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Diagnostic approach to penile pain and engorged superficial dorsal vein in a young male. 年轻男性阴茎疼痛及浅背静脉充血的诊断方法。
IF 2.8 2区 医学 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2024-12-30 DOI: 10.1016/j.jvsv.2024.102164
Amarseen Mikael, Steven Elias
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引用次数: 0
Ultrasound characteristics and risk factors of female patients with pelvic varicose veins and concomitant chronic pelvic pain. 女性盆腔静脉曲张伴慢性盆腔疼痛的超声特征及危险因素分析。
IF 2.8 2区 医学 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2024-12-27 DOI: 10.1016/j.jvsv.2024.102165
Binyu Zheng, Gaorui Liu, Yong Liu

Objective: The study aims to elucidate clinical and ultrasonographic characteristics of female patients diagnosed with pelvic varicose veins (PVVs) and to assess potential risk factors associated with incidences of chronic pelvic pain (CPP) in this population.

Methods: Clinical and ultrasound data were retrospectively collected from female patients with PVVs at Beijing Shijitan Hospital between December 2017 and October 2022. Patient cohorts were divided into two groups based on whether they had been experiencing non-periodic pelvic pain over 6 months, consistent with the symptoms of CPP. Comparative analyses were conducted between the two groups, utilizing both univariate and multivariate logistic regression methodologies to identify risk factors for CPP.

Results: The study included a total of 236 patients: 89 patients in the CPP group and 147 patients in the non-CPP group. No statistically significant differences were found between the two groups with regard to demographic parameters including age, height, weight, age of menarche, and number of pregnancies and births. However, the CPP group showed a higher menstrual volume score and a greater incidence of varicose veins, coupled with a lower body mass index. Transabdominal ultrasonography revealed that patients with CPP had a significantly larger diameter in the left ovarian vein (LOV) (6.2 ± 1.9 mm vs 5.0 ±2.3 mm; P < .05), and a higher prevalence of left internal iliac vein incompetence (21.3% vs 8.8%). Moreover, positive rates for LOV incompetence were markedly higher (94.4% vs 23.1%; P < .05), even in the absence of left common iliac vein compression and nutcracker phenomenon. Multivariate logistic regression analysis discerned that the LOV reflux (odds ratio [OR], 9.102; 95% confidence interval [CI], 4.578-18.099; P < .05), lower body mass index (OR, 0.646; 95% CI, 0.502-0.83; P < .05), elevated menstrual bleeding (OR, 1.182; 95% CI, 1.131-1.234; P < .05), and concomitant varicose veins (OR, 3.140; 95% CI, 1.067-9.273; P < .05) are independent risk factors for the manifestations of CPP in our patient cohorts.

Conclusions: Ultrasonography serves as an efficacious modality for evaluating abdomino-pelvic vascular pathology in patients with PVVs. Notably, LOV and internal iliac vein incompetence emerge as independent risk factors for CPP, thus offering a pivotal point of reference for clinical diagnosis and therapeutic management of PVVs.

目的:探讨女性盆腔静脉曲张(PVV)患者的临床及超声特征,探讨该人群慢性盆腔疼痛(CPP)发生的潜在危险因素。方法:回顾性收集2017年12月至2022年10月北京世纪坛医院女性PVV患者的临床和超声资料。根据患者是否在6个月内经历过非周期性盆腔疼痛(与CPP症状一致),将患者队列分为两组。在两组之间进行比较分析,使用单变量和多变量逻辑回归方法来确定CPP的危险因素。结果:(1)共纳入236例患者,其中CPP组89例,非CPP组147例。两组在年龄、身高、体重、月经初潮年龄、怀孕和分娩次数等人口统计学参数方面无统计学差异。然而,CPP组表现出更高的月经量评分和更高的静脉曲张发生率,并伴有较低的体重指数(BMI)。(2)经腹超声检查显示,CPP患者卵巢左静脉直径明显增大(6.2±1.9 mm vs 5.0±2.3mm)。结论:超声检查可作为评估PVV患者腹盆腔血管病理的有效手段。值得注意的是,卵巢左静脉和髂内静脉功能不全成为CPP的独立危险因素,为PVV的临床诊断和治疗管理提供了关键参考点。
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引用次数: 0
The natural history of portal venous system aneurysms. 门静脉系统动脉瘤的自然史。
IF 2.8 2区 医学 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2024-12-27 DOI: 10.1016/j.jvsv.2024.102163
Mary A Binko, Elizabeth A Andraska, Katherine M Reitz, Robert M Handzel, Michael J Singh, Natalie D Sridharan, Rabih A Chaer, Eric S Hager

Background: Portal venous system aneurysms (PVAs) are increasingly diagnosed on cross-sectional computed tomography imaging. However, the natural history of these aneurysms is poorly understood, and reports are limited to small case series.

Methods: Terms relevant to PVAs were searched in radiology reports (2010-2022), with PVA presence confirmed by manual review. PVA were defined as a diameter greater than 1.5 cm in patients without cirrhosis and 1.9 cm in those with cirrhosis. Aneurysm growth was defined as greater than 20% increase in size, whereas aneurysm regression was defined as greater than 20% decrease in size. Patient demographics, comorbid conditions, and PVA outcomes were abstracted. Univariate statistics were used to compare groups.

Results: Thirty-eight aneurysms with radiographic follow up were identified in 35 patients, involving the portal vein (n = 18; 47.4%), splenic vein (n = 10; 26.3%), superior mesenteric vein (n = 3; 7.9%), and portal confluence (n = 7; 18.4%). Although 12 (31.6%) were idiopathic, the remaining 26 (68.4%) were associated with portal hypertension (n = 20; 52.6%) and prior liver transplant (n = 4; 10.5%). The median growth was 0.2 cm (range, -2.6 to 2.4 cm) over median follow up over 5.0 years (range, 0.3-16.6 years). Five PVAs (13.2%) regressed and were largely idiopathic (80.0%; P = .03). Thirteen PVAs (34.2%) grew and were associated with portal hypertension (n = 11; 84.6%; P = .003) and thrombosis (n = 6; 46.2%; P = .05). Nine PVAs (23.7%) thrombosed, predominantly in males (n =7; 77.8%). The median growth was 1.0 cm (range, -0.7 to 1.9 cm). Three patients (33.3%) were symptomatic from PVA thrombosis including abdominal pain (n = 2; 22.2%), intestinal ischemia (n = 1; 11.1%), and variceal bleeding (n = 2; 22.2%). Four patients (44.4%) were treated with anticoagulation. No aneurysms ruptured. Of the 58 PVAs initially identified with and without radiographic follow up, five (8.6%) underwent intervention with a median diameter of 4.0 cm (range, 3.4-5 cm). Intervention included vein ligation (n = 1; 20.0%), aneurysmorrhaphy (n = 1; 20.0%), and aneurysmectomy (n = 3; 60.0%). There was one case of aneurysm recurrence 20 years following resection and one postoperative mortality.

