LILLE-4 vs. LILLE-7 to predict short-term mortality in patients with severe alcoholic hepatitis

IF 3.7 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY Annals of hepatology Pub Date : 2024-02-01 DOI:10.1016/j.aohep.2024.101458
Claudia L. Dorantes-Nava , María F. Higuera-de la Tijera , Alfredo Servín-Caamaño , Gabriela Gutiérrez-Reyes , Miguel Y. Carmona-Castillo , Sandra Teutli-Carrion , Ernesto J. Medina-Avalos , José L. Pérez-Hernández
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Abstract

Introduction and Objectives

Alcoholic hepatitis (AH) is an acute liver inflammation associated with excessive alcohol consumption. The pharmacological treatment for AH is corticosteroids. There is a study that has proposed calculating the Lille model on day 4 (Lille-4), which apparently has comparable accuracy to the Lille model calculated on day 7 (Lille-7). However, this finding has not been validated. Therefore our objective is to determine if Lille-4 is equivalent to Lille-7 in predicting 28-day mortality in patients with probable severe alcoholic hepatitis (AH) as defined by the 2016 consortium criteria sponsored by NIAAA.

Materials and Patients

Observational, prospective, ambidirectional, analytical cohort study conducted from January 2010 to April 2023. We collected clinical and biochemical variables upon admission, calculated Lille models, assessed response and 28-day mortality. Comparative analyses were performed based on survival versus mortality. Sensitivity, specificity, PPV, NPV, and accuracy of the models were calculated.

Results

A total of 327 patients were included, 297 (90.8%) being male. Mean age was 43.4±9.3 years. The 50th percentile for alcohol consumption was 320 g/day (5th-95th percentile: 100.8-662). At day 28, 207 patients (63.3%) died. Upon admission, the patients who died showed a significant difference compared to survivors in: Maddrey (90 [95%CI: 81-99] vs. 70 [95%CI:65-75]; p<0.0001); ABIC (8.8±1.8 vs. 8.1±1.3; p<0.0001); MELD (32±8 vs. 27±4; p<0.0001); MELD-Na (33±6 vs. 30±4; p<0.0001). Lille-7 model had an AUROC of 0.71 [0.65-0.77], where a value >0.45 had a sensitivity (S) of 78% and specificity (E) of 45% in predicting early mortality. Lille-4 model had an AUROC of 0.68 [0.63-0.74], where a value >0.45 had an S of 81% and E of 54% (Figure 1).

Conclusions

Lille-7 is the model with the highest accuracy, according to the obtained AUROC, for predicting early mortality in severe alcoholic hepatitis (AH). Therefore, the determination of total bilirubin should not be done prematurely (before day 7), and steroid therapy should be provided to patients for up to 7 days to classify treatment response.

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LILLE-4 与 LILLE-7 预测重症酒精性肝炎患者短期死亡率的比较
导言和目的酒精性肝炎(AH)是一种与过度饮酒有关的急性肝脏炎症。治疗酒精性肝炎的药物是皮质类固醇。有一项研究建议在第 4 天计算里尔模型(Lille-4),其准确性显然与第 7 天计算的里尔模型(Lille-7)相当。然而,这一发现尚未得到验证。因此,我们的目标是确定 Lille-4 与 Lille-7 在预测由 NIAAA 赞助的 2016 年联盟标准所定义的可能重度酒精性肝炎(AH)患者的 28 天死亡率方面是否相当。我们收集了入院时的临床和生化变量,计算了里尔模型,评估了反应和 28 天死亡率。根据存活率与死亡率进行了比较分析。结果 共纳入 327 例患者,其中 297 例(90.8%)为男性。平均年龄为(43.4±9.3)岁。酒精消耗量的第 50 百分位数为 320 克/天(第 5-95 百分位数:100.8-662)。第 28 天,207 名患者(63.3%)死亡。入院时,死亡患者与存活患者相比,在以下方面存在显著差异:Maddrey(90 [95%CI: 81-99] vs. 70 [95%CI:65-75]; p<0.0001);ABIC(8.8±1.8 vs. 8.1±1.3;p<0.0001);MELD(32±8 vs. 27±4;p<0.0001);MELD-Na(33±6 vs. 30±4;p<0.0001)。Lille-7模型的AUROC为0.71 [0.65-0.77],其中0.45的值在预测早期死亡率方面的灵敏度(S)为78%,特异度(E)为45%。里尔-4 模型的 AUROC 为 0.68 [0.63-0.74],其中值为 0.45 的 S 为 81%,E 为 54%(图 1)。因此,不应过早(在第 7 天前)测定总胆红素,应为患者提供长达 7 天的类固醇治疗,以对治疗反应进行分类。
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来源期刊
Annals of hepatology
Annals of hepatology 医学-胃肠肝病学
CiteScore
7.90
自引率
2.60%
发文量
183
审稿时长
4-8 weeks
期刊介绍: Annals of Hepatology publishes original research on the biology and diseases of the liver in both humans and experimental models. Contributions may be submitted as regular articles. The journal also publishes concise reviews of both basic and clinical topics.
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