Abstract

The Michigan Department of Health and Human Services implemented and evaluated two initiatives designed to enhance provider knowledge of patients appropriate for breast and/or ovarian cancer genetic risk assessment and hereditary breast and ovarian cancer (HBOC) syndrome testing. The first initiative targeted select providers who had diagnosed patients meeting HBOC risk criteria. Specifically, the initiative used 2008–2009 state cancer registry data to identify all providers who had diagnosed breast cancers in women ≤50 years of age, male breast cancers, and ovarian cancers in four health systems with newly established cancer genetics clinics. Using a method coined bidirectional reporting (BDR), reports highlighting how many of these cases each provider had seen were generated and mailed. Reports on 475 cancers (9.5% of the 5005 cases statewide meeting criteria) were sent to 69 providers with information about how and why to refer such patients for genetic counseling. Providers who received a report were contacted to assess whether the reports increased awareness or resulted in action (genetic counseling/referral). Based on the few responses received, despite multiple attempts to contact, and attrition rate, it is not possible to ascertain the impact of this initiative on providers. However the project resulted in the MDHHS identifying which providers see the largest proportion of at-risk patients, creating an opportunity to target those providers with HBOC education efforts. The second initiative involved creating and broadly disseminating an online, interactive case-based educational module to increase awareness and referral decisions for HBOC using high- and low-risk patient scenarios. A total of 1835 unique users accessed the module in a one year. Collectively the users viewed topic pages 2724 times and the interactive case studies 1369 times. Point of care tools (fact sheets) were viewed 1624 times and downloaded 764 times. Satisfaction among the subset of users applying for continuing medical education credit was high. The online educational module had a much broader reach than the bidirectional reporting initiative but to a self-selected audience. Combining targeted and broad-based provider education efforts may be a better way to increase HBOC awareness in the target audience, starting with those providers seeing the largest proportion of patients at risk.

Highlights

  • Healthy People 2020 includes a genomics objective that aims to “increase the proportion of women with a family history of breast and/or ovarian cancer who receive genetic counseling” [1]

  • 5%–10% of cases of breast cancers and 15% of invasive ovarian cancers are related to hereditary breast and ovarian cancer syndrome (HBOC) [2]

  • Using Michigan Cancer Surveillance Program (MCSP) data, in 2008–2009 there were 5005 cancers that were appropriate for genetic counseling (GC) based on HBOC referral guidelines

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Summary

Introduction

Healthy People 2020 includes a genomics objective that aims to “increase the proportion of women with a family history of breast and/or ovarian cancer who receive genetic counseling” [1]. HBOC are available and are quite different from population screening guidelines for breast and ovarian cancer [3,4]. The discovery that mutations in two genes, BRCA1 and BRCA2 [9,10], are associated with HBOC led to the availability of genetic testing to identify individuals at risk in the mid-1990s. Various organizations began to develop strategies for educating providers about how to identify at-risk individuals and referral guidelines for genetic counseling and testing [11,12]

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