Rapid Identification and Phenotyping of Nonalcoholic Fatty Liver Disease Patients Using an Automated Algorithmic Approach in Diverse, Urban Healthcare Systems

Author:

Basile Anna O.ORCID,Verma AnuragORCID,Tang Leigh Anne,Serper MarinaORCID,Scanga Andrew,Farrell Ava,Destin Brittney,Carr Rotonya M.ORCID,Anyanwu-Ofili Anuli,Rajagopal GunaretnamORCID,Krikhely Abraham,Bessler Marc,Reilly Muredach P.ORCID,Ritchie Marylyn D.ORCID,Denny JoshuaORCID,Tatonetti Nicholas P.ORCID,Wattacheril JuliaORCID

Abstract

AbstractBackground and AimsNonalcoholic Fatty Liver Disease (NAFLD) is the most common global cause of chronic liver disease. Therapeutic interventions are rapidly advancing for its inflammatory phenotype, nonalcoholic steatohepatitis (NASH). Diagnosis codes alone fail to accurately recognize at-risk patients. The objective of the present work is to identify NAFLD patients within large electronic health record (EHR) databases for targeted intervention based on clinically relevant phenotypes.MethodsWe present a rule-based phenotype algorithm for the rapid identification of NAFLD patients developed using EHRs from 5.8 million adult patients at Columbia University Irving Medical Center (CUIMC). The algorithm was developed using the Observational Medical Outcomes Partnership (OMOP) Common Data Model, and queries multiple structured and unstructured data elements, including diagnosis codes, laboratory measurements, radiology and pathology modalities.ResultsOur approach identified 16,060 CUIMC NAFLD patients with 170 having a biopsy-proven NASH diagnosis. Fibrosis scoring on patients without histology identified 943 with scores indicative of advanced fibrosis (FIB-4, APRI, NAFLD) in 2 of the scoring metrics. The algorithm was validated at two independent healthcare systems, University of Pennsylvania Healthcare System (UPHS) and Vanderbilt Medical Center (VUMC), where 20,779 and 19,575 NAFLD patients were identified, respectively. Clinical chart review identified a high positive predictive value (PPV) for the algorithm across all healthcare systems: 91% at CUIMC, 75% at UPHS, and 85% at VUMC.ConclusionsOur rule-based algorithm provides an accurate, automated approach for rapidly identifying and sub-phenotyping NAFLD patients within a large EHR system. This highlights the clinical potential algorithms have in discovering NAFLD patients at highest risk for disease progression for diagnostic and therapeutic intervention.Data Transparency StatementAlgorithmic code is available for academic, non-commercial collaborations by request to the corresponding authors.What You Need to KnowBackground and ContextNAFLD is the leading form of liver disease worldwide with a rising prevalence in the population. Current means of identification are complex and dependent on provider recognition of clinical risk factors.New FindingsWe present an accurate (mean PPV=84%) and cross-institution validated, rule-based algorithm for the high-throughput, rapid identification of NAFLD patients across diverse EHR systems comprising approximately 12.1 million patients. The majority of patients were previously unidentified.LimitationsInaccessible imaging and histologic data (performed outside the healthcare system) limited our ability to verify hepatic steatosis and resulted in low sensitivity for the final step of the algorithm.ImpactOur NAFLD algorithm provides an accurate means of rapidly identifying NAFLD in large EHR systems to target patients at greatest risk for disease progression and clinical outcomes towards diagnostic and therapeutic interventions.Short SummaryNAFLD, the leading cause of liver disease globally, is often under-recognized in at-risk individuals. Here we present a rapid, non-invasive algorithm for identifying patients within large health systems who are at greatest risk for disease progression and clinical decompensation for diagnostic and therapeutic intervention.

Publisher

Cold Spring Harbor Laboratory

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3