Conclusions: Two-thirds of PVAa, including those with size greater than 3 cm, remain stable on surveillance. Although annual surveillance is initially recommended to confirm PVA stability, interval imaging can be subsequently extended given low growth rates. Over 20% of PVAs thrombosed, but none ruptured. Although we did not observe any cases of rupture, the devastating consequences of rupture necessitate consideration of surgical intervention for large symptomatic PVAs.

背景:门静脉系统动脉瘤(PVA)越来越多地被诊断为横断面计算机断层扫描(CT)。然而,这些动脉瘤的自然历史知之甚少,报道仅限于小病例系列。方法:检索2010-2022年放射学报告中与PVA相关的术语,并通过人工审查确认PVA的存在。无肝硬化患者的PVA直径大于1.5 cm,肝硬化患者的PVA直径大于1.9 cm。动脉瘤生长被定义为体积增大20%以上,而动脉瘤消退被定义为体积减小20%以上。患者统计资料、合并症和PVA结果被抽象化。采用单变量统计进行组间比较。结果:35例患者经x线随访发现动脉瘤38个,其中门静脉18个,占47.4%,脾静脉10个,占26.3%,肠系膜上静脉3个,占7.9%,门静脉汇合处7个,占18.4%。其中12例(31.6%)为特发性,其余26例(68.4%)与门静脉高压症(n=20, 52.6%)和既往肝移植(n=4, 10.5%)相关。中位生长为0.2厘米(-2.6-2.4厘米),中位随访超过5.0年(0.3-16.6年)。5例(13.2%)PVA复发,多数为特发性(80.0%,p=0.03)。13例(34.2%)PVA增大并合并门静脉高压症(n=11、84.6%,p=0.003)和血栓形成(n=6、46.2%,p=0.05)。9例(23.7%)PVA血栓形成,主要为男性(n=7, 77.8%)。中位生长为1.0 cm (-0.7-1.9 cm)。3例(33.3%)患者有PVA血栓形成的症状,包括腹痛(n=2, 22.2%)、肠缺血(n=1, 11.1%)和静脉曲张出血(n=2, 22.2%)。4例(44.4%)患者接受抗凝治疗。无动脉瘤破裂。在最初确定的58例PVA中,有或没有x线随访,5例(8.6%)接受了中位直径为4.0 cm (3.4-5 cm)的干预。干预措施包括静脉结扎(n=1, 20.0%)、动脉瘤吻合(n=1, 20.0%)和动脉瘤切除术(n=3, 60.0%)。术后20年动脉瘤复发1例,术后死亡1例。结论:三分之二的PVA(包括大于3cm的PVA)在监测中保持稳定。虽然最初建议进行年度监测以确认PVA的稳定性,但考虑到低生长速率,可以延长间隔成像时间。超过20%的PVA血栓形成,但没有破裂。虽然我们没有观察到任何破裂的病例,但破裂的破坏性后果需要考虑对大面积症状性PVA进行手术干预。
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引用次数: 0
Predicting lack of clinical improvement following varicose vein ablation using machine learning. 使用机器学习预测静脉曲张消融后缺乏临床改善。
IF 2.8 2区 医学 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2024-12-26 DOI: 10.1016/j.jvsv.2024.102162
Ben Li, Naomi Eisenberg, Derek Beaton, Douglas S Lee, Leen Al-Omran, Duminda N Wijeysundera, Mohamad A Hussain, Ori D Rotstein, Charles de Mestral, Muhammad Mamdani, Graham Roche-Nagle, Mohammed Al-Omran
<p><strong>Objective: </strong>Varicose vein ablation is generally indicated in patients with active/healed venous ulcers. However, patient selection for intervention in individuals without venous ulcers is less clear. Tools that predict lack of clinical improvement (LCI) after vein ablation may help guide clinical decision-making but remain limited. We developed machine learning (ML) algorithms that predict 1-year LCI after varicose vein ablation.</p><p><strong>Methods: </strong>The Vascular Quality Initiative database was used to identify patients who underwent endovenous or surgical varicose vein treatment for Clinical-Etiological-Anatomical-Pathophysiological (CEAP) C2 to C4 disease between 2014 and 2024. We identified 226 predictive features (111 preoperative [demographic/clinical], 100 intraoperative [procedural], and 15 postoperative [immediate postoperative course/complications]). The primary outcome was 1-year LCI, defined as a preoperative Venous Clinical Severity Score (VCSS) minus postoperative VCSS of ≤0, indicating no clinical improvement after vein ablation. The data were divided into training (70%) and test (30%) sets. Six ML models were trained using preoperative features with 10-fold cross-validation (Extreme Gradient Boosting [XGBoost], random forest, Naïve Bayes classifier, support vector machine, artificial neural network, and logistic regression). The primary model evaluation metric was area under the receiver operating characteristic curve (AUROC). The algorithm with the best performance was further trained using intraoperative and postoperative features. The focus was on preoperative features, whereas intraoperative and postoperative features were of secondary importance, because preoperative predictions offer the most potential to mitigate risk, such as deciding whether to proceed with intervention. Model calibration was assessed using calibration plots, and the accuracy of probabilistic predictions was evaluated with Brier scores. Performance was evaluated across subgroups based on age, sex, race, ethnicity, rurality, median Area Deprivation Index, prior ipsilateral varicose vein ablation, location of primary vein treated, and treatment type.</p><p><strong>Results: </strong>Overall, 33,924 patients underwent varicose vein treatment (30,602 endovenous [90.2%] and 3322 surgical [9.8%]) during the study period and 5619 (16.6%) experienced 1-year LCI. Patients who developed the primary outcome were older, more likely to be socioeconomically disadvantaged, and less likely to use compression therapy routinely. They also had less severe disease as characterized by lower preoperative VCSS, Varicose Vein Symptom Questionnaire scores, and CEAP classifications. The best preoperative prediction model was XGBoost, achieving an AUROC of 0.94 (95% confidence interval [CI], 0.93-0.95). In comparison, logistic regression had an AUROC of 0.71 (95% CI, 0.70-0.73). The XGBoost model had marginally improved performance at the intraoperative
