Department of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Clinical Trials Methods and Outcomes Lab, Palliative and Advanced Illness Research (PAIR) Center, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Sci Rep. 2023 Apr 21;13(1):6570. doi: 10.1038/s41598-023-33425-3.
The currently recommended dose of dexamethasone for patients with severe or critical COVID-19 is 6 mg per day (mg/d) regardless of patient features and variation. However, patients with severe or critical COVID-19 are heterogenous in many ways (e.g., age, weight, comorbidities, disease severity, and immune features). Thus, it is conceivable that a standardized dosing protocol may not be optimal. We assessed treatment effect heterogeneity in the COVID STEROID 2 trial, which compared 6 mg/d to 12 mg/d, using a causal inference framework with Bayesian Additive Regression Trees, a flexible modeling method that detects interactive effects and nonlinear relationships among multiple patient characteristics simultaneously. We found that 12 mg/d of dexamethasone, relative to 6 mg/d, was probably associated with better long-term outcomes (days alive without life support and mortality after 90 days) among the entire trial population (i.e., no signals of harm), and probably more beneficial among those without diabetes mellitus, that were older, were not using IL-6 inhibitors at baseline, weighed less, or had higher level respiratory support at baseline. This adds more evidence supporting the use of 12 mg/d in practice for most patients not receiving other immunosuppressants and that additional study of dosing could potentially optimize clinical outcomes.
目前建议的 COVID-19 重症或危重症患者地塞米松剂量为每天 6 毫克(mg/d),无论患者特征和变异如何。然而,COVID-19 重症或危重症患者在许多方面存在异质性(例如年龄、体重、合并症、疾病严重程度和免疫特征)。因此,可以想象,标准化的给药方案可能不是最佳的。我们使用因果推理框架和贝叶斯加性回归树(一种灵活的建模方法,可以同时检测多个患者特征之间的交互作用和非线性关系)评估了 COVID STEROID 2 试验中的治疗效果异质性,该试验比较了 6 毫克/天和 12 毫克/天。我们发现,与 6 毫克/天相比,12 毫克/天的地塞米松可能与整个试验人群的长期结局(无生命支持的存活天数和 90 天后的死亡率)更好相关(即无危害信号),并且在没有糖尿病、年龄较大、基线时不使用白细胞介素-6 抑制剂、体重较轻或基线时呼吸支持水平较高的患者中可能更有益。这为大多数未接受其他免疫抑制剂治疗的患者在实践中使用 12 毫克/天提供了更多证据,并表明进一步研究剂量可能会优化临床结局。