Evaluating the cost-effectiveness of medical interventions, particular
ly pharmaceuticals, has been the focus of much debate in this country
over the past few years. Although the support for efficient utilizatio
n of monies is widespread, the delicate balance between optimizing pat
ient outcome with the costs to do so in high-risk patients is especial
ly difficult. Although research in the field of cost-effectiveness is
widespread, at present there are few guidelines in this country. Furth
ermore, the introduction of bias is a serious concern in the interpret
ation and validation of studies, often limiting their utility. Guideli
nes that can be implemented to minimize bias in economic research have
been identified to include administrative, methodology-based, and eth
ical parameters. The standardization and implementation of such guidel
ines can reduce bias in economic research and optimize study validity.
This review focuses on these issues and suggests that initial steps t
o produce unbiased economic research include total disclosure, appropr
iate comparator selection, complete release of all relevant data, and
the cooperation of all involved parties.