Tocilizumab Administration for COVID-19 Pneumonia: A Single Center Experience Description

G. Palmer, N. Meyer, F. Jamous
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Abstract

Rationale: We aim to describe the clinical characteristics and outcomes of patients who received Tocilizumab for COVID-19 pneumonia at our institution between March 20 and October 26, 2020. Methods: In this single center, retrospective, observational study, we identified 55 adults admitted with COVID-19 pneumonia who received Tocilizumab. Demographic data, symptoms, laboratory values, treatments, and clinical outcomes were collected. Data was compared between those who received Tocilizumab and all patients admitted with COVID-19. Primary outcome was 28-day mortality. Secondary outcomes included role of concomitant steroid use and change in eosinophil counts, ferritin, AST, CRP and D-Dimer values. Results: Of the 589 patients admitted with COVID-19 pneumonia, 55 received Tocilizumab as part of their treatment course. Patient demographics of those who received Tocilizumab include a mean age of 58 years with 73% male, 51% with diabetes, and 58% with hypertension. 4/55 (7.3%) were immunocompromised. Common presenting symptoms on admission were fever (62%), cough (78%) and dyspnea (89%). 35/55 (64%) were admitted to the ICU during their hospitalization;their mean P/F ratio was 127. Tocilizumab was administered on average admission day 4 (1-19). A second dose was given to 17 (31%) of patients, with 11 given the following day. Average hospital length of stay (LOS) postadministration was 17 days. Average white blood cell (WBC) count on day of Tocilizumab administration was 11, with an absolute lymphocyte count of 0.96. Mean IL-6 on hospital admission was 48.3. Two days post Tocilizumab administration there was a peak in ferritin, percent eosinophils, and AST. Both two-and five-day post-Tocilizumab CRP levels decreased while D-Dimer increased (Table 1). All Tocilizumab patients received antibiotics. In addition, three received hydroxychloroquine, 16 Remdesivir, and 51 convalescent plasma. 31 (56%) received steroids. On Day 2, those who did not receive steroids had, on average, more than double the percent of eosinophils in their blood (3.21% vs 1.53%). This difference decreased by Day 5. In time period of interest, COVID-19 admission mortality was 63/589 (10.6%) and 40/77 (52%) for mechanically ventilated patients. For Tocilizumab recipients, 25/55 patients were mechanically ventilated and 12/25 (48%) died. Overall, 28-day mortality was 11/55 (20%), with hospital mortality up to 16/55 (29%). This was similar to our larger cohort ICU mortality of 29.3%. Conclusion: Tocilizumab recipients in our cohort had a mortality similar to overall COVID ICU mortality. It appeared to be well tolerated except for an increase in eosinophilia if with no concomitant steroid use.
托珠单抗治疗COVID-19肺炎:单中心经验描述
理由:我们的目标是描述2020年3月20日至10月26日期间在我们机构接受Tocilizumab治疗COVID-19肺炎患者的临床特征和结局。方法:在这项单中心、回顾性、观察性研究中,我们确定了55名接受托珠单抗治疗的成人COVID-19肺炎患者。收集人口统计数据、症状、实验室值、治疗和临床结果。将接受Tocilizumab治疗的患者与所有入院的COVID-19患者的数据进行比较。主要终点为28天死亡率。次要结局包括伴随使用类固醇的作用以及嗜酸性粒细胞计数、铁蛋白、AST、CRP和d -二聚体值的变化。结果:在589例入院的COVID-19肺炎患者中,55例接受了Tocilizumab作为其治疗过程的一部分。接受Tocilizumab的患者人口统计数据包括平均年龄58岁,73%为男性,51%患有糖尿病,58%患有高血压。4/55(7.3%)免疫功能低下。入院时常见的症状为发热(62%)、咳嗽(78%)和呼吸困难(89%)。35/55(64%)住院期间入住ICU,平均P/F为127。Tocilizumab在平均入院第4天(1-19)给予。17名(31%)患者接受了第二剂治疗,11名患者在第二天接受了第二剂治疗。给药后平均住院时间为17天。给药当天平均白细胞(WBC)计数为11,绝对淋巴细胞计数为0.96。入院时平均IL-6为48.3。托珠单抗给药2天后,铁蛋白、嗜酸性粒细胞百分比和AST达到峰值。托珠单抗给药2天和5天后,CRP水平均下降,而d -二聚体升高(表1)。所有托珠单抗患者均接受抗生素治疗。另外,3例接受羟氯喹治疗,16例接受瑞德西韦治疗,51例接受恢复期血浆治疗。31例(56%)接受类固醇治疗。在第2天,那些没有接受类固醇治疗的人血液中嗜酸性粒细胞的比例平均增加了一倍多(3.21%比1.53%)。这种差异在第5天减小。在感兴趣的时间段内,机械通气患者的入院死亡率为63/589(10.6%),40/77(52%)。对于托珠单抗接受者,25/55的患者进行机械通气,12/25(48%)死亡。总的来说,28天死亡率为11/55(20%),住院死亡率高达16/55(29%)。这与我们的ICU大队列死亡率29.3%相似。结论:在我们的队列中,托珠单抗受者的死亡率与COVID - ICU的总死亡率相似。如果不同时使用类固醇,除了嗜酸性粒细胞增多外,它似乎是耐受性良好的。
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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