E-ISSN: 1305-3612
Reproducibility and variability of very low dose hepatic perfusion CT in metastatic liver disease
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Abdominal Imaging - Original Article
VOLUME: 22 ISSUE: 6
P: 495-500
November 2016

Reproducibility and variability of very low dose hepatic perfusion CT in metastatic liver disease

Diagn Interv Radiol 2016;22(6):495-500
DOI: 10.5152/dir.2016.16612
Osman Melih Topcuoğlu 1
Muşturay Karçaaltıncaba 2
Deniz Akata 2
Mustafa Nasuh Özmen 2
1. Department of Radiology, Yeditepe University School of Medicine, İstanbul, Turkey
2. Department of Radiology, Hacettepe University School of Medicine, Ankara, Turkey
No information available.
No information available
Received Date: 24.12.2015
Accepted Date: 20.04.2016
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ABSTRACT

PURPOSE:

We aimed to determine the intra- and interobserver agreement on the software analysis of very low dose hepatic perfusion CT (pCT).

METHODS:

A total of 53 pCT examinations were obtained from 21 patients (16 men, 5 women; mean age, 60.4 years) with proven liver metastasis from various primary cancers. The pCT examinations were analyzed by two readers independently and perfusion parameters were noted for whole liver, whole metastasis, metastasis wall, and normal-looking liver (liver tissue without metastasis) in regions of interest (ROIs). Readers repeated the analysis after an interval of one month. Intra- and interobserver agreements were assessed with intraclass correlation coefficients (ICC) and Bland-Altman statistics.

RESULTS:

The mean ICCs of all ROIs between readers were 0.91, 0.93, 0.86, 0.45, 0.53, and 0.66 for blood flow (BF), blood volume (BV), permeability, arterial liver perfusion (ALP), portal venous perfusion (PVP) and hepatic perfusion index (HPI), respectively. The mean ICCs of all ROIs between readings were 0.86, 0.91, 0.81, 0.53, 0.56, and 0.71 for BF, BV, permeability, ALP, PVP, and HPI, respectively. There was greater agreement on the parameters measured for the whole metastasis than on the parameters measured for the metastasis wall. The effective dose of all perfusion CT studies was 2.9 mSv.

CONCLUSION:

There is greater intra- and interobserver agreement for BF and BV than for permeability, ALP, PVP, and HPI at very low dose hepatic pCT. Permeability, ALP, PVP, and HPI parameters cannot be used in clinical practice for hepatic pCT with an effective dose of 2.9 mSv.