Electronic medical record documentation of germline genetic evaluations in patients with ovarian cancer

J Genet Couns. 2024 Apr;33(2):314-321. doi: 10.1002/jgc4.1731. Epub 2023 May 15.

Abstract

Germline genetic evaluation is indicated for all patients with epithelial ovarian cancer (EOC). For testing to have clinical utility, results must be documented within the electronic medical record (EMR) and accessible to providers at the point of care, which can be challenging in the context of current EMR limitations and genetic testing processes. We examined the receipt of genetics services and EMR capture of genetic testing results in patients with EOC. We conducted a retrospective chart review to examine germline genetic evaluations among patients with EOC seen by a gynecologic or medical oncologist at the University of Pennsylvania in 2016. EMRs were reviewed to determine: (1) if patients were referred for genetic evaluation; (2) if genetic testing was performed; (3) if results were documented in office notes, scanned third-party test reports, and/or the EMR problem list; (4) if provider notes correctly listed the variant classification. Overall, 413 (62%) of patients had documented genetic testing. Genetic testing was documented in almost all provider notes (96%) and the majority of scanned EMR reports (64%). Pathogenic variants were found in 119 (29%) individuals; the majority (70%) had genetic testing documented within EMR problem lists. Provider notes were highly accurate in describing variant classification. In this study, genetic testing was performed and documented in the EMR for most EOC patients. Approximately one-third of those tested did not have scanned test reports specifying variant found, limiting the utility of test results for cascade testing and therapeutic decisions.

Keywords: cascade testing; genetic testing; referral practices.

MeSH terms

  • Adult
  • Aged
  • Documentation / methods
  • Electronic Health Records*
  • Female
  • Genetic Testing* / methods
  • Germ Cells
  • Germ-Line Mutation
  • Humans
  • Middle Aged
  • Ovarian Neoplasms* / genetics
  • Retrospective Studies