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Combination therapy with fosfomycin for Staphylococcus aureus bacteraemia or endocarditis: a systematic review and meta-analysis of randomized trials.

Publication ,  Journal Article
Mourad, A; Parsons, JB; Skalla, LA; Holland, TL; Jenkins, TC
Published in: JAC Antimicrob Resist
June 2025

BACKGROUND AND OBJECTIVES: Fosfomycin combination therapy for Staphylococcus aureus bacteraemia or endocarditis has been evaluated, but studies were limited by small sample sizes. We sought to conduct a systematic review and meta-analysis of randomized controlled trials (RCTs) to establish robust efficacy and safety estimates of fosfomycin combination therapy in this patient population. DATA SOURCES: MEDLINE, Embase, Cochrane Library and Web of Science databases were searched from inception through September 2024 (PROSPERO CRD42024583822). STUDY ELIGIBILITY: RCTs comparing fosfomycin combination with standard-of-care antibiotics in patients with S. aureus bacteraemia or endocarditis were included. Two independent reviewers screened studies for inclusion. ASSESSMENT OF RISK OF BIAS: Risk of bias was assessed using the revised Cochrane RoB 2 tool. DATA SYNTHESIS AND ANALYSIS: Treatment effects were estimated with pooled risk ratios (RRs) using random effects meta-analysis. Heterogeneity between studies was assessed with Cochran's Q-statistic and I 2 test. RESULTS: Of 437 articles identified, three RCTs met inclusion criteria. Primary outcome of treatment success or cure was not meta-analysed due to clinical heterogeneity. Combination therapy did not significantly improve mortality (RR 0.85; 95% CI, 0.28-2.52; I2  = 27.8%) or persistent bacteraemia (RR 0.34; 95% CI, 0.04-2.59; I2  = 0%). Participants receiving combination therapy had more adverse events leading to treatment discontinuation, but this was not statistically significant (RR 1.84; 95% CI, 0.36-9.36; I2  = 18%). CONCLUSIONS: In this meta-analysis of three RCTs, fosfomycin combination therapy for S. aureus bacteraemia or endocarditis did not significantly improve patient outcomes and may be associated with higher rates of adverse events.

Duke Scholars

Published In

JAC Antimicrob Resist

DOI

EISSN

2632-1823

Publication Date

June 2025

Volume

7

Issue

3

Start / End Page

dlaf101

Location

England

Related Subject Headings

  • 3214 Pharmacology and pharmaceutical sciences
  • 3207 Medical microbiology
  • 3202 Clinical sciences
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Mourad, A., Parsons, J. B., Skalla, L. A., Holland, T. L., & Jenkins, T. C. (2025). Combination therapy with fosfomycin for Staphylococcus aureus bacteraemia or endocarditis: a systematic review and meta-analysis of randomized trials. JAC Antimicrob Resist, 7(3), dlaf101. https://doi.org/10.1093/jacamr/dlaf101
Mourad, Ahmad, Joshua B. Parsons, Lesley A. Skalla, Thomas L. Holland, and Timothy C. Jenkins. “Combination therapy with fosfomycin for Staphylococcus aureus bacteraemia or endocarditis: a systematic review and meta-analysis of randomized trials.JAC Antimicrob Resist 7, no. 3 (June 2025): dlaf101. https://doi.org/10.1093/jacamr/dlaf101.
Mourad A, Parsons JB, Skalla LA, Holland TL, Jenkins TC. Combination therapy with fosfomycin for Staphylococcus aureus bacteraemia or endocarditis: a systematic review and meta-analysis of randomized trials. JAC Antimicrob Resist. 2025 Jun;7(3):dlaf101.
Mourad, Ahmad, et al. “Combination therapy with fosfomycin for Staphylococcus aureus bacteraemia or endocarditis: a systematic review and meta-analysis of randomized trials.JAC Antimicrob Resist, vol. 7, no. 3, June 2025, p. dlaf101. Pubmed, doi:10.1093/jacamr/dlaf101.
Mourad A, Parsons JB, Skalla LA, Holland TL, Jenkins TC. Combination therapy with fosfomycin for Staphylococcus aureus bacteraemia or endocarditis: a systematic review and meta-analysis of randomized trials. JAC Antimicrob Resist. 2025 Jun;7(3):dlaf101.
Journal cover image

Published In

JAC Antimicrob Resist

DOI

EISSN

2632-1823

Publication Date

June 2025

Volume

7

Issue

3

Start / End Page

dlaf101

Location

England

Related Subject Headings

  • 3214 Pharmacology and pharmaceutical sciences
  • 3207 Medical microbiology
  • 3202 Clinical sciences