Venous Segmental Flow Changes after Superficial Venous Intervention Demonstrating by Quantitative Phase-Contrast Magnetic Resonance Analysis: Preliminary Data from a Longitudinal Cohort Study
by
,
Chien-Wei Chen
1,2
,
Yuan-Hsi Tseng
3,
Chih-Chen Kao
2,4,5,
Yeh Giin Ngo
2,3,
Chung-Yuan Lee
2,3,
Teng-Yao Yang
2,6,
Yu-Hui Lin
6 and
Yao-Kuang Huang
2,4,5,*,† 1
Department of Diagnostic Radiology, Chia Yi Chang Gung Memorial Hospital, Chiayi 61363, Taiwan
2
College of Medicine, Chang Gung University, Taoyuan 33302, Taiwan
3
Department of Obstetrics and Gynecology, Chia Yi Chang Gung Memorial Hospital, Chiayi 61363, Taiwan
4
Division of Thoracic and Cardiovascular Surgery, Chia Yi Chang Gung Memorial Hospital, Chiayi 61363, Taiwan
5
Division of Thoracic and Cardiovascular Surgery, Chia Yi Hospital, MOHW, Chiayi 61363, Taiwan
6
Cardiology, Chia Yi Chang Gung Memorial Hospital, Chiayi 61363, Taiwan
*
Author to whom correspondence should be addressed.
†
Current address: Department of Cardiovascular Surgery, Chia Yi Chang Gung Memorial Hospital, No. 8, West Section, Jiapu Road., Puzi City, Chiayi 61363, Taiwan.
J. Pers. Med. 2022, 12(6), 1000; https://doi.org/10.3390/jpm12061000
Submission received: 5 April 2022
/
Revised: 11 June 2022
/
Accepted: 16 June 2022
/
Published: 19 June 2022
(This article belongs to the Special Issue Chronic Vascular Disease and Personalized Medicine: Unraveling New Horizons)
Abstract
:The effects of superficial venous intervention on hemodynamics can be quantified using two-dimensional phase-contrast magnetic resonance imaging (2D PC-MRI). Twelve patients received pre- and postintervention 2D PC-MRI analysis using quantitative hemodynamic parameters. Fifteen healthy volunteers served as controls. The 2D PC-MRI results of the target limbs (limbs scheduled for intervention for venous reflux) differed from those of the controls in terms of stroke volume (SV), forward flow volume (FFV), absolute stroke volume (ASV), and mean flux (MF) in all venous segments. The velocity time integral (VTI) and mean velocity (MV) of the popliteal vein (PV) segments were similar between the target limbs and controls preoperatively. After intervention, the target limbs exhibited an increase in VTI and MV in the femoral vein (FV) and PV segments. We compared the target and nontreated limbs of the individual patients preoperatively and postoperatively to minimalize individual bias. All QFlow parameter ratios in the FV segment increased after venous intervention (VTI, p = 0.025; MV, p = 0.024). In the PV segment, FFV and ASV increased significantly (p = 0.035 and 0.024, respectively). After interventions, the volume (FFV and ASV) of the PV segment and the efficiency (VTI and MV) of the FV segment significantly increased.
1. Introduction
Few objective diagnostic modalities for venous disorders are currently available. The magnetic resonance angiography (MRA) using gated three-dimensional (3D) turbo spin-echo short tau inversion recovery (TSE-STIR) sequence has been used to diagnose leg venous diseases since 2017 and was demonstrated to be efficacious in combination with ultrasonography (US) in a preliminary report [1,2,3]. The morphology of the entire venous anatomy of lower extremities, particularly that of the low-flow superficial venous system and pelvic collaterals in various diseases, can be observed through 3D imaging without a contrast medium or radiation [4,5]. Gated 3D-TSE-STIR MRA combing with hemodynamic analysis, by using two-dimensional (2D) phase-contrast (PC) magnetic resonance imaging (MRI) scanning, has been the standard preoperative evaluation method for the venous diseases of the legs at our institution [4,5,6,7,8,9,10]. In this study, we explored the role of 2D PC-MRI quantitative analysis plus gated 3D-TSE-STIR MRA in managing leg venous diseases and investigated the hemodynamic effects of superficial venous interventions involving the truncal ablation of the diseased great saphenous vein.
2. Materials and Methods
2.1. Patients
The Institutional Review Board of Chang Gung Memorial Hospital approved this study (numbers 201802137B0, 201901058B0, and 202100938B0). This study enrolled consecutive patients evaluated for the venous pathology of their lower extremities through non-contrast MRI, including gated 3D-TSE-STIR MRA and 2D PC-MRI scanning, at a tertiary hospital between April 2017 and October 2021. We prospectively collected and retrospectively analyzed their clinical data. All patients were suspected to have venous pathology in their lower extremities. Initially, 271 patients (including 15 healthy volunteers) were evaluated, and 21 patients were excluded. The exclusion criteria were being pregnant, having restless legs, having extreme arrhythmia, being morbidly obese, and having ferromagnetic devices incompatible with MRI. In the remaining 250 patients, anatomic evaluation was performed using gated 3D-TSE-STIR MRA and hemodynamic evaluation was performed using 2D PC-MRI quantitative analysis. On the basis of their symptoms and MRI schedule indication, the 250 patients were divided into five groups, namely superficial venous varicose with venous reflux, stasis leg ulcers, swollen legs favoring venous occlusion, other presentation, and healthy volunteers (Figure 1). According to the 2D PC-MRI analysis, 116 patients had venous reflux in their legs. A total of 60 patients received superficial venous interventions and 12 underwent postintervention gated 3D-TSE-STIR MRA plus 2D PC-MRI analysis.
