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The antipyretic effectiveness of dipyrone in the intensive care unit: A retrospective cohort study

INTRODUCTION: Dipyrone (metamizol) is regularly used in critical care for pain and fever treatment, especially in Germany and Spain. However, indication for antipyretic therapy in critically ill patients is currently unclear and data for both the risk and benefit of dipyrone treatment in the intensi...

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Autores principales: Gillmann, Hans-Jörg, Reichart, Jessica, Leffler, Andreas, Stueber, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8912151/
https://www.ncbi.nlm.nih.gov/pubmed/35271621
http://dx.doi.org/10.1371/journal.pone.0264440
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author Gillmann, Hans-Jörg
Reichart, Jessica
Leffler, Andreas
Stueber, Thomas
author_facet Gillmann, Hans-Jörg
Reichart, Jessica
Leffler, Andreas
Stueber, Thomas
author_sort Gillmann, Hans-Jörg
collection PubMed
description INTRODUCTION: Dipyrone (metamizol) is regularly used in critical care for pain and fever treatment, especially in Germany and Spain. However, indication for antipyretic therapy in critically ill patients is currently unclear and data for both the risk and benefit of dipyrone treatment in the intensive care environment are scarce. We hypothesized that antipyretic efficiency of dipyrone would not exceed antipyretic efficiency of acetaminophen. We therefore aimed to compare temperature courses in critically ill patients receiving either intravenous dipyrone, acetaminophen or no antipyretic medication. MATERIAL AND METHODS: We included 937 intensive care unit (ICU) patients with body temperature recordings of at least 37.5°C. We investigated temperature decrease associated with dipyrone or acetaminophen and additionally compared it to an untreated control group. RESULTS: Within the eight-hour study interval, maximum body temperature decrease in patients without antipyretic medication was -0.6°C (IQR: -1.0 to -0.4°C; n = 315). Maximal decrease in body temperature was higher both with dipyrone (-0.8°C (IQR: -1.2 to -0.4°C); p = 0.016; n = 341) and acetaminophen (-0.9°C (IQR: -1.6 to -0.6°C); p<0.001; n = 71), but did not differ between dipyrone and acetaminophen (p = 0.066). As compared to untreated patients, dipyrone only led to a marginal additional decrease in body temperature of only -0.1°C. Maximum of antipyretic effectiveness was reached four hours after administration. CONCLUSION: Antipyretic effectiveness of dipyrone in ICU patients may be overestimated. Given the lack of prospective data, clinical evidence for antipyretic dipyrone therapy in the ICU is insufficient and warrants further critical evaluation.
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spelling pubmed-89121512022-03-11 The antipyretic effectiveness of dipyrone in the intensive care unit: A retrospective cohort study Gillmann, Hans-Jörg Reichart, Jessica Leffler, Andreas Stueber, Thomas PLoS One Research Article INTRODUCTION: Dipyrone (metamizol) is regularly used in critical care for pain and fever treatment, especially in Germany and Spain. However, indication for antipyretic therapy in critically ill patients is currently unclear and data for both the risk and benefit of dipyrone treatment in the intensive care environment are scarce. We hypothesized that antipyretic efficiency of dipyrone would not exceed antipyretic efficiency of acetaminophen. We therefore aimed to compare temperature courses in critically ill patients receiving either intravenous dipyrone, acetaminophen or no antipyretic medication. MATERIAL AND METHODS: We included 937 intensive care unit (ICU) patients with body temperature recordings of at least 37.5°C. We investigated temperature decrease associated with dipyrone or acetaminophen and additionally compared it to an untreated control group. RESULTS: Within the eight-hour study interval, maximum body temperature decrease in patients without antipyretic medication was -0.6°C (IQR: -1.0 to -0.4°C; n = 315). Maximal decrease in body temperature was higher both with dipyrone (-0.8°C (IQR: -1.2 to -0.4°C); p = 0.016; n = 341) and acetaminophen (-0.9°C (IQR: -1.6 to -0.6°C); p<0.001; n = 71), but did not differ between dipyrone and acetaminophen (p = 0.066). As compared to untreated patients, dipyrone only led to a marginal additional decrease in body temperature of only -0.1°C. Maximum of antipyretic effectiveness was reached four hours after administration. CONCLUSION: Antipyretic effectiveness of dipyrone in ICU patients may be overestimated. Given the lack of prospective data, clinical evidence for antipyretic dipyrone therapy in the ICU is insufficient and warrants further critical evaluation. Public Library of Science 2022-03-10 /pmc/articles/PMC8912151/ /pubmed/35271621 http://dx.doi.org/10.1371/journal.pone.0264440 Text en © 2022 Gillmann et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Gillmann, Hans-Jörg
Reichart, Jessica
Leffler, Andreas
Stueber, Thomas
The antipyretic effectiveness of dipyrone in the intensive care unit: A retrospective cohort study
title The antipyretic effectiveness of dipyrone in the intensive care unit: A retrospective cohort study
title_full The antipyretic effectiveness of dipyrone in the intensive care unit: A retrospective cohort study
title_fullStr The antipyretic effectiveness of dipyrone in the intensive care unit: A retrospective cohort study
title_full_unstemmed The antipyretic effectiveness of dipyrone in the intensive care unit: A retrospective cohort study
title_short The antipyretic effectiveness of dipyrone in the intensive care unit: A retrospective cohort study
title_sort antipyretic effectiveness of dipyrone in the intensive care unit: a retrospective cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8912151/
https://www.ncbi.nlm.nih.gov/pubmed/35271621
http://dx.doi.org/10.1371/journal.pone.0264440
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