Division of HepatologyDepartment of MedicineAlbert Einstein College of MedicineBronxNYUSA.
Division of Blood Banking/Transfusion MedicineDepartment of PathologyAlbert Einstein College of MedicineBronxNYUSA.
Hepatol Commun. 2020 Dec 5;5(3):424-433. doi: 10.1002/hep4.1648. eCollection 2021 Mar.
The novel coronavirus severe acute respiratory syndrome coronavirus 2 (SARS-CoV2) is the causative agent of coronavirus disease 2019 (COVID-19). The presenting symptoms of this virus are variable, and there is an increasing body of literature on risk factors for mortality. The aim of this study was to evaluate the effect of initial aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels and preexisting liver disease, including cirrhosis, in a cohort of patients admitted with COVID-19 infection at a tertiary care hospital network in the Bronx, New York. We reviewed 3,352 patients who had a positive SARS-CoV2 nasal swab, were over 18 years of age, and had an associated inpatient admission and discharge (or death) to the Montefiore Medical Center from February 28, 2020, to May 22, 2020. Of these, 39/86 (45%) patients died when the initial ALT was >5 times the upper limit of normal (ULN); 115/230 (50%) patients died when the initial AST was >3 times the ULN. The mortality of patients without preexisting liver disease was 26.6% compared to a mortality rate of 29.5% in patients with liver disease. Subgroup analysis showed a mortality of 36.1% in the patients with cirrhosis. Cirrhosis conferred a hazard ratio for mortality of 1.67 (95% confidence interval, 1.09, 2.55; = 0.019). The baseline Model for End-Stage Liver Disease score was not prognostic in the cirrhosis cohort. There was no statistical difference between mortality in patients with a history of compensated or decompensated cirrhosis. The most common cause of death in the cirrhosis cohort was respiratory failure. : COVID-19 hepatitis may lead to poor outcomes in patients who are hospitalized for the disease. Patients with cirrhosis are at a higher risk of COVID-19-related mortality.
新型冠状病毒严重急性呼吸综合征冠状病毒 2(SARS-CoV2)是 2019 年冠状病毒病(COVID-19)的病原体。该病毒的临床表现多种多样,越来越多的文献报道了其死亡的相关危险因素。本研究旨在评估在纽约布朗克斯一家三级护理医院网络中,因 COVID-19 感染住院的患者队列中,初始天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)水平以及先前存在的肝脏疾病(包括肝硬化)的影响。我们回顾了 2020 年 2 月 28 日至 2020 年 5 月 22 日期间,在蒙蒂菲奥里医疗中心因 SARS-CoV2 鼻拭子阳性、年龄大于 18 岁且有相关住院和出院(或死亡)的 3352 例患者。其中,当初始 ALT >5 倍正常值上限(ULN)时,39/86(45%)例患者死亡;当初始 AST >3 倍 ULN 时,115/230(50%)例患者死亡。无先前肝脏疾病的患者死亡率为 26.6%,而有肝脏疾病的患者死亡率为 29.5%。亚组分析显示,肝硬化患者的死亡率为 36.1%。肝硬化使死亡率的危险比为 1.67(95%置信区间,1.09,2.55;P = 0.019)。肝硬化组基线终末期肝病模型评分对预后无预测价值。有或无代偿性或失代偿性肝硬化病史的患者死亡率无统计学差异。肝硬化组最常见的死亡原因是呼吸衰竭。COVID-19 肝炎可能导致因疾病住院的患者预后不良。肝硬化患者 COVID-19 相关死亡率较高。