Streeter J E, Dayton P A
University of North Carolina and North Carolina State University, Chapel Hill, NC.
Med Phys. 2012 Jun;39(6Part27):3953. doi: 10.1118/1.4736133.
Medical ultrasound has long been used in clinical applications both as a primary modality and as a supplement to other diagnostic procedures. The basis for ultrasound imaging is the transmission of high frequency (megaHertz) sound waves that propagate through tissue. These sound waves backscatter from the interfaces between tissue components with different acoustic properties and are detected by the imaging system, allowing the creation of images based on tissue characteristics and spatial location. Thus, traditional ultrasound has focused primarily on the imaging of anatomical structures and analysis of blood flow in large vessels. Unfortunately, blood is a weak scatterer, which can make vascular diagnostic applications (example: echocardiography) challenging especially with larger patients. Contrast agents help to improve on this shortcoming by enhancing the visualization of blood flow, thus improving the quality of diagnostics. The use of contrast agents for ultrasound was first reported in 1968 when Gramiak and Shah discovered that there was an increased backscatter of ultrasound caused by injected microbubbles. This is because the mismatch in acoustic impedance (a function of an object's density and compressibility) between the microbubble gas core and blood (or tissue) is several orders of magnitude, which results in substantially higher scattering from a bubble than an equivalent volume of tissue or blood. Additionally, microbubbles oscillate in response to an ultrasound field, and respond non-linearly to acoustic pulses even at low energies, unlike tissue. The non-linear property of microbubbles in an ultrasound field allows for the use of various pulsing and signal processing strategies to detect the backscattered signal from contrast agents and segment it from tissue, thus providing a high contrast-to- noise ratio. Due to these unique acoustic properties, a clinical ultrasound system can detect even single microbubble contrast agents, providing exquisite sensitivity and the ability to perform advanced diagnostic procedures. Over the last several decades, ultrasound contrast agents have been improved for enhanced stability and increased persistence times. Although preclinical studies as well as clinical use in Europe and Asia strongly suggest that the use of contrast ultrasound can substantially improve diagnostic capabilities in both cardiology and radiology applications, contrast use in the US is still very limited. Obstacles to the widespread use of microbubbles include safety concerns, the need for optimization of approaches for contrast use, and general understanding of their potential by physicians. This course covers the basic principles of contrast agents used in ultrasound imaging including their stability, shell properties and their behavior within an acoustic field. In addition, we will cover many new techniques that are being evaluated in preclinical studies including: p er fus ion-based techniques, molecular imaging, gene therapy, drug delivery, and acoustic angiography. Finally, basic safety concerns and biological effects will be reviewed.
医学超声长期以来一直作为主要方式以及其他诊断程序的补充应用于临床。超声成像的基础是高频(兆赫兹)声波在组织中传播。这些声波从具有不同声学特性的组织成分之间的界面反向散射,并由成像系统检测到,从而能够根据组织特征和空间位置创建图像。因此,传统超声主要专注于解剖结构成像和大血管内血流分析。不幸的是,血液是一种弱散射体,这使得血管诊断应用(例如:超声心动图)具有挑战性,尤其是对于体型较大的患者。造影剂通过增强血流可视化来帮助改善这一缺点,从而提高诊断质量。1968年,格拉米亚克和沙阿首次报道了超声造影剂的使用,当时他们发现注入的微泡会导致超声反向散射增加。这是因为微泡气体核心与血液(或组织)之间的声阻抗不匹配(物体密度和可压缩性的函数)相差几个数量级,这导致气泡的散射比相同体积的组织或血液高得多。此外,微泡会响应超声场而振荡,并且即使在低能量下也会对声脉冲产生非线性响应,这与组织不同。超声场中微泡的非线性特性允许使用各种脉冲和信号处理策略来检测来自造影剂的反向散射信号并将其与组织区分开来,从而提供高对比度噪声比。由于这些独特的声学特性,临床超声系统甚至可以检测到单个微泡造影剂,提供极高的灵敏度并能够执行先进的诊断程序。在过去几十年中,超声造影剂在稳定性和持续时间方面得到了改进。尽管临床前研究以及在欧洲和亚洲的临床应用强烈表明,超声造影剂的使用可以显著提高心脏病学和放射学应用中的诊断能力,但在美国,造影剂的使用仍然非常有限。微泡广泛应用的障碍包括安全问题、造影剂使用方法的优化需求以及医生对其潜力的普遍了解。本课程涵盖超声成像中使用的造影剂的基本原理,包括其稳定性、外壳特性及其在声场中的行为。此外,我们将介绍许多正在临床前研究中评估的新技术,包括:基于灌注的技术、分子成像、基因治疗、药物递送和声血管造影。
a. 什么是微泡造影剂?
b. 微泡的特性
c. 安全问题和生物学效应
a. 谐波和次谐波成像技术
b. 脉冲反转技术
a. 传统方法(心血管、腹部)
b. 先进的灌注成像技术
a. 超声分子成像
b. 基因治疗
c. 药物递送
d. 声血管造影。