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Article

Stasis Leg Ulcers: Venous System Revises by Triggered Angiography Non-Contrast-Enhanced Sequence Magnetic Resonance Imaging

1
Department of Diagnostic Radiology, Chang Gung Memorial Hospital, Chang-Gung University, Chiayi 61363, Taiwan
2
Department of Cardiovascular Surgery, Wound and Vascular Center, 6 West Section, Chang Gung Memorial Hospital, Chia-Yi 61363, Taiwan
3
Division of Thoracic and Cardiovascular Surgery, Chiayi Chang Gung Memorial Hospital, College of Medicine Chia-Yi and Chang Gung University, Taoyuan 61363, Taiwan
4
Institute of Imaging and Biomedical Photonics, National Chiao Tung University, Tainan 71150, Taiwan
*
Author to whom correspondence should be addressed.
Diagnostics 2020, 10(9), 707; https://doi.org/10.3390/diagnostics10090707
Received: 31 July 2020 / Revised: 29 August 2020 / Accepted: 15 September 2020 / Published: 17 September 2020
(This article belongs to the Special Issue New Trends in Vascular Imaging)
Objectives: The distribution of venous pathology in stasis leg ulcers is unclear. The main reason for this uncertainty is the lack of objective diagnostic tools. To fill this gap, we assessed the effectiveness of triggered angiography non-contrast-enhanced (TRANCE)-magnetic resonance imaging (MRI) in determining the venous status of patients with stasis leg ulcers. Methods: This prospective observational study included the data of 23 patients with stasis leg ulcers who underwent TRANCE-MRI between April 2017 and May 2020; the data were retrospectively analyzed. TRANCE MRI utilizes differences in vascular signal intensity during the cardiac cycle for subsequent image subtraction, providing not only a venogram but also an arteriogram without the use of contrast agents or radiation. Results: TRANCE MRI revealed that the stasis leg ulcers of nine of the 23 patients could be attributed to valvular insufficiency and venous occlusion (including deep venous thrombosis [DVT], May–Thurner syndrome, and other external compression). Moreover, TRANCE MRI demonstrated no venous pathology in five patients (21.7%). We analyzed TRANCE MRI hemodynamic parameters, namely stroke volume, forward flow volume, backward flow volume, regurgitant fraction, absolute volume, mean flux, stroke distance, and mean velocity, in the external iliac vein, femoral vein, popliteal vein, and great saphenous vein (GSV) in three of the patients with valvular insufficiency and three of those with venous occlusion. We found that the mean velocity and stroke volume in the GSV was higher than that in the popliteal vein in all patients with venous valvular insufficiency. Conclusions: Stasis leg ulcers may have no underlying venous disease and could be confirmed by TRANCE-MRI. TRANCE MRI has good Interrater reliability between Duplex study in greater saphenous venous insufficiency. It also potentially surpasses existing diagnostic modalities in terms of distinguishable hemodynamic figures. Accordingly, TRANCE-MRI is a safe and useful tool for examining stasis leg ulcers and is extensively applied currently. View Full-Text
Keywords: MRI; non-contrast; phase contrast; venography; TRANCE; stasis ulcer; chronic wound MRI; non-contrast; phase contrast; venography; TRANCE; stasis ulcer; chronic wound
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MDPI and ACS Style

Chen, C.-W.; Tseng, Y.-H.; Wong, M.Y.; Wu, C.-M.; Lin, B.-S.; Huang, Y.-K. Stasis Leg Ulcers: Venous System Revises by Triggered Angiography Non-Contrast-Enhanced Sequence Magnetic Resonance Imaging. Diagnostics 2020, 10, 707. https://doi.org/10.3390/diagnostics10090707

AMA Style

Chen C-W, Tseng Y-H, Wong MY, Wu C-M, Lin B-S, Huang Y-K. Stasis Leg Ulcers: Venous System Revises by Triggered Angiography Non-Contrast-Enhanced Sequence Magnetic Resonance Imaging. Diagnostics. 2020; 10(9):707. https://doi.org/10.3390/diagnostics10090707

Chicago/Turabian Style

Chen, Chien-Wei, Yuan-Hsi Tseng, Min Y. Wong, Chao-Ming Wu, Bor-Shyh Lin, and Yao-Kuang Huang. 2020. "Stasis Leg Ulcers: Venous System Revises by Triggered Angiography Non-Contrast-Enhanced Sequence Magnetic Resonance Imaging" Diagnostics 10, no. 9: 707. https://doi.org/10.3390/diagnostics10090707

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