Khan Sarah N, McWilliams Justin P, Bista Biraj B, Kee Stephen, Finn J Paul
Department of Radiological Sciences, University of California at Los Angeles, Peter V. Ueberroth Building Suite 3371, 10945 Le Conte Ave, Los Angeles, CA 90095-7206.
Radiol Cardiothorac Imaging. 2020 Apr 30;2(2):e190077. doi: 10.1148/ryct.2020190077. eCollection 2020 Apr.
To perform a preliminary comparison of the sensitivity and positive predictive value of ferumoxytol-enhanced MR angiography with those of CT angiography for detection of pulmonary arteriovenous malformations (AVMs) in hereditary hemorrhagic telangiectasia (HHT).
Institutional review board approval and informed patient consent were obtained. Ten patients with pulmonary AVMs who had undergone CT of the chest within 12 months underwent MRI of the chest and abdomen with ferumoxytol at 3.0 T at a dose of 4 mg per kilogram of body weight. Consensus review of MR and CT images assessed the presence and characteristics of pulmonary AVMs, image quality, vessel visibility, and artifact grade.
Forty-three AVMs were detected, 13 native and 30 recanalized. Twenty-one AVMs had a feeding artery diameter of greater than 2 mm, of which detection occurred in 19 (at MRI and CT), in two (at MRI only), and zero (at CT only). Twenty-two AVMs had a feeding artery diameter of less than or equal to 2 mm, of which detection occurred in 16 (at MRI and CT), six (at CT only), and zero (at MRI only). For the entire cohort, the sensitivity of ferumoxytol-enhanced MRI using CT as the reference standard was 85.4% (35 of 41), and the positive predictive value was 100% (35 of 35). No significant difference was found between CT and MRI in AVM size, feeding artery and draining vein diameter, and artifact score ( >.05 for all).
Initial results suggest that ferumoxytol-enhanced MRI is a feasible alternative to CT for detection of pulmonary AVM in HHT, while avoiding repeated exposure to radiation, nephrotoxic contrast material, or gadolinium-based contrast agent.© RSNA, 2020.
对利用菲洛培南增强磁共振血管造影术(MR angiography)与CT血管造影术检测遗传性出血性毛细血管扩张症(HHT)患者肺动静脉畸形(AVM)的敏感性和阳性预测值进行初步比较。
获得机构审查委员会批准并取得患者知情同意。10例患有肺AVM且在12个月内接受过胸部CT检查的患者,接受了3.0 T的菲洛培南增强胸部和腹部MRI检查,剂量为每千克体重4 mg。对MR和CT图像进行共识性评估,以确定肺AVM的存在、特征、图像质量、血管可视性和伪影等级。
共检测到43个AVM,其中13个为原发性,30个为再通性。21个AVM的供血动脉直径大于2 mm,其中19个(MRI和CT均检测到)、2个(仅MRI检测到)、0个(仅CT检测到)。22个AVM的供血动脉直径小于或等于2 mm,其中16个(MRI和CT均检测到)、6个(仅CT检测到)、0个(仅MRI检测到)。对于整个队列,以CT作为参考标准,菲洛培南增强MRI的敏感性为85.4%(41个中的35个),阳性预测值为100%(35个中的35个)。CT和MRI在AVM大小、供血动脉和引流静脉直径以及伪影评分方面均无显著差异(所有P>.05)。
初步结果表明,菲洛培南增强MRI是检测HHT患者肺AVM的一种可行的替代CT的方法,同时避免了反复暴露于辐射、肾毒性造影剂或钆基造影剂。©RSNA,2020年。