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المؤلفElmekaty, Eman Zeyad I.
المؤلفMaklad, Aya
المؤلفAbouelhassan, Rawan
المؤلفMunir, Waqar
المؤلفIbrahim, Mohamed Izham Mohamed
المؤلفNair, Arun
المؤلفAlibrahim, Rim
المؤلفIqbal, Fatima
المؤلفAl Bishawi, Ahmad
المؤلفAbdelmajid, Alaaeldin
المؤلفAboukamar, Mohamed
المؤلفHadi, Hamad Abdel
المؤلفKhattab, Mohammed Abu
المؤلفAl Soub, Hussam
المؤلفAl Maslamani, Muna
تاريخ الإتاحة2023-05-24T10:12:18Z
تاريخ النشر2023-01-26
اسم المنشورFrontiers in Microbiology
المعرّفhttp://dx.doi.org/10.3389/fmicb.2023.1098703
الاقتباسElmekaty, E. Z. I., Maklad, A., Abouelhassan, R., Munir, W., Ibrahim, M. I. M., Nair, A., ... & Al Maslamani, M. (2023). Evaluation of anakinra in the management of patients with COVID-19 infection: A randomized clinical trial. Frontiers in Microbiology, 14.
الرقم المعياري الدولي للكتاب1664-302X
معرّف المصادر الموحدhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85147657343&origin=inward
معرّف المصادر الموحدhttp://hdl.handle.net/10576/43437
الملخصBackground: The global COVID-19 pandemic led to substantial clinical and economic outcomes with catastrophic consequences. While the majority of cases has mild to moderate disease, minority of patients progress into severe disease secondary to the stimulation of the immune response. The hyperinflammatory state contributes towards progression into multi-organ failure which necessitates suppressive therapy with variable outcomes. This study aims to explore the safety and efficacy of anakinra in COVID-19 patients with severe disease leading to cytokine release syndromes. Methods: In this open-label, multi-center, randomized clinical trial, patients with confirmed COVID-19 infection with evidence of respiratory distress and signs of cytokine release syndrome were randomized in 1:1 ratio to receive either standard of care (SOC) or anakinra (100 mg subcutaneously every 12 h for 3 days then 100 mg subcutaneously once daily for 4 days) in addition to SOC. The primary outcome was treatment success at day 14 as defined by the WHO clinical progression score of ≤3. Primary analysis was based upon intention-to-treat population, with value of p of <0.05. Results: Out 327 patients screened for eligibility, 80 patients were recruited for the study. The mean age was 49.9 years (SD = 11.7), with male predominance at 82.5% (n = 66). The primary outcome was not statistically different (87.5% (n = 35) in anakinra group vs. 92.5% (n = 37) in SOC group, p = 0.712; OR = 1.762 (95%CI: 0.39–7.93). The majority of reported adverse events were mild in severity and not related to the study treatment. Elevated aspartate aminotransferase was the only significant adverse event which was not associated with discontinuation of therapy. Conclusion: In patients with severe COVID-19 infection, the addition of anakinra to SOC treatment was safe but was not associated with significant improvement according to the WHO clinical progression scale. Further studies are warranted to explore patients’ subgroups characteristics that might benefit from administered therapy. Clinical Trial Registration: Trial registration at ClinicalTrials.gov, identifier: NCT04643678.
راعي المشروعThis study was funded by the Medical Research Center at Hamad Medical Corporation, Qatar (MRC-01-20-1095).
اللغةen
الناشرFrontiers Media S.A.
الموضوعanakinra
COVID-19
cytokine release syndrome
interlukin-1 inhibitor
pneumonia
SARS-CoV-2
العنوانEvaluation of anakinra in the management of patients with COVID-19 infection: A randomized clinical trial
النوعArticle
رقم المجلد14
dc.accessType Open Access


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