目的:静脉曲张消融通常适用于活动性/已愈合的静脉溃疡患者。然而,对没有静脉溃疡的个体进行干预的患者选择尚不清楚。预测静脉消融后缺乏临床改善(LCI)的工具可能有助于指导临床决策,但仍然有限。我们开发了机器学习(ML)算法来预测静脉曲张消融后1年的LCI。方法:使用血管质量倡议(VQI)数据库识别2014-2024年间因临床-病因-解剖-病理生理(CEAP) C2-C4疾病接受静脉内或手术静脉曲张治疗的患者。我们确定了226个预测特征(术前111个[人口学/临床],术中100个[程序],术后15个[术后病程/并发症])。主要终点为1年LCI,定义为术前静脉临床严重程度评分(VCSS)减去术后VCSS≤0,表明静脉消融后无临床改善。数据分为训练集(70%)和测试集(30%)。使用10倍交叉验证的术前特征(Extreme Gradient Boosting [XGBoost]、随机森林、Naïve贝叶斯分类器、支持向量机、人工神经网络和逻辑回归)训练6个ML模型。主要模型评价指标为受试者工作特征曲线下面积(AUROC)。利用术中、术后特征对表现最佳的算法进行进一步训练。重点是术前特征,而术中和术后特征是次要的,因为术前预测提供了最大的降低风险的潜力,例如决定是否继续进行干预。模型校正采用校正图进行评估,概率预测的准确性采用Brier评分进行评估。根据年龄、性别、种族、民族、农村、中位面积剥夺指数、既往同侧静脉曲张消融、主静脉治疗位置和治疗类型对亚组的疗效进行评估。结果:总体而言,在研究期间,33,924例患者接受了静脉曲张治疗(30,602例(90.2%)静脉内治疗,3,322例(9.8%)手术治疗),5,619例(16.6%)经历了1年的LCI。出现主要结局的患者年龄较大,更有可能处于社会经济不利地位,并且不太可能常规使用压迫治疗。他们的病情也较轻,其特点是术前VCSS、VVSymQ评分和CEAP分类较低。最佳术前预测模型为XGBoost, AUROC (95% CI)为0.94(0.93-0.95)。相比之下,logistic回归的AUROC (95% CI)为0.71(0.70-0.73)。XGBoost模型在术中和术后阶段的表现略有改善,AUROC (95% CI)均为0.97(0.96-0.98)。校正图显示预测和观察到的事件概率吻合良好,Brier评分分别为0.12(术前)、0.11(术中)和0.10(术后)。在前10个预测因素中,有7个是术前特征,包括VCSS、VVSymQ评分、CEAP分类、静脉曲张消融史、大隐静脉血栓、深静脉返流。模型的性能在所有子组中都保持稳健。结论:我们建立的ML模型可以准确预测CEAP C2-C4疾病静脉内和手术静脉曲张治疗后的结果,优于logistic回归。这些算法在指导患者咨询和围手术期风险降低策略以预防静脉曲张消融后LCI方面具有重要的应用潜力。
{"title":"Predicting lack of clinical improvement following varicose vein ablation using machine learning.","authors":"Ben Li, Naomi Eisenberg, Derek Beaton, Douglas S Lee, Leen Al-Omran, Duminda N Wijeysundera, Mohamad A Hussain, Ori D Rotstein, Charles de Mestral, Muhammad Mamdani, Graham Roche-Nagle, Mohammed Al-Omran","doi":"10.1016/j.jvsv.2024.102162","DOIUrl":"10.1016/j.jvsv.2024.102162","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;Varicose vein ablation is generally indicated in patients with active/healed venous ulcers. However, patient selection for intervention in individuals without venous ulcers is less clear. Tools that predict lack of clinical improvement (LCI) after vein ablation may help guide clinical decision-making but remain limited. We developed machine learning (ML) algorithms that predict 1-year LCI after varicose vein ablation.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;The Vascular Quality Initiative database was used to identify patients who underwent endovenous or surgical varicose vein treatment for Clinical-Etiological-Anatomical-Pathophysiological (CEAP) C2 to C4 disease between 2014 and 2024. We identified 226 predictive features (111 preoperative [demographic/clinical], 100 intraoperative [procedural], and 15 postoperative [immediate postoperative course/complications]). The primary outcome was 1-year LCI, defined as a preoperative Venous Clinical Severity Score (VCSS) minus postoperative VCSS of ≤0, indicating no clinical improvement after vein ablation. The data were divided into training (70%) and test (30%) sets. Six ML models were trained using preoperative features with 10-fold cross-validation (Extreme Gradient Boosting [XGBoost], random forest, Naïve Bayes classifier, support vector machine, artificial neural network, and logistic regression). The primary model evaluation metric was area under the receiver operating characteristic curve (AUROC). The algorithm with the best performance was further trained using intraoperative and postoperative features. The focus was on preoperative features, whereas intraoperative and postoperative features were of secondary importance, because preoperative predictions offer the most potential to mitigate risk, such as deciding whether to proceed with intervention. Model calibration was assessed using calibration plots, and the accuracy of probabilistic predictions was evaluated with Brier scores. Performance was evaluated across subgroups based on age, sex, race, ethnicity, rurality, median Area Deprivation Index, prior ipsilateral varicose vein ablation, location of primary vein treated, and treatment type.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Overall, 33,924 patients underwent varicose vein treatment (30,602 endovenous [90.2%] and 3322 surgical [9.8%]) during the study period and 5619 (16.6%) experienced 1-year LCI. Patients who developed the primary outcome were older, more likely to be socioeconomically disadvantaged, and less likely to use compression therapy routinely. They also had less severe disease as characterized by lower preoperative VCSS, Varicose Vein Symptom Questionnaire scores, and CEAP classifications. The best preoperative prediction model was XGBoost, achieving an AUROC of 0.94 (95% confidence interval [CI], 0.93-0.95). In comparison, logistic regression had an AUROC of 0.71 (95% CI, 0.70-0.73). The XGBoost model had marginally improved performance at the intraoperative ","PeriodicalId":17537,"journal":{"name":"Journal of vascular surgery. Venous and lymphatic disorders","volume":" ","pages":"102162"},"PeriodicalIF":2.8,"publicationDate":"2024-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142895768","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}
引用次数: 0
Safety assessment of cyanoacrylate closure for treatment of varicose veins in a large-scale national survey in Japan. 在日本进行的一项大规模全国调查中,氰基丙烯酸酯治疗静脉曲张的安全性评价。
IF 2.8 2区 医学 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2024-12-18 DOI: 10.1016/j.jvsv.2024.102160
Michihisa Umetsu, Masayuki Hirokawa, Eri Fukaya, Eiichi Teshima, Hitoshi Kusagawa, Toshiya Nishibe, Makoto Mo, Tomohiro Ogawa

