Non-contrast enhanced visualization of the equine foot vasculature in a cadaver model using time-of-flight sequence.

Objective The objective of this study was to establish a non-contrast enhanced MR angiography (NC-MRA) sequence for the equine foot (EF) using a post-mortem angiography model.Materials And Methods Time-of-flight (TOF) sequences were tested using variable parameter settings and 3 slice orientations during vascular perfusion of frozen-thawed cadaver EF with paraffine oil. Transverse and dorsal orientations were planned perpendicular or parallel to the sublamellar vascular plexus at the dorsal aspect of P3, or approximately perpendicular to the coronary plexus. Visibility of the coronary plexus, sublamellar plexus, palmar plexus, terminal arch and its respective branches, solar plexus, and the marginal circumflex vessels was evaluated in a total of 74 sequences.Results Twelve EF of 10 horses were scanned. Visibility of vessels as small as the sublamellar plexus was best achieved by 3D-TOF sequences in transverse and dorsal orientations with the following parameters: pixel size 0.34 × 0.48 mm, slice thickness 0.2 mm, interslice gap 0.2 mm, TR/TE 21.2/4.7 ms, flip angle 16°, TONE ramp 70%, acquisition time 22.05 min. Only for the sublamellar plexus, the transverse acquisition showed a slightly better visualization than the dorsal acquisition, however the latter could include nearly the entire EF in the field of view with the same acquisition time.Conclusion And Discussion 3D-TOF allowed visualization down to at least the sublamellar venous plexus which is reported to have diameters of approximately 0.45 mm. The post-mortem model facilitated establishment of a TOF sequence without the need for experimental animals.

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Publication Details

Journal
Open Access CRIS of the University of Bern
Published
2025-07-18
DOI
https://doi.org/10.48620/90678
Primary Topic
Peripheral Artery Disease Management
Type
article
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article

Non-contrast enhanced visualization of the equine foot vasculature in a cadaver model using time-of-flight sequence.

Open Access CRIS of the University of Bern
Peripheral Artery Disease Management
article

Non-contrast enhanced visualization of the equine foot vasculature in a cadaver model using time-of-flight sequence.

article en

Abstract

Objective The objective of this study was to establish a non-contrast enhanced MR angiography (NC-MRA) sequence for the equine foot (EF) using a post-mortem angiography model.Materials And Methods Time-of-flight (TOF) sequences were tested using variable parameter settings and 3 slice orientations during vascular perfusion of frozen-thawed cadaver EF with paraffine oil. Transverse and dorsal orientations were planned perpendicular or parallel to the sublamellar vascular plexus at the dorsal aspect of P3, or approximately perpendicular to the coronary plexus. Visibility of the coronary plexus, sublamellar plexus, palmar plexus, terminal arch and its respective branches, solar plexus, and the marginal circumflex vessels was evaluated in a total of 74 sequences.Results Twelve EF of 10 horses were scanned. Visibility of vessels as small as the sublamellar plexus was best achieved by 3D-TOF sequences in transverse and dorsal orientations with the following parameters: pixel size 0.34 × 0.48 mm, slice thickness 0.2 mm, interslice gap 0.2 mm, TR/TE 21.2/4.7 ms, flip angle 16°, TONE ramp 70%, acquisition time 22.05 min. Only for the sublamellar plexus, the transverse acquisition showed a slightly better visualization than the dorsal acquisition, however the latter could include nearly the entire EF in the field of view with the same acquisition time.Conclusion And Discussion 3D-TOF allowed visualization down to at least the sublamellar venous plexus which is reported to have diameters of approximately 0.45 mm. The post-mortem model facilitated establishment of a TOF sequence without the need for experimental animals.

Open Access CRIS of the University of Bern
Faculty of Public Health (GB), Clinical Research Management (US)
Openalex Percentile: Top 37%
Peripheral Artery Disease Management
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