The University of Texas Medical Branch, Galveston, TX 77555-0735, USA.
J Vasc Surg. 2011 Jan;53(1 Suppl):44S-46S. doi: 10.1016/j.jvs.2010.06.177. Epub 2010 Sep 27.
The use of radiation for medical purposes falls under the purview of the Food and Drug Administration (FDA) and individual states. Enhanced regulations are in place to promote the right exam for the right reason at the right time for every patient exposed to medical x-rays.
The February 2010 FDA initiative to reduce unnecessary radiation exposure from fluoroscopy, CT, and nuclear medicine studies is reviewed along with regulations currently in place.
Facilities granting privileges to physicians performing fluoroscopic procedures need to ensure appropriate education so they can assess individual patient risk and benefit on a case-by-case basis. These are guidelines with individual states controlling requirements.
Regulation of education, training, and credentialing for physician operators of fluoroscopic equipment is currently controlled by individual states and is not uniform. There are strong indications that the FDA and or the Joint Commission will become increasingly involved to increase documentation of patient exposure and safety.
医疗辐射的使用属于食品和药物管理局(FDA)和各个州的监管范围。强化法规的目的是为每个接受医疗 X 射线检查的患者在适当的时间、出于适当的原因进行适当的检查。
审查了 FDA 于 2010 年 2 月发起的降低透视、CT 和核医学研究中不必要辐射暴露的倡议,以及现行法规。
授予医生进行透视程序特权的医疗机构需要确保适当的教育,以便他们能够根据具体情况评估每个患者的风险和收益。这些是有个别州控制要求的指南。
透视设备医师操作人员的教育、培训和认证的监管目前由各州控制,并不统一。有强烈迹象表明,FDA 和/或联合委员会将越来越多地参与,以增加对患者暴露和安全的记录。