Evidence map›Paper›PMID 39652885›Full record

Trial reportJAMA2025

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

Paul Dark, Anower Hossain, Daniel F McAuley, David Brealey, Gordon Carlson, Jonathan C Clayton, Timothy W Felton, Belinder K Ghuman, Anthony C Gordon, Thomas P Hellyer and 23 more

Erratum issuedAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 60 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

60 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Efficacy and Safety of Procalcitonin-Guided Antibiotic Therapy versus Standard of Care for Sepsis: A Systematic Review and Meta-Analysis.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2026
    Pooled it
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  17. What's Hot This Year in ID Clinical Science 2025.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

33 authors.

Paul DarkDivision of Immunology, Immunity to Infection and Respiratory Medicine, University of Manchester, Critical Care Unit, Northern Care Alliance NHS Foundation Trust, Salford Care Organization, Greater Manchester, United Kingdom.
Anower HossainWarwick Medical School, Clinical Trials Unit, University of Warwick, Coventry, United Kingdom.
Daniel F McAuleyWellcome Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Sciences, Queens University Belfast, Belfast, United Kingdom.
David BrealeyUniversity College London Hospitals NHS Foundation Trust, United Kingdom.
Gordon CarlsonNational Intestinal Failure Centre, Northern Care Alliance NHS Foundation Trust, Salford Care Organization, Greater Manchester, United Kingdom.
Jonathan C ClaytonDepartment of Clinical Biochemistry, Lancashire Teaching Hospitals NHS Foundation Trust, Sharoe Green Lane, Fulwood, Preston Lancashire, United Kingdom.
Timothy W FeltonRespiratory Academic Group, Division of Immunology, Immunity to Infection and Respiratory Medicine, University of Manchester, Wythenshawe Hospital, Manchester, United Kingdom.
Belinder K GhumanWarwick Medical School, Clinical Trials Unit, University of Warwick, Coventry, United Kingdom.
Anthony C GordonDivision of Anaesthetics, Pain Medicine and Intensive Care, Faculty of Medicine, Imperial College London, London, United Kingdom.
Thomas P HellyerNewcastle upon Tyne Hospitals NHS Foundation Trust, United Kingdom.
Nazir I LoneAnaesthesia, Critical Care and Pain Medicine, Usher Institute, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh Royal Infirmary, Edinburgh, United Kingdom.
Uzma ManazarWarwick Medical School, Clinical Trials Unit, University of Warwick, Coventry, United Kingdom.
Gillian RichardsWarwick Medical School, Clinical Trials Unit, University of Warwick, Coventry, United Kingdom.
Iain J McCullaghNewcastle upon Tyne Hospitals NHS Foundation Trust, United Kingdom.
Ronan McMullanWellcome Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Sciences, Queens University Belfast, Belfast, United Kingdom.
James J McNameeRoyal Victoria Hospital Belfast, Belfast, United Kingdom.
Hannah C McNeilWarwick Medical School, Clinical Trials Unit, University of Warwick, Coventry, United Kingdom.
Paul R MounceyClinical Trials Unit, Intensive Care National Audit and Research Centre, Napier House, London, United Kingdom.
Micheal J NaisbittSalford Royal Hospital, Manchester, United Kingdom.
Robert J ParkerLiverpool University NHS Foundation Trust, Aintree University Hospital, Liverpool, United Kingdom.
Ruth L PooleCEDAR, Cardiff and Vale University Health Board, Wales, United Kingdom.
Anthony J RostronUniversity of Newcastle, Newcastle Upon Tyne, United Kingdom.
Mervyn SingerCentre for Intensive Care Medicine, Experimental and Translational Medicine, Division of Medicine, Faculty of Medical Sciences, University College London, London, United Kingdom.
Matt D StevensonSheffield Centre for Health and Related Research, Regent Court, Sheffield, United Kingdom.
Tim S WalshAnaesthesia, Critical Care and Pain Medicine, Usher Institute, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh Royal Infirmary, Edinburgh, United Kingdom.
Ingeborg D WeltersRoyal Liverpool University Hospital, Liverpool, United Kingdom.
Tony WhitehouseInstitute of Inflammation and Ageing, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, Birmingham, United Kingdom.
Simon WhiteleySt James's University Hospital, Leeds, United Kingdom.
Peter WilsonClinical Microbiology, University College London Hospitals NHS Foundation Trust, London, United Kingdom.
Keith K YoungWarwick Medical School, Clinical Trials Unit, University of Warwick, Coventry, United Kingdom.
Gavin D PerkinsWarwick Medical School, Clinical Trials Unit, University of Warwick, Coventry, United Kingdom.
Ranjit LallWarwick Medical School, Clinical Trials Unit, University of Warwick, Coventry, United Kingdom.
ADAPT-Sepsis Collaborators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: For hospitalized critically ill adults with suspected sepsis, procalcitonin (PCT) and C-reactive protein (CRP) monitoring protocols can guide the duration of antibiotic therapy, but the evidence of the effect and safety of these protocols remains uncertain. Objective: To determine whether decisions based on assessment of CRP or PCT safely results in a reduction in the duration of antibiotic therapy. Design, Setting, and Participants: A multicenter, intervention-concealed randomized clinical trial, involving 2760 adults (≥18 years), in 41 UK National Health Service (NHS) intensive care units, requiring critical care within 24 hours of initiating intravenous antibiotics for suspected sepsis and likely to continue antibiotics for at least 72 hours. Intervention: From January 1, 2018, to June 5, 2024, 918 patients were assigned to the daily PCT-guided protocol, 924 to the daily CRP-guided protocol, and 918 assigned to standard care. Main Outcomes and Measures: The primary outcomes were total duration of antibiotics (effectiveness) and all-cause mortality (safety) to 28 days. Secondary outcomes included critical care unit data and hospital stay data. Ninety-day all-cause mortality was also collected. Results: Among the randomized patients (mean age 60.2 [SD, 15.4] years; 60.3% males), there was a significant reduction in antibiotic duration from randomization to 28 days for those in the daily PCT-guided protocol compared with standard care (mean duration, 10.7 [SD, 7.6] days for standard care and 9.8 [SD, 7.2] days for PCT; mean difference, 0.88 days; 95% CI, 0.19 to 1.58, P = .01). For all-cause mortality up to 28 days, the daily PCT-guided protocol was noninferior to standard care, where the noninferiority margin was set at 5.4% (19.4% [170 of 878] of patients receiving standard care; 20.9% [184 of 879], PCT; absolute difference, 1.57; 95% CI, -2.18 to 5.32; P = .02). No difference was found in antibiotic duration for standard care vs daily CRP-guided protocol (mean duration, 10.6 [7.7] days for CRP; mean difference, 0.09; 95% CI, -0.60 to 0.79; P = .79). For all-cause mortality, the daily CRP-guided protocol was inconclusive compared with standard care (21.1% [184 of 874] for CRP; absolute difference, 1.69; 95% CI, -2.07 to 5.45; P = .03). Conclusions and Relevance: 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. Trial Registration: isrctn.org Identifier: ISRCTN47473244.

Indexed as

Anti-Bacterial AgentsC-Reactive ProteinProcalcitoninSepsisAdministration, IntravenousAdultAgedBiomarkersCritical IllnessDuration of TherapyFemaleHumansIntensive Care UnitsLength of StayMaleMiddle AgedAnti-Bacterial AgentsBiomarkersC-Reactive ProteinProcalcitonin

Identifiers

PMID39652885
PMCPMC11862976

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.