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Evaluation
of State Prescription Drug Programs:
Lessons for Medicare
Increasing
seniors' access to prescription drugs is a top policy priority for
the American people, the Administration, and members of Congress.
Both parties have proposed legislation that would add a prescription-drug
component to Medicare, albeit with very different structures. Many
questions about the design and implementation of a Medicare drug
benefit need to be answered.
States
have been administering public prescription drug programs in some
form since 1975. Their experiences with various program designs
can provide valuable information to federal policymakers designing
a drug benefit. To assess how states have expanded access to prescription
drugs while trying to control costs, The Robert Wood Johnson Foundation's
Changes in Health Care Financing and Organization (HCFO) program
convened a small meeting of state and federal policymakers, researchers,
and analysts. The participants generated many important questions.
Therefore, through this special topic solicitation, the HCFO program
encourages research assessing the effect of state prescription drug
programs on costs and access to care and on the implications of
these programs for Medicare.
Although
we are interested in evaluating state programs themselves, we are
hoping to solicit proposals that would relate lessons learned from
these evaluations to the design and implementation of a Medicare
drug benefit. Thus, the proposed findings from these projects should
be put in the context of implications for Medicare, including:
- The
effect of implementing similar design elements on beneficiary
access, out-of-pocket costs, and the cost to public payors;
- The
effect on the private market, including drug company costs, research
and development, and pharmacy benefit managers; and,
- The
degree to which adopting certain program elements would mean a
fundamental change in Medicare's structure (e.g., introducing
a means-testing component into a program that was heretofore an
entitlement program).
The
following questions are intended to suggest the types of issues
we are interested in funding. They are not meant to be a complete
list. Moreover, each question does not necessarily represent a stand-alone
research project. Projects submitted under this solicitation should
follow the regular HCFO application instructions.
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What have states done to expand access to prescription drugs?
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How have states been able to control costs?
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Which mechanisms have been most effective at expanding access
while controlling costs?
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How has participation in state programs been affected by different
components of program design and operation (e.g. eligibility determination,
cost sharing, means testing, formulary structure)?
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How do beneficiaries' out-of-pocket costs vary with the interventions
that have been tried?
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How do a state's program design and operation affect utilization
of prescription drugs and other health care services?
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What has been the experience of private discount card programs
administered by pharmaceutical companies? Who enrolled in these
programs?
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How do private discount card programs affect consumers' utilization,
cost, and access?
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How do state programs and private discount cards affect drug companies
(e.g. costs, research, and development budgets)?
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What effect do they have on overall prescription drug costs?
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How do the design and operation of state programs and private
discount cards affect physicians' prescribing patterns?
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