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Permissive versus restrictive temperature thresholds in critically ill children with fever and infection: a multicentre randomized clinical pilot trial
BACKGROUND: Fever 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 cu...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407208/ https://www.ncbi.nlm.nih.gov/pubmed/30845977 http://dx.doi.org/10.1186/s13054-019-2354-4 |
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author | Peters, Mark J. Woolfall, Kerry Khan, Imran Deja, Elisabeth Mouncey, Paul R. Wulff, Jerome Mason, Alexina Agbeko, Rachel S. Draper, Elizabeth S. Fenn, Blaise Gould, Doug W. Koelewyn, Abby Klein, Nigel Mackerness, Christine Martin, Sian O’Neill, Lauran Ray, Samiran Ramnarayan, Padmanabhan Tibby, Shane Thorburn, Kentigern Tume, Lyvonne Watkins, Jason Wellman, Paul Harrison, David A. Rowan, Kathryn M. |
author_facet | Peters, Mark J. Woolfall, Kerry Khan, Imran Deja, Elisabeth Mouncey, Paul R. Wulff, Jerome Mason, Alexina Agbeko, Rachel S. Draper, Elizabeth S. Fenn, Blaise Gould, Doug W. Koelewyn, Abby Klein, Nigel Mackerness, Christine Martin, Sian O’Neill, Lauran Ray, Samiran Ramnarayan, Padmanabhan Tibby, Shane Thorburn, Kentigern Tume, Lyvonne Watkins, Jason Wellman, Paul Harrison, David A. Rowan, Kathryn M. |
author_sort | Peters, Mark J. |
collection | PubMed |
description | BACKGROUND: Fever 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. METHODS: An 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. RESULTS: One 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. CONCLUSION: Uncertainty 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 REGISTRATION: ISRCTN16022198. Registered on 14 August 2017. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-019-2354-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6407208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64072082019-03-21 Permissive versus restrictive temperature thresholds in critically ill children with fever and infection: a multicentre randomized clinical pilot trial Peters, Mark J. Woolfall, Kerry Khan, Imran Deja, Elisabeth Mouncey, Paul R. Wulff, Jerome Mason, Alexina Agbeko, Rachel S. Draper, Elizabeth S. Fenn, Blaise Gould, Doug W. Koelewyn, Abby Klein, Nigel Mackerness, Christine Martin, Sian O’Neill, Lauran Ray, Samiran Ramnarayan, Padmanabhan Tibby, Shane Thorburn, Kentigern Tume, Lyvonne Watkins, Jason Wellman, Paul Harrison, David A. Rowan, Kathryn M. Crit Care Research BACKGROUND: Fever 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. METHODS: An 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. RESULTS: One 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. CONCLUSION: Uncertainty 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 REGISTRATION: ISRCTN16022198. Registered on 14 August 2017. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-019-2354-4) contains supplementary material, which is available to authorized users. BioMed Central 2019-03-07 /pmc/articles/PMC6407208/ /pubmed/30845977 http://dx.doi.org/10.1186/s13054-019-2354-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Peters, Mark J. Woolfall, Kerry Khan, Imran Deja, Elisabeth Mouncey, Paul R. Wulff, Jerome Mason, Alexina Agbeko, Rachel S. Draper, Elizabeth S. Fenn, Blaise Gould, Doug W. Koelewyn, Abby Klein, Nigel Mackerness, Christine Martin, Sian O’Neill, Lauran Ray, Samiran Ramnarayan, Padmanabhan Tibby, Shane Thorburn, Kentigern Tume, Lyvonne Watkins, Jason Wellman, Paul Harrison, David A. Rowan, Kathryn M. Permissive versus restrictive temperature thresholds in critically ill children with fever and infection: a multicentre randomized clinical pilot trial |
title | Permissive versus restrictive temperature thresholds in critically ill children with fever and infection: a multicentre randomized clinical pilot trial |
title_full | Permissive versus restrictive temperature thresholds in critically ill children with fever and infection: a multicentre randomized clinical pilot trial |
title_fullStr | Permissive versus restrictive temperature thresholds in critically ill children with fever and infection: a multicentre randomized clinical pilot trial |
title_full_unstemmed | Permissive versus restrictive temperature thresholds in critically ill children with fever and infection: a multicentre randomized clinical pilot trial |
title_short | Permissive versus restrictive temperature thresholds in critically ill children with fever and infection: a multicentre randomized clinical pilot trial |
title_sort | permissive versus restrictive temperature thresholds in critically ill children with fever and infection: a multicentre randomized clinical pilot trial |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407208/ https://www.ncbi.nlm.nih.gov/pubmed/30845977 http://dx.doi.org/10.1186/s13054-019-2354-4 |
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