HEPATIC ENHANCEMENT DURING HELICAL CT - A COMPARISON OF MODERATE RATEUNIPHASIC AND BIPHASIC CONTRAST INJECTION PROTOCOLS

Citation
Ba. Birnbaum et al., HEPATIC ENHANCEMENT DURING HELICAL CT - A COMPARISON OF MODERATE RATEUNIPHASIC AND BIPHASIC CONTRAST INJECTION PROTOCOLS, American journal of roentgenology, 165(4), 1995, pp. 853-858
Citations number
17
Categorie Soggetti
Radiology,Nuclear Medicine & Medical Imaging
ISSN journal
0361803X
Volume
165
Issue
4
Year of publication
1995
Pages
853 - 858
Database
ISI
SICI code
0361-803X(1995)165:4<853:HEDHC->2.0.ZU;2-1
Abstract
OBJECTIVE. The purpose of this study was to compare the degree and tim ing of peak hepatic enhancement, optimal scanning intervals, and optim al delay times of moderate-rate uniphasic and biphasic contrast materi al injection protocols for hepatic helical CT. MATERIALS AND METHODS. One hundred fifty patients were randomized into three injection protoc ols, receiving 42.3 g iodine (150 ml iothalamate meglumine) delivered using 3 ml/sec uniphasic, 2 ml/sec uniphasic, or biphasic (3 ml/sec [5 0 ml], 1 ml/sec [100 ml]) technique. Statistically fitted aortic and h epatic enhancement curves were generated from dynamic incremental CT d ata for each patient. Protocols were compared by maximum hepatic enhan cement, and contrast enhancement indices were modeled for a 38-sec hel ical acquisition. RESULTS. The 3 ml/sec and 2 ml/sec uniphasic protoco ls produced higher peak hepatic enhancement (64 +/- 15 H and 62 +/- 15 H [mean +/- 1 SD]) than the 3 ml/sec biphasic protocol (52 +/- 10 H; p < .001). Contrast enhancement indices for the 3 ml/sec uniphasic and 2 ml/sec uniphasic protocols (385 +/- 398 H/sec and 397 +/- 412 H/sec ) were significantly greater than the index for the 3 ml/sec biphasic protocol (123 +/- 194 H/sec; p < .0001) at a 50-H threshold, Optimal s can delay times were 50 +/- 8, 75 +/- 7, and 119 +/- 8 sec, respective ly, for the 3 ml/sec uniphasic, 2 mllsec uniphasic, and 3 ml/sec bipha sic techniques. CONCLUSION. The moderate-rate uniphasic injections stu died provided greater hepatic enhancement throughout the helical acqui sition without requiring the prohibitively long delay time necessitate d by the moderate-rate biphasic injection. These findings differ from prior results that showed that a uniphasic injection may provide compa rable levels of hepatic enhancement when compared with a high-flow-rat e biphasic injection.