2.2. MRI Acquisition and Phase-Contrast Hemodynamic Analysis
MRI was performed using a 1.5 T MRI scanner (Philips Ingenia, Philips Healthcare, Best, The Netherlands). During the examination, the patient must be equipped with an electrocardiography detector and a respiration detector. Technicians use the gating method to detect the heart rhythm and then use the heart synchronization method to obtain MRI images in the supine position (Figure 2). Gated 3D-TSE-STIR MRA imaging was performed using the following parameters: repetition time, 1 beat; echo time, 85 ms; inversion recovery delay time, 160 ms; voxel size, 1.7 mm × 1.7 mm × 4 mm; and field of view, 360 mm × 320 mm. STIR provides extra background suppression because of the additional suppression of the fat and bones. When systolic triggering was applied, the arteries appeared black. The imaging process yielded a 3D data set of the venous system. A trans-axial PC-MRI scan was routinely performed at the aortic bifurcation level to determine the triggering time for imaging acquisition. Hemodynamic analysis using 2D PC-MRI scanning was performed by the following parameters: repetition time, shortest; echo time, shortest; flip angle, 20 degrees; 25 im-ages/period; acquisition matrix, 324 × 324; slice thickness, 5 mm; pixel size, 0.33 mm × 0.33 mm; and velocity encoding, 80 cm/s. Trans-axial scanning of 2D PC-MRI was performed at the venous segments, including the inferior vena cava, external iliac veins (EIVs), femoral vein (FV), popliteal vein (PV), and great saphenous veins (GSV). By drawing the region of interest (ROI) on the vascular lumens (covering the whole lumen), the hemodynamic parameters will be generated by measuring the phase-shifting information of voxels within the ROI. All of the hemodynamic parameters are shown as follows: stroke volume (SV: the net volume of blood that passes through the contour of ROI during one heartbeat), forward flow volume (FFV: the volume of blood that passes through the contour of ROI in the positive direction (toward head direction) during one heartbeat), absolute stroke volume (ASV: the absolute value of forwarding flow volume plus the absolute value of backward flow volume), mean flux (MF: stroke amount × heartbeat/60 (one-heartbeat)), velocity time integral (VTI, also known as stroke distance: the net distance that blood proceeds in the vessel during one heartbeat), and mean velocity (MV: stroke distance × heartbeat/60 (one-heartbeat)). The whole process of non-contrast MRI requires 25 min for imaging acquisition, reconstructing imaging, and hemodynamic analysis.
2.3. Statistical Analysis
Continuous variables (age and hemodynamic parameters) were analyzed using an unpaired two-tailed Student’s t test or one-way analysis of variance, and discrete variables (sex, substance usage, comorbidities, and intervention history) were compared using a two-tailed Fisher’s exact test. All statistical analyses were performed using Stata statistics and data analysis (version 8.0; Stata Corporation, College Station, TX, USA). The results are presented as means and standard deviations. Statistical significance was defined as p < 0.05.
3. Results
A total of 60 patients received superficial venous interventions and 12 received postintervention gated 3D-TSE-STIR MRA plus 2D PC-MRI analysis. Table 1 lists the sex, age, comorbidities, morbid leg, Clinical–Etiology–Anatomy–Pathophysiology classification, preop venous clinical severity score (VCSS), wound status, and interventions of the 12 patients. Four patients presented at the clinic with static leg ulcers, and their VCSS ranged from 7 to 20. They all had primary reflux limited to the superficial leg veins and received unilateral truncal ablation by either radiofrequency, laser (Wolf ARC catheters), or cyanoacrylate ablation (VenaSeal). The 12 patients underwent 2D PC-MRI analysis pre-operatively and then received a second 2D PC-MRI analysis from the third to sixth months after the superficial venous intervention. The 15 healthy volunteers received 2D PC-MRI analysis as the control.
3.1. Comparison between Target Limbs and Health Control by 2D PC-MRI Quantitative Analysis: Preintervention and Postintervention
The target limbs with venous reflux exhibited different 2D PC-MRI patterns from those of the healthy controls in terms of SV, forward flow volume (FFV), ASV, and MF in all venous segments (Table 2).
The VTI and MV of the PV segment were similar between the target limbs and those of the healthy controls preoperatively. After intervention, the treated limbs exhibited increased VTI and MV in the FV/PV segment, and the difference between the treated limbs and healthy controls was significant (Table 3).
3.2. Ratio of Target Limb to Nontreated Limb in Each Individual: Effects of Venous Intervention
To minimalize individual bias, we compared the targeted and nontreated limbs of the individual patients preoperatively and postoperatively (Table 4). The EIV segment differed in terms of all 2D PC-MRI parameter ratios (targeted limbs to nontreated limbs) after venous intervention. All 2D PC-MRI parameter ratios (SV, FFV, ASV, MF, VTI, and MV) in the FV segment increased after venous intervention, and VTI (p = 0.025) and MV (p = 0.024) increased significantly. In the PV segment, the SV ratio increased (p = 0.058) and FFV and ASV increased significantly (p = 0.035 and 0.024, respectively). The MF, VTI, and MV ratio in the PV segment increased after intervention (p = 0.059, 0.08, and 0.082, respectively). All 2D PC-MRI parameter ratios decreased significantly in the GSV segments, indicating the effectiveness of ablation.
4. Discussion
Arterial disorders, such as occlusion and aneurysmal changes, are easily diagnosed and treated. Unlike arterial lesions, venous disorders are complex, have slow therapeutic responses, and often present as a sentinel of neoplasm, hypercoagulation, infection, and autoimmune disorders. Superficial venous reflux, mostly involving GSV reflux, is the most frequent form of venous insufficiency in symptomatic patients and is often responsible for varicose veins and stasis ulcers of the lower extremities. The introduction of endovenous techniques almost 20 years ago changed the treatment of varicose veins [11,12,13]. Minimally invasive technology, such as segmental radiofrequency, hemoglobin-specific lasers, water-specific lasers, endovenous steam, and mechanochemical and cyanoacrylate ablation, has been proven to be safe and is becoming more popular than the standard surgical method (high ligation and stripping) [11,14,15,16,17,18,19].
