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5.4 Radiation protection situation

in brachytherapy

Fourteen inspections were carried out in brachytherapy

in 2014 (about 22% of the centres).

5.4.1 Worker radiation protection

Themajority of the centres have put in place appropriate

measures for:

having a PCR designated by the employer (100% of

the centres);

defining the PCR’s duties (100% of the centres) and

resources (100% of the centres) ;

passive dosimetry monitoring of workers that could

be exposed (100% of the centres);

active dosimetry monitoring of personnel working in

controlled areas (95% of the centres).

The organisation put in place by the brachytherapy units

for worker radiation protection is judged satisfactory.

93% of the brachytherapy units inspected in 2014 have

a PCR dedicated to this activity. The inspectors noted

that the necessarymeans for fulfilling their assignments

were available in 100%of the centres inspected in 2014.

Training actions for paramedical personnel are held at

the required frequency on the whole. However, training

in worker radiation protection is rarely provided for

physicians andmedical physicists. The radiationprotection

of nurses present in the brachytherapy unit, when they

belong to a structure other than the radiotherapy centre

concerned, needs to be improved (training, dosimetric

monitoring, analysis of working practices and conditions).

The external technical verifications of radiation protection

are carried out in 86% of the centres inspected. Only

63%of the centres inspected perform internal technical

verifications and produce a technical schedule for the

verifications.

Progress is required in the performance of analyses of

working practices and conditions (carried out in 8% of

the centres inspected in 2014).

5.4.2 Radiation protection of patients

The treatment quality and safety

management system

Themajority of the centres have put in place appropriate

measures for:

appointing the manager of the treatment quality and

safety management system (93% of the centres);

producing the document management procedure;

internal communication.

The inspections performed since 2013 have shown that

two requirements concerning the implementation of the

care quality and safety management system have not

been satisfactorily met. They concern the formalising

of process mapping which is only carried out in 64% of

the inspected centres, and the conducting of the analysis

of risks run by the brachytherapy patient.

Although the brachytherapy units are assisted by

the external-beam radiotherapy departments in the

deployment of the quality approach, further progress

is required.

Training and information

Training in patient radiation protection hasmade progress

and is carried out in 89%of the centres inspected in 2014.

Themandatory inclusion of the necessary information in

the report formedical procedures using ionising radiation

was not considered satisfactory for the inspections carried

out in 2014. More specifically, in 62% of the centres

the reports did not contain any information on the

identification of the treatment device.

Maintenance and quality controls

In 2014, themajority of the centres had an inventory of the

medical devices and a register for recordingmaintenance

operations and quality controls. In 20%of the inspected

centres however, the organisation for carrying out and

tracking maintenance operations and quality controls

remains to be finalised. It was notedmore specifically that

the traceability of the internal verifications andmaintenance

operations is not always ensured satisfactorily.

In the absence of an ANSMdecision defining the quality

controls for brachytherapy devices, the nature of the

quality controls results from past practices and is based

on recommendations provided by devicemanufacturers

or professionals.

Maintenance of the HDR and PDR afterloaders is ensured

by themanufacturers. More specifically, themanufacturers

perform the afterloader operating verifications when the

sources are replaced. The brachytherapy units rely on

these verifications to guarantee correct operation of the

devices. The source activity is verified at each delivery

and source removal verifications are also carried out.

315

CHAPTER 09:

MEDICAL USES OF IONISING RADIATION

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