Objective: Cyanoacrylate closure (CAC) is a minimally invasive technique for treating axial venous reflux. However, the incidence of serious adverse events (AEs) related to CAC is concerning. With an increasing number of patients undergoing CAC and insufficient safety data in Japan, this study aimed to investigate the safety profile of CAC, focusing on the types and incidence of AEs.

Methods: A nationwide survey was conducted by the Japanese Regulatory Committee for Endovascular Treatment of Varicose Veins between November 2023 and December 2023. Data were collected from 1017 institutions, covering 24,209 patients who underwent CAC at 335 institutions between January 2020 and October 2023. Thromboembolism, phlebitis, hypersensitivity reactions, granuloma formation, infection, bleeding, death, and need for glue resection were documented as unfavorable events or outcomes.

Results: Venous thromboembolism developed in 142 patients (0.59%). Pulmonary embolism, proximal deep vein thrombosis, and ablation-related thrombus extension developed in 3 (0.01%), 9 (0.04%), and 95 (0.39%) patients, respectively. Localized phlebitis that required additional treatment was observed in 1656 patients (6.8%). Of the localized hypersensitivity cases, 960 (58%) required oral antihistamines and 268 (16%) required oral and/or intravenous steroids. Furthermore, 65 patients (0.27%) developed systemic hypersensitivity that required systemic steroids. No patients developed a stroke or anaphylaxis. One patient died owing to pulmonary embolism. Glue resection was performed in nine patients with delayed infection (n = 4), hypersensitivity reactions (n = 4), or a foreign body granuloma (n = 1). The incidence of hypersensitivity reactions was similar among institutions. However, the incidence of thrombosis-related events significantly differed between the high-volume and low-volume institutions. The incidence of proximal deep vein thrombosis (0.13% vs 0.01%; P < .001; odds ratio, 12.5; 95% confidence interval, 2.6-60.3) and ablation-related thrombus extension (0.73% vs 0.30%; P < .001; odds ratio, 2.5; 95% confidence interval, 1.66-3.77) was significantly higher in low-volume institutions than in high-volume centers.

Conclusions: A nationwide survey of CAC for varicose veins in Japan demonstrated that it was a safe procedure with a low rate of serious AEs, such as venous thromboembolism. However, hypersensitivity reactions requiring steroid administration and systemic allergic reactions were observed in some patients.

目的:氰基丙烯酸酯封闭术(CAC)是一种治疗轴静脉回流的微创技术。然而,与CAC相关的严重不良事件(ae)的发生率令人担忧。由于日本接受CAC的患者越来越多,安全性数据不足,本研究旨在调查CAC的安全性,重点关注ae的类型和发生率。方法:日本血管内治疗静脉曲张监管委员会于2023年11月至2023年12月进行了一项全国性调查。数据收集自1017家机构,涵盖了2020年1月至2023年10月期间在335家机构接受CAC治疗的24209名患者。血栓栓塞、静脉炎、过敏反应、肉芽肿形成、感染、出血、死亡和需要胶切除被记录为不良事件/结果。结果:142例(0.59%)发生静脉血栓栓塞(VTE)。肺栓塞、近端深静脉血栓形成(DVT)和消融相关血栓延伸(ARTE)分别在3例(0.01%)、9例(0.04%)和95例(0.39%)患者中发生。1656例(6.8%)患者出现需要额外治疗的局限性静脉炎。在局部过敏病例中,960例(58%)需要口服抗组胺药,268例(16%)需要口服和/或静脉注射类固醇。此外,65名患者(0.27%)出现全身性过敏,需要全身性类固醇。没有患者发生中风或过敏反应。1例患者死于肺栓塞。9例迟发性感染(n = 4)、超敏反应(n = 4)或异物肉芽肿(n = 1)患者行胶切术。各机构间超敏反应的发生率相似。然而,血栓相关事件的发生率在高容量和低容量机构之间存在显著差异。近端DVT发生率(0.13% vs. 0.01%;P < 0.001;优势比[OR], 12.5;95%可信区间[CI], 2.6-60.3)和ARTE (0.73% vs. 0.30%;P < 0.001;或者,2.5;95% CI, 1.66-3.77)在低容量机构中显著高于在高容量中心。结论:在日本,一项针对静脉曲张的CAC全国调查表明,这是一种安全的手术,严重ae(如静脉血栓栓塞)发生率低。然而,在一些患者中观察到需要类固醇治疗的超敏反应和全身过敏反应。
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引用次数: 0
Noncontrast MRI-based machine learning and radiomics signature can predict the severity of primary lower limb lymphedema. 基于非对比MRI的机器学习和放射组学特征可以预测原发性下肢淋巴水肿的严重程度。
IF 2.8 2区 医学 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2024-12-16 DOI: 10.1016/j.jvsv.2024.102161
Jie Ren, Xingpeng Li, Mengke Liu, Tingting Cui, Jia Guo, Rongjie Zhou, Kun Hao, Rengui Wang, Yunlong Yue

Objective: According to International Lymphology Society guidelines, the severity of lymphedema is determined by the difference in volume between the affected limb and the healthy side divided by the volume of the healthy side. However, this method of measuring volume is time consuming, laborious, and has certain errors in clinical applications. Therefore, this study aims to explore whether machine learning radiomics features based on noncontrast magnetic resonance imaging (MRI) can predict the severity of primary lower limb lymphedema.

