Department of Neurology, Southern California Permanente Medical Group, Los Angeles, USA; Department of Clinical Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, USA.
Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, USA.
Int J Infect Dis. 2023 Jan;126:87-93. doi: 10.1016/j.ijid.2022.11.017. Epub 2022 Nov 18.
To assess whether escalating to high-dose corticosteroids or anakinra compared with continuing low-dose corticosteroids reduced mortality in patients with severe COVID-19 whose respiratory function deteriorated while receiving dexamethasone 6 mg daily.
We conducted a retrospective cohort study between March 1 to December 31, 2020, of hospitalized patients with confirmed COVID-19 pneumonia. In-hospital death was analyzed using logistic regression with inverse probability of treatment weighting of receiving anakinra, high-dose corticosteroid (dexamethasone >10 mg daily), or remaining on low-dose corticosteroids on the day of first respiratory deterioration.
We analyzed 6671 patients whose respiratory status deteriorated while receiving dexamethasone 6 mg daily for COVID-19 pneumonia, of whom 6265 stayed on low-dose corticosteroids, 232 were escalated to high-dose corticosteroids, and 174 to anakinra in addition to corticosteroids. The propensity score-adjusted odds of death were higher in the anakinra (odds ratio [OR] 1.76; 95% CI 1.13-2.72) and high-dose corticosteroid groups (OR 1.53; 95% CI 1.14-2.07) compared with those who continued low-dose corticosteroids on the day of respiratory deterioration. The odds of hospital-acquired infections were also higher in the anakinra (OR 2.00; 95% CI 1.28-3.11) and high-dose corticosteroid groups (OR 1.43; 95% CI 1.00-2.04) compared with low-dose corticosteroid group.
Our findings do not support escalating patients with COVID-19 pneumonia who deteriorate on low-dose corticosteroids to high-dose corticosteroids or anakinra.
评估在接受每日 6 毫克地塞米松治疗的 COVID-19 患者呼吸功能恶化时,与继续低剂量皮质类固醇相比,升级为高剂量皮质类固醇或阿那白滞素是否降低死亡率。
我们对 2020 年 3 月 1 日至 12 月 31 日期间住院的确诊 COVID-19 肺炎患者进行了回顾性队列研究。使用逻辑回归分析在第一天呼吸恶化时接受阿那白滞素、高剂量皮质类固醇(地塞米松> 10 毫克/天)或继续低剂量皮质类固醇治疗的患者的院内死亡率。
我们分析了 6671 名因 COVID-19 肺炎而接受每日 6 毫克地塞米松治疗时呼吸状况恶化的患者,其中 6265 名继续使用低剂量皮质类固醇,232 名升级为高剂量皮质类固醇,174 名除皮质类固醇外还使用阿那白滞素。与呼吸恶化当天继续低剂量皮质类固醇相比,阿那白滞素(优势比 [OR] 1.76;95%CI 1.13-2.72)和高剂量皮质类固醇组(OR 1.53;95%CI 1.14-2.07)的死亡可能性更高。与低剂量皮质类固醇组相比,阿那白滞素(OR 2.00;95%CI 1.28-3.11)和高剂量皮质类固醇组(OR 1.43;95%CI 1.00-2.04)的医院获得性感染的可能性也更高。
我们的研究结果不支持将 COVID-19 肺炎恶化的患者升级为高剂量皮质类固醇或阿那白滞素。