By contrast, with advancements in the minimally invasive techniques of venous surgery, little progress has been made in terms of diagnostic methods. In addition, no objective tool for the assessment of the post-venous intervention of the lower limbs is currently available [20]. US is a frequently used tool for the initial diagnosis of venous diseases of the legs and to assess the results of venous intervention. However, it is operator dependent and provides minimal information regarding the pelvic area. Conventional venography is the first objective tool for the detection of venous lesions; however, its invasiveness prevents its widespread use. Computed tomography (CT) venography is useful for the exclusion of pulmonary embolism in patients with signs of thrombosis in the legs and abdominal lesions, but it cannot replace US for the detection of deep venous thrombosis in the legs [21,22]. Injected contrast media are often unevenly distributed through the venous system during CT venogram acquisition. In CT venography, contrast media are injected into morbid limbs to optimize venous image quality, which may harm morbid legs.
Numerous MRA techniques are used to reconstruct vascular structures. Developed in 1998, time-of-flight MRA was the earliest technique for evaluating arterial pathology [23]. However, it requires considerable time to produce an entire image of the lower extremity and has thus become less clinically applicable [24,25,26]. MRA with gadolinium-based contrast media is a rapid method of imaging the lower extremities [27,28]. However, gadolinium-based contrast media might cause nephrogenic sclerosing fibrosis [29,30]. The gated 3D-TSE MRA technique, which is used to identify differences in the vascular signal intensity during the cardiac cycle through image subtraction, was first applied in 1985 [31]. Gated 3D-TSE MRA has frequently been used to diagnose cranial neurologic diseases and most arterial diseases; however, it has few known applications for venous pathology and particularly for the lower extremities [32,33,34,35]. We demonstrated that gated 3D-TSE-STIR MRA, plus the STIR sequence to provide additional background subtraction of bone and soft tissue, offers several advantages in evaluating lower extremity venous pathology. First, it provides an objective 3D model of the venous morphology, including the pelvis and caves. Second, it does not require venipuncture, radiation, or contrast medium injection. Third, as this study demonstrated, hemodynamics can be recorded and evaluated when required.
We evaluated legs with venous reflux scheduled for GSV truncal ablation (target legs) through gated 3D-TSE-STIR MRA plus 2D PC-MRI scanning and compared the resulting data with those of healthy controls. The target legs exhibited higher SV, FFV, ASV, and MF values in all venous segments, which is consistent with our previous findings (Table 2). VTI and MV were higher in the GSV segments of the target limbs (p = 0.055 and 0.044, respectively) but similar in the PV segments (p = 0.223 and 0.201, respectively). After truncal ablation, the VTI and MV in the PV segment of target limbs became higher than those of the controls (p = 0.001 and 0.001, respectively; Table 3). These results suggest that increasing the volume may lead to more efficient and faster transport though the PV after ablation of the diseased GSV. We compared the target and nontreated limbs of the individual patients preoperatively and postoperatively to minimalize individual bias (Table 4). We observed that the FFV and ASV increased significantly in the PV segment after intervention (p = 0.035 and 0.024, respectively), with similar FFV and ASV values in the EIV segments. VTI and MV increased in the FV segment more than they did in the PV segment (p = 0.025 and 0.024 vs. p = 0.08 and 0.082, respectively). These results indicate faster and more efficient volume transport though the FV segments after the intervention. A less significant increase in VTI and MV in the PV segment suggests higher complexity in the pathophysiology of the interaction between the perforator veins and lessor saphenous systems.
We used gated 3D-TSE-STIR MRA and 2D PC-MRI quantitative analysis to manage patients receiving scheduled truncal ablation for superficial venous reflux. We compared 2D PC-MRI patterns among the target limbs, nontarget limbs, and the limbs of the healthy controls after intervention. The 2D PC-MRI parameters were higher in the target limbs with reflux than in those of the healthy controls. The volume (FFV and ASV) of the PV segment and the efficiency (VTI and MV) of the FV segment increased significantly after superficial venous reflux intervention.
There are several technical issues of 2D PC-MRI to be discussed. First, this study proposes an application of 2D PC-MRI in lower extremity venous disease, which is still poorly reported and not widely understood. This study performed hemodynamic analysis using 2D PC-MRI scanning on axial planes of the venous segments. By drawing the region of interest (ROI) on the vascular lumens (covering the whole lumen), the hemodynamic parameters will be generated by measuring the phase-shifting information of voxels within the ROI. When using quantitative 2D PC-MRI analysis for evaluating the superficial venous system, stroke volume reflects the net volume of blood that passes through the contour of ROI during one heartbeat. As well as that, forward flow volume reflects the volume of blood that passes through the contour of ROI only in the positive direction (toward the head direction) during one heartbeat. Second, venous flow is phasic, frequently a combination of cardiac and respiratory cycles. Making acquisitions during a cardiac cycle may give a random value. To determine the correct time during the repeat processes for imaging acquisition, technicians use the gating method to detect the heart and respiratory cycles. Thus, MRI data from the consistent phase can be acquired. Another issue is that venous flow is sensitive to muscle contractions, especially in the popliteal vein. In our experience, in most cases, the lower extremity venous system can be imaged clearly by MRI in the supine position without being affected by muscle contractions. Our MRI protocol adopts the supine position because this position is often used as the standard position for imaging acquisitions. In our experience, the entire venous system of the lower extremities can be displayed clearly without being affected by muscle contractions in most cases. Third, beyond the presented result, we performed the statistical analysis to compare the difference between the target limb and the contralateral leg during the initial investigation. However, our data showed no significant difference between the target limb and the contralateral leg. We suspect it may be due to some subjects having venous reflux in both legs. Thus, we compared the differences between the diseased leg and the healthy controls and between the diseased leg and the treated leg.
Study Limitations
The major limitations of this study are its nonrandomized design and small sample size. Although we performed the MRI on 271 subjects, only 12 subjects completed the postintervention MRI. Larger sample sizes, long follow-up intervals for clinical correlations, and a randomized study design may provide more solid results.
5. Conclusions
Gated 3D-TSE-STIR MRA plus 2D PC-MRI quantitative analysis is helpful in venous disorders and has a novel application in postop hemodynamic records after venous intervention. After the truncal ablation of the diseased GSV, the volume (FFV and ASV) of the PV segment and the efficiency (VTI and MV) of the FV segment increased significantly.
