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COVID-19-associated ARDS treated with DEXamethasone (CoDEX): study design and rationale for a randomized trial.

Publication ,  Journal Article
Tomazini, BM; Maia, IS; Bueno, FR; Silva, MVAO; Baldassare, FP; Costa, ELV; Moura, RAB; Honorato, MO; Costa, AN; Cavalcanti, AB; Rosa, RG ...
Published in: Rev Bras Ter Intensiva
2020

OBJECTIVE: The infection caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spreads worldwide and is considered a pandemic. The most common manifestation of SARS-CoV-2 infection (coronavirus disease 2019 - COVID-19) is viral pneumonia with varying degrees of respiratory compromise and up to 40% of hospitalized patients might develop acute respiratory distress syndrome. Several clinical trials evaluated the role of corticosteroids in non-COVID-19 acute respiratory distress syndrome with conflicting results. We designed a trial to evaluate the effectiveness of early intravenous dexamethasone administration on the number of days alive and free of mechanical ventilation within 28 days after randomization in adult patients with moderate or severe acute respiratory distress syndrome due to confirmed or probable COVID-19. METHODS: This is a pragmatic, prospective, randomized, stratified, multicenter, open-label, controlled trial including 350 patients with early-onset (less than 48 hours before randomization) moderate or severe acute respiratory distress syndrome, defined by the Berlin criteria, due to COVID-19. Eligible patients will be randomly allocated to either standard treatment plus dexamethasone (Intervention Group) or standard treatment without dexamethasone (Control Group). Patients in the intervention group will receive dexamethasone 20mg intravenous once daily for 5 days, followed by dexamethasone 10mg IV once daily for additional 5 days or until intensive care unit discharge, whichever occurs first. The primary outcome is ventilator-free days within 28 days after randomization, defined as days alive and free from invasive mechanical ventilation. Secondary outcomes are all-cause mortality rates at day 28, evaluation of the clinical status at day 15 assessed with a 6-level ordinal scale, mechanical ventilation duration from randomization to day 28, Sequential Organ Failure Assessment Score evaluation at 48 hours, 72 hours and 7 days and intensive care unit -free days within 28.

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Published In

Rev Bras Ter Intensiva

DOI

EISSN

1982-4335

Publication Date

2020

Volume

32

Issue

3

Start / End Page

354 / 362

Location

Brazil

Related Subject Headings

  • Time Factors
  • Respiratory Distress Syndrome
  • Respiration, Artificial
  • Randomized Controlled Trials as Topic
  • Prospective Studies
  • Pragmatic Clinical Trials as Topic
  • Pandemics
  • Organ Dysfunction Scores
  • Multicenter Studies as Topic
  • Intensive Care Units
 

Citation

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Tomazini, B. M., Maia, I. S., Bueno, F. R., Silva, M. V. A. O., Baldassare, F. P., Costa, E. L. V., … em nome dos investigadores da COALIZÃO COVID-19 BRASIL III, . (2020). COVID-19-associated ARDS treated with DEXamethasone (CoDEX): study design and rationale for a randomized trial. Rev Bras Ter Intensiva, 32(3), 354–362. https://doi.org/10.5935/0103-507X.20200063
Tomazini, Bruno Martins, Israel Silva Maia, Flavia Regina Bueno, Maria Vitoria Aparecida Oliveira Silva, Franca Pellison Baldassare, Eduardo Leite Vieira Costa, Ricardo Antonio Bonifácio Moura, et al. “COVID-19-associated ARDS treated with DEXamethasone (CoDEX): study design and rationale for a randomized trial.Rev Bras Ter Intensiva 32, no. 3 (2020): 354–62. https://doi.org/10.5935/0103-507X.20200063.
Tomazini BM, Maia IS, Bueno FR, Silva MVAO, Baldassare FP, Costa ELV, et al. COVID-19-associated ARDS treated with DEXamethasone (CoDEX): study design and rationale for a randomized trial. Rev Bras Ter Intensiva. 2020;32(3):354–62.
Tomazini, Bruno Martins, et al. “COVID-19-associated ARDS treated with DEXamethasone (CoDEX): study design and rationale for a randomized trial.Rev Bras Ter Intensiva, vol. 32, no. 3, 2020, pp. 354–62. Pubmed, doi:10.5935/0103-507X.20200063.
Tomazini BM, Maia IS, Bueno FR, Silva MVAO, Baldassare FP, Costa ELV, Moura RAB, Honorato MO, Costa AN, Cavalcanti AB, Rosa RG, Avezum Á, Veiga VC, Lopes RD, Damiani LP, Machado FR, Berwanger O, Azevedo LCPD, em nome dos investigadores da COALIZÃO COVID-19 BRASIL III. COVID-19-associated ARDS treated with DEXamethasone (CoDEX): study design and rationale for a randomized trial. Rev Bras Ter Intensiva. 2020;32(3):354–362.

Published In

Rev Bras Ter Intensiva

DOI

EISSN

1982-4335

Publication Date

2020

Volume

32

Issue

3

Start / End Page

354 / 362

Location

Brazil

Related Subject Headings

  • Time Factors
  • Respiratory Distress Syndrome
  • Respiration, Artificial
  • Randomized Controlled Trials as Topic
  • Prospective Studies
  • Pragmatic Clinical Trials as Topic
  • Pandemics
  • Organ Dysfunction Scores
  • Multicenter Studies as Topic
  • Intensive Care Units