Methods: A retrospective analysis of 119 patients with primary lower limb lymphedema. The enrolled patients were divided into a nonsevere group (mild and moderate) and a severe group. Using the semiautomatic threshold method in ITK-snap software on the patient's noncontrast MRI, we filled the area between the subcutaneous tissue and muscle of the edematous site. The PyRadiomics software package was used to extract radiomic features. The radiomic features were analyzed using the t test or Mann-Whitney test. Subsequently, Pearson correlation testing and least absolute shrinkage and selection operator screening were performed. Using Scikit-learn, the remaining features were used to construct five models: logistic regression, support vector machine, random Forest, ExtraTrees, and light gradient boosting machine. The predictive performance were evaluated by the receiver operating characteristic curve, and the sensitivity and specificity of these measures were calculated. The predictive curve was used to evaluate the performance of the predictive model in guiding decisions for nonsevere and severe lymphedema patients.

Results: The enrolled patients including 28 patients with mild lymphedema (grade I), 38 patients with moderate lymphedema (grade II), and 53 patients with severe lymphedema (grade III) was conducted. A total of 1196 features were extracted, and after Pearson correlation testing and least absolute shrinkage and selection operator screening, 21 nonzero features were selected. The ExtraTree model performed the best, with an area under the curve of 0.974 (95% confidence interval, 0.9437-1.0000) in the training set, a sensitivity of 89.2%, and a specificity of 95.7%. In the test set, these values were 0.938 (95% confidence interval, 0.8539-1.0000), 75%, and 100%, respectively. The decision curve showed that when the predicted probability was between 16% and 78%, the net benefit of the ExtraTree model was greater than that of the two extreme curves, indicating strong clinical value in guiding decisions for nonsevere and severe lymphedema patients.

Conclusions: All five models performed well in distinguishing between the nonsevere group and the severe group. Noncontrast MRI-based machine learning radiomics signature can predict the severity of primary lower limb lymphedema.

目的:根据国际淋巴学会的指南,淋巴水肿的严重程度由患肢与健康侧体积之差除以健康侧体积来确定。然而,这种测量体积的方法耗时,费力,并且在临床应用中存在一定的误差。因此,本研究旨在探讨基于非对比磁共振成像(NCMRI)的机器学习放射组学特征是否可以预测原发性下肢淋巴水肿的严重程度。方法:对119例原发性下肢淋巴水肿患者进行回顾性分析。入组患者分为非重度组(轻度和中度)和重度组。采用患者NCMRI ITK-snap软件中的半自动阈值法,对水肿部位皮下组织与肌肉之间的区域进行填充。使用PyRadiomics软件包提取放射学特征。放射学特征分析采用t检验或Mann-Whitney检验。随后进行Pearson相关检验和Lasso筛选。使用Scikit-learn,剩余的特征被用来构建五个模型:Logistic回归、支持向量机、随机森林、ExtraTrees和光梯度增强机。采用受试者工作特征曲线(ROC)评价预测效果,并计算这些指标的敏感性和特异性。预测曲线用于评估预测模型在指导非严重和严重淋巴水肿患者决策中的性能。结果:纳入的患者包括轻度(I级)淋巴水肿患者28例,中度(II级)淋巴水肿患者38例,重度(III级)淋巴水肿患者53例。共提取了1196个特征,经过Pearson相关检验和Lasso筛选,筛选出21个非零特征。ExtraTree模型表现最好,在训练集中的AUC为0.974 (95% CI: 0.9437-1.0000),灵敏度为89.2%,特异性为95.7%。在测试集中,这些值分别为0.938 (95% CI: 0.8539-1.0000)、75%和100%。决策曲线显示,当预测概率在16% ~ 78%之间时,ExtraTree模型的净收益大于两个极值曲线的净收益,对非重度和重度淋巴水肿患者的决策具有较强的临床指导价值。结论:5种模型均能较好地区分非重度组和重度组。基于NCMRI的机器学习放射组学特征可以预测原发性下肢淋巴水肿的严重程度。
{"title":"Noncontrast MRI-based machine learning and radiomics signature can predict the severity of primary lower limb lymphedema.","authors":"Jie Ren, Xingpeng Li, Mengke Liu, Tingting Cui, Jia Guo, Rongjie Zhou, Kun Hao, Rengui Wang, Yunlong Yue","doi":"10.1016/j.jvsv.2024.102161","DOIUrl":"10.1016/j.jvsv.2024.102161","url":null,"abstract":"<p><strong>Objective: </strong>According to International Lymphology Society guidelines, the severity of lymphedema is determined by the difference in volume between the affected limb and the healthy side divided by the volume of the healthy side. However, this method of measuring volume is time consuming, laborious, and has certain errors in clinical applications. Therefore, this study aims to explore whether machine learning radiomics features based on noncontrast magnetic resonance imaging (MRI) can predict the severity of primary lower limb lymphedema.</p><p><strong>Methods: </strong>A retrospective analysis of 119 patients with primary lower limb lymphedema. The enrolled patients were divided into a nonsevere group (mild and moderate) and a severe group. Using the semiautomatic threshold method in ITK-snap software on the patient's noncontrast MRI, we filled the area between the subcutaneous tissue and muscle of the edematous site. The PyRadiomics software package was used to extract radiomic features. The radiomic features were analyzed using the t test or Mann-Whitney test. Subsequently, Pearson correlation testing and least absolute shrinkage and selection operator screening were performed. Using Scikit-learn, the remaining features were used to construct five models: logistic regression, support vector machine, random Forest, ExtraTrees, and light gradient boosting machine. The predictive performance were evaluated by the receiver operating characteristic curve, and the sensitivity and specificity of these measures were calculated. The predictive curve was used to evaluate the performance of the predictive model in guiding decisions for nonsevere and severe lymphedema patients.</p><p><strong>Results: </strong>The enrolled patients including 28 patients with mild lymphedema (grade I), 38 patients with moderate lymphedema (grade II), and 53 patients with severe lymphedema (grade III) was conducted. A total of 1196 features were extracted, and after Pearson correlation testing and least absolute shrinkage and selection operator screening, 21 nonzero features were selected. The ExtraTree model performed the best, with an area under the curve of 0.974 (95% confidence interval, 0.9437-1.0000) in the training set, a sensitivity of 89.2%, and a specificity of 95.7%. In the test set, these values were 0.938 (95% confidence interval, 0.8539-1.0000), 75%, and 100%, respectively. The decision curve showed that when the predicted probability was between 16% and 78%, the net benefit of the ExtraTree model was greater than that of the two extreme curves, indicating strong clinical value in guiding decisions for nonsevere and severe lymphedema patients.</p><p><strong>Conclusions: </strong>All five models performed well in distinguishing between the nonsevere group and the severe group. Noncontrast MRI-based machine learning radiomics signature can predict the severity of primary lower limb lymphedema.</p>","PeriodicalId":17537,"journal":{"name":"Journal of vascular surgery. Venous and lymphatic disorders","volume":" ","pages":"102161"},"PeriodicalIF":2.8,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142854677","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}
引用次数: 0
Corrigendum.
IF 2.8 2区 医学 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2024-12-06 DOI: 10.1016/j.jvsv.2024.102008
{"title":"Corrigendum.","authors":"","doi":"10.1016/j.jvsv.2024.102008","DOIUrl":"10.1016/j.jvsv.2024.102008","url":null,"abstract":"","PeriodicalId":17537,"journal":{"name":"Journal of vascular surgery. Venous and lymphatic disorders","volume":" ","pages":"102008"},"PeriodicalIF":2.8,"publicationDate":"2024-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142801455","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}
引用次数: 0
Intracardiopulmonary migration of inferior vena cava filters: An updated systematic review. 下腔静脉滤器的心肺内迁移:最新的系统综述。
IF 2.8 2区 医学 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2024-11-28 DOI: 10.1016/j.jvsv.2024.102009
Yifei Bai, Kai Wang, Tongqing Xue, Zhongzhi Jia

