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D.410

ACTIVITY ESTIMATION IN PATIENTS SUBMITTED TO RADIOIODINE

THERAPY FOR HYPERTHYROIDISM

A. Ostinelli

* , a ,

M. Duchini

a ,

V. Conti

a ,

P. Bonfanti

a ,

S. Ross

i b ,

M. Cacciatori

a .

a

A. O. Sant’Anna, Como, Italy;

b

Università Insubria, Como, Italy

Introduction:

The 131I administered activities for the hyperthyroidism treat-

ments are very high, with significant residual amounts in the following days.

This paper proposes a mathematical algorithm that correlates patient ac-

tivities and external measurements. The results are supported by clinical

and experimental validations.

Materials and Methods:

The mathematical model is based on the rela-

tionship between activity, H*(10) rate, gamma constant and source-

detector distance (d), without considering both the distribution of iodine

and uptake through the tissues. An effective distance (deff) was intro-

duced, adding a contribution dx to d, evaluating both the mean depth of

the 131I 3D distribution and the photon-tissues interaction. Two measure-

ments are required at known distances (d1 and d2). Applying the inverse

square law to H*(10) rates and assuming C

=

(dH*2/dt)0.5/(dH*1/dt)0.5 and

d1

+

dx

=

C(d2

+

dx); the residual activity is: F2dH*(10)/dt(d/gamma con-

stant) where F

=

(d

+

dx)/d.

Results:

This model was validated by clinical trials, comparing the admin-

istered activities with the calculated ones. Comparing these results with

the activities estimated by single measurements, the average deviation from

the expected values decreases from 11% to 0.5%. Additional measure-

ments were performed at the discharge time and four days after, with an

11.3% and 43.0% excreted mean activity. dx is about the radiopharmaceu-

tical depth within the patient, with 82

±

40, 56

±

46 and 34

±

36 mm average

values at 0.5, 4 and 72 hours respectively. This decrease may be due to the

gradual iodine capture by thyroid.

Conclusions:

This study proved the validity of the theoretical-experimental

approach, providing a good estimation of the residual activity and an ef-

fective radiation protection tool.

http://dx.doi.org/10.1016/j.ejmp.2016.01.417

D.411

“OPERRA” PROJECT ON PRIORITIES FOR RESEARCH IN THE FIELD OF

RADIATION PROTECTION: DEVELOPMENT OF A SURVEY

A. Palma *

, a ,

S. Bouffler

b ,

M. Coeck

c ,

S. Della Monaca

a ,

P. Fattibene

a ,

S. Grande

a ,

N. Impens

c ,

G. Meskens

c ,

I. Pecchia

a ,

T. Perko

c ,

A. Rosi

a ,

F. Rollinger

d ,

S. Salomaa

e ,

L. Sirkka

e ,

M.A. Tabocchini

a ,

C. Turcanu

c ,

M. Grigion

i a .

a

Dipartimento di Tecnologie e Salute, Istituto Superiore di Sanità,

Roma, Italy;

b

Centre for Radiation, Chemical and Environmental Hazards, Public

Health England, Didcot, UK;

c

SCK CEN Belgian Nuclear Research Centre, Mol,

Belgium;

d

Institut de Radioprotection e de Surete Nucleaire, Fontenay-aux-Roses,

France;

e

STUK – Radiation and Nuclear Safety Authority, Helsinki, Finland

Introduction:

The EC OPERRA project (Open Project for the European Ra-

diation Research Area) aims to create an innovative mechanism for the

implementation of an instrument of joint programming that can be applied

to all fields of research in radiation protection. In particular, the Task Group

(TG) 4.3 aims to identify national and international stakeholders and to

collect and analyse their opinions on research priorities in radiation pro-

tection. Within this TG, the ISS (TG 4.3.2 leader) has coordinated the creation

of a survey in electronic format.

Materials and Methods:

The survey has been developed by the tool ZEF

Evaluation Engine. Data analysis was performed by using ZEF, EXCEL and

SPSS software.

The questionnaire was organised with an initial section containing the syn-

ergistic priorities common to the European platforms MELODI, ALLIANCE,

NERIS and EURADOS. The next four sections contained questions ex-

tracted respectively from each platform Strategic Research Agenda. Finally,

other sections were devoted to issues related to ethical aspects of radia-

tion protection, risk communication and risk perception, and education and

training.

