In this Section |
232140 Pre-operative breast MRI and treatment outcomes: A cost-effectiveness analysisMonday, November 8, 2010
Background: Nearly 12% of American women will be treated for invasive breast cancer during their lifetimes. Breast magnetic resonance imaging (BMRI) may improve surgical planning and outcomes. There is concern regarding treatment delay and increased rate of mastectomy in practices utilizing universal BMRI.
Objective: To assess the costs, risks, and benefits associated with universal BMRI in early stage breast cancer compared to no further imaging prior to local therapy, over five years. Design: Decision tree model Data Sources: Clinical trials, meta-analyses, government-sponsored research studies Target Population: Women diagnosed with Stage I or II invasive breast cancer Perspective: Payer Intervention: Breast magnetic resonance imagery Outcome Measures: Life-years saved, costs incurred Base-Case Analysis: BMRI was projected to have almost no effect on 5-year survival compared to no BMRI. The incremental cost-effectiveness ratio was $203 per life-year saved. BMRI was always more expensive and is more effective approximately half of the time. Sensitivity Analysis: Deterministic sensitivity analyses indicated that results were most sensitive to changes in the probabilities of 5-year survival. Probabilistic sensitivity analyses showed uncertainty did not influence the conclusions of the cost-effectiveness analysis. Limitations: Costs, risks, and benefits associated with additional BMRI findings and decreased quality of life due to unnecessary mastectomy were beyond the scope of this analysis. Neo-adjuvant therapies were not considered in the model. Conclusions: Universal BMRI is a costly addition to pre-treatment planning and results in no significant benefits to the patient. Payers should ensure that BMRI is indicated prior to authorizing payment.
Learning Areas:
Public health or related researchLearning Objectives: Keywords: Breast Cancer, Cost-Effectiveness
Presenting author's disclosure statement:
Qualified on the content I am responsible for because: Delta Omega student nominee 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.
Back to: 3071.0: Delta Omega Poster Session II
|