PURPOSE: To investigate the use of gadolinium as a computed tomographic (CT
) contrast agent.
MATERIALS AND METHODS: In vitro attenuation measurements of multiple diluti
ons of gadodiamide and ioversol were compared. In three pigs, 50-mL boluses
of undiluted gadodiamide were injected intravenously at 2 mL/sec, and repe
ated single-level scans were obtained through the lung bases, liver, and ki
dneys. The doses of 0.8-1.0 mmol of gadolinium per kilogram of body weight
were approximately three times the highest doses currently used in patients
. Enhancement was determined from attenuation measurements in the aorta, pu
lmonary arteries, liver, and kidneys.
RESULTS: In vitro, the attenuation of undiluted gadodiamide (3,069 HU) was
equivalent to that of ioversol diluted to 106 mg of iodine per milliliter a
nd at equimolar concentrations was 50% greater than that of ioversol. The m
agnitude of and time to peak enhancement were 141 HU and 27 seconds (n = 3)
for the aorta; 168 HU and 21 seconds (n = 3) for the pulmonary arteries; 2
3 HU and 65 seconds (n = 2) for the liver; and 63 HU and 32 seconds (n = 1)
for the kidneys. Time-attenuation curves revealed a useful duration of enh
ancement of 20-30 seconds for the aorta and pulmonary arteries.
CONCLUSION: Gadolinium produces good vascular enhancement, adequate renal e
nhancement, and suboptimal hepatic enhancement. Further study is needed to
determine the safety of the gadolinium dose required to produce similar enh
ancement in patients.