This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
1. Introduction
Chronic venous insufficiency (CVI) is a common condition caused by dysfunctional valves in the venous circulation system [1]. The lack of muscular support in the lower extremity superficial veins leads to a higher incidence of varicose veins (VVs), which is nearly 2% per year [2], higher in the lower extremities [3, 4].
VVs result from a complex pathophysiology, with saphenofemoral junction (SFJ) reflux alone responsible for 75% of cases. Additional contributing factors include venous hypertension, valvular incompetence, vein wall changes, inflammation, and shear stress alterations [4–6].
First-line management consists of the use of compression stockings, modified lifestyle, and exercise regimens [7]. Open vein surgery was previously used but had significant disadvantages [5, 7]. Currently, minimally invasive procedures like endovenous radiofrequency ablation, trans-catheter-guided sclerotherapy, and endovenous laser treatment (EVLT) are preferred [8–10]. EVLT, in particular, uses thermal energy in an outpatient setting, guided by Duplex Ultrasound, and presents fewer complications compared to traditional methods [7, 11].
Although existing research indicates that EVLT is a safe and effective treatment for VVs, there is a paucity of data on long-term outcomes concerning symptom relief, recurrence rates, and patient satisfaction. This study’s objective is to examine these long-term results to evaluate EVLT’s efficacy and safety more comprehensively, considering the significant impact of CVI on healthcare systems.
2. Materials and Methods
2.1. Study Design and Patient Selection
In this retrospective cohort study, 68 patients with great saphenous vein (GSV) insufficiency and reflux, who were treated by EVLT between the years of 2008 and 2016, were included. The diagnosis was made using Duplex Ultrasound, with reflux defined as the reverse flow lasting more than 0.5 seconds. In our study, Hach’s classification system was employed to rate the severity of primary varicosities in the GSV. The grading scale is as follows: a score of 4 indicates varices near the groin area, 3 signifies varices around the midthigh region, 2 denotes varices in the upper calf area, 1 represents varices near the ankle, and a score of 0 is given when no varices are visible [12]. Patients were qualified for inclusion in the study if they presented with VVs accompanied by GSV reflux and were not pregnant. Exclusion criteria included age less than 18 years; patients with prior interventions on GSV; a poor health condition which was defined as the inability to perform required tasks physically, mentally, or socially; deep vein incompetency; superficial thrombophlebitis; nonhealing ulcers; nonpalpable pedal pulses; and extremely tortuous GSVs.
2.2. Data Collection
The radiological intervention and duplex ultrasound were conducted by expert radiologists, and data collection was undertaken by a physician. Data were collected and recorded in the patients’ case report form. Patients underwent evaluations preprocedure, followed by postprocedure assessments at one week, one month, three months, and six months to discern short-term outcomes. The length of long-term follow-up, however, varied from 5 to 12 years across patients.
2.3. Outcomes of Study
The study focused on the diameter of the GSV, GSV reflux, the signs and symptoms, and the patients’ quality of life (QoL) as variables of interest.
2.4. Device Description and Procedure
A preprocedural duplex ultrasound was conducted to determine the severity and tortuosity of GSV. This entails a comprehensive examination of crucial metrics like the length of time for venous reflux, the size of the veins, and the extent of vein twisting. These factors are vital because prolonged reflux duration, larger vein diameters, and heightened vein tortuosity suggest more severe venous disease. The procedure was performed using the 25 W 940 nm diode laser in continuous mode, causing thermal damage with a 1-3 mm per minute withdrawal rate.
The procedure was conducted under duplex ultrasound guidance in a conscious sedation environment. Initially, the leg was prepared and draped, followed by a targeted puncture of the GSV at the knee level, utilizing an ultrasound probe encased in a sterile cover for precision. The puncture site was carefully chosen for its proximity to the distal limit of venous reflux. Local anesthesia was administered using a 0.1–0.2% lidocaine solution provided by AstraZeneca, Wilmington, DE, USA. A 5-French (Fr) catheter was then inserted into the GSV, aided by a guidewire for exact positioning, as visualized under duplex ultrasound imaging. The catheter was advanced to a location 2 cm below the SFJ. Following this, a 600-micron laser fiber was threaded through the introducer sheath of the catheter, aiming towards the SFJ. Duplex ultrasound imaging verified the laser fiber’s precise placement, supplemented by the transdermal visibility of the laser’s aiming beam. The power settings for GSV less than 6, 6-8, and higher in diameter were 8, 10, and 12 W, respectively. The laser’s energy damaged the vascular endothelium and caused venous obliteration.
