Warshauer D M, Hiken J N, Molina P L, Hackney S L, Bellinger D A, Lee J K
Department of Radiology, University of North Carolina School of Medicine, Chapel Hill 27599-7510, USA.
Radiology. 1995 Nov;197(2):365-8. doi: 10.1148/radiology.197.2.7480678.
To investigate the effect of glucagon on the timing and degree of hepatic enhancement at computed tomography.
Each of 11 dogs underwent injection of contrast material at two uniphasic rates (0.5 mL/sec and 1.5 mL/sec) with without previous intravenous administration of 0.5 mg of glucagon. Scans were obtained at a single intrahepatic level every 3.5 seconds for 120-160 seconds. Attenuation values in the liver, aorta, portal vein, and inferior vena cava (IVC) were measured.
Glucagon administration was associated with greater hepatic enhancement throughout the study: Peak hepatic enhancement was greater at contrast injection rates of 0.5 mL/sec (P = .021) and 1.5 mL/sec (P = .0001). Peak hepatic enhancement also occurred earlier during the glucagon runs. Portal vein enhancement was greater during the glucagon runs at an injection rate of 1.5 mL/sec (P = .032). IVC enhancement was greater during the nonglucagon runs at 0.5 mL/sec (P = .013) and at 1.5 mL/sec (P = .005).
Intravenous administration of glucagon before contrast material injection produces greater and more rapid hepatic enhancement in a canine model.