Daptomycin versus Vancomycin for the Treatment of Methicillin-Resistant Staphylococcus aureus Bloodstream Infection with or without Endocarditis: A Systematic Review and Meta-Analysis

被引:41
作者
Maraolo, Alberto Enrico [1 ]
Giaccone, Agnese [2 ]
Gentile, Ivan [2 ]
Saracino, Annalisa [3 ]
Bavaro, Davide Fiore [3 ]
机构
[1] Cotugno Hosp, AORN Colli, Div Infect Dis 1, I-80131 Naples, Italy
[2] Univ Naples Federico II, Dept Clin Med & Surg, Sect Infect Dis, I-80131 Naples, Italy
[3] Univ Bari, Dept Biomed Sci & Human Oncol, Clin Infect Dis, I-70121 Bari, Italy
来源
ANTIBIOTICS-BASEL | 2021年 / 10卷 / 08期
关键词
daptomycin; vancomycin; MRSA; Staphylococcus aureus; bloodstream infection; endocarditis; MINIMUM INHIBITORY CONCENTRATION; GREATER-THAN-1; MG/L; GENDER-DIFFERENCES; DISEASES SOCIETY; BACTEREMIA; MORTALITY; ASSOCIATION; OUTCOMES; GENTAMICIN; GUIDELINES;
D O I
10.3390/antibiotics10081014
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Methicillin-resistant Staphylococcus aureus (MRSA) is an important cause of invasive infections, mainly bloodstream infections (BSI) with or without endocarditis. The purpose of this meta-analysis was to compare vancomycin, the mainstay treatment, with daptomycin as therapeutic options in this context. Materials: PubMed, Embase and the Cochrane Database were searched from their inception to 15 February 2020. The primary outcome was all-cause mortality. Secondary outcomes included clinical failure, infection recurrence, persistence of infection, length-of-stay, antibiotic discontinuation due to adverse events (AEs) and 30-day re-admission. This study was registered with PROSPERO, CRD42020169413. Results: Eight studies (1226 patients, 554 vs. 672 in daptomycin vs. vancomycin, respectively) were included. No significant difference in terms of overall mortality was observed [odds ratio (OR) 0.73, 95% confidence interval (CI) 0.40-1.33, I-2 = 67%]. Daptomycin was associated with a significantly reduced risk of clinical failure (OR 0.58, 95% CI 0.38-0.89, I-2 = 60%), as confirmed by pooling adjusted effect sizes (adjusted OR against the use of vancomycin 1.94, 95%CI 1.33-1.82, I-2 = 41%), and was linked with fewer treatment-limiting AEs (OR 0.15, 95%CI 0.06-0.36, I-2 = 19%). No difference emerged between the two treatments as secondary outcomes. Results were not robust to unmeasured confounding (E-value lower than 95% CI 1.00 for all-cause mortality). Conclusions: Against MRSA BSI, with or without endocarditis, daptomycin seems to be associated with a lower risk of clinical failure and treatment-limiting AEs compared with vancomycin. Further studies are needed to better characterize the differences between the two drugs.
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