Sunday, August 20, 2006

Using information to measure benefits

by Aidan Hollis
One of the most common criticisms of drug prize plans like HR417 is that they would require a tremendous amount of information to be able to allocate prizes correctly. However, as an article in the NYTimes ("Smart Care via a Mouse, but What Will It Cost?") discusses today, exactly such information is becoming available.

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The technology backbone for more efficient health care markets is being called the “national health information network.” Such a network — with patient records stripped of their personal identifiers — is intended to someday allow doctors, nurses, researchers and ordinary people to track the outcome of various therapies, drugs and devices.

The idea is that they could tap into a public Web site to sift through health databases that are based on millions of records, updated regularly. Clever software would help them to understand what works and what doesn’t — and to seek answers about side effects, recovery times and vitamin regimens. A result, health experts say, is that fewer decisions about how to treat patients would be based on studies by drug companies and medical device makers, as they often are now.
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The information system described would be ideal for measuring the benefits of specific drugs.

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