Logan Hubbard, Sipan Mathevosian, Takegawa Yoshida, Cameron Hassani, Mohammad H Jalili, J Paul Finn, Arash Bedayat
{"title":"阿魏木糖醇增强MR血管造影对肾功能受损患者主动脉支架内漏的评价。","authors":"Logan Hubbard, Sipan Mathevosian, Takegawa Yoshida, Cameron Hassani, Mohammad H Jalili, J Paul Finn, Arash Bedayat","doi":"10.1016/j.clinimag.2024.110383","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate ferumoxytol-enhanced magnetic resonance angiography (FE-MRA) for assessment of endoleaks in patients with abdominal aortic aneurysms (AAA) and chronic kidney disease (CKD) status post endovascular aneurysm repair (EVAR).</p><p><strong>Methods: </strong>Of 1854 patients who underwent FE-MRA at a single institution between 03/21/2014 and 08/21/2023, 21 patients with a history of AAA and CKD status post EVAR were retrospectively identified (IRB #13-001341). Multiplanar pre- and post-contrast HASTE, T1-VIBE, and high-resolution breath-held 3D MRA sequences were obtained, where a dose of 4 mg/kg of Ferumoxytol was infused over six minutes. All examinations were performed on either a Siemens 3.0 T Prisma Fit, a Siemens 3.0 T TIM Trio, or a Siemens 1.5 T Avanto MRI scanner. Image post-processing was performed using OsiriX and Vitrea software for endoleak identification and display.</p><p><strong>Results: </strong>Twenty-six FE-MRA examinations were completed, where 24 were fully diagnostic and 2 were limited by metal artifact. Three patients underwent one follow-up examination, while one patient underwent two follow-up examinations. Endoleaks were identified in seven patients: one Type Ia, two Type Ib, and four Type II. The Type Ia endoleak patient received follow-up imaging two years after initial imaging. A Type II endoleak patient received follow-up imaging six months and one year after initial imaging. In both cases, the Type I and Type II endoleaks were reproducibly visualized. No contrast reactions occurred.</p><p><strong>Conclusion: </strong>For patients with a history of AAA and CKD status post EVAR, FE-MRA is a safe, practical and effective imaging solution for evaluation of Type I and Type II endoleaks.</p>","PeriodicalId":50680,"journal":{"name":"Clinical Imaging","volume":"118 ","pages":"110383"},"PeriodicalIF":1.8000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluation of aortic stent endoleaks in the renally impaired patient with ferumoxytol-enhanced MR angiography.\",\"authors\":\"Logan Hubbard, Sipan Mathevosian, Takegawa Yoshida, Cameron Hassani, Mohammad H Jalili, J Paul Finn, Arash Bedayat\",\"doi\":\"10.1016/j.clinimag.2024.110383\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>To evaluate ferumoxytol-enhanced magnetic resonance angiography (FE-MRA) for assessment of endoleaks in patients with abdominal aortic aneurysms (AAA) and chronic kidney disease (CKD) status post endovascular aneurysm repair (EVAR).</p><p><strong>Methods: </strong>Of 1854 patients who underwent FE-MRA at a single institution between 03/21/2014 and 08/21/2023, 21 patients with a history of AAA and CKD status post EVAR were retrospectively identified (IRB #13-001341). Multiplanar pre- and post-contrast HASTE, T1-VIBE, and high-resolution breath-held 3D MRA sequences were obtained, where a dose of 4 mg/kg of Ferumoxytol was infused over six minutes. All examinations were performed on either a Siemens 3.0 T Prisma Fit, a Siemens 3.0 T TIM Trio, or a Siemens 1.5 T Avanto MRI scanner. Image post-processing was performed using OsiriX and Vitrea software for endoleak identification and display.</p><p><strong>Results: </strong>Twenty-six FE-MRA examinations were completed, where 24 were fully diagnostic and 2 were limited by metal artifact. Three patients underwent one follow-up examination, while one patient underwent two follow-up examinations. Endoleaks were identified in seven patients: one Type Ia, two Type Ib, and four Type II. The Type Ia endoleak patient received follow-up imaging two years after initial imaging. A Type II endoleak patient received follow-up imaging six months and one year after initial imaging. In both cases, the Type I and Type II endoleaks were reproducibly visualized. 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引用次数: 0
