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of the radiation beam and the use of the adjacent rooms,

including those vertically above and below the treatment

room. This study shouldbe included in the file presented to

support the application for a license to use a radiotherapy

installation, examined by ASN.

In addition, safety systems must indicatemachine status

(operating or not) and must switch off the beam in an

emergency or if the door to the irradiation room is opened.

3.2.2 Technical rules applicable to brachytherapy

installations

The rules for radioactive source management in

brachytherapy are comparable to those defined for all

sealed sources, regardless of their use.

Low Dose-Rate brachytherapy

In cases where permanent implant techniques are used

(seeds of iodine-125 in particular for treating prostate

cancer), the applications are carried out in the operating

theatre with ultrasonography monitoring, and do

not require hospitalisation in a room with radiation

protection.

Pulsed Dose-Rate brachytherapy

This technique uses source afterloaders (generally 18.5GBq

of iridium-192). The treatment takes place in hospital

rooms with radiological protection appropriate for the

maximum activity of the radioactive source used.

High Dose-Rate brachytherapy

As the maximum activity used is high (370 GBq of

iridium-192 or 91GBq of cobalt-60), irradiation can only

be carried out in a roomwith a configuration comparable

to that of an external beam radiotherapy room.

4. BLOOD PRODUCT IRRADIATORS

4.1 Description

The irradiation of blood products is used to prevent post-

transfusion reactions in blood-transfusion patients. The

blood bag is irradiated with an average dose of about

20 to 25 grays. Irradiation is ensured by a self-shielded

device (radiological protection by lead), therefore it can

be installed in a roomwhich does not require additional

radiation protection. Depending on the models, the

irradiators are equipped either with radioactive sources

(1, 2 or 3 sources of caesium-137) with a unit activity of

about 60 terabecquerels (TBq) or with electrical X-ray

generators.

The policy initiated in 2009 to gradually replace the

source-equipped irradiators by X-ray generators has

reversed the composition of the equipment pool which

now comprises more X-ray generators than irradiators

with sources. As at 1st November 2015, the irradiator

pool comprised 30 machines, 5 of which are equipped

with radioactive sources (including one irradiator

undergoing decommissioning), that is to say 16% of

the irradiator pool.

4.2 Technical rules applicable

to facilities

Ablood product irradiatormust be installed in a dedicated

room designed to provide physical protection (fire,

flooding, break-in, etc.). Access to the device, which

must have a lockable control console, must be limited

to authorised persons only.

The layout of irradiators equipped with X-ray generators

must comply with the provisions of ASN’s new technical

resolution 2013-DC-0349 of 4th June 2013 (see

chapter 3). This resolution requires that the layout

and access to the facilities comply with the radiation

protection rules set by French Standard NFC 15-160

in its March 2011 version.

5. THE STATE OF RADIATION

PROTECTION IN THE MEDICAL

SECTOR

Radiation protection in the medical sector concerns

patients receiving treatment or undergoing diagnostic

examinations, health professionals (physicians, medical

physicists,medical radiation technologists, nurses, nursing

auxiliaries, etc.) using or participating in the use of ionising

radiation, and also the population, such as members of

the public who can be present within a health facility,

or population groups that could be exposed to waste or

effluents from nuclear medicine units.

Since 2008, ASNhas periodically produced documents

presenting a national synthesis of themain lessons learned

from inspections, based on indicators that determine

compliance with the regulatory radiation protection

requirements. These syntheses enable the state of radiation

protection in the different areas (radiotherapy, nuclear

medicine, interventional radiology, etc.) to be assessed for

publication in the annual report. The syntheses are based

on the findings established during the year preceding

their publication. ASN also publishes annual or several-

year national appraisals of inspection results; they are

available at

www.asn.fr

.

306

CHAPTER 09:

MEDICAL USES OF IONISING RADIATION

ASN report on the state of nuclear safety and radiation protection in France in 2015