The efficacy and safety of adjunctive corticosteroids in the treatment of tuberculous pleurisy: a systematic review and meta-analysis

被引:16
|
作者
Xie, Shuanshuan [1 ]
Lu, Lin [2 ]
Li, Ming [1 ]
Xiong, Mengting [3 ]
Zhou, Shunping [4 ]
Zhang, Guoliang [1 ]
Peng, Aimei [1 ]
Wang, Changhui [1 ]
机构
[1] Tongji Univ, Shanghai Peoples Hosp 10, Dept Resp Med, Shanghai, Peoples R China
[2] Fudan Univ, North Huashan Hosp, Dept Nephrol, Shanghai, Peoples R China
[3] Fudan Univ, Pudong Hosp, Dept Cardiol Med, Shanghai, Peoples R China
[4] Tongji Univ, Yangpu Hosp, Sch Med, Dept Cardiol Med, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
tuberculous pleurisy; corticosteroid; pleural fluid; pleural thickening; pleural adhesion; DOUBLE-BLIND; QUALITY; TRIAL; BIAS;
D O I
10.18632/oncotarget.18160
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To evaluate the efficacy and safety of adjunctive corticosteroids in the treatment of patients with tuberculous pleurisy. Methods: The PubMed, Cochrane, Medline, Embase, Web of Science and Chinese National Knowledge Infrastructure were searched. Clinical trials of corticosteroids compared with control were eligible for inclusion. Results: Ten studies (6 randomized controlled trials [RCTs] and 4 non-RCTs) with 957 participants met the inclusion criteria. Compared to the controls (placebos or non-steroids), adjunctive corticosteroid use reduced the risk of residual pleural fluid after 4 weeks and the number of days to symptom improvement; however, there was no convincing evidence to support the positive effects of corticosteroids over the long term (8 weeks) on residual pleural fluid, pleural thickening, or pleural adhesions, and there was no statistical difference between the corticosteroid group and control group with respect to 7-days relief of the clinical symptoms or death from any cause. In addition, more adverse events were observed in patients who received corticosteroids than in those in the control group. Conclusions: Our results suggest that adjunctive corticosteroid use did not improve long-term efficacy and might induce more adverse events, although the risk of residual pleural fluid at 4 weeks and the number of days to symptom improvement were reduced.
引用
收藏
页码:83315 / 83322
页数:8
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