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Παρασκευή 1 Ιουνίου 2018

Task-based quantification of image quality using a model observer in abdominal CT: a multicentre study

Abstract

Objective

We investigated the variability in diagnostic information inherent in computed tomography (CT) images acquired at 68 different CT units, with the selected acquisition protocols aiming to answer the same clinical question.

Methods

An anthropomorphic abdominal phantom with two optional rings was scanned on 68 CT systems from 62 centres using the local clinical acquisition parameters of the portal venous phase for the detection of focal liver lesions. Low-contrast detectability (LCD) was assessed objectively with channelised Hotelling observer (CHO) using the receiver operating characteristic (ROC) paradigm. For each lesion size, the area under the ROC curve (AUC) was calculated and considered as a figure of merit. The volume computed tomography dose index (CTDIvol) was used to indicate radiation dose exposure.

Results

The median CTDIvol used was 5.8 mGy, 10.5 mGy and 16.3 mGy for the small, medium and large phantoms, respectively. The median AUC obtained from clinical CT protocols was 0.96, 0.90 and 0.83 for the small, medium and large phantoms, respectively.

Conclusions

Our study used a model observer to highlight the difference in image quality levels when dealing with the same clinical question. This difference was important and increased with growing phantom size, which generated large variations in patient exposure. In the end, a standardisation initiative may be launched to ensure comparable diagnostic information for well-defined clinical questions. The image quality requirements, related to the clinical question to be answered, should be the starting point of patient dose optimisation.

Key Points

Model observers enable to assess image quality objectively based on clinical tasks.

Objective image quality assessment should always include several patient sizes.

Clinical diagnostic image quality should be the starting point for patient dose optimisation.

Dose optimisation by applying DRLs only is insufficient for ensuring clinical requirements.



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