Ruth P Lim1,2,3, Emma Hornsey1, Dinesh Ranatunga1,2, Huming Hao4, Lucy McKenna1, Julie Smith1, Tim Spelman5, Jason Chuen3,4, and Mark Goodwin1,2
1Radiology, Austin Health, Melbourne, Australia, 2Radiology, The University of Melbourne, Melbourne, Australia, 3Surgery, The University of Melbourne, Melbourne, Australia, 4Surgery, Austin Health, Melbourne, Australia, 5Centre for Population Health, Burnet Institute, Melbourne, Australia
Synopsis
Venous
mapping is important in end stage renal disease patients requiring vascular
access for hemodialysis. We compare image quality (IQ) and measured vessel
caliber of FSE based non-contrast MRV (NC-MRV) to contrast-enhanced MRV (CE-MRV) and
US in available segments in 10 healthy volunteers. Central and arm vein IQ was diagnostic, but forearm
vein IQ was suboptimal, inferior to CE-MRV. No difference in vessel caliber
between sequences was demonstrated for most segments between NC-MRV and CE-MRV, but both
MRV techniques yielded significantly larger caliber measurements than US,
raising concern regarding application of MRV-derived measurements to clinical
practice.Purpose
Venous
mapping is important in end stage renal disease patients requiring hemodialysis
for vascular access planning, to establish vessel caliber and patency
1. Ultrasound (US) is performed first
line, but is difficult for central veins. Contrast-enhanced MRV (CE-MRV) is
undesirable due to risk of Nephrogenic Systemic Fibrosis
2. Our purpose was to evaluate image
quality (IQ) and measured vessel caliber of central and upper extremity veins with
a non-contrast MRV (NC-MRV) protocol, with comparison to CE-MRV and US measurements
in healthy volunteers.
Methods
Following
informed consent, 10 healthy volunteers (3M, 7F, mean 36y) underwent bilateral
NC-MRV and CE-MRV at 1.5T (Avanto, Siemens) in a single visit. NC-MRV comprised
2D and 3D bSSFP imaging of the chest, followed by 2-station fast spin echo MRV
(FSE-MRV), based on a fresh blood imaging technique3. Upper FSE-MRV station (SVC to elbow) was performed with
respiratory navigator in an oblique coronal plane, and lower station (forearm)
in an oblique sagittal plane. Subsequently, 2 station CE-MRV images were
acquired in identical orientation, 3 minutes post injection of 0.2 mmol/kg
gadobenate dimeglumine (Multihance, Bracco) into a hand vein, with breath-holding
for the upper station. Sequence parameters are provided in Table 1. Bilateral
upper limb B-mode US from proximal arm to wrist was performed within 7 days of
MR (Philips IU22, linear 15-7 array transducer), with measurements made by an
experienced sonographer. A tourniquet was employed for lower MRV stations and
US.
Anonymized
MR images were independently evaluated by two vascular radiologists on a PACS
workstation (Impax, Agfa). Up to 27 segments were evaluated, including central
(SVC, brachiocephalic, subclavian and axillary) and superficial arm/forearm veins
(basilic, cephalic, and medial antebrachial veins where present). IQ was scored
on a 5-point scale (0=non-diagnostic, 2= sufficient for diagnosis, 4= excellent
IQ). For both MR techniques and US, caliber was measured for veins larger than
3mm diameter. IQ and caliber measurements were combined across readers and
compared with the Wilcoxon signed rank test.
Results
All
subjects successfully completed both MR and US. Overall, 471 segments were graded
for IQ with NC-MRV and 468 with CE-MRV. Mean IQ was diagnostic for both
sequences (
Figures 1 and 2), but statistically significantly superior for CE-MRV versus NC-MRV
(
Table 2). CE-MRV was superior for central and forearm veins, with forearm
segments suboptimally visualized (mean IQ score <2) with NC-MRV. Mean IQ was
higher for NC-MRV for arm veins, approaching statistical significance. Difficulties
encountered with both techniques were: assessment of the proximal humeral basilic
vein related to patient positioning, and separating target veins from adjacent
vessels in the upper limb. Vessel blurring was the main artifact reported
limiting NC-MRV image quality, particularly for forearm segments, with flow
dephasing in central segments in 2 subjects. Poor fat suppression and
low SNR were cited as reasons for poor IQ for CE-MRV for distal segments.
Caliber
measurements were performed in 383 NC-MRV and 371 CE-MRV segments, with no
overall significant difference in caliber between sequences. NC-MRV mean
measurements were 0.1mm larger than CE-MRV in the arm, with no
significant differences observed in central and forearm regions. A 0.6mm
greater mean caliber for NC-MRV was observed for the distal humeral basilic vein, with no other significant segmental differences between NC-MRV and CE-MRV
measurements (
Table 3). 261 vessel segments were measured at US, with both
NC-MRV and CE-MRV measurements significantly larger than US measurements
(NC-MRV 8.5±5.2mm, CE-MRV 8.3±5.2mm, US 4.5±1.8mm, both p <0.001).
Discussion/ Conclusion
A
non-contrast assessment of the upper extremity and central veins is desirable
in patients with end stage renal disease for vascular access planning. Previous
preliminary work demonstrated superior visualization of the arm veins with FSE-MRV
in volunteers compared with 2D-TOF4.
Similarly, superior venous IQ has been described using a balanced SSFP
technique against CE-MRV5. In
our study, IQ was inferior for NC-MRV for central and forearm veins. Vessel
blurring in the phase encoding direction, related to interecho spacing and echo
train length with FSE imaging6,
was the major factor impacting IQ.
Optimization
with increased acceleration factors to minimize echo train length, in
combination with 3T imaging, may engender improvements in image quality and
spatial resolution.
We
demonstrated comparable venous caliber of most segments for NC-MRV and CE-MRV,
with small (<1mm) but significant differences observed in the basilic vein in
the arm. Both MRV techniques yielded significantly
larger vessel caliber than US measurements, as has been reported for bSSFP
NC-MRV7, with direct US
transducer pressure, patient positioning, temporal variation and MR spatial
resolution limitations potential factors. These results are concerning if MRV
is to be applied in clinical practice.
Acknowledgements
This work was supported by a grant from the Austin Medical Research Foundation.References
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