Interleukin-6 Receptor Antagonists in Critically Ill Patients with Covid-19
Autor: | Gordon, A.C., Mouncey, P.R., Al-Beidh, F., Rowan, K.M., Nichol, A.D., Arabi, Y.M., Annane, D., Beane, A., Bentum-Puijk, W. van, Berry, L.R., Bhimani, Z., Bonten, M.J.M., Bradbury, C.A., Brunkhorst, F.M., Buzgau, A., Cheng, A.C., Detry, M.A., Duffy, E.J., Estcourt, L.J., Fitzgerald, M., Goossens, H., Haniffa, R., Higgins, A.M., Hills, T.E., Horvat, C.M., Lamontagne, F., Lawler, P.R., Leavis, H.L., Linstrum, K.M., Litton, E., Lorenzi, E., Marshall, J.C., Mayr, F.B., McAuley, D.F., McGlothlin, A., McGuinness, S.P., McVerry, B.J., Montgomery, S.K., Morpeth, S.C., Murthy, S., Orr, K., Parke, R.L., Parker, J.C., Patanwala, A.E., Pettilä, V., Rademaker, E., Santos, M.S., Saunders, C.T., Seymour, C.W., Shankar-Hari, M., Sligl, W.I., Turgeon, A.F., Turner, A.M., Veerdonk, F.L. van de, Zarychanski, R., Green, C., Lewis, R.J., Angus, D.C., McArthur, C.J., Berry, S., Schouten, J.A., Pickkers, P., Webb, S.A., Derde, L.P.G. |
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Přispěvatelé: | Université de Versailles Saint-Quentin-en-Yvelines - UFR Sciences de la santé Simone Veil (UVSQ Santé), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), REMAP-CAP Investigators, Pour la France: Bruno Megarbane, Inserm U1144, European Project: 602386,EC:FP7:HEALTH,FP7-HEALTH-2013-INNOVATION-1,CREDITS4HEALTH(2013), European Project: 602525,EC:FP7:HEALTH,FP7-HEALTH-2013-INNOVATION-1,PREPARE(2014), NIHR, National Institute for Health Research, Gordon, Anthony C [0000-0002-0419-547X], Mouncey, Paul R [0000-0002-8510-8517], Beane, Abi [0000-0001-7046-1580], Bradbury, Charlotte A [0000-0001-5248-8165], Detry, Michelle A [0000-0002-2794-1439], Duffy, Eamon J [0000-0002-4515-5116], Estcourt, Lise J [0000-0003-4309-9162], Haniffa, Rashan [0000-0002-8288-449X], Higgins, Alisa M [0000-0001-8295-7559], Hills, Thomas E [0000-0003-0322-5822], Horvat, Christopher M [0000-0002-1593-2252], Lawler, Patrick R [0000-0001-5155-5071], Litton, Edward [0000-0002-5125-6829], Mayr, Florian B [0000-0002-2298-9011], McVerry, Bryan J [0000-0002-1175-4874], Patanwala, Asad E [0000-0003-3999-4703], Saunders, Christina T [0000-0003-4325-9568], Shankar-Hari, Manu [0000-0002-5338-2538], Angus, Derek C [0000-0002-7026-5181], Derde, Lennie PG [0000-0002-3577-5629], Apollo - University of Cambridge Repository, Investigators, REMAP-CAP, HAL UVSQ, Équipe, Credits-based, people-centric approach for the adoption of healthy life-styles and balanced Mediterranean diet in the frame of social participation and innovation for health promotion. - CREDITS4HEALTH - - EC:FP7:HEALTH2013-09-01 - 2016-08-31 - 602386 - VALID, Platform foR European Preparedness Against (Re-)emerging Epidemics - PREPARE - - EC:FP7:HEALTH2014-02-01 - 2019-01-31 - 602525 - VALID |
Rok vydání: | 2021 |
Předmět: |
Male
[SDV]Life Sciences [q-bio] lnfectious Diseases and Global Health Radboud Institute for Molecular Life Sciences [Radboudumc 4] 030204 cardiovascular system & hematology law.invention chemistry.chemical_compound 0302 clinical medicine Randomized controlled trial law Interquartile range middle aged Credible interval Odds Ratio odds ratio 030212 general & internal medicine Hospital Mortality humans 11 Medical and Health Sciences adult Hazard ratio Covid19 General Medicine Middle Aged Intensive care unit 3. Good health [SDV] Life Sciences [q-bio] aged Intensive Care Units Antibodies Monoclonal Humanized/adverse effects COVID-19/complications Original Article Female Adult medicine.medical_specialty Critical Care Critical Illness Antibodies Monoclonal Humanized 03 medical and health sciences Tocilizumab male Internal medicine General & Internal Medicine medicine Humans Aged hospital mortality business.industry SARS-CoV-2 COVID-19 Odds ratio Receptors Interleukin-6 Respiration Artificial COVID-19 Drug Treatment Coronavirus Sarilumab lnfectious Diseases and Global Health Radboud Institute for Health Sciences [Radboudumc 4] chemistry Receptors Interleukin-6/antagonists & inhibitors REMAP-CAP Investigators interleukin-6 receptor antagonists coronavirus disease business |
