Anakinra after treatment with corticosteroids alone or with tocilizumab in patients with severe COVID‑19 pneumonia and moderate hyperinflammation. A retrospective cohort study: comment
Autor: | Ismael Francisco Aomar-Millán, Juan Salvatierra, Úrsula Torres-Parejo, Naya Faro-Miguez, José Luis Callejas-Rubio, Ángel Ceballos-Torres, María Teresa Cruces-Moreno, Francisco Javier Gómez-Jiménez, José Hernández-Quero, Francisco Anguita-Santos |
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Rok vydání: | 2021 |
Předmět: |
musculoskeletal diseases
Male medicine.medical_specialty Coronavirus disease 2019 (COVID-19) Ce - Letter to the Editor MEDLINE Hyperinflammation 030204 cardiovascular system & hematology Antibodies Monoclonal Humanized Methylprednisolone 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Tocilizumab Internal medicine Internal Medicine medicine Humans In patient 030212 general & internal medicine Glucocorticoids Aged Retrospective Studies Aged 80 and over Anakinra business.industry COVID-19 Retrospective cohort study Middle Aged medicine.disease Im - Original COVID-19 Drug Treatment Survival Rate Interleukin 1 Receptor Antagonist Protein Pneumonia Cytokine storm syndrome Treatment Outcome chemistry Spain Antirheumatic Agents Emergency Medicine Drug Therapy Combination Female business After treatment medicine.drug |
Zdroj: | Internal and Emergency Medicine |
ISSN: | 1970-9366 1828-0447 |
DOI: | 10.1007/s11739-021-02663-6 |
Popis: | Introduction Little evidence appears to exist for the use of anakinra, a recombinant interleukin-1 receptor antagonist, after non-response to treatment with corticosteroids alone or combined with tocilizumab in patients with severe COVID-19 pneumonia and moderate hyperinflammatory state. Patients and Methods A retrospective observational cohort study was carried out involving 143 patients with severe COVID-19 pneumonia and moderate hyperinflammation. They received standard therapy along with pulses of methylprednisolone (group 1) or methylprednisolone plus tocilizumab (group 2), with the possibility of receiving anakinra (group 3) according to protocol. The aim of this study was to assess the role of anakinra in the clinical course (death, admission to the intensive care ward) during the first 60 days after the first corticosteroid pulse. Clinical, laboratory, and imaging characteristics as well as infectious complications were also analyzed. Results 74 patients (51.7%) in group 1, 59 (41.3%) patients in group 2, and 10 patients (7%) in group 3 were included. 8 patients (10.8%) in group 1 died, 6 (10.2%) in group 2, and 0 (0%) in group 3. After adjustment for age and clinical severity indices, treatment with anakinra was associated with a reduced risk of mortality (adjusted hazard ratio 0.518, 95% CI 0.265–0.910; p = 0.0437). Patients in group 3 had a lower mean CD4 count after 3 days of treatment. No patients in this group presented infectious complications. Conclusions In patients with moderate hyperinflammatory state associated with severe COVID-19 pneumonia, treatment with anakinra after non-response to corticosteroids or corticosteroids plus tocilizumab therapy may be an option for the management of these patients and may improve their prognosis. |
Databáze: | OpenAIRE |
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