摘要
目的:评估铁氧体增强磁共振血管造影(FE-MRA)在评估腹主动脉瘤(AAA)患者内漏和血管内动脉瘤修补术(EVAR)后慢性肾病(CKD)状态方面的应用:在2014年3月21日至2023年8月21日期间,在一家机构接受FE-MRA检查的1854名患者中,回顾性地确定了21名有AAA病史和EVAR术后有慢性肾脏病(CKD)的患者(IRB #13-001341)。在六分钟内输注 4 毫克/千克 Ferumoxytol 的剂量后,获得了多平面对比前后 HASTE、T1-VIBE 和高分辨率呼吸保持三维 MRA 序列。所有检查均在西门子 3.0 T Prisma Fit、西门子 3.0 T TIM Trio 或西门子 1.5 T Avanto MRI 扫描仪上进行。使用 OsiriX 和 Vitrea 软件进行图像后处理,以识别和显示内漏:完成了 26 次 FE-MRA 检查,其中 24 次完全确诊,2 次受到金属伪影的限制。三名患者接受了一次随访检查,一名患者接受了两次随访检查。在七名患者中发现了内漏:一名 Ia 型,两名 Ib 型,四名 II 型。Ia 型内漏患者在初次成像两年后接受了随访成像。一名 II 型内漏患者在初次成像六个月和一年后接受了随访成像。在这两个病例中,Ⅰ型和Ⅱ型内漏均可重复观察到。结论:对于 EVAR 后有 AAA 病史和 CKD 状态的患者,FE-MRA 是评估 I 型和 II 型内漏的一种安全、实用和有效的成像解决方案。
Evaluation of aortic stent endoleaks in the renally impaired patient with ferumoxytol-enhanced MR angiography.
Purpose: To evaluate ferumoxytol-enhanced magnetic resonance angiography (FE-MRA) for assessment of endoleaks in patients with abdominal aortic aneurysms (AAA) and chronic kidney disease (CKD) status post endovascular aneurysm repair (EVAR).
Methods: Of 1854 patients who underwent FE-MRA at a single institution between 03/21/2014 and 08/21/2023, 21 patients with a history of AAA and CKD status post EVAR were retrospectively identified (IRB #13-001341). Multiplanar pre- and post-contrast HASTE, T1-VIBE, and high-resolution breath-held 3D MRA sequences were obtained, where a dose of 4 mg/kg of Ferumoxytol was infused over six minutes. All examinations were performed on either a Siemens 3.0 T Prisma Fit, a Siemens 3.0 T TIM Trio, or a Siemens 1.5 T Avanto MRI scanner. Image post-processing was performed using OsiriX and Vitrea software for endoleak identification and display.
Results: Twenty-six FE-MRA examinations were completed, where 24 were fully diagnostic and 2 were limited by metal artifact. Three patients underwent one follow-up examination, while one patient underwent two follow-up examinations. Endoleaks were identified in seven patients: one Type Ia, two Type Ib, and four Type II. The Type Ia endoleak patient received follow-up imaging two years after initial imaging. A Type II endoleak patient received follow-up imaging six months and one year after initial imaging. In both cases, the Type I and Type II endoleaks were reproducibly visualized. No contrast reactions occurred.
Conclusion: For patients with a history of AAA and CKD status post EVAR, FE-MRA is a safe, practical and effective imaging solution for evaluation of Type I and Type II endoleaks.
期刊介绍:
The mission of Clinical Imaging is to publish, in a timely manner, the very best radiology research from the United States and around the world with special attention to the impact of medical imaging on patient care. The journal''s publications cover all imaging modalities, radiology issues related to patients, policy and practice improvements, and clinically-oriented imaging physics and informatics. The journal is a valuable resource for practicing radiologists, radiologists-in-training and other clinicians with an interest in imaging. Papers are carefully peer-reviewed and selected by our experienced subject editors who are leading experts spanning the range of imaging sub-specialties, which include:
-Body Imaging-
Breast Imaging-
Cardiothoracic Imaging-
Imaging Physics and Informatics-
Molecular Imaging and Nuclear Medicine-
Musculoskeletal and Emergency Imaging-
Neuroradiology-
Practice, Policy & Education-
Pediatric Imaging-
Vascular and Interventional Radiology