Objective: Intracardiopulmonary migration of an inferior vena cava (IVC) filter is an uncommon but potentially life-threatening complication. A previous systematic review including data through 2008 found that the most common cause for migration was operator error and that open thoracotomy was the best first option for management. The aim of this study was to assess the clinical presentation and causes of intracardiopulmonary filter migration, as well as the most commonly used management strategies over the past 15 years.

Methods: A systematic search of the literature was conducted to identify studies pertaining to intracardiopulmonary IVC filter migration that were published between November 2008 and June 2024, and data were collected regarding clinical presentation, complications, type and location of filter migration, and management strategies.

Results: A total of 156 cases of intracardiopulmonary migration of IVC filters were identified in 88 publications. Of the 66 patients whose symptoms status was listed, 50 patients had symptoms and 16 patients were asymptomatic. In the remaining patients, the symptom status was not listed. The most frequently reported symptom was chest pain (68.0%; 34/50). Of the 156 patients, 34 (22.8%) experienced intracardiopulmonary migration of the entire filter body, and the remaining 122 (78.2%) experienced filter fracture with migration of the fractured struts. Complications were reported in 30.1% of patients (47/156); these complications included myocardial injury (n = 37), damage of tricuspid valve (n = 12), and hemopericardium (n = 21). Endovascular (16 filters and 56 struts) or surgical (13 filters and 16 struts) retrieval was the primary management strategy for intracardiopulmonary migration of the filter or fractured strut.

Conclusions: The main cause of intracardiopulmonary migration of an IVC filter is filter fracture. Endovascular retrieval is gradually becoming the preferred management option for intracardiopulmonary migration of IVC filters.

