Knuttinen Martha-Grace, Karow Jillian, Mar Winnie, Golden Margaret, Xie Karen L
Department of Radiology, University of Illinois Hospital and Health Sciences System, Chicago, Illinois, United States.
J Clin Imaging Sci. 2014 Nov 29;4:63. doi: 10.4103/2156-7514.145860. eCollection 2014.
Magnetic resonance angiography (MRA) provides noninvasive visualization of the vascular supply of soft tissue masses and vascular pathology, without harmful radiation. This is important for planning an endovascular intervention, and helps to evaluate the efficiency and effectiveness of the treatment. MRA with conventional extracellular contrast agents relies on accurate contrast bolus timing, limiting the imaging window to first-pass arterial phase. The recently introduced blood pool contrast agent (BPCA), gadofosveset trisodium, reversibly binds to human serum albumin, resulting in increased T1 relaxivity and prolonged intravascular retention time, permitting both first-pass and steady-state phase high-resolution imaging. In our practice, high-quality MRA serves as a detailed "roadmap" for the needed endovascular intervention. Cases of aortoiliac occlusive disease, inferior vena cava thrombus, pelvic congestion syndrome, and lower extremity arteriovenous malformation are discussed in this article. MRA was acquired at 1.5 T with an 8-channel phased array coil after intravenous administration of gadofosveset (0.03 mmol/kg body weight), at the first-pass phase. In the steady-state, serial T1-weighted 3D spoiled gradient echo images were obtained with high resolution. All patients underwent digital subtraction angiography (DSA) and endovascular treatment. MRA and DSA findings of vascular anatomy and pathology are discussed and correlated. BPCA-enhanced MRA provides high-quality first-pass and steady-state vascular imaging. This could increase the diagnostic accuracy and create a detailed map for pre-intervention planning. Understanding the pharmacokinetics of BPCA and being familiar with the indications and technique of MRA are important for diagnosis and endovascular intervention.
磁共振血管造影(MRA)可对软组织肿块的血管供应和血管病变进行无创可视化成像,且无有害辐射。这对于规划血管内介入治疗很重要,并有助于评估治疗的效率和效果。使用传统细胞外造影剂的MRA依赖于精确的造影剂团注时间,将成像窗口限制在首次通过动脉期。最近引入的血池造影剂(BPCA)——钆布醇三钠,可与人血清白蛋白可逆性结合,导致T1弛豫率增加和血管内滞留时间延长,从而允许进行首次通过和稳态期的高分辨率成像。在我们的实践中,高质量的MRA可作为所需血管内介入治疗的详细“路线图”。本文讨论了主髂动脉闭塞性疾病、下腔静脉血栓、盆腔淤血综合征和下肢动静脉畸形的病例。静脉注射钆布醇(0.03 mmol/kg体重)后,在首次通过期使用8通道相控阵线圈于1.5 T下进行MRA检查。在稳态下,以高分辨率获取一系列T1加权三维扰相梯度回波图像。所有患者均接受了数字减影血管造影(DSA)和血管内治疗。对MRA和DSA在血管解剖和病理方面的发现进行了讨论并相互关联。BPCA增强MRA可提供高质量的首次通过和稳态血管成像。这可以提高诊断准确性,并为介入前规划创建详细的图谱。了解BPCA的药代动力学并熟悉MRA的适应症和技术对于诊断和血管内介入治疗很重要。