Clinical Study
A Phantom Study and a Retrospective Clinical Analysis to Investigate the Impact of a New Image Processing Technology on Radiation Dose and Image Quality during Hepatic Embolization

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Abstract

Purpose

To investigate changes in radiation dose and image quality using phantoms and hepatic embolization procedures performed with a new image processing technology (ClarityIQ) for a single-plane flat-detector–based interventional fluoroscopy system.

Materials and Methods

Phantom study was performed using acrylic sheets simulating different patient sizes. Air kerma rates (AKRs) were compared for different fluoroscopy modes and magnification modes without and with ClarityIQ. Repeat hepatic embolization procedures performed on the same lobe of the liver in the same patient by the same interventional radiologist between January 2013 and July 2014 without and with ClarityIQ were evaluated retrospectively. This included treatment of 33 hepatic lobes in 26 patients. Cumulative air kerma (CAK), kerma–area product (KAP), and factors affecting radiation dose were extracted from study metadata and compared. Blinded randomized image quality review was performed on arteriograms using a five-point scale.

Results

The phantom study revealed a significantly lower AKR (P < .005) with ClarityIQ. Repeated-measures analysis revealed a significant effect of ClarityIQ (P ≤ .001) on CAK and KAP, with reductions ranging between 9% and 85% (median, 67%) and between 5% and 89% (median, 75%), respectively, on a case-by-case basis. Mean reductions in CAK and KAP were 279 mGy and 134,030 mGy·cm2, respectively. Image quality review scores were significantly lower (P ≤ .001) with ClarityIQ, effecting visualization of tumor vasculature and appearance of noise texture.

Conclusions

ClarityIQ resulted in radiation dose reduction in the phantom study and in the hepatic embolization procedures, but with a decrease in subjective perceptions of image quality.

Section snippets

Materials and Methods

All data were acquired from two single-plane flat-detector interventional fluoroscopy systems (Allura Xper FD20; Philips), labeled in the present paper as system 1 and system 2. System 2 was upgraded with ClarityIQ image processing technology in December 2013. System 1, installed in December 2009, and system 2, installed in April 2011, operated on similar software versions before the ClarityIQ upgrade of system 2 (version 8.1.3) during the course of the study period. Both systems had identical

Phantom Study

The maximum percentage error values between the system-reported AKR and measured AKR at the interventional reference point were 25.7% (ratio, 1.3; mean AKR error, 1.2 mGy/min; range, 0.0–6.7 mGy/min) for system 1 and 14.0% (ratio, 1.2; mean AKR error, 1.3 mGy/min; range, 0.0–5.1 mGy/min) and 19.0% (ratio, 1.2; mean AKR error, 0.4 mGy/min; range, 0.0–1.7 mGy/min) for system 2 before and after the upgrade with ClarityIQ technology, respectively. The discrepancy between measured and indicated CAK

Discussion

The present study demonstrates that ClarityIQ technology resulted in a reduction in radiation dose indicators based on controlled phantom experiments and a retrospective analysis of clinical procedures. Any reduction in radiation dose for such procedures will reduce the likelihood of tissue reactions and will decrease the occupational exposure to the staff (23), in addition to the reduction in occupational exposure achieved by following the standard as-low-as-reasonably-achievable principles.

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    None of the authors have identified a conflict of interest.

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