6. Patents
Invention I740594 in the Taiwan Intellectual property Office, from 21 September 2021 to 3 August 2040.
Supplementary Materials
The following are available online at https://www.mdpi.com/article/10.3390/jpm12061000/s1, Video S1: Pre-op and Post-op evaluation of venous ulcer by quantitative phase contrast MRI.
Author Contributions
Conception and design: Y.-K.H. and C.-W.C.; analysis and interpretation: Y.-K.H., C.-W.C., C.-C.K. and Y.G.N.; data collection: C.-W.C., Y.-H.T., C.-Y.L. and T.-Y.Y.; writing the article: Y.-K.H. and C.-W.C.; statistical analysis: C.-W.C. and Y.-H.L.; overall responsibility: Y.-K.H. and C.-W.C. All authors have read and agreed to the published version of the manuscript.
Funding
This study was supported by Chang Gung Memorial Hospital (Contract Nos. CORPG6G0091, CORPG6G0092, CORPG6D0292, CMRPG6K0341, CMRPG6K0342, CMRPG6L0351).
Institutional Review Board Statement
The Institutional Review Board (IRB) of Chang Gung Memorial Hospital approved this study (numbers 201802137B0, 201901058B0, and 202100938B0).
Informed Consent Statement
Informed consent was obtained from all subjects involved in the study.
Data Availability Statement
The data presented in this study are available on request from the corresponding author. The data are not publicly available due to ethical restrictions.
Acknowledgments
We acknowledge Wallace Academic.
Conflicts of Interest
The authors declare no conflict of interest.
Abbreviations
| 2D | two-dimensional |
| 3D | three-dimensional |
| ASV | absolute stroke volume |
| CT | computed tomography |
| CTA | computed tomography angiography |
| DVT | deep venous thrombosis |
| EIV | external iliac vein |
| FFV | forward flow volume |
| FOV | field of view |
| FV | femoral vein |
| GSV | great saphenous vein |
| IR | inversion recovery |
| IRB | institutional review board |
| MF | mean flux |
| MRA | magnetic resonance angiography |
| MRI | magnetic resonance imaging |
| MV | mean velocity |
| PC | phase-contrast |
| PV | popliteal vein |
| STIR | short tau inversion recovery |
| SV | stroke volume |
| TOF | time-of-flight |
| TSE | turbo spin-echo |
| VTI | velocity time integral |
References
- Huang, Y.K.; Tseng, Y.H.; Lin, C.H.; Tsai, Y.H.; Hsu, Y.C.; Wang, S.C.; Chen, C.W. Evaluation of venous pathology of the lower extremities with triggered angiography non-contrast-enhanced magnetic resonance imaging. BMC Med. Imaging 2019, 19, 96. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Hsu, Y.C.; Huang, Y.K.; Hsu, L.S.; Chen, P.Y.; Chen, C.W. Using non-contrast-enhanced magnetic resonance venography for the evaluation of May-Thurner syndrome in patients with renal insufficiency: A case report. Medicine 2019, 98, e18427. [Google Scholar] [CrossRef] [PubMed]
- Chen, C.W.; Ting, H.; Chen, P.Y.; Weng, J.C.; Hsu, Y.C.; Wang, S.C.; Tseng, Y.H.; Huang, Y.K. Usefulness of triggered non-contrast-enhanced magnetic resonance angiography in assessing lower extremity venous disease. Medicine 2021, 100, e25809. [Google Scholar] [CrossRef] [PubMed]
- 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. [Google Scholar] [CrossRef]
- Chen, C.W.; Tseng, Y.H.; Lin, C.C.; Kao, C.C.; Wong, M.Y.; Lin, B.S.; Huang, Y.K. Novel Diagnostic Options without Contrast Media or Radiation: Triggered Angiography Non-Contrast-Enhanced Sequence Magnetic Resonance Imaging in Treating Different Leg Venous Diseases. Diagnostics 2020, 10, 355. [Google Scholar] [CrossRef]
- Chen, C.W.; Tseng, Y.H.; Fang, Y.F.; Wong, M.Y.; Lin, Y.H.; Huang, Y.K. Superficial Venous Reflux Intervention Guided by Triggered Angiography Non-Contrast-Enhanced Sequence Magnetic Resonance Imaging: Different QFlow Pattern from Health Controls. J. Pers. Med. 2021, 11, 751. [Google Scholar] [CrossRef]
- Tseng, Y.H.; Chen, C.W.; Wong, M.Y.; Yang, T.Y.; Lin, B.S.; Ting, H.; Huang, Y.K. Discriminating Reflux from Non-Reflux Diseases of Superficial Veins in Legs by Novel Non-Contrast MR with QFlow Technique. J. Pers. Med. 2021, 11, 242. [Google Scholar] [CrossRef]
- Tseng, Y.H.; Chen, C.W.; Wong, M.Y.; Yang, T.Y.; Lin, Y.H.; Lin, B.S.; Huang, Y.K. Reduced External Iliac Venous Blood Flow Rate Is Associated with Asymptomatic Compression of the Common Iliac Veins. Medicina 2021, 57, 835. [Google Scholar] [CrossRef]
- Chen, C.W.; Fang, Y.F.; Tseng, Y.H.; Wong, M.Y.; Lin, Y.H.; Hsu, Y.C.; Lin, B.S.; Huang, Y.K. A Novel Tool for a Challenging Disease: Stasis Leg Ulcers Assessed Using QFlow in Triggered Angiography Noncontrast Enhanced Magnetic Resonance Imaging. J. Pers. Med. 2021, 11, 857. [Google Scholar] [CrossRef]
- Lin, B.S.; Chen, C.W.; Zhou, S.K.; Tseng, Y.H.; Wang, S.C.; Huang, Y.K. Evaluation of static ulcer on lower extremities using wireless wearable near-infrared spectroscopy device: Effect of deep venous thrombosis on TRiggered Angiography Non-Contrast-Enhanced sequence magnetic resonance imaging. Phlebology 2020, 35, 814–823. [Google Scholar] [CrossRef]
- Kursat Bozkurt, A.; Lawaetz, M.; Danielsson, G.; Lazaris, A.M.; Pavlovic, M.; Olariu, S.; Rasmussen, L. European College of Phlebology guideline for truncal ablation. Phlebology 2020, 35, 73–83. [Google Scholar] [CrossRef] [PubMed]
