Clinical frailty, and not features of acute infection, is associated with late mortality in COVID-19: a retrospective cohort study.
Clinical frailty, and not features of acute infection, is associated with late mortality in COVID-19: a retrospective cohort study.
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DOI:
10.1002/jcsm.12966
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发表时间:
2022-06
期刊:
影响因子:
--
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中科院分区:
文献类型:
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Coronavirus disease 2019 (COVID‐19) is associated with excess mortality after hospital discharge. Identification of patients at increased risk of death following hospital discharge is needed to guide clinical monitoring and early intervention. Herein, we aimed to identify predictors of early vs. late mortality in COVID‐19 patients. A total of 471 patients with polymerase chain reaction‐confirmed COVID‐19 were followed up for 9 months [median (inter‐quartile range) of follow‐up time: 271 (14) days] after hospital admission. COVID‐19‐related signs and symptoms, laboratory features, co‐morbidities, Coronavirus Clinical Characterisation Consortium (4C) mortality and Clinical Frailty Scale (CFS) scores were analysed by logistic regression for association with early (28 day) vs. late mortality. Receiver operating characteristic (ROC) analysis was used to determine the discriminative value of 4C and CFS scores for early vs. late mortality. A total of 120 patients died within 28 days from hospital admission. Of the remaining 351 patients, 41 died within the next 8 months. Respiratory failure, systemic inflammation, and renal impairment were associated with early mortality, while active cancer and dementia were associated with late mortality, after adjustment for age and sex. 4C mortality score and CFS were associated with both early [odds ratio (OR) (95% confidence interval—CI): 4C: 1.34 (1.25–1.45); CFS: 1.49 (1.33–1.66)] and late [OR (95% CI): 4C: 1.23 (1.12–1.36); CFS: 2.04 (1.62–2.56)] mortality. After adjustment for CFS, the association between 4C and late mortality was lost. By ROC analysis, 4C mortality score was superior to CFS for 28 day mortality [area under the curve (AUC) (95% CI): 0.779 (0.732–0.825) vs. 0.723 (0.673–0.773), respectively; P = 0.039]. In contrast, CFS had higher predictive value for late mortality compared with 4C mortality score [AUC (95% CI): 0.830 (0.776–0.883) vs. 0.724 (0.650–0.798), respectively; P = 0.007]. In our cohort, late mortality in COVID‐19 patients is more strongly associated with premorbid clinical frailty than with severity of the acute infection phase.
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DOI:
10.3390/medsci9010006
发表时间:
2021-02-04
期刊:
Medical sciences (Basel, Switzerland)
影响因子:
--
作者:
Baker KF;Hanrath AT;van der Loeff IS;Tee SA;Capstick R;Marchitelli G;Li A;Barr A;Eid A;Ahmed S;Bajwa D;Mohammed O;Alderson N;Lendrem C;Lendrem DW;Covid-Control Group;Covid-Clinical Group;Pareja-Cebrian L;Welch A;Field J;Payne BAI;Taha Y;Price DA;Gibbins C;Schmid ML;Hunter E;Duncan CJA
通讯作者:
Duncan CJA
影响因子:
20.3
作者:
Giannis D;Allen SL;Tsang J;Flint S;Pinhasov T;Williams S;Tan G;Thakur R;Leung C;Snyder M;Bhatia C;Garrett D;Cotte C;Isaacs S;Gugerty E;Davidson A;Marder GS;Schnitzer A;Goldberg B;McGinn T;Davidson KW;Barish MA;Qiu M;Zhang M;Goldin M;Matsagkas M;Arnaoutoglou E;Spyropoulos AC
通讯作者:
Spyropoulos AC
DOI:
10.1136/bmj.i2375
发表时间:
2016-05-17
期刊:
BMJ (Clinical research ed.)
影响因子:
--
作者:
Prescott HC;Osterholzer JJ;Langa KM;Angus DC;Iwashyna TJ
通讯作者:
Iwashyna TJ
影响因子:
9.6
作者:
Ferrante, Lauren E.;Pisani, Margaret A.;Gill, Thomas M.
通讯作者:
Gill, Thomas M.
影响因子:
3
作者:
BOZDOGAN, H
通讯作者:
BOZDOGAN, H