颅内应用Stroop试验筛选轻度肝性脑病合并非酒精性肝硬化患者的外部验证

IF 2.5 Q2 GASTROENTEROLOGY & HEPATOLOGY
Ting-Ting Jiang, Xiao-Li Liu, Hao Yu, Ya-Xuan Sun, Jia-Yan Zhou, Zhi-Yun Yang, Guang Chen
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引用次数: 0

摘要

背景:神经认知障碍,包括轻度肝性脑病(MHE)和显性肝性脑病,是所有类型的原发性肝病(如乙型肝炎、胆管炎和自身免疫性肝炎)最常见的并发症之一。EncephalApp Stroop测试是一种基于智能手机应用程序的测试,可以节省MHE筛查的时间。然而,酒精性肝硬化患者与非酒精性肝硬化患者的神经认知功能障碍不同,因此MHE诊断的临界值可能会被夸大。目的:验证Stroop试验在非酒精性肝硬化患者中的应用价值。方法:外部验证在国家传染病中心(北京)进行。年龄在18 - 65岁之间、自愿参加研究并提供知情同意书的肝硬化患者被纳入研究。采用肝性脑病心理测量评分(PHES)作为MHE的标准诊断标准。然后在iPad上进行EncephalApp Stroop测试,包括两个测试阶段(“关闭”和“打开”),以测量患者区分数字和字母的能力。以PHES为标准,从曲线下面积(AUC)、敏感性、特异性、阳性预测值和阴性预测值等方面评价EncephalApp Stroop试验的性能。结果:共有160例非酒精性肝硬化患者纳入本验证研究,其中87例(54.4%)无MHE患者和73例(45.6%)有MHE患者。以PHES为金标准,EncephalApp Stroop试验在“关闭”时间[AUC: 0.85, 95%可信区间(CI): 0.79-0.91]和“打开+关闭”时间(AUC: 0.85, 95%CI: 0.80-0.91)方面对非酒精性肝硬化患者表现良好;然而,“关闭”会话的总运行量(AUC: 0.61, 95%CI: 0.52-0.69),“打开”会话的总运行量(AUC: 0.57, 95%CI: 0.48-0.65)和“打开-关闭”时间(AUC: 0.54, 95%CI: 0.44-0.63)相对较低。最佳截断点分别为“off”时间> 101.93秒和“on + off”时间> 205.86秒,灵敏度分别为0.84和0.90,特异性分别为0.77和0.71,阳性预测值分别为0.75和0.72,假阳性预测值分别为0.85和0.89。结论:我们的研究结果表明,在酒精性和非酒精性在世患者之间使用EncephalApp Stroop工具筛查MHE时,应该使用不同的截止点,这是在推广到整个慢性肝病人群中筛查神经认知障碍之前的关键检查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
External validation of EncephalApp Stroop test to screen minimal hepatic encephalopathy patients with nonalcoholic cirrhosis.

Background: Neurocognitive impairment, including minimal hepatic encephalopathy (MHE) and overt hepatic encephalopathy, is one of the most common complications of all types of primary liver diseases, such as hepatitis B, biliary cholangitis, and autoimmune hepatitis. The EncephalApp Stroop test is a smartphone application-based test that is time-saving for MHE screening. However, neurocognitive impairment is different between alcoholic cirrhosis patients and nonalcoholic cirrhosis patients, so the cutoff value for MHE diagnosis might be inflated.

Aim: To validate the Stroop test in nonalcoholic cirrhosis patients.

Methods: This external validation was performed at the National Center for Infectious Diseases (Beijing). Liver cirrhosis patients aged between 18 and 65 years who voluntarily enrolled in the study and provided signed informed consent were included. The Psychometric Hepatic Encephalopathy Score (PHES) test was used as the standard diagnostic criterion for MHE. The EncephalApp Stroop test was then performed on the iPad, including two sessions of tests ("off" and "on") to measure patients' ability to differentiate between numbers and letters. We assessed the performance of the EncephalApp Stroop test in terms of the area under the curve (AUC), sensitivity, specificity, positive predictive value, and negative predictive value, with the PHES as the standard criterion.

Results: A total of 160 nonalcoholic cirrhosis patients were included in this validation study, including 87 (54.4%) patients without MHE and 73 (45.6%) patients with MHE. Taking the PHES as the gold standard, the EncephalApp Stroop test performed well for nonalcoholic liver cirrhosis patients in terms of "off" time [AUC: 0.85, 95% confidence interval (CI): 0.79-0.91] and "on + off" time (AUC: 0.85, 95%CI: 0.80-0.91); however, total runs of "off" session (AUC: 0.61, 95%CI: 0.52-0.69), total runs of "on" session (AUC: 0.57, 95%CI: 0.48-0.65), and "on - off" time (AUC: 0.54, 95%CI: 0.44-0.63) were comparatively low. The optimal cutoff points were "off" time > 101.93 seconds and "on + off" time > 205.86 seconds, with sensitivities of 0.84 and 0.90, specificities of 0.77 and 0.71, positive predictive values of 0.75 and 0.72, and false-positive values of 0.85 and 0.89, respectively.

Conclusion: Our results suggest that different cutoffs should be used for the EncephalApp Stroop tool for MHE screening between alcoholic and nonalcoholic living patients, which is a critical check before generalization to screen for neurocognitive impairment among the whole population of chronic liver diseases.

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来源期刊
World Journal of Hepatology
World Journal of Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
4.10
自引率
4.20%
发文量
172
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