Effect of high


Journal

The European respiratory journal
ISSN: 1399-3003
Titre abrégé: Eur Respir J
Pays: England
ID NLM: 8803460

Informations de publication

Date de publication:
08 2022
Historique:
received: 18 09 2021
accepted: 02 12 2021
pubmed: 18 12 2021
medline: 9 8 2022
entrez: 17 12 2021
Statut: epublish

Résumé

Low-dose dexamethasone demonstrated clinical improvement in patients with coronavirus disease 2019 (COVID-19) needing oxygen therapy; however, evidence on the efficacy of high-dose dexamethasone is limited. We performed a randomised, open-label, controlled trial involving hospitalised patients with confirmed COVID-19 pneumonia needing oxygen therapy. Patients were randomly assigned in a 1:1 ratio to receive low-dose dexamethasone (6 mg once daily for 10 days) or high-dose dexamethasone (20 mg once daily for 5 days, followed by 10 mg once daily for an additional 5 days). The primary outcome was clinical worsening within 11 days since randomisation. Secondary outcomes included 28-day mortality, time to recovery and clinical status at day 5, 11, 14 and 28 on an ordinal scale ranging from 1 (discharged) to 7 (death). A total of 200 patients (mean±sd age 64±14 years; 62% male) were enrolled. 32 (31.4%) out of 102 patients enrolled in the low-dose group and 16 (16.3%) out of 98 in the high-dose group showed clinical worsening within 11 days since randomisation (rate ratio 0.427, 95% CI 0.216-0.842; p=0.014). The 28-day mortality was 5.9% in the low-dose group and 6.1% in the high-dose group (p=0.844). There was no significant difference in time to recovery, and in the seven-point ordinal scale at days 5, 11, 14 and 28. Among hospitalised COVID-19 patients needing oxygen therapy, high dose of dexamethasone reduced clinical worsening within 11 days after randomisation, compared with low dose.

Sections du résumé

BACKGROUND
Low-dose dexamethasone demonstrated clinical improvement in patients with coronavirus disease 2019 (COVID-19) needing oxygen therapy; however, evidence on the efficacy of high-dose dexamethasone is limited.
METHODS
We performed a randomised, open-label, controlled trial involving hospitalised patients with confirmed COVID-19 pneumonia needing oxygen therapy. Patients were randomly assigned in a 1:1 ratio to receive low-dose dexamethasone (6 mg once daily for 10 days) or high-dose dexamethasone (20 mg once daily for 5 days, followed by 10 mg once daily for an additional 5 days). The primary outcome was clinical worsening within 11 days since randomisation. Secondary outcomes included 28-day mortality, time to recovery and clinical status at day 5, 11, 14 and 28 on an ordinal scale ranging from 1 (discharged) to 7 (death).
RESULTS
A total of 200 patients (mean±sd age 64±14 years; 62% male) were enrolled. 32 (31.4%) out of 102 patients enrolled in the low-dose group and 16 (16.3%) out of 98 in the high-dose group showed clinical worsening within 11 days since randomisation (rate ratio 0.427, 95% CI 0.216-0.842; p=0.014). The 28-day mortality was 5.9% in the low-dose group and 6.1% in the high-dose group (p=0.844). There was no significant difference in time to recovery, and in the seven-point ordinal scale at days 5, 11, 14 and 28.
CONCLUSIONS
Among hospitalised COVID-19 patients needing oxygen therapy, high dose of dexamethasone reduced clinical worsening within 11 days after randomisation, compared with low dose.

Identifiants

pubmed: 34916266
pii: 13993003.02518-2021
doi: 10.1183/13993003.02518-2021
pmc: PMC8678498
pii:
doi:

Substances chimiques

Dexamethasone 7S5I7G3JQL
Oxygen S88TT14065

Banques de données

ClinicalTrials.gov
['NCT04726098']
EudraCT
['EudraCT2020-005702-25']

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright ©The authors 2022.

Déclaration de conflit d'intérêts

Conflict of interest: The authors declare the absence of conflict of interests.

Auteurs

Manuel Taboada (M)

Dept of Anesthesiology and Intensive Care Medicine, Clinical University Hospital of Santiago, Sanitary Research Institute of Santiago (IDIS), Santiago de Compostela, Spain manutabo@yahoo.es.

Nuria Rodríguez (N)

Dept of Pneumology, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

Pablo Manuel Varela (PM)

Dept Internal Medicine, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

María Teresa Rodríguez (MT)

Dept Pharmacology, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

Romina Abelleira (R)

Dept of Pneumology, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

Amara González (A)

Dept Internal Medicine, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

Ana Casal (A)

Dept of Pneumology, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

José Antonio Díaz Peromingo (JA)

Dept Internal Medicine, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

Adriana Lama (A)

Dept of Pneumology, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

María Jesús Domínguez (MJ)

Dept Internal Medicine, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

Carlos Rábade (C)

Dept of Pneumology, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

Emilio Manuel Páez (EM)

Dept Internal Medicine, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

Vanessa Riveiro (V)

Dept of Pneumology, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

Hadrián Pernas (H)

Dept Internal Medicine, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

María Del Carmen Beceiro (MDC)

Dept Internal Medicine, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

Valentín Caruezo (V)

Dept of Anesthesiology and Intensive Care Medicine, Clinical University Hospital of Santiago, Sanitary Research Institute of Santiago (IDIS), Santiago de Compostela, Spain.

Alberto Naveira (A)

Dept of Anesthesiology and Intensive Care Medicine, Clinical University Hospital of Santiago, Sanitary Research Institute of Santiago (IDIS), Santiago de Compostela, Spain.

Agustín Cariñena (A)

Dept of Anesthesiology and Intensive Care Medicine, Clinical University Hospital of Santiago, Sanitary Research Institute of Santiago (IDIS), Santiago de Compostela, Spain.

Teresa Cabaleiro (T)

Research Methodology Unit, Fundación Instituto de Investigaciones Sanitarias (FIDIS), Santiago de Compostela, Spain.

Ana Estany-Gestal (A)

Research Methodology Unit, Fundación Instituto de Investigaciones Sanitarias (FIDIS), Santiago de Compostela, Spain.

Irene Zarra (I)

Dept Pharmacology, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

Antonio Pose (A)

Dept Internal Medicine, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

Luis Valdés (L)

Dept of Pneumology, Clinical University Hospital of Santiago, Santiago de Compostela, Spain.

Julián Álvarez-Escudero (J)

Dept of Anesthesiology and Intensive Care Medicine, Clinical University Hospital of Santiago, Sanitary Research Institute of Santiago (IDIS), Santiago de Compostela, Spain.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH