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Too Much Information?
By Cheryl Herlihy
In its recent release, the U.S. Government Accountability Office made a significant finding, stating that too much medical data is being collected by Medicare. We all know it is being collected, and now we know more. The GAO found:
Medicare beneficiaries have received bills totaling nearly $11 billion for just one month of medical data.
Medicare beneficiaries received more than 26 million requests for medical information, many from private vendors, between September 2007 and December 2008.
Using a small amount of information, private health insurance companies were able to identify about 36,000 patients who were new to the health plan.
According to the GAO report, it is “difficult to assess the extent to which the current system provides enough information to satisfy beneficiaries’ needs.” It is further stated in the report that, “it would be challenging to use Medicare’s data holdings to assess whether the health care system’s collection of and access to medical data benefits beneficiaries.”
In order to address the GAO’s concern, the Centers for Medicare and Medicaid Services (CMS) has proposed several reforms. These include creating a standardized summary of the information to enable beneficiaries to make better-informed medical decisions. The changes also allow CMS to solicit information from Medicare providers to tailor the benefit to meet beneficiaries’ medical needs.
So what’s wrong with too much information? We don’t know! It is extremely difficult to determine what constitutes too much information. Since there are no baseline data, it is impossible to quantify the amount of information being collected.
We also don’t know the full extent of the data being collected. Currently, information on both Medicare beneficiaries and their doctors are in the
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