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Published on: September 4, 2017
Mean glandular dose in digital mammography: a dose calculation method comparison
Moayyad E Suleiman1, Patrick C Brennan1, Mark F McEntee1
1The University of Sydney , Faculty of Health Sciences, M205, Cumberland Campus, 75 East Street, Lidcombe, New South Wales 2141, Australia.
Digital mammography organ dose estimates show significant bias compared to calculated doses, varying by manufacturer. This highlights potential over or underestimation risks when relying solely on organ dose for patient radiation exposure audits.
Area of Science:
- Medical Physics
- Radiology
- Radiation Dosimetry
Background:
- Accurate estimation of mean glandular dose (MGD) is crucial for mammography quality assurance and patient safety.
- Digital Imaging and Communication in Medicine (DICOM) headers contain valuable data for dose assessment.
- Existing methods for calculating MGD include those by Dance et al., Wu et al., and Boone et al.
Purpose of the Study:
- To analyze the agreement between organ dose estimates and calculated doses from clinical digital mammography data.
- To investigate potential biases in organ dose estimation across different digital mammography unit manufacturers.
Main Methods:
- Extracted DICOM header information from 52,405 anonymized mammograms.
- Filtered data for specific breast thicknesses (20-110 mm) and excluded cases with breast implants.
- Calculated MGD using Dance, Wu, and Boone methods; employed Bland-Altman analysis and regression to assess agreement.
Main Results:
- Statistically significant bias was observed between organ dose and calculated doses.
- Bias varied by manufacturer: Philips showed the lowest bias (overestimating Dance by 0.03 mGy), while GE exhibited the highest (overestimating Wu by 0.20 mGy).
- Hologic and Fujifilm organ doses underestimated calculated doses by 0.07 mGy and 0.09 mGy, respectively.
Conclusions:
- Organ dose estimates derived from mammography units disagree with calculated doses.
- Manufacturer-specific biases necessitate caution when using organ dose for rapid dose audits.
- Potential over- or underestimation errors must be considered in reported results based on organ dose alone.
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