3.8 Article

Clinical impact of combination therapy with baricitinib, remdesivir, and dexamethasone in patients with severe COVID-19

期刊

RESPIRATORY INVESTIGATION
卷 59, 期 6, 页码 799-803

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ELSEVIER
DOI: 10.1016/j.resinv.2021.07.004

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Coronavirus disease 2019; Severe acute respiratory syndrome coronavirus 2; Acute respiratory distress syndrome; Adverse event; Efficacy

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The study indicates that combination therapy with BRD is effective in treating severe COVID-19, with a low incidence rate of adverse events. It can significantly reduce the need for invasive mechanical ventilation and shorten the hospitalization duration for patients.
Background: Coronavirus disease 2019 (COVID-19) has spread worldwide and is also an important disease in Japan. Thus, the optimal treatment strategy for severe COVID-19 should be established urgently. The effects of combination treatment with baricitinib-a Janus kinase inhibitor, remdesivir, and dexamethasone (BRD) are unknown. Methods: Patients who received combination therapy with BRD at the Japanese Red Cross Medical Center were enrolled in the study. All patients received baricitinib (<= 14 d), remdesivir (<= 10 d), and dexamethasone (<= 10 d). The efficacy and adverse events were evaluated. Results: In total, 44 patients with severe COVID-19 were enrolled in this study. The 28-d mortality rate was low at 2.3% (1/44 patients). The need for invasive mechanical ventilation was avoided in most patients (90%, 17/19 patients). Patients who received BRD therapy had a median hospitalization duration of 11 d, time to recovery of 9 d, duration of intensive care unit stay of 6 d, duration of invasive mechanical ventilation of 5 d, and duration of supplemental oxygen therapy of 5 d. Adverse events occurred in 15 patients (34%). Liver dysfunction, thrombosis, iliopsoas hematoma, renal dysfunction, ventilator- associated pneumonia, infective endocarditis, and herpes zoster occurred in 11%, 11%, 2%, 2%, 2%, 2%, and 2% of patients, respectively. Conclusions: Combination therapy with BRD was effective in treating severe COVID-19, and the incidence rate of adverse events was low. The results of the present study are encouraging; however, further randomized clinical studies are needed. (C) 2021 The Japanese Respiratory Society. Published by Elsevier B.V. All rights reserved.

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