Enhanced family history-based algorithms increase the identification of individuals meeting criteria for genetic testing of hereditary cancer syndromes but would not reduce disparities on their own

Richard L. Bradshaw, Kensaku Kawamoto, Jemar R. Bather, Melody S. Goodman, Wendy K. Kohlmann, Daniel Chavez-Yenter, Molly Volkmar, Rachel Monahan, Kimberly A. Kaphingst, Guilherme Del Fiol

Research output: Contribution to journalArticlepeer-review

Abstract

Objective: This study aimed to 1) investigate algorithm enhancements for identifying patients eligible for genetic testing of hereditary cancer syndromes using family history data from electronic health records (EHRs); and 2) assess their impact on relative differences across sex, race, ethnicity, and language preference. Materials and Methods: The study used EHR data from a tertiary academic medical center. A baseline rule-base algorithm, relying on structured family history data (structured data; SD), was enhanced using a natural language processing (NLP) component and a relaxed criteria algorithm (partial match [PM]). The identification rates and differences were analyzed considering sex, race, ethnicity, and language preference. Results: Among 120,007 patients aged 25–60, detection rate differences were found across all groups using the SD (all P < 0.001). Both enhancements increased identification rates; NLP led to a 1.9 % increase and the relaxed criteria algorithm (PM) led to an 18.5 % increase (both P < 0.001). Combining SD with NLP and PM yielded a 20.4 % increase (P < 0.001). Similar increases were observed within subgroups. Relative differences persisted across most categories for the enhanced algorithms, with disproportionately higher identification of patients who are White, Female, non-Hispanic, and whose preferred language is English. Conclusion: Algorithm enhancements increased identification rates for patients eligible for genetic testing of hereditary cancer syndromes, regardless of sex, race, ethnicity, and language preference. However, differences in identification rates persisted, emphasizing the need for additional strategies to reduce disparities such as addressing underlying biases in EHR family health information and selectively applying algorithm enhancements for disadvantaged populations. Systematic assessment of differences in algorithm performance across population subgroups should be incorporated into algorithm development processes.

Original languageEnglish (US)
Article number104568
JournalJournal of Biomedical Informatics
Volume149
DOIs
StatePublished - Jan 2024

Keywords

  • Algorithm development
  • Electronic health records
  • Genetic testing
  • Healthcare disparities
  • Hereditary cancer syndromes

ASJC Scopus subject areas

  • Health Informatics
  • Computer Science Applications

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