Association between β-lactam exposure and clearance of bacteraemia and acute kidney injury in patients with methicillin-resistant Staphylococcus aureus bloodstream infections-a post hoc analysis of the CAMERA2 trial.

Clin Microbiol InfectApr 12, 2026 (epub)

Neta Petersiel, Amy Legg, Sean W X Ong et al.

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In 30 seconds

This post hoc analysis of the CAMERA2 randomized trial examined whether the timing and duration of β-lactam exposure were associated with bacteraemia clearance and acute kidney injury (AKI) in patients with methicillin-resistant Staphylococcus aureus bloodstream infection. Compared with no β-lactam, early, late, and throughout exposure were each associated with faster clearance; adjusted hazard ratios were 1.59 (1.16-2.19), 1.62 (1.14-2.31), and 1.85 (1.36-2.52), respectively. Late and throughout exposure were also associated with higher adjusted odds of AKI, whereas early exposure was not clearly associated with increased AKI.

Key findings

  • Compared with no β-lactam, early exposure was associated with faster bacteraemia clearance (adjusted hazard ratio 1.59 [1.16-2.19]).
  • Late and throughout β-lactam exposure were associated with faster clearance, with adjusted hazard ratios of 1.62 (1.14-2.31) and 1.85 (1.36-2.52), respectively.
  • Adjusted AKI odds were higher with late exposure (OR 6.01 [1.61-29.60]) and throughout exposure (OR 7.93 [2.43-36.30]); early exposure had an OR of 1.24 (0.27-6.60).

Why it matters

The analysis highlights a potential trade-off between microbiological response and renal harm that may depend on β-lactam exposure duration. It also suggests that empiric-period exposure and continued combination treatment should not be assumed to have the same risk profile. These findings can inform interpretation of combination-therapy evidence, while remaining hypothesis-generating because they come from a post hoc analysis.

What to keep in mind

This was a post hoc analysis, and the exposure groups were not randomized comparisons; the associations therefore do not establish that β-lactam duration caused the observed outcomes.

Source

Published in Clin Microbiol Infect. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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