Cargando…
A biomarker-based age, biomarkers, clinical history, sex (ABCS)-mortality risk score for patients with coronavirus disease 2019
BACKGROUND: Early identification and timely therapeutic strategies for potential critical patients with coronavirus disease 2019 (COVID-19) are of crucial importance to reduce mortality. We aimed to develop and validate a prediction tool for 30-day mortality for these patients on admission. METHODS:...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940919/ https://www.ncbi.nlm.nih.gov/pubmed/33708857 http://dx.doi.org/10.21037/atm-20-6205 |
_version_ | 1783662046577950720 |
---|---|
author | Jiang, Meng Li, Changli Zheng, Li Lv, Wenzhi He, Zhigang Cui, Xinwu Dietrich, Christoph F. |
author_facet | Jiang, Meng Li, Changli Zheng, Li Lv, Wenzhi He, Zhigang Cui, Xinwu Dietrich, Christoph F. |
author_sort | Jiang, Meng |
collection | PubMed |
description | BACKGROUND: Early identification and timely therapeutic strategies for potential critical patients with coronavirus disease 2019 (COVID-19) are of crucial importance to reduce mortality. We aimed to develop and validate a prediction tool for 30-day mortality for these patients on admission. METHODS: Consecutive hospitalized patients admitted to Tongji Hospital and Hubei Xinhua Hospital from January 1 to March 10, 2020, were retrospective analyzed. They were grouped as derivation and external validation set. Multivariate Cox regression was applied to identify the risk factors associated with death, and a nomogram was developed and externally validated by calibration plots, C-index, Kaplan-Meier curves and decision curve. RESULTS: Data from 1,717 patients at the Tongji Hospital and 188 cases at the Hubei Xinhua Hospital were included in our study. Using multivariate Cox regression with backward stepwise selection of variables in the derivation cohort, age, sex, chronic obstructive pulmonary disease (COPD), as well as seven biomarkers (aspartate aminotransferase, high-sensitivity C-reactive protein, high-sensitivity troponin I, white blood cell count, lymphocyte count, D-dimer, and procalcitonin) were incorporated in the model. An age, biomarkers, clinical history, sex (ABCS)-mortality score was developed, which yielded a higher C-index than the conventional CURB-65 score for predicting 30-day mortality in both the derivation cohort {0.888 [95% confidence interval (CI), 0.869–0.907] vs. 0.696 (95% CI, 0.660–0.731)} and validation cohort [0.838 (95% CI, 0.777–0.899) vs. 0.619 (95% CI, 0.519–0.720)], respectively. Furthermore, risk stratified Kaplan-Meier curves showed good discriminatory capacity of the model for classifying patients into distinct mortality risk groups for both derivation and validation cohorts. CONCLUSIONS: The ABCS-mortality score might be offered to clinicians to strengthen the prognosis-based clinical decision-making, which would be helpful for reducing mortality of COVID-19 patients. |
format | Online Article Text |
id | pubmed-7940919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-79409192021-03-10 A biomarker-based age, biomarkers, clinical history, sex (ABCS)-mortality risk score for patients with coronavirus disease 2019 Jiang, Meng Li, Changli Zheng, Li Lv, Wenzhi He, Zhigang Cui, Xinwu Dietrich, Christoph F. Ann Transl Med Original Article BACKGROUND: Early identification and timely therapeutic strategies for potential critical patients with coronavirus disease 2019 (COVID-19) are of crucial importance to reduce mortality. We aimed to develop and validate a prediction tool for 30-day mortality for these patients on admission. METHODS: Consecutive hospitalized patients admitted to Tongji Hospital and Hubei Xinhua Hospital from January 1 to March 10, 2020, were retrospective analyzed. They were grouped as derivation and external validation set. Multivariate Cox regression was applied to identify the risk factors associated with death, and a nomogram was developed and externally validated by calibration plots, C-index, Kaplan-Meier curves and decision curve. RESULTS: Data from 1,717 patients at the Tongji Hospital and 188 cases at the Hubei Xinhua Hospital were included in our study. Using multivariate Cox regression with backward