Treatment protocols, disease understanding, and viral characteristics changed over the course of the COVID-19 pandemic; as a result, the risks associated with patient comorbidities and biomarkers also changed. We add to the conversation regarding inflammation, hemostasis and vascular function in COVID-19 by performing a time-varying observational analysis of over 4000 patients hospitalized for COVID-19 in a New York City hospital system from March 2020 to August 2021. To perform this analysis, we apply tree-based generalized additive models with temporal interactions which recover discontinuous risk changes caused by discrete protocols changes. We find that the biomarkers of thrombosis increasingly predicted mortality from March 2020 to August 2021, while the association between biomarkers of inflammation and thrombosis weakened. Beyond COVID-19, this presents a straightforward methodology to estimate unknown and discontinuous time-varying effects.
翻译:在COVID-19大流行期间,治疗规程、疾病理解和病毒特征发生了变化;因此,与病人的发病率和生物标志有关的风险也发生了变化;在COVID-19中,我们通过对从2020年3月至2021年8月在纽约市医院系统中住院治疗COVID-19的4 000多名病人进行时间变化式的观察分析,增加了关于COVID-19的炎症、河麻洲和血管功能的对话;为了进行这一分析,我们采用了基于树的通用添加剂模型,并采用时间互动模式,恢复了离散规改变引起的不连续的风险变化;我们发现血栓生物标志越来越多地预测2020年3月至2021年8月的死亡率,而炎症生物标志与血栓的联系则减弱了;除了COVID-19,这是估算未知和不连续的时间变化效应的简单方法。