Algorithm to Identify Type 2 Diabetes Using Electronic Health Record and Self-Reported Data.

IF 1.7 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Metabolic syndrome and related disorders Pub Date : 2025-05-01 Epub Date: 2025-04-07 DOI:10.1089/met.2024.0133
Ben T Varghese, Marlene E Girardo, Ruchi Gupta, Karen M Fischer, Madison Duellman, Michelle M Mielke, Aoife M Egan, Janet E Olson, Adrian Vella, Kent R Bailey, Sagar B Dugani
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Abstract

Aims: Identifying participants with type 2 diabetes (T2D) based only on electronic health record (EHR) or self-reported data has limited accuracy. Therefore, the objective of the study was to develop an algorithm using EHR and self-reported data to identify participants with and without T2D. Methods: We included participants enrolled in the Mayo Clinic Biobank. At enrollment, participants completed a baseline questionnaire on health conditions, including T2D, and provided access to their EHR data. T2D status was based on self-report and EHR data (International Classification of Diseases codes, hemoglobin A1c [HbA1c], plasma glucose, and glucose-regulating medications) within 5 years prior to and 2 months after enrollment. Participants who self-reported T2D but lacked corroborating EHR data were categorized separately ("only self-reported T2D"). After identifying participants with T2D, we identified participants without T2D based on normal HbA1c and plasma glucose. Participants who self-reported the absence of T2D but lacked corroborating EHR data were categorized separately ("only self-reported no T2D"). Using manual chart reviews (gold standard), we calculated the positive and negative predictive values (NPV) to identify T2D. Results: Of 57,000 participants, the algorithm classified participants as having T2D (n = 6,238), no T2D (n = 38,883), "only self-reported T2D" (n = 757), and "only self-reported no-T2D" (n = 9,759). The algorithm had a high positive predictive value (96.0% [91.5%-98.5%]), NPV (100% [98.0%-100%]), and accuracy (99.5% [98.3%-99.8%]). Participant age (median [range]) ranged from 52 (18-98) years (only self-reported T2D) to 67 (19-99) years (T2D) (P < 0.0001), and the proportion of women ranged from 45.3% (T2D) to 69.6% (only self-reported no T2D) (P < 0.0001). Most participants were of the White race (84.0%-92.7%) and non-Hispanic ethnicity (97.6%-98.6%). Conclusions: In this study, we developed an algorithm to accurately identify participants with and without T2D, which may be generalizable to cohorts with linked EHR data.

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利用电子健康记录和自我报告数据识别2型糖尿病的算法
目的:仅根据电子健康记录(EHR)或自我报告的数据识别2型糖尿病(T2D)参与者的准确性有限。因此,本研究的目的是开发一种使用电子病历和自我报告数据的算法来识别患有和不患有T2D的参与者。方法:我们纳入了梅奥诊所生物库的参与者。在入组时,参与者完成了一份关于健康状况的基线问卷,包括T2D,并提供了他们的电子病历数据。T2D状态基于入组前5年和入组后2个月内的自我报告和EHR数据(国际疾病分类代码、血红蛋白A1c [HbA1c]、血糖和血糖调节药物)。自我报告T2D但缺乏确凿电子病历数据的参与者被单独分类(“仅自我报告T2D”)。在确定T2D患者后,我们根据正常的HbA1c和血糖来确定没有T2D的患者。自我报告无T2D但缺乏确凿电子病历数据的参与者被单独分类(“仅自我报告无T2D”)。使用手工图表回顾(金标准),我们计算了阳性和阴性预测值(NPV)来识别T2D。结果:在57,000名参与者中,该算法将参与者分为有T2D (n = 6238)、无T2D (n = 38,883)、“仅自我报告T2D”(n = 757)和“仅自我报告无T2D”(n = 9,759)。该算法具有较高的阳性预测值(96.0%[91.5% ~ 98.5%])、NPV(100%[98.0% ~ 100%])和准确率(99.5%[98.3% ~ 99.8%])。参与者年龄(中位[范围])从52(18-98)岁(仅自我报告T2D)到67(19-99)岁(T2D) (P < 0.0001),女性比例从45.3% (T2D)到69.6%(仅自我报告无T2D) (P < 0.0001)。大多数参与者是白人(84.0%-92.7%)和非西班牙裔(97.6%-98.6%)。结论:在本研究中,我们开发了一种算法来准确识别患有和不患有T2D的参与者,该算法可以推广到具有相关电子病历数据的队列。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Metabolic syndrome and related disorders
Metabolic syndrome and related disorders MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.40
自引率
0.00%
发文量
74
审稿时长
6-12 weeks
期刊介绍: Metabolic Syndrome and Related Disorders is the only peer-reviewed journal focusing solely on the pathophysiology, recognition, and treatment of this major health condition. The Journal meets the imperative for comprehensive research, data, and commentary on metabolic disorder as a suspected precursor to a wide range of diseases, including type 2 diabetes, cardiovascular disease, stroke, cancer, polycystic ovary syndrome, gout, and asthma. Metabolic Syndrome and Related Disorders coverage includes: -Insulin resistance- Central obesity- Glucose intolerance- Dyslipidemia with elevated triglycerides- Low HDL-cholesterol- Microalbuminuria- Predominance of small dense LDL-cholesterol particles- Hypertension- Endothelial dysfunction- Oxidative stress- Inflammation- Related disorders of polycystic ovarian syndrome, fatty liver disease (NASH), and gout
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