Evaluation of family health history collection methods impact on data and risk assessment outcomes.

Journal Article (Journal Article)

Information technology applications for patient-collection of family health history (FHH) increase identification of elevated-risk individuals compared to usual care. It is unknown if the method of collection impacts data collected or if simply going directly to the patient is what makes the difference. The objective of this study was to examine differences in data detail and risk identification rates between FHH collection directly from individuals using paper-based forms and an interactive web-based platform. This is a non-randomized epidemiologic study in Singaporean population from 2016 to 2018. Intervention was paper-based versus web-based interactive platform for FHH collection. Participant demographics, FHH detail, and risk assessment results were analyzed. 882 participants enrolled in the study, 481 in the paper-based group and 401 in the web-based group with mean (SD) age of 45.4 (12.98) years and 47.5% male. Web-based FHH collection participants had an increased number of conditions per relative (p-value <0.001), greater frequency of reporting age of onset (p-value <0.001), and greater odds of receiving ≥1 risk recommendation both overall (OR: 3.99 (2.41, 6.59)) and within subcategories of genetic counselling for hereditary cancer syndromes (p-value = 0.041) and screening and prevention for breast (p-value = 0.002) and colon cancer (p-value = 0.005). This has significant implications for clinical care and research efforts where FHH is being assessed. Using interactive information technology platforms to collect FHH can improve the completeness of the data collected and result in increased rates of risk identification. Methods of data collection to maximize benefit should be taken into account in future studies and clinical care.

Full Text

Duke Authors

Cited Authors

  • Wu, RR; Sultana, R; Bylstra, Y; Jamuar, S; Davila, S; Lim, WK; Ginsburg, GS; Orlando, LA; Yeo, KK; Cook, SA; Tan, P

Published Date

  • June 2020

Published In

Volume / Issue

  • 18 /

Start / End Page

  • 101072 -

PubMed ID

  • 32181122

Pubmed Central ID

  • 32181122

International Standard Serial Number (ISSN)

  • 2211-3355

Digital Object Identifier (DOI)

  • 10.1016/j.pmedr.2020.101072

Language

  • eng

Conference Location

  • United States