Jacobson P D, Rosenquist C J
RAND Corp., Santa Monica, Calif. 90406-2138.
JAMA. 1988 Sep 16;260(11):1586-92.
This case study of the public policy implications of introducing a new technology in radiology, namely, low-osmolar contrast media (LOCM), raises the issues of whether and how to place appropriate limits on new technologies. Although these contrast media represent small episodic costs, they may add up to an aggregate expenditure of nearly $1 billion per year if used for all contrast injections. As a result, this technology raises a number of important medical, economic, legal, and public policy questions. Our cost-effectiveness analysis and an analysis of the medical evidence suggest that LOCM should be limited to high-risk patients. We discuss in this article how the legal system might respond to such limitations, and we consider various public policy options for adopting restrictions on use. We conclude that the medical profession should take the lead in developing protocols for appropriate assessment, reimbursement, and use of LOCM.
本案例研究探讨了放射学领域引入一项新技术——低渗造影剂(LOCM)所带来的公共政策影响,提出了是否以及如何对新技术进行适当限制的问题。尽管这些造影剂单次使用成本较低,但如果用于所有造影剂注射,每年的总支出可能接近10亿美元。因此,这项技术引发了一些重要的医学、经济、法律和公共政策问题。我们的成本效益分析以及对医学证据的分析表明,低渗造影剂应仅限于高危患者使用。我们在本文中讨论了法律体系可能如何应对此类限制,并考虑了采取使用限制措施的各种公共政策选择。我们得出结论,医学专业应率先制定有关低渗造影剂适当评估、报销和使用的方案。