Abstract
Background: The reduced renal function has prognostic significance in COVID and it has been linked to mortality in the general population. Reduced renal function is prevalent in older age and thus we set out to better understand its effect on mortality.
Methods: Patient clinical and demographic data was taken from the COVID-19 in
Older People (COPE) study during two periods (February-June 2020 and October
10 2020-March 2021, respectively). Kidney function on admission was measured using estimated glomerular filtration rate (eGFR). The primary outcomes were time to mortality and 28-day mortality. Secondary outcome was length of hospital stay. Data were analysed with multilevel Cox proportional hazards regression, and multilevel logistic regression and adjusted for individual patient clinical and demographic characteristics.
Results: 1,802 patients (55.0% male; median [IQR] 80 [73-86] years) were included in the study. 28-day mortality was 42.3% (n=742). 48% (n=801) had evidence of renal impairment on admission. Using a time-to-event analysis, reduced renal function was associated with increased in-hospital mortality (compared to eGFR ≥60 [Stage 1&2]): eGFR 45-59 [Stage 3a] aHR=1.26 (95%CI 1.02-1.55); eGFR 30-44 [Stage 3b] aHR=1.41 (95%CI 1.14-1.73); eGFR 1-29 [Stage 4&5] aHR=1.42 (95%CI 1.13-1.80). In the co-primary outcome of 28-day mortality, mortality was associated with: Stage 3a adjusted odds ratio (aOR)=1.18 (95%CI 0.88-1.58), Stage 3b aOR=1.40 (95%CI 1.03-1.89); and Stage 4&5 aOR=1.65 (95%CI 1.16-2.35).
Conclusion: eGFR on admission is a good independent predictor of mortality in
hospitalised older patients with COVID-19 population. We found evidence of a dose29 response between reduced renal function and increased mortality.
Methods: Patient clinical and demographic data was taken from the COVID-19 in
Older People (COPE) study during two periods (February-June 2020 and October
10 2020-March 2021, respectively). Kidney function on admission was measured using estimated glomerular filtration rate (eGFR). The primary outcomes were time to mortality and 28-day mortality. Secondary outcome was length of hospital stay. Data were analysed with multilevel Cox proportional hazards regression, and multilevel logistic regression and adjusted for individual patient clinical and demographic characteristics.
Results: 1,802 patients (55.0% male; median [IQR] 80 [73-86] years) were included in the study. 28-day mortality was 42.3% (n=742). 48% (n=801) had evidence of renal impairment on admission. Using a time-to-event analysis, reduced renal function was associated with increased in-hospital mortality (compared to eGFR ≥60 [Stage 1&2]): eGFR 45-59 [Stage 3a] aHR=1.26 (95%CI 1.02-1.55); eGFR 30-44 [Stage 3b] aHR=1.41 (95%CI 1.14-1.73); eGFR 1-29 [Stage 4&5] aHR=1.42 (95%CI 1.13-1.80). In the co-primary outcome of 28-day mortality, mortality was associated with: Stage 3a adjusted odds ratio (aOR)=1.18 (95%CI 0.88-1.58), Stage 3b aOR=1.40 (95%CI 1.03-1.89); and Stage 4&5 aOR=1.65 (95%CI 1.16-2.35).
Conclusion: eGFR on admission is a good independent predictor of mortality in
hospitalised older patients with COVID-19 population. We found evidence of a dose29 response between reduced renal function and increased mortality.
Original language | English |
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Article number | 119 |
Number of pages | 8 |
Journal | BMC Geriatrics |
Volume | 22 |
Issue number | 1 |
Early online date | 12 Feb 2022 |
DOIs | |
Publication status | Published - 12 Feb 2022 |
Keywords
- COVID-19
- chronic kidney failure
- eGFR
- mortality
- dose-response