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Discontinuing vs continuing ACEIs and ARBs in hospitalized patients with COVID-19 according to disease severity: Insights from the BRACE CORONA trial.
Macedo, Ariane Vieira Scarlatelli; de Barros E Silva, Pedro Gabriel Melo; de Paula, Thiago Ceccatto; Moll-Bernardes, Renata Junqueira; Mendonça Dos Santos, Tiago; Mazza, Lilian; Feldman, Andre; Arruda, Guilherme D Andréa Saba; de Albuquerque, Denílson Campos; de Sousa, Andrea Silvestre; de Souza, Olga Ferreira; Gibson, C Michael; Granger, Christopher B; Alexander, John H; Lopes, Renato D.
  • Macedo AVS; D'Or Institute for Research and Education (IDOR), Rio de Janeiro, Brazil; Hospital São Luiz Jabaquara, São Paulo, Brazil; Programa de Pós-Graduação em Medicina Translacional, Universidade Federal de São Paulo, São Paulo, Brazil; Brazilian Clinical Research Institute, São Paulo, Brazil.
  • de Barros E Silva PGM; Brazilian Clinical Research Institute, São Paulo, Brazil; Centro Universitário São Camilo, São Paulo, Brazil.
  • de Paula TC; Hospital São Luiz Jabaquara, São Paulo, Brazil; Brazilian Clinical Research Institute, São Paulo, Brazil.
  • Moll-Bernardes RJ; D'Or Institute for Research and Education (IDOR), Rio de Janeiro, Brazil.
  • Mendonça Dos Santos T; Brazilian Clinical Research Institute, São Paulo, Brazil; Insper Institute of Education and Research, São Paulo, Brazil.
  • Mazza L; Brazilian Clinical Research Institute, São Paulo, Brazil.
  • Feldman A; D'Or Institute for Research and Education (IDOR), Rio de Janeiro, Brazil; Hospital São Luiz Anália Franco, São Paulo, Brazil.
  • Arruda GDAS; D'Or Institute for Research and Education (IDOR), Rio de Janeiro, Brazil; Hospital São Luiz São Caetano, São Caetano do Sul, Brazil.
  • de Albuquerque DC; D'Or Institute for Research and Education (IDOR), Rio de Janeiro, Brazil; Universidade do Estado do Rio de Janeiro (UERJ), Rio de Janeiro, Brazil.
  • de Sousa AS; D'Or Institute for Research and Education (IDOR), Rio de Janeiro, Brazil; Evandro Chagas National Institute of Infectious Diseases, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil; Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil.
  • de Souza OF; D'Or Institute for Research and Education (IDOR), Rio de Janeiro, Brazil; Rede D'Or São Luiz (RDSL), São Paulo, Brazil; Hospital Copa D'Or, Rio de Janeiro, Brazil.
  • Gibson CM; Harvard Medical School, Boston, MA, USA.
  • Granger CB; Duke Clinical Research Institute, Duke University Medical Center, Durham, NC, USA.
  • Alexander JH; Duke Clinical Research Institute, Duke University Medical Center, Durham, NC, USA.
  • Lopes RD; D'Or Institute for Research and Education (IDOR), Rio de Janeiro, Brazil; Programa de Pós-Graduação em Medicina Translacional, Universidade Federal de São Paulo, São Paulo, Brazil; Brazilian Clinical Research Institute, São Paulo, Brazil; Rede D'Or São Luiz (RDSL), São Paulo, Brazil; Duke Clinical R
Am Heart J ; 249: 86-97, 2022 07.
Статья в английский | MEDLINE | ID: covidwho-1777919
ABSTRACT

BACKGROUND:

We explored the effect of discontinuing versus continuing angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin II receptor blockers (ARBs) on clinical outcomes in patients with COVID-19 according to baseline disease severity.

METHODS:

We randomized 659 patients with a confirmed diagnosis of COVID-19 and classified them as having mild or moderate COVID-19 disease severity at hospital presentation using blood oxygen saturation and lung imaging. The primary outcome was the mean ratio of number of days alive and out of the hospital at 30 days according to disease severity.

RESULTS:

At presentation, 376 patients (57.1%) had mild and 283 (42.9%) had moderate COVID-19. In patients with mild disease, there was no significant difference in the number of days alive and out of the hospital between ACEI/ARB discontinuation (mean 23.5 [SD 6.3] days) and continuation (mean 23.8 [SD 6.5] days), with a mean ratio of 0.98 (95% CI 0.92-1.04). However, in patients with moderate disease, there were fewer days alive and out of the hospital with ACEI/ARB discontinuation (mean 19.6 [SD 9.5] days) than continuation (mean 21.6 [SD 7.6] days), with a mean ratio of 0.90 (95% CI 0.81-1.00; P-interaction = .01). The impact of discontinuing versus continuing ACEIs/ARBs on days alive and out of hospital through 30 days differed according to baseline COVID-19 disease severity.

CONCLUSIONS:

Unlike patients with mild disease, patients with moderate disease who continued ACEIs/ARBs had more days alive and out of hospital through 30 days than those who discontinued ACEIs/ARBs. This suggests that ACEIs/ARBs should be continued for patients with moderate COVID-19 disease severity. CLINICAL TRIAL REGISTRATION ClinicalTrials.gov (NCT04364893).
Тема - темы

Полный текст: Имеется в наличии Коллекция: Международные базы данных база данных: MEDLINE Основная тема: COVID-19 / Hypertension Тип исследования: Экспериментальные исследования / Прогностическое исследование / Рандомизированные контролируемые испытания Пределы темы: Люди Язык: английский Журнал: Am Heart J Год: 2022 Тип: Статья Аффилированная страна: J.ahj.2022.04.001

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Полный текст: Имеется в наличии Коллекция: Международные базы данных база данных: MEDLINE Основная тема: COVID-19 / Hypertension Тип исследования: Экспериментальные исследования / Прогностическое исследование / Рандомизированные контролируемые испытания Пределы темы: Люди Язык: английский Журнал: Am Heart J Год: 2022 Тип: Статья Аффилированная страна: J.ahj.2022.04.001