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Copyright ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Radiology. Mar 28, 2020; 12(3): 18-28
Published online Mar 28, 2020. doi: 10.4329/wjr.v12.i3.18
Review of imaging and endovascular intervention of iliocaval venous compression syndrome
Ming Ren Toh, Duke-NUS Medical School, Singapore 544886, Singapore
Tjun Yip Tang, Department of Vascular surgery, Singapore General Hospital, Singapore 169608, Singapore
Han Hui Mervin Nathan Lim, Yong Yoo Ling School of Medicine, Singapore 117597, Singapore
Nanda Venkatanarasimha, Department of Radiology, Singapore General Hospital, Singapore 169608, Singapore
Karthikeyan Damodharan, Department of Radiology, SengKang General Hospital, Singapore 544886, Singapore
ORCID number: Ming Ren Toh (0000-0002-7019-9743); Tjun Yip Tang (0000-0002-8524-7912); Han Hui Mervin Nathan Lim (0000-0002-8587-0624); Nanda Venkatanarasimha (0000-0001-7377-4881); Karthikeyan Damodharan (0000-0002-0655-6021).
Author contributions: Toh MR, Lim HHMN, Tang TY, Venkatanarasimha N and Damodharan K researched literature and conceived the study; Toh MR wrote the first draft of the manuscript; all authors reviewed and edited the manuscript and approved the final version of the manuscript.
Conflict-of-interest statement: Authors declare no conflict of interests for this article.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Corresponding author: Karthikeyan Damodharan, MBBS, Doctor, Department of Radiology, SengKang General Hospital, 10 Sengkang E Way, Singapore 544886, Singapore. karthikeyan.damodharan@singhealth.com.sg
Received: December 7, 2019
Peer-review started: December 7, 2019
First decision: December 25, 2019
Revised: January 4, 2020
Accepted: January 13, 2020
Article in press: January 13, 2020
Published online: March 28, 2020
Processing time: 81 Days and 10.5 Hours

Abstract

Iliocaval venous compression syndrome (ICS) is the extrinsic compression of the common iliac vein by the overlying iliac artery against the vertebra. Chronic compression can lead to venous stenosis and stasis, which manifests as chronic venous disease and treatment resistance. Therefore, early recognition of ICS and prompt treatment are essential. Clinical presentations of ICS can be ambiguous and diagnosis requires a high index of suspicion with the relevant imaging studies. The initial imaging test is typically a Duplex ultrasound for vessel assessment and pelvic ultrasound to exclude a compressive mass, which is followed by computed tomography (CT) or magnetic resonance (MR) venography. CT and MRI can identify the anatomical causes for venous compression. In patients with high clinical suspicion for ICS, negative findings on CT and MR venography would still warrant further investigations. Definitive diagnosis can be established using catheter-based venography complemented with intravascular ultrasonography but the nature of their invasiveness limits its utility as a routine imaging modality. In this review paper, we will discuss the evidence, utility and limitations of the existing imaging modalities and endovascular intervention used in the management of ICS.

Key Words: Iliocaval venous compression syndrome; Duplex ultrasound; Intravascular ultrasound; Computed tomography venography; Magnetic resonance venography; Endovascular stent

Core tip: Imaging modalities are crucial to the diagnosis of iliocaval compressions. In this review, we will explore the various imaging modalities and their associated signs of iliocaval compressions, advantages/disadvantages, and sensitivity/specificity. We will also discuss their utility in the diagnosis and management of this condition. Main aim is to raise awareness among the general practitioners and specialists, facilitate the prompt diagnosis and treatment of patients with acute/chronic leg swelling secondary to iliocaval venous compressions.



INTRODUCTION

Iliocaval venous compression syndrome (ICS) is the extrinsic compression of the iliocaval veins by the arterial system against the adjacent bony structures. These veins include the infrahepatic inferior vena cava, common, external and internal iliac veins. A well-recognized variant of ICS is May-Thurner syndrome (MTS), where the left common iliac vein (CIV) is compressed by the overlying right common iliac artery against the fifth lumbar vertebrae. Constant pulsations from the arteries will evoke a sustained inflammatory response within the compressed veins. Reactive hyperplasia of the venous wall will lead to formation of spurs and intimal fibrosis, which leads to venous stenosis and predispose to venous thrombosis[1,2].

EPIDEMIOLOGY AND CLINICAL PRESENTATIONS
Epidemiology and risk factors

ICS is predominantly seen in women (72%-74%) in their second to fourth decade of life; females also tend to develop more severe compression than males[3-6]. The exact prevalence of ICS is not known, especially since most patients are asymptomatic. Nonetheless, growing evidence suggests that it is not as uncommon as previously thought[1,6]. Significant venous obstruction, defined as a stenosis diameter or cross sectional area (CSA) greater than 50% on computed tomography/magnetic resonance imaging (CT/MRI) venography and intravascular ultrasound (IVUS) respectively[7], was seen in 25%-37% of patients with advanced venous diseases (C4-6)[7,8]. Iliac vein compression is also prevalent among asymptomatic patients; a study on MTS incidence among patients admitted for non-venous complaints showed that almost a quarter of the cohort had significant compression of the left iliac vein[9]. Generally, patients would remain asymptomatic until exposure to stress such as surgery and prolonged bed rest[5]. Other factors associated with symptomatic ICS include spinal deformities such as exaggerated lordosis and scoliosis, oral contraceptive use, post-partum and multiparous[10-12]. When symptoms do emerge, they may present as deep vein thrombosis and chronic venous disease.

