Observational studyCritical care (London, England)2025
Mortality and antibiotic timing in deep learning-derived surviving sepsis campaign risk groups: a multicenter study.
Observational study in Critical care (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Nanomaterial-nucleic acid probe synergy: accelerating rapid pathogen detection and antimicrobial susceptibility testing in bloodstream infections.Folia microbiologica · 2026Review
- Integrating Precision Sepsis Risk Stratification Into Systems-Based Antimicrobial Stewardship.Open forum infectious diseases · 2026Article
- Sepsis, Patient Monitoring and Nursing Research.Journal of multidisciplinary healthcare · 2026Article
- Immunometabolic Reprogramming in Experimental Sepsis: A Driver of Multiple Organ Dysfunction Syndrome.Journal of inflammation research · 2026Review
- Artificial intelligence-assisted phenotyping of sepsis: Research progress, clinical challenges, and translational prospects.Digital healthReview
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9 authors.
Funding
Abstract
backgroundThe current Surviving Sepsis Campaign (SSC) guidelines provide recommendations on timing of administering antibiotics in sepsis patients based on probability of sepsis and presence of shock. However, there have been minimal efforts to stratify patients objectively into these groups and describe patient outcomes as a function of antibiotic timing recommendations based on risk stratification using this approach.
methodsWe conducted an observational cohort study using prospectively applied patient data from two large health systems using patient encounters between 2016 and 2024. At the time of clinical suspicion of sepsis, two deep learning (DL) models were used to stratify patients objectively into groups analogous to the SSC risk groups, based on a patient's likelihood of having sepsis and likelihood of developing shock. These risk groups were: (1) shock likely to develop and sepsis probable, (2) shock likely to develop and sepsis possible, (3) shock unlikely to develop and sepsis probable, and (4) shock unlikely to develop and sepsis possible. The primary outcome was short-term mortality, a composite of in-hospital mortality and transition to hospice care, across each risk group.
resultsWe identified 34,087 adult patients with potential sepsis. At the development site, risk group mortality rates (%) and median time to antibiotics [IQR] were as follows: (1) 23.2%, 1.7 [1.0-3.1] hours; (2) 17.7%, 3.0 [1.7-6.2] hours; (3) 5.0%, 2.8 [1.5-5.1] hours; and (4) 1.9%, 4.6 [2.7-8.0] hours. Results from the validation site were similar. Mortality rates were similar for patients with possible sepsis unlikely to develop shock regardless of antibiotic administration within 1, 3 or more hours from triage. For patients with probable sepsis at the development site, regardless of risk of shock, mortality was significantly lower if antibiotics were administered within the first hour from triage.
conclusionsOur data suggest that patients who are at low risk of developing shock and possible sepsis had similar rates of mortality in the 1-hour vs. > 1-hour and 3-hour vs. > 3-hour time to antibiotic administration groups. Thus, a more lenient time to antibiotic administration could allow for more detailed evaluations and judicious administration of antibiotics without impacting patient mortality. Patients with probable sepsis had lower mortality if antibiotics were administered within 1 h from triage, regardless of risk of shock. Additional prospective studies are required to validate these findings and guide optimal antibiotic timing in patients with suspected sepsis.
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