TY - JOUR
T1 - Cefazolin for Methicillin-Susceptible Staphylococcus aureus Bacteremia
AU - Lee, Todd C
AU - Barina, Lauren A
AU - Walls, Genevieve
AU - Goodman, Anna L
AU - Yahav, Dafna
AU - Cheng, Matthew P
AU - Bonten, Marc
AU - Bowen, Asha C
AU - Boyles, Tom
AU - Daneman, Nick
AU - Ekkelenkamp, Miquel B
AU - Ghanem-Zoubi, Nesrin
AU - Hensgens, Marjolein P M
AU - Jager, Nynke G L
AU - Kaasch, Achim J
AU - Kouijzer, Ilse J E
AU - Lewis, Roger J
AU - Lumley, Thomas
AU - Lye, David C
AU - McDonald, Emily G
AU - McKew, Genevieve
AU - McLean, Alistair R D
AU - McMullan, Brendan J
AU - McQuilten, Zoe K
AU - Morpeth, Susan C
AU - Paterson, David L
AU - Roberts, Jason A
AU - Robinson, J Owen
AU - Saito, Hiroki
AU - Scarborough, Matthew
AU - Ten Oever, Jaap
AU - Turner, Rebecca M
AU - Tverring, Jonas
AU - van Hal, Sebastiaan J
AU - Webb, Steve A
AU - Whiteway, Lynda M
AU - Arias, Cesar A
AU - Henderson, Andrew
AU - Heriot, George S
AU - Snelling, Tom L
AU - Afra, Kevin
AU - Ali, Shabinah S
AU - Amit, Sharon
AU - Anagnostou, Nicholas A
AU - Archuleta, Sophia
AU - Aston, Stephen J
AU - Athan, Eugene
AU - Baharav, Nadav
AU - Ten Doesschate, Thijs
AU - van Welzen, Berend J
N1 - Publisher Copyright:
Copyright © 2026 Massachusetts Medical Society.
PY - 2026/6/18
Y1 - 2026/6/18
N2 - BACKGROUND: Staphylococcus aureus bacteremia is associated with high mortality. Whether cefazolin or an antistaphylococcal penicillin should be preferred for the treatment of methicillin-susceptible S. aureus bacteremia is unclear. METHODS: In an ongoing international Bayesian adaptive platform trial, we conducted an open-label, randomized comparison of cefazolin with an antistaphylococcal penicillin (flucloxacillin or cloxacillin) in adult patients with penicillin-resistant, methicillin-susceptible S. aureus bacteremia. The primary outcome, which was evaluated with a hierarchical Bayesian logistic-regression model, was death from any cause within 90 days after enrollment in the platform. We assessed the posterior probability of the noninferiority of cefazolin to flucloxacillin or cloxacillin (with the criterion for noninferiority prespecified as an adjusted odds ratio of <1.2, which approximates an absolute difference in mortality of <2.5 percentage points if mortality in the antistaphylococcal-penicillin group is 15%), as well as the posterior probability of superiority (with the criterion of an adjusted odds ratio of <1.0). Secondary safety outcomes included the development of acute kidney injury within 14 days. RESULTS: This domain of the ongoing trial was conducted between February 17, 2022, and August 7, 2024, by which time the criterion for noninferiority had been met. Mortality at 90 days among adults who could be evaluated was 15.0% (97 deaths among 645 patients) in the cefazolin group and 17.0% (109 deaths among 642 patients) in the antistaphylococcal-penicillin group (adjusted odds ratio, 0.81; 95% credible interval, 0.59 to 1.12; probability of noninferiority, 99.2%; probability of superiority, 89.8%). Acute kidney injury occurred in 92 of 660 patients (13.9%) in the cefazolin group, as compared with 127 of 648 (19.6%) in the antistaphylococcal-penicillin group (adjusted odds ratio, 0.67; 95% credible interval, 0.50 to 0.89; probability of superiority, 99.7%). CONCLUSIONS: In patients with methicillin-susceptible S. aureus bacteremia, cefazolin was noninferior to flucloxacillin or cloxacillin with respect to 90-day mortality and was associated with a lower incidence of acute kidney injury. (Funded by the National Health and Medical Research Council and others; SNAP ClinicalTrials.gov number, NCT05137119.).
AB - BACKGROUND: Staphylococcus aureus bacteremia is associated with high mortality. Whether cefazolin or an antistaphylococcal penicillin should be preferred for the treatment of methicillin-susceptible S. aureus bacteremia is unclear. METHODS: In an ongoing international Bayesian adaptive platform trial, we conducted an open-label, randomized comparison of cefazolin with an antistaphylococcal penicillin (flucloxacillin or cloxacillin) in adult patients with penicillin-resistant, methicillin-susceptible S. aureus bacteremia. The primary outcome, which was evaluated with a hierarchical Bayesian logistic-regression model, was death from any cause within 90 days after enrollment in the platform. We assessed the posterior probability of the noninferiority of cefazolin to flucloxacillin or cloxacillin (with the criterion for noninferiority prespecified as an adjusted odds ratio of <1.2, which approximates an absolute difference in mortality of <2.5 percentage points if mortality in the antistaphylococcal-penicillin group is 15%), as well as the posterior probability of superiority (with the criterion of an adjusted odds ratio of <1.0). Secondary safety outcomes included the development of acute kidney injury within 14 days. RESULTS: This domain of the ongoing trial was conducted between February 17, 2022, and August 7, 2024, by which time the criterion for noninferiority had been met. Mortality at 90 days among adults who could be evaluated was 15.0% (97 deaths among 645 patients) in the cefazolin group and 17.0% (109 deaths among 642 patients) in the antistaphylococcal-penicillin group (adjusted odds ratio, 0.81; 95% credible interval, 0.59 to 1.12; probability of noninferiority, 99.2%; probability of superiority, 89.8%). Acute kidney injury occurred in 92 of 660 patients (13.9%) in the cefazolin group, as compared with 127 of 648 (19.6%) in the antistaphylococcal-penicillin group (adjusted odds ratio, 0.67; 95% credible interval, 0.50 to 0.89; probability of superiority, 99.7%). CONCLUSIONS: In patients with methicillin-susceptible S. aureus bacteremia, cefazolin was noninferior to flucloxacillin or cloxacillin with respect to 90-day mortality and was associated with a lower incidence of acute kidney injury. (Funded by the National Health and Medical Research Council and others; SNAP ClinicalTrials.gov number, NCT05137119.).
KW - Acute Kidney Injury/chemically induced
KW - Aged
KW - Anti-Bacterial Agents/therapeutic use
KW - Bacteremia/drug therapy
KW - Bayes Theorem
KW - Cefazolin/therapeutic use
KW - Cloxacillin/therapeutic use
KW - Female
KW - First Generation Cephalosporins/adverse effects
KW - Floxacillin/therapeutic use
KW - Humans
KW - Incidence
KW - Male
KW - Middle Aged
KW - Staphylococcal Infections/drug therapy
KW - Staphylococcus aureus/drug effects
KW - Treatment Outcome
U2 - 10.1056/NEJMoa2506905
DO - 10.1056/NEJMoa2506905
M3 - Article
C2 - 42308484
SN - 0028-4793
VL - 394
SP - 2329
EP - 2339
JO - The New England journal of medicine
JF - The New England journal of medicine
IS - 23
ER -