Division of Cardiovascular Medicine, Henry Ford Hospital, Detroit, MI, USA.
Department of Pulmonary and Critical Care Medicine, University of Arizona, Tucson, AZ, USA.
J Intensive Care Med. 2023 Nov;38(11):1042-1050. doi: 10.1177/08850666231180528. Epub 2023 Jun 12.
Acute respiratory distress syndrome (ARDS) with oliguria is associated with increased mortality. Interleukin-6 (IL-6) plays an integral role in the pathophysiology of both disease processes. Patients who experience severe COVID-19 have demonstrated higher IL-6 levels compared to baseline, and use of tocilizumab has demonstrated efficacy in such cohorts. We set out to investigate the relationship between tocilizumab use, COVID-19 ARDS, low urine output, and mortality.
Retrospective cohort review of adult patients aged ≥ 18 years with COVID-19 and moderate or severe ARDS, admitted to the intensive care unit (ICU) of a tertiary referral center in metropolitan Detroit. Patients were analyzed based on presence of oliguria (defined as ≤ 0.7 mL/kg/h) on the day of intubation and exposure to tocilizumab while inpatient. The primary outcome was inpatient mortality.
One hundred and twenty-eight patients were analyzed, 103 (80%) with low urine output, of whom 30 (29%) received tocilizumab. In patients with low urine output, risk factors associated with mortality on univariate analysis included Black race ( = .028), lower static compliance ( = .015), and tocilizumab administration ( = .002). Tocilizumab (odds ratio 0.245, 95% confidence interval 0.079-0.764, = .015) was the only risk factor independently associated with survival on multivariate logistic regression analysis.
In this retrospective cohort review of patients hospitalized with COVID-19 and moderate or severe ARDS, tocilizumab administration was independently associated with survival in patients with low urine output ≤ 0.7 mL/kg/h on the day of intubation. Prospective studies are needed to investigate the impact of urine output on efficacy of interleukin-targeted therapies in the management of ARDS.
伴有少尿的急性呼吸窘迫综合征(ARDS)与死亡率增加有关。白细胞介素-6(IL-6)在这两种疾病过程的病理生理学中都起着重要作用。与基线相比,患有严重 COVID-19 的患者表现出更高的 IL-6 水平,而托珠单抗的使用已证明在这些队列中有效。我们着手研究托珠单抗的使用、COVID-19 ARDS、少尿和死亡率之间的关系。
回顾性分析了底特律大都市三级转诊中心重症监护病房(ICU)收治的年龄≥18 岁的 COVID-19 合并中度或重度 ARDS 的成年患者。根据插管当天少尿(定义为≤0.7 mL/kg/h)和住院期间接受托珠单抗的情况对患者进行分析。主要结局为住院死亡率。
共分析了 128 例患者,其中 103 例(80%)出现少尿,其中 30 例(29%)接受了托珠单抗治疗。在少尿的患者中,单因素分析与死亡率相关的危险因素包括黑人种族( = .028)、静态顺应性较低( = .015)和托珠单抗的使用( = .002)。托珠单抗(比值比 0.245,95%置信区间 0.079-0.764, = .015)是多变量逻辑回归分析中唯一与生存相关的独立危险因素。
在这项对 COVID-19 住院患者的回顾性队列研究中,与插管当天尿量≤0.7 mL/kg/h 的少尿患者相比,托珠单抗的使用与低尿量患者的生存独立相关。需要前瞻性研究来研究尿输出对白细胞介素靶向治疗在 ARDS 管理中的疗效的影响。