Clinical presentations

Prolonged venous stenosis causes venous stasis which in turn predisposes individuals to acute deep vein thrombosis and chronic venous diseases[3]. Patients with ICS are more likely to develop deep vein thrombosis (OR = 9.5, P < 0.001), typically after an inciting prothrombotic event such as prolonged immobility and pregnancy which may worsen the venous compression[13,14]. Standard systemic anticoagulation is usually inadequate in these patients due to extensive clot burden, warranting more aggressive intervention such as intravascular thrombolysis[15]. In spite of prompt and adequate treatment, they are more likely to develop post-treatment sequalae such as re-thrombosis (RR = 2.8, P = 0.04) and post-thrombotic syndrome if the underlying anatomic variant is not corrected[16,17].

Besides deep vein thrombosis, patients may suffer with symptoms of leg pain, heaviness and swelling usually worse by the end of the day. Chronic venous disease develops from complex processes such as venous reflux and obstruction, with varying clinical severity depending on the presence of telangiectasia (C1), varicose veins (C2), edema (C3), pigmentation (C4a), lipodermatosclerosis (C4b) and venous ulcers (C5-6)[18]. Although reflux from incompetent valves is the predominant pathophysiology of chronic venous disease, venous obstruction is a common and aggravating factor that should be addressed[19]. In a cohort of 4026 patients with chronic venous disease, significant (greater than 50%) venous obstruction warranting stent placement was noted in 879 patients, of which almost half (n = 319) were due to extrinsic iliac venous compression[20]. Not only is venous compression a common contributor of chronic venous disease, it is also associated with more severe disease, in part due to the raised venous ambulatory pressure[21]. Class C4-6 disease occurred in 35% of patients with venous obstruction[20], compared to 3%-6% of the general population (i.e., patients with chronic venous disease unselected for a specific pathophysiology)[22,23]. In addition, disease with untreated venous compression is more resistant to conventional treatment such as vein ligation and stripping[5].

Given the poor disease and treatment outcomes associated with ICS, early recognition and prompt treatment are essential. Making this diagnosis requires a high index of suspicion, particularly in young to middle-aged women presenting with acute deep vein thrombosis and unilateral stigmata of chronic venous disease[24]. Other features that may require further investigations include presence of varicosities on the abdominal wall, groin or thigh, persistence or recurrence of condition despite appropriate treatment.

DIAGNOSTIC IMAGING STUDIES

Investigations are targeted at the identification of the site and severity of the stenosis. Sites of compression in ICS include inferior vena cava (50%), common iliac (32%), external iliac (7%) and common femoral veins (11%)[25]. Another common site is the confluence of external and internal iliac veins but the exact prevalence is not known. Severity of the stenosis can be represented in relation to the reference diameter and CSA. Traditionally, stenosis greater than 50% has been considered as significant stenosis requiring stenting[19]. This cut-off was recently corroborated by a prospective study which reported CSA stenosis greater than 54% to be the best predictor of post-treatment response[26]. Reference diameter and CSA are determined from the non-stenosed segments proximal or distal to the stenosis, or from the contralateral non-stenosed vein[27]. Reference diameters from the literature include 24 mm for the inferior vena cava[28], 16 mm for the CIV[29], 14 mm for the external iliac vein (EIV)[30], and 10-12 mm for the common femoral vein[27,31,32]. Reference areas can be calculated from the diameters or directly measured from the axial cross-sectional images on IVUS.

Ultrasonography

Duplex ultrasound is the best initial test because it is fast, easily accessible and non-invasive. With the patient supine, the external iliac, common iliac and inferior vena cava are visualized with a 2 to 5 MHz curvilinear transducer[25]. The iliocaval vessels are imaged using different views at the paraumbilical, midline and adjacent to the line connecting the superior iliac spine to the umbilicus[25]. Site of stenosis is identified by the presence of abnormal Doppler signal and flow patterns such as post-stenotic turbulence and slow flow[25]. Indirect signs of stenosis include pre-stenotic vein dilation, absent respiratory variations, flow reversal, and poor response to both flow augmentation and Valsalva maneuver[8,33]. Degree of stenosis is then determined based on the peak vein velocity of the post-stenotic and pre-stenotic segments, and the percent reduction in vein diameter when compared with the normal lumen[14]. Significant stenosis is defined as a peak vein velocity ratio greater than 2.0 or vein diameter greater than 50%[25]. Transvaginal ultrasound has been reliably used for evaluating the internal iliac veins[34]. In comparison, transabdominal ultrasound is unsuitable for proximal iliocaval vessels which are deep in the pelvis and may be obscured by the intraabdominal fats and bowel gas[33]. Moreover, indirect signs are often absent; the sensitivity of flow reversal and absent respiratory variations in the detection of significant iliocaval obstruction are only 7.9% and 23.7% respectively while both have a specificity of 100%[7]. Hence, patients with a negative ultrasound study should be referred for further imaging such as CT and MRI before confirming the diagnosis[7,8]. Whilst Duplex ultrasound is operator dependent, it remains a reliable initial investigation in high volume centres.

CT venography

CT venogram of the pelvis is used in the diagnosis of ICS. Patients are given intravenous contrast at a rate of 4 to 5 mL/s followed by 20-50 mL of saline and venous phase imaging is obtained generally after 60-80 s delay[8,22]. Timing of the imaging sequence may require optimization to obtain maximal contrast opacification of the target veins. The scan coverage extends from the infrarenal segment of the vena cava to the common femoral veins. The degree of stenosis is then derived either by comparing the smallest diameter of the vein with the normal diameter caudal to the obstruction, or with the corresponding contralateral healthy vein segment[7].

