Prescription Drug Insurance Coverage, Drug Utilization, and Cost-Related Non-Adherence


Book Description

This paper uses the substantial increase in prescription drug insurance coverage from the adoption of Part D to generate new estimates the impact of coverage on drug utilization and cost-related non-adherence. The analysis uses detailed panel data on the elderly before and after the implementation of Part D drawn from the 2005 and 2007 Prescription Drug Study (PDS), administered as a supplement to the Health and Retirement Study (HRS), a large nationally representative survey of Americans aged 50 and older. Fixed-effect estimates suggest that gaining coverage results in a 15 percent increase in utilization. These results are consistent with the lower end of estimates in the literature. Gaining coverage also is associated with a 20-50 percent reduction in the incidence of cost-related non-adherence. However, even among the uninsured, only a relatively small proportion of drugs (12 percent) are associated with episodes of cost-related non-adherence. So, these large reductions apply to a small slice of all drugs.




Making Medicines Affordable


Book Description

Thanks to remarkable advances in modern health care attributable to science, engineering, and medicine, it is now possible to cure or manage illnesses that were long deemed untreatable. At the same time, however, the United States is facing the vexing challenge of a seemingly uncontrolled rise in the cost of health care. Total medical expenditures are rapidly approaching 20 percent of the gross domestic product and are crowding out other priorities of national importance. The use of increasingly expensive prescription drugs is a significant part of this problem, making the cost of biopharmaceuticals a serious national concern with broad political implications. Especially with the highly visible and very large price increases for prescription drugs that have occurred in recent years, finding a way to make prescription medicinesâ€"and health care at largeâ€"more affordable for everyone has become a socioeconomic imperative. Affordability is a complex function of factors, including not just the prices of the drugs themselves, but also the details of an individual's insurance coverage and the number of medical conditions that an individual or family confronts. Therefore, any solution to the affordability issue will require considering all of these factors together. The current high and increasing costs of prescription drugsâ€"coupled with the broader trends in overall health care costsâ€"is unsustainable to society as a whole. Making Medicines Affordable examines patient access to affordable and effective therapies, with emphasis on drug pricing, inflation in the cost of drugs, and insurance design. This report explores structural and policy factors influencing drug pricing, drug access programs, the emerging role of comparative effectiveness assessments in payment policies, changing finances of medical practice with regard to drug costs and reimbursement, and measures to prevent drug shortages and foster continued innovation in drug development. It makes recommendations for policy actions that could address drug price trends, improve patient access to affordable and effective treatments, and encourage innovations that address significant needs in health care.




Closing the Medicare Part D Coverage Gap


Book Description

The standard Medicare Part D benefit structure contains a gap in coverage (or so-called "doughnut hole") which requires beneficiaries to pay 100% of the cost for prescription drugs until they reach the catastrophic coverage phase. This coverage gap has been linked to a financial burden for beneficiaries resulting in poor medication adherence and other cost-related access problems. Under the 2010 Affordable Care Act (ACA) reform, the coverage gap has been gradually phasing out since 2011 such that beneficiaries will only pay 25% of drug costs by 2020. This study evaluated the impact of closing the coverage gap under the ACA by conducting three separate studies using data from the 2008-2015 Medicare Current Beneficiary Survey. Outcomes assessed included the utilization of and expenditures for prescription drugs, as well as cost-related access problems. Chapter 3 (Manuscript #1) analyzes trends in the distribution of beneficiaries in each benefit phase, prescription drug utilization, and expenditures among Part D beneficiaries not receiving the Low-Income Subsidy (LIS). After the ACA, the proportion of beneficiaries reaching the catastrophic coverage threshold increased (from 4% in 2010 to 6% in 2015), and they reached the threshold earlier in the year. The overall number of 30-day drug fills also increased after the ACA, although no significant changes in the number of 30-day drug fills were seen among those reaching the catastrophic coverage threshold. Total drug spending steadily increased after the ACA, with the largest increase seen in those reaching the catastrophic threshold; however, out-of-pocket spending significantly decreased among all beneficiaries (17% decrease in 2015 compared to 2009). Chapter 4 (Manuscript #2) evaluates the effects of the ACA coverage gap reform on drug utilization and expenditures using a difference-in-differences study design. Over the first five years after implementation of the ACA, out-of-pocket drug spending significantly decreased among non-LIS beneficiaries (treatment) relative to LIS beneficiaries (control), with growing decreases over time (average decreases of $41 in 2011 versus $135 in 2015). This was particularly noticeable among those who reached the coverage gap but not the catastrophic threshold. Despite seemingly large reductions in cost-sharing in the coverage gap, there were no significant changes in the number of 30-day drug fills and total drug spending after the ACA reform between non-LIS and LIS beneficiaries. Chapter 5 (Manuscript #3) evaluates the effects of the ACA coverage gap reform on cost-related access problems among beneficiaries using a difference-in-differences study design. Cost-related access problems were estimated by the likelihood of having cost-related nonadherence (CRN) or the adoption of drug cost-reduction strategies (CRS) by beneficiaries. Compared to LIS beneficiaries, no significant changes in CRN were seen among non-LIS beneficiaries after the ACA; furthermore, the likelihood of adopting CRS increased by 4 percentage points for non-LIS beneficiaries relative to LIS beneficiaries. Although the ACA reform has helped reduce out-of-pocket drug costs for beneficiaries by gradually reducing the beneficiary cost-sharing rate in the Part D coverage gap, the significant reduction in cost-sharing rate did not translate into an increased use of prescription drugs or resolved cost-related access problems for beneficiaries. Additionally, this study provides evidence of increased Part D spending, which has been a growing concern for the Medicare program. The findings of this study provide empirical evidence on the effects of closing the Part D coverage gap and address gaps in the limited existing literature. Overall, although the ACA decreased out-of-pocket drug costs, this study suggests additional initiatives will be needed to provide better protection against the cost of prescription drugs for Part D beneficiaries.




