Engel M E, Matchaba P T, Volmink J
Faculty of Health Sciences, University of Cape Town, Department of Medicine, J47 Old Main Building, Groote Schuur Hospital, Observatory, South Africa, 7925.
Cochrane Database Syst Rev. 2007 Oct 17(4):CD001876. doi: 10.1002/14651858.CD001876.pub2.
Corticosteroids used in addition to antituberculous therapy have been reported to benefit people with tuberculous pleurisy. However, research findings are inconsistent, raising doubt as to whether such treatment is worthwhile. Concern also exists regarding the potential adverse effects of corticosteroids, especially in HIV-positive people.
To evaluate the effects of adding corticosteroids to drug regimens for tuberculous pleural effusion.
In May 2007, we searched the Cochrane Infectious Diseases Group Specialized Register, CENTRAL (The Cochrane Library 2007, Issue 2), MEDLINE, EMBASE, LILACS, Current Controlled Trials, and reference lists of articles.
Randomized and quasi-randomized controlled trials comparing any corticosteroid with no treatment, placebo, or other active treatment (both groups should receive the same antituberculous drug regimen) in people diagnosed with tuberculous pleurisy.
Two authors independently assessed trial methodological quality and extracted data. Data were analysed using relative risks (RR) and weighted mean difference (WMD) with 95% confidence intervals (CI). The fixed-effect model was applied in the absence of statistically significant heterogeneity.
Six trials with 633 participants met the inclusion criteria; one trial included only HIV-positive people. Compared to control, corticosteroid use was associated with less residual pleural fluid at four weeks (RR 0.76, 95% CI 0.62 to 0.94; 394 participants, 3 trials) and reduced pleural thickening (RR 0.69, 95% CI 0.51 to 0.94; 309 participants, 4 trials). We found no evidence of an effect of corticosteroids on death from any cause (194 participants, 1 trial), respiratory function (191 participants, 2 trials), residual pleural fluid at eight weeks (399 participants, 4 trials), or pleural adhesions (123 participants, 2 trials). Although discontinuation of treatment due to adverse events was more frequent in participants receiving corticosteroids than placebo (RR 2.80, 95% CI 1.12 to 6.98; 586 participants, 6 trials), the effects were generally mild. The risk of Kaposi sarcoma may be increased in HIV-positive people receiving corticosteroids (RR 13.00, 95% CI 0.74 to 227.63; 194 participants, 1 trial).
AUTHORS' CONCLUSIONS: There are insufficient data to support evidence-based recommendations regarding the use of adjunctive corticosteroids in people with tuberculous pleurisy. Randomized controlled trials that are sufficiently powered to evaluate the effects of corticosteroids on both morbidity and mortality are needed. The effects of corticosteroids on HIV-related complications, such as Kaposi sarcoma, should be assessed in people co-infected with HIV.
据报道,在抗结核治疗的基础上加用皮质类固醇对结核性胸膜炎患者有益。然而,研究结果并不一致,这让人怀疑这种治疗是否值得。同时,人们也担心皮质类固醇的潜在不良反应,尤其是在艾滋病毒呈阳性的人群中。
评估在结核性胸腔积液的药物治疗方案中加用皮质类固醇的效果。
2007年5月,我们检索了Cochrane传染病组专业注册库、CENTRAL(Cochrane图书馆2007年第2期)、MEDLINE、EMBASE、LILACS、当前对照试验以及文章的参考文献列表。
在诊断为结核性胸膜炎的患者中,比较任何皮质类固醇与不治疗、安慰剂或其他活性治疗(两组应接受相同的抗结核药物治疗方案)的随机和半随机对照试验。
两位作者独立评估试验方法的质量并提取数据。使用相对风险(RR)和加权平均差(WMD)及95%置信区间(CI)进行数据分析。在无统计学显著异质性的情况下应用固定效应模型。
六项试验共633名参与者符合纳入标准;一项试验仅纳入了艾滋病毒呈阳性的人群。与对照组相比,使用皮质类固醇在四周时胸腔积液残留较少(RR 0.76,95%CI 0.62至0.94;394名参与者,3项试验),胸膜增厚减轻(RR 0.69,95%CI 0.51至0.94;309名参与者,4项试验)。我们没有发现皮质类固醇对任何原因导致的死亡(194名参与者,1项试验)、呼吸功能(191名参与者,2项试验)、八周时胸腔积液残留(399名参与者,4项试验)或胸膜粘连(123名参与者,2项试验)有影响的证据。尽管接受皮质类固醇治疗的参与者因不良事件停药的频率高于安慰剂组(RR 2.80,95%CI 1.12至6.98;586名参与者,6项试验),但影响通常较轻。接受皮质类固醇治疗的艾滋病毒呈阳性人群患卡波西肉瘤的风险可能会增加(RR 13.00,95%CI 0.74至227.63;194名参与者,1项试验)。
没有足够的数据支持关于在结核性胸膜炎患者中使用辅助皮质类固醇的循证推荐。需要有足够效力来评估皮质类固醇对发病率和死亡率影响的随机对照试验。应在艾滋病毒合并感染人群中评估皮质类固醇对艾滋病毒相关并发症(如卡波西肉瘤)的影响。