Pub Date : 2025-02-11DOI: 10.1016/j.jvsv.2025.102211
Megan Lombardi, Julia Glass, Suman Wasan, William Marston
Objective: Acute iliofemoral deep vein thrombosis (IFDVT) in young adults and adolescents is a cause of lower extremity pain and edema that may lead to chronic debilitating symptoms. Treatment options include pharmaco-mechanical thrombectomy, stent placement, and anticoagulation. The lack of long-term data in young patients after venous stenting leads to variability in treatment and reluctance to employ stents in this population. The purpose of this study is to review the etiology and incidence of post-thrombotic syndrome (PTS) along with the role of intervention in young patients after IFDVT.
Methods: Patients presenting with acute IFDVT were identified retrospectively through Peripheral Vascular Lab databases. IFDVT was defined as any thrombus believed to be <1 month old involving the common femoral or more proximal veins. Charts were reviewed to identify demographics, risk factors for venous thrombosis, relevant laboratory data, treatment provided for the DVT, and patient outcomes.
Results: Forty-nine patients under age 25 were identified with acute IFDVT and no other acute illness or trauma precipitating thrombosis. Forty patients (81%) were female. Thirty-three patients (58.1%) identified as White, 10 (28%) as Black and five (9.3%) as Hispanic. Hypercoagulable states were identified in 25 patients (51%) with Factor V deficiency (9 patients) and antiphospholipid antibodies (6 patients) being the most common. Intervention was performed in 36 patients (73.5%), which consisted of pharmaco-mechanical thrombectomy with balloon angioplasty in 22 patients and with stent placement in 14. One year after IFDVT, 19 patients (43.2%) reported no PTS symptoms, 10 (22.7%) reported mild symptoms, and 15 (34.1%) reported moderate or severe symptoms. Recurrent IFDVT occurred in 18% of patients at 1 year and 26.2% at 3 years after IFDVT.
Conclusions: Acute IFDVT in young patients occurs typically in females, the majority of whom are found to have a hypercoagulable state. Most of this cohort were treated without venous stenting. However, significant PTS and recurrent IFDVT occurred frequently after the initial event, suggesting that aggressive treatment is warranted. This is an understudied patient population in whom the role of intervention and stenting is unclear, suggesting that focused study in larger cohorts is required to improve treatment recommendations.
{"title":"Acute iliofemoral deep venous thrombosis in adolescents and young adults is associated with hypercoagulable states and a significant incidence of post-thrombotic syndrome.","authors":"Megan Lombardi, Julia Glass, Suman Wasan, William Marston","doi":"10.1016/j.jvsv.2025.102211","DOIUrl":"10.1016/j.jvsv.2025.102211","url":null,"abstract":"<p><strong>Objective: </strong>Acute iliofemoral deep vein thrombosis (IFDVT) in young adults and adolescents is a cause of lower extremity pain and edema that may lead to chronic debilitating symptoms. Treatment options include pharmaco-mechanical thrombectomy, stent placement, and anticoagulation. The lack of long-term data in young patients after venous stenting leads to variability in treatment and reluctance to employ stents in this population. The purpose of this study is to review the etiology and incidence of post-thrombotic syndrome (PTS) along with the role of intervention in young patients after IFDVT.</p><p><strong>Methods: </strong>Patients presenting with acute IFDVT were identified retrospectively through Peripheral Vascular Lab databases. IFDVT was defined as any thrombus believed to be <1 month old involving the common femoral or more proximal veins. Charts were reviewed to identify demographics, risk factors for venous thrombosis, relevant laboratory data, treatment provided for the DVT, and patient outcomes.</p><p><strong>Results: </strong>Forty-nine patients under age 25 were identified with acute IFDVT and no other acute illness or trauma precipitating thrombosis. Forty patients (81%) were female. Thirty-three patients (58.1%) identified as White, 10 (28%) as Black and five (9.3%) as Hispanic. Hypercoagulable states were identified in 25 patients (51%) with Factor V deficiency (9 patients) and antiphospholipid antibodies (6 patients) being the most common. Intervention was performed in 36 patients (73.5%), which consisted of pharmaco-mechanical thrombectomy with balloon angioplasty in 22 patients and with stent placement in 14. One year after IFDVT, 19 patients (43.2%) reported no PTS symptoms, 10 (22.7%) reported mild symptoms, and 15 (34.1%) reported moderate or severe symptoms. Recurrent IFDVT occurred in 18% of patients at 1 year and 26.2% at 3 years after IFDVT.</p><p><strong>Conclusions: </strong>Acute IFDVT in young patients occurs typically in females, the majority of whom are found to have a hypercoagulable state. Most of this cohort were treated without venous stenting. However, significant PTS and recurrent IFDVT occurred frequently after the initial event, suggesting that aggressive treatment is warranted. This is an understudied patient population in whom the role of intervention and stenting is unclear, suggesting that focused study in larger cohorts is required to improve treatment recommendations.</p>","PeriodicalId":17537,"journal":{"name":"Journal of vascular surgery. Venous and lymphatic disorders","volume":" ","pages":"102211"},"PeriodicalIF":2.8,"publicationDate":"2025-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143414556","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-05DOI: 10.1016/j.jvsv.2025.102208