stepwise selection of variables in the derivation cohort, age, sex, chronic obstructive pulmonary disease (COPD), as well as seven biomarkers (aspartate aminotransferase, high-sensitivity C-reactive protein, high-sensitivity troponin I, white blood cell count, lymphocyte count, D-dimer, and procalcitonin) were incorporated in the model. An age, biomarkers, clinical history, sex (ABCS)-mortality score was developed, which yielded a higher C-index than the conventional CURB-65 score for predicting 30-day mortality in both the derivation cohort {0.888 [95% confidence interval (CI), 0.869–0.907] vs. 0.696 (95% CI, 0.660–0.731)} and validation cohort [0.838 (95% CI, 0.777–0.899) vs. 0.619 (95% CI, 0.519–0.720)], respectively. Furthermore, risk stratified Kaplan-Meier curves showed good discriminatory capacity of the model for classifying patients into distinct mortality risk groups for both derivation and validation cohorts. CONCLUSIONS: The ABCS-mortality score might be offered to clinicians to strengthen the prognosis-based clinical decision-making, which would be helpful for reducing mortality of COVID-19 patients. AME Publishing Company 2021-02 /pmc/articles/PMC7940919/ /pubmed/33708857 http://dx.doi.org/10.21037/atm-20-6205 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Jiang, Meng Li, Changli Zheng, Li Lv, Wenzhi He, Zhigang Cui, Xinwu Dietrich, Christoph F. A biomarker-based age, biomarkers, clinical history, sex (ABCS)-mortality risk score for patients with coronavirus disease 2019 |
title | A biomarker-based age, biomarkers, clinical history, sex (ABCS)-mortality risk score for patients with coronavirus disease 2019 |
title_full | A biomarker-based age, biomarkers, clinical history, sex (ABCS)-mortality risk score for patients with coronavirus disease 2019 |
title_fullStr | A biomarker-based age, biomarkers, clinical history, sex (ABCS)-mortality risk score for patients with coronavirus disease 2019 |
title_full_unstemmed | A biomarker-based age, biomarkers, clinical history, sex (ABCS)-mortality risk score for patients with coronavirus disease 2019 |
title_short | A biomarker-based age, biomarkers, clinical history, sex (ABCS)-mortality risk score for patients with coronavirus disease 2019 |
title_sort | biomarker-based age, biomarkers, clinical history, sex (abcs)-mortality risk score for patients with coronavirus disease 2019 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940919/ https://www.ncbi.nlm.nih.gov/pubmed/33708857 http://dx.doi.org/10.21037/atm-20-6205 |
work_keys_str_mv | AT jiangmeng abiomarkerbasedagebiomarkersclinicalhistorysexabcsmortalityriskscoreforpatientswithcoronavirusdisease2019 AT lichangli abiomarkerbasedagebiomarkersclinicalhistorysexabcsmortalityriskscoreforpatientswithcoronavirusdisease2019 AT zhengli abiomarkerbasedagebiomarkersclinicalhistorysexabcsmortalityriskscoreforpatientswithcoronavirusdisease2019 AT lvwenzhi abiomarkerbasedagebiomarkersclinicalhistorysexabcsmortalityriskscoreforpatientswithcoronavirusdisease2019 AT hezhigang abiomarkerbasedagebiomarkersclinicalhistorysexabcsmortalityriskscoreforpatientswithcoronavirusdisease2019 AT cuixinwu abiomarkerbasedagebiomarkersclinicalhistorysexabcsmortalityriskscoreforpatientswithcoronavirusdisease2019 AT dietrichchristophf abiomarkerbasedagebiomarkersclinicalhistorysexabcsmortalityriskscoreforpatientswithcoronavirusdisease2019 AT jiangmeng biomarkerbasedagebiomarkersclinicalhistorysexabcsmortalityriskscoreforpatientswithcoronavirusdisease2019 AT lichangli biomarkerbasedagebiomarkersclinicalhistorysexabcsmortalityriskscoreforpatientswithcoronavirusdisease2019 AT zhengli biomarkerbasedagebiomarkersclinicalhistorysexabcsmortalityriskscoreforpatientswithcoronavirusdisease2019 AT lvwenzhi biomarkerbasedagebiomarkersclinicalhistorysexabcsmortalityriskscoreforpatientswithcoronavirusdisease2019 AT hezhigang biomarkerbasedagebiomarkersclinicalhistorysexabcsmortalityriskscoreforpatientswithcoronavirusdisease2019 AT cuixinwu biomarkerbasedagebiomarkersclinicalhistorysexabcsmortalityriskscoreforpatientswithcoronavirusdisease2019 AT dietrichchristophf biomarkerbasedagebiomarkersclinicalhistorysexabcsmortalityriskscoreforpatientswithcoronavirusdisease2019 |