背景:下腔静脉(IVC)滤过物的心肺内移位是一种罕见但可能危及生命的并发症。之前的一项系统综述(包括2008年的数据)发现,最常见的移位原因是操作人员的失误,开胸手术是治疗的最佳首选。目的:评价15年来心肺内滤过物迁移的临床表现和原因,以及最常用的治疗策略。患者和方法:系统检索了2008年11月至2024年6月期间发表的关于心肺内IVC滤过器迁移的研究,收集了有关滤过器迁移的临床表现、并发症、类型和位置以及管理策略的数据。结果:88篇文献共发现156例下腔静脉滤过器心肺内移位。列出症状状态的66例患者中,有症状的50例,无症状的16例。其余患者未列出症状状态。最常见的症状是胸痛(68.0%,34/50)。156例患者中,34例(22.8%)出现了整个滤过体的心肺内移位,其余122例(78.2%)出现了滤过体骨折伴骨折支移位。30.1%的患者出现并发症(47/156);这些并发症包括心肌损伤(n = 37)、三尖瓣损伤(n = 12)和心包积血(n = 21)。血管内(16个滤过器和56支支)或手术(13个滤过器和16支支)取出是滤过器心肺内移位或支架断裂的主要处理策略。结论:导致下腔静脉滤过器肺内移位的主要原因是滤过器断裂。血管内回收正逐渐成为首选的管理方案,为心脏内肺脏内迁移的IVC过滤器。
{"title":"Intracardiopulmonary migration of inferior vena cava filters: An updated systematic review.","authors":"Yifei Bai, Kai Wang, Tongqing Xue, Zhongzhi Jia","doi":"10.1016/j.jvsv.2024.102009","DOIUrl":"10.1016/j.jvsv.2024.102009","url":null,"abstract":"<p><strong>Objective: </strong>Intracardiopulmonary migration of an inferior vena cava (IVC) filter is an uncommon but potentially life-threatening complication. A previous systematic review including data through 2008 found that the most common cause for migration was operator error and that open thoracotomy was the best first option for management. The aim of this study was to assess the clinical presentation and causes of intracardiopulmonary filter migration, as well as the most commonly used management strategies over the past 15 years.</p><p><strong>Methods: </strong>A systematic search of the literature was conducted to identify studies pertaining to intracardiopulmonary IVC filter migration that were published between November 2008 and June 2024, and data were collected regarding clinical presentation, complications, type and location of filter migration, and management strategies.</p><p><strong>Results: </strong>A total of 156 cases of intracardiopulmonary migration of IVC filters were identified in 88 publications. Of the 66 patients whose symptoms status was listed, 50 patients had symptoms and 16 patients were asymptomatic. In the remaining patients, the symptom status was not listed. The most frequently reported symptom was chest pain (68.0%; 34/50). Of the 156 patients, 34 (22.8%) experienced intracardiopulmonary migration of the entire filter body, and the remaining 122 (78.2%) experienced filter fracture with migration of the fractured struts. Complications were reported in 30.1% of patients (47/156); these complications included myocardial injury (n = 37), damage of tricuspid valve (n = 12), and hemopericardium (n = 21). Endovascular (16 filters and 56 struts) or surgical (13 filters and 16 struts) retrieval was the primary management strategy for intracardiopulmonary migration of the filter or fractured strut.</p><p><strong>Conclusions: </strong>The main cause of intracardiopulmonary migration of an IVC filter is filter fracture. Endovascular retrieval is gradually becoming the preferred management option for intracardiopulmonary migration of IVC filters.</p>","PeriodicalId":17537,"journal":{"name":"Journal of vascular surgery. Venous and lymphatic disorders","volume":" ","pages":"102009"},"PeriodicalIF":2.8,"publicationDate":"2024-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142755318","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}
引用次数: 0
Long-term outcomes of stenting superior cava and brachio-cephalic vein occlusion in hemodialysis patients with arteriovenous fistulas. 动静脉瘘血液透析患者上腔静脉和臂-脑静脉闭塞支架植入术的长期疗效。
IF 2.8 2区 医学 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2024-11-20 DOI: 10.1016/j.jvsv.2024.102007
Florent Porez, Reuben Veerapen, Stéphanie Delelis, Sarah Kirat, Eric Braunberger, Gilles Lerussi, Bruno Delelis
<p><strong>Objective: </strong>Central vein occlusion (CVO) is a significant complication in patients undergoing chronic hemodialysis, often leading to dialysis inefficacy, disabling symptoms, and, most critically, major risk of access failure. Although stenting has been proposed as a technique to maintain vascular access patency following the recanalization of occluded central veins, the data supporting its long-term efficacy remains limited. This study aims to evaluate the long-term effectiveness of stenting occluded superior vena cava (SVC) and/or brachiocephalic veins to preserve vascular access patency, ensure continued dialysis efficacy, and relieve SVC syndrome.</p><p><strong>Methods: </strong>This study retrospectively reviewed all hemodialysis patients who underwent stent placement for CVO between January 2017 and August 2024 at two vascular centers in Reunion Island. The primary endpoints of the study were the primary, assisted primary, and secondary patency rates of the vascular circuit during follow-up. Additionally, patient demographics, medical comorbidities, postoperative complications, definitive access abandonment, and reinterventions were analyzed.</p><p><strong>Results: </strong>This study included 21 patients with a mean age of 67 years. CVO stenting initially provided symptomatic relief for all patients, resolving symptoms such as SVC or arm swelling in symptomatic patients. Over a median follow-up period of 41 months (range, 3-80 months), the primary patency rates were 67% at 12 months, 42% at 24 months, and 38% at 36 months, whereas the secondary patency rates were 90%, 79%, and 60% at these same intervals. Twelve patients (62%) experienced clinically significant stent restenosis, necessitating one or several additional percutaneous transluminal angioplasties during follow-up, whereas five patients (24%) developed acute access thrombosis requiring thrombectomy and percutaneous transluminal angioplasty, with central stent involved for three patients. Three patients (14%) required extra-anatomic bypasses due to definitive stent occlusion, five patients (14%) had definitive access failure, and five patients (24%) died from unrelated causes.</p><p><strong>Conclusions: </strong>This review suggests that hemodialysis patients with symptomatic CVO can often be successfully recanalized and treated with stenting, leading to symptom resolution and, importantly, achieving promising secondary patency rates. Our long-term results highlight the necessity for regular reintervention and close follow-up, as a significant number of patients will experience restenosis, and ultimately definitive access failure. Therefore, CVO stenting should be considered a temporary solution, although for some patients, this strategy may prove highly effective, maintaining long-term patency without any restenosis.</p><p><strong>Clinical relevance: </strong>We studied central vein stenting for 21 hemodialysis patients with a mean follow-up of 41 months. Long-t
背景:中心静脉闭塞(CVO)是慢性血液透析患者的一个重要并发症,通常会导致透析效果不佳、致残症状,最关键的是,还存在通路失败的重大风险。虽然支架植入术被认为是在闭塞的中心静脉再通之后保持血管通路通畅的一种技术,但支持其长期疗效的数据仍然有限。本研究旨在评估对闭塞的上腔静脉(SVC)和/或肱静脉(BCV)进行支架植入以保持血管通路通畅、确保持续透析疗效并缓解 SVC 综合征的长期有效性:本研究回顾性分析了2017年1月至2024年8月期间在留尼汪岛两家血管中心因中心静脉闭塞而接受支架置入术的所有血液透析患者。研究的主要终点是随访期间血管回路的主要、辅助主要和次要通畅率。此外,还分析了患者的人口统计学、医学合并症、术后并发症、最终通路放弃和再次干预:本研究共纳入 21 名患者,平均年龄为 67 岁。CVO支架植入术最初缓解了所有患者的症状,解决了无症状患者的上腔静脉或手臂肿胀等症状。中位随访时间为 41 个月(范围:3-80 个月),12 个月时的一次通畅率为 67%,24 个月时为 42%,36 个月时为 38%,而相同时间间隔内的二次通畅率分别为 90%、79% 和 60%。有 12 名患者(62%)出现了临床意义上的支架再狭窄,需要在随访期间进行一次或多次经皮腔内血管成形术(PTA),有 5 名患者(24%)出现了急性入路血栓,需要进行血栓切除术和 PTA,其中 3 名患者的中心支架受到了牵连。3名患者(14%)因确定性支架闭塞而需要解剖外搭桥,5名患者(14%)确定性通路失败,5名患者(24%)死于无关原因:本综述表明,有症状的中心静脉闭塞血液透析患者通常可以通过支架治疗成功实现再通畅,从而缓解症状,更重要的是,二次通畅率也很可观。我们的长期研究结果强调了定期再介入和密切随访的必要性,因为相当多的患者会出现再狭窄,最终导致通路失败。因此,CVO 支架植入术应被视为一种临时解决方案,尽管对某些患者来说,这种策略可能被证明非常有效,能保持长期通畅,且不会出现任何再狭窄。
{"title":"Long-term outcomes of stenting superior cava and brachio-cephalic vein occlusion in hemodialysis patients with arteriovenous fistulas.","authors":"Florent Porez, Reuben Veerapen, Stéphanie Delelis, Sarah Kirat, Eric Braunberger, Gilles Lerussi, Bruno Delelis","doi":"10.1016/j.jvsv.2024.102007","DOIUrl":"10.1016/j.jvsv.2024.102007","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;Central vein occlusion (CVO) is a significant complication in patients undergoing chronic hemodialysis, often leading to dialysis inefficacy, disabling symptoms, and, most critically, major risk of access failure. Although stenting has been proposed as a technique to maintain vascular access patency following the recanalization of occluded central veins, the data supporting its long-term efficacy remains limited. This study aims to evaluate the long-term effectiveness of stenting occluded superior vena cava (SVC) and/or brachiocephalic veins to preserve vascular access patency, ensure continued dialysis efficacy, and relieve SVC syndrome.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;This study retrospectively reviewed all hemodialysis patients who underwent stent placement for CVO between January 2017 and August 2024 at two vascular centers in Reunion Island. The primary endpoints of the study were the primary, assisted primary, and secondary patency rates of the vascular circuit during follow-up. Additionally, patient demographics, medical comorbidities, postoperative complications, definitive access abandonment, and reinterventions were analyzed.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;This study included 21 patients with a mean age of 67 years. CVO stenting initially provided symptomatic relief for all patients, resolving symptoms such as SVC or arm swelling in symptomatic patients. Over a median follow-up period of 41 months (range, 3-80 months), the primary patency rates were 67% at 12 months, 42% at 24 months, and 38% at 36 months, whereas the secondary patency rates were 90%, 79%, and 60% at these same intervals. Twelve patients (62%) experienced clinically significant stent restenosis, necessitating one or several additional percutaneous transluminal angioplasties during follow-up, whereas five patients (24%) developed acute access thrombosis requiring thrombectomy and percutaneous transluminal angioplasty, with central stent involved for three patients. Three patients (14%) required extra-anatomic bypasses due to definitive stent occlusion, five patients (14%) had definitive access failure, and five patients (24%) died from unrelated causes.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;This review suggests that hemodialysis patients with symptomatic CVO can often be successfully recanalized and treated with stenting, leading to symptom resolution and, importantly, achieving promising secondary patency rates. Our long-term results highlight the necessity for regular reintervention and close follow-up, as a significant number of patients will experience restenosis, and ultimately definitive access failure. Therefore, CVO stenting should be considered a temporary solution, although for some patients, this strategy may prove highly effective, maintaining long-term patency without any restenosis.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Clinical relevance: &lt;/strong&gt;We studied central vein stenting for 21 hemodialysis patients with a mean follow-up of 41 months. Long-t","PeriodicalId":17537,"journal":{"name":"Journal of vascular surgery. Venous and lymphatic disorders","volume":" ","pages":"102007"},"PeriodicalIF":2.8,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142693134","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}
引用次数: 0
Efficacy of complex decongestive therapy on venous flow, internal saphenous diameter, edema, fat mass of the limbs and quality of life in patients with chronic venous insufficiency: A randomized clinical trial. 复合减充血疗法对慢性静脉功能不全患者的静脉流量、隐静脉内径、水肿、肢体脂肪量和生活质量的疗效:随机临床试验。
IF 2.8 2区 医学 Q2 PERIPHERAL VASCULAR DISEASE Pub Date : 2024-11-13 DOI: 10.1016/j.jvsv.2024.102005
Ana Martín Jiménez, Beatriz María Bermejo Gil, Alejandro Santos-Lozano, Francisco Jose Pinto-Fraga, Carolina García Barroso, Leonardo Raul Vittori, Aurymar Fraino, Héctor Menéndez Alegre