Slade Smith, Hayden Butts, Jack Owens, Sara Matheson, Mary Meghan Dickerson, Arjun Jayaraj
<p><strong>Objective: </strong>Venous stenting has become the standard of care for patients with iliofemoral venous stenosis who have failed conservative therapy. Although outcome data following such stenting exist for Wallstents and Wallstent-Zenith (Z) stent combination, such data for dedicated stents is sparse outside of industry-sponsored trials. This study aims to address this gap by comparing the outcomes of matched cohorts of limbs that underwent stenting with either the Medtronic Abre stent (Medtronic Inc), the Bard Venovo stent (Becton, Dickinson, and Co), or Wallstent-Z stent combination (Boston Scientific; Cook Medical Inc).</p><p><strong>Methods: </strong>Contemporaneously entered data on matched cohorts of patients who underwent stenting from 2016 to 2022 for quality of life (QoL)-impairing iliofemoral venous stenosis (not occlusion) after failing conservative therapy was analyzed. The venous clinical severity score (VCSS, 0-27), grade of swelling (GOS, 0-4), visual analog scale pain score (VAS pain score, 0-10), and CIVIQ-20 QoL scores were evaluated initially and post stenting to assess the effects of stenting. Analysis of variance and paired t-tests were used to compare clinical and QoL variables, whereas Kaplan-Meier analysis was used to examine primary, primary-assisted, and secondary stent patencies, with log-rank test used to discriminate between different curves.</p><p><strong>Results: </strong>There were a total of 198 limbs that had undergone stenting, including 68 in the Abre, 60 in the Venovo and 70 in the Wallstent-Z stent groups. The median age for the entire cohort was 65 years (range, 21-101 years). The cohort included 141 women and 57 men. Left laterality (112 limbs) was more common than right laterality (86 limbs). Post-thrombotic syndrome was seen in 146 limbs and nonthrombotic iliac vein lesions/May-Thurner syndrome in 52 limbs. The median body mass index was 35 kg/m<sup>2</sup>. Median follow-up was 20 months. For the entire cohort, post stenting, VCSS improved from 6 to 4.5 at 3 months (P < .0001), further improved to 4 at 6 months (P < .0001), and remained at 4 at 12 months (P < .0001) and 24 months (P < .0001). GOS for the entire cohort improved from 3 to 1 at 3 months (P < .0001) and remained at 1 at 6 months, (P < .0001), 12 months (P < .0001), and 24 months (P < .0001). VAS pain score for the entire cohort improved from 8 to 2 at 3 months (P < .0001), increased to 3 at 6 months (P < .0001) before dropping to 2 at 12 months (P < .0001), and remained at 2 at 24 months (P < .0001). The CIVIQ-20 score for the entire cohort improved from 61 to 38 (P < .0001) over the duration of follow-up. The primary patencies for the Abre, Bard, and Wallstent-Z stent groups at 32 months were 93%, 86%, and 92%, respectively (P = .37). Primary assisted patencies for all three groups at 32 months was 100% (P = .08). There were no stent occlusions in any of the groups. Reintervention was pursued for QoL-impairing recurrent clinica
{"title":"Outcomes following stenting for symptomatic chronic iliofemoral venous stenosis - a comparison of three stent types.","authors":"Slade Smith, Hayden Butts, Jack Owens, Sara Matheson, Mary Meghan Dickerson, Arjun Jayaraj","doi":"10.1016/j.jvsv.2025.102208","DOIUrl":"10.1016/j.jvsv.2025.102208","url":null,"abstract":"<p><strong>Objective: </strong>Venous stenting has become the standard of care for patients with iliofemoral venous stenosis who have failed conservative therapy. Although outcome data following such stenting exist for Wallstents and Wallstent-Zenith (Z) stent combination, such data for dedicated stents is sparse outside of industry-sponsored trials. This study aims to address this gap by comparing the outcomes of matched cohorts of limbs that underwent stenting with either the Medtronic Abre stent (Medtronic Inc), the Bard Venovo stent (Becton, Dickinson, and Co), or Wallstent-Z stent combination (Boston Scientific; Cook Medical Inc).</p><p><strong>Methods: </strong>Contemporaneously entered data on matched cohorts of patients who underwent stenting from 2016 to 2022 for quality of life (QoL)-impairing iliofemoral venous stenosis (not occlusion) after failing conservative therapy was analyzed. The venous clinical severity score (VCSS, 0-27), grade of swelling (GOS, 0-4), visual analog scale pain score (VAS pain score, 0-10), and CIVIQ-20 QoL scores were evaluated initially and post stenting to assess the effects of stenting. Analysis of variance and paired t-tests were used to compare clinical and QoL variables, whereas Kaplan-Meier analysis was used to examine primary, primary-assisted, and secondary stent patencies, with log-rank test used to discriminate between different curves.