Development of a computable phenotype using electronic health records for venous thromboembolism in medical inpatients: the Medical Inpatient Thrombosis and Hemostasis study

被引:4
作者
Thomas, Ryan M. [1 ,2 ]
Wilkinson, Katherine [3 ]
Koh, Insu [3 ]
Li, Ang [4 ]
Warren, Janine S. A. [1 ]
Roetker, Nicholas S. [5 ]
Smith, Nicholas L. [6 ,7 ,8 ]
Holmes, Chris E. [1 ,2 ]
Plante, Timothy B. [1 ,2 ]
Repp, Allen B. [1 ,2 ]
Cushman, Mary [1 ,2 ]
Zakai, Neil A. [1 ,2 ,9 ]
机构
[1] Univ Vermont, Larner Coll Med, Dept Med, Burlington, VT USA
[2] Univ Vermont, Med Ctr, Burlington, VT USA
[3] Univ Vermont, Larner Coll Med, Dept Pathol & Lab Med, Burlington, VT USA
[4] Baylor Univ, Med Ctr, Dept Med, Houston, TX USA
[5] Hennepin Healthcare Res Inst, Chron Dis Res Grp, Minneapolis, MN USA
[6] Univ Washington, Dept Epidemiol, Seattle, WA USA
[7] Kaiser Permanente Washington, Kaiser Permanente Washington Hlth Res Inst, Seattle, WA USA
[8] Seattle Epidemiol Res & Informat Ctr, Dept Vet Affairs fice Res & Dev, Seattle, WA USA
[9] Univ Vermont, Larner Coll Med, Colchester Res Facil, 360 South Pk Dr, Colchester, VT 05446 USA
基金
美国国家卫生研究院;
关键词
International Classi; fication of Diseases; predictive value of; tests; venous thromboembolism; CODES; ACCURACY; VALIDITY; CARE;
D O I
10.1016/j.rpth.2023.100162
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Accurate and efficient methods to identify venous thromboembolism (VTE) events in hospitalized people are needed to support large-scale studies. Validated computable phenotypes using a specific combination of discrete, searchable elements in electronic health records to identify VTE and distinguish between hospital-acquired (HA)-VTE and present-on-admission (POA)-VTE would greatly facilitate the study of VTE, obviating the need for chart review. Objectives: To develop and validate computable phenotypes for POA-and HA-VTE in adults hospitalized for medical reasons. Methods: The population included admissions to medical services from 2010 to 2019 at an academic medical center. POA-VTE was defined as VTE diagnosed within 24 hours of admission, and HA-VTE as VTE identified more than 24 hours after admission. Using discharge diagnosis codes, present-on-admission flags, imaging procedures, and medication administration records, we iteratively developed computable phenotypes for POA-VTE and HA-VTE. We assessed the performance of the phenotypes using manual chart review and survey methodology. Results: Among 62,468 admissions, 2693 had any VTE diagnosis code. Using survey methodology, 230 records were reviewed to validate the computable phenotypes. Based on the computable phenotypes, the incidence of POA-VTE was 29.4 per 1000 admissions and that of HA-VTE was 3.6 per 1000 admissions. The POA-VTE comput-able phenotype had positive predictive value and sensitivity of 88.8% (95% CI, 79.8%-94.0%) and 99.1% (95% CI, 94.0%-99.8%), respectively. Corresponding values for the HA-VTE computable phenotype were 84.2% (95% CI, 60.8%-94.8%) and 72.3% (95% CI, 40.9%-90.8%). Conclusion: We developed computable phenotypes for HA-VTE and POA-VTE with adequate positive predictive value and sensitivity. This phenotype can be used in electronic health record data-based research.
引用
收藏
页数:8
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