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Efficacy of Doxycycline for Mild-to-Moderate Community-Acquired Pneumonia in Adults: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

医学 内科学 强力霉素 随机对照试验 肺炎 罗红霉素 社区获得性肺炎 不利影响 置信区间 优势比 左氧氟沙星 外科 红霉素 抗生素 生物 微生物学
作者
Sang‐Ho Choi,Antoni Cesar,Timothy Arthur Chandos Snow,Naveed Saleem,Nishkantha Arulkumaran,Mervyn Singer
出处
期刊:Clinical Infectious Diseases [Oxford University Press]
卷期号:76 (4): 683-691 被引量:20
标识
DOI:10.1093/cid/ciac615
摘要

Abstract Background Doxycycline has been recommended as a treatment option for non-severe community-acquired pneumonia (CAP) in adults. We sought to review the evidence for the efficacy of doxycycline in adult patients with mild-to-moderate CAP. Methods We performed a systematic review and meta-analysis of randomized controlled trials (RCTs) of doxycycline versus comparator to assess the clinical efficacy. The primary outcome was the clinical cure rate. Random effects model meta-analyses were used to generate pooled odds ratio (OR) and evaluate heterogeneity (I2). Risk of bias (RoB) and quality of evidence (QoE) were evaluated using the Cochrane Risk of Bias 2.0 tool and GRADE methods, respectively. Results We included 6 RCTs with 834 clinically evaluable patients. The trials were performed between 1984 and 2004. Comparators were 3 macrolides (roxithromycin, spiramycin, and erythromycin) and 3 fluoroquinolones (ofloxacin, fleroxacin, and levofloxacin). Four trials had an overall high RoB. The clinical cure rate was similar between the doxycycline and comparator groups (87.2% [381/437] vs 82.6% [328/397]; OR 1.29 [95% confidence interval {CI}: .73–2.28]; I2 = 30%; low QoE). Subgroup analysis of two studies with a low RoB showed significantly higher clinical cure rates in the doxycyline group (87.1% [196/225] vs 77.8% [165/212]; OR 1.92 [95% CI: 1.15–3.21]; P = .01; I2 = 0%). Adverse event rates were comparable between the doxycycline and comparator groups. Conclusions The efficacy of doxycycline was comparable to macrolides or fluoroquinolones in mild-to-moderate CAP and thus represents a viable treatment option. Considering the lack of recent trials, it warrants large-scale clinical trials.
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