- Nijsten, T.; van den Bos, R.R.; Goldman, M.P.; Kockaert, M.A.; Proebstle, T.M.; Rabe, E.; Sadick, N.S.; Weiss, R.A.; Neumann, M.H. Minimally invasive techniques in the treatment of saphenous varicose veins. J. Am. Acad. Dermatol. 2009, 60, 110–119. [Google Scholar] [CrossRef] [PubMed]
- Gonzalez-Zeh, R.; Armisen, R.; Barahona, S. Endovenous laser and echo-guided foam ablation in great saphenous vein reflux: One-year follow-up results. J. Vasc. Surg. 2008, 48, 940–946. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Woodburn, K.R. Endothermal ablation for the treatment of clinically significant incompetent lower limb perforating veins: Factors influencing the early outcomes. Phlebology 2021, 36, 127–134. [Google Scholar] [CrossRef]
- O’Banion, L.A.; Reynolds, K.B.; Kochubey, M.; Cutler, B.; Tefera, E.A.; Dirks, R.; Kiguchi, M.M. A comparison of cyanoacrylate glue and radiofrequency ablation techniques in the treatment of superficial venous reflux in CEAP 6 patients. J. Vasc. Surg. Venous Lymphat. Disord. 2021, 9, 1215–1221. [Google Scholar] [CrossRef] [PubMed]
- Dimech, A.P.; Cassar, K. Efficacy of Cyanoacrylate Glue Ablation of Primary Truncal Varicose Veins Compared to Existing Endovenous Techniques: A Systematic Review of the Literature. Surg. J. 2020, 6, e77–e86. [Google Scholar] [CrossRef]
- Aherne, T.M.; Ryan, E.J.; Boland, M.R.; McKevitt, K.; Hassanin, A.; Tubassam, M.; Tang, T.Y.; Walsh, S. Concomitant vs. Staged Treatment of Varicose Tributaries as an Adjunct to Endovenous Ablation: A Systematic Review and Meta-Analysis. Eur. J. Vasc. Endovasc. Surg. 2020, 60, 430–442. [Google Scholar] [CrossRef]
- Garcia-Madrid, C.; Pastor Manrique, J.O.; Gomez-Blasco, F.; Sala Planell, E. Update on endovenous radio-frequency closure ablation of varicose veins. Ann. Vasc. Surg. 2012, 26, 281–291. [Google Scholar] [CrossRef]
- Feliciano, B.A.; Dalsing, M.C. Varicose vein: Current management. Adv. Surg. 2011, 45, 45–62. [Google Scholar] [CrossRef]
- Nelzen, P.O.; Skoog, J.; Lassvik, C.; Lanne, T.; Zachrisson, H. Prediction of Post-interventional Outcome in Great Saphenous Vein Incompetence: The Role of Venous Plethysmography with Selective Superficial Vein Occlusion. Eur. J. Vasc. Endovasc. Surg. 2016, 52, 377–384. [Google Scholar] [CrossRef] [Green Version]
- Ciccotosto, C.; Goodman, L.R.; Washington, L.; Quiroz, F.A. Indirect CT venography following CT pulmonary angiography: Spectrum of CT findings. J. Thorac. Imaging 2002, 17, 18–27. [Google Scholar] [CrossRef] [PubMed]
- Duwe, K.M.; Shiau, M.; Budorick, N.E.; Austin, J.H.; Berkmen, Y.M. Evaluation of the lower extremity veins in patients with suspected pulmonary embolism: A retrospective comparison of helical CT venography and sonography. 2000 ARRS Executive Council Award I. American Roentgen Ray Society. Am. J. Roentgenol. 2000, 175, 1525–1531. [Google Scholar] [CrossRef] [PubMed]
- Yucel, E.K.; Kaufman, J.A.; Geller, S.C.; Waltman, A.C. Atherosclerotic occlusive disease of the lower extremity: Prospective evaluation with two-dimensional time-of-flight MR angiography. Radiology 1993, 187, 637–641. [Google Scholar] [CrossRef]
- Suttmeyer, B.; Teichgraber, U.; Thomas, A.; Rathke, H.; Albrecht, L.; Jonczyk, M.; Verba, M.; Guttler, F.; Schnackenburg, B.; Hamm, B.; et al. Non-invasive ECG-triggered 2D TOF MR angiography of the pelvic and leg arteries in an open 1.0-tesla high-field MRI system in comparison to conventional DSA. Biomed. Tech. Biomed. Eng. 2014, 59, 29–37. [Google Scholar] [CrossRef] [PubMed]
- Harigai, M.; Okada, T.; Umeoka, S.; Nagayama, S.; Tanaka, E.; Fujimoto, K.; Kido, A.; Takeda, K.; Togashi, K.; Sakai, Y. Non-contrast-enhanced MR venography of the upper limb: A comparative study of acquisitions with fresh blood imaging vs. time-of-flight methods. Clin. Imaging 2012, 36, 496–501. [Google Scholar] [CrossRef] [PubMed]
- Steffens, J.C.; Link, J.; Schwarzenberg, H.; Mueller-Huelsbeck, S.; Brinkmann, G.; Heller, M. Lower extremity occlusive disease: Diagnostic imaging with a combination of cardiac-gated 2D phase-contrast and cardiac-gated 2D time-of-flight MRA. J. Comput. Assist. Tomogr. 1999, 23, 7–12. [Google Scholar] [CrossRef] [PubMed]
- Gurel, K.; Gurel, S.; Karavas, E.; Buharalioglu, Y.; Daglar, B. Direct contrast-enhanced MR venography in the diagnosis of May-Thurner syndrome. Eur. J. Radiol. 2011, 80, 533–536. [Google Scholar] [CrossRef] [PubMed]
- Ruehm, S.G.; Zimny, K.; Debatin, J.F. Direct contrast-enhanced 3D MR venography. Eur. Radiol. 2001, 11, 102–112. [Google Scholar] [CrossRef]
- Alfano, G.; Fontana, F.; Ferrari, A.; Solazzo, A.; Perrone, R.; Giaroni, F.; Torricelli, P.; Cappelli, G. Incidence of nephrogenic systemic fibrosis after administration of gadoteric acid in patients on renal replacement treatment. Magn. Reason. Imaging 2020, 70, 1–4. [Google Scholar] [CrossRef]
