Abstract

BackgroundInfections due to methicillin-resistant Staphylococcus aureus (MRSA) cause serious health risks and significant economic burdens and the preferred drugs are still controversial.MethodsWe performed a network meta-analysis (NMA) to compare the efficacy and safety of antibiotics used to treat inpatients with complicated skin and soft structure infections (cSSSI) or hospital-acquired or ventilator-associated pneumonia (HAP/VAP). We also developed a decision tree model to assess the cost-effectiveness of antibiotics.ResultsForty-nine randomized controlled trials met the inclusion criteria (34 for cSSSI, 15 for HAP/VAP) and compared the efficacy and safety of 16 antibiotics. For cSSSI, NMA indicated that for clinical cure, linezolid was superior than vancomycin (odds ratio (OR) 1.55, 95% confidence interval (CI) 1.19–2.02), while tedizolid (OR 1.39, CI 0.70–2.76) was similar to vancomycin. In terms of safety, there were no significant differences between any two interventions on total adverse events. Based on drug and hospital costs in America, the incremental cost-effectiveness ratios (ICERs) per life-year saved for linezolid and tedizolid compared with vancomycin were US$2833 and US$5523. For HAP/VAP, there were no significant effects either for clinical cure or for safety endpoints between linezolid and vancomycin in NMA. ICERs per life-year saved for linezolid compared with vancomycin were US$2185.ConclusionIn these clinical trials, considering efficacy, safety, and cost-effectivenes, linezolid and tedizolid showed their superiority in MRSA cSSSI; while linezolid might be recommended to treat MRSA pneumonia. Although vancomycin was not cost-effective in pharmacoeconomic evaluation, it is still the first-line treatment for MRSA infection in the clinical practice. This study might provide new insights of therapeutic choices for patients with MRSA infections whilst awaiting the arrival of higher quality evidence.

Highlights

  • Methicillin-resistant Staphylococcus aureus (MRSA) infections have posed a global threat since the end of the last century

  • In the latest decade, minimum inhibitory concentration (MIC) ‘creep’ among susceptible strains to vancomycin has been observed among methicillin-resistant Staphylococcus aureus (MRSA) isolates in USA, this has been consistently associated with increased mortality [6, 7]

  • The eligible comparison networks with MRSA complicated skin and soft structure infections (cSSSI) and pneumonia respectively are shown in Figs. 2 and 3

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Summary

Introduction

Methicillin-resistant Staphylococcus aureus (MRSA) infections have posed a global threat since the end of the last century. MRSA infections cause increased mortality, cost burden and longer hospital stay [1]. The Infectious Diseases Society of America (IDSA) [4] published clinical practice guidelines for the treatment of MRSA infections, providing a practical basis for management. The glycopeptide vancomycin has been recommended by IDSA guidelines of MRSA treatment for many decades due to its excellent antibacterial activity [5]. In the latest decade, minimum inhibitory concentration (MIC) ‘creep’ among susceptible strains to vancomycin has been observed among MRSA isolates in USA, this has been consistently associated with increased mortality [6, 7]. Infections due to methicillin-resistant Staphylococcus aureus (MRSA) cause serious health risks and significant economic burdens and the preferred drugs are still controversial

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