Premium
Meta‐analysis of trials comparing cefazolin to antistaphylococcal penicillins in the treatment of methicillin‐sensitive Staphylococcus aureus bacteraemia
Author(s) -
Rindone Joseph P.,
Mellen Chadwick K.
Publication year - 2018
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1111/bcp.13554
Subject(s) - cefazolin , medicine , confidence interval , meta analysis , staphylococcus aureus , penicillin , adverse effect , relative risk , staphylococcal infections , surgery , antibiotics , microbiology and biotechnology , biology , genetics , bacteria
Aims The objective of this study was to determine the effectiveness and safety of cefazolin vs. antistaphylococcal penicillin (ASP) in the treatment of methicillin‐sensitive Staphylococcus aureus (MSSA) bacteraemia. Methods The databases of PubMed, Embase and Cochrane Central were used to identify comparative trials of cefazolin vs. ASP in MSSA bacteraemia. Meta‐analysis of included trials was performed to assess any differences regarding mortality, clinical cure, recurrence and withdrawal from adverse effects between groups. Data were analysed using fixed effect model. Studies were weighted using Mantel–Haenszel methodology. Heterogeneity was calculated using the I 2 statistic. Results Nine retrospective and one prospective trials were identified involving 4728 patients, 2954 with ASP and 1774 with cefazolin. Meta‐analysis showed a lower mortality rate with cefazolin vs. ASP using fixed effect model [risk ratio (RR) 0.78, 95% confidence interval (CI) 0.69–0.88, P < 0.0001] with borderline high heterogeneity (I 2 = 51%). Clinical cure was noted more often with cefazolin (RR 1.09, 95% CI 1.02–1.17, P = 0.02), although no difference was noted with relapse (RR 1.29, 95% CI 0.96–1.74 P = 0.09). Analysis also showed more withdrawals from adverse events with ASP vs. cefazolin (RR 0.27, 95% CI 0.16–0.47, P < 0.00001). A minority of patients enrolled in these trials were admitted to the intensive care unit or had endocarditis (11.4% with ASP and 9% with cefazolin). Conclusion Our meta‐analysis of retrospective data demonstrate that cefazolin is more effective and safer ASP in patients with MSSA bacteraemia from various causes. Low quality of trials, borderline high heterogeneity, and possible publication bias may limit the validity of our findings. Randomized trials are needed to confirm these findings.