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Comparison of 12 surrogates to characterize CT radiation risk across a clinical population
Comparison of 12 surrogates to characterize CT radiation risk across a clinical population
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Comparison of 12 surrogates to characterize CT radiation risk across a clinical population
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Comparison of 12 surrogates to characterize CT radiation risk across a clinical population
Comparison of 12 surrogates to characterize CT radiation risk across a clinical population

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Comparison of 12 surrogates to characterize CT radiation risk across a clinical population
Comparison of 12 surrogates to characterize CT radiation risk across a clinical population
Journal Article

Comparison of 12 surrogates to characterize CT radiation risk across a clinical population

2021
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Overview
Objectives Quantifying radiation burden is essential for justification, optimization, and personalization of CT procedures and can be characterized by a variety of risk surrogates inducing different radiological risk reflections. This study compared how twelve such metrics can characterize risk across patient populations. Methods This study included 1394 CT examinations (abdominopelvic and chest). Organ doses were calculated using Monte Carlo methods. The following risk surrogates were considered: volume computed tomography dose index (CTDI vol ), dose-length product (DLP), size-specific dose estimate (SSDE), DLP-based effective dose (ED k ), dose to a defining organ (OD D ), effective dose and risk index based on organ doses (ED OD , RI), and risk index for a 20-year-old patient (RI rp ). The last three metrics were also calculated for a reference ICRP-110 model (OD D,0 , ED 0 , and RI 0 ). Lastly, motivated by the ICRP, an adjusted-effective dose was calculated as E D r = RI R I rp × E D OD . A linear regression was applied to assess each metric’s dependency on RI. The results were characterized in terms of risk sensitivity index (RSI) and risk differentiability index (RDI). Results The analysis reported significant differences between the metrics with ED r showing the best concordance with RI in terms of RSI and RDI. Across all metrics and protocols, RSI ranged between 0.37 (SSDE) and 1.29 (RI 0 ); RDI ranged between 0.39 (ED k ) and 0.01 (ED r ) cancers × 10 3 patients × 100 mGy. Conclusion Different risk surrogates lead to different population risk characterizations. ED r exhibited a close characterization of population risk, also showing the best differentiability. Care should be exercised in drawing risk predictions from unrepresentative risk metrics applied to a population. Key Points • Radiation risk characterization in CT populations is strongly affected by the surrogate used to describe it. • Different risk surrogates can lead to different characterization of population risk. • Healthcare professionals should exercise care in ascribing an implicit risk to factors that do not closely reflect risk.