Unlike Duplex ultrasound, CT venogram allows a clearer visualization of the anatomic compression sites and collaterals, which indicates the hemodynamic significance of the stenosis (Figure 1A)[27,35]. CT also serves to rule out other causes of the compression such as pelvic tumors and ascites (Figure 1B)[35]. CT is relatively less operator dependent compared to ultrasound. Significant reduction in vessel calibre or complete venous occlusion can be visualized on CT imaging. Indirect signs such as enlarged paravertebral and internal iliac veins resultant of prominent collateral drainage, also support the diagnosis of iliocaval venous compression. Unfortunately, these anatomical changes represent late stage disease. In two small retrospective studies, CT venography (CTV) was reported to have both high sensitivity and specificity in detecting iliac vein compression[29,36]. However, patients in these studies presented with acute deep vein thrombosis of the lower limbs, which is an advanced stage of iliocaval venous compression where the veins are severely stenosed or completely occluded. Earlier signs such as intraluminal webs or scarring, vein wall thickening and partial luminal occlusion cannot be seen on CT imaging. Spurs and webs can serve as nidus for thrombosis. Early detection of these changes is crucial given that patients with such changes would benefit most from thrombolytic therapy[37,38]. Left undetected and untreated, these would progress and further impair venous drainage, eventually manifesting as symptoms of venous incompetence.

Figure 1
Figure 1 Axial Computed tomography venography image. A: Axial computed tomography venography image showing compression of the left common iliac vein (arrow) between the right common iliac artery and the lumbar vertebral body; B: Extraluminal compression of the external iliac veins (arrows) from an ovarian tumor (asterixis).

Hence in our opinion, CT has limited sensitivity in the diagnosis of early ICS. Its main utility is to diagnose advanced disease and to exclude compressive pelvic masses prior to the use of invasive imaging and therapy. The diagnostic performance of CTV in patients with IVCS leading to chronic venous insufficiency remains unknown.

CT is readily available in most centres and can be used in patients with metallic implants and iliac vascular stents. Unfortunately, CT imaging requires administration of contrast and radiation, which may be contraindicated in patients with chronic renal failure and pregnancy. In these instances, MRV may be considered. An alternative is the dual energy CT which offers the advantage of better contrast opacification at relatively lower contrast dose compared to conventional single energy CT, which may be acceptable to patients with chronic renal failure. dual energy CT also reduces streak/beam hardening artefacts from iodinated contrast and metal implants such as previous stents. Hence, it is useful in assessing the patency of previously stented veins[39].

MR venography

Similar to CT, MRV is non-invasive, operator-independent and allows identification of venous stenosis or occlusion, and collaterals[19]. MRV can be performed either with injection of Gadolinium contrast to opacify the veins or using non contrast techniques such as two- or three-dimensional time of flight sequence. An example of stenosis demonstrated on non-contrast MRV is seen in Figure 2. Unlike CTV, contrast-enhanced MRV can demonstrate intraluminal webs, partial occlusion or venous wall thickening due to superior soft tissue resolution[40]. Increasingly, studies have advocated using MRV to confirm the diagnosis of iliocaval compression[4,41-43], in part due to its success in diagnosing pelvic venous thrombosis[44,45]. Without direct comparison with catheter-based venography, the sensitivity and specificity of MRV in the diagnosis of ICS are not yet known and MRV should not be used in place of catheter-based venography[24]. Furthermore, the degree of venous compression on MRV can vary over time; a retrospective study on 36 MTS patients revealed that the venous compression vary significantly from 12% increase to 69% decrease between the index and follow-up MRV studies[30]. This variability might be explained by the dependence of compression on the hydration status and study position of the patient. In most centers, the CTV/MRV protocol requires patients to fast overnight. Consequently, the patient is dehydrated and the veins are collapsed, which may be misinterpreted as stenotic. The supine position adopted during the scans further contributes to extrinsic narrowing of the veins. Behzadi et al[46] demonstrated an increase in the common femoral vein area on MRV (59 ± 21 mm2 when supine and dehydrated) with a prone/decubitus position (83 ± 35 mm2) and hydration (123 ± 44 mm2)[46]. To avoid false positive findings, the patient may be hydrated intravenously prior to the study and kept prone/decubitus during the study.

Figure 2
Figure 2 Magnetic resonance venography image. A: Magnetic resonance venography image of the stenosed left common iliac vein (arrow); B: Axial image of the left common iliac artery (asterisk) compressing against the left common iliac vein (arrowhead). Under magnetic resonance venography, venous blood generates high signal intensity (hyperintense) while arterial blood is suppressed (hypointense).

Practical limitations of MRV include the cost, availability and the contraindications in patients with metallic spinal fixation devices in the lower lumbar spine or iliac vein stents due to image degradation by artefacts from the metal implants. Non contrast MRV images are also easily degraded, by arterial pulsation artefacts and breathing movement artefacts. In our experience, a negative MRV or CTV study should still be confirmed with invasive imaging (catheter-based venography and IVUS) if the clinical suspicion of ICS is high due to potential missed diagnoses on CTV/MRV (Figure 3A, 3B).