</p><p><strong>Results: </strong>There were a total of 198 limbs that had undergone stenting, including 68 in the Abre, 60 in the Venovo and 70 in the Wallstent-Z stent groups. The median age for the entire cohort was 65 years (range, 21-101 years). The cohort included 141 women and 57 men. Left laterality (112 limbs) was more common than right laterality (86 limbs). Post-thrombotic syndrome was seen in 146 limbs and nonthrombotic iliac vein lesions/May-Thurner syndrome in 52 limbs. The median body mass index was 35 kg/m<sup>2</sup>. Median follow-up was 20 months. For the entire cohort, post stenting, VCSS improved from 6 to 4.5 at 3 months (P < .0001), further improved to 4 at 6 months (P < .0001), and remained at 4 at 12 months (P < .0001) and 24 months (P < .0001). GOS for the entire cohort improved from 3 to 1 at 3 months (P < .0001) and remained at 1 at 6 months, (P < .0001), 12 months (P < .0001), and 24 months (P < .0001). VAS pain score for the entire cohort improved from 8 to 2 at 3 months (P < .0001), increased to 3 at 6 months (P < .0001) before dropping to 2 at 12 months (P < .0001), and remained at 2 at 24 months (P < .0001). The CIVIQ-20 score for the entire cohort improved from 61 to 38 (P < .0001) over the duration of follow-up. The primary patencies for the Abre, Bard, and Wallstent-Z stent groups at 32 months were 93%, 86%, and 92%, respectively (P = .37). Primary assisted patencies for all three groups at 32 months was 100% (P = .08). There were no stent occlusions in any of the groups. Reintervention was pursued for QoL-impairing recurrent clinica","PeriodicalId":17537,"journal":{"name":"Journal of vascular surgery. Venous and lymphatic disorders","volume":" ","pages":"102208"},"PeriodicalIF":2.8,"publicationDate":"2025-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143374438","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-05DOI: 10.1016/j.jvsv.2025.102207
Leizhi Ku, Di Huang, Ming Qi
{"title":"Successful endovascular treatment of post-traumatic iliac arteriovenous fistula.","authors":"Leizhi Ku, Di Huang, Ming Qi","doi":"10.1016/j.jvsv.2025.102207","DOIUrl":"10.1016/j.jvsv.2025.102207","url":null,"abstract":"","PeriodicalId":17537,"journal":{"name":"Journal of vascular surgery. Venous and lymphatic disorders","volume":" ","pages":"102207"},"PeriodicalIF":2.8,"publicationDate":"2025-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143374440","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-29DOI: 10.1016/j.jvsv.2025.102199
Colin M Cleary, Emily Orosco, James Gallagher, James Gallagher, Mouhanad Ayach, Kaveh Davoudi, Allison Bailey, Parth Shah, Elizabeth Aitcheson, Ya-Huei Li, Kristy Wrana, Edward D Gifford
Objectives: Chronic anticoagulation for atrial fibrillation, a history of venous thromboembolism, and after heart valve replacement is often stopped or bridged for surgery. Our institutional practice is to continue anticoagulation through ambulatory phlebectomy (AP) procedures. As such, we aimed to compare postprocedure bleeding and major adverse events in patients on anticoagulation who received AP compared with patients not on anticoagulation.
Methods: We included all patients who required AP from January 2016 to February 2023. Given the low frequency of chronic anticoagulation during the study period, as defined as patients on anticoagulation ≥30 days before index procedure and not held through the procedure, a propensity score match of 16 demographic parameters was performed to better match patients. After propensity matching, we compared the frequency and quality of postprocedural bleeding (none, incisional, large volume), extent of postprocedural ecchymosis (none, minimal, moderate, significant), and pain (minimal, moderate, severe) on follow-up examination with a provider. Thirty-day emergency department (ED) visits and major adverse cardiac events were also recorded for each patient. Continuous variables were compared using independent t tests or Mann-Whitney U tests, and categorical variables were compared using a χ2 or Fisher's exact test.
Results: In total, 1853 patients received AP from four outpatient offices during the study period, 101 (5.5%) of whom were on chronic anticoagulation. Seventy patients for each group were propensity score matched in key demographics including age, gender, body mass index, Clinical-Etiology-Anatomy-Pathophysiology classification, prior vein procedures, concomitant laser procedures, number of phlebectomies performed, and comorbidities like history of deep vein thrombosis, pulmonary embolism, and peripheral arterial disease. There were no intraoperative major bleeding events. Patients on chronic anticoagulation were not more likely to have increased postprocedural bleeding (2.9% vs 0%; P = .496), significant ecchymosis (4.5% vs 1.5%; P = .671), severe pain on follow-up (1.4% vs 0%; P = .604), or increased likelihood of postprocedural cellulitis (1.4% vs 0%; P = 1.000). There were no instances of 30-day ED visits or major adverse cardiac events. Within patients on anticoagulation, use of rivaroxaban (8%) had higher incidence of bleeding than those on apixaban or warfarin (0%); however, these findings were not significant.
Conclusions: AP while continuing chronic anticoagulation did not result in an increased rate of bleeding, ED visits, or major adverse events. It is likely safe to continue anticoagulation throughout these outpatient procedures.
