首页> 美国卫生研究院文献>The International Journal of Angiology : Official Publication of the International College of Angiology Inc >French Oak Wood (Quercus robur) Extract (Robuvit) in Primary Lymphedema: A Supplement Pilot Registry Evaluation
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French Oak Wood (Quercus robur) Extract (Robuvit) in Primary Lymphedema: A Supplement Pilot Registry Evaluation

机译:原发性淋巴水肿中的法国栎木(栎栎)提取物(Robuvit):补充飞行员注册表评估

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摘要

The aim of this pilot supplement study was the evaluation of an oak wood extract (Robuvit, Quercus robur [QR], Horphag Research) in an 8-week registry study on lymphatic signs in primary lymphedema.Subjects with primary lymphedema confined to a single leg without skin changes or ulcerations were followed for at least 8 weeks. Lymphedema was mainly present distally (below the knee). Three groups were formed: one group used only the standard management for lymphedema; one used the same management plus 300 mg Robuvit; and one used the standard management plus 600 mg of Robuvit.The three groups were comparable. After 8 weeks the variation in leg volume was on average −6.2% with standard management, −15% in the QR 300 mg group, and −18.9% in the 600 mg group. The edema score was also significantly lower at 8 weeks in the two QR groups. The variation in proteins in the interstitial fluid in comparison with initial values was −14.8% in controls in comparison with −29.9% in QR 300 mg group and −36.9% in QR 600 mg group. Skin flux significantly improved (increased) in the two QR groups. Ultrasound pretibial skin thickness was decreased on average 6% in controls versus 10.3% in the low-dose QR group and 11.8% in the higher dose group. Perimalleolar thickness was decreased 7% in controls and more in the two QR groups. Ankle circumference was decreased 4.4% in controls and more in the two supplement groups.This pilot registry indicates that Robuvit can be effective in the management of primary lymphedema. More patients and longer evaluation periods are needed.
机译:这项初步补充研究的目的是在一项为期8周的注册表研究中评估橡树提取物(Robuvit,Quercus robur [QR],Horphag Research),以评估原发性淋巴水肿的淋巴体征。没有皮肤变化或溃疡的情况持续了至少8周。淋巴水肿主要存在于远端(膝盖以下)。分为三组:一组仅对淋巴水肿进行标准处理;另一组仅对淋巴水肿进行标准处理。一位使用相同的管理方法加上300毫克的Robuvit;一组使用标准管理加600毫克Robuvit。三组具有可比性。 8周后,标准治疗下腿部体积的平均变化为-6.2%,QR 300mg组为-15%,600μg组为-18.9%。两个QR组在第8周时的水肿评分也显着降低。与对照组相比,对照组中组织液中蛋白质的变化与初始值相比为-14.8%,QR 300 mg组为-29.9%,QR 600 mg组为-36.9%。在两个QR组中,皮肤通量显着改善(增加)。对照组的超声前胫骨皮肤厚度平均降低了6%,而低剂量QR组的超声前皮肤厚度平均降低了10.3%,高剂量组的超声前庭皮肤厚度降低了11.8%。对照组的周唇厚度减少了7%,而两个QR组则增加了。对照组的踝关节圆周下降了4.4%,而两个补充组的踝关节圆周下降了更多。该试验性注册表表明Robuvit可以有效治疗原发性淋巴水肿。需要更多的患者和更长的评估期。

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