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Utility of an A ustralasian registry for children undergoing radiation treatment
Author(s) -
Ahern Verity
Publication year - 2014
Publication title -
journal of medical imaging and radiation oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.31
H-Index - 43
eISSN - 1754-9485
pISSN - 1754-9477
DOI - 10.1111/1754-9485.12215
Subject(s) - medicine , cancer registry , disease registry , audit , radiation therapy , medical diagnosis , pediatrics , disease , cancer , family medicine , surgery , pathology , management , economics
The aim of this study was to evaluate the utility of an A ustralasian registry (‘the Registry’) for children undergoing radiation treatment ( RT ). Methods Children under the age of 16 years who received a course of radiation between J anuary 1997 and D ecember 2010 and were enrolled on the Registry form the subjects of this study. Results A total of 2232 courses of RT were delivered, predominantly with radical intent (87%). Registrations fluctuated over time, but around one‐half of children diagnosed with cancer undergo a course of RT . The most prevalent age range at time of RT was 10–15 years, and the most common diagnoses were central nervous system tumours (34%) and acute lymphoblastic leukaemia (20%). Conclusions The Registry provides a reflection of the patterns of care of children undergoing RT in A ustralia and a mechanism for determining the resources necessary to manage children by RT (human, facilities and emerging technologies, such as proton therapy). It lacks the detail to provide information on radiotherapy quality and disease outcomes which should be the subject of separate audit studies. The utility of the Registry has been hampered by its voluntary nature and varying needs for consent. Completion of registry forms is a logical requirement for inclusion in the definition of a subspecialist in paediatric radiation oncology.