- Schieda, N.; Maralani, P.J.; Hurrell, C.; Tsampalieros, A.K.; Hiremath, S. Updated Clinical Practice Guideline on Use of Gadolinium-Based Contrast Agents in Kidney Disease Issued by the Canadian Association of Radiologists. Can. Assoc. Radiol. J. 2019, 70, 226–232. [Google Scholar] [CrossRef] [Green Version]
- Meuli, R.A.; Wedeen, V.J.; Geller, S.C.; Edelman, R.R.; Frank, L.R.; Brady, T.J.; Rosen, B.R. MR gated subtraction angiography: Evaluation of lower extremities. Radiology 1986, 159, 411–418. [Google Scholar] [CrossRef] [PubMed]
- Gutzeit, A.; Sutter, R.; Froehlich, J.M.; Roos, J.E.; Sautter, T.; Schoch, E.; Giger, B.; Wyss, M.; Graf, N.; von Weymarn, C.; et al. ECG-triggered non-contrast-enhanced MR angiography (TRANCE) versus digital subtraction angiography (DSA) in patients with peripheral arterial occlusive disease of the lower extremities. Eur. Radiol. 2011, 21, 1979–1987. [Google Scholar] [CrossRef] [PubMed]
- Khan, F.; Seyam, M.; Sharma, N.; Ud Din, M.; Bansal, V. New Horizons for Diagnostic Pitfalls of Cerebral Venous Thrombosis: Clinical Utility of a Newly Developed Cerebral Venous Thrombosis Diagnostic Score: A Case Report and Literature Review. Am. J. Case Rep. 2021, 22, e932123. [Google Scholar] [CrossRef] [PubMed]
- Spadaro, A.; Scott, K.R.; Koyfman, A.; Long, B. Cerebral venous thrombosis: Diagnosis and management in the emergency department setting. Am. J. Emerg. Med. 2021, 47, 24–29. [Google Scholar] [CrossRef]
- Algin, O.; Koc, U.; Yalcin, N. Cerebrospinal fluid velocity changes of idiopathic scoliosis: A preliminary study on 3-T PC-MRI and 3D-SPACE-VFAM data. Child’s Nerv. Syst. 2021, 38, 379–386. [Google Scholar] [CrossRef]
Figure 1.
Cohorts of the study.
Figure 2.
Typical stasis leg ulcer with venous reflux in the gaiter area (Also seen in Video S1). (A) Wet and nonhealing stasis leg ulcer. Black Arrow: unhealed venous ulcer with cellulitis. (B) Preintervention: The gated 3D-TSE-STIR MRA demonstrates the venous anatomy both leg veins. The white arrow indicates the diseased great saphenous vein of the wounded leg. (C) Postintervention: gated 3D-TSE-STIR MRA. The red arrow indicates the diseased great saphenous vein occluded. (D) Stasis leg ulcer healed after truncal ablation. Gated 3D-TSE-STIR MRA for venous systems. Black arrow: healed ulcers.
Figure 2.
Typical stasis leg ulcer with venous reflux in the gaiter area (Also seen in Video S1). (A) Wet and nonhealing stasis leg ulcer. Black Arrow: unhealed venous ulcer with cellulitis. (B) Preintervention: The gated 3D-TSE-STIR MRA demonstrates the venous anatomy both leg veins. The white arrow indicates the diseased great saphenous vein of the wounded leg. (C) Postintervention: gated 3D-TSE-STIR MRA. The red arrow indicates the diseased great saphenous vein occluded. (D) Stasis leg ulcer healed after truncal ablation. Gated 3D-TSE-STIR MRA for venous systems. Black arrow: healed ulcers.
Table 1.
Demographic data of the 12 patients have TRANCE MR venous mapping pre and post interventions.
Table 1.
Demographic data of the 12 patients have TRANCE MR venous mapping pre and post interventions.
| No | Age | Sex | Comorbidities | Target Legs | Main Symptoms | C in CEAP | E in CEAP | A in CEAP | P in CEAP | Wound Location | VCSS | Surgical Intervention |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | 59 | F | DM | Left | Wound | C6 | Ep | GSVa, GSVb, SSV, CPV | Pr | gaiter area | 19 | A.R.C catheter ablation |
| 2 | 50 | M | Nil | Right | Wound | C6 | Ep | GSVa, GSVb | Pr | gaiter area | 13 | A.R.C catheter ablation |
| 3 | 48 | F | Nil | Left | pain, swelling | C5 | Ep | GSVa, GSVb | Pr | nil | 10 | A.R.C catheter ablation |
| 4 | 61 | F | Cervix cancer | Left | pain, claudication | C5 | Ep | GSVa, GSVb, LSV | Pr | nil | 9 | Atoven cathter ablation, sclerotherapy |
| 5 | 55 | F | Cholesteremia, Hepatitis B | Left | pain, swelling, mild skin hyperpigmentation | C5 | Ep | GSVa, GSVb | Pr | nil | 7 | A.R.C catheter ablation |
| 6 | 56 | F | Hypertension, tongue SCC | Left | swelling | C5 | Ep | GSV, LSV | Pr | nil | 10 | A.R.C catheter ablation |
| 7 | 65 | F | Nil | Left | cramping pain, heat | C5 | Ep | GSVa, GSVa, GSVbLSV | Pr | nil | 7 | Venaseal |
| 8 | 59 | F | Nil | Right | red swelling, itchy patches | C5 | Ep | GSVa, GSVb | Pr | nil | 7 | Venaseal |
| 9 | 43 | M | DM, Hypertension | Right | Wound, pain | C6 | Ep | GSVa, GSVb, LSV | Pr | gaiter area | 17 | A.R.C catheter ablation |
| 10 | 72 | F | DM, Hypertension | Left | swelling | C5 | Ep | GSVa, GSVb, LSV | Pr | nil | 10 | A.R.C catheter ablation |
| 11 | 59 | M | Nil | Left | cramping | C5 | Ep | GSVa, GSVb | Pr | nil | 8 | Atoven catheter ablation, sclerotherapy |
| 12 | 65 | F | Renal insufficiency, DM, Hypertension, Hepatitis C | Right | Wound, pain | C6 | Ep | GSV, SSV | Pr | gaiter | 20 | A.R.C catheter ablation |
AASV: anterior accessory saphenous vein; CEAP: Clinical-Etiology-Anatomy-Pathophysiology; CHF: congestive heart failure; CPV: calf perforator vein; CVA: cerebral vascular accident; DM: diabetes mellitus; F: female; HTN: hypertension; GSVa: great saphenous vein above knee; GSVb: great saphenous vein below knee; M: male; MR: mitral regurgitation; SSV: short saphenous vein.