Objective: Demonstrate the effectiveness of complex decongestive therapy (CDT) in patients with chronic venous insufficiency (CVI).

Methods: A single-blind randomized controlled trial was conducted, where the participants were patients with CVI (n = 21/42) were assigned randomly to an experimental group (n = 11/22) or a control group (n = 9/18). A treatment of CDT (manual lymphatic drainage, intermittent pneumatic presotherapy, bilayer bandage) was applied to the experimental group for 4 weeks 2 days per week and no treatment was applied to the control group. The patients were evaluated at baseline (t0), 1 week after finishing the intervention (t1), and 6 weeks after the intervention (t2). The effectiveness of the treatment on symptoms and quality of life (QoL) (heaviness, pain and Chronic Venous Insufficiency Quality of Life [CIVIQ-20] questionary), edema, venous flow, and impedanciometry measurements was evaluated.

Results: An improvement in the patient's QoL was observed: there was a decrease in symptoms such as heaviness and pain, an increase in the average velocity of the left femoral vein and left internal saphenous vein (ISV), a decrease in the ISV diameter in both extremities and a decrease in body mass index and fat mass in both extremities. These results were maintained when following up at 6 weeks, except for the improvement of QoL.

Conclusions: CDT treatment improves the CIVIQ-20 and Venous Clinical Severity Scores. It also improves symptoms (pain and heaviness), venous flow velocity (superficial veins and deep veins [common femoral vein, femoral vein, popliteal vein]) and decreases body mass index, fat mass, and ISV diameter.

目的:展示复合减充血疗法(CDT)对慢性静脉功能不全(CVI)患者的有效性:证明复合减充血疗法(CDT)对慢性静脉功能不全(CVI)患者的有效性:进行单盲随机对照试验,参与者为 CVI 患者(21/42),随机分配到实验组(11/22)或对照组(9/18)。实验组接受 CDT 治疗(手动淋巴引流 (MDL)、间歇性气压预治疗 (IPP)、双层绷带 (BB)),为期 4 周,每周两天;对照组不接受任何治疗。分别在基线(t0)、干预结束后 1 周(t1)和干预结束后 6 周(t2)对患者进行评估。评估了治疗对症状和 QoL(乏力、疼痛和 CIVIQ-20 问卷)、水肿、静脉流量(VF)和阻抗测量的效果:患者的 QoL 有所改善:沉重感和疼痛等症状减轻,左股静脉(LFV)和左大隐静脉(LISV)的平均流速增加,双侧肢体的大隐静脉内径(ISVD)减小,双侧肢体的体重指数和脂肪量(FM)减少。结论:CDT 治疗可改善 QoL:结论:CDT 治疗可改善 CVI 患者的 QoL(CIVIQ-20、VCSS)。结论:CDT 治疗可改善 CVI 患者的 QoL(CIVIQ-20、VCSS),还可改善症状(疼痛和沉重感)、VF 速度(浅静脉 [ISV] 和深静脉 [股总静脉 (CFV)、股静脉 (FV)、腘静脉 (PV)]),降低体重指数 (BMI)、脂肪量 (FM) 和 ISVD。
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Journal of vascular surgery. Venous and lymphatic disorders
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