Optimal injection rate of ultrasound contrast agent for evaluation of focal liver lesions using an automatic power injector: a pilot study
© The Author(s) 2016
Received: 18 May 2015
Accepted: 18 May 2016
Published: 17 June 2016
To determine the optimal bolus injection rate of ultrasound (US) contrast agent in vascular imaging for focal liver lesions.
Thirteen patients with 13 focal liver lesions (5 hepatocellular carcinomas (HCCs) with cirrhosis, 4 liver metastases, 2 hemangiomas, 1 intrahepatic cholangiocarcinoma, 1 focal nodular hyperplasia) received two bolus injections of Sonazoid (at 0.5 and 2.0 mL/s) using an automatic power injector. The lesion-to-liver contrast ratio at peak enhancement was quantitatively evaluated. Enhancement of the lesions compared to liver parenchyma was assessed by two independent readers using a five-point scale and qualitatively evaluated by receiver operating characteristic (ROC) analysis.
For all lesions, the contrast ratio was not significantly different between the two injection rates. For HCCs, the contrast ratio was higher at 0.5 mL/s (7.41 ± 6.56) than at 2.0 mL/s (4.28 ± 4.66, p = 0.025). For all lesions, the mean area under the ROC curve (AUC) was not significantly different between the two injection rates. For HCCs, the AUC was greater at 0.5 mL/s than at 2.0 mL/s (AUC: 0.86, p = 0.013).
In contrast-enhanced US, an injection rate of 0.5 mL/s is superior to an injection rate of 2.0 mL/s for the quantitative and qualitative analysis of HCCs in the cirrhotic liver.
KeywordsUltrasound Contrast Injection rate Focal liver lesion Power injector
Current low-mechanical index (low-MI) techniques for contrast-enhanced ultrasound (CEUS) using second-generation microbubble agents have advantages in the characterization of focal liver lesions (FLLs), including the real-time observation of continuous hemodynamic changes in hepatic lesions (Claudon et al. 2013). However, to our knowledge, there is little agreement concerning the appropriate injection rate for microbubble agents in CEUS, despite the fact that there have been many studies regarding the injection rate of contrast media in dynamic computed tomography (CT) (Tublin et al. 1999) and magnetic resonance (MR) imaging (Schmid-Tannwald et al. 2012).
We have therefore conducted a prospective pilot study to determine both qualitatively and quantitatively the optimal bolus injection rate of US contrast agent in vascular imaging for the evaluation of FLLs, with the ultimate goal of establishing suitable protocols for the examination of patients with FLLs.
Thirteen consecutive patients (2 men and 11 women; age, 67.5 ± 10.4 years (mean ± standard deviation); body weight, 51.9 ± 9.4 kg; and height, 151.8 ± 8.0 cm) with FLLs to be evaluated by CEUS were enrolled as the subjects of this pilot study. Five subjects had hepatocellular carcinoma (HCC) with cirrhosis, 4 had liver metastasis (2 from pancreatic neuroendocrine tumor and 2 from breast cancer), 2 had hemangioma, 1 had cholangiocarcinoma, and 1 had focal nodular hyperplasia (FNH).
The diagnosis of HCC, as well as liver cirrhosis, all metastases, and cholangiocarcinoma, was based on the findings of needle biopsy (21-gauge Majima needle; Top Surgical Manufacturing, Tokyo, Japan). The diagnosis of hemangioma and FNH was based on a combination of imaging findings: a classic contrast enhancement pattern observed on CEUS, with peripheral nodular enhancement or tiny enhancing dots in the early phase and persistent enhancement or centripetal fill-in enhancement in the late and postvascular phases for hemangioma (Claudon et al. 2013), and with a hypervascular appearance with the presence of stellate lesional vessels with a centrifugal filling direction in the early phase and persistent enhancement in the late and postvascular phases for FNH (Claudon et al. 2013).
A diagnostic US system (TSU-A500, Aplio™ 500; Toshiba Medical System Corporation, Tochigi, Japan) with a 3.75-MHz convex transducer (PVT-375BT; Toshiba) was used in this study. The imaging mode was wideband harmonic imaging (commercial name “Pulse subtraction”) with transmission and reception frequencies of 1.75 and 3.5 MHz, respectively.
All subjects were fasted overnight. All US scans were performed by the same sonologist (M.A.) with 5 years of experience in standard US and CEUS. The probe was held steady during acquisition while the subject was breathing shallowly and evenly in order to obtain a single image showing the largest plane through the lesion and including adjacent liver parenchyma.
Examination recording and timing were triggered immediately after the contrast agent was injected. The acquisition time for the raw data was 1 min. The use of low-MI nonlinear imaging (MI < 0.2) allowed the microbubbles to be visualized nondestructively with simultaneous low-MI B-mode anatomic imaging displayed side by side.