Table 2.
Hemodynamics parameter between target limb (before intervention) and healthy controls.
| QFlow | Segments | Target Limb before Interventions | Heathy Controls | p Value | ||
|---|---|---|---|---|---|---|
| Mean | SD | Mean | SD | |||
| Stroke volume (SV), mL | ||||||
| EIV | 5.898 | 2.200 | 3.751 | 1.386 | < 0.001 | |
| FV | 1.728 | 0.801 | 1.124 | 0.511 | 0.004 | |
| PV | 1.095 | 0.446 | 0.602 | 0.338 | < 0.001 | |
| GSV | 0.936 | 0.518 | 0.310 | 0.219 | 0.001 | |
| Forward flow volume (FFV), mL | ||||||
| EIV | 5.932 | 2.172 | 3.872 | 1.506 | 0.001 | |
| FV | 1.731 | 0.797 | 1.139 | 0.505 | 0.004 | |
| PV | 1.102 | 0.441 | 0.614 | 0.331 | < 0.001 | |
| GSV | 0.941 | 0.513 | 0.321 | 0.209 | 0.001 | |
| Absolute stroke volume (ASV), mL | ||||||
| EIV | 5.956 | 2.154 | 4.022 | 1.602 | 0.002 | |
| FV | 1.734 | 0.792 | 1.155 | 0.502 | 0.005 | |
| PV | 1.108 | 0.437 | 0.625 | 0.325 | < 0.001 | |
| GSV | 0.947 | 0.507 | 0.334 | 0.199 | 0.001 | |
| Mean flux (MF), mL/s | ||||||
| EIV | 6.641 | 2.958 | 4.144 | 1.752 | 0.015 | |
| FV | 1.979 | 1.019 | 1.224 | 0.604 | 0.003 | |
| PV | 1.223 | 0.544 | 0.661 | 0.401 | < 0.001 | |
| GSV | 1.037 | 0.524 | 0.336 | 0.240 | 0.001 | |
| Velocity time integral (VTI), cm | ||||||
| EIV | 6.653 | 2.114 | 3.856 | 1.764 | < 0.001 | |
| FV | 4.190 | 2.219 | 3.004 | 1.677 | 0.057 | |
| PV | 1.464 | 0.948 | 1.154 | 0.704 | 0.233 | |
| GSV | 2.768 | 1.853 | 1.570 | 1.256 | 0.055 | |
| Mean velocity (MV), cm/s | ||||||
| EIV | 7.288 | 2.123 | 12.630 | 49.991 | 0.715 | |
| FV | 4.694 | 2.574 | 3.251 | 1.859 | 0.040 | |
| PV | 1.611 | 1.094 | 1.241 | 0.765 | 0.201 | |
| GSV | 3.088 | 2.088 | 1.669 | 1.272 | 0.044 | |
EIV: external iliac vein; GSV: great saphenous vein; FV: femoral vein; PV: popliteal vein.
Table 3.
Hemodynamics parameter between target limb (after intervention) and healthy controls.
| QFlow | Segments | Target Limb after Interventions | Heathy Cotrols | p Value | ||
|---|---|---|---|---|---|---|
| Mean | SD | Mean | SD | |||
| Stroke volume (SV), mL | ||||||
| EIV | 6.334 | 2.093 | 3.751 | 1.386 | < 0.001 | |
| FV | 2.671 | 1.560 | 1.124 | 0.511 | 0.006 | |
| PV | 1.750 | 0.928 | 0.602 | 0.338 | 0.001 | |
| GSV | 0.054 | 0.070 | 0.310 | 0.219 | < 0.001 | |
| Forward flow volume (FFV), mL | ||||||
| EIV | 6.413 | 2.025 | 3.872 | 1.506 | < 0.001 | |
| FV | 2.843 | 1.360 | 1.139 | 0.505 | 0.001 | |
| PV | 1.750 | 0.928 | 0.614 | 0.331 | 0.001 | |
| GSV | 0.096 | 0.046 | 0.321 | 0.209 | < 0.001 | |
| Absolute stroke volume (ASV), mL | ||||||
| EIV | 6.490 | 1.979 | 4.022 | 1.602 | < 0.001 | |
| FV | 2.849 | 1.353 | 1.155 | 0.502 | 0.001 | |
| PV | 1.750 | 0.928 | 0.625 | 0.325 | 0.001 | |
| GSV | 0.186 | 0.067 | 0.334 | 0.199 | 0.001 | |
| Mean flux (MF), mL/s | ||||||
| EIV | 7.276 | 2.959 | 4.144 | 1.752 | 0.004 | |
| FV | 3.245 | 1.728 | 1.224 | 0.604 | 0.002 | |
| PV | 1.989 | 1.125 | 0.661 | 0.401 | 0.002 | |
| GSV | 0.049 | 0.059 | 0.336 | 0.240 | < 0.001 | |
| Velocity time integral (VTI), cm | ||||||
| EIV | 5.673 | 1.806 | 3.856 | 1.764 | 0.004 | |
| FV | 6.225 | 4.332 | 3.004 | 1.677 | 0.027 | |
| PV | 1.959 | 0.580 | 1.154 | 0.704 | 0.001 | |
| GSV | 0.063 | 0.439 | 1.570 | 1.256 | < 0.001 | |
| Mean velocity (MV), cm/s | ||||||
| EIV | 6.373 | 2.224 | 12.630 | 49.991 | 0.669 | |
| FV | 7.160 | 5.292 | 3.251 | 1.859 | 0.028 | |
| PV | 2.188 | 0.747 | 1.241 | 0.765 | 0.001 | |
| GSV | 0.081 | 0.386 | 1.669 | 1.272 | < 0.001 | |
EIV: external iliac vein; GSV: great saphenous vein; FV: femoral vein; PV: popliteal vein.
