BH GSO IEC 61267:2016
IEC 61267:2005
Bahraini Standard
Current Edition
·
Approved on
08 February 2016
Medical diagnostic X-ray equipment - Radiation conditions for use in the determination of characteristics
BH GSO IEC 61267:2016 Files
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BH GSO IEC 61267:2016 Scope
This International Standard applies to test procedures which, for the determination of
characteristics of systems or components of medical diagnostic X-RAY EQUIPMENT, require
well-defined RADIATION CONDITIONS.
Except for mammography, this standard does not apply to conditions where discontinuities in
radiation absorption of elements are deliberately used to modify properties of the RADIATION
BEAM (for example by rare earth filters).
RADIATION CONDITIONS as used for screen-film sensitometry are not covered in this standard.
NOTE Screen-film sensitometry is the subject of the ISO 9236 series.
This standard deals with methods for generating RADIATION BEAMS with RADIATION CONDITIONS
which can be used under test conditions typically found in test laboratories or in
manufacturing facilities for the determination of characteristics of medical diagnostic X-RAY
EQUIPMENT.
Examples of such RADIATION QUALITIES are RADIATION BEAMS emerging through the filtration
from the X-RAY SOURCE ASSEMBLY. RADIATION CONDITIONS represent the more general case,
where SCATTERED RADIATION emerges from an EXIT SURFACE of a PATIENT or a PHANTOM. This
requires a well defined geometrical arrangement.
The most complete specification of RADIATION FIELDS is given by the spectral distribution of the
photon fluence. Since the measurement of X-RAY SPECTRA is a demanding task, this standard
expresses RADIATION QUALITIES in terms of the X-RAY TUBE VOLTAGE, the first and second HALFVALUE
LAYER. In the case of RADIATION CONDITIONS, specifications are performed additionally in
terms of PHANTOM properties and geometry.
The attempt to characterize a spectral distribution just by means of the X-RAY TUBE VOLTAGE,
the first and possibly the second HALF-VALUE LAYER is thus a compromise between the
mutually conflicting requirements of avoiding excessive efforts for establishing a RADIATION
QUALITY and of the complete absence of any ambiguity in the definition of a RADIATION
QUALITY. Due to differences in the design and the age of X-RAY TUBES in terms of anode angle,
anode roughening and INHERENT FILTRATION, two RADIATION QUALITIES produced at a given XRAY
TUBE VOLTAGE having the same first HALF-VALUE LAYER can still have quite different
spectral distributions. Given the inherent ambiguity in the characterization of RADIATION
QUALITY, it is essential that further tolerances introduced by allowing certain ranges of values,
e.g. for X-RAY TUBE VOLTAGE and first HALF-VALUE LAYER, must be sufficiently small not to
jeopardise the underlying objective of this standard. This standard is to ensure that
measurements of the properties of medical diagnostic equipment should produce consistent
results if RADIATION QUALITIES or RADIATION CONDITIONS in compliance with this standard are
used.
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