Ammi Azzdine Y, Lindner Jonathan R, Zhao Yan, Porter Thomas, Siegel Robert, Kaul Sanjiv
Azzdine Y. Ammi, PhD, Knight Cardiovascular Institute, UHN-62, Oregon Health & Science University, 3181 SW Sam Jackson Park Rd., Portland, OR 97239, USA, Tel.: +1 503 494 8750, Fax: +1 503 494 8550, E-mail:
Thromb Haemost. 2015 Jun;113(6):1357-69. doi: 10.1160/TH14-03-0286. Epub 2015 Mar 26.
Ultrasound and microbubble (MB) contrast agents accelerate clot lysis, yet clinical trials have been performed without defining optimal acoustic conditions. Our aim was to assess the effect of acoustic pressure and frequency on the extent and spatial location of clot lysis. Clots from porcine blood were created with a 2-mm central lumen for infusion of lipid-shelled perfluorocarbon MBs (1×10(7) ml(-1)) or saline. Therapeutic ultrasound at 0.04, 0.25, 1.05, or 2.00 MHz was delivered at a wide range of peak rarefactional acoustic pressure amplitudes (PRAPAs). Ultrasound was administered over 20 minutes grouped on-off cycles to allow replenishment of MBs. The region of lysis was quantified using contrast-enhanced ultrasound imaging. In the absence of MBs, sonothrombolysis did not occur at any frequency. Sonothrombolysis was also absent in the presence of MBs despite their destruction at 0.04 and 2.00 MHz. It occurred at 0.25 and 1.05 MHz in the presence of MBs for PRAPAs > 1.2 MPa and increased with PRAPA. At 0.25 MHz the clot lysis was located in the far wall. At 1.05 MHz, however, there was a transition from far to near wall as PRAPA was increased. The area of clot lysis measured by ultrasound imaging correlated with that by micro-CT and quantification of debris in the effluent. In conclusion, sonothrombolysis with MBs was most efficient at 0.25 MHz. The spatial location of sonothrombolysis varies with pressure and frequency indicating that the geometric relation between therapeutic probe and vascular thrombosis is an important variable for successful lysis clinically.
超声与微泡(MB)造影剂可加速血栓溶解,但此前的临床试验并未确定最佳声学条件。我们的目的是评估声压和频率对血栓溶解程度及空间位置的影响。用猪血液制备含2毫米中央腔的血栓,用于注入脂质壳全氟碳微泡(1×10⁷个/毫升)或生理盐水。以0.04、0.25、1.05或2.00兆赫的治疗性超声在很宽范围的峰值稀疏声压幅度(PRAPA)下进行照射。超声以20分钟的开-关周期进行给药,以便微泡得到补充。使用超声造影成像对溶解区域进行定量。在没有微泡的情况下,任何频率下均未发生超声溶栓。尽管微泡在0.04和2.00兆赫下被破坏,但在有微泡存在时也未发生超声溶栓。在有微泡存在的情况下,当PRAPA>1.2兆帕时,在0.25和1.05兆赫发生了超声溶栓,且随PRAPA增加而增加。在0.25兆赫时,血栓溶解位于远壁。然而,在1.05兆赫时,随着PRAPA增加,血栓溶解从远壁向近壁转变。超声成像测量的血栓溶解面积与微计算机断层扫描测量的面积以及流出物中碎片的定量结果相关。总之,微泡超声溶栓在0.25兆赫时效率最高。超声溶栓的空间位置随压力和频率而变化,这表明治疗探头与血管血栓之间的几何关系是临床上成功溶解血栓的一个重要变量。