Figure 3
Figure 3 Computed tomography venography and intravascular ultrasound. A: Normal filling of the left common iliac vein (arrow) on computed tomography venography; B: Obvious stenosis on intravascular ultrasound for a patient with May-Thurner syndrome.
Catheter-based venography

Catheter-based venography is generally regarded as the gold-standard diagnostic test for ICS, as it has been around for the longest period and is used for planning the treatment[24]. Venous access is via the ipsilateral popliteal or femoral vein and the imaged venous segments include the inferior vena cava, CIV, EIV and common femoral vein[27]. Location and degree of narrowing can be assessed directly (Figure 4A). To improve the diagnostic accuracy, venography is performed in at least two orthogonal views beyond the standard anteroposterior, such as left, right anterior oblique and cranial caudal views[1]; single plane venography has low sensitivity (45%) in detecting venous stenosis above 70%[47]. However, the acquisition of additional views will require higher doses of radiation and contrast, thus this is not routinely done in clinical practice[47]. Instead, the diagnosis of ICS can be inferred in the presence of other supporting signs such as collaterals (Figure 4B) and raised pressure gradients (greater than 2 mmHg) across the stenosed sites[25,47]. Unlike the previous diagnostic modalities discussed, digital subtraction venography is usually performed as part of the planned endovascular intervention, given its invasiveness and the significant amount of iodinated contrast and radiation administered.

Figure 4
Figure 4 Digital subtraction angiography images. A: Digital subtraction angiography images obtained during revascularization showing left proximal common iliac vein stenosis (arrow) with formation of collaterals (arrowhead); B: Digital subtraction angiography images obtained during revascularization showing dilation post-stenting.
IVUS

IVUS is usually performed after catheter based venography to improve the diagnostic accuracy[47]. After venography, the lesions are crossed with a diagnostic 4 French (F) catheter and hydrophilic guide wire (usually 035” Glide wire, Terumo, Japan) under fluoroscopic guidance into guide the distal inferior vena cava (IVC). After exchanging for a stiffer guidewire (HI-TORQUE SupracoreTM Abbott Medical, United States) the access sheath is upsized to 9F to accomadate the IVUS catheter. A 10 MHz IVUS transducer catheter (VolcanoTM, Philips Healthcare, Netherlands) is inserted over the guide wire into the distal IVC. A preliminary pull back scan of the iliac and femoral veins is performed to get a quick overview of the lesions under Xray fluoroscopy. The IVUS catheter is reintroduced into the IVC and crosss sectional measurements of the distal IVC, proximal CIV, mid CIV, distal CIV at the confluence, proximal, mid and distal EIV and the common femoral veins are measured using the IVUS. In our experience, IVUS provides the most accurate estimate of the severity and extent of the venous lesions as well as the diameters of the normal iliac veins. The combination of high probe frequency and close luminal distance facilitates high-resolution imaging of the stenosis (Figure 5A)[25]. This improves the detection of finer endoluminal venous lesions and features such as webs, trabeculations and spur morphologies, which might be missed on catheter-based venography[47]. Up to one-third of venous compressions detected on IVUS were missed on initial CT venography[24,27]. Besides having a greater sensitivity, IVUS allows for a more accurate measurement of the stenosed vein diameter and cross-sectional area[1,27,45]; a study comparing IVUS and single-plane catheter-based venography found the stenotic area directly measured in IVUS was more severe than that derived in venography (80% vs 50%)[47]. Similarly, another study comparing IVUS and multiplanar venography reported 33% underestimation of stenosis diameter by venography[27]. This underestimation was attributed to the non-circular geometry of the stenosed lumens which are only seen on certain views. Since IVUS examines each segment with a full 360-degree field of view, it is better able to identify these lesions than multiplanar venography[47]. The recent VIDIO trial comparing multiplanar venography (MPV) with IVUS for the diagnosis and treatment of iliofemoral stenosis showed that IVUS was more sensitive than MPV and that clinical improvement post stenting was best predicted by IVUS baseline measurement of the venous CSA[26].

Figure 5
Figure 5 Intravascular ultrasound. A: Intravascular ultrasound showing stenosis at the left proximal common iliac vein; B: Intravascular ultrasound showing dilatation post-stenting. Intravascular ultrasound allows for direct imaging of the stenosis and evaluation of post-stenting vein diameter.

Routine use of IVUS may allow for better detection hence treatment of iliocaval stenotic lesions (Figure 5B). Precise vessel diameter and lesion length measurement facilitate the choice of stents with the appropriate diameter and length. IVUS also guides the precise deployment of the stent to ensure adequate coverage of the lesion. This is especially important for lesions near the iliac vein confluence, which may be difficult to ascertain on venography alone. IVUS helps to avoid unwanted “jailing” of the origin of the contralateral CIV and undercoverage of lesion, which risks early restenosis. Once the stent is deployed, IVUS can be used to ensure adequate stent apposition to the venous wall. However, IVUS is limited by the image artefacts such as acoustic shadowing from calcification and stent struts which can obscure the underlying venous walls. Image quality in IVUS is also impaired by rotational distortion artefacts created during manoeuvres in tortuous vessels, and multiple circular echoes from reverberating ultrasound beams[48].

MANAGEMENT

Endovascular intervention has become the established treatment for IVCS. Intervention is usually performed during the same session as venography with IVUS. An appropriately sized balloon is placed across the lesion and pre-dilatation of the vessel is performed to allow stent deployment. Stents are crucial for deep venous work due to the high tendency of stenotic fibrotic veins to recoil after balloon dilation. Stenotic veins managed with balloon angioplasty alone have high rates of reocclusion[49,50], with a 5-year cumulative patency rate of only 18%[51]. An oversized stent (usually 20%) is then deployed across with combined fluoroscopic and IVUS guidance to ensure adequate coverage of the lesion. Alternatives to endovascular interventions include open surgical approaches such as dissection and reconstruction of the diseased veins. However, these procedures are associated with higher morbidity and only indicated in patients with long-segment venous obstruction (e.g., extended femorocaval occlusions) or endovascular angioplasty failure[52].