{"title":"Continuation of anticoagulation through ambulatory phlebectomy does not impact postoperative bleeding risk.","authors":"Colin M Cleary, Emily Orosco, James Gallagher, James Gallagher, Mouhanad Ayach, Kaveh Davoudi, Allison Bailey, Parth Shah, Elizabeth Aitcheson, Ya-Huei Li, Kristy Wrana, Edward D Gifford","doi":"10.1016/j.jvsv.2025.102199","DOIUrl":"10.1016/j.jvsv.2025.102199","url":null,"abstract":"<p><strong>Objectives: </strong>Chronic anticoagulation for atrial fibrillation, a history of venous thromboembolism, and after heart valve replacement is often stopped or bridged for surgery. Our institutional practice is to continue anticoagulation through ambulatory phlebectomy (AP) procedures. As such, we aimed to compare postprocedure bleeding and major adverse events in patients on anticoagulation who received AP compared with patients not on anticoagulation.</p><p><strong>Methods: </strong>We included all patients who required AP from January 2016 to February 2023. Given the low frequency of chronic anticoagulation during the study period, as defined as patients on anticoagulation ≥30 days before index procedure and not held through the procedure, a propensity score match of 16 demographic parameters was performed to better match patients. After propensity matching, we compared the frequency and quality of postprocedural bleeding (none, incisional, large volume), extent of postprocedural ecchymosis (none, minimal, moderate, significant), and pain (minimal, moderate, severe) on follow-up examination with a provider. Thirty-day emergency department (ED) visits and major adverse cardiac events were also recorded for each patient. Continuous variables were compared using independent t tests or Mann-Whitney U tests, and categorical variables were compared using a χ<sup>2</sup> or Fisher's exact test.</p><p><strong>Results: </strong>In total, 1853 patients received AP from four outpatient offices during the study period, 101 (5.5%) of whom were on chronic anticoagulation. Seventy patients for each group were propensity score matched in key demographics including age, gender, body mass index, Clinical-Etiology-Anatomy-Pathophysiology classification, prior vein procedures, concomitant laser procedures, number of phlebectomies performed, and comorbidities like history of deep vein thrombosis, pulmonary embolism, and peripheral arterial disease. There were no intraoperative major bleeding events. Patients on chronic anticoagulation were not more likely to have increased postprocedural bleeding (2.9% vs 0%; P = .496), significant ecchymosis (4.5% vs 1.5%; P = .671), severe pain on follow-up (1.4% vs 0%; P = .604), or increased likelihood of postprocedural cellulitis (1.4% vs 0%; P = 1.000). There were no instances of 30-day ED visits or major adverse cardiac events. Within patients on anticoagulation, use of rivaroxaban (8%) had higher incidence of bleeding than those on apixaban or warfarin (0%); however, these findings were not significant.</p><p><strong>Conclusions: </strong>AP while continuing chronic anticoagulation did not result in an increased rate of bleeding, ED visits, or major adverse events. It is likely safe to continue anticoagulation throughout these outpatient procedures.</p>","PeriodicalId":17537,"journal":{"name":"Journal of vascular surgery. Venous and lymphatic disorders","volume":" ","pages":"102199"},"PeriodicalIF":2.8,"publicationDate":"2025-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143074942","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-29DOI: 10.1016/j.jvsv.2025.102200
Alexandr Kuperin, Evgeny Seliverstov, Evgeny An, Igor Lebedev, Igor Zolotukhin
Objectives: The aim of the study was to assess the mechanical thrombectomy (MT) and catheter-directed thrombolysis (CDT) use in patients with deep vein thrombosis (DVT) in tertiary care.
Methods: We conducted a single-center retrospective cohort study. A tertiary hospital database from January 2022 to December 2023 was analyzed. All records of patients referred for DVT were extracted. The collected data included general patient information, medical history, results of physical examination, duplex ultrasound, and laboratory analyses. We assessed indications and contraindications for MT and CDT considering possible benefits and risks. We have identified patients who could be eligible for this technique.
Results: A total of 2427 patients with DVT were referred to hospital from January 2022 to December 2023. Among them, 961 patients (39.6%) had no indications for hospital admission or refused it and were recommended to receive anticoagulation on an outpatient basis, and 1466 patients (60.4%) were admitted to the hospital. Among the hospitalized patients, 1277 had a proximal DVT and 189 had a distal DVT. The number of patients with iliofemoral DVT was 451 (18.6%). We found only 82 cases (3.4%) that could be potentially eligible for endovascular thrombectomy considering all possible indications and contraindications. Two attempts and 14 successful procedures were conducted during the period of the study.
Conclusions: The number of patients with DVT who could be eligible for MT and CDT in a tertiary hospital is low.
{"title":"Mechanical thrombectomy and catheter directed thrombolysis utilization in patients with deep vein thrombosis: Analysis of a database of a tertiary hospital.","authors":"Alexandr Kuperin, Evgeny Seliverstov, Evgeny An, Igor Lebedev, Igor Zolotukhin","doi":"10.1016/j.jvsv.2025.102200","DOIUrl":"10.1016/j.jvsv.2025.102200","url":null,"abstract":"<p><strong>Objectives: </strong>The aim of the study was to assess the mechanical thrombectomy (MT) and catheter-directed thrombolysis (CDT) use in patients with deep vein thrombosis (DVT) in tertiary care.</p><p><strong>Methods: </strong>We conducted a single-center retrospective cohort study. A tertiary hospital database from January 2022 to December 2023 was analyzed. All records of patients referred for DVT were extracted. The collected data included general patient information, medical history, results of physical examination, duplex ultrasound, and laboratory analyses. We assessed indications and contraindications for MT and CDT considering possible benefits and risks. We have identified patients who could be eligible for this technique.</p><p><strong>Results: </strong>A total of 2427 patients with DVT were referred to hospital from January 2022 to December 2023. Among them, 961 patients (39.6%) had no indications for hospital admission or refused it and were recommended to receive anticoagulation on an outpatient basis, and 1466 patients (60.4%) were admitted to the hospital. Among the hospitalized patients, 1277 had a proximal DVT and 189 had a distal DVT. The number of patients with iliofemoral DVT was 451 (18.6%). We found only 82 cases (3.4%) that could be potentially eligible for endovascular thrombectomy considering all possible indications and contraindications. Two attempts and 14 successful procedures were conducted during the period of the study.</p><p><strong>Conclusions: </strong>The number of patients with DVT who could be eligible for MT and CDT in a tertiary hospital is low.</p>","PeriodicalId":17537,"journal":{"name":"Journal of vascular surgery. Venous and lymphatic disorders","volume":" ","pages":"102200"},"PeriodicalIF":2.8,"publicationDate":"2025-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143074945","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-29DOI: 10.1016/j.jvsv.2025.102198
Ana Clarice de Carvalho Bacelar, E M Netto, N Barreto, R Neves, C Heine, P Botelho, C S C B Almeida, E Ramalho, R Aras
Background: Despite advances in wound care, the dressing and management of chronic ulcers on lower limbs remains unsatisfactory. The simplicity, cost effectiveness, and diverse application possibilities of ultrasound-guided foam sclerotherapy make it an attractive and effective approach to treat patients with no access to or contraindications to more invasive methods. We sought to evaluate the healing rate of chronic venous ulcers (Clinical, Etiological, Anatomical, Pathophysiological [CEAP] C6) in patients treated with ultrasound guided foam sclerotherapy.