During the laser therapy, the total energy delivered averaged
2.5. Postprocedural Follow-Up
In this study, postprocedural management entailed a combined application of compression bandages and class 2 compression stockings exerting a pressure of 30-40 mmHg, implemented for one week postprocedure. The therapeutic effectiveness was assessed by evaluating the persistence of symptoms, occlusion of the GSV, and recanalization via duplex ultrasound. Immediate postprocedural assessments were conducted, followed by additional evaluations at intervals of one week, one month, three months, and six months. Long-term follow-ups were performed once within a timeframe of 5- to 12-year postprocedure.
Measurements of the GSV diameter were standardized across three segments: 2 cm distal to the SFJ for the proximal segment, at the midpoint between the knee and groin for the middle segment, and 2 cm proximal to the medial malleolus for the distal segment. To ensure consistency, all measurements were taken with the patient standing, during morning hours to account for circadian rhythm influences on venous diameter. The same ultrasound equipment and probe were used throughout, with measurements conducted by the same trained examiner. Additionally, calipers were positioned anteroposteriorly in each measurement to maintain uniformity in the methodology.
2.6. Quality-of-Life Questionnaire
Two questionnaires were used to assess the QoL in the study participants. The Medical Outcomes Study Short Form 36 Health Survey (SF-36 Iranian version questionnaire) [13] was selected to evaluate general QoL, and the Aberdeen Varicose Vein Questionnaire (AVVQ) [14] was chosen to assess disease-specific QoL in patients with VVs.
2.7. Statistics
Descriptive results were shown as
2.8. Ethics
Written consent was obtained from all patients. This study was approved by the ethics committee of a university-affiliated hospital.
3. Results
3.1. Demographic Characteristics
Sixty-eight patients with a mean age of 52.4 (±12.4) years (25-82), including 45 men (66.2%) and 23 women (33.8%), were included in this study. In our patient group, we noted an equal distribution of VVs, with 50% of the patients displaying the condition on the right side and the remaining 50% showing symptoms on the left side. In this study, it was discovered that 27 out of 68 patients (39.7%) held jobs that involved continuous standing for over one hour throughout the day. Table 1 provides a comprehensive overview of the associated conditions and risk factors.
Table 1
Demographic and baseline characteristics of patients undergoing endovenous laser treatment for varicose veins.
Variables | |
Age, | |
Gender, M/F no. (%) | 45/23 (66.2/38.2) |
BMI, mean (kg/m2) | |
Previous pregnancy, no. (%) | 21 (30.9) |
Previous family history, no. (%) | 11 (16.2%) |
Smoking, no. (%) | 14 (20.6) |
Job status, no. (%) | |
Moderate standing | 38 (60.3) |
Too much standing | 27 (39.7) |
Previous medical history, no. (%) | |
DVT | 10 (14.7) |
Spontaneous bleeding | 11 (16.2) |
DM | 3 (4.4) |
Foot ulcer | 15 (22.1) |
Foot edema | 55 (80.9) |
Clinical manifestations, no. (%) | |
Dull pain | 2 (2.9) |
Feeling heavy | 12 (17.6) |
Burning or irritating pain | 5 (7.4) |
Cramp | 2 (2.9) |
Physical exam, no. (%) | |
Healed venous ulcer | 28 (41.2) |
Active venous ulcer | 17 (25) |
Skin changes | 35 (51.5) |
Edema | 56 (82.4) |
Abbreviations: SD: standard deviation; M: male; F: female; no.: number; BMI: body mass index; kg: kilograms; DVT: deep vein thrombosis; DM: diabetes mellitus.
3.2. Short-Term Follow-Up
In the six-month follow-up of this research, we observed a notable decrease in the mean diameter of the GSV across all participants. The mean diameter of the proximal GSV segment reduced from
Table 2
Comparison of mean great saphenous vein diameter in proximal, middle, and distal segments in varicose vein patients undergoing endovenous laser treatment: short-term follow-up results.
