Constraints on Formulary Design Under the Affordable Care Act
1Department of Economics, University of North Carolina at Greensboro, Greensboro, NC, USA.
Health Economics
|February 25, 2017
Summary
The Affordable Care Act
Area of Science:
- Health policy
- Pharmaceutical economics
- Insurance regulation
Background:
- The Affordable Care Act mandates essential health benefits (EHB) for health insurance marketplace plans.
- EHB requirements influence prescription drug coverage but not cost-sharing or utilization management.
- Understanding the impact of these regulations on drug formularies is crucial for assessing healthcare access and costs.
Purpose of the Study:
- To analyze the effect of essential health benefits (EHB) requirements on prescription drug formularies in health insurance marketplace plans.
- To determine how EHB mandates influence the number of drugs covered, cost-sharing, and utilization management practices.
- To investigate the mechanisms driving changes in formularies post-EHB implementation.
Main Methods:
- Analysis of a comprehensive dataset of U.S. health insurance formularies.
- Econometric modeling to assess the impact of EHB on formulary size and drug placement.
- Comparative analysis using Medicare Advantage plan formularies and drugs not meeting EHB criteria.
Main Results:
- Mandatory coverage of one additional drug increased average formularies by 0.22 drugs (3.3%).
- Newly covered drugs are 22.3 percentage points more likely to face utilization management.
- EHB requirements also increase the likelihood of drugs being placed on higher, more expensive formulary tiers.
Conclusions:
- Essential health benefits (EHB) requirements significantly alter prescription drug formularies.
- Insurers respond to EHB by expanding formulary size and increasing utilization management for newly covered drugs.
- Findings suggest regulatory mandates, rather than consumer demand or market entry effects, drive these formulary changes.
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