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    A controlled trial of value-based insurance design - the MHealthy: Focus on Diabetes (FOD) trial

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    Authors
    Spaulding, Alicen
    Fendrick, A. Mark
    Herman, William H.
    Stevenson, James G.
    Smith, Dean G.
    Chernew, Michael E.
    Parsons, Dawn M.
    Bruhnsen, Keith
    Rosen, Allison B.
    UMass Chan Affiliations
    Department of Quantitative Health Sciences
    Document Type
    Journal Article
    Publication Date
    2009-04-09
    Keywords
    Bioinformatics
    Biostatistics
    Epidemiology
    Health Services Research
    
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    Abstract
    BACKGROUND: Diabetes affects over 20 million Americans, resulting in substantial morbidity, mortality, and costs. While medications are the cornerstone of secondary prevention, many evidence-based therapies are underutilized, and patients often cite out-of-pocket costs as the reason. Value-based insurance design (VBID) is a 'clinically sensitive' refinement to benefit design which links patient cost-sharing to therapy value; the more clinically beneficial (and valuable) a therapy is for a patient, the lower that patient's cost-sharing should be. We describe the design and implementation of MHealthy: Focus on Diabetes (FOD), a prospective, controlled trial of targeted co-payment reductions for high value, underutilized therapies for individuals with diabetes. METHODS: The FOD trial includes 2,507 employees and dependents with diabetes insured by one large employer. Approximately 81% are enrolled in a single independent-practice association model health maintenance organization. The control group includes 8,637 patients with diabetes covered by other employers and enrolled in the same managed care organization. Both groups received written materials about the importance of adherence to secondary prevention therapies, while only the intervention group received targeted co-payment reductions for glycemic agents, antihypertensives, lipid-lowering agents, antidepressants, and diabetic eye exams. Primary outcomes include medication uptake and adherence. Secondary outcomes include health care utilization and expenditures. An interrupted time series, control group design will allow rigorous assessment of the intervention's impact, while controlling for unrelated temporal trends. Individual patient-level baseline data are presented. DISCUSSION: To our knowledge, this is the first prospective controlled trial of co-payment reductions targeted to high-value services for high-risk patients. It will provide important information on feasibility of implementation and effectiveness of VBID in a real-world setting. This program has the potential for broad dissemination to other employers and insurers wishing to improve the value of their health care spending.
    Source
    Implement Sci. 2009 Apr 7;4:19. Link to article on publisher's site
    DOI
    10.1186/1748-5908-4-19
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/47797
    PubMed ID
    19351413
    Related Resources
    Link to Article in PubMed
    Rights
    © 2009 Spaulding et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
    ae974a485f413a2113503eed53cd6c53
    10.1186/1748-5908-4-19
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    Population and Quantitative Health Sciences Publications

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