Following the endovascular interventions, most patients would experience prompt and sustained relief from symptoms/signs of pain and swelling (Figure 6). In a study by Raju et al[53] on 304 limbs with symptomatic chronic venous insufficiency, the endovascular interventions of stenting and ballooning achieved complete pain relief and ulcer resolution in 62%-71% of the patients at 24 mo of follow up[53]. In another large cohort study by Peter et al[6] on 982 limbs, 5-year cumulative rates of complete relief of pain and swelling were 62% and 58% respectively[54]. In most centers, the diseased veins would remain patent for sustained periods. In a recent meta-analysis of stent efficacy in iliofemoral venous compression, patency rates at 1 year were 96% for non-thrombotic and 79%-87% for thrombotic lesions[55]. In the longer term, patency rate at 5 years ranges from 70%-84%[56]. Predominant factors associated with higher failure rates include the presence of thrombosis (26.7, P < 0.001), degree of occlusion (OR = 8.3, P < 0.001) and stent extension to below the inguinal ligament (OR = 5.5, P < 0.001)[54,56,57].

Figure 6
Figure 6 Marked hyperpigmentation and swelling of the legs in a patient with May-Thurner syndrome which showed significant resolution as early as three months after endovascular stenting was performed. A: Pre-Stenting; B: Three months post-stenting.
CONCLUSION

Iliocaval venous compressions are common. Fortunately, they usually remain silent until secondary insults are superimposed. Venous diseases with underlying venous compressions often have severe features such as extensive disease and resistance to treatment. Therefore, early recognition and prompt treatment are essential[58]. Duplex ultrasonography is the most convenient initial test but negative findings should be followed with CTV or MRV to better visualize the more proximal vessels and rule out other causes of extrinsic compression. Patients with negative findings on non-invasive imaging should still proceed with invasive imaging if the clinical suspicion for compressions remains high. Conversely, for patients with low clinical suspicion of ICS, further testing beyond the non-invasive testing is not recommended.