Zdroj: | New England Journal of Medicine New England Journal of Medicine, Massachusetts Medical Society, 2021, 384 (16), pp.1491-1502. ⟨10.1056/NEJMoa2100433⟩ McAuley, D & Writing Committee, REMAP-CAP 2021, ' Interleukin-6 Receptor Antagonists in Critically Ill Patients with Covid-19 ', New England Journal of Medicine . https://doi.org/10.1056/NEJMoa2100433 2021, ' Interleukin-6 Receptor Antagonists in Critically Ill Patients with Covid-19 ', New England Journal of Medicine, vol. 384, no. 16, pp. 1491-1502 . https://doi.org/10.1056/NEJMoa2100433 The New England Journal of Medicine, 384, 16, pp. 1491-1502 The New England Journal of Medicine, 384, 1491-1502 NEW ENGLAND JOURNAL OF MEDICINE REMAP-CAP Investigators, Felton, T & Dark, P 2021, ' Interleukin-6 Receptor Antagonists in Critically Ill Patients with Covid-19 ', The New England Journal of Medicine, vol. 384, no. 16, pp. 1491-1502 . https://doi.org/10.1056/NEJMoa2100433 The New England Journal of Medicine |
ISSN: | 1533-4406 0028-4793 |
Popis: | BACKGROUNDThe efficacy of interleukin-6 receptor antagonists in critically ill patients with coronavirus disease 2019 (Covid-19) is unclear.METHODSWe evaluated tocilizumab and sarilumab in an ongoing international, multifactorial, adaptive platform trial. Adult patients with Covid-19, within 24 hours after starting organ support in the intensive care unit (ICU), were randomly assigned to receive tocilizumab (8 mg per kilogram of body weight), sarilumab (400 mg), or standard care (control). The primary outcome was respiratory and cardiovascular organ support–free days, on an ordinal scale combining in-hospital death (assigned a value of −1) and days free of organ support to day 21. The trial uses a Bayesian statistical model with predefined criteria for superiority, efficacy, equivalence, or futility. An odds ratio greater than 1 represented improved survival, more organ support–free days, or both.RESULTSBoth tocilizumab and sarilumab met the predefined criteria for efficacy. At that time, 353 patients had been assigned to tocilizumab, 48 to sarilumab, and 402 to control. The median number of organ support–free days was 10 (interquartile range, −1 to 16) in the tocilizumab group, 11 (interquartile range, 0 to 16) in the sarilumab group, and 0 (interquartile range, −1 to 15) in the control group. The median adjusted cumulative odds ratios were 1.64 (95% credible interval, 1.25 to 2.14) for tocilizumab and 1.76 (95% credible interval, 1.17 to 2.91) for sarilumab as compared with control, yielding posterior probabilities of superiority to control of more than 99.9% and of 99.5%, respectively. An analysis of 90-day survival showed improved survival in the pooled interleukin-6 receptor antagonist groups, yielding a hazard ratio for the comparison with the control group of 1.61 (95% credible interval, 1.25 to 2.08) and a posterior probability of superiority of more than 99.9%. All secondary analyses supported efficacy of these interleukin-6 receptor antagonists.CONCLUSIONSIn critically ill patients with Covid-19 receiving organ support in ICUs, treatment with the interleukin-6 receptor antagonists tocilizumab and sarilumab improved outcomes, including survival. (REMAP-CAP ClinicalTrials.gov number, NCT02735707. opens in new tab.) |
Databáze: | OpenAIRE |
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