CEUS examinations were performed at a rate of 10 frames per second and with a dynamic range of 60 dB. The receive gain, image depth, and transmit focus were optimized for each subject. When the examination was completed, the raw data were stored in a workstation (UltraExtend FX; Toshiba). Initial quantification was performed using US quantification software (CHI-Q; Toshiba).
Region of interest (ROI) analysis
Quantitative perfusion parameter analysis
Qualitative visual analysis
Two experienced sonologists (M.A. and S.O.) involved in the study qualitatively assessed the degree of lesion conspicuity as compared to adjacent liver parenchyma in CEUS images during all vascular phases. The two sonologists performed assessment independently and were blinded to the injection rate used.
All image cine clips were reviewed at the workstation (UltraExtend FX; Toshiba). The degree of lesion conspicuity was visually scored in comparison to adjacent liver parenchyma using a five-point scale: 5 (excellent), contrast enhancement provided optimal information for establishing a diagnosis; 4 (good), contrast enhancement provided adequate information for establishing a diagnosis; 3 (fair), contrast enhancement provided acceptable information for establishing a diagnosis, but image quality was unsatisfactory; 2 (poor), contrast enhancement did not provide adequate information for establishing a diagnosis; and 1 (none), no enhancement was observed.
The results were expressed as mean ± standard deviation. The quantitative perfusion parameter analysis results for the two injection rates were compared using the two-tailed Student’s t test. The conspicuity of each lesion at each injection rate and for each reviewer was evaluated by receiver operating characteristic (ROC) analysis. The area under the ROC curve (AUC) was calculated for each reviewer and for each injection rate. The two-tailed Student’s t test was also used to test for differences in the AUCs. A p value of less than 0.05 was considered to be statistically significant. All statistical analyses were performed using a computer software package (JMP® version 11; SAS Institute Japan Ltd., Tokyo, Japan).
For all lesions, no significant difference in the mean AUC was observed between the two injection rates. For HCC, the mean AUC was greater for injection at 0.5 mL/s than for injection at 2.0 mL/s (AUC: 0.86, p = 0.013) (Fig. 4).
An important advantage of CEUS is the ability to assess contrast enhancement patterns in real time with a much higher temporal resolution than is possible with other imaging modalities. It may therefore seem that there is no need to define an optimal injection protocol, unlike the case for CT or MR imaging.
In fact, one set of clinical CEUS guidelines for the liver simply states that ultrasound contrast agent should be administered as a bolus injection followed by a 0.9 % normal saline flush (Claudon et al. 2013). Another states that contrast agent should be administered by bolus injection within 2 s, followed by flushing with 10 mL of normal saline (Jang et al. 2013). We basically agree with these guidelines, but we also feel that it is important to conduct studies to determine whether it is possible to develop optimal CEUS examination protocols, particularly with regard to the injection of contrast agent.
The results of this pilot study showed that, for all lesions, no significant differences were observed between the two injection rates in both quantitative and qualitative analysis. However, for HCC in the cirrhotic liver, an injection rate of 0.5 mL/s was found to be significantly superior to an injection rate of 2.0 mL/s in both quantitative and qualitative analysis.
Elucidating the mechanisms responsible for the finding that a slow injection rate is superior only for HCC in patients with a cirrhotic liver may be important in CEUS examinations for the characterization of FLLs. In general, it is said that as the liver becomes cirrhotic, the hepatic blood flow balance changes from “portal vein dominant” to “hepatic artery dominant” (Kleber et al. 1999). Thus, we assume that the arterial enhancement of HCC can be masked by that of adjacent liver parenchyma and that this phenomenon is expressed more strongly at a faster injection rate because the time to peak intensity is significantly shorter for a fast injection rate than a slow injection rate. Our visual assessment and ROC analysis results support this theory.
Our study has several limitations. First, the number of subjects was relatively small, although the number is probably sufficient for a pilot study. Second, pathologic confirmation was not obtained for a minority of the lesions, although all subjects did undergo confirmatory imaging examinations.
In conclusion, in CEUS examinations, an injection rate of 0.5 mL/s was found to be significantly superior to an injection rate of 2.0 mL/s for the quantitative and qualitative analysis of HCC in the cirrhotic liver. The use of a slow injection rate may improve the diagnostic accuracy of CEUS for HCC in patients with cirrhosis of the liver.
KS and MK contributed in developing the study design, performed clinical examination, and drafting the manuscript. MK and SO performed observer study. HT, FM, YK, YF, TS, and IN contributed in assessing the imaging findings, reviewing the literatures, and performing statistical analysis. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Human rights statement and informed consent
All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2008 (5). The study protocol was approved by the Institutional Review Board of Tokyo Medical University. Informed consent was obtained from all subjects at the time of scanning after the nature of the procedure was fully explained.
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