Footnotes

Manuscript source: Invited manuscript

Specialty type: Radiology, nuclear medicine and medical imaging

Country of origin: Singapore

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References
1.  DeRubertis B, Patel R, Chaar CIO. May-Thurnesr Syndrome: Diagnosis and Management. In: Chaar CIO. Current Management of Venous Diseases. Cham: Springer International Publishing. Chaar CIO. 2018;463-477.  [PubMed]  [DOI]  [Cited in This Article: ]
2.  Mitsuoka H, Ohta T, Hayashi S, Yokoi T, Arima T, Asamoto K, Nakano T. Histological study on the left common iliac vein spur. Ann Vasc Dis. 2014;7:261-265.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 16]  [Cited by in F6Publishing: 17]  [Article Influence: 1.7]  [Reference Citation Analysis (0)]
3.  Moudgill N, Hager E, Gonsalves C, Larson R, Lombardi J, DiMuzio P. May-Thurner syndrome: case report and review of the literature involving modern endovascular therapy. Vascular. 2009;17:330-335.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 81]  [Cited by in F6Publishing: 83]  [Article Influence: 5.9]  [Reference Citation Analysis (0)]
4.  O'Sullivan GJ, Semba CP, Bittner CA, Kee ST, Razavi MK, Sze DY, Dake MD. Endovascular management of iliac vein compression (May-Thurner) syndrome. J Vasc Interv Radiol. 2000;11:823-836.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 300]  [Cited by in F6Publishing: 263]  [Article Influence: 11.0]  [Reference Citation Analysis (1)]
5.  Cockett FB, Thomas ML, Negus D. Iliac vein compression.--Its relation to iliofemoral thrombosis and the post-thrombotic syndrome. Br Med J. 1967;2:14-19.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 180]  [Cited by in F6Publishing: 157]  [Article Influence: 2.8]  [Reference Citation Analysis (0)]
6.  Peters M, Syed RK, Katz M, Moscona J, Press C, Nijjar V, Bisharat M, Baldwin D. May-Thurner syndrome: a not so uncommon cause of a common condition. Proc (Bayl Univ Med Cent). 2012;25:231-233.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 35]  [Cited by in F6Publishing: 29]  [Article Influence: 2.4]  [Reference Citation Analysis (0)]
7.  Sermsathanasawadi N, Pruekprasert K, Pitaksantayothin W, Chinsakchai K, Wongwanit C, Ruangsetakit C, Mutirangura P. Prevalence, risk factors, and evaluation of iliocaval obstruction in advanced chronic venous insufficiency. J Vasc Surg Venous Lymphat Disord. 2019;7:441-447.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 11]  [Cited by in F6Publishing: 16]  [Article Influence: 3.2]  [Reference Citation Analysis (0)]
8.  Marston W, Fish D, Unger J, Keagy B. Incidence of and risk factors for iliocaval venous obstruction in patients with active or healed venous leg ulcers. J Vasc Surg. 2011;53:1303-1308.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 73]  [Cited by in F6Publishing: 76]  [Article Influence: 5.8]  [Reference Citation Analysis (0)]
9.  Kibbe MR, Ujiki M, Goodwin AL, Eskandari M, Yao J, Matsumura J. Iliac vein compression in an asymptomatic patient population. J Vasc Surg. 2004;39:937-943.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 336]  [Cited by in F6Publishing: 335]  [Article Influence: 16.8]  [Reference Citation Analysis (0)]
10.  Murphy EH, Davis CM, Journeycake JM, DeMuth RP, Arko FR. Symptomatic ileofemoral DVT after onset of oral contraceptive use in women with previously undiagnosed May-Thurner Syndrome. J Vasc Surg. 2009;49:697-703.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 52]  [Cited by in F6Publishing: 55]  [Article Influence: 3.7]  [Reference Citation Analysis (0)]
11.  Wax JR, Pinette MG, Rausch D, Cartin A. May-Thurner syndrome complicating pregnancy: a report of four cases. J Reprod Med. 2014;59:333-336.  [PubMed]  [DOI]  [Cited in This Article: ]
12.  Oteros Fernández R, Bravo Rodríguez F, Delgado Acosta F, González Barrios I. [May-Thurner syndrome and surgery for scoliosis]. Radiologia. 2008;50:245-247.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 13]  [Cited by in F6Publishing: 16]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
13.  Jin S, Sun Z, Li X, Jian T, Jin X, Li S, Wang G, Ma C, Cui K, Xu P. May-Thurner syndrome and the risk of pulmonary embolism in patients with acute deep venous thrombosis. J Vasc Surg Venous Lymphat Disord. 2018;6:433-440.e1.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 7]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
14.  Oguzkurt L, Ozkan U, Ulusan S, Koc Z, Tercan F. Compression of the left common iliac vein in asymptomatic subjects and patients with left iliofemoral deep vein thrombosis. J Vasc Interv Radiol. 2008;19:366-70; quiz 371.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 76]  [Cited by in F6Publishing: 80]  [Article Influence: 5.0]  [Reference Citation Analysis (1)]
15.  Ezhumalai B, Mathur A. May-Thurner syndrome needs to be ruled out in unexplained left-sided deep venous thrombosis: Three-tiered endovascular therapy is warranted. IHJ Cardiovascular Case Reports (CVCR). 2018;2:73-76.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 2]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
16.  Hartung O, Benmiloud F, Barthelemy P, Dubuc M, Boufi M, Alimi YS. Late results of surgical venous thrombectomy with iliocaval stenting. J Vasc Surg. 2008;47:381-387.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 75]  [Cited by in F6Publishing: 59]  [Article Influence: 3.7]  [Reference Citation Analysis (0)]
17.  Alshabatat AO, Barbati ME, Alzoubi O, Jalaie H, Wittens CHA. The Role of May-Thurner Syndrome in Recurrent Thrombosis after Catheter-Directed Thrombolysis of Deep Vein Thrombosis. Ann Vasc Surg. 2019;54:276-281.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 6]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
18.  Radhakrishnan N, George D, Jayakrishnan R, Sumi S, Kartha CC. Vein Size and Disease Severity in Chronic Venous Diseases. Int J Angiol. 2018;27:185-189.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 5]  [Article Influence: 0.8]  [Reference Citation Analysis (0)]
19.  Neglén P, Thrasher TL, Raju S. Venous outflow obstruction: An underestimated contributor to chronic venous disease. J Vasc Surg. 2003;38:879-885.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 174]  [Cited by in F6Publishing: 146]  [Article Influence: 7.0]  [Reference Citation Analysis (0)]
20.  Raju S, Neglen P. High prevalence of nonthrombotic iliac vein lesions in chronic venous disease: a permissive role in pathogenicity. J Vasc Surg. 2006;44:136-43; discussion 144.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 274]  [Cited by in F6Publishing: 251]  [Article Influence: 13.9]  [Reference Citation Analysis (0)]
