Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Department of Gastroenterology and Hepatology, Guangzhou Eighth People's Hospital, Guangzhou, Guangdong Province, China.
Clin Infect Dis. 2021 Aug 2;73(3):e594-e601. doi: 10.1093/cid/ciaa1710.
Limited prior data suggest that preexisting liver disease is associated with adverse outcomes among patients with coronavirus disease 2019 (COVID-19). Fibrosis-4 (FIB-4) is a noninvasive index of readily available laboratory measurements that represents hepatic fibrosis. We evaluated the association between FIB-4 at the early stage of infection and COVID-19 outcomes.
FIB-4 was evaluated at admission in a cohort of 267 patients admitted with early-stage COVID-19 confirmed through reverse-transcription polymerase chain reaction assay. Hazard of ventilator use and of high-flow oxygen was estimated using Cox regression models controlled for covariates. Risks of progression to severe disease and of death/prolonged hospitalization were estimated using multivariable logistic regression models.
Forty-one (15%) patients progressed to severe disease, 36 (14%) required high-flow oxygen support, 10 (4%) required mechanical ventilator support, and 1 died. FIB-4 between 1.45 and 3.25 was associated with a greater than 5-fold (95% confidence interval [CI], 1.2-28) increased hazard of high-flow oxygen use, a greater than 4-fold (95% CI, 1.5-14.6) increased odds of progression to severe disease, and an over 3-fold (95% CI, 1.4-7.7) increased odds of death or prolonged hospitalization. FIB-4 >3.25 was associated with a greater than 12-fold (95% CI, 2.3-68. 7) increased hazard of high-flow oxygen use and an over 11-fold (95% CI, 3.1-45) increased risk of progression to severe disease. All associations were independent of sex, number of comorbidities, and inflammatory markers (D-dimer, C-reactive protein).
FIB-4 at the early-stage of COVID-19 had an independent and dose-dependent association with adverse outcomes during hospitalization. FIB-4 provided significant prognostic value for estimating adverse outcomes among COVID-19 patients.
有限的先前数据表明,在患有 2019 年冠状病毒病(COVID-19)的患者中,预先存在的肝脏疾病与不良结局相关。纤维化 4 指数(FIB-4)是一种易于获得的实验室测量的非侵入性指数,代表肝纤维化。我们评估了感染早期 FIB-4 与 COVID-19 结局之间的关系。
在通过逆转录聚合酶链反应检测确诊的 267 例早期 COVID-19 住院患者中评估了 FIB-4。使用 Cox 回归模型估计了使用呼吸机和高流量氧气的风险,并控制了协变量。使用多变量逻辑回归模型估计了向严重疾病进展和死亡/延长住院时间的风险。
41 名(15%)患者进展为严重疾病,36 名(14%)需要高流量氧气支持,10 名(4%)需要机械通气支持,1 名死亡。FIB-4 在 1.45 至 3.25 之间与高流量氧气使用的风险增加 5 倍以上(95%置信区间[CI],1.2-28),进展为严重疾病的风险增加 4 倍以上(95%CI,1.5-14.6),死亡或延长住院时间的风险增加 3 倍以上(95%CI,1.4-7.7)。FIB-4>3.25 与高流量氧气使用的风险增加 12 倍以上(95%CI,2.3-68.7)和进展为严重疾病的风险增加 11 倍以上(95%CI,3.1-45)相关。所有关联均独立于性别、合并症数量和炎症标志物(D-二聚体、C 反应蛋白)。
COVID-19 早期的 FIB-4 与住院期间的不良结局具有独立且剂量依赖性的关联。FIB-4 为估计 COVID-19 患者的不良结局提供了重要的预后价值。