Despite the rise and impact of methicillin-resistant Staphylococcus aureus, methicillin-susceptible S. aureus (MSSA) continues to contribute to the overall burden of S. aureus infections, representing Ն50% of clinical S. aureus strains (1-3) with known appreciable mortality outcomes (4, 5). Prevailing evidence supports the use of semisynthetic penicillins, such as oxacillin or nafcillin, or the first-generation cephalosporin cefazolin in preference to vancomycin as optimal therapy for MSSA bloodstream infections (BSI) (6-11). Moreover, an early switch from vancomycin to either nafcillin or cefazolin with definitive MSSA identification was associated with a 69% risk reduction in 30-day in-hospital mortality in a recent retrospective cohort study (11).Cefazolin offers a convenient dosing scheme with a favorable adverse event profile, allowing many institutions to consider its use in the management of MSSA infections (12). However, deepseated infections with a high burden of S. aureus have been shown to overproduce certain types of -lactamases, rendering cefazolin inactive and thus resulting in possible treatment failure (13-15). Furthermore, current practice guidelines, such as those for infective endocarditis, suggest reserving the use of cefazolin for patients with nonanaphylactoid-type penicillin allergies (7). As a result, clinician preference for either nafcillin or oxacillin for more severe or deep-seated MSSA infection has evolved in practice, while the use of cefazolin in this setting remains controversial (12,16,17). The purpose of this study was to evaluate and compare treatment outcomes using cefazolin or oxacillin for MSSA BSI, including deep-seated sources of infection.(Portions of this paper were presented as a poster at the 54th Interscience Conference on Antimicrobial Agents and Chemotherapy, 5 to 9 September 2014, Washington, DC.)
MATERIALS AND METHODS
Study design.From January 2010 to April 2013, a retrospective cohort study was conducted at Rush University Medical Center (RUMC) and Northwestern Memorial Hospital (NMH), two tertiary care academic medical centers in Chicago, IL. The study methods were reviewed and approved by the institutional review boards at RUMC, NMH, and Midwestern University. Adult patients who received in-hospital definitive treatment with cefazolin or oxacillin within 48 h of finalized blood cultures with MSSA were eligible for inclusion in the study. Patients were included only once, and only the first (index) in-hospital admission during the study period was evaluated. The index blood culture was the first blood culture growing MSSA during the index admission. Patients were excluded if they (i) were Ͻ18 years of age, (ii) received antibiotics other than cefazolin or oxacillin for definitive treatment of an MSSA BSI, (iii) received Ն5 days of an empirical antibiotic agent active against MSSA prior to definitive treatment with cefazolin or oxacillin, (iv) had a docu-