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Therapeutic plasma exchange in patients with sepsis: Secondary analysis of a cluster‐randomized controlled trial
INTRODUCTION: Sepsis is life‐threatening organ dysfunction caused by infection‐related inflammatory response. Therapeutic plasma exchange (TPE) can remove inflammatory mediators and benefit patients in different disease settings. However, no solid evidence showed the efficacy and safety of TPE in se...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092885/ https://www.ncbi.nlm.nih.gov/pubmed/36314372 http://dx.doi.org/10.1002/jca.22027 |
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author | Luo, Xiang Li, Xiaoling Lai, Xiaoyan Ke, Lu Zhou, Jing Liu, Man Cao, Longxiang Fu, Lingyan |
author_facet | Luo, Xiang Li, Xiaoling Lai, Xiaoyan Ke, Lu Zhou, Jing Liu, Man Cao, Longxiang Fu, Lingyan |
author_sort | Luo, Xiang |
collection | PubMed |
description | INTRODUCTION: Sepsis is life‐threatening organ dysfunction caused by infection‐related inflammatory response. Therapeutic plasma exchange (TPE) can remove inflammatory mediators and benefit patients in different disease settings. However, no solid evidence showed the efficacy and safety of TPE in sepsis. METHODS: This study was a secondary analysis of a randomized controlled trial. Critically ill patients with sepsis were divided into two groups according to whether treated with TPE. The primary outcome was the delta Sequential Organ Failure Assessment (SOFA) score from days 1 to 7. Secondary outcomes included new‐onset organ failure, intensive care unit (ICU)‐free and alive days to day 28, and 28‐day mortality. Propensity score‐matched (PSM) analysis was applied to control confounders. Analysis of covariance (ANCOVA) and logistic regression were used to assess the association between TPE and selected outcomes. RESULTS: Among the 2772 critically ill patients enrolled in the trial, 742 patients with sepsis were selected and 22 patients received TPE were matched with 22 control patients. No significant difference was found in the delta SOFA score and 28‐day mortality between TPE group and control group. The ICU‐free and alive days in the TPE group were significantly shorter than the control group. CONCLUSIONS: TPE may be not associated with improvement of organ failure and mortality in critically ill patients with sepsis and may be associated with a prolonged ICU stay. |
format | Online Article Text |
id | pubmed-10092885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100928852023-04-13 Therapeutic plasma exchange in patients with sepsis: Secondary analysis of a cluster‐randomized controlled trial Luo, Xiang Li, Xiaoling Lai, Xiaoyan Ke, Lu Zhou, Jing Liu, Man Cao, Longxiang Fu, Lingyan J Clin Apher Research Articles INTRODUCTION: Sepsis is life‐threatening organ dysfunction caused by infection‐related inflammatory response. Therapeutic plasma exchange (TPE) can remove inflammatory mediators and benefit patients in different disease settings. However, no solid evidence showed the efficacy and safety of TPE in sepsis. METHODS: This study was a secondary analysis of a randomized controlled trial. Critically ill patients with sepsis were divided into two groups according to whether treated with TPE. The primary outcome was the delta Sequential Organ Failure Assessment (SOFA) score from days 1 to 7. Secondary outcomes included new‐onset organ failure, intensive care unit (ICU)‐free and alive days to day 28, and 28‐day mortality. Propensity score‐matched (PSM) analysis was applied to control confounders. Analysis of covariance (ANCOVA) and logistic regression were used to assess the association between TPE and selected outcomes. RESULTS: Among the 2772 critically ill patients enrolled in the trial, 742 patients with sepsis were selected and 22 patients received TPE were matched with 22 control patients. No significant difference was found in the delta SOFA score and 28‐day mortality between TPE group and control group. The ICU‐free and alive days in the TPE group were significantly shorter than the control group. CONCLUSIONS: TPE may be not associated with improvement of organ failure and mortality in critically ill patients with sepsis and may be associated with a prolonged ICU stay. John Wiley & Sons, Inc. 2022-10-31 2023-02 /pmc/articles/PMC10092885/ /pubmed/36314372 http://dx.doi.org/10.1002/jca.22027 Text en © 2022 The Authors. Journal of Clinical Apheresis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Luo, Xiang Li, Xiaoling Lai, Xiaoyan Ke, Lu Zhou, Jing Liu, Man Cao, Longxiang Fu, Lingyan Therapeutic plasma exchange in patients with sepsis: Secondary analysis of a cluster‐randomized controlled trial |
title | Therapeutic plasma exchange in patients with sepsis: Secondary analysis of a cluster‐randomized controlled trial |
title_full | Therapeutic plasma exchange in patients with sepsis: Secondary analysis of a cluster‐randomized controlled trial |
title_fullStr | Therapeutic plasma exchange in patients with sepsis: Secondary analysis of a cluster‐randomized controlled trial |
title_full_unstemmed | Therapeutic plasma exchange in patients with sepsis: Secondary analysis of a cluster‐randomized controlled trial |
title_short | Therapeutic plasma exchange in patients with sepsis: Secondary analysis of a cluster‐randomized controlled trial |
title_sort | therapeutic plasma exchange in patients with sepsis: secondary analysis of a cluster‐randomized controlled trial |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092885/ https://www.ncbi.nlm.nih.gov/pubmed/36314372 http://dx.doi.org/10.1002/jca.22027 |
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