Extremity exposure in nuclear medicine therapy with 90Y-labelled substances - Results of the ORAMED project


Autoria(s): Rimpler A.; Barth I.; Ferrari P.; Baechler S.; Carnicer A.; Donadille L.; Fulop M.; Ginjaume M.; Mariotti M.; Sans-Merce M.; Gualdrini G.; Krim S.; Ortega X.; Ruiz N.; Vanhavere F.
Data(s)

2011

Resumo

90Y-labelled radiopharmaceuticals offer promising prospects for radionuclide therapies of tumours, e.g. radioimmunotherapies (RIT), (EANM, 2007), peptide receptor radiotherapies (PRRT), (Otte et al., 1998), and selective internal radiotherapies (SIRT), (Salem and Thurston, 2006). 90Y, an almost pure high-energy beta radiation emitter (Eβ,max = 2.28 MeV), is a favourable radionuclide for therapeutic purposes. However, when preparing and performing these therapies, high activities of 90Y (>1 GBq) are to be manipulated and technicians, physicians and nurses may receive high skin exposures to the hands. If radiation protection standards are low, the exposure of staff can exceed the annual skin dose limit of 500 mSv. Within a particular work package (WP4) of the ORAMED project, comprehensive measurements in nuclear medicine departments of several hospitals in 6 European countries were carried out. The study focussed on 90Y-labelled substances such as Zevalin® and DOTATOC to achieve a representative database on staff exposure. This paper summarises the most important results and conclusions for individual monitoring of skin exposure of staff.

Identificador

http://serval.unil.ch/?id=serval:BIB_B15AD2CF1269

isbn:1350-4487

doi:10.1016/j.radmeas.2011.05.068

isiid:000297881400020

Idioma(s)

en

Fonte

ORAMED 2011, International Workshop on Optimization of Radiation Protection of Medical Staff

Tipo

info:eu-repo/semantics/conferenceObject

inproceedings