Managed Care Pharmacy Practice


Book Description

Managed Care Pharmacy Practice, Second Edition offers information critical to the development and operation of a managed care pharmacy program. The text also covers the changes that have taken place within the delivery of pharmacy services, as well as the evolving role of pharmacists.










Rare Diseases and Orphan Products


Book Description

Rare diseases collectively affect millions of Americans of all ages, but developing drugs and medical devices to prevent, diagnose, and treat these conditions is challenging. The Institute of Medicine (IOM) recommends implementing an integrated national strategy to promote rare diseases research and product development.




Handbook of Pharmaceutical Public Policy


Book Description

Get an invaluable view of the impact of economics and politics on pharmaceuticals in the United States Pharmacy and pharmaceutical drug use are highly regulated and the various regulatory forces interact with diverse goals. Pharmaceutical Public Policy is a comprehensive review of the legislation, trends, business developments, and policy interpretations that have shaped drug use during the last 50 years. This unique single source explains drug regulatory activity, the major insurance and payment systems, and the impact of economics and politics on drug use in the United States. Leading experts provide a thorough and objective look at public policy issues, making this text perfect for upper level undergraduate and graduate level pharmacy, medical, and public health educators and students. Pharmacists and pharmacy students must learn more than just the physical sciences and clinical aspects of the pharmaceutical industry. The rationale for policies, rules, and regulations is integral to understanding how to best serve patients and make the entire pharmaceutical sector more equitable and cost-effective. Pharmaceutical Public Policy examines the most pressing issues facing the industry, including control of the rising costs for drugs and ensuring correct drug usage by patients. This insightful text offers an in depth perspective of the policies and the debates that surround them. Chapters are well-referenced and many include helpful figures and tables to illustrate facts and ideas. Topics in Pharmaceutical Public Policy include: pharmacy law and regulation Medicare and prescription drug coverage FDA drug approval process Medicaid and prescription drugs public health pharmacy Department of Veterans Affairs pharmacy programs Department of Defense pharmacy programs innovative state drug program practices state and federal regulation of pharmacy the future of the pharmaceutical industry managed care pharmacy PBM’s (pharmacy benefit managers) risk minimization importation and reimportation biotechnology and pharmacogenetics policy and issues product promotion competition between drugs drug insurance design patient compliance abuse of prescription drugs health care systems and insurance in Europe much more Pharmaceutical Public Policy is a one-of-a-kind resource that explains just who the players are and the complexity of the issues that are examined in most pharmaceutical policy debates, and is perfect for pharmacy students, educators, other health professionals, trade association leaders, and policymakers.




The Price of Global Health


Book Description

The Price of Global Health is the first book of its kind: an in-depth but straightforward exploration of the pharmaceutical pricing strategy process, its underlying market access, general business and ethical considerations, and its implications for payers, physicians and patients. It is a much needed and invaluable resource for anybody interested, involved in or affected by the development, funding and use of prescription drugs. In particular, it is of critical importance to pharmaceutical company executives and other leaders and professionals in commercialization and drug development, including marketing, business development, market access and pricing, clinical development, drug discovery, regulatory affairs, health outcomes, market research and public affairs.