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Optimized diagnosis-based comorbidity measures for all-cause mortality prediction in a national population-based ICU population

BACKGROUND: We aimed to optimize prediction of long-term all-cause mortality of intensive care unit (ICU) patients, using quantitative register-based comorbidity information assessed from hospital discharge diagnoses prior to intensive care treatment. MATERIAL AND METHODS: Adult ICU admissions durin...

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Autores principales: Aronsson Dannewitz, Anna, Svennblad, Bodil, Michaëlsson, Karl, Lipcsey, Miklos, Gedeborg, Rolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535950/
https://www.ncbi.nlm.nih.gov/pubmed/36203163
http://dx.doi.org/10.1186/s13054-022-04172-0
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author Aronsson Dannewitz, Anna
Svennblad, Bodil
Michaëlsson, Karl
Lipcsey, Miklos
Gedeborg, Rolf
author_facet Aronsson Dannewitz, Anna
Svennblad, Bodil
Michaëlsson, Karl
Lipcsey, Miklos
Gedeborg, Rolf
author_sort Aronsson Dannewitz, Anna
collection PubMed
description BACKGROUND: We aimed to optimize prediction of long-term all-cause mortality of intensive care unit (ICU) patients, using quantitative register-based comorbidity information assessed from hospital discharge diagnoses prior to intensive care treatment. MATERIAL AND METHODS: Adult ICU admissions during 2006 to 2012 in the Swedish intensive care register were followed for at least 4 years. The performance of quantitative comorbidity measures based on the 5-year history of number of hospital admissions, length of stay, and time since latest admission in 36 comorbidity categories was compared in time-to-event analyses with the Charlson comorbidity index (CCI) and the Simplified Acute Physiology Score (SAPS3). RESULTS: During a 7-year period, there were 230,056 ICU admissions and 62,225 deaths among 188,965 unique individuals. The time interval from the most recent hospital stays and total length of stay within each comorbidity category optimized mortality prediction and provided clear separation of risk categories also within strata of age and CCI, with hazard ratios (HRs) comparing lowest to highest quartile ranging from 1.17 (95% CI: 0.52–2.64) to 6.41 (95% CI: 5.19–7.92). Risk separation was also observed within SAPS deciles with HR ranging from 1.07 (95% CI: 0.83–1.38) to 3.58 (95% CI: 2.12–6.03). CONCLUSION: Baseline comorbidity measures that included the time interval from the most recent hospital stay in 36 different comorbidity categories substantially improved long-term mortality prediction after ICU admission compared to the Charlson index and the SAPS score. Trial registration ClinicalTrials.gov ID NCT04109001, date of registration 2019-09-26 retrospectively. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-022-04172-0.
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spelling pubmed-95359502022-10-07 Optimized diagnosis-based comorbidity measures for all-cause mortality prediction in a national population-based ICU population Aronsson Dannewitz, Anna Svennblad, Bodil Michaëlsson, Karl Lipcsey, Miklos Gedeborg, Rolf Crit Care Research BACKGROUND: We aimed to optimize prediction of long-term all-cause mortality of intensive care unit (ICU) patients, using quantitative register-based comorbidity information assessed from hospital discharge diagnoses prior to intensive care treatment. MATERIAL AND METHODS: Adult ICU admissions during 2006 to 2012 in the Swedish intensive care register were followed for at least 4 years. The performance of quantitative comorbidity measures based on the 5-year history of number of hospital admissions, length of stay, and time since latest admission in 36 comorbidity categories was compared in time-to-event analyses with the Charlson comorbidity index (CCI) and the Simplified Acute Physiology Score (SAPS3). RESULTS: During a 7-year period, there were 230,056 ICU admissions and 62,225 deaths among 188,965 unique individuals. The time interval from the most recent hospital stays and total length of stay within each comorbidity category optimized mortality prediction and provided clear separation of risk categories also within strata of age and CCI, with hazard ratios (HRs) comparing lowest to highest quartile ranging from 1.17 (95% CI: 0.52–2.64) to 6.41 (95% CI: 5.19–7.92). Risk separation was also observed within SAPS deciles with HR ranging from 1.07 (95% CI: 0.83–1.38) to 3.58 (95% CI: 2.12–6.03). CONCLUSION: Baseline comorbidity measures that included the time interval from the most recent hospital stay in 36 different comorbidity categories substantially improved long-term mortality prediction after ICU admission compared to the Charlson index and the SAPS score. Trial registration ClinicalTrials.gov ID NCT04109001, date of registration 2019-09-26 retrospectively. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-022-04172-0. BioMed Central 2022-10-06 /pmc/articles/PMC9535950/ /pubmed/36203163 http://dx.doi.org/10.1186/s13054-022-04172-0 Text en © The Author(s) 2022 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
Aronsson Dannewitz, Anna
Svennblad, Bodil
Michaëlsson, Karl
Lipcsey, Miklos
Gedeborg, Rolf
Optimized diagnosis-based comorbidity measures for all-cause mortality prediction in a national population-based ICU population
title Optimized diagnosis-based comorbidity measures for all-cause mortality prediction in a national population-based ICU population
title_full Optimized diagnosis-based comorbidity measures for all-cause mortality prediction in a national population-based ICU population
title_fullStr Optimized diagnosis-based comorbidity measures for all-cause mortality prediction in a national population-based ICU population
title_full_unstemmed Optimized diagnosis-based comorbidity measures for all-cause mortality prediction in a national population-based ICU population
title_short Optimized diagnosis-based comorbidity measures for all-cause mortality prediction in a national population-based ICU population
title_sort optimized diagnosis-based comorbidity measures for all-cause mortality prediction in a national population-based icu population
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535950/
https://www.ncbi.nlm.nih.gov/pubmed/36203163
http://dx.doi.org/10.1186/s13054-022-04172-0
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