Location (no.) | Time session | Pairwise comparison | |||
Proximal (55) | Preprocedure | <0.001 | Preprocedure vs. | ||
Short-term F/U | 1 w | ||||
1 m | |||||
3 m | |||||
6 m | |||||
Middle (48) | Preprocedure | <0.001 | Preprocedure vs. | ||
Short-term F/U | 1 w | ||||
1 m | |||||
3 m | |||||
6 m | |||||
Distal (44) | Preprocedure | <0.001 | Preprocedure vs. | ||
Short-term F/U | 1 w | ||||
1 m | |||||
3 m | |||||
6 m |
Abbreviations: no.: number; SD: standard deviation; F/U: follow-up; w: week; m: month; vs.: versus; IQR: interquartile range.
There were significant changes in the Hach classifications from before the procedure to the subsequent follow-up periods (
[figure(s) omitted; refer to PDF]
3.3. Long-Term Follow Up
The mean duration of follow-up was
Across all patients, the average diameter of the proximal segment of the GSV dropped from
Table 3
Comparison of mean great saphenous vein diameter in proximal, middle, and distal segments in varicose vein patients undergoing endovenous laser treatment: long-term follow-up results.
Location (no.) | Time session | ||
Proximal (64) | Preprocedure | <0.001 | |
Long-term F/U | |||
Middle (65) | Preprocedure | <0.001 | |
Long-term F/U | |||
Distal (66) | Preprocedure | <0.001 | |
Long-term F/U |
Abbreviations: no.: number; SD: standard deviation; F/U: follow-up; w: week; m: month; vs.: versus; IQR: interquartile range.
3.3.1. Quality of Life (QoL)
The results of the disease-specific questionnaire (AVVQ) demonstrated the substantial positive impact of EVLT in the long-term management of VVs. Additional and comprehensive information can be found in Supplementary Material Table 1.
The SF-36 results also demonstrate significant improvement in QoL across all domains except emotional well-being (Table 4).
Table 4
Comparing quality of life (QoL) changes in patients with varicose veins before and after endovenous laser treatment: insights from SF-36 questionnaire subscales.
Items | Before procedure, | After long-term follow-up, | |
Physical functioning | <0.001 | ||
Role limitations due to physical health | <0.001 | ||
Role limitations due to emotional problems | 0.001 | ||
Energy/fatigue | 0.091 | ||
Emotional well-being | 0.12 | ||
Social functioning | <0.001 | ||
Pain | <0.001 | ||
General health | 0.009 | ||
Total physical score | <0.001 | ||
Total mental score | <0.001 | ||
Total QoL score | <0.001 |
Abbreviations: SD: standard deviation; QoL: quality of life; IQR: interquartile range.
3.3.2. Recurrence Rate
Considering that recanalization and reflux are acknowledged as types of recurrence, in the latest follow-up, GSV reflux and recanalization were seen in 23 out of 68 patients (33.8%). A more detailed examination of the data reveals that the minimum incidence of GSV reflux occurred one-month postprocedure, with only 3 reported cases. Among the 23 patients who developed GSV reflux, 7 instances occurred within six-month postintervention, while the remaining 16 cases were identified during the extended follow-up period. Our evaluation revealed no significant difference in the baseline Hach classification and proximal GSV diameter, near the groin, between patients with and without disease recurrence, with respective mean diameters of
Table 5
Comparison of preprocedure great saphenous vein diameter between patients with recurrent varicose veins and those without recurrence during the latest follow-up.
GSV segment | Patients with recurrence, | Patients without recurrence, | |
Proximal | 0.5 | ||
Middle | 0.03 | ||
Distal | 0.056 |
Abbreviations: GSV: great saphenous vein; SD: standard deviation; mm: millimeter; IQR: interquartile range.
Totally 45 patients did not show recurrence in the last follow-up; among them, the data of follow-up time was determined in 43 patients. These 43 patients were followed up for
4. Discussion
EVLT is a minimally invasive and safe treatment option for patients with refractory VVs offering several benefits compared to conventional surgical treatments [15, 16]. Short-term outcomes of EVLT have been reported to be excellent, with an occlusion rate of over 90% and minimal complications [17, 18]. However, there is limited research on the long-term efficacy of laser therapy for treating VVs.
In a randomized clinical trial (RCT) study [19], patients were followed up for 5 years after treatment. The study revealed that EVLT was more effective compared to surgery.
