Hoertel Nicolas, Sánchez-Rico Marina, Vernet Raphaël, Beeker Nathanaël, Neuraz Antoine, Alvarado Jesús M, Daniel Christel, Paris Nicolas, Gramfort Alexandre, Lemaitre Guillaume, Salamanca Elisa, Bernaux Mélodie, Bellamine Ali, Burgun Anita, Limosin Frédéric
Département de Psychiatrie, AP-HP.Centre, Hôpital Corentin-Celton, Issy-les-Moulineaux, France.
Institut de Psychiatrie et Neurosciences de Paris, Université de Paris, INSERM, Paris, France.
Br J Clin Pharmacol. 2021 Oct;87(10):3766-3775. doi: 10.1111/bcp.14784. Epub 2021 Mar 10.
To examine the association between dexamethasone use and mortality among patients hospitalized for COVID-19.
We examined the association between dexamethasone use and mortality at AP-HP Greater Paris University hospitals. Study baseline was defined as the date of hospital admission. The primary endpoint was time to death. We compared this endpoint between patients who received dexamethasone and those who did not in time-to-event analyses adjusted for patient characteristics (such as age, sex and comorbidity) and clinical and biological markers of clinical severity of COVID-19, and stratified by the need for respiratory support, i.e. mechanical ventilation or oxygen. The primary analysis was a multivariable Cox regression model.
Of 12 217 adult patients hospitalized with a positive COVID-19 reverse transcriptase-polymerase chain reaction test, 171 (1.4%) received dexamethasone orally or by intravenous perfusion during the visit. Among patients who required respiratory support, the end-point occurred in 10/63 (15.9%) patients who received dexamethasone and 298/1129 (26.4%) patients who did not. In this group, there was a significant association between dexamethasone use and reduced mortality in the primary analysis (hazard ratio, 0.46; 95% confidence interval 0.22-0.96, P = .039). Among patients who did not require respiratory support, there was no significant association between dexamethasone use and the endpoint.
In this multicentre observational study, dexamethasone use administered either orally or by intravenous injection at a cumulative dose between 60 mg and 150 mg was associated with reduced mortality among patients with COVID-19 requiring respiratory support.
研究因新型冠状病毒肺炎(COVID-19)住院患者使用地塞米松与死亡率之间的关联。
我们在巴黎公立医院集团(AP-HP)的大学医院研究了地塞米松使用与死亡率之间的关联。研究基线定义为入院日期。主要终点是死亡时间。在针对患者特征(如年龄、性别和合并症)以及COVID-19临床严重程度的临床和生物学标志物进行调整的事件发生时间分析中,我们比较了接受地塞米松治疗的患者和未接受地塞米松治疗的患者的这一终点,并根据呼吸支持需求进行分层,即机械通气或吸氧。主要分析采用多变量Cox回归模型。
在12217例COVID-19逆转录聚合酶链反应检测呈阳性的住院成年患者中,171例(1.4%)在就诊期间口服或静脉输注了地塞米松。在需要呼吸支持的患者中,接受地塞米松治疗的10/63例(15.9%)患者和未接受地塞米松治疗的298/1129例(26.4%)患者出现了终点事件。在该组中进行的主要分析显示,地塞米松使用与死亡率降低之间存在显著关联(风险比,0.46;95%置信区间0.22 - 0.96,P = 0.039)。在不需要呼吸支持的患者中,地塞米松使用与终点事件之间无显著关联。
在这项多中心观察性研究中,口服或静脉注射累积剂量在60毫克至150毫克之间的地塞米松与需要呼吸支持的COVID-19患者死亡率降低相关。