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The attributable mortality of sepsis for acute kidney injury: a propensity-matched analysis based on multicenter prospective cohort study

BACKGROUND: Both sepsis and AKI are diseases of major concern in intensive care unit (ICU). This study aimed to evaluate the excess mortality attributable to sepsis for acute kidney injury (AKI). METHODS: A propensity score-matched analysis on a multicenter prospective cohort study in 18 Chinese ICU...

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Autores principales: Jia, Hui-Miao, Jiang, Yi-Jia, Zheng, Xi, Li, Wen, Wang, Mei-Ping, Xi, Xiu-Ming, Li, Wen-Xiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9848315/
https://www.ncbi.nlm.nih.gov/pubmed/36637012
http://dx.doi.org/10.1080/0886022X.2022.2162415
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author Jia, Hui-Miao
Jiang, Yi-Jia
Zheng, Xi
Li, Wen
Wang, Mei-Ping
Xi, Xiu-Ming
Li, Wen-Xiong
author_facet Jia, Hui-Miao
Jiang, Yi-Jia
Zheng, Xi
Li, Wen
Wang, Mei-Ping
Xi, Xiu-Ming
Li, Wen-Xiong
author_sort Jia, Hui-Miao
collection PubMed
description BACKGROUND: Both sepsis and AKI are diseases of major concern in intensive care unit (ICU). This study aimed to evaluate the excess mortality attributable to sepsis for acute kidney injury (AKI). METHODS: A propensity score-matched analysis on a multicenter prospective cohort study in 18 Chinese ICUs was performed. Propensity score was sequentially conducted to match AKI patients with and without sepsis on day 1, day 2, and day 3–5. The primary outcome was hospital death of AKI patients. RESULTS: A total of 2008 AKI patients (40.9%) were eligible for the study. Of the 1010 AKI patients with sepsis, 619 (61.3%) were matched to 619 AKI patients in whom sepsis did not develop during the screening period of the study. The hospital mortality rate of matched AKI patients with sepsis was 205 of 619 (33.1%) compared with 150 of 619 (24.0%) for their matched AKI controls without sepsis (p = 0.001). The attributable mortality of total sepsis for AKI patients was 9.1% (95% CI: 4.8–13.3%). Of the matched patients with sepsis, 328 (53.0%) diagnosed septic shock. The attributable mortality of septic shock for AKI was 16.2% (95% CI: 11.3–20.8%, p < 0.001). Further, the attributable mortality of sepsis for AKI was 1.4% (95% CI: 4.1–5.9%, p = 0.825). CONCLUSIONS: The attributable hospital mortality of total sepsis for AKI were 9.1%. Septic shock contributes to major excess mortality rate for AKI than sepsis. REGISTRATION FOR THE MULTICENTER PROSPECTIVE COHORT STUDY: registration number ChiCTR-ECH-13003934
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spelling pubmed-98483152023-01-19 The attributable mortality of sepsis for acute kidney injury: a propensity-matched analysis based on multicenter prospective cohort study Jia, Hui-Miao Jiang, Yi-Jia Zheng, Xi Li, Wen Wang, Mei-Ping Xi, Xiu-Ming Li, Wen-Xiong Ren Fail Clinical Study BACKGROUND: Both sepsis and AKI are diseases of major concern in intensive care unit (ICU). This study aimed to evaluate the excess mortality attributable to sepsis for acute kidney injury (AKI). METHODS: A propensity score-matched analysis on a multicenter prospective cohort study in 18 Chinese ICUs was performed. Propensity score was sequentially conducted to match AKI patients with and without sepsis on day 1, day 2, and day 3–5. The primary outcome was hospital death of AKI patients. RESULTS: A total of 2008 AKI patients (40.9%) were eligible for the study. Of the 1010 AKI patients with sepsis, 619 (61.3%) were matched to 619 AKI patients in whom sepsis did not develop during the screening period of the study. The hospital mortality rate of matched AKI patients with sepsis was 205 of 619 (33.1%) compared with 150 of 619 (24.0%) for their matched AKI controls without sepsis (p = 0.001). The attributable mortality of total sepsis for AKI patients was 9.1% (95% CI: 4.8–13.3%). Of the matched patients with sepsis, 328 (53.0%) diagnosed septic shock. The attributable mortality of septic shock for AKI was 16.2% (95% CI: 11.3–20.8%, p < 0.001). Further, the attributable mortality of sepsis for AKI was 1.4% (95% CI: 4.1–5.9%, p = 0.825). CONCLUSIONS: The attributable hospital mortality of total sepsis for AKI were 9.1%. Septic shock contributes to major excess mortality rate for AKI than sepsis. REGISTRATION FOR THE MULTICENTER PROSPECTIVE COHORT STUDY: registration number ChiCTR-ECH-13003934 Taylor & Francis 2023-01-13 /pmc/articles/PMC9848315/ /pubmed/36637012 http://dx.doi.org/10.1080/0886022X.2022.2162415 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Jia, Hui-Miao
Jiang, Yi-Jia
Zheng, Xi
Li, Wen
Wang, Mei-Ping
Xi, Xiu-Ming
Li, Wen-Xiong
The attributable mortality of sepsis for acute kidney injury: a propensity-matched analysis based on multicenter prospective cohort study
title The attributable mortality of sepsis for acute kidney injury: a propensity-matched analysis based on multicenter prospective cohort study
title_full The attributable mortality of sepsis for acute kidney injury: a propensity-matched analysis based on multicenter prospective cohort study
title_fullStr The attributable mortality of sepsis for acute kidney injury: a propensity-matched analysis based on multicenter prospective cohort study
title_full_unstemmed The attributable mortality of sepsis for acute kidney injury: a propensity-matched analysis based on multicenter prospective cohort study
title_short The attributable mortality of sepsis for acute kidney injury: a propensity-matched analysis based on multicenter prospective cohort study
title_sort attributable mortality of sepsis for acute kidney injury: a propensity-matched analysis based on multicenter prospective cohort study
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9848315/
https://www.ncbi.nlm.nih.gov/pubmed/36637012
http://dx.doi.org/10.1080/0886022X.2022.2162415
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