Divisions of Cardiology (T.S.M., A.S.B., M.J.C., A.G.H., C.J.L., E.D.M., W.S.P., J.R.R., D.R.T., J.C.T., R.K.H.), Johns Hopkins University School of Medicine, Baltimore, MD.
Department of Medicine, and Department of Pathology (L.J.S.), Johns Hopkins University School of Medicine, Baltimore, MD.
Circulation. 2021 Feb 9;143(6):553-565. doi: 10.1161/CIRCULATIONAHA.120.050543. Epub 2020 Nov 13.
Knowledge gaps remain in the epidemiology and clinical implications of myocardial injury in coronavirus disease 2019 (COVID-19). We aimed to determine the prevalence and outcomes of myocardial injury in severe COVID-19 compared with acute respiratory distress syndrome (ARDS) unrelated to COVID-19.
We included intubated patients with COVID-19 from 5 hospitals between March 15 and June 11, 2020, with troponin levels assessed. We compared them with patients from a cohort study of myocardial injury in ARDS and performed survival analysis with primary outcome of in-hospital death associated with myocardial injury. In addition, we performed linear regression to identify clinical factors associated with myocardial injury in COVID-19.
Of 243 intubated patients with COVID-19, 51% had troponin levels above the upper limit of normal. Chronic kidney disease, lactate, ferritin, and fibrinogen were associated with myocardial injury. Mortality was 22.7% among patients with COVID-19 with troponin under the upper limit of normal and 61.5% for those with troponin levels >10 times the upper limit of normal (<0.001). The association of myocardial injury with mortality was not statistically significant after adjusting for age, sex, and multisystem organ dysfunction. Compared with patients with ARDS without COVID-19, patients with COVID-19 were older and had higher creatinine levels and less favorable vital signs. After adjustment, COVID-19-related ARDS was associated with lower odds of myocardial injury compared with non-COVID-19-related ARDS (odds ratio, 0.55 [95% CI, 0.36-0.84]; =0.005).
Myocardial injury in severe COVID-19 is a function of baseline comorbidities, advanced age, and multisystem organ dysfunction, similar to traditional ARDS. The adverse prognosis of myocardial injury in COVID-19 relates largely to multisystem organ involvement and critical illness.
在 2019 年冠状病毒病(COVID-19)中,心肌损伤的流行病学和临床意义仍存在知识空白。我们旨在确定与 COVID-19 无关的急性呼吸窘迫综合征(ARDS)相比,重症 COVID-19 中心肌损伤的患病率和结局。
我们纳入了 2020 年 3 月 15 日至 6 月 11 日期间 5 家医院中接受插管治疗的 COVID-19 患者,评估了他们的肌钙蛋白水平。我们将其与 ARDS 中心肌损伤队列研究中的患者进行了比较,并对与心肌损伤相关的住院内死亡这一主要结局进行了生存分析。此外,我们还进行了线性回归,以确定 COVID-19 中心肌损伤相关的临床因素。
在 243 例接受插管治疗的 COVID-19 患者中,51%的患者肌钙蛋白水平高于正常值上限。慢性肾脏病、乳酸、铁蛋白和纤维蛋白原与心肌损伤相关。肌钙蛋白水平在正常值上限以下的 COVID-19 患者的死亡率为 22.7%,而肌钙蛋白水平>正常值上限 10 倍的患者的死亡率为 61.5%(<0.001)。在校正年龄、性别和多系统器官功能障碍后,心肌损伤与死亡率的相关性无统计学意义。与非 COVID-19 相关的 ARDS 患者相比,COVID-19 相关的 ARDS 患者年龄更大,肌酐水平更高,生命体征更差。调整后,COVID-19 相关 ARDS 与非 COVID-19 相关 ARDS 相比,心肌损伤的可能性更低(比值比,0.55[95%置信区间,0.36-0.84];=0.005)。
重症 COVID-19 中的心肌损伤是基线合并症、高龄和多系统器官功能障碍的结果,与传统 ARDS 相似。COVID-19 中心肌损伤的不良预后主要与多系统器官受累和危重病有关。