拼凑:填补基因检测监管难题的最新建议。

Annals of health law Pub Date : 2012-01-01
Serra J Schlanger
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引用次数: 0

摘要

基因信息不同于其他医学信息,因此需要特殊保护的想法导致了一个监管难题,即基因检测目前在三个不同的计划下受到监管。虽然有2000多种疾病的基因检测,但这些检测中只有不到10%经过临床有效性或实用性审查。最近一些基因检测公司的行动促使联邦政府提议修改现行的监管计划。本文讨论了当前的框架和最近的发展,然后研究了实施这些拟议变更所面临的一些问题和挑战。作者评估了提案和竞争利益,以建议如何最好地规范基因检测,以满足行业,临床医生,研究人员,患者和消费者的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Putting together the pieces: recent proposals to fill in the genetic testing regulatory puzzle.

The idea that genetic information is different from other medical information and therefore needs special protection has led to a regulatory puzzle where genetic testing is currently regulated under three separate schemes. Although genetic tests for over 2,000 diseases are available, less than 10% of these tests have been reviewed for clinical validity or utility. Recent action by some genetic testing companies has prompted the federal government to propose changes to the current regulatory scheme. This article discusses the current framework and the recent developments before examining some of the concerns and challenges that face the implementation of these proposed changes. The author evaluates the proposals and competing interests in order to suggest how genetic testing may best be regulated to meet the needs of the industry, clinicians, researchers, patients, and consumers.

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