Key result
In a 1.4 million patient nationwide cohort, ACEi/ARB use was associated with a reduced risk of hospitalization or death for COVID-19 (OR 0.86; 95% CI 0.81-0.91).
Why the study?
RAAS inhibitors improve cardiorenal outcomes, but concerns arose regarding an increased risk of incident hospitalization and death from COVID-19.
Does RAASi use increase the risk of COVID-19 hospitalization or death in patients with cardiorenal disease?
Cohort (n=1,387,746)
Yes
Does RAASi use increase the risk of COVID-19 hospitalization or death in patients with cardiorenal disease?
Answers are grounded in this paper and cite their sources.
Use of RAAS inhibitors is not associated with an increased risk of COVID-19 hospitalization or death, supporting their continued use in patients with cardiorenal disease during the pandemic.
AIMS: Renin-angiotensin-aldosterone system inhibitors (RAASi) improve outcomes in cardiorenal disease but concerns have been raised over increased risk of incident hospitalization and death from coronavirus disease 2019 (COVID-19). We investigated the association between use of angiotensin-converting enzyme inhibitors (ACEi), angiotensin receptor blockers (ARBs) or mineralocorticoid receptor antagonists (MRAs) and COVID-19 hospitalization/death in a large nationwide population. METHODS AND RESULTS: Patients with hypertension, heart failure, diabetes, kidney disease, or ischaemic heart disease registered in the Swedish National Patient Registry until 1 February 2020 were included and followed until 31 May 2020. COVID-19 cases were defined based on hospitalization/death for COVID-19. Multivariable logistic and Cox regressions were fitted to investigate the association between ACEi/ARB and MRA and risk of hospitalization/death for COVID-19 in the overall population, and of all-cause mortality in COVID-19 cases. We performed consistency analysis to quantify the impact of potential unmeasured confounding. Of 1 387 746 patients (60% receiving ACEi/ARB and 5.8% MRA), 7146 (0.51%) had incident hospitalization/death from COVID-19. After adjustment for 45 variables, ACEi/ARB use was associated with a reduced risk of hospitalization/death for COVID-19 (odds ratio 0.86, 95% confidence interval 0.81-0.91) in the overall population, and with reduced mortality in COVID-19 cases (hazard ratio 0.89, 95% confidence interval 0.82-0.96). MRA use was not associated with risk of any outcome. Consistency analysis showed that unmeasured confounding would need to be large for there to be harmful signals associated with RAASi use. CONCLUSIONS: In a 1.4 million nationwide cohort, use of RAASi was not associated with increased risk of hospitalization for or death from COVID-19.
No takes yet. Share an insight, caveat, or question.
Savarese et al. (2020) conducted a cohort in Hypertension, heart failure, diabetes, kidney disease, or ischaemic heart disease (n=1,387,746). ACEi/ARB use vs. Non-use was evaluated on Hospitalization or death for COVID-19 (OR 0.86, 95% CI 0.81-0.91). In a 1.4 million patient nationwide cohort, ACEi/ARB use was associated with a reduced risk of hospitalization or death for COVID-19 (OR 0.86; 95% CI 0.81-0.91).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: