Chen Haojun, Liu Qianqian, Chen Zhanguo, Li Congrong
Department of Laboratory Medicine, Renmin Hospital of Wuhan University, Wuhan 430060, Hubei, China.
Department of Respiratory Medicine, Chengdu First People's Hospital, Chengdu 610041, Sichuan, China; Department of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu 610041, Sichuan, China.
J Infect Chemother. 2017 May;23(5):278-285. doi: 10.1016/j.jiac.2017.01.005. Epub 2017 Feb 13.
Meta-analyses that ignore the full programme of clinical trials may lead to a misleading interpretation. We did a comprehensive meta-analysis to explore the efficacy of sulbactam for the treatment of Acinetobacter baumannii complex infection. We searched electronic databases, including Pubmed and Embase up to April 24, 2016, to identify relevant published trials. Clinical trial registries were likewise searched to identify completed unpublished studies. Primary outcomes of interest were the clinical and microbiological efficacy and in-hospital mortality. Effect model was based on heterogeneity across studies. Altogether 12 observational trials, comprising about 1500 patients, were included. Compared with control group, the clinical response (OR 1.16, 95% CI 0.77-1.75), bacteriological response (OR 1.71, 95% CI 0.89-3.29) and in-hospital mortality (OR 0.76, 95% CI 0.57-1.01) of sulbactam-based therapy group achieved similar therapeutic in A. baumannii complex infection. Subgroup analysis showed the clinical response (OR 1.66, 95% CI 1.11-2.48) of A. baumannii complex infection favored high-dose sulbactam group. In conclusion, our findings suggested that the overall therapy effect of sulbactam was no more superior than alternative therapeutics. However, when taking consideration of the dose factor, we found that high dosage regimen of sulbactam showed an obvious advantage in the treatment of A. baumannii complex infection.
忽略完整临床试验方案的荟萃分析可能会导致误导性的解释。我们进行了一项全面的荟萃分析,以探讨舒巴坦治疗鲍曼不动杆菌复合感染的疗效。我们检索了电子数据库,包括截至2016年4月24日的PubMed和Embase,以确定相关的已发表试验。同样检索了临床试验注册库,以确定已完成的未发表研究。感兴趣的主要结局是临床和微生物学疗效以及住院死亡率。效应模型基于各研究之间的异质性。共纳入12项观察性试验,约1500例患者。与对照组相比,舒巴坦治疗组在鲍曼不动杆菌复合感染中的临床反应(OR 1.16,95%CI 0.77-1.75)、细菌学反应(OR 1.71,95%CI 0.89-3.29)和住院死亡率(OR 0.76,95%CI 0.57-1.01)达到了相似的治疗效果。亚组分析显示,鲍曼不动杆菌复合感染的临床反应(OR 1.66,95%CI 1.11-2.48)有利于高剂量舒巴坦组。总之,我们的研究结果表明,舒巴坦的总体治疗效果并不优于其他治疗方法。然而,考虑到剂量因素,我们发现高剂量舒巴坦方案在治疗鲍曼不动杆菌复合感染方面显示出明显优势。