21.  Nicolaides AN, Hussein MK, Szendro G, Christopoulos D, Vasdekis S, Clarke H. The relation of venous ulceration with ambulatory venous pressure measurements. J Vasc Surg. 1993;17:414-419.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 224]  [Cited by in F6Publishing: 131]  [Article Influence: 4.2]  [Reference Citation Analysis (0)]
22.  Jawien A, Grzela T, Ochwat A. Prevalence of chronic venous insufficiency in men and women in Poland: multicentre cross-sectional study in 40,095 patients. Phlebology. 2003;18:110-122.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 84]  [Cited by in F6Publishing: 86]  [Article Influence: 10.8]  [Reference Citation Analysis (0)]
23.  Carpentier PH, Maricq HR, Biro C, Ponçot-Makinen CO, Franco A. Prevalence, risk factors, and clinical patterns of chronic venous disorders of lower limbs: a population-based study in France. J Vasc Surg. 2004;40:650-659.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 237]  [Cited by in F6Publishing: 209]  [Article Influence: 10.5]  [Reference Citation Analysis (0)]
24.  Birn J, Vedantham S. May-Thurner syndrome and other obstructive iliac vein lesions: meaning, myth, and mystery. Vasc Med. 2015;20:74-83.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 71]  [Cited by in F6Publishing: 76]  [Article Influence: 7.6]  [Reference Citation Analysis (0)]
25.  Labropoulos N, Borge M, Pierce K, Pappas PJ. Criteria for defining significant central vein stenosis with duplex ultrasound. J Vasc Surg. 2007;46:101-107.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 134]  [Cited by in F6Publishing: 133]  [Article Influence: 7.8]  [Reference Citation Analysis (0)]
26.  Gagne PJ, Gasparis A, Black S, Thorpe P, Passman M, Vedantham S, Marston W, Iafrati M. Analysis of threshold stenosis by multiplanar venogram and intravascular ultrasound examination for predicting clinical improvement after iliofemoral vein stenting in the VIDIO trial. J Vasc Surg Venous Lymphat Disord. 2018;6:48-56.e1.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 55]  [Cited by in F6Publishing: 77]  [Article Influence: 11.0]  [Reference Citation Analysis (0)]
27.  Gagne PJ, Tahara RW, Fastabend CP, Dzieciuchowicz L, Marston W, Vedantham S, Ting W, Iafrati MD. Venography versus intravascular ultrasound for diagnosing and treating iliofemoral vein obstruction. J Vasc Surg Venous Lymphat Disord. 2017;5:678-687.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 102]  [Cited by in F6Publishing: 131]  [Article Influence: 18.7]  [Reference Citation Analysis (0)]
28.  Ouriel K, Greenberg RK, Green RM, Massullo JM, Goines DR. A volumetric index for the quantification of deep venous thrombosis. J Vasc Surg. 1999;30:1060-1066.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 15]  [Cited by in F6Publishing: 16]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]
29.  Oguzkurt L, Tercan F, Pourbagher MA, Kizilkilic O, Turkoz R, Boyvat F. Computed tomography findings in 10 cases of iliac vein compression (May-Thurner) syndrome. Eur J Radiol. 2005;55:421-425.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 72]  [Cited by in F6Publishing: 73]  [Article Influence: 3.7]  [Reference Citation Analysis (0)]
30.  McDermott S, Oliveira G, Ergül E, Brazeau N, Wicky S, Oklu R. May-Thurner syndrome: can it be diagnosed by a single MR venography study? Diagn Interv Radiol. 2013;19:44-48.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 16]  [Cited by in F6Publishing: 28]  [Article Influence: 2.3]  [Reference Citation Analysis (0)]
31.  Fronek A, Criqui MH, Denenberg J, Langer RD. Common femoral vein dimensions and hemodynamics including Valsalva response as a function of sex, age, and ethnicity in a population study. J Vasc Surg. 2001;33:1050-1056.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 105]  [Cited by in F6Publishing: 101]  [Article Influence: 4.4]  [Reference Citation Analysis (0)]
32.  Hertzberg BS, Kliewer MA, DeLong DM, Lalouche KJ, Paulson EK, Frederick MG, Carroll BA. Sonographic assessment of lower limb vein diameters: implications for the diagnosis and characterization of deep venous thrombosis. AJR Am J Roentgenol. 1997;168:1253-1257.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 55]  [Cited by in F6Publishing: 43]  [Article Influence: 1.6]  [Reference Citation Analysis (0)]
33.  Butros SR, Liu R, Oliveira GR, Ganguli S, Kalva S. Venous compression syndromes: clinical features, imaging findings and management. Br J Radiol. 2013;86:20130284.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 89]  [Cited by in F6Publishing: 109]  [Article Influence: 9.9]  [Reference Citation Analysis (0)]
34.  Whiteley MS, Dos Santos SJ, Harrison CC, Holdstock JM, Lopez AJ. Transvaginal duplex ultrasonography appears to be the gold standard investigation for the haemodynamic evaluation of pelvic venous reflux in the ovarian and internal iliac veins in women. Phlebology. 2015;30:706-713.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 49]  [Cited by in F6Publishing: 44]  [Article Influence: 4.4]  [Reference Citation Analysis (0)]
35.  Brinegar KN, Sheth RA, Khademhosseini A, Bautista J, Oklu R. Iliac vein compression syndrome: Clinical, imaging and pathologic findings. World J Radiol. 2015;7:375-381.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 82]  [Cited by in F6Publishing: 88]  [Article Influence: 9.8]  [Reference Citation Analysis (0)]
36.  Chung JW, Yoon CJ, Jung SI, Kim HC, Lee W, Kim YI, Jae HJ, Park JH. Acute iliofemoral deep vein thrombosis: evaluation of underlying anatomic abnormalities by spiral CT venography. J Vasc Interv Radiol. 2004;15:249-256.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 137]  [Cited by in F6Publishing: 124]  [Article Influence: 6.2]  [Reference Citation Analysis (0)]
37.  Wojcik K, Milburn J, Vidal G, Steven A. Carotid Webs: Radiographic Appearance and Significance. Ochsner J. 2018;18:115-120.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 11]  [Cited by in F6Publishing: 12]  [Article Influence: 2.0]  [Reference Citation Analysis (0)]
38.  Mickley V, Schwagierek R, Rilinger N, Görich J, Sunder-Plassmann L. Left iliac venous thrombosis caused by venous spur: treatment with thrombectomy and stent implantation. J Vasc Surg. 1998;28:492-497.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 129]  [Cited by in F6Publishing: 112]  [Article Influence: 4.3]  [Reference Citation Analysis (0)]
