Liming Wei1, Xiaoyue Zhou2, and Jungong Zhao1
1Shanghai Jiaotong University affiliated Sixth People's Hospital, Shanghai, China, 2MR Collaboration, Siemens Healthcare Ltd., Shanghai, China, Shanghai, China
Synopsis
Early diagnosis and aggressive management are critical to
mitigate the devastating natural history of Critical limb ischemia (CLI). Computed tomography angiography (CTA) and
contrast-enhanced magnetic resonance angiography (CE-MRA) are established
methods in the diagnostic workup of PAD. However, the high incidence of
infrapopliteal disease in CLI and the calcified nature of these vessels in
patients suffering from diabetes mellitus are problems even for the dual-energy
CT. In addition, diabetic patients with CLI frequently experience several
comorbidities, which can hamper administration of iodinated contrast media and
lead to contrast-induced nephropathy. What’s more, the high prevalence of
chronic renal impairment in diabetic patients with CLI and CE-MRA studies often
place such patients at an increased risk of nephrogenic systemic fibrosis.
Quiescent-interval single-shot (QISS)-MRA is a robust non-enhanced MRA method
that has shown promising results at 1.5 T and 3 T. Here, we wished to evaluate
the image quality and diagnostic accuracy of QISS-MRA at 3 T in diabetic
patients with CLI compared with CE-MRA with calf compression, with digital
subtraction angiography (DSA) serving as the standard reference.
Introduction
Early diagnosis and aggressive management of critical
limb ischemia (CLI)
are critical to mitigate this condition’s devastating
natural history. Computed tomography angiography (CTA) and contrast-enhanced
magnetic resonance angiography (CE-MRA) are established methods for diagnosing
peripheral arterial disease. However, calcified infrapopliteal vessels, which
are commonly found in diabetic patients suffering from peripheral arterial
disease, are not imaged well on CT and even on dual-energy CT. In addition,
diabetic patients with CLI frequently experience renal dysfunction, which can
prohibit administration of both iodinated and gadolinium contrasts.
Quiescent-interval single-shot (QISS)-MRA is a robust non-enhanced MRA method
that has shown promising results on 1.5T and 3T scanners. In this study, we aim
ed to evaluate the image quality and diagnostic accuracy of QISS-MRA at 3T in
diabetic patients with CLI and to compare it with CE-MRA with calf compression.
method
Thirty-seven diabetic patients with CLI underwent
QISS-MRA, CE-MRA, and DSA, the last of which served as the standard of
reference. QISS-MRA was undertaken on a 3T
system (MAGNETOM Verio, Siemens Healthcare, Erlangen, Germany) using a
combination of superficial body array matrix coils for the abdomen and pelvis,
a 36-element peripheral angiography matrix coil, and a large 4-channel flex coil
(Fig. 1-2). A prototype QISS sequence was applied. The phase of magnetization
preparation was followed by a quiescent interval of 226 ms, during which no
excitation took place. The following imaging parameters were used: field of
view, 400 × 266 mm2; axial plane; 2D; matrix, 400 × 260; measured
voxel size, 1.0 × 1.0 × 3.0 mm3; reconstructed voxel size, 0.5 × 0.5
× 3 mm3; repetition time, 813 ms; echo time, 1.45 ms; flip angles
per slab of 60°; generalized autocalibrating partially parallel acquisitions (GRAPPA)
with an acceleration factor of 2; partial Fourier acquisition in the
phase-encoding direction, 5/8. To span the entire arterial system from the
pelvis to the feet, we acquired eight groups of 70 slices with a slice
thickness of 3.0 mm and an overlap of 0.6 mm. Image quality (five-point Likert scale) and stenosis severity (five-point
grading scale) for QISS-MRA and CE-MRA were evaluated by two blinded readers.
DSA results served as the reference for stenosis severity. Per-segment and
per-region sensitivity, specificity, positive predictive value (PPV) and
negative predictive value (NPV) were calculated.results
Image quality of QISS-MRA and CE-MRA in all 1147 segments
was evaluated. Stenosis severity was assessed on QISS-MRA and CE-MRA and was
analyzed in 654 vessel segments. Image quality of QISS-MRA was lower compared
with CE-MRA in the pelvic region (p<0.001 in both reader 1 and reader 2) and
thigh region (p=0.033 in reader 1 and p = 0.018 in reader 2), whereas in the
calf region, the image quality of QISS-MRA was better than CE-MRA (p=0.009 in
reader 1 and p=0.001 in reader 2). In segment-based and region-based analyses,
there was no difference between QISS-MRA and CE-MRA in sensitivity (89.5% vs.
90.3%, p=0.774 in reader 1 and 87.6% vs, 90.6%, p=0.266 in reader 2) and
specificity (94.2% vs. 92.9%, p=0.513 in reader 1 and 92.9% vs. 92.9%, p=1.000
in reader 2). Region-based analyses also showed that QISS-MRA and CE-MRA
yielded similar sensitivity and specificity values in all regions except the
pelvis where a difference in specificity was observed (95.5% vs. 84.8%,
p=0.041).discussion
In the present study, QISS-MRA generated good-quality
images in diabetic patients with CLI. The image quality of QISS-MRA was
comparable with that of CE-MRA, and was particularly good in the distal thigh
and calf. Using DSA as the reference standard, the diagnostic accuracy of
QISS-MRA was high. In QISS-MRA, a pre-saturation pulse is used inferior to the
slice to suppress the signal from venous blood. However, venous overlap was
found frequently in pelvic and calf stations upon study commencement. We
attempted to adjust the venous pre-saturation slab thickness for pelvic
(100mm), thigh and calf stations (40mm), which resulted in remarkable venous
suppression. Meanwhile, the venous contamination was eliminated at calf station
on QISS-MRA. Another challenge of QISS-MRA in diabetic patients with CLI is
motion artifact. QISS-MRA has a longer scan time than CE-MRA, so the tendency
for diabetic patients with CLI to move their legs caused by pain at rest can
result in degradation of image quality.conclusion
QISS-MRA performed very well in diabetic patients with
CLI and may be a good alternative for patients with contraindications to
CE-MRA. QISS may be particularly useful for the diagnosis of diabetic
peripheral vascular disease which preferentially involves arteries below the
knee with lower-limb ulceration or other risk factors.Acknowledgements
No acknowledgement found.References
No reference found.