The diameter of the GSV is a critical determinant in predicting the occurrence of reflux. According to previous research, a GSV diameter exceeding 5.05 millimeters is the strongest predictor of reflux [20]. In the current study, across all patients, we observed a notable reduction in the mean GSV diameters from the initial pretreatment measurements to the most recent follow-up. Specifically, the average diameters decreased from
Both EVLT and surgery are effective short-term treatments that improve the patients’ QoL and symptoms. However, in the long term, patients who underwent EVLT had better clinical outcomes and higher satisfaction levels compared with surgery [21]. All patients demonstrated symptom improvement after the procedure, with significant improvements in QoL observed in various areas, except for emotional well-being, which showed a less pronounced enhancement.
According to a systematic review study conducted by Kheirelseid et.al in 2018 [22], which included all clinical trial studies that compared long-term outcomes of EVLT and surgical treatments for VVs, the recurrence rates for EVLT (36.6%) and surgical treatments (33.3%) were not significantly different, a finding that aligns with the results of the current study.
O’Donnell et al. conducted an additional systematic review [23], which examined the incidence of VV recurrence following EVLT in comparison to ligation and stripping (L & S). This analysis encompassed all RCTs with a follow-up period of at least 2 years. The study revealed that the overall recurrence rate for VVs was 22% for both EVLT and ligation and stripping (L & S), indicating a comparable rate of recurrence over time for both treatment methods.
Importantly, it should be noted that a significant majority (70%) of the patients did not experience disease recurrence. The follow-up period, averaging 9 years, was extensive, with nearly half of the patients undergoing monitoring for over a decade without recorded instances of recurrence.
Unlike previous studies [24], this study revealed a significant difference in the mean diameter of the GSV between patients who experienced a recurrence and those who did not. Specifically, patients with recurrence had a larger average diameter in the middle part of the GSV before treatment compared to nonrecurrence patients (
While previous research has shown a correlation between being female and the onset of VVs [25], the present study yielded contrasting results. Specifically, a notable increase in the occurrence of VVs among men was observed, along with a higher chance of recurrence after treatment (
Although our follow-up schedule lacks regular intervals, it is essential to highlight the substantial duration of our follow-up, extending beyond 10 years for nearly half of our patients. This extended period confers a significant advantage to our study, providing valuable insights into long-term patient outcomes. In our long-term study, all patients showed a significant reduction in average GSV diameter that was concurrent and associated with improved general and disease-specific QoL scores. These outcomes demonstrate the enduring effectiveness of EVLT.
This study has several limitations that must be acknowledged. The absence of a control group treated with a classic method and the lack of randomized patient selection preclude a direct comparison with EVLT outcomes. Another constraint is the small sample size. Furthermore, the lack of a regular basis in our long-term follow-up and the variability in follow-up durations may potentially affect the robustness of the results; however, it is important to note that our patients were followed up at least 5 years, and this could be considered as a reasonable long follow-up time.
It should be taken into account that regarding our study starting date, we utilized a lower-wavelength laser for patients’ treatment, a choice that might be less common nowadays. Recent devices utilize physical parameters linked to increased photocoagulation effectiveness. Advancements in technology might have prompted interventional radiologists to opt for more advanced lasers over a decade. Furthermore, as modern techniques continue to evolve, it is reasonable to anticipate that patients treated with contemporary devices may exhibit even more favorable long-term outcomes in the coming years.
Nonetheless, the pivotal focus of our study centers on the extended duration follow-up, encompassing the assessment of patient symptoms, laser effectiveness, and patients’ QoL. Further research involving a larger cohort and more strictly defined follow-up periods, and the inclusion of a control group subjected to alternate treatments, is imperative to validate these results and assess the enduring effectiveness of the intervention.
5. Conclusion
This study highlights the potential of EVLT as a highly effective solution for long-term complications and recurrence rates associated with the treatment of VVs. This minimally invasive technique has been shown to significantly reduce patient symptoms and improve QoL.
Ethical Approval
This study was approved by the ethics committee of a university-affiliated hospital (Tehran University of Medical Science, TUMS).
Consent
Written consent was obtained from all patients.
[1] R. T. Eberhardt, J. D. Raffetto, "Chronic venous insufficiency," Circulation, vol. 111 no. 18, pp. 2398-2409, DOI: 10.1161/01.CIR.0000164199.72440.08, 2005.
[2] E. Rabe, G. Berboth, F. Pannier, "Epidemiology of chronic venous diseases," Wiener Medizinische Wochenschrift (1946), vol. 166 no. 9-10, pp. 260-263, DOI: 10.1007/s10354-016-0465-y, 2016.
