TY - JOUR
T1 - Association Between Baseline Use of Angiotensin-Converting Enzyme Inhibitors and Angiotensin Receptor Blockers and Death Among Patients Tested for COVID-19
AU - Thomas, Sarah A.
AU - Puskarich, Michael
AU - Pulia, Michael S.
AU - Meltzer, Andrew C.
AU - Camargo, Carlos A.
AU - Courtney, D. Mark
AU - Nordenholz, Kristen E.
AU - Kline, Jeffrey A.
AU - Kabrhel, Christopher
N1 - Funding Information:
Dr Puskarich's institution received grant funding for clinical trials of losartan for COVID‐19 (Bill and Melinda Gates Foundation, Minnesota Partnership for Biotechnology and Medical Genomics).
Publisher Copyright:
© 2021, The American College of Clinical Pharmacology.
PY - 2022/6
Y1 - 2022/6
N2 - Angiotensin-converting enzyme inhibitor (ACEI) and angiotensin receptor blocker (ARB) drugs may modify risk associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Therefore, we assessed whether baseline therapy with ACEIs or ARBs was associated with lower mortality, respiratory failure (noninvasive ventilation or intubation), and renal failure (new renal replacement therapy) in SARS-CoV-2-positive patients. This retrospective registry-based observational cohort study used data from a national database of emergency department patients tested for SARS-CoV-2. Symptomatic emergency department patients were accrued from January to October 2020, across 197 hospitals in the United States. Multivariable analysis using logistic regression evaluated end points among SARS-CoV-2–positive cases, focusing on ACEIs/ARBs and adjusting for covariates. Model performance was evaluated using the c statistic for discrimination and Cox plotting for calibration. A total of 13 859 (99.9%) patients had known mortality status, of whom 2045 (14.8%) died. Respiratory failure occurred in 2485/13 880 (17.9%) and renal failure in 548/13 813 (4.0%) patients with available data. ACEI/ARB status was associated with a 25% decrease in mortality odds (odds ratio [OR], 0.75; 95%CI, 0.59-0.94; P =.011; c =.82). ACEIs/ARBs were not significantly associated with respiratory failure (OR, 0.89; 95%CI, 0.78-1.06; P =.206) or renal failure (OR, 0.75; 95%CI, 0.55-1.04; P =.083). Adjusting for covariates, baseline ACEI/ARB was associated with 25% lower mortality in SARS-CoV-2–positive patients. The potential mechanism for ACEI/ARB mortality modification requires further exploration.
AB - Angiotensin-converting enzyme inhibitor (ACEI) and angiotensin receptor blocker (ARB) drugs may modify risk associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Therefore, we assessed whether baseline therapy with ACEIs or ARBs was associated with lower mortality, respiratory failure (noninvasive ventilation or intubation), and renal failure (new renal replacement therapy) in SARS-CoV-2-positive patients. This retrospective registry-based observational cohort study used data from a national database of emergency department patients tested for SARS-CoV-2. Symptomatic emergency department patients were accrued from January to October 2020, across 197 hospitals in the United States. Multivariable analysis using logistic regression evaluated end points among SARS-CoV-2–positive cases, focusing on ACEIs/ARBs and adjusting for covariates. Model performance was evaluated using the c statistic for discrimination and Cox plotting for calibration. A total of 13 859 (99.9%) patients had known mortality status, of whom 2045 (14.8%) died. Respiratory failure occurred in 2485/13 880 (17.9%) and renal failure in 548/13 813 (4.0%) patients with available data. ACEI/ARB status was associated with a 25% decrease in mortality odds (odds ratio [OR], 0.75; 95%CI, 0.59-0.94; P =.011; c =.82). ACEIs/ARBs were not significantly associated with respiratory failure (OR, 0.89; 95%CI, 0.78-1.06; P =.206) or renal failure (OR, 0.75; 95%CI, 0.55-1.04; P =.083). Adjusting for covariates, baseline ACEI/ARB was associated with 25% lower mortality in SARS-CoV-2–positive patients. The potential mechanism for ACEI/ARB mortality modification requires further exploration.
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U2 - 10.1002/jcph.2015
DO - 10.1002/jcph.2015
M3 - Article
C2 - 34921684
AN - SCOPUS:85124550290
SN - 0091-2700
VL - 62
SP - 777
EP - 782
JO - Journal of clinical pharmacology
JF - Journal of clinical pharmacology
IS - 6
ER -