A randomized controlled trial of renin-angiotensin-aldosterone system inhibitor management in patients admitted in hospital with COVID-19

Data de publicação: Data Ahead of Print:

Autores da FMUP

  • João Pedro Melo Marques Pinho Ferreira

    Autor

Participantes de fora da FMUP

  • Sharma, A
  • Elharram, M
  • Afilalo, J
  • Flannery, A
  • Afilalo, M
  • Tselios, C
  • Ni, JY
  • Ezekowitz, JA
  • Cheng, MP
  • Ambrosy, AP
  • Zannad, F
  • Brophy, JM
  • Giannetti, N
  • Bessissow, A
  • Kronfli, N
  • Marelli, A
  • Aziz, H
  • Alqahtani, M
  • Aflaki, M
  • Craig, M
  • Lopes, RD

Unidades de investigação

Abstract

Background Renin-angiotensin aldosterone system inhibitors (RAASi) are commonly used among patients hospitalized with a severe acute respiratory syndrome coronavirus 2 infection coronavirus disease 2019 (COVID-19). We evaluated whether continuation versus discontinuation of RAASi were associated with short term clinical or biochemical outcomes. Methods The RAAS-COVID-19 trial was a randomized, open label study in adult patients previously treated with RAASi who are hospitalized with COVID-19 (NCT04508985). Participants were randomized 1:1 to discontinue or continue RAASi. The primary outcome was a global rank score calculated from baseline to day 7 (or discharge) incorporating clinical events and biomarker changes. Global rank scores were compared between groups using the Wilcoxon test statistic and the negative binomial test (using incident rate ratio [IRR]) and the intention-to-treat principle. Results Overall, 46 participants were enrolled; 21 participants were randomized to discontinue RAASi and 25 to continue. Patients' mean age was 71.5 years and 43.5% were female. Discontinuation of RAASi, versus continuation, resulted in a non-statistically different mean global rank score (discontinuation 6 [standard deviation [SD] 6.3] vs continuation 3.8 (SD 2.5); P = .60). The negative binomial analysis identified that discontinuation increased the risk of adverse outcomes (IRR 1.67 [95% CI 1.06-2.62]; P = .027); RAASi discontinuation increased brain natriuretic peptide levels (% change from baseline: + 16.7% vs-27.5%; P = .024) and the incidence of acute heart failure (33% vs 4.2%, P = .016). Conclusion RAASi continuation in participants hospitalized with COVID-19 appears safe; discontinuation increased brain natriuretic peptide levels and may increase risk of acute heart failure; where possible, RAASi should be continued.

Dados da publicação

ISSN/ISSNe:
1097-6744, 0002-8703

American Heart Journal  Mosby Inc.

Tipo:
Article
Páginas:
76-89
Link para outro recurso:
www.scopus.com

Citações Recebidas na Web of Science: 11

Citações Recebidas na Scopus: 13

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Keywords

  • Adult; Aged; Aldosterone; Angiotensin Receptor Antagonists; Angiotensin-Converting Enzyme Inhibitors; Antihypertensive Agents; COVID-19; Female; Heart Failure; Hospitals; Humans; Natriuretic Peptide, Brain; Renin-Angiotensin System; acetylsalicylic acid; angiotensin receptor antagonist; anti-SARS-CoV-2 agent; anticoagulant agent; antihypertensive agent; antineoplastic agent; beta adrenergic receptor blocking agent; biological marker; brain natriuretic peptide; C reactive protein; calcium channel blocking agent; dexamethasone; dipeptidyl carboxypeptidase inhibitor; glucose; hemoglobin; hydroxymethylglutaryl coenzyme A reductase inhibitor; mineralocorticoid antagonist; nonsteroid antiinflammatory agent; potassium; sodium; troponin; troponin I; warfarin; aldosterone; angiotensin receptor antagonist; antihypertensive agent; brain natriuretic peptide; dipeptidyl carboxypeptidase inhibitor; acute heart failure; acute heart infarction; acute kidney failure; adverse drug reaction; African Amer

Financiamento

Proyectos asociados

Dapagliflozin, Spironolactone or Both for HFpEF (SOGALDI-PEF) - NCT05676684

Investigador Principal: João Pedro Melo Marques Pinho Ferreira

Ensaio Clínico Académico (SOGALDI-PEF) . AstraZeneca . 2022

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