{"title":"Tocilizumab Treatment for Hospitalized Patients with Severe Covid-19 Pneumonia: A Retrospective Case-Control Study","authors":"A. Alsaeedi","doi":"10.19080/IJOPRS.2021.04.555646","DOIUrl":null,"url":null,"abstract":"Background: Tocilizumab, through the blocking of interleukin-6 receptors, is hypothesized to be effective in the treatment of severe coronavirus disease 2019 (COVID-19). However, data on tocilizumab use in this setting is conflicting. Objective: To evaluate the effect of tocilizumab treatment on the outcomes of patients with severe COVID-19 pneumonia. Methods: A retrospective case-control study including 168 patients hospitalized with severe COVID-19 pneumonia at Al-Jahra hospital, Kuwait, from April 1st to June 30th. All patients received standard of care treatment. Patients in the tocilizumab group received tocilizumab infusion. The primary outcomes were death, need for mechanical ventilation and the proportion of patients with clinical improvement. The incidence of adverse events was monitored. Results: Need for mechanical ventilation was higher in the tocilizumab group (48% vs. 24.3%, p=0.002). Clinical improvement was lower (54.1% vs. 71.4%) and number of deaths were higher (29.6% vs. 10%) in the tocilizumab group (p=0.009). There was no difference in the mean survival time between tocilizumab and control group (17.7 days vs. 19.2 days). There was no significant difference between the two groups regarding the incidence of infections (6.1% vs. 2.9%, p=0.471). Conclusion: Our results suggest that use of tocilizumab in severe COVID-19 pneumonia does not provide clinical or mortality benefit. However, further research is needed to determine the ideal utilization of tocilizumab in the setting of severe COVID-19 disease.","PeriodicalId":257243,"journal":{"name":"International Journal of Pulmonary & Respiratory Sciences","volume":"31 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Pulmonary & Respiratory Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.19080/IJOPRS.2021.04.555646","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Tocilizumab, through the blocking of interleukin-6 receptors, is hypothesized to be effective in the treatment of severe coronavirus disease 2019 (COVID-19). However, data on tocilizumab use in this setting is conflicting. Objective: To evaluate the effect of tocilizumab treatment on the outcomes of patients with severe COVID-19 pneumonia. Methods: A retrospective case-control study including 168 patients hospitalized with severe COVID-19 pneumonia at Al-Jahra hospital, Kuwait, from April 1st to June 30th. All patients received standard of care treatment. Patients in the tocilizumab group received tocilizumab infusion. The primary outcomes were death, need for mechanical ventilation and the proportion of patients with clinical improvement. The incidence of adverse events was monitored. Results: Need for mechanical ventilation was higher in the tocilizumab group (48% vs. 24.3%, p=0.002). Clinical improvement was lower (54.1% vs. 71.4%) and number of deaths were higher (29.6% vs. 10%) in the tocilizumab group (p=0.009). There was no difference in the mean survival time between tocilizumab and control group (17.7 days vs. 19.2 days). There was no significant difference between the two groups regarding the incidence of infections (6.1% vs. 2.9%, p=0.471). Conclusion: Our results suggest that use of tocilizumab in severe COVID-19 pneumonia does not provide clinical or mortality benefit. However, further research is needed to determine the ideal utilization of tocilizumab in the setting of severe COVID-19 disease.
背景:托珠单抗通过阻断白细胞介素-6受体,被推测可有效治疗2019年严重冠状病毒病(COVID-19)。然而,托珠单抗在这种情况下的使用数据是相互矛盾的。目的:评价托珠单抗治疗对重症COVID-19肺炎患者预后的影响。方法:对4月1日至6月30日在科威特Al-Jahra医院收治的168例重症COVID-19肺炎患者进行回顾性病例对照研究。所有患者均接受标准护理治疗。托珠单抗组患者接受托珠单抗输注。主要结局为死亡、机械通气需求和临床改善患者比例。监测不良事件的发生率。结果:托珠单抗组机械通气需求较高(48% vs. 24.3%, p=0.002)。托珠单抗组的临床改善较低(54.1%对71.4%),死亡人数较高(29.6%对10%)(p=0.009)。托珠单抗组和对照组的平均生存时间没有差异(17.7天对19.2天)。两组感染发生率无显著差异(6.1% vs. 2.9%, p=0.471)。结论:我们的研究结果表明,在重症COVID-19肺炎中使用托珠单抗并没有提供临床或死亡率方面的益处。然而,需要进一步的研究来确定托珠单抗在严重COVID-19疾病背景下的理想应用。