39.  Machida H, Tanaka I, Fukui R, Shen Y, Ishikawa T, Tate E, Ueno E. Dual-Energy Spectral CT: Various Clinical Vascular Applications. Radiographics. 2016;36:1215-1232.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 64]  [Cited by in F6Publishing: 75]  [Article Influence: 10.7]  [Reference Citation Analysis (0)]
40.  Arnoldussen CW, de Graaf R, Wittens CH, de Haan MW. Value of magnetic resonance venography and computed tomographic venography in lower extremity chronic venous disease. Phlebology. 2013;28 Suppl 1:169-175.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 50]  [Cited by in F6Publishing: 51]  [Article Influence: 4.6]  [Reference Citation Analysis (0)]
41.  Wolpert LM, Rahmani O, Stein B, Gallagher JJ, Drezner AD. Magnetic resonance venography in the diagnosis and management of May-Thurner syndrome. Vasc Endovascular Surg. 2002;36:51-57.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 106]  [Cited by in F6Publishing: 90]  [Article Influence: 4.1]  [Reference Citation Analysis (0)]
42.  Fraser DG, Moody AR, Morgan PS, Martel A. Iliac compression syndrome and recanalization of femoropopliteal and iliac venous thrombosis: a prospective study with magnetic resonance venography. J Vasc Surg. 2004;40:612-619.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 35]  [Cited by in F6Publishing: 35]  [Article Influence: 1.8]  [Reference Citation Analysis (0)]
43.  Hurst DR, Forauer AR, Bloom JR, Greenfield LJ, Wakefield TW, Williams DM. Diagnosis and endovascular treatment of iliocaval compression syndrome. J Vasc Surg. 2001;34:106-113.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 135]  [Cited by in F6Publishing: 136]  [Article Influence: 5.9]  [Reference Citation Analysis (0)]
44.  Gurel K, Gurel S, Karavas E, Buharalıoglu Y, Daglar B. Direct contrast-enhanced MR venography in the diagnosis of May-Thurner syndrome. Eur J Radiol. 2011;80:533-536.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 25]  [Cited by in F6Publishing: 27]  [Article Influence: 2.1]  [Reference Citation Analysis (0)]
45.  Asciutto G, Mumme A, Marpe B, Köster O, Asciutto KC, Geier B. MR venography in the detection of pelvic venous congestion. Eur J Vasc Endovasc Surg. 2008;36:491-496.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 76]  [Cited by in F6Publishing: 64]  [Article Influence: 4.0]  [Reference Citation Analysis (0)]
46.  Behzadi AH, Khilnani NM, Zhang W, Bares AJ, Boddu SR, Min RJ, Prince MR. Pelvic cardiovascular magnetic resonance venography: venous changes with patient position and hydration status. J Cardiovasc Magn Reson. 2019;21:3.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 6]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
47.  Neglén P, Raju S. Intravascular ultrasound scan evaluation of the obstructed vein. J Vasc Surg. 2002;35:694-700.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 300]  [Cited by in F6Publishing: 246]  [Article Influence: 11.2]  [Reference Citation Analysis (0)]
48.  McLafferty RB. The role of intravascular ultrasound in venous thromboembolism. Semin Intervent Radiol. 2012;29:10-15.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 33]  [Cited by in F6Publishing: 24]  [Article Influence: 2.0]  [Reference Citation Analysis (0)]
49.  Juhan C, Hartung O, Alimi Y, Barthélemy P, Valerio N, Portier F. Treatment of nonmalignant obstructive iliocaval lesions by stent placement: mid-term results. Ann Vasc Surg. 2001;15:227-232.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 31]  [Cited by in F6Publishing: 32]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
50.  Neglén P, Raju S. Balloon dilation and stenting of chronic iliac vein obstruction: technical aspects and early clinical outcome. J Endovasc Ther. 2000;7:79-91.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 101]  [Cited by in F6Publishing: 105]  [Article Influence: 4.4]  [Reference Citation Analysis (0)]
51.  Whittemore AD, Donaldson MC, Polak JF, Mannick JA. Limitations of balloon angioplasty for vein graft stenosis. J Vasc Surg. 1991;14:340-345.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 73]  [Cited by in F6Publishing: 73]  [Article Influence: 2.2]  [Reference Citation Analysis (0)]
52.  Garg N, Gloviczki P, Karimi KM, Duncan AA, Bjarnason H, Kalra M, Oderich GS, Bower TC. Factors affecting outcome of open and hybrid reconstructions for nonmalignant obstruction of iliofemoral veins and inferior vena cava. J Vasc Surg. 2011;53:383-393.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 89]  [Cited by in F6Publishing: 70]  [Article Influence: 5.0]  [Reference Citation Analysis (0)]
53.  Raju S, Owen S, Neglen P. The clinical impact of iliac venous stents in the management of chronic venous insufficiency. J Vasc Surg. 2002;35:8-15.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 23]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
54.  Neglén P, Hollis KC, Olivier J, Raju S. Stenting of the venous outflow in chronic venous disease: long-term stent-related outcome, clinical, and hemodynamic result. J Vasc Surg. 2007;46:979-990.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 468]  [Cited by in F6Publishing: 447]  [Article Influence: 26.3]  [Reference Citation Analysis (0)]
55.  Razavi MK, Jaff MR, Miller LE. Safety and Effectiveness of Stent Placement for Iliofemoral Venous Outflow Obstruction: Systematic Review and Meta-Analysis. Circ Cardiovasc Interv. 2015;8:e002772.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 129]  [Cited by in F6Publishing: 179]  [Article Influence: 22.4]  [Reference Citation Analysis (0)]
56.  Souto Barros F, Salles-Cunha SX, Roelke LH, Morais Filho Dd, Paula Brandão NAd, Pontes SM. Arterial Compression of Left Iliac Veins: Five-Year Patency Rates of Endovascular Treatment. JVU. 2018;42:11-17.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Cited by in F6Publishing: 1]  [Article Influence: 0.2]  [Reference Citation Analysis (0)]
57.  Avgerinos ED, Saadeddin Z, Abou Ali AN, Pandya Y, Hager E, Singh M, Al-Khoury G, Makaroun MS, Chaer RA. Outcomes and predictors of failure of iliac vein stenting after catheter-directed thrombolysis for acute iliofemoral thrombosis. J Vasc Surg Venous Lymphat Disord. 2019;7:153-161.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 15]  [Cited by in F6Publishing: 21]  [Article Influence: 4.2]  [Reference Citation Analysis (0)]
58.  Kim JY, Choi D, Guk Ko Y, Park S, Jang Y, Lee DY. Percutaneous treatment of deep vein thrombosis in May-Thurner syndrome. Cardiovasc Intervent Radiol. 2006;29:571-575.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 47]  [Cited by in F6Publishing: 40]  [Article Influence: 2.2]  [Reference Citation Analysis (0)]