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Effect of different corticosteroid regimes for hospitalised patients with exacerbated COPD: pooled analysis of individual participant data from the REDUCE and CORTICO-COP trials
BACKGROUND: Systemic corticosteroid administration for severe acute exacerbations of COPD (AECOPD) reduces the duration of hospital stays. Corticosteroid-sparing regimens have showed non-inferiority to higher accumulated dose regimens regarding re-exacerbation risk in patients with AECOPD. However,...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138920/ https://www.ncbi.nlm.nih.gov/pubmed/34020641 http://dx.doi.org/10.1186/s12931-021-01745-5 |
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author | Sivapalan, Pradeesh Rutishauser, Jonas Ulrik, Charlotte Suppli Leuppi, Jörg D. Pedersen, Lars Mueller, Beat Eklöf, Josefin Biering-Sørensen, Tor Gottlieb, Vibeke Armbruster, Karin Janner, Julie Moberg, Mia Lapperre, Therese S. Nielsen, Thyge L. Browatzki, Andrea Mathioudakis, Alexander Vestbo, Jørgen Schüetz, Philipp Jensen, Jens-Ulrik |
author_facet | Sivapalan, Pradeesh Rutishauser, Jonas Ulrik, Charlotte Suppli Leuppi, Jörg D. Pedersen, Lars Mueller, Beat Eklöf, Josefin Biering-Sørensen, Tor Gottlieb, Vibeke Armbruster, Karin Janner, Julie Moberg, Mia Lapperre, Therese S. Nielsen, Thyge L. Browatzki, Andrea Mathioudakis, Alexander Vestbo, Jørgen Schüetz, Philipp Jensen, Jens-Ulrik |
author_sort | Sivapalan, Pradeesh |
collection | PubMed |
description | BACKGROUND: Systemic corticosteroid administration for severe acute exacerbations of COPD (AECOPD) reduces the duration of hospital stays. Corticosteroid-sparing regimens have showed non-inferiority to higher accumulated dose regimens regarding re-exacerbation risk in patients with AECOPD. However, it remains unclear whether 14-day or 2–5-day regimens would result in shorter admission durations and changes in mortality risk. We explored this by analysing the number of days alive and out of hospital based on two randomised controlled trials with different corticosteroid regimens. METHODS: We pooled individual patient data from the two available multicentre randomised trials on corticosteroid-sparing regimens for AECOPD: the REDUCE (n = 314) and CORTICO-COP (n = 318) trials. In the 14-day regimen group, patients were older, fewer patients received pre-treatment with antibiotics and more patients received pre-treatment with systemic corticosteroids. Patients randomly allocated to the 14-day and 2–5-day regimens were compared, with adjustment for baseline differences. RESULTS: The number of days alive and out of hospital within 14 days from recruitment was higher for the 2–5 day regimen group (mean 8.4 days; 95% confidence interval [CI] 8.0–8.8) than the 14-day regimen patient group (4.2 days; 95% CI3.4–4.9; p < 0.001). The 14-day AECOPD group had longer hospital stays (mean difference, 5.4 days [standard error ± 0.6]; p < 0.0001) and decreased likelihood of discharge within 30 days (hazard ratio [HR] 0.5; 95% CI 0.4–0.6; p < 0.0001). Comparing the 14-day regimen and the 2–5 day regimen group showed no differences in the composite endpoint ‘death or ICU admission’ (odds ratio [OR] 1.4; 95% CI 0.8–2.3; p = 0.15), new or aggravated hypertension (OR 1.5; 95% CI 0.9–2.7; p = 0.15), or mortality risk (HR 0.8; 95% CI 0.4–1.5; p = 0.45) during the 6-month follow-up period. CONCLUSION: 14-day corticosteroid regimens were associated with longer hospital stays and fewer days alive and out of hospital within 14 days, with no apparent 6-month benefit regarding death or admission to ICU in COPD patients. Our results favour 2–5 day regimens for treating COPD exacerbations. However, prospective studies are needed to validate these findings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-021-01745-5. |
format | Online Article Text |
