Evidence map›Paper›PMID 30845977›Full record

Trial reportCritical care (London, England)2019

Permissive versus restrictive temperature thresholds in critically ill children with fever and infection: a multicentre randomized clinical pilot trial.

Mark J Peters, Kerry Woolfall, Imran Khan, Elisabeth Deja, Paul R Mouncey, Jerome Wulff, Alexina Mason, Rachel S Agbeko, Elizabeth S Draper, Blaise Fenn and 16 more

Open access · goldAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Critical care (London, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 10% of its field
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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 citations in OpenAlex.

  1. Pooled it
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  6. Nursing management decisions in fever: a mixed-methods approach to understanding.International journal of nursing studies advances · 2026
    Article
  7. Protocolized Evaluation of Permissive Blood Pressure Targets Versus Usual Care (PRESSURE): Statistical Analysis Plan for the PRESSURE Trial.Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies · 2026
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors at 8 institutions in 2 countries.

Mark J PetersRespiratory, Critical Care and Anaesthesia Unit, Paediatric Intensive Care, UCL Great Ormond Street Institute of Child Health, 30 Guildford Street, London, WC1N 1EH, UK. mark.peters@ucl.ac.uk.ORCID 0000-0003-3653-4808
Kerry WoolfallDepartment of Psychological Sciences, North West Hub for Trials Methodology, University of Liverpool, Liverpool, UK.
Imran KhanClinical Trials Unit, Intensive Care National Audit and Research Centre, London, UK.
Elisabeth DejaDepartment of Psychological Sciences, North West Hub for Trials Methodology, University of Liverpool, Liverpool, UK.
Paul R MounceyClinical Trials Unit, Intensive Care National Audit and Research Centre, London, UK.
Jerome WulffClinical Trials Unit, Intensive Care National Audit and Research Centre, London, UK.
Alexina MasonClinical Trials Unit, Intensive Care National Audit and Research Centre, London, UK.
Rachel S AgbekoNHS Foundation Trust, Newcastle, UK.
Elizabeth S DraperDepartment of Health Sciences, University of Leicester, Leicester, UK.
Blaise FennPatient and Parent representative, London, UK.
Doug W GouldClinical Trials Unit, Intensive Care National Audit and Research Centre, London, UK.
Abby KoelewynClinical Trials Unit, Intensive Care National Audit and Research Centre, London, UK.
Nigel KleinInfection, Inflammation and Rheumatology, UCL Great Ormond Street Institute of Child Health, London, UK.
Christine MackernessNHS Foundation Trust, Newcastle, UK.
Sian MartinClinical Trials Unit, Intensive Care National Audit and Research Centre, London, UK.
Lauran O'NeillPaediatric Intensive Care Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Samiran RayRespiratory, Critical Care and Anaesthesia Unit, Paediatric Intensive Care, UCL Great Ormond Street Institute of Child Health, 30 Guildford Street, London, WC1N 1EH, UK.
Padmanabhan RamnarayanRespiratory, Critical Care and Anaesthesia Unit, Paediatric Intensive Care, UCL Great Ormond Street Institute of Child Health, 30 Guildford Street, London, WC1N 1EH, UK.
Shane TibbyEvelina Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Kentigern ThorburnAlder Hey Children's Hospital NHS Foundation Trust, Liverpool, UK.
Lyvonne TumeFaculty of Health and Applied Sciences, University of the West of England, Glenside Campus, Bristol, UK.
Jason WatkinsInstitute of Cellular Medicine, Newcastle University, Newcastle, UK.
Paul WellmanEvelina Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, London, UK.
David A HarrisonClinical Trials Unit, Intensive Care National Audit and Research Centre, London, UK.
Kathryn M RowanClinical Trials Unit, Intensive Care National Audit and Research Centre, London, UK.
FEVER Investigators on behalf of the Paediatric Intensive Care Society Study Group (PICS-SG)
Intensive Care National Audit & Research Centre · GBUniversity of Liverpool · GBGreat Ormond Street Hospital · GBGuy's and St Thomas' NHS Foundation Trust · GBGreat Ormond Street Hospital for Children NHS Foundation Trust · GBNewcastle upon Tyne Hospitals NHS Foundation Trust · GBUniversity of Leicester · GBUniversity of the West of England · GB

Funding

Department of Health HTA/15/44/01Health Technology Assessment Programme 15/44/01
6 · The paper itself

Abstract

backgroundFever improves pathogen control at a significant metabolic cost. No randomized clinical trials (RCT) have compared fever treatment thresholds in critically ill children. We performed a pilot RCT to determine whether a definitive trial of a permissive approach to fever in comparison to current restrictive practice is feasible in critically ill children with suspected infection.

methodsAn open, parallel-group pilot RCT with embedded mixed methods perspectives study in four UK paediatric intensive care units (PICUs) and associated retrieval services. Participants were emergency PICU admissions aged > 28 days to < 16 years receiving respiratory support and supplemental oxygen. Subjects were randomly assigned to permissive (antipyretic interventions only at ≥ 39.5 °C) or restrictive groups (antipyretic interventions at ≥ 37.5 °C) whilst on respiratory support. Parents were invited to complete a questionnaire or take part in an interview. Focus groups were conducted with staff at each unit. Outcomes were measures of feasibility: recruitment rate, protocol adherence and acceptability, between group separation of temperature and safety.

resultsOne hundred thirty-eight children met eligibility criteria of whom 100 (72%) were randomized (11.1 patients per month per site) without prior consent (RWPC). Consent to continue in the trial was obtained in 87 cases (87%). The mean maximum temperature (95% confidence interval) over the first 48 h was 38.4 °C (38.2-38.6) in the restrictive group and 38.8 °C (38.6-39.1) in the permissive group, a mean difference of 0.5 °C (0.2-0.8). Protocol deviations were observed in 6.8% (99/1438) of 6-h time periods and largely related to patient comfort in the recovery phase. Length of stay, duration of organ support and mortality were similar between groups. No pre-specified serious adverse events occurred. Staff (n = 48) and parents (n = 60) were supportive of the trial, including RWPC. Suggestions were made to only include invasively ventilated children for the duration of intubation.

conclusionUncertainty around the optimal fever threshold for antipyretic intervention is relevant to many emergency PICU admissions. A more permissive approach was associated with a modest increase in mean maximum temperature. A definitive trial should focus on the most seriously ill cases in whom antipyretics are rarely used for their analgesic effects alone.

trial registrationISRCTN16022198 . Registered on 14 August 2017.

Indexed as

Threshold Limit ValuesTreatment OutcomeChildChild, PreschoolCritical IllnessFemaleFeverFocus GroupsHumansInfantInfectionsIntensive Care Units, PediatricMalePilot ProjectsSurveys and QuestionnairesUnited KingdomAntipyreticsClinical trialFeverInfectionPaediatric intensive careParacetamolSepsis

Identifiers

PMID30845977
PMCPMC6407208
OpenAlexW2923151879

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.