Stakeholders to which the survey should be sent were identified from contact

lists provided by the four platforms and by contacting the presidents of

international scientific associations, the representatives of international

organisations, etc. Each of them has been asked to spread the survey link

to their members and/or advertise on their websites.

Results and Conclusion:

In the present work, some key results related to

the synergistic priorities will be shown and discussed. The importance/

feasibility ranking was used for gathering opinion on these topics. Most

responses came from those with interests in low dose risk and dosimetry.

A complete analysis of the results is available on MELODI website

( http://www.melodi-online.eu )

. A selection of such synergistic topics was

recommended as the focus of the second OPERRA call for research proposals.

http://dx.doi.org/10.1016/j.ejmp.2016.01.418

D.412

QUALITY ASSURANCE AND MANAGEMENT PROGRAM OF INDIVIDUAL

AND ENVIRONMENTAL RADIATION PROTECTION EQUIPMENT IN A ISO

9001: 2008 QUALITY MANAGEMENT SYSTEM

M. Paolucci *, R. Di Lorenzo, A. Didona.

USL Umbria 2 – Servizio Di Fisica

Medica, Foligno, Italy

Purpose:

USL 2 Umbria was born in 2013 by merging 2 health care insti-

tutions; it’s organized into 6 districts and 8 regional hospitals, where the

Medical Physics Department started a Quality Assurance (QA) and man-

agement system of Personal Protective Equipment (PPE) and mobile radiation

shields, by placing them in the ISO 9001: 2008 Quality Management System.

Materials and Methods:

A multidisciplinary workgroup, including the De-

partment of Diagnostic Imaging and Therapeutics and all departments and

structures where radiation sources are used, was created. We started with

census and efficiency check of all the equipment, through a dedicated QA

program on all USL 2 Umbria radiological sites, in collaboration with tech-

nician staff.

Subsequently a protocol for periodic functional and quality tests and a man-

agement procedure were established and a list with minimum necessary

equipment for each radiological site was prescribed.

Results:

The Quality Management System was implemented over a period

of about two years, establishing a management and monitoring paper-

work, a program of audits and periodic QA tests on all the equipment, in

order to ensure their correct efficiency, in compliance with regulatory

requirements.

During the QA campaign 483 PPE were tested, 5% of which was replaced

with new equipment as resulted not suitable. We also disposed of 46 PPE

unused because clearly damaged, following an internal procedure accord-

ing to Italian legislation D. Lgs. 152/06. Furthermore a routine sanitization

procedure for each PPE was established for their correct maintenance and

conservation.

Conclusion:

The results led to an optimization of the equipment distri-

bution, highlighting the need of continuous checks in order to provide a

proper protection against ionizing radiation during clinical activities for pa-

tients and operators.

http://dx.doi.org/10.1016/j.ejmp.2016.01.419

D.413

ISO 17025 ACCREDITATION EXPERIENCE OF AN INDIVIDUAL MONITORING

SERVICE

F. Rossi *, L. Fedeli, L. Noferini, M. Fedi, A. Falivene.

Fisica Sanitaria AOU

Careggi, Firenze, Italy

Introduction:

The European directives, according to ICRP recommenda-

tions, state that for people occupationally exposed to ionizing radiation a

monitoring of absorbed dose is needed, the measuring instrument is called

dosimeter. A service, called IMS (Individual Monitoring Service), is thus

needed, providing not only the instruments but also calibrations, trace-

ability of the name of worker related to dosimeter ID, proper storage of

dose data, and so on. The Directive states that each member State shall

develop approval procedures to state whether an IMS is or not suitable for

its purpose. Italy is actually without any kind of approval procedure. Fur-

thermore, the EC document RP160 states guidelines for IMSs, requiring

compliance to ISO 17025 standard to fulfill adequate quality levels.

Materials and Methods:

Our IMS was updated to make it compliant with

ISO 17025 standard. This involved: instrument maintenance, human re-

source proper training, operative procedures, traceability, calibrations,

software, data recording and dose reporting. The updating was very time-

consuming, involving six persons two of them medical physicists.

e121

Abstracts/Physica Medica 32 (2016) e116–e123