4.6 Article

Clinical utility of family history for cancer screening and referral in primary care: A report from the Family Healthware Impact Trial

期刊

GENETICS IN MEDICINE
卷 13, 期 11, 页码 956-965

出版社

NATURE PUBLISHING GROUP
DOI: 10.1097/GIM.0b013e3182241d88

关键词

family history; risk assessment; early detection of cancer; neoplasms; health knowledge; attitudes; practice

资金

  1. Centers for Disease Control and Prevention
  2. Association for Prevention Teaching and Research [U50/CCU300860 TS-1216]
  3. American Association of Medical Colleges [U36/CCU319276 MM-0789, U36/CCU319276 MM0630]
  4. National Cancer Institute [K07 CA086958, K07 CA131103]

向作者/读者索取更多资源

Purpose: To assess the effectiveness of computerized familial risk assessment and tailored messages for identifying individuals for targeted cancer prevention strategies and motivating behavior change. Methods: We conducted a randomized clinical trial in primary care patients aged 35-65 years using Family Healthware, a self-administered, internet-based tool that collects family history for six common diseases including breast cancer, colon cancer, and ovarian cancer, stratifies risk into three tiers, and provides tailored prevention messages. Cancer screening adherence and consultation were measured at baseline and 6-month follow-up. Results: Of 3283 participants, 34% were at strong or moderate risk of at least one of the cancers. Family Healthware identified additional participants for whom earlier screening (colon cancer, 4.4%; breast cancer, women ages: 35-39 years, 9%) or genetic assessment (colon cancer, 2.5%; breast cancer, 10%; and ovarian cancer, 4%) may be indicated. Fewer than half were already adherent with risk-based screening. Screening adherence improved for all risk categories with no difference between intervention and control groups. Consultation with specialists did not differ between groups. Conclusion: Family Healthware identified patients for intensified cancer prevention. Engagement of clinicians and patients, integration with clinical decision support, and inclusion of nonfamilial risk factors may be necessary to achieve the full potential of computerized risk assessment. Genet Med 2011:13(11):956-965.

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