Methods: From January 2018 to December 2020, 279 patients (336 legs) classified at the first consultation as stage 6 for CEAP disease were followed during treatment of axial venous reflux in saphenous and tributary veins with polidocanol (Aethosxysklerol) foam and evaluated at 52 weeks for complete healing rates or ≥50% ulcer size reduction, using Kaplan-Meier statistics and Cox regression to study the influence of covariates.
Results: The average age of the 279 patients was 55 years. Of these, 156 (56%) showed complete healing in 52 weeks and 89 (32%) achieved a wound area reduction of >50%. Ulcer size, severity, lymphedema, and reduced dorsiflexion of the ankle were significantly associated with healing difficulty. Time of ulcer progression up to beginning of treatment (P < .01), ulcer size (P = .01), lymphedema (P = .006), reduced dorsiflexion of the ankle (P = .01), and age ≥65 years (P = .003) were significantly associated with difficulty in healing. Patients with a mean Venous Clinical Severity Score of 18.7 had a better prognosis (18.7 vs 22.5; P < .001).
Conclusions: Most patients with chronic venous ulcers (CEAP 6) treated with foam sclerotherapy achieved healing or significant improvement within 52 weeks. Healing was highly influenced by time until treatment, ulcer size, reduced dorsiflexion of the ankle and/or lymphedema presence, and the use of compression therapy.
{"title":"Promising results of ultrasound guided foam sclerotherapy for treating chronic venous ulcers.","authors":"Ana Clarice de Carvalho Bacelar, E M Netto, N Barreto, R Neves, C Heine, P Botelho, C S C B Almeida, E Ramalho, R Aras","doi":"10.1016/j.jvsv.2025.102198","DOIUrl":"10.1016/j.jvsv.2025.102198","url":null,"abstract":"<p><strong>Background: </strong>Despite advances in wound care, the dressing and management of chronic ulcers on lower limbs remains unsatisfactory. The simplicity, cost effectiveness, and diverse application possibilities of ultrasound-guided foam sclerotherapy make it an attractive and effective approach to treat patients with no access to or contraindications to more invasive methods. We sought to evaluate the healing rate of chronic venous ulcers (Clinical, Etiological, Anatomical, Pathophysiological [CEAP] C6) in patients treated with ultrasound guided foam sclerotherapy.</p><p><strong>Methods: </strong>From January 2018 to December 2020, 279 patients (336 legs) classified at the first consultation as stage 6 for CEAP disease were followed during treatment of axial venous reflux in saphenous and tributary veins with polidocanol (Aethosxysklerol) foam and evaluated at 52 weeks for complete healing rates or ≥50% ulcer size reduction, using Kaplan-Meier statistics and Cox regression to study the influence of covariates.</p><p><strong>Results: </strong>The average age of the 279 patients was 55 years. Of these, 156 (56%) showed complete healing in 52 weeks and 89 (32%) achieved a wound area reduction of >50%. Ulcer size, severity, lymphedema, and reduced dorsiflexion of the ankle were significantly associated with healing difficulty. Time of ulcer progression up to beginning of treatment (P < .01), ulcer size (P = .01), lymphedema (P = .006), reduced dorsiflexion of the ankle (P = .01), and age ≥65 years (P = .003) were significantly associated with difficulty in healing. Patients with a mean Venous Clinical Severity Score of 18.7 had a better prognosis (18.7 vs 22.5; P < .001).</p><p><strong>Conclusions: </strong>Most patients with chronic venous ulcers (CEAP 6) treated with foam sclerotherapy achieved healing or significant improvement within 52 weeks. Healing was highly influenced by time until treatment, ulcer size, reduced dorsiflexion of the ankle and/or lymphedema presence, and the use of compression therapy.</p>","PeriodicalId":17537,"journal":{"name":"Journal of vascular surgery. Venous and lymphatic disorders","volume":" ","pages":"102198"},"PeriodicalIF":2.8,"publicationDate":"2025-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143074956","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-19DOI: 10.1016/j.jvsv.2025.102192
Görkem Yiğit, Ufuk Türkmen
Objective: This study aimed to examine the early clinical outcomes of AngioJet rheolytic thrombectomy (RT) in patients with acute bilateral iliofemoral deep vein thrombosis (IFDVT), with a specific focus on the incidence of post-thrombotic syndrome.
