Sánchez-Montalvá Adrián, Sellarés-Nadal Júlia, Espinosa-Pereiro Juan, Fernández-Hidalgo Nuria, Pérez-Hoyos Santiago, Salvador Fernando, Durà Xavier, Miarons Marta, Antón Andrés, Eremiev-Eremiev Simeón, Sempere-González Abiu, Monforte-Pallarés Arnau, Bosch-Nicolau Pau, Augustin Salvador, Sampol Júlia, Guillén-Del-Castillo Alfredo, Almirante Benito
Infectious Diseases Department, Vall d'Hebron University Hospital, Universitat Autònoma de Barcelona, Barcelona, Spain.
International Health Program of the Catalan Institut of Health (PROSICS), Barcelona, Spain.
Med Clin (Engl Ed). 2022 Jun 10;158(11):509-518. doi: 10.1016/j.medcle.2021.06.023. Epub 2022 Jun 18.
Modulation of the immune system to prevent lung injury is being widely used against the new coronavirus disease (COVID-19). The primary endpoint was mortality at 7 days after tocilizumab administration. Secondary endpoints were admission to the intensive care unit, development of ARDS and respiratory insufficiency among others.
We report the preliminary results from the Vall d'Hebron cohort study at Vall d'Hebron University Hospital, in Barcelona (Spain), including all consecutive patients who had a confirmed SARS-CoV-2 infection and who were treated with tocilizumab until March 25th.
82 patients with COVID-19 received at least one dose of tocilizumab. The mean (± SD) age was 59.1 (19.8) years, 63% were male, 22% were of non-Spanish ancestry, and the median (IQR) age-adjusted Charlson index at baseline was 3 (1-4) points. Respiratory failure and ARDS developed in 62 (75.6%) and 45 (54.9%) patients, respectively. Median time from symptom onset to ARDS development was 8 (5-11) days. Mortality at 7 days was 26.8%. Hazard ratio for mortality was 3.3; 95% CI, 1.3-8.5 (age-adjusted hazard ratio for mortality 2.1; 95% CI, 0.8-5.8) if tocilizumab was administered after the onset of ARDS.
Early administration of tocilizumab in patients needing oxygen supplementation may be critical to patient recovery. Our preliminary data could inform bedside decisions until more data regarding the precise timing in of initiation of the treatment with tocilizumab.
调节免疫系统以预防肺损伤正被广泛用于对抗新型冠状病毒病(COVID-19)。主要终点是托珠单抗给药后7天的死亡率。次要终点包括入住重症监护病房、发生急性呼吸窘迫综合征(ARDS)和呼吸功能不全等。
我们报告了西班牙巴塞罗那市瓦尔德希伯伦大学医院进行的瓦尔德希伯伦队列研究的初步结果,该研究纳入了所有连续确诊感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)且接受托珠单抗治疗直至3月25日的患者。
82例COVID-19患者接受了至少一剂托珠单抗。平均(±标准差)年龄为59.1(19.8)岁,63%为男性,22%为非西班牙裔,基线时年龄调整后的Charlson指数中位数(四分位间距)为3(1 - 4)分。分别有62例(75.6%)和45例(54.9%)患者发生呼吸衰竭和ARDS。从症状出现到发生ARDS的中位时间为8(5 - 11)天。7天死亡率为26.8%。如果在ARDS发作后给予托珠单抗,死亡风险比为3.3;95%置信区间为1.3 - 8.5(年龄调整后的死亡风险比为2.1;95%置信区间为0.8 - 5.8)。
对于需要吸氧的患者,早期给予托珠单抗可能对患者康复至关重要。在获得更多关于托珠单抗治疗起始精确时机的数据之前,我们的初步数据可为临床决策提供参考。