id | pubmed-8138920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81389202021-05-21 Effect of different corticosteroid regimes for hospitalised patients with exacerbated COPD: pooled analysis of individual participant data from the REDUCE and CORTICO-COP trials Sivapalan, Pradeesh Rutishauser, Jonas Ulrik, Charlotte Suppli Leuppi, Jörg D. Pedersen, Lars Mueller, Beat Eklöf, Josefin Biering-Sørensen, Tor Gottlieb, Vibeke Armbruster, Karin Janner, Julie Moberg, Mia Lapperre, Therese S. Nielsen, Thyge L. Browatzki, Andrea Mathioudakis, Alexander Vestbo, Jørgen Schüetz, Philipp Jensen, Jens-Ulrik Respir Res Research BACKGROUND: Systemic corticosteroid administration for severe acute exacerbations of COPD (AECOPD) reduces the duration of hospital stays. Corticosteroid-sparing regimens have showed non-inferiority to higher accumulated dose regimens regarding re-exacerbation risk in patients with AECOPD. However, it remains unclear whether 14-day or 2–5-day regimens would result in shorter admission durations and changes in mortality risk. We explored this by analysing the number of days alive and out of hospital based on two randomised controlled trials with different corticosteroid regimens. METHODS: We pooled individual patient data from the two available multicentre randomised trials on corticosteroid-sparing regimens for AECOPD: the REDUCE (n = 314) and CORTICO-COP (n = 318) trials. In the 14-day regimen group, patients were older, fewer patients received pre-treatment with antibiotics and more patients received pre-treatment with systemic corticosteroids. Patients randomly allocated to the 14-day and 2–5-day regimens were compared, with adjustment for baseline differences. RESULTS: The number of days alive and out of hospital within 14 days from recruitment was higher for the 2–5 day regimen group (mean 8.4 days; 95% confidence interval [CI] 8.0–8.8) than the 14-day regimen patient group (4.2 days; 95% CI3.4–4.9; p < 0.001). The 14-day AECOPD group had longer hospital stays (mean difference, 5.4 days [standard error ± 0.6]; p < 0.0001) and decreased likelihood of discharge within 30 days (hazard ratio [HR] 0.5; 95% CI 0.4–0.6; p < 0.0001). Comparing the 14-day regimen and the 2–5 day regimen group showed no differences in the composite endpoint ‘death or ICU admission’ (odds ratio [OR] 1.4; 95% CI 0.8–2.3; p = 0.15), new or aggravated hypertension (OR 1.5; 95% CI 0.9–2.7; p = 0.15), or mortality risk (HR 0.8; 95% CI 0.4–1.5; p = 0.45) during the 6-month follow-up period. CONCLUSION: 14-day corticosteroid regimens were associated with longer hospital stays and fewer days alive and out of hospital within 14 days, with no apparent 6-month benefit regarding death or admission to ICU in COPD patients. Our results favour 2–5 day regimens for treating COPD exacerbations. However, prospective studies are needed to validate these findings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-021-01745-5. BioMed Central 2021-05-21 2021 /pmc/articles/PMC8138920/ /pubmed/34020641 http://dx.doi.org/10.1186/s12931-021-01745-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Sivapalan, Pradeesh Rutishauser, Jonas Ulrik, Charlotte Suppli Leuppi, Jörg D. Pedersen, Lars Mueller, Beat Eklöf, Josefin Biering-Sørensen, Tor Gottlieb, Vibeke Armbruster, Karin Janner, Julie Moberg, Mia Lapperre, Therese S. Nielsen, Thyge L. Browatzki, Andrea Mathioudakis, Alexander Vestbo, Jørgen Schüetz, Philipp Jensen, Jens-Ulrik Effect of different corticosteroid regimes for hospitalised patients with exacerbated COPD: pooled analysis of individual participant data from the REDUCE and CORTICO-COP trials |
title | Effect of different corticosteroid regimes for hospitalised patients with exacerbated COPD: pooled analysis of individual participant data from the REDUCE and CORTICO-COP trials |
title_full | Effect of different corticosteroid regimes for hospitalised patients with exacerbated COPD: pooled analysis of individual participant data from the REDUCE and CORTICO-COP trials |
title_fullStr | Effect of different corticosteroid regimes for hospitalised patients with exacerbated COPD: pooled analysis of individual participant data from the REDUCE and CORTICO-COP trials |
title_full_unstemmed | Effect of different corticosteroid regimes for hospitalised patients with exacerbated COPD: pooled analysis of individual participant data from the REDUCE and CORTICO-COP trials |
title_short | Effect of different corticosteroid regimes for hospitalised patients with exacerbated COPD: pooled analysis of individual participant data from the REDUCE and CORTICO-COP trials |
title_sort | effect of different corticosteroid regimes for hospitalised patients with exacerbated copd: pooled analysis of individual participant data from the reduce and cortico-cop trials |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138920/ https://www.ncbi.nlm.nih.gov/pubmed/34020641 http://dx.doi.org/10.1186/s12931-021-01745-5 |
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