Methods: From March 2021 to August 2023, 16 consecutive patients with acute bilateral IFDVT treated with AngioJet RT at our center were evaluated. Primary outcomes include patency of the target veins, development of post-thrombotic syndrome, recurrent DVT, and procedure-related death. Secondary outcomes included minor or major bleeding, acute kidney injury, documented hemoglobinuria, cardiac event, pulmonary embolism, limb loss, and death.
Results: The mean age of the patients was 69 ± 12 years (range, 53-87 years). Malignancy and recent major surgery were the most prevalent risk factors, each observed in 25% of patients (n = 4). Technical success, complete clot removal, and alleviation of symptoms were achieved in all patients (n = 16; 100%). In one-quarter of the patients (n = 4), transient hemoglobinuria was observed following the procedure. This complication resolved spontaneously after adequate fluid replenishment. Minor bleeding occurred in three patients (19%), whereas no patients had major bleeding complication. There was one postoperative acute kidney injury and transient bradycardia (6%). Three patients died after the procedures (19%). One patient (6%) developed postoperative massive pulmonary embolism. The mean follow-up was 11 ± 6 months (range, 5-19 months). The primary patency rate was 92% and 91%, respectively, 6 and 12 months after procedures. One patient had reocclusion during the follow-up.
Conclusions: AngioJet RT applied to patients with bilateral IFDVT provides a promising picture, providing a patent vein lumen with high procedural success and achieving convincing early symptomatic improvement in severely symptomatic patients with impaired quality of life. In this early case series, the feasibility of the AngioJet device in elderly cases appears to be a significant problem. Therefore, patient selection is essential.
{"title":"A preliminary experience on the efficacy, safety, and short-term results in the treatment of acute bilateral iliofemoral deep vein thrombosis with the Angiojet rheolytic thrombectomy.","authors":"Görkem Yiğit, Ufuk Türkmen","doi":"10.1016/j.jvsv.2025.102192","DOIUrl":"10.1016/j.jvsv.2025.102192","url":null,"abstract":"<p><strong>Objective: </strong>This study aimed to examine the early clinical outcomes of AngioJet rheolytic thrombectomy (RT) in patients with acute bilateral iliofemoral deep vein thrombosis (IFDVT), with a specific focus on the incidence of post-thrombotic syndrome.</p><p><strong>Methods: </strong>From March 2021 to August 2023, 16 consecutive patients with acute bilateral IFDVT treated with AngioJet RT at our center were evaluated. Primary outcomes include patency of the target veins, development of post-thrombotic syndrome, recurrent DVT, and procedure-related death. Secondary outcomes included minor or major bleeding, acute kidney injury, documented hemoglobinuria, cardiac event, pulmonary embolism, limb loss, and death.</p><p><strong>Results: </strong>The mean age of the patients was 69 ± 12 years (range, 53-87 years). Malignancy and recent major surgery were the most prevalent risk factors, each observed in 25% of patients (n = 4). Technical success, complete clot removal, and alleviation of symptoms were achieved in all patients (n = 16; 100%). In one-quarter of the patients (n = 4), transient hemoglobinuria was observed following the procedure. This complication resolved spontaneously after adequate fluid replenishment. Minor bleeding occurred in three patients (19%), whereas no patients had major bleeding complication. There was one postoperative acute kidney injury and transient bradycardia (6%). Three patients died after the procedures (19%). One patient (6%) developed postoperative massive pulmonary embolism. The mean follow-up was 11 ± 6 months (range, 5-19 months). The primary patency rate was 92% and 91%, respectively, 6 and 12 months after procedures. One patient had reocclusion during the follow-up.</p><p><strong>Conclusions: </strong>AngioJet RT applied to patients with bilateral IFDVT provides a promising picture, providing a patent vein lumen with high procedural success and achieving convincing early symptomatic improvement in severely symptomatic patients with impaired quality of life. In this early case series, the feasibility of the AngioJet device in elderly cases appears to be a significant problem. Therefore, patient selection is essential.</p>","PeriodicalId":17537,"journal":{"name":"Journal of vascular surgery. Venous and lymphatic disorders","volume":" ","pages":"102192"},"PeriodicalIF":2.8,"publicationDate":"2025-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11875154/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143007753","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
