Philips Ultrasound, Bothell, WA, USA.
Ultrasonics. 2012 Jan;52(1):12-9. doi: 10.1016/j.ultras.2011.06.003. Epub 2011 Jun 13.
The objective of this study was to assess in vitro the impact of ultrasound scanner settings and contrast bolus volume on time-intensity curves formed from dynamic contrast-enhanced ultrasound image loops. An indicator-dilution experiment was developed with an in vitro flow phantom setup used with SonoVue contrast agent (Bracco SpA, Milan, Italy). Imaging was performed with a Philips iU22 scanner and two transducers (L9-3 linear and C5-1 curvilinear). The following ultrasound scanner settings were investigated, along with contrast bolus volume: contrast-specific nonlinear pulse sequence, gain, mechanical index, focal zone depth, acoustic pulse center frequency and bandwidth. Four parameters (rise time, mean transit time, peak intensity, and area under the curve) were derived from time-intensity curves which were obtained after pixel by pixel linearization of log-compressed data (also referred to as video data) included in a region of interest. Rise time was found to be the parameter least impacted by changes to ultrasound scanner settings and contrast bolus volume; the associated coefficient of variation varied between 0.7% and 6.9% while it varied between 0.8% and 19%, 12% and 71%, and 9.2% and 66%, for mean transit time, peak intensity, and area under the curve, respectively. The present study assessed the impact of ultrasound scanner settings and contrast bolus volume on time-intensity curve analysis. One should be aware of these issues to standardize their technique in each specific organ of interest and to achieve accurate, sensitive, and reproducible data using dynamic contrast-enhanced ultrasound. One way to mitigate the impact of ultrasound scanner settings in longitudinal, multi-center quantitative dynamic contrast-enhanced ultrasound studies may be to prohibit any adjustments to those settings throughout a given study. Further clinical studies are warranted to confirm the reproducibility and diagnostic or prognostic value of time-intensity curve parameters measurements in a particular clinical scenario of interest, for example that of cancer patients undergoing vascular targeting therapies.
本研究旨在评估超声扫描仪设置和对比剂团注体积对动态对比增强超声图像循环形成的时间-强度曲线的体外影响。采用 SonoVue 对比剂(意大利米兰 Bracco SpA)的体外流动体模装置开发了指示剂稀释实验。使用飞利浦 iU22 扫描仪和两个换能器(L9-3 线性和 C5-1 曲线)进行成像。研究了以下超声扫描仪设置以及对比剂团注体积:对比特异性非线性脉冲序列、增益、机械指数、焦点深度、声脉冲中心频率和带宽。从时间-强度曲线中得出了四个参数(上升时间、平均渡越时间、峰值强度和曲线下面积),这些曲线是通过对感兴趣区域内的视频数据进行逐像素线性化获得的。上升时间是受超声扫描仪设置和对比剂团注体积变化影响最小的参数;其相关变异系数在 0.7%至 6.9%之间变化,而平均渡越时间、峰值强度和曲线下面积的变异系数分别在 0.8%至 19%、12%至 71%和 9.2%至 66%之间变化。本研究评估了超声扫描仪设置和对比剂团注体积对时间-强度曲线分析的影响。在使用动态对比增强超声进行标准化技术和实现准确、敏感和可重复的数据时,应该意识到这些问题。在纵向、多中心定量动态对比增强超声研究中,一种减轻超声扫描仪设置影响的方法可能是在整个特定研究中禁止对这些设置进行任何调整。有必要进行进一步的临床研究,以确认时间-强度曲线参数测量在特定感兴趣的临床情况下(例如接受血管靶向治疗的癌症患者)的可重复性和诊断或预后价值。