P188 Tick tock...where and when can we give toc? Review of COVID-19 patients receiving tocilizumab in a non critical care setting

K. Aiken, M. Wilson, E. Keelan
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Abstract

IntroductionThe REMAP-CAP trial demonstrated the positive effects of interleukin-6 receptor antagonists (tocilizumab and sarilumab), on mortality in COVID-19 patients managed in a critical care setting.1 Prior to this, adjuvant drug therapies such as remdesivir and dexamethasone have shown limited benefits regarding COVID-19 related mortality in patients requiring non-invasive respiratory, managed in non-critical care settings.During the pandemic the Mater Hospital, Belfast was designed as the local COVID-19 centre. Prior to January 2021 standard ward level care included IV antibiotics, IV remdesivir, oral dexamethasone and non-invasive ventilation. Continuous positive airway pressure was used first line (commenced when FiO2 requirements exceeded 4L/min via nasal cannula). After the release of the Department of Health’s position statement regarding tocilizumab for COVID-19 patients on respiratory support, a decision was taken to use tocilizumab off license in a non-critical care setting.Our hypothesis was that COVID-19 positive patients on non-invasive ventilation who received tocilizumab in addition to standard care would have reduced hospital mortality compared with standard care alone. The REMAP-CAP trial administered tocilizumab to COVID-19 patients in a critical care setting, however we postulated that those ‘less unwell’ patients requiring ward level respiratory support but not ‘critical care’ could still benefit.MethodsPatients commenced on tocilizumab in a non-critical care setting were identified and followed up prospectively. A control group receiving ward level standard care was established retrospectively.ResultsForty patients were recruited into both the control and treatment groups. Results were analysed using Chi-squared statistics on Microsoft Excel. The primary outcome, namely;hospital mortality, demonstrated a significant difference between the groups (p=0.048) with no discernible difference in side effect profile.ConclusionThis data supports the use of tocilizumab in patients with COVID-19 disease, noting its positive effect on hospital mortality for COVID-19 patients on non-invasive respiratory support but not requiring critical care. Moreover, the limited side effect profile witnessed suggests tocilizumab can be safely administered in a non-critical care setting.ReferenceGordon AC, Mouncey PR, Al-Beidh F, Rowan KM, Nichol AD, Arabi YM, et al. Interleukin-6 receptor antagonists in critically ill patients with COVID-19–preliminary report. medRxiv. 2021.
P188嘀嗒……我们可以在什么地方和什么时候交货?在非重症监护环境中接受托珠单抗治疗的COVID-19患者综述
REMAP-CAP试验证明了白细胞介素-6受体拮抗剂(托珠单抗和沙伐单抗)对重症监护下COVID-19患者死亡率的积极影响在此之前,瑞德西韦和地塞米松等辅助药物治疗对需要非侵入性呼吸的患者的COVID-19相关死亡率显示出有限的益处,并在非重症监护环境中进行管理。在大流行期间,贝尔法斯特Mater医院被设计为当地的COVID-19中心。2021年1月之前,标准病房级护理包括静脉注射抗生素、静脉注射瑞德西韦、口服地塞米松和无创通气。第一时间使用持续气道正压通气(当FiO2要求超过4L/min时通过鼻插管开始)。在卫生部发布关于托珠单抗用于COVID-19患者呼吸支持的立场声明后,决定在非重症监护环境中使用托珠单抗。我们的假设是,接受无创通气的COVID-19阳性患者在接受托珠单抗治疗的同时接受标准治疗,与单独接受标准治疗相比,住院死亡率会降低。REMAP-CAP试验对危重监护环境中的COVID-19患者施用tocilizumab,但我们假设那些需要病房呼吸支持但不需要危重监护的“不太不适”患者仍然可以受益。方法确定在非重症监护环境中开始使用托珠单抗的患者并进行前瞻性随访。回顾性建立接受病区标准护理的对照组。结果共纳入对照组和治疗组各40例。使用Microsoft Excel进行卡方统计分析。主要结局,即住院死亡率,显示两组之间有显著差异(p=0.048),副作用方面无明显差异。结论:该数据支持在COVID-19患者中使用tocilizumab,并指出其对COVID-19患者的住院死亡率有积极影响,无需无创呼吸支持,但不需要重症监护。此外,有限的副作用表明tocilizumab可以在非重症监护环境中安全使用。参考文献gordon AC, Mouncey PR, al - beh F, Rowan KM, Nichol AD, Arabi YM,等。covid -19重症患者白细胞介素-6受体拮抗剂初步报告medRxiv。2021.
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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