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Association of Renin Angiotensin Aldosterone System Inhibitors and Outcomes of Hospitalized Patients With COVID-19.
Gupta, Neha; Settle, Lisa; Brown, Brent R; Armaignac, Donna L; Baram, Michael; Perkins, Nicholas E; Kaufman, Margit; Melamed, Roman R; Christie, Amy B; Danesh, Valerie C; Denson, Joshua L; Cheruku, Sreekanth R; Boman, Karen; Bansal, Vikas; Kumar, Vishakha K; Walkey, Allan J; Domecq, Juan P; Kashyap, Rahul; Aston, Christopher E.
  • Gupta N; Department of Pediatrics, Division of Pediatric Critical Care, University of Oklahoma College of Medicine, Oklahoma City, OK.
  • Settle L; Department of Pediatrics, University of Oklahoma College of Medicine, Oklahoma City, OK.
  • Brown BR; Department of Medicine, Division of Pulmonary Critical Care, University of Oklahoma College of Medicine, Oklahoma City, OK.
  • Armaignac DL; Center for Advanced Analytics, Baptist Health South Florida, Coral Gables, FL.
  • Baram M; Department of Medicine, Thomas Jefferson University, Philadelphia, PA.
  • Perkins NE; Department of Medicine, Division of Hospital Medicine, Prisma Health, Greenville, SC.
  • Kaufman M; Departments of Anesthesiology and Critical Care Medicine, Englewood Health, Englewood, NJ.
  • Melamed RR; Department of Critical Care, Abbott Northwestern Hospital, Allina Health, Minneapolis, MN.
  • Christie AB; Department of Critical Care, Atrium Health Navicent, Macon, GA.
  • Danesh VC; Center for Applied Health Research, Baylor Scott & White Health, Dallas, TX.
  • Denson JL; Section of Pulmonary Diseases, Critical Care, and Environmental Medicine, Tulane University School of Medicine, New Orleans, LA.
  • Cheruku SR; Department of Anesthesiology and Pain Management, UT Southwestern Medical Center, Dallas, TX.
  • Boman K; Society of Critical Care Medicine, Mount Prospect, IL.
  • Bansal V; Department of Anesthesia and Perioperative Medicine, Mayo Clinic, Rochester, MN.
  • Kumar VK; Society of Critical Care Medicine, Mount Prospect, IL.
  • Walkey AJ; Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, and Evans Center of Implementation and Improvement Sciences, Department of Medicine, Boston University School of Medicine, Boston, MA.
  • Domecq JP; Division of Nephrology and Hypertension, Department of Internal Medicine, Mayo Clinic, Rochester, MN.
  • Kashyap R; Department of Anesthesia and Perioperative Medicine, Mayo Clinic, Rochester, MN.
  • Aston CE; Biomedical and Behavioral Methodology Core, Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, OK.
Crit Care Med ; 50(10): e744-e758, 2022 10 01.
Article in English | MEDLINE | ID: covidwho-1961176
ABSTRACT

OBJECTIVES:

To determine the association of prior use of renin-angiotensin-aldosterone system inhibitors (RAASIs) with mortality and outcomes in hospitalized patients with COVID-19.

DESIGN:

Retrospective observational study.

SETTING:

Multicenter, international COVID-19 registry.

SUBJECTS:

Adult hospitalized COVID-19 patients on antihypertensive agents (AHAs) prior to admission, admitted from March 31, 2020, to March 10, 2021.

INTERVENTIONS:

None. MEASUREMENTS AND MAIN

RESULTS:

Data were compared between three groups patients on RAASIs only, other AHAs only, and those on both medications. Multivariable logistic and linear regressions were performed after controlling for prehospitalization characteristics to estimate the effect of RAASIs on mortality and other outcomes during hospitalization. Of 26,652 patients, 7,975 patients were on AHAs prior to hospitalization. Of these, 1,542 patients (19.3%) were on RAASIs only, 3,765 patients (47.2%) were on other AHAs only, and 2,668 (33.5%) patients were on both medications. Compared with those taking other AHAs only, patients on RAASIs only were younger (mean age 63.3 vs 66.9 yr; p < 0.0001), more often male (58.2% vs 52.4%; p = 0.0001) and more often White (55.1% vs 47.2%; p < 0.0001). After adjusting for age, gender, race, location, and comorbidities, patients on combination of RAASIs and other AHAs had higher in-hospital mortality than those on RAASIs only (odds ratio [OR] = 1.28; 95% CI [1.19-1.38]; p < 0.0001) and higher mortality than those on other AHAs only (OR = 1.09; 95% CI [1.03-1.15]; p = 0.0017). Patients on RAASIs only had lower mortality than those on other AHAs only (OR = 0.87; 95% CI [0.81-0.94]; p = 0.0003). Patients on ACEIs only had higher mortality compared with those on ARBs only (OR = 1.37; 95% CI [1.20-1.56]; p < 0.0001).

CONCLUSIONS:

Among patients hospitalized for COVID-19 who were taking AHAs, prior use of a combination of RAASIs and other AHAs was associated with higher in-hospital mortality than the use of RAASIs alone. When compared with ARBs, ACEIs were associated with significantly higher mortality in hospitalized COVID-19 patients.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Drug Treatment / Hypertension Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Adult / Humans / Male / Middle aged Language: English Journal: Crit Care Med Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Drug Treatment / Hypertension Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Adult / Humans / Male / Middle aged Language: English Journal: Crit Care Med Year: 2022 Document Type: Article