较皮质类固醇加抗结核治疗与单纯抗结核治疗在临床诊断为结核性脑膜炎的患者中的效果,并将死亡和/或残疾作为结局指标。
我们独立评估检索结果和方法学质量,并独立提取数据。我们使用相对风险(RR)及95%置信区间(CI)和固定效应模型分析数据。我们还进行了完全病例分析和最佳-最差情况分析。
7项试验涉及1140名参与者(411人死亡)符合纳入标准。所有试验均使用地塞米松或泼尼松龙。总体而言,皮质类固醇降低了死亡风险(RR 0.78,95% CI 0.67至0.91;1140名参与者,7项试验)。三项试验中关于致残性残留神经功能缺损的数据表明,皮质类固醇降低了死亡或致残性残留神经功能缺损的风险(RR 0.82,95% CI 0.70至0.97;720名参与者,3项试验)。不良事件包括胃肠道出血、细菌和真菌感染以及高血糖,但症状较轻且可治疗。
皮质类固醇应常规用于HIV阴性的结核性脑膜炎患者,以降低幸存者中的死亡率和致残性残留神经功能缺损。然而,对于HIV阳性者,没有足够的证据支持或反驳类似结论。