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首页> 外文期刊>Angiology: the Journal of Vascular Diseases >Chronic venous insufficiency: worldwide results of the RELIEF study. Reflux assEssment and quaLity of lIfe improvEment with micronized Flavonoids.
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Chronic venous insufficiency: worldwide results of the RELIEF study. Reflux assEssment and quaLity of lIfe improvEment with micronized Flavonoids.

机译:慢性静脉功能不全:RELIEF研究的全球结果。微粉化类黄酮的反流评估和质量改进。

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摘要

Chronic venous insufficiency (CVI) results in considerable morbidity and may seriously affect patients' quality of life. The RELIEF (Reflux assEssment and quaLity of life improvEment with micronized Flavonoids) Study was a prospective controlled study designed to assess differences in the severity and in the evolution of symptoms and signs of CVI according to presence or not of venous reflux. Patients were thus separated into 2 comparative groups: those presenting venous reflux and those without venous reflux. The design of the study was multicentric and international, carried out in 23 countries over 2 years, in which 5,052 symptomatic patients assigned to classes C0 to C4 (on the basis of CEAP clinical classification) were enrolled. Patients were treated with micronized purified flavonoid fraction (MPFF), consisting of 450 mg of micronized diosmin and 50 mg of flavonoids expressed in hesperidin over 6 months. In order to document changes in the quality of life of these patients during MPFF treatment, a new validated Quality of Life Questionnaire specific to CVI (CIVIQ) was used. The study also set out to gather epidemiologic data including the prevalence of venous reflux in symptomatic patients. The RELIEF study provided important information about the epidemiology and clinical manifestations of CVI. Of particular interest was the observation that venous reflux was found to be absent in 57% of patients diagnosed as suffering from CVI belonging to CEAP classes C0 to C4. A positive relationship between symptoms of CVI (pain, leg heaviness, sensation of swelling, and cramps) and presence of venous reflux was found in the RELIEF study: symptoms were more frequent and more severe at presentation in patients with venous reflux. Moreover, during MPFF treatment, all symptoms showed a greater decrease in the group without venous reflux compared with the other group. This difference in the evolution of symptoms between the 2 groups was significant for pain, sensation of swelling, and cramps. Regarding leg heaviness and signs such as edema (assessed by leg circumference), patients improved equally independently of the presence or not of venous reflux. The significant and progressive improvement in the signs of CVI was reflected in significant changes in the clinical class of the CEAP classification, ie, from more severe to less severe stages. Continuous clinical improvement was found throughout the study and after treatment with MPFF for 6 months, the clinical scores of all symptoms and signs had significantly decreased (p=0.0001 versus DO) in both groups. This improvement was also associated with a significant and continuous progression in the quality of life scores of all patients. Age of patients, average time since diagnosis, and presence of venous reflux increased with the severity of the disease. The relationship shown in this study between these parameters and clinical CEAP classification reflects the progressive nature of CVI. Despite obvious symptoms of CVI, a very low percentage (21.8%) of the "intention-to-treat" (ITT) population had previously been treated. This was the case whether venous reflux was present or not.
机译:慢性静脉功能不全(CVI)导致相当大的发病率,并可能严重影响患者的生活质量。 RELIEF(微粉化类黄酮的返流评估和生活质量改善)研究是一项前瞻性对照研究,旨在根据静脉回流的存在与否评估CVI的严重程度以及症状和体征变化。因此,将患者分为两个比较组:出现静脉反流的患者和没有静脉反流的患者。这项研究的设计是多中心的和国际性的,历时2年,在23个国家/地区进行,纳入了5052名有症状的患者,其分类为C0至C4级(根据CEAP临床分类)。患者用微粉化的纯化黄酮类成分(MPFF)进行治疗,其中包含450毫克微粉化的薯di和6个月中橙皮苷中表达的50毫克类黄酮。为了记录这些患者在MPFF治疗期间的生活质量变化,使用了针对CVI(CIVIQ)的新的经过验证的生活质量调查表。该研究还着手收集流行病学数据,包括有症状患者的静脉反流患病率。 RELIEF研究提供了有关CVI的流行病学和临床表现的重要信息。特别令人感兴趣的是,发现被诊断患有CEAP C0至C4类CVI的患者中57%没有静脉回流。在RELIEF研究中发现CVI症状(疼痛,腿部沉重,肿胀感和抽筋)与静脉反流的存在呈正相关:静脉反流患者的症状在出现时更为频繁和严重。此外,在MPFF治疗期间,与另一组相比,无静脉反流的组中所有症状均表现出更大的减轻。两组之间症状演变的这种差异对于疼痛,肿胀感和抽筋很明显。关于腿部沉重和水肿等症状(通过腿围评估),无论是否存在静脉回流,患者均得到同等程度的改善。 CVI征象的显着和逐步改善反映在CEAP分类的临床类别的显着变化中,即从较重的阶段转变为较轻的阶段。在整个研究中发现持续的临床改善,MPFF治疗6个月后,两组所有症状和体征的临床评分均显着降低(相对于DO,p = 0.0001)。这种改善还与所有患者生活质量评分的持续显着提高有关。患者的年龄,诊断以来的平均时间以及静脉回流的存在随着疾病的严重程度而增加。这些参数与临床CEAP分类之间的关系显示出CVI的进行性。尽管有明显的CVI症状,但之前接受“意向治疗”(ITT)人群的比例非常低(21.8%)。无论是否存在静脉回流都是这种情况。

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