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The efficacy of anakinra compared to standard care of treatment for COVID-19: a meta-analysis

BACKGROUND/AIM: As SARS-CoV-2 continues to spread worldwide, this study brings to light the link that anakinra, a recombinant IL-1 receptor antagonist, has in averting grave clinical outcomes. The objectives of this meta-analysis are to investigate the effects of anakinra in interventional groups co...

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Autores principales: MALIK, Hamna, BINT ABDUL JABBAR, Hira, LATIF, Farah, SARFRAZ, Azza, SARFRAZ, Zouina, SARFRAZ, Muzna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific and Technological Research Council of Turkey (TUBITAK) 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390186/
https://www.ncbi.nlm.nih.gov/pubmed/36326309
http://dx.doi.org/10.55730/1300-0144.5345
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author MALIK, Hamna
BINT ABDUL JABBAR, Hira
LATIF, Farah
SARFRAZ, Azza
SARFRAZ, Zouina
SARFRAZ, Muzna
author_facet MALIK, Hamna
BINT ABDUL JABBAR, Hira
LATIF, Farah
SARFRAZ, Azza
SARFRAZ, Zouina
SARFRAZ, Muzna
author_sort MALIK, Hamna
collection PubMed
description BACKGROUND/AIM: As SARS-CoV-2 continues to spread worldwide, this study brings to light the link that anakinra, a recombinant IL-1 receptor antagonist, has in averting grave clinical outcomes. The objectives of this meta-analysis are to investigate the effects of anakinra in interventional groups compared to control/standard of care groups on mortality along with the provision of a prevalence estimate of the variables associated with death (C-reactive protein-CRP, ferritin, acute respiratory distress syndrome-ARDS). MATERIALS AND METHODS: According to the PRISMA 2020 statement guidelines, a systematic search was conducted from December 19, 2020, until December 10, 2021, with keywords including COVID-19, coronavirus, SARS-CoV-2, anakinra, mortality, across the following databases: PubMed/MEDLINE, Scopus, Web of Science, CINAHL Plus, and Cochrane. A random-effects model was applied using RevMan 5.4 for all statistical analyses. RESULTS: The meta-analysis pooled in 1297 participants with 565 (43.6%) patients in the anakinra group. When comparing to the control/standard of care group, the anakinra group had a much lower risk of death (RR = 0.47. 95% CI = 0.37–0.59, Z = 6.44; P < 0.001). In addition to the risk of death being reduced by around 50% in the interventional group, prognostic indicators such as CRP and ferritin were improved with fewer occurrences of severe ARDS. CONCLUSION: Patients with COVID-19 pneumonia may be treated with anakinra as a safe and viable treatment modality to defer adverse outcomes such as a death in the 28-day period. Despite an auspicious premise, our findings must be used with caution as adequately powered randomized, placebo-controlled trials are required to corroborate these findings.
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spelling pubmed-103901862023-08-01 The efficacy of anakinra compared to standard care of treatment for COVID-19: a meta-analysis MALIK, Hamna BINT ABDUL JABBAR, Hira LATIF, Farah SARFRAZ, Azza SARFRAZ, Zouina SARFRAZ, Muzna Turk J Med Sci Research Article BACKGROUND/AIM: As SARS-CoV-2 continues to spread worldwide, this study brings to light the link that anakinra, a recombinant IL-1 receptor antagonist, has in averting grave clinical outcomes. The objectives of this meta-analysis are to investigate the effects of anakinra in interventional groups compared to control/standard of care groups on mortality along with the provision of a prevalence estimate of the variables associated with death (C-reactive protein-CRP, ferritin, acute respiratory distress syndrome-ARDS). MATERIALS AND METHODS: According to the PRISMA 2020 statement guidelines, a systematic search was conducted from December 19, 2020, until December 10, 2021, with keywords including COVID-19, coronavirus, SARS-CoV-2, anakinra, mortality, across the following databases: PubMed/MEDLINE, Scopus, Web of Science, CINAHL Plus, and Cochrane. A random-effects model was applied using RevMan 5.4 for all statistical analyses. RESULTS: The meta-analysis pooled in 1297 participants with 565 (43.6%) patients in the anakinra group. When comparing to the control/standard of care group, the anakinra group had a much lower risk of death (RR = 0.47. 95% CI = 0.37–0.59, Z = 6.44; P < 0.001). In addition to the risk of death being reduced by around 50% in the interventional group, prognostic indicators such as CRP and ferritin were improved with fewer occurrences of severe ARDS. CONCLUSION: Patients with COVID-19 pneumonia may be treated with anakinra as a safe and viable treatment modality to defer adverse outcomes such as a death in the 28-day period. Despite an auspicious premise, our findings must be used with caution as adequately powered randomized, placebo-controlled trials are required to corroborate these findings. Scientific and Technological Research Council of Turkey (TUBITAK) 2022-01-25 /pmc/articles/PMC10390186/ /pubmed/36326309 http://dx.doi.org/10.55730/1300-0144.5345 Text en © TÜBİTAK https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License.
spellingShingle Research Article
MALIK, Hamna
BINT ABDUL JABBAR, Hira
LATIF, Farah
SARFRAZ, Azza
SARFRAZ, Zouina
SARFRAZ, Muzna
The efficacy of anakinra compared to standard care of treatment for COVID-19: a meta-analysis
title The efficacy of anakinra compared to standard care of treatment for COVID-19: a meta-analysis
title_full The efficacy of anakinra compared to standard care of treatment for COVID-19: a meta-analysis
title_fullStr The efficacy of anakinra compared to standard care of treatment for COVID-19: a meta-analysis
title_full_unstemmed The efficacy of anakinra compared to standard care of treatment for COVID-19: a meta-analysis
title_short The efficacy of anakinra compared to standard care of treatment for COVID-19: a meta-analysis
title_sort efficacy of anakinra compared to standard care of treatment for covid-19: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390186/
https://www.ncbi.nlm.nih.gov/pubmed/36326309
http://dx.doi.org/10.55730/1300-0144.5345
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