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Validity of an automated algorithm using diagnosis and procedure codes to identify decompensated cirrhosis using electronic health records

机译:使用诊断和程序代码通过电子健康记录识别失代偿性肝硬化的自动算法的有效性

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摘要

Viral hepatitis-induced cirrhosis can progress to decompensated cirrhosis. Clinical decompensation represents a milestone event for the patient with cirrhosis, yet there remains uncertainty regarding precisely how to define this important phenomenon. With the development of broader treatment options for cirrhotic hepatitis patients, efficient identification of liver status before evolving to decompensated cirrhosis could be life-saving, but research on the topic has been limited by inconsistencies across studies, populations, and case-confirmation methods. We sought to determine whether diagnosis/procedure codes drawn from electronic health records (EHRs) could be used to identify patients with decompensated cirrhosis. In our first step, chart review was used to determine liver status (compensated cirrhosis, decompensated cirrhosis, non-cirrhotic) in patients from the Chronic Hepatitis Cohort Study. Next, a hybrid approach between Least Absolute Shrinkage and Selection Operator regression and Classification Regression Trees models was used to optimize EHR-based identification of decompensated cirrhosis, based on 41 diagnosis and procedure codes. These models were validated using tenfold cross-validation; method accuracy was evaluated by positive predictive values (PPVs) and area under receiver operating characteristic (AUROC) curves. Among 296 patients (23 with hepatitis B, 268 with hepatitis C, and 5 co-infected) with a 2:1 ratio of biopsy-confirmed cirrhosis to noncirrhosis, chart review identified 127 cases of decompensated cirrhosis (Kappa=0.88). The algorithm of five liver-related conditions—liver transplant, hepatocellular carcinoma, esophageal varices complications/procedures, ascites, and cirrhosis—yielded a PPV of 85% and an AUROC of 92%. A hierarchical subset of three conditions (hepatocellular carcinoma, ascites, and esophageal varices) demonstrated a PPV of 81% and an AUROC of 86%. Given the excellent predictive ability of our model, this EHR-based automated algorithm may be used to successfully identify patients with decompensated cirrhosis. This algorithm may contribute to timely identification and treatment of viral hepatitis patients who have progressed to decompensated cirrhosis.
机译:病毒性肝炎引起的肝硬化可发展为代偿性肝硬化。临床代偿失调是肝硬化患者的一个里程碑事件,但是对于如何定义这一重要现象仍然存在不确定性。随着针对肝硬化性肝炎患者的更广泛治疗选择的发展,在发展为代偿性肝硬化之前有效地鉴定肝脏状况可能会挽救生命,但该主题的研究受到研究,人群和病例确认方法不一致的限制。我们试图确定是否可以使用从电子健康记录(EHR)中提取的诊断/程序代码来识别失代偿性肝硬化患者。在我们的第一步中,使用图表审查来确定来自慢性肝炎队列研究的患者的肝脏状况(代偿性肝硬化,代偿性肝硬化,非肝硬化)。接下来,基于41种诊断和程序代码,使用最小绝对收缩和选择算子回归与分类回归树模型之间的混合方法来优化基于EHR的代偿性肝硬化识别。这些模型使用十倍交叉验证进行了验证。通过正预测值(PPV)和接收器工作特征(AUROC)曲线下的面积评估方法的准确性。在296例活检证实的肝硬化与非肝硬化比率为2:1的患者中(23例为乙型肝炎,268例为丙型肝炎,5例合并感染),图表审查确定了127例失代偿性肝硬化(Kappa = 0.88)。五个与肝脏相关的疾病(肝脏移植,肝细胞癌,食道静脉曲张并发症/手术,腹水和肝硬化)的算法产生的PPV为85%,AUROC为92%。三种疾病(肝细胞癌,腹水和食管静脉曲张)的分层子集显示PPV为81%,AUROC为86%。鉴于我们模型的出色预测能力,这种基于EHR的自动化算法可用于成功识别失代偿性肝硬化患者。该算法可能有助于及时识别和治疗已发展为代偿性肝硬化的病毒性肝炎患者。

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