<p><strong>Objective: </strong>The International Society of Lymphology proposed a grading standard for lymphedema in 2020 based on the percent increase in the volume of the affected limb compared to that of the healthy limb. However, this method is cumbersome and time consuming to measure and calculate, and a standardized formula across different institutions is not available. Therefore, the aim of this study was to investigate the value of nonenhanced magnetic resonance imaging (MRI) for grading primary lower extremity lymphedema (PLEL).</p><p><strong>Methods: </strong>This retrospective study included 124 consecutive patients with unilateral PLEL from 2021 to 2023. All patients were categorized into three groups, mild (n = 43), moderate (n = 41), and severe (n = 40), according to the 2020 International Society of Lymphology grading standard. From the lymphedema involvement range (vertical range: whole lower extremity, only thigh, only calf and ankle; transversal range: ≤25% of the cross-section, 26%-50%, 51%-75%, and >75%), MRI signs of lymphedema (parallel lines sign, grid sign, honeycomb sign, band sign, crescent sign, lymphatic lake sign, and nebula sign), and lymphedema measurements (total diameter, total circumference, and total area of the affected limb; diameter and area of the bone, muscle, subcutaneous fat, and subcutaneous soft tissues on the affected limb; circumference of the bone and muscle on the affected limb; thickness of skin; thickness of band sign; thickness of crescent sign) were recorded and statistically analysed in the three groups of patients.</p><p><strong>Results: </strong>The statistically significant differences in the indicators among the three groups were as follows: vertical and transversal ranges of lymphedema, parallel lines sign, grid sign, honeycomb sign, band sign, crescent sign, and lymphatic lake sign, total diameter, total circumference, total area, diameter and area of the subcutaneous fat, diameter and area of the subcutaneous soft tissues, thickness of skin, thickness of band sign and crescent sign (P < .05). The receiver operating characteristic curve showed that the highest area under the curve for each parameter for identifying patients in the mild and nonmild (including moderate and severe) groups was in the following order: diameter of the subcutaneous fat > area of the subcutaneous fat > thickness of the skin (P < .05). The receiver operating characteristic curve showed that the highest under the curve for each parameter used to identify patients in the severe and nonsevere (including mild and moderate) groups was in the following order: diameter of the subcutaneous fat > area of the subcutaneous fat > thickness of the crescent sign.</p><p><strong>Conclusions: </strong>The parallel lines sign is a characteristic indicator for diagnosing patients with a mild disease, the grid sign is a characteristic indicator for diagnosing patients with a moderate disease, the lymphatic lake sign and crescent sig
目的:国际淋巴学会(International Society of Lymphology, ISL)提出了2020年淋巴水肿的分级标准,以患肢体积比健康肢体积增加百分比为标准。然而,这种方法测量和计算繁琐且耗时,并且没有跨不同机构的标准化公式。因此,本研究的目的是探讨非增强MRI对原发性下肢淋巴水肿(PLEL)分级的价值。方法:本回顾性研究纳入了2021年至2023年连续124例单侧PLEL患者。所有患者按照2020 ISL分级标准分为轻度(n=43)、中度(n=41)和重度(n=40)三组。从淋巴水肿受累范围来看(垂直范围:整个下肢,仅大腿,仅小腿和脚踝;横断面范围:≤25%横截面,26%-50%,51-75%,>75%),MRI淋巴水肿征象(平行线征、网格征、蜂窝征、带状征、新月形征、淋巴湖征、星云征),淋巴水肿测量(患肢总直径、总周长、总面积;患肢骨、肌肉、皮下脂肪和皮下软组织的直径和面积;患肢骨和肌肉的周长;皮肤厚度;带号厚度;记录三组患者月牙征厚度,并进行统计学分析。结果:三组间各项指标差异有统计学意义:淋巴水肿、平行线征、网格征、蜂窝征、带状征、新月征、淋巴湖征的纵横范围,皮下脂肪的总直径、总周长、总面积、直径和面积,皮下软组织的直径和面积,皮肤的厚度,带状征和新月征的厚度(皮下脂肪bbb的P面积)皮肤的厚度(皮下脂肪bbb的P面积)新月征的厚度(皮下脂肪bbb的P面积)。结论:(1)平行线标志是诊断轻度疾病的特征指标,网格标志是诊断中度疾病的特征指标,淋巴湖标志和新月标志是诊断重度疾病的特征指标,蜂窝标志和带状标志是诊断中重度疾病的特征指标。(ii)皮肤厚度、带状征、新月形征随病情加重而逐渐增加。(iii)皮下脂肪直径和面积对PLEL分级的效果最佳。(iv)非增强MRI可作为分级PLEL的更好和标准化的工具。
{"title":"The value of nonenhanced magnetic resonance imaging in the grading of primary lower extremity lymphedema.","authors":"Jia Guo, Xingpeng Li, Mengke Liu, Wenbin Shen, Yunlong Yue, Rengui Wang","doi":"10.1016/j.jvsv.2025.102168","DOIUrl":"10.1016/j.jvsv.2025.102168","url":null,"abstract":"<p><strong>Objective: </strong>The International Society of Lymphology proposed a grading standard for lymphedema in 2020 based on the percent increase in the volume of the affected limb compared to that of the healthy limb. However, this method is cumbersome and time consuming to measure and calculate, and a standardized formula across different institutions is not available. Therefore, the aim of this study was to investigate the value of nonenhanced magnetic resonance imaging (MRI) for grading primary lower extremity lymphedema (PLEL).</p><p><strong>Methods: </strong>This retrospective study included 124 consecutive patients with unilateral PLEL from 2021 to 2023. All patients were categorized into three groups, mild (n = 43), moderate (n = 41), and severe (n = 40), according to the 2020 International Society of Lymphology grading standard. From the lymphedema involvement range (vertical range: whole lower extremity, only thigh, only calf and ankle; transversal range: ≤25% of the cross-section, 26%-50%, 51%-75%, and >75%), MRI signs of lymphedema (parallel lines sign, grid sign, honeycomb sign, band sign, crescent sign, lymphatic lake sign, and nebula sign), and lymphedema measurements (total diameter, total circumference, and total area of the affected limb; diameter and area of the bone, muscle, subcutaneous fat, and subcutaneous soft tissues on the affected limb; circumference of the bone and muscle on the affected limb; thickness of skin; thickness of band sign; thickness of crescent sign) were recorded and statistically analysed in the three groups of patients.