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Meta-analysis finds no clear difference between amoxicillin and other antibiotics for community-acquired pneumonia

Meta-analysis finds no clear difference between amoxicillin and other antibiotics for…
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Key Takeaway
Consider amoxicillin as a reasonable option for community-acquired pneumonia, but recognize the evidence does not show clear superiority over other antibiotics.

This systematic review and meta-analysis evaluated amoxicillin and amoxicillin-clavulanate versus other antibiotics or placebo for community-acquired pneumonia in adults and children. The primary outcome was clinical resolution or clinical failure. The authors found no evidence of a differential effect on clinical resolution when comparing amoxicillin to other antibiotics, or when comparing amoxicillin-clavulanate to other antibiotics. For clinical failure with amoxicillin, the evidence was unclear, and the authors could not rule out clinically important benefits or harms. A comparison between amoxicillin and amoxicillin-clavulanate in adults also showed no evidence of a differential effect.

The authors noted key limitations, including a small number of trials and substantial heterogeneity in the comparators used across study settings. The analysis did not report on adverse events, serious adverse events, discontinuations, or tolerability.

Given these limitations, the clinical relevance is restrained. The findings suggest that amoxicillin and amoxicillin-clavulanate may be reasonable options, but the evidence does not establish clear superiority over other antibiotics for community-acquired pneumonia.

Study Details

Study typeMeta analysis
Sample sizen = 15
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
OBJECTIVES: The aim of this study is to evaluate existing evidence on the effectiveness of amoxicillin and amoxicillin-clavulanate for community-acquired pneumonia in children and adults. DESIGN: Systematic review and meta-analysis. DATA SOURCES: PubMed, Cochrane Library, Web of Science and Ovid-MEDLINER were searched with no language restrictions through 16 July 2024. ELIGIBILITY CRITERIA: We included studies comparing the effectiveness of amoxicillin or amoxicillin-clavulanate versus other antibiotics or placebo. DATA EXTRACTION AND SYNTHESIS: Only randomised controlled trials comparing amoxicillin or amoxicillin-clavulanate with another antibiotic or placebo with a primary outcome of clinical resolution or clinical failure were eligible for our review. We used random-effects and fixed-effects logistic regression models to estimate the pooled treatment effect size. Heterogeneity of the studies was evaluated using the τ statistic. We performed an unplanned frequentist random-effects network meta-analysis for the indirect comparison between amoxicillin and amoxicillin-clavulanate. The revised Cochrane risk of bias tool for randomised trials was used to assess and categorise studies into low risk of bias, some concerns or high risk of bias. RESULTS: We extracted data from 44 studies including 45 400 patients. We found no evidence of a differential effect on clinical resolution when comparing amoxicillin with other antibiotics (n=15 trials; pooled OR 0.88; 95% CI 0.56 to 1.38, where >1 favours amoxicillin) or amoxicillin-clavulanate with other antibiotics (n=17; OR 0.89; 95% CI 0.76 to 1.04). Similarly, evidence of difference in clinical failure between amoxicillin and other antibiotics was unclear and unable to rule out clinically important benefits or harms (n=8; OR 0.76; 95% CI 0.55 to 1.06, where <1 favours amoxicillin). We found no evidence of a differential effect on clinical resolution between adults treated with amoxicillin and amoxicillin-clavulanate (n=28; OR 1.04; 95% CI 0.64 to 1.70, where >1 favours amoxicillin-clavulanate). Sixty-three per cent and 29% of amoxicillin and amoxicillin-clavulanate studies, respectively, had low risk of bias according to the Cochrane risk of bias tool for randomised trials. CONCLUSIONS: Current evidence is unclear as to whether amoxicillin or amoxicillin-clavulanate differs from other antibiotics, or from each other, in the treatment of community-acquired pneumonia, owing to the small number of trials and substantial heterogeneity in comparators used across study settings. PROSPERO REGISTRATION NUMBER: CRD42024568554.
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