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• Update recommendations for improving radiation protection of<br />

patients.<br />

• Provide feedback for the needed development of the IAEA<br />

reporting and learning system SAFRAD.<br />

The duration of this phase is one calendar year.<br />

Who can participate?<br />

Participation in the project is voluntary, and withdrawal is<br />

permitted at any stage of the project.<br />

Medical facilities performing FGI procedures from all IAEA<br />

Member States can participate. There is no limitation on the<br />

number of facilities that can participate.<br />

Different departments/ functional units of the same hospital may<br />

register independently or may provide a coordinated response. The<br />

same applies to facilities from a region or a country – coordinated<br />

data submission from the existing local, national or regional<br />

registries is also welcome.<br />

A participating medical facility should perform<br />

complex FGI procedures of at least one of the<br />

following groups/ types of procedures on a<br />

regular basis:<br />

• Cardiac interventions, such as: percutaneous<br />

coronary intervention (PCI); and especially<br />

chronic total occlusion (CTO); transcatheter<br />

valve implantations; cardiac ablation;<br />

percutaneous repair of septal defects.<br />

• Neurovascular interventions, such as:<br />

intracranial or spinal embolization;<br />

intracranial and extracranial angioplasty,<br />

stenting and stent-assisted coiling;<br />

endovascular treatment of stroke;<br />

vertebroplasty/ kyphoplasty and vertebral<br />

augmentation with an implant; radiofrequency<br />

spine tumor ablation.<br />

• Abdominal and thoracic interventions, such<br />

as: endovascular aneurysm repair (EVAR);<br />

transjugular intrahepatic portosystemic shunt<br />

(TIPS); transcatheteral embolisation in the<br />

abdomen and pelvis; hepatic chemo/radioembolization<br />

(TACE and SIRT); treatment<br />

of arterial stenoses or occlusive disease<br />

in the abdomen or pelvis; percutaneous<br />

transhepatic biliary drainage (PTCD) and<br />

stenting; bronchial artery embolization;<br />

endovascular central venous reconstruction.<br />

A participating medical facility should nominate<br />

a Facility coordinator who will coordinate data<br />

collection within the facility and be responsible<br />

for submission of deidentified data to the<br />

IAEA. Facility coordinators will receive detailed<br />

instructions and online support from the IAEA<br />

coordinator. They will also be invited to attend<br />

trainings and meetings organized by the IAEA. As the trainings<br />

and data submission will be in English, coordinators should have<br />

sufficient proficiency in this specific language.<br />

The medical facility is responsible for adhering to the local rules<br />

and obtaining needed ethical approval for participation in this<br />

study.<br />

ISRRT members are encouraged to participate in this important<br />

study. For more information please use the links listed above.<br />

Representatives attending the IAEA Technical Meeting on<br />

Radiation Protection in Fluoroscopically Guided Interventional<br />

(FGI) Procedures.<br />

ISRRT NEWSLETTER | APRIL <strong>2022</strong><br />

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