2.
Determine typical patient exposure levels
for standard radiographic exams and fluoroscopy,
3. Assess fluoroscopic contrast and spatial
resolution,
5.
4. Evaluate radiographic image quality, and
Review processor quality control procedures.
These quality assurance efforts are beyond the scope of
this report.
The performance levels cited from Reference 1 do not
apply to non-certified components.
In the absence of
specific state regulations
for these
certified component performance
levels
components,
should be
considered "ideal"
may not be
goals for this type of equipment, but
achievable
due to design limitations.
In addition to survey data, records should also be
maintained on:
(a) the manufacturer, model number, and serial
number of the transformer/generator and
control console,
(b) the manufacturer, model type and serial numbers
of the x-ray tube housing and insert,
(c) the model type and the serial number of the
collimator, and
(d) the manufacturer, model type and serial number
of the x-ray image intensifier.
Outlines of these records and survey data are at the end
of each "part"
of this report.
Unless specifically noted in the text or outline,
each parameter should be checked at least annually or
after machine repairs or
replacement) which could affect
used equipment
adjustments (e.g., x-ray tube
performance. Heavily
checks.
may require more frequent (semi-annual)
Measurements of parameters such as the half-value
layer (HVL), the source-to-image receptor distance (SID),
etc.
that are common to all four
radiological
are discussed in detail in Part I -- Medical
systems
Installations.
Recommended modifications
Radiographic
in the
measurement methods for
unique types of radiological
equipment are listed in the section where the unique type
of equipment is discussed.
2
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