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微粉化纯化黄酮类成分:关于其在慢性静脉功能不全、静脉溃疡和痔疮治疗中应用的综述

Micronised purified flavonoid fraction: a review of its use in chronic venous insufficiency, venous ulcers and haemorrhoids.

作者信息

Lyseng-Williamson Katherine A, Perry Caroline M

机构信息

Adis International Limited, Mairangi Bay, Auckland, New Zealand.

出版信息

Drugs. 2003;63(1):71-100. doi: 10.2165/00003495-200363010-00005.

Abstract

Micronised purified flavonoid fraction (MPFF) [Daflon 500 mg], an oral phlebotropic drug consisting of 90% micronised diosmin and 10% flavonoids expressed as hesperidin, improves venous tone and lymphatic drainage, and reduces capillary hyperpermeability by protecting the microcirculation from inflammatory processes. The absorption of diosmin is improved by its micronisation to particles with a diameter <2 microm. Compared with placebo, MPFF 500 mg twice daily significantly decreased ankle or calf circumference, and improved many symptoms of chronic venous insufficiency (CVI) and plethysmographic parameters in two randomised, double-blind, 2-month studies. Improvement in symptoms was parallelled by an improvement in health-related quality of life in a nonblind, 6-month trial. Significantly more venous leg ulcers </=10 cm in diameter completely healed with MPFF 500 mg twice daily plus standard management (compression and local treatment) for 2-6 months than with standard management alone or with placebo in a nonblind and a double-blind trial. The addition of MPFF to standard management was cost effective in a retrospective pharmacoeconomic analysis of the 6-month trial. Compared with placebo, the duration and/or intensity of individual symptoms of grade 1 or 2 acute internal haemorrhoids improved significantly with 3 tablets of MPFF 500 mg twice daily for 4 days then 2 tablets of MPFF 500 mg twice daily for 3 days. Two tablets of MPFF 500 mg daily for 60 or 83 days reduced the frequency, duration and/or severity of acute haemorrhoidal symptoms and improved the overall signs and symptoms of chronic (recurrent) haemorrhoids compared with placebo. Compared with a control group, MPFF significantly reduced the risk of secondary bleeding after elective haemorrhoidectomy. In clinical trials, MPFF had a tolerability profile similar to that of placebo; the most frequently reported adverse events were gastrointestinal and autonomic in nature. In conclusion, MPFF is a well established and well tolerated treatment option in patients with CVI, venous ulcers, or acute or chronic internal haemorrhoids. MPFF is indicated as a first-line treatment of oedema and the symptoms of CVI in patients in any stage of the disease. In more advanced disease stages, MPFF may be used in conjunction with sclerotherapy, surgery and/or compression therapy, or as an alternative treatment when surgery is not indicated or is unfeasible. The healing of venous ulcers </=10 cm in diameter is accelerated by the addition of MPFF to standard venous ulcer management. MPFF may reduce the frequency, duration and/or intensity of symptoms of grade 1 or 2 acute internal haemorrhoids, and also the severity of the signs and symptoms of chronic haemorrhoids.

摘要

微粉化纯化黄酮组分(MPFF)[爱脉朗500毫克],一种口服的促静脉血循环药物,由90%的微粉化地奥司明和10%以橙皮苷表示的黄酮类化合物组成,可改善静脉张力和淋巴引流,并通过保护微循环免受炎症过程影响来降低毛细血管通透性。地奥司明微粉化至直径<2微米的颗粒后,其吸收得到改善。在两项随机、双盲、为期2个月的研究中,与安慰剂相比,每日两次服用500毫克MPFF可显著减小脚踝或小腿周长,并改善慢性静脉功能不全(CVI)的多种症状以及体积描记参数。在一项为期6个月的非盲试验中,症状改善的同时,与健康相关的生活质量也得到了改善。在一项非盲试验和一项双盲试验中,与单独使用标准治疗(加压和局部治疗)或安慰剂相比,每日两次服用500毫克MPFF加标准治疗2 - 6个月,直径≤10厘米的静脉性腿部溃疡完全愈合的比例显著更高。在对为期6个月试验的回顾性药物经济学分析中,在标准治疗中添加MPFF具有成本效益。与安慰剂相比,对于1级或2级急性内痔,每日两次服用3片500毫克MPFF,共4天,然后每日两次服用2片500毫克MPFF,共3天,个体症状的持续时间和/或强度显著改善。与安慰剂相比,每日两次服用2片500毫克MPFF,共60或83天,可降低急性痔症状的频率、持续时间和/或严重程度,并改善慢性(复发性)痔的总体体征和症状。与对照组相比,MPFF显著降低了择期痔切除术后继发性出血的风险。在临床试验中,MPFF的耐受性与安慰剂相似;最常报告的不良事件本质上是胃肠道和自主神经系统方面的。总之,MPFF是CVI、静脉溃疡或急性或慢性内痔患者中一种成熟且耐受性良好的治疗选择。MPFF被指定为疾病任何阶段患者水肿和CVI症状的一线治疗药物。在疾病的更晚期阶段,MPFF可与硬化疗法、手术和/或加压疗法联合使用,或在不适合或不可行手术时作为替代治疗。在标准静脉溃疡治疗中添加MPFF可加速直径≤10厘米的静脉溃疡愈合。MPFF可降低1级或2级急性内痔症状的频率、持续时间和/或强度,以及慢性痔体征和症状的严重程度。

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