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Category: AllSummer ShortsAugust 8, 2008
Health policy news isn't exactly beach reading, so we've decided to offer a series of short items just to keep you current…
Grace-Marie Turner Recent News Articles and Studies Politicians Note: Drug Reimportation is Waning PRESCRIPTION DRUGS Politicians Note: Drug Reimportation is Waning Prescription drug importation introduces major public health risks with minimal, if any, cost savings, writes White. When Americans turn to Canada or Europe for drugs, it's not always clear whether the medicine they receive is safe and genuine. By contrast, thanks to America's robust regulation regime and guarded supply chains, 99% of the drugs sold in the U.S. are safe and real, according to the World Health Organization. What's more, prescription drugs are cheaper and more easily available than ever before. Prescription drug importation has actually declined over the last few years and importation programs established by various states and cities in the U.S. have been shut down for lack of demand. Illinois, for example, saw just 3,689 residents use its importation program -- or 0.02% of the state population. As hundreds of thousands of visitors descend on Beijing for the Olympic Games, they might consider steering clear of military-owned hospitals where they could run the risk of being treated with substandard or counterfeit medicines, writes AEI's Roger Bate. The Chinese military operates outside of the law, running counterfeiting networks even though such profit-making military enterprises are technically illegal. Biosimilars: Policy, clinical, and regulatory considerations An abbreviated regulatory pathway for the approval of biosimilars and a process for safely demonstrating the therapeutic interchangeability of these proteins has the potential to provide meaningful cost savings, writes Gottlieb. (Biosimilars are biopharmaceuticals that are considered similar in composition to an innovator product but not necessarily clinically interchangeable.) The economic advantage to patients of greater access to biopharmaceuticals can translate into important public health benefits. But the legal and regulatory status of biosimilars remains to be resolved in the U.S. as policymakers address the scientific and policy issues surrounding product manufacturing, patent terms, and clinical use. STATE ISSUES Biotech at Risk for Broadside Hit A recent bill passed by the Massachusetts legislature may inadvertently harm patients as well as one of the state's most-bustling industries, writes Pipes. Among other provisions, the bill would require public disclosure when payments of $50 or more are made between pharmaceutical research firms and health care providers. The new law poses a serious threat to the state's role in clinical trials and academic research. Fears of biotechnology firms choosing to do business elsewhere are also real and their absence would create a gaping hole in the state's economy, writes Pipes. Whereas Massachusetts lost 100,000 private-sector jobs between 2000 and 2005, the biotechnology industry created 6,100 jobs. If Gov. Deval Patrick doesn't veto the bill by Aug. 13, the law will put a needless chill on clinical research and pharmaceutical innovation in the Commonwealth. State Health Care Reform: A Brief Guide to Risk Adjustment in Consumer-Driven Health Insurance Markets Risk adjustment can improve the functioning of consumer-centered health insurance markets, writes Haislmaier. Well-designed risk adjustment mechanisms would give health plans the right incentives to provide better value to both healthier and sicker enrollees. While policymakers can design and implement risk-adjustment mechanisms that work either prospectively or retrospectively, retrospective approaches, such as risk-transfer pools for health insurers, are somewhat easier to design, can be implemented in a shorter time, and are less likely to develop significant operational problems over time. HEALTH CARE REFORM The Patient Centric Health Leadership Forum: Towards a Critical Path for Patient-Centered Medicine Policy changes are needed to support the inevitable move toward patient-centric medicine, and speakers described both the threats posed by inaction and the need for policy change at a conference sponsored by CMPI. The report builds on discussions with health policy experts, including the Galen Institute's Grace-Marie Turner, and describes personalized medicine initiatives already in place in three American cities. But personalized health care faces stiff resistance from the prevailing political winds that push for a bigger government role in how healthcare is paid for and delivered. "A single-payer government-run system won't achieve the kind of personalized medicine we're talking about," said Mark McClellan, former head of the Centers for Medicare and Medicaid Services and a contributor to the report. "Who" not "How": The Real First Step in Health Care Reform The days of a trusted primary care doctor are numbered, writes Dr. Kelleher. The first step in returning sanity to American health care must be to decrease the need for volume-based primary care by increasing reimbursement for personalized quality care, thereby fostering the creation of a true "medical home." By increasing reimbursements, doctors gain the ability to spend more time with their patients to assess problems and concerns, discuss how lifestyle choices affect patients' risk of disease, and to reinforce the value of routine screening and prevention measures. Fundamental changes in payment systems, tax structure, and tort reforms will also be needed to support patient-centered care. If changes are not swiftly and effectively implemented over the next decade, patients' best advocate for comprehensive care will become extinct. MEDICARE Medicare: Covert Testing Exposes Weaknesses in the Durable Medical Equipment Supplier Screening Process The Centers for Medicare and Medicaid Service's oversight of suppliers of durable medical equipment is inadequate to prevent fraud and abuse, according to this GAO report. Specifically, weaknesses in the enrollment and inspection process have allowed sham companies to fraudulently bill Medicare for unnecessary or nonexistent supplies. GAO investigators easily set up two fictitious companies using undercover names and bank accounts and were approved for Medicare billing privileges despite having no clients and no inventory. Once criminals have similarly created fictitious companies, they typically steal or illegally buy Medicare beneficiary numbers and physician identification numbers and use them to repeatedly submit clams. (Nonetheless, Congress voted before leaving for recess to block administration efforts to curtail the fraud and abuse.) Upcoming Events Oklahoma Health Care Reform Task Force Meeting Differing Approaches to a National Crisis: Presidential Candidates' Health Care Plans Debated Health Policy Matters is a weekly newsletter containing summaries of timely and informative studies and articles on free-market health reform. It features a commentary by Grace-Marie Turner on the major developments and issues of the week as well as summaries of writings by participants in the Health Policy Consensus Group and other articles of interest from the health policy world, plus announcements of coming events. Health Policy Matters is published by the Galen Institute, a not-for-profit public policy organization specializing in information and education on health policy. For more information about the newsletter and our organization, please visit our website at www.galen.org. If you wish to subscribe to this free weekly newsletter, update your address, or be removed from our list, please send an e-mail message to galen@galen.org. The views expressed in this newsletter are the opinions of the authors and do not necessarily reflect the views of the Galen Institute or its directors. |
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