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Medicare News

Fraud Grows as Private Managed Care Takes Over More Medicaid, Medicare Patients

Wall Street Journal looks at new types of fraud; CVS pays millions for over-billing Medicaid

March 19, 2008 – The Wall Street Journal today asserts that as the government shoves more Medicaid and Medicare beneficiaries to private sector managed care plans, new types of fraud are emerging. This report hits on the same day as the report that the giant pharmacy chain CVS agreed to pay nearly $37 million to settle claims that it fraudulently billed Medicaid. The WSJ also examined the growing practice of hospitals to reuse medical devices that have designated for one time use.

 

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Increase in Medicare, Medicaid Managed Care Plans Has Led to 'More Complex' Health Care Fraud, Wall Street Journal Reports

The Wall Street Journal on Wednesday examined how as the private sector is increasingly providing more Medicare and Medicaid services, new types of fraud are "cropping up that are harder to spot, more complicated to prosecute and potentially more harmful to patients," prompting the federal government to increase scrutiny of managed care.

 

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States and the federal government began shifting Medicaid and Medicare beneficiaries to managed care plans in the 1990s to control program costs, and many believed the shift also would reduce fraud because "companies would have strong incentives to prevent overbilling by doctors, hospitals and other medical providers -- and to avoid cheating the government themselves," the Journal reports.

However, some states reduced the number of health care fraud investigators, and a recent federal review of health programs for low-income children found that states mostly rely on HMOs to regulate themselves.

The Journal reports that traditional fraud prevention for government programs consisted of "policing doctors, hospitals, dialysis centers and the like to catch overcharges or billing for treatment never provided."

CVS to pay $37 million to settle Medicaid suit - Pharmacy chain accused of switching to more expensive drug

March 19, 2008 – “CVS Caremark Corp., one of the nation's largest pharmacy chains, has agreed to pay nearly $37 million to the federal government, 23 states and the District of Columbia to settle claims that it fraudulently billed Medicaid for a more expensive form of a drug used to treat ulcers and heartburn,” reports Monifa Thomas in the Chicago Sun Times.

“The settlement announced Tuesday resolves a whistleblower lawsuit filed five years ago by Northbrook pharmacist Bernard Lisitza, who also brought similar claims against Omnicare Inc. in an unrelated lawsuit that was settled for $49.5 million in 2006. “ Read the rest of the story…

However, according to the Journal, "[m]anaged care fraudsters profit by ... shortchanging patients or physicians to cut costs while collecting preset fees from the government," as well as by "refus[ing] to enroll unhealthy people, skimp[ing] on paying doctors or deny[ing] patients care." Regulators say "they are realizing they must become more attuned to more-complex scams carried out by sophisticated corporations," the Journal reports.

The Journal also profiled several fraud cases in Pennsylvania, California, New York, Texas and Virginia that "have provided a wakeup call for regulators" and "illustrate the potential for fraud and authorities' growing understanding of its scope" (Francis, Wall Street Journal, 3/19).

Click here to WSJ Link, which is subscription.

Wall Street Journal Examines Cost-Reducing Practice of Reusing Some Products

The Wall Street Journal on Wednesday examined efforts by some U.S. hospitals to reduce health care costs by recycling certain medical devices that have been labeled for single use. According to the Journal, the practice is legal as long as hospitals follow FDA regulations for reprocessing devices, such as scissors, clinical scrubs and sharp blades used by surgeons to cut through bones.

However, the Journal reports that the process, "which involves shipping devices to reprocessing facilities to be cleansed, sterilized and tested for reuse, has raised concerns about safety." Manufacturers of the devices say their products are not designed to withstand the strong chemicals and sterilization methods used at reprocessing plants. In addition, devices with porous surfaces or small gaps could still contain traces of blood, tissue or other bodily fluids that could transmit viral and bacterial infections, manufacturers say.

Hospitals, reprocessing firms and environmental groups say that reprocessed devices are just as safe as new devices because of modern sterilization methods. Supporters of the practice also say that recycled devices cost 40% to 60% less and reduce medical waste at landfills by thousands of tons.

Kenneth Kizer -- a consultant and former undersecretary for health at the U.S. Department of Veterans Affairs, who testified last year at a congressional hearing on the issue -- said the agency could save as much as $30 million in 2008 by using reprocessed devices.

Kizer said, "Single-use labeling is a real scam for a lot of devices, and by not using reprocessed devices where possible, it is wasteful and not environmentally responsive, since these items have to be disposed of as biomedical waste."

He added, "The reuse of medical devices that are labeled for single use only is a well-established and safe practice regulated by the FDA and utilized by most of the top-ranked hospitals in the country."

In addition, a Government Accountability Office report released in January that analyzed eight years of FDA data concluded that there is no evidence reprocessed single-use medical devices increase health risks for patients.

As many as 100 single-use devices, or 2% of all single-use devices, currently are reprocessed for further use.

The Journal reports that while the GAO study "tilts the debate strongly in favor of reprocessing and opens the door to more widespread use," device manufacturers "are sticking to their guns" and are lobbying several states to pass legislation that would require hospitals and other care providers to obtain "informed consent" from patients before reprocessed devices are used in medical procedures (Landro, Wall Street Journal, 3/19).

 

"Reprinted with permission from kaisernetwork.org You can view the entire Kaiser Daily Health Policy Report, search the archives, and sign up for email delivery at www.kaisernetwork.org/dailyreports/healthpolicy. The Kaiser Daily Health Policy Report is published for kaisernetwork.org, a free service of The Henry J. Kaiser Family Foundation. © 2006 Advisory Board Company and Kaiser Family Foundation. All rights reserved.”

 

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