[3] M. Chwała, W. Szczeklik, M. Szczeklik, T. Aleksiejew-Kleszczyński, M. Jagielska-Chwała, "Varicose veins of lower extremities, hemodynamics and treatment methods," Advances in Clinical and Experimental Medicine, vol. 24 no. 1,DOI: 10.17219/acem/31880, 2015.
[4] N. Labropoulos, A. K. Tassiopoulos, A. F. Bhatti, L. Leon, "Development of reflux in the perforator veins in limbs with primary venous disease," Journal of Vascular Surgery, vol. 43 no. 3, pp. 558-562, DOI: 10.1016/j.jvs.2005.11.046, 2006.
[5] K. Firouznia, H. Ghanaati, M. Hedayati, M. Shakiba, A. H. Jalali, R. Mirsharifi, A. Dargahi, "Endovenous laser treatment (EVLT) for the saphenous reflux and varicose veins: a follow-up study," Journal of Medical Imaging and Radiation Oncology, vol. 57 no. 1, pp. 15-20, DOI: 10.1111/j.1754-9485.2012.02457.x, 2013.
[6] J. J. Bergan, G. W. Schmid-Schönbein, P. D. Smith, A. N. Nicolaides, M. R. Boisseau, B. Eklof, "Chronic venous disease," The New England Journal of Medicine, vol. 355 no. 5, pp. 488-498, DOI: 10.1056/NEJMra055289, 2006.
[7] O. Ahadiat, S. Higgins, A. Ly, A. Nazemi, A. Wysong, "Review of endovenous thermal ablation of the great saphenous vein: endovenous laser therapy versus radiofrequency ablation," Dermatologic Surgery, vol. 44 no. 5, pp. 679-688, DOI: 10.1097/DSS.0000000000001478, 2018.
[8] J. Brittenden, D. Cooper, M. Dimitrova, G. Scotland, S. C. Cotton, A. Elders, G. MacLennan, C. R. Ramsay, J. Norrie, J. M. Burr, B. Campbell, P. Bachoo, I. Chetter, M. Gough, J. Earnshaw, T. Lees, J. Scott, S. A. Baker, E. Tassie, J. Francis, M. K. Campbell, "Five-year outcomes of a randomized trial of treatments for varicose veins," The New England Journal of Medicine, vol. 381 no. 10, pp. 912-922, DOI: 10.1056/NEJMoa1805186, 2019.
[9] S. Vemulapalli, K. Parikh, R. Coeytaux, V. Hasselblad, A. McBroom, A. Johnston, G. Raitz, M. J. Crowley, K. R. Lallinger, W. S. Jones, G. D. Sanders, "Systematic review and meta-analysis of endovascular and surgical revascularization for patients with chronic lower extremity venous insufficiency and varicose veins," American Heart Journal, vol. 196, pp. 131-143, DOI: 10.1016/j.ahj.2017.09.017, 2018.
[10] S. Vahaaho, K. Halmesmaki, A. Alback, E. Saarinen, M. Venermo, "Five-year follow-up of a randomized clinical trial comparing open surgery, foam sclerotherapy and endovenous laser ablation for great saphenous varicose veins," The British Journal of Surgery, vol. 105 no. 6, pp. 686-691, DOI: 10.1002/bjs.10757, 2018.
[11] R. J. Darwood, N. Theivacumar, D. Dellagrammaticas, A. I. Mavor, M. J. Gough, "Randomized clinical trial comparing endovenous laser ablation with surgery for the treatment of primary great saphenous varicose veins," The British Journal of Surgery, vol. 95 no. 3, pp. 294-301, DOI: 10.1002/bjs.6101, 2008.
[12] W. Hach, Phlebography and sonography of the veins, 1997.
[13] A. Montazeri, A. Goshtasebi, M. Vahdaninia, B. Gandek, "The short form health survey (SF-36): translation and validation study of the Iranian version," Quality of Life Research, vol. 14 no. 3, pp. 875-882, DOI: 10.1007/s11136-004-1014-5, 2005.
[14] A. M. Garratt, L. M. Macdonald, D. A. Ruta, I. T. Russell, J. K. Buckingham, Z. H. Krukowski, "Towards measurement of outcome for patients with varicose veins," Quality in Health Care, vol. 2 no. 1,DOI: 10.1136/qshc.2.1.5, 1993.
