Vascular Surgery Department, University Hospital Clinico San Carlos, Madrid, Spain.
Medical Physics Service, Hospital Clínico San Carlos and IdISSC, Madrid, Spain; Radiology Department, Complutense University, Madrid, Spain.
Eur J Vasc Endovasc Surg. 2020 Dec;60(6):837-842. doi: 10.1016/j.ejvs.2020.08.006. Epub 2020 Sep 8.
The International Commission on Radiological Protection (ICRP) has highlighted the large number of medical specialties using fluoroscopy outside imaging departments without programmes of radiation protection (RP) for patients and staff. Vascular surgery is one of these specialties and endovascular aneurysm repair (EVAR) is one of the most challenging procedures requiring RP guidance and optimisation actions. The recent European Directive on Basic Safety Standards requires the use and regular update of diagnostic reference levels (DRL) for interventional procedures. The objective of the study was to know the doses of patients undergoing EVAR with mobile Xray systems and with hybrid rooms (fixed Xray systems), to obtain national DRLs and suggest optimisation actions.
The Spanish Chapter of Endovascular Surgery launched a national survey that involved hospitals for 10 autonomous communities representing the 77% of the Spanish population (46.7 million inhabitants). Patient dose values from mobile Xray systems were available from nine hospitals (sample of 165 EVAR procedures) and data from hybrid rooms, from seven hospitals, with dosimetric data from 123 procedures. The initial national DRLs have been obtained, as the third quartile of the median values from the different centres involved in the survey.
The proposed national DRLs are 278 Gy cm for hybrid rooms and 87 Gy cm for mobile Xray systems, and for cumulative air kerma (cumulative AK) at the patient entrance reference point, 1403 mGy for hybrid rooms, and 292 mGy for mobile systems.
An audit of patient doses for EVAR procedures to identify optimised imaging protocol strategies is needed. It is also appropriate to evaluate the diagnostic information required for EVAR procedures. The increase by a factor of 3.2 (for kerma area product) and 4.8 (for cumulative AK) in the DRLs needs to be justified when the procedures are performed in the hybrid rooms rather than with mobile Xray systems.
国际辐射防护委员会(ICRP)强调了许多在影像部门之外使用透视设备但没有为患者和工作人员提供放射防护(RP)计划的医学专业。血管外科学就是其中之一,而血管内动脉瘤修复术(EVAR)是最具挑战性的手术之一,需要 RP 指导和优化措施。最近的欧洲基本安全标准指令要求介入性手术使用和定期更新诊断参考水平(DRL)。该研究的目的是了解在移动 X 射线系统和混合手术室(固定 X 射线系统)中接受 EVAR 的患者的剂量,获得国家 DRL 并提出优化措施。
西班牙血管外科学分会发起了一项全国性调查,涉及代表西班牙 77%人口(4.67 亿居民)的 10 个自治区的医院。来自九个医院的移动 X 射线系统的患者剂量值(样本为 165 例 EVAR 手术)和来自七个医院的混合手术室的数据,其中 123 例手术有剂量数据。已经获得了初步的国家 DRL,即参与调查的不同中心中位数的第三四分位数。
提出的国家 DRL 为混合手术室 278 Gy·cm,移动 X 射线系统 87 Gy·cm,患者入口参考点的累积空气比释动能(cumulative AK)为混合手术室 1403 mGy,移动系统 292 mGy。
需要对 EVAR 手术的患者剂量进行审核,以确定优化的成像方案策略。还需要评估 EVAR 手术所需的诊断信息。在混合手术室而不是移动 X 射线系统中进行手术时,DRL 增加 3.2 倍(对于比释动能面积乘积)和 4.8 倍(对于累积 AK)需要有合理的依据。