Tuddenham W J
Radiology. 1979 Jun;131(3):579-88. doi: 10.1148/131.3.579.
The problem of federal regulation of radiologic practice is examined via an in-depth analysis of the Proposed Recommendations for Diagnostic Radiology Facility Quality Assurance Programs as published in the Federal Register by the Commissioner of Food and Drugs. It is shown that the need for such recommendations is not established, that the program proposed by the Commissioner is potentially burdensome for the radiologist, that it does not address the most significant causes of unnecessary patient irradiation, and that the benefits expected to derive from it are, in fact, negligible. This is not to denigrate the value of well-conceived quality assurance efforts, and measures are suggested that might more reasonably be expected to reduce the radiation exposure of the public. The radiologist is urged to 1) conduct his practice in as faultless a manner as possible; and 2) exercise his right to respond to proposals of the federal regulatory agencies.
通过对食品药品专员在《联邦公报》上发布的《诊断放射学设施质量保证计划建议》进行深入分析,探讨了联邦对放射学实践的监管问题。结果表明,此类建议的必要性并未确立,专员提议的计划可能给放射科医生带来负担,该计划未涉及不必要的患者辐射的最主要原因,且预期从中获得的益处实际上微不足道。这并非诋毁精心构思的质量保证工作的价值,并提出了一些有望更合理地减少公众辐射暴露的措施。敦促放射科医生:1)尽可能以完美无缺的方式开展业务;2)行使其对联邦监管机构提议做出回应的权利。