[15] P. Yao, T. Mukhdomi, Varicose Vein Endovenous Laser Therapy, 2023.
[16] Y. Pan, J. Zhao, J. Mei, M. Shao, J. Zhang, "Comparison of endovenous laser ablation and high ligation and stripping for varicose vein treatment: a meta-analysis," Phlebology, vol. 29 no. 2, pp. 109-119, DOI: 10.1177/0268355512473911, 2014.
[17] R. J. Min, S. E. Zimmet, M. N. Isaacs, M. D. Forrestal, "Endovenous laser treatment of the incompetent greater saphenous vein," Journal of Vascular and Interventional Radiology, vol. 12 no. 10, pp. 1167-1171, DOI: 10.1016/S1051-0443(07)61674-1, 2001.
[18] T. M. Proebstle, H. A. Lehr, A. Kargl, C. Espinola-Klein, W. Rother, S. Bethge, J. Knop, "Endovenous treatment of the greater saphenous vein with a 940-nm diode laser: thrombotic occlusion after endoluminal thermal damage by laser-generated steam bubbles," Journal of Vascular Surgery, vol. 35 no. 4, pp. 729-736, DOI: 10.1067/mva.2002.121132, 2002.
[19] T. Wallace, J. El-Sheikha, S. Nandhra, C. Leung, A. Mohamed, A. Harwood, G. Smith, D. Carradice, I. Chetter, "Long-term outcomes of endovenous laser ablation and conventional surgery for great saphenous varicose veins," The British Journal of Surgery, vol. 105 no. 13, pp. 1759-1767, DOI: 10.1002/bjs.10961, 2018.
[20] J. H. Joh, H. C. Park, "The cutoff value of saphenous vein diameter to predict reflux," Journal of the Korean Surgical Society, vol. 85 no. 4, pp. 169-174, DOI: 10.4174/jkss.2013.85.4.169, 2013.
[21] B. Siribumrungwong, P. Noorit, C. Wilasrusmee, J. Attia, A. Thakkinstian, "A systematic review and meta-analysis of randomised controlled trials comparing endovenous ablation and surgical intervention in patients with varicose vein," European Journal of Vascular and Endovascular Surgery, vol. 44 no. 2, pp. 214-223, DOI: 10.1016/j.ejvs.2012.05.017, 2012.
[22] E. A. H. Kheirelseid, G. Crowe, R. Sehgal, D. Liakopoulos, H. Bela, E. Mulkern, C. McDonnell, M. O'Donohoe, "Systematic review and meta-analysis of randomized controlled trials evaluating long-term outcomes of endovenous management of lower extremity varicose veins," Journal of Vascular Surgery. Venous and Lymphatic Disorders, vol. 6 no. 2, pp. 256-270, DOI: 10.1016/j.jvsv.2017.10.012, 2018.
[23] T. F. O'Donnell, E. M. Balk, M. Dermody, E. Tangney, M. D. Iafrati, "Recurrence of varicose veins after endovenous ablation of the great saphenous vein in randomized trials," Journal of Vascular Surgery. Venous and Lymphatic Disorders, vol. 4 no. 1, pp. 97-105, DOI: 10.1016/j.jvsv.2014.11.004, 2016.
[24] N. S. Theivacumar, D. Dellagrammaticas, R. J. Beale, A. I. Mavor, M. J. Gough, "Factors influencing the effectiveness of endovenous laser ablation (EVLA) in the treatment of great saphenous vein reflux," European Journal of Vascular and Endovascular Surgery, vol. 35 no. 1, pp. 119-123, DOI: 10.1016/j.ejvs.2007.08.010, 2008.
[25] M. R. Antani, J. B. Dattilo, Varicose Veins, 2023.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Copyright © 2024 Hossein Ghanaati et al. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
Introduction. This study investigates the long-term effectiveness and safety of endovenous laser treatment (EVLT) for chronic venous insufficiency (CVI), a condition commonly caused by dysfunctional valves in the venous circulation system. Materials and Methods. In this retrospective cohort study, patients underwent EVLT and were followed up for successive short intervals and one last time after a median duration of 9-year postprocedural. Pre- and postprocedure duplex ultrasound was used to assess changes in the great saphenous vein (GSV) diameter, reflux, and saphenofemoral junction incompetence. Quality of life was evaluated using the SF-36 and Aberdeen Varicose Vein Questionnaire (AVVQ). Results. Sixty-eight patients with a mean age of
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer