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Sepsis & septic shock · Duration of antibiotic therapy

ADAPT-Sepsis randomised trial

Biomarker-Guided Antibiotic Duration for Hospitalized Patients With Suspected Sepsis

ADAPT-Sepsis trial design and results
Design Multicentre randomised clinical trial
Treatment Daily procalcitonin-guided or C-reactive protein-guided antibiotic discontinuation protocol
Control Standard care
Population Hospitalised patients with suspected sepsis, mean age 60.2, 60.3% male
Follow-up 28 days
Primary endpoint Total antibiotic duration and 28-day all-cause mortality
Result A daily procalcitonin-guided protocol significantly reduced total antibiotic duration from randomisation to day 28 compared with standard care, without evidence of harm on mortality.
Secondary endpoints 28-day all-cause mortality, ICU and hospital length of stay, adverse events

Care guided by measurement of PCT reduces antibiotic duration safely compared with standard care, but CRP does not. All-cause mortality for CRP was inconclusive.

The trial authors, in the published abstract

How it has aged

Biomarker-guided stopping has a long history of small positive trials and limited uptake. Whether procalcitonin adds anything to simply stopping at seven days, as BALANCE supports, is the question this design cannot answer.

Publications

Biomarker-Guided Antibiotic Duration for Hospitalized Patients With Suspected Sepsis: The ADAPT-Sepsis Randomized Clinical Trial

Dark P, Hossain A, McAuley DF, et al. Biomarker-Guided Antibiotic Duration for Hospitalized Patients With Suspected Sepsis: The ADAPT-Sepsis Randomized Clinical Trial. JAMA 2025 Feb 25;333(8):682-693.

  • Significant reduction in total antibiotic duration
  • No signal of harm in 28-day mortality