Implications of Medicare Part D
About This Event

The launch of the Medicare Part D program to cover prescription drugs for seniors was one of the biggest changes in entitlement spending since the 1960s. What has the impact of this program been on patients and the U.S. health care system? Emerging data on the pharmaceutical industry in particular and the overall health care economy in general have allowed researchers to begin to answer this question. At this event, Lambert van der Walde of the Centers for Medicare & Medicaid Services will deliver special remarks, and leading academics will discuss initial studies of the effect of Part D on the use and pricing of prescription drugs. This newly generated data should inform assessment of the current program and suggest the changes, if any, that deserve consideration.

Agenda
8:45 a.m.
Registration
9:00
Introduction:
9:15
Special Remarks:
Lambert van der Walde, Centers for Medicare & Medicaid Services
"An Overview of the Part D Program"
10:15
Panelists:
Mark Duggan, University of Maryland
Dana Goldman, RAND Corporation
Helen Levy, University of Michigan
David Weir, University of Michigan
Discussant:
Moderator:

12:00 p.m. Adjournment

Event Summary

 

Surprise: Medicare's Prescription Drug Benefit Is Delivering Drugs, Preserving Incentives for Drug Development

 

 

WASHINGTON, OCTOBER 16, 2008--Medicare's "Part D" prescription drug benefit fosters true consumer choice, Lambert van der Walde of the Centers for Medicare and Medicaid Services said at an AEI conference on October 14. He reported that while only 7 percent of Medicare enrollees chose the congressionally formulated structure, more than 64 percent--10.5 million people--were willing to pay higher premiums for what they perceived as greater benefits.

This would come as a surprise to those who skeptically observed Part D's implementation in 2006. With a projected cost of $780 billion over ten years, Part D was the largest expansion of Medicare since the 1960s. Many feared that it would create mass confusion among the elderly and produce huge increases in pharmaceutical prices. Now, two years after its implementation, academic studies show that those fears were misplaced.  Most seniors have been able to navigate the program easily, and more seniors now have drug coverage than in the past.

Helen Levy and David Weir of the University of Michigan presented data showing a decrease in the share of senior citizens with no drug coverage from 23 percent before Part D to only 7 percent afterward. However, they cautioned that while Part D lowered out-of-pocket costs when compared with no coverage, it was still no substitute for employer-based coverage, which saved its beneficiaries an average of $7 dollars more per medication than Part D.

But beyond this domestic success, is Part D the best model of reform available? How does Part D's performance compare to the European approach to prescription drug benefits? An early criticism of Part D was that without the government directly purchasing from and negotiating with pharmaceutical companies--as is the practice in many European countries--drug prices would only continue their record rise. Not true, asserted the University of Maryland's Mark Duggan. Plans are free to create incentives for their enrollees to move between comparable drugs within a therapeutic class, as long as at least two drugs are covered in each class. This provides pharmaceutical companies with an incentive to lower their prices in the form of a larger share of the market, measured by the number of enrollees. Duggan presented data that demonstrated the success of Part D in decreasing drug prices by 12 percent, augmenting the out-of-pocket savings of subsidies alone.

Further, the European model uses the breadth of the government's control over health care provision to force drug prices down in negotiations. Dana Goldman of the RAND Corporation argues that while this resulted in a 23 percent decrease in drug prices overall in Europe, it has an inevitable negative effect on pharmaceutical research and development. Goldman measured the consequences of decreased innovation in terms of projected decreases in life expectancy in the absence of a robust drug pipeline. His data suggests a decrease of one-fifth of a year of life for current generations, increasing to seven-tenths of a year of life by 2060. Medicare Part D lowers the cost of drugs to consumers through government subsidies, not price controls. While this saddles current generations with an immediate cost, Goldman said that it is "buying future innovation, so it's not such a bad thing, this liability we're passing on."

 --KRISTIN VISWANATHAN

For video, audio, presentations, and event information, visit www.aei.org/event1814/.

AEI's AEI Studies on Medicare Reform series includes several volumes on the scope of Medicare's problems and how to fix them. The Health Policy Outlook series includes several issues on Medicare, including a recent edition by Joseph Antos on why health reformers seem to neglect Medicare.

The AEI Press recently published Innovation and Technology Adoption in Health Care Markets, by Anupam B. Jena and Tomas J. Philipson. This volume explores why cost-control measures like those in Europe may suppress the innovation and development of the life-saving drugs of the future.

For media inquiries, contact Véronique Rodman at 202.862.4870 or vrodman@aei.org.

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AEI Participants

 

Joseph
Antos

  • Mr. Antos's research focuses on the economics of health policy—including Medicare and broader health system reform, health care financing, health insurance regulation, and the uninsured—and federal budget policy. He has written and spoken extensively on the Medicare drug benefit and has led a team of experienced independent actuaries and cost estimators in a study to evaluate various proposals to extend health coverage to the uninsured. His work on the country’s budget crisis includes a detailed plan to achieve fiscal stability and economic growth developed in conjunction with AEI colleagues.  


    Joseph Antos is also a commissioner of the Maryland Health Services Cost Review Commission and a health adviser to the Congressional Budget Office.  Before joining AEI, Mr. Antos was Assistant Director for Health and Human Resources at the Congressional Budget Office.




    Watch Mr. Antos in an interview with Bill Erwin of the Alliance for Health Reform on "Will Health Reform Reduce the Federal Deficit?"

    nullFollow Joseph Antos on Twitter

  • Phone: 202-862-5938
    Email: jantos@aei.org
  • Assistant Info

    Name: Catherine Griffin
    Phone: 2028625920
    Email: catherine.griffin@aei.org

 

John E.
Calfee
  • Economist John E. Calfee (1941-2011) studied the pharmaceutical industry and the Food and Drug Administration (FDA), along with the economics of tobacco, tort liability, and patents. He previously worked at the Federal Trade Commission's Bureau of Economics. He had also taught marketing and consumer behavior at the business schools of the University of Maryland at College Park and Boston University. While Mr. Calfee's writings are mostly on pharmaceutical markets and FDA regulation, his academic articles and opinion pieces covered a variety of topics, from patent law and tort liability to advertising and consumer information. His books include Prices, Markets, and the Pharmaceutical Revolution (AEI Press, 2000) and Biotechnology and the Patent System (AEI Press, 2007). Mr. Calfee wrote regularly for AEI's Health Policy Outlook series. He testified before Congress and federal agencies on various topics, including alcohol advertising; biodefense vaccine research; international drug prices; and FDA oversight of drug safety.

 

Tomas J.
Philipson
  • Tomas J. Philipson is a visiting scholar at AEI and the Daniel Levin Chair in the Irving B. Harris Graduate School of Public Policy as well as an associate member of the department of economics at the University of Chicago. He was a senior health care adviser to the 2008 presidential campaign of John McCain and served in the Bush administration as the senior economic adviser to the commissioner of the Food and Drug Administration from 2003 to 2004 and subsequently as the senior economic adviser to the administrator of the Centers for Medicare & Medicaid Services from 2004 to 2005. Mr. Philipson is an editor of Forum for Health Economics & Policy and is on the editorial board of Health Economics and The European Journal of Health Economics. He has twice been the recipient of the highest honor of his field, the Kenneth Arrow Award from the International Health Economics Association, in 2000 and 2006.  Mr. Philipson is the cofounder of Precision Health Economics, is an adviser to the Gerson Lehrman Group, and is a consultant for Compass-Lexecon and Analysis Group.
  • Email: tomas.philipson@aei.org
  • Assistant Info

    Name: Gregory Lane
    Phone: 2028624879
    Email: greg.lane@aei.org
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