by Tim Leiner
Department of Radiology, Maastricht University Hospital
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Contrast-enhanced MR angiography (CE-MRA) is more sensitive and specific for diagnosis and preinterventional work-up of Periferal Arterial Disease (PAD) compared to Duplex (1).
CE-MRA detects more patent arteries than IA-DSA in patients with chronic critical ischemia and can modify the choice of therapeutic strategy in these patients (2). It is important to distinguish between patients with intermittend claudication and patients with chronic critical ischemia because they need a different imaging approach. In this overview guidelines are given how to tailor the MRA-examination by optimizing the use of surface coils, k-space filling, spatial resolution and contrast delivery. |
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Periferal Arterial Occlusive Disease |
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Intermittend claudicationIntermittend claudication is a benign form of periferal arterial occlusive disease.
Typically these patients have 'single level' disease usually an isolated stenosis in the iliac or femoral artery. When MRA is performed in these patients perfect imaging of lower leg and feet is not the issue since no surgeon will perform a infragenual procedure in patients with these complaints. |
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Chronic critical ischemiaIn patients with chronic critical ischemia
however, there is rest pain and/or tissue loss.
They typically have 'multi level' disease with bilateral, severe stenoses or occlusions in multiple arteries and segments. |
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In these patients it is the job of MRA to find patent arteries in the lower leg or feet for bypass surgery with or without PTA. |
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How to optimize the Imaging Protocol |
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Equipment requirementsCentric k-spacing provides the capability to acquire the optimal part of the central k-space during the arterial-phase of contrast enhancement in a short time-period. The remaining time is used for increasing spatial resolution. Venous enhancement will not be of much of a problem because if the outer k-space is filled with data this does not add much to the contrast in the image. |
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Surface coils |
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Spatial resolutionAs a rule of thumb you need at least 3 pixels per vessel-diameter in order to reliably differentiate between <50% versus >50% stenosis. |
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Planning the seriesThe CE-MRA series can be planned on a rough TOF-serie that gives you a good idea where the vessels of interest are located. |
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At the crural level especially if the pedal arch has to be included a large box will be needed. The spatial resolution at this level has to be high. This results in more thin slices and a longer scan time. How to beat venous enhancement in the lower leg when there is a longer scantime is explained later. |
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Contrast bolus-timing |
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Injection protocolIn patients with intermittent claudication a one-step examination with imaging of 3 sequential stations is optimal. |
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Tips and Tricks in MRA |
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How to beat venous enhancement in lower legs1. Prolong the arterio-venous (AV) window by venous compression. Use a midfemoral compression with a pressure cuff at 50-60 mmHg. A normal blood pressure cuff without the metal parts usually works fine. |
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Centric k-spacing not availableAt the iliac level centric k-spacing is not necessary. Linear filling of k-space works good at this level and provides the advance that the sequence can be started in front of the arrival of the contrast-bolus. |
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3-station coil not availableA 3-station coil is optimal for MRA from the aorta to the feet. If not available use as many surface coils as possible. Synergy body and synergy spine coils are very helpfull, |
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Problems with breath-holdThe most important issue in MRA of the aorta and iliac arteries is that the patient manages to hold his breath. A lower resolution breath-hold scan is superior to a higher resolution scan with breathing artifacts. |
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Peripheral Arterial Disease: Comparison of Color Duplex US and Contrast-enhanced MR Angiography for Diagnosis
Radiology 2005;235:699-708. by Tim Leiner, MD, PhD et al. -
Comparison of Contrast-Enhanced Magnetic Resonance Angiography and Digital Subtraction Angiography in Patients With Chronic Critical Ischemia and Tissue Loss.
Investigative Radiology. 39(7):435-444, July 2004. by Leiner, Tim MD, PhD et al.