</p><p><strong>Results: </strong>The statistically significant differences in the indicators among the three groups were as follows: vertical and transversal ranges of lymphedema, parallel lines sign, grid sign, honeycomb sign, band sign, crescent sign, and lymphatic lake sign, total diameter, total circumference, total area, diameter and area of the subcutaneous fat, diameter and area of the subcutaneous soft tissues, thickness of skin, thickness of band sign and crescent sign (P < .05). The receiver operating characteristic curve showed that the highest area under the curve for each parameter for identifying patients in the mild and nonmild (including moderate and severe) groups was in the following order: diameter of the subcutaneous fat > area of the subcutaneous fat > thickness of the skin (P < .05). The receiver operating characteristic curve showed that the highest under the curve for each parameter used to identify patients in the severe and nonsevere (including mild and moderate) groups was in the following order: diameter of the subcutaneous fat > area of the subcutaneous fat > thickness of the crescent sign.</p><p><strong>Conclusions: </strong>The parallel lines sign is a characteristic indicator for diagnosing patients with a mild disease, the grid sign is a characteristic indicator for diagnosing patients with a moderate disease, the lymphatic lake sign and crescent sig","PeriodicalId":17537,"journal":{"name":"Journal of vascular surgery. Venous and lymphatic disorders","volume":" ","pages":"102168"},"PeriodicalIF":2.8,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11872591/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143007755","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective: This study sought to investigate the changes in plasma D-dimer levels during catheter-directed thrombolysis (CDT) in patients with acute lower extremity deep venous thrombosis (DVT), analyze imaging results, and assess their clinical implications.
Methods: We retrospectively analyzed 62 patients diagnosed with acute lower extremity DVT who underwent CDT between March 2019 and December 2022. Plasma D-dimer levels were measured before CDT, at regular intervals after CDT, and at the end of CDT. Lower limb venography was performed every 2 days during CDT to assess the thrombus clearance rate and level of thrombus dissolution. Statistical analyses were conducted to observe the D-dimer concentration changes and analyze the correlation between D-dimer concentration and thrombus clearance rate. Additionally, a receiver operating characteristic curve was constructed to determine the diagnostic performance of D-dimer in assessing the efficacy of thrombolysis, including the calculation of the area under the curve, sensitivity, specificity, and optimal cut-off value.
Results: During CDT for acute lower extremity DVT, plasma D-dimer levels rapidly increased, peaking on CDT day 1, and then gradually decreased, followed by a rapid decline, but remained slightly elevated compared with normal levels. There was a positive correlation between D-dimer levels and thrombolysis efficacy (r = 0.809; P = .00). The linear regression equation for this correlation was Y = 0.161 + 0.028X. The area under the curve of D-dimer was 0.95, with a cut-off value of 9.935 mg/L (sensitivity, 93.2%; specificity, 95.4%).
Conclusions: Plasma D-dimer concentration can serve as an indicator for evaluating the efficacy of thrombolysis during CDT in acute lower extremity DVT.
{"title":"Plasma D-dimer changes and clinical value in acute lower extremity deep venous thrombosis treated with catheter-directed thrombolysis.","authors":"Jixu Wang, Yide Zheng, Yongzhong Yu, Xiaowen Fan, Shaofei Xu","doi":"10.1016/j.jvsv.2025.102167","DOIUrl":"10.1016/j.jvsv.2025.102167","url":null,"abstract":"<p><strong>Objective: </strong>This study sought to investigate the changes in plasma D-dimer levels during catheter-directed thrombolysis (CDT) in patients with acute lower extremity deep venous thrombosis (DVT), analyze imaging results, and assess their clinical implications.</p><p><strong>Methods: </strong>We retrospectively analyzed 62 patients diagnosed with acute lower extremity DVT who underwent CDT between March 2019 and December 2022. Plasma D-dimer levels were measured before CDT, at regular intervals after CDT, and at the end of CDT. Lower limb venography was performed every 2 days during CDT to assess the thrombus clearance rate and level of thrombus dissolution. Statistical analyses were conducted to observe the D-dimer concentration changes and analyze the correlation between D-dimer concentration and thrombus clearance rate. Additionally, a receiver operating characteristic curve was constructed to determine the diagnostic performance of D-dimer in assessing the efficacy of thrombolysis, including the calculation of the area under the curve, sensitivity, specificity, and optimal cut-off value.</p><p><strong>Results: </strong>During CDT for acute lower extremity DVT, plasma D-dimer levels rapidly increased, peaking on CDT day 1, and then gradually decreased, followed by a rapid decline, but remained slightly elevated compared with normal levels. There was a positive correlation between D-dimer levels and thrombolysis efficacy (r = 0.809; P = .00). The linear regression equation for this correlation was Y = 0.161 + 0.028X. The area under the curve of D-dimer was 0.95, with a cut-off value of 9.935 mg/L (sensitivity, 93.2%; specificity, 95.4%).</p><p><strong>Conclusions: </strong>Plasma D-dimer concentration can serve as an indicator for evaluating the efficacy of thrombolysis during CDT in acute lower extremity DVT.</p>","PeriodicalId":17537,"journal":{"name":"Journal of vascular surgery. Venous and lymphatic disorders","volume":" ","pages":"102167"},"PeriodicalIF":2.8,"publicationDate":"2025-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11875163/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143007754","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}