我们在COVID患者中使用tocilizumab的方案是否足够?

A. Dominguez Barahona, S. Gonzalez Suarez, MA Toledo Davia, C. Blázquez Romero, L. Torralba Fernández, R. López Álvarez, C. Jiménez Méndez, P. Moya Gómez
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The incessant publication of new studies assessing its effectiveness and the ideal time of use means that in-hospital protocols are constantly being reviewed and updated.Aim and objectivesTo describe the clinical characteristics of hospitalised patients with SARS-CoV-2 pneumonia treated with TCZ and their evolution, and to compare our results with those of the primary endpoint (28-day mortality) of the RECOVERY study.Material and methodsRetrospective observational study of patients administered TCZ between October 2020 and February 2021 in a tertiary hospital. Criteria for TCZ use were PAFI <300 and meeting two of the following three criteria: C-reactive protein (CRP) >150 mg/L, D-dimer >1500 ng/mL and ferritin >2000 ng/mL, and not having contraindications for its use.Each patient received a single dose of 400 mg if weight <75 kg and 600 mg if weight >75 kg.Demographic data, comorbidities and days from symptom onset to TCZ administration were collected. 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引用次数: 0

摘要

背景和重要性tocilizumab (TCZ)已成为管理SARS-CoV-2肺炎患者肺部高炎症的关键支柱。评估其有效性和理想使用时间的新研究的不断发表意味着医院内的协议不断被审查和更新。目的和目的描述使用TCZ治疗的SARS-CoV-2肺炎住院患者的临床特征及其演变,并将我们的结果与RECOVERY研究的主要终点(28天死亡率)进行比较。材料与方法回顾性观察研究某三级医院2020年10月至2021年2月接受TCZ治疗的患者。TCZ的使用标准为PAFI 150 mg/L, d -二聚体>1500 ng/mL,铁蛋白>2000 ng/mL,无使用禁忌症。如果体重为75公斤,每位患者接受单次剂量400毫克。收集人口统计数据、合并症和从症状出现到服用TCZ的天数。随访分析数据(TCZ给药前后(15天)CRP、d -二聚体、铁蛋白)。以28天死亡率评价临床进展。统计分析:Stata/MP v16.0。定量变量比较采用学生t检验。结果纳入39例患者,男性25例(64.1%),中位年龄74岁(IQR 61 ~ 80)。61.5%患有高血压,33.3%患有肥胖症,41%患有糖尿病,17.9%患有慢性肾病,12.8%患有心脏病。从症状出现到服用TCZ的中位时间为10 (IQR 7-15)天。TCZ给药前和15天的中位数分别为:152.5 mg/L (IQR 89-220.8)和1.7 mg/L (IQR 0.65-4.2) CRP (p300和CRP >75 mg/L,无使用禁忌症。在随后的研究中,我们将测试这一更新是否有助于改善死亡率结果。参考文献和/或致谢利益冲突无利益冲突
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4CPS-036 Is our protocol for the use of tocilizumab in COVID patients adequate?
Background and importanceTocilizumab (TCZ) has been a key pillar in the management of pulmonary hyperinflammation in patients with SARS-CoV-2 pneumonia. The incessant publication of new studies assessing its effectiveness and the ideal time of use means that in-hospital protocols are constantly being reviewed and updated.Aim and objectivesTo describe the clinical characteristics of hospitalised patients with SARS-CoV-2 pneumonia treated with TCZ and their evolution, and to compare our results with those of the primary endpoint (28-day mortality) of the RECOVERY study.Material and methodsRetrospective observational study of patients administered TCZ between October 2020 and February 2021 in a tertiary hospital. Criteria for TCZ use were PAFI <300 and meeting two of the following three criteria: C-reactive protein (CRP) >150 mg/L, D-dimer >1500 ng/mL and ferritin >2000 ng/mL, and not having contraindications for its use.Each patient received a single dose of 400 mg if weight <75 kg and 600 mg if weight >75 kg.Demographic data, comorbidities and days from symptom onset to TCZ administration were collected. Follow-up of analytical data (CRP, D-dimer and ferritin pre- and post- (15 days) TCZ administration). Clinical evolution was evaluated by mortality rate at 28 days.Statistical analysis: Stata/MP v16.0. Student’s t-test was used for comparison of quantitative variables.Results39 patients were included, 25 (64.1%) were male, median age 74 (IQR 61–80) years. 61.5% had hypertension, 33.3% obesity, 41% diabetes mellitus, 17.9% chronic kidney disease, 12.8% heart disease. The median time from symptom onset to TCZ administration was 10 (IQR 7–15) days.The medians prior to and at 15 days of TCZ administration were, respectively: 152.5 mg/L (IQR 89–220.8) and 1.7 mg/L (IQR 0.65–4.2) CRP (p<0.001);2300 ng/mL (IQR 11 959–4889) and 1124 ng/mL (IQR 567–1439) D-dimer (p=0.1726);1242 ng/mL (IQR 647–2705) and 851 ng/mL (IQR 268–1384) ferritin (p=0.1294). Mortality at 28 days was 64.1%.Conclusion and relevanceOur sample size is smaller than that of the RECOVERY study;however, the days of symptoms until TCZ administration (10 vs 9) and the median CRP prior to TCZ (143 vs 152.5 mg/L) in both studies are very similar. Our mortality is much higher (64.1% vs 29%). We found a statistically significant difference between our pre- and post-CRP data.With this result, the in-hospital protocol was modified and new criteria for TCZ administration in COVID patients became oxygen saturation <92% or PAFI >300 and CRP >75 mg/L, with no contraindications for use.In subsequent studies we will test whether this update helps to improve mortality outcomes.References and/or acknowledgementsConflict of interestNo conflict of interest
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