Published online Mar 28, 2017. doi: 10.4329/wjr.v9.i3.143
Peer-review started: October 9, 2016
First decision: November 29, 2016
Revised: December 30, 2016
Accepted: January 16, 2017
Article in press: January 18, 2017
Published online: March 28, 2017
Processing time: 170 Days and 7 Hours
To evaluate the feasibility of reducing the dose of iodinated contrast agent in computed tomography pulmonary angiography (CTPA).
One hundred and twenty-seven patients clinically suspected of having pulmonary embolism underwent spiral CTPA, out of whom fifty-seven received 75 mL and the remaining seventy a lower dose of 60 mL of contrast agent. Both doses were administered in a multiphasic injection. A minimum opacification threshold of 250 Hounsfield units (HU) in the main pulmonary artery is used for assessing the technical adequacy of the scans.
Mean opacification was found to be positively correlated to patient age (Pearson’s correlation 0.4255, P < 0.0001) and independent of gender (male:female, 425.6 vs 450.4, P = 0.34). When age is accounted for, the study and control groups did not differ significantly in their mean opacification in the main (436.8 vs 437.9, P = 0.48), left (416.6 vs 419.8, P = 0.45) or the right pulmonary arteries (417.3 vs 423.5, P = 0.40). The number of sub-optimally opacified scans (the mean opacification in the main pulmonary artery < 250 HU) did not differ significantly between the study and control groups (7 vs 10).
A lower dose of iodine contrast at 60 mL can be feasibly used in CTPA without resulting in a higher number of sub-optimally opacified scans.
Core tip: Computed tomography pulmonary angiography scanning using a lower dose of contrast agent (60 mL) is proposed. Comparisons were made to patients in a control group who have received a standard dose of contrast medium (75 mL) at our Trust. There is no statistical difference in the degree of opacification in the main pulmonary artery between the two groups. The rate of rejection due to inadequate opacification is not affected by the reduction in contrast dose. The feasibility of using a reduced contrast dose at 60 mL is clearly demonstrated.