302399
Screening Mammography Rate Before and After the 2009 USPSTF Guideline: An Interrupted Time Series Analysis
Study Design: We used the Interrupted-Time-Series (ITS) design with a non-equivalent dependent variable and segmented regression analysis to evaluate the longitudinal effects of the 2009 USPSTF guideline changes on utilization of breast cancer screening.
Principal Findings: Our initial findings show that the release of 2009 USPSTF guideline results in a sharp drop of 8.3 per 1000 Medicare-eligible women (p-value <0.0001). The rate increases at a pace of 0.3 per month (p-value <0.001), and by the end of 2011, the rate has returned to the pre-2009 guideline level. When stratified by age groups, the guideline shows a stronger effect for women age 70 and older than age 65-69. The rate of pap test shows a similar pattern but less drastic post-2009 USPSTF guideline.
Conclusion: Consistent with most previous studies that used pre-post comparison, we found the screening mammography rate did not change in the long run after the 2009 guideline. But our study further reveals the incremental effect of policy changes overall and for different age groups. It appears important for policy organizations to issue concordant, rather than competing guidelines to effect changes in population care.
Learning Areas:
Biostatistics, economicsConduct evaluation related to programs, research, and other areas of practice
Public health or related organizational policy, standards, or other guidelines
Learning Objectives:
Compare mammography rate before and after 2009 USPSTF guideline using 2004-2011 Medicare claims data
Keyword(s): Cancer and Women’s Health, Medicare
Qualified on the content I am responsible for because: I have published extensively on the economics and utilization of diagnostic imaging and have been supported by external funding for this research. My recent research has focused specifically on screening programs to include mammography and low-dose CT lung screening.
Any relevant financial relationships? No
I agree to comply with the American Public Health Association Conflict of Interest and Commercial Support Guidelines, and to disclose to the participants any off-label or experimental uses of a commercial product or service discussed in my presentation.