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Published on: May 26, 2022
Inpatient Omission of Angiotensin-Converting Enzyme Inhibitors and Angiotensin Receptor Blockers Is Associated With
Christopher Oddy1, Jonathan Allington1, James McCaul1
1St. Helier Hospital, London, United Kingdom.
Insights
Continuing ACE inhibitors and ARBs in hospitalized COVID-19 patients is crucial. Missing doses of these medications was linked to higher mortality and worse clinical outcomes in patients with COVID-19.
Area of Science:
- Cardiology
- Infectious Diseases
- Pharmacology
Background:
- Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) targets the human angiotensin-converting enzyme 2 (ACE2) receptor.
- The use of ACE inhibitors and angiotensin receptor blockers (ARBs) in patients with COVID-19 raised clinical concerns during the 2020 pandemic.
- Previous meta-analyses indicated no worsening of clinical outcomes with ACE inhibitors/ARBs in SARS-CoV-2 infection, but direct evidence on inpatient use during acute illness was limited.
Purpose of the Study:
- To investigate the impact of inpatient ACE inhibitor/ARB use on morbidity and mortality in hospitalized COVID-19 patients.
- To evaluate the safety and clinical outcomes associated with continuing or discontinuing ACE inhibitors/ARBs during acute COVID-19 illness.
Main Methods:
- A retrospective cohort analysis included 612 adult patients admitted to the hospital with COVID-19.
- Patients were categorized based on their established use of ACE inhibitors/ARBs.
- Linear and logistic regression models were used to explore relationships, controlling for known confounders.
Main Results:
- Of 612 patients, 151 (24.7%) were on ACE inhibitors/ARBs.
- Discontinuation of ACE inhibitors/ARBs was a significant predictor of worsened outcomes.
- Missed doses were strongly associated with increased mortality (OR, 9.59), higher National Early Warning Score 2 (OR, 1.66), greater oxygen requirements (OR, 3.00), and elevated C-reactive protein levels (OR, 1.83).
Conclusions:
- Missed doses of ACE inhibitors/ARBs in hospitalized COVID-19 patients correlate with increased morbidity and mortality.
- Current practice of continuing ACE inhibitor/ARB therapy during acute illness, with careful monitoring and timely reinitiation, is supported by these findings.
- The study advocates for limiting drug omission to acute contraindications and resuming therapy when safe.
Purpose:
Due to the affinity of severe acute respiratory syndrome coronavirus 2 for the human angiotensin-converting enzyme 2 (ACE2) receptor, use of ACE inhibitors and angiotensin receptor blockers (ARBs) has been a major concern for clinicians during the 2020 pandemic. Meta-analyses have affirmed that these agents do not worsen clinical outcomes in patients with severe acute respiratory syndrome coronavirus 2 infection. To date, only a limited number of studies have directly evaluated the safety of inpatient prescription of ACE inhibitors/ARBs during acute coronavirus disease 2019 (COVID-19) illness.
Methods:
A retrospective cohort analysis was conducted to investigate the impact of inpatient provision of ACE inhibitors/ARBs on morbidity and mortality in patients admitted to the hospital with COVID-19. Relationships were explored by using linear and logistic regression.
Findings:
A total of 612 adult patients met the inclusion criteria, of whom 151 (24.7%) patients were established on ACE inhibitors/ARBs. Despite correction for known confounders, discontinuation of ACE inhibitors/ARBs was highly predictive of worsened outcomes in COVID-19. The proportion of doses omitted in the hospital was significantly associated with increased mortality (OR, 9.59; 95% CI, 2.55-36.09; P < 0.001), maximum National Early Warning Score 2 (OR, 1.66; 95% CI, 1.27-2.17; P < 0.001), maximum oxygen requirements (OR, 3.00; 95% CI, 1.83-4.91; P < 0.001), and maximum C-reactive protein concentration (OR, 1.83; 95% CI, 1.06-3.17; P = 0.030).
Implications:
Our data show a strong association between missed ACE inhibitor/ARB doses with increased morbidity and mortality. The available evidence supports continuation of currently accepted practice surrounding ACE inhibitor/ARB therapy in acute illness, which is to limit drug omission to established acute contraindications, to actively monitor such decisions, and to restart therapy as soon as it is safe to do so. (Clin Ther. 2021;43:e97-e110) © 2021 Elsevier HS Journals, Inc.
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