Table 4.
Parameter ratio of target to non-treated limb: before and after intervention.
| QFlow | Segments | Ratio before Interventions | Ratio after Interventions | p Value | ||
|---|---|---|---|---|---|---|
| Mean | SD | Mean | SD | |||
| Stroke volume (SV), mL | ||||||
| EIV | 0.984 | 0.330 | 0.912 | 0.298 | 0.437 | |
| FV | 1.124 | 0.342 | 1.522 | 1.061 | 0.164 | |
| PV | 1.115 | 0.589 | 1.799 | 0.955 | 0.058 | |
| GSV | 2.829 | 2.393 | 0.362 | 0.861 | 0.007 | |
| Forward flow volume (FFV), mL | ||||||
| EIV | 0.918 | 0.344 | 0.897 | 0.314 | 0.835 | |
| FV | 0.966 | 0.410 | 1.593 | 1.081 | 0.125 | |
| PV | 1.065 | 0.482 | 1.793 | 0.956 | 0.035 | |
| GSV | 2.515 | 2.080 | 0.336 | 0.416 | 0.002 | |
| Absolute stroke volume (ASV), mL | ||||||
| EIV | 0.958 | 0.334 | 0.888 | 0.326 | 0.456 | |
| FV | 1.103 | 0.337 | 1.652 | 1.035 | 0.056 | |
| PV | 1.026 | 0.409 | 1.788 | 0.957 | 0.024 | |
| GSV | 2.029 | 1.834 | 0.499 | 0.562 | 0.014 | |
| Mean flux (MF), mL/s | ||||||
| EIV | 0.984 | 0.329 | 0.913 | 0.301 | 0.446 | |
| FV | 1.121 | 0.346 | 1.631 | 0.976 | 0.053 | |
| PV | 1.117 | 0.588 | 1.791 | 0.943 | 0.059 | |
| GSV | 2.941 | 2.599 | 0.347 | 0.807 | 0.008 | |
| Velocity time integral (VTI), cm | ||||||
| EIV | 1.041 | 0.401 | 1.054 | 0.425 | 0.938 | |
| FV | 1.060 | 0.298 | 1.806 | 1.107 | 0.025 | |
| PV | 1.150 | 0.800 | 1.793 | 0.826 | 0.080 | |
| GSV | 1.482 | 1.033 | 0.421 | 0.911 | 0.027 | |
| Mean velocity (MV), cm/s | ||||||
| EIV | 1.042 | 0.401 | 1.053 | 0.424 | 0.945 | |
| FV | 1.059 | 0.298 | 1.799 | 1.091 | 0.024 | |
| PV | 1.150 | 0.807 | 1.788 | 0.816 | 0.082 | |
| GSV | 1.483 | 1.039 | 0.423 | 0.916 | 0.027 | |
EIV: external iliac vein; GSV: great saphenous vein; FV: femoral vein; PV: popliteal vein.
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Chen, C.-W.; Tseng, Y.-H.; Kao, C.-C.; Ngo, Y.G.; Lee, C.-Y.; Yang, T.-Y.; Lin, Y.-H.; Huang, Y.-K. Venous Segmental Flow Changes after Superficial Venous Intervention Demonstrating by Quantitative Phase-Contrast Magnetic Resonance Analysis: Preliminary Data from a Longitudinal Cohort Study. J. Pers. Med. 2022, 12, 1000. https://doi.org/10.3390/jpm12061000
AMA Style
Chen C-W, Tseng Y-H, Kao C-C, Ngo YG, Lee C-Y, Yang T-Y, Lin Y-H, Huang Y-K. Venous Segmental Flow Changes after Superficial Venous Intervention Demonstrating by Quantitative Phase-Contrast Magnetic Resonance Analysis: Preliminary Data from a Longitudinal Cohort Study. Journal of Personalized Medicine. 2022; 12(6):1000. https://doi.org/10.3390/jpm12061000
Chicago/Turabian StyleChen, Chien-Wei, Yuan-Hsi Tseng, Chih-Chen Kao, Yeh Giin Ngo, Chung-Yuan Lee, Teng-Yao Yang, Yu-Hui Lin, and Yao-Kuang Huang. 2022. "Venous Segmental Flow Changes after Superficial Venous Intervention Demonstrating by Quantitative Phase-Contrast Magnetic Resonance Analysis: Preliminary Data from a Longitudinal Cohort Study" Journal of Personalized Medicine 12, no. 6: 1000. https://doi.org/10.3390/jpm12061000
APA StyleChen, C.-W., Tseng, Y.-H., Kao, C.-C., Ngo, Y. G., Lee, C.-Y., Yang, T.-Y., Lin, Y.-H., & Huang, Y.-K. (2022). Venous Segmental Flow Changes after Superficial Venous Intervention Demonstrating by Quantitative Phase-Contrast Magnetic Resonance Analysis: Preliminary Data from a Longitudinal Cohort Study. Journal of Personalized Medicine, 12(6), 1000. https://doi.org/10.3390/jpm12061000
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