Pycnogenol® 可缓解糖尿病患者的慢性静脉功能不全 (CVI):一项补充剂登记研究。

IF 1.8 4区 医学 Q2 SURGERY Minerva Surgery Pub Date : 2024-09-11 DOI:10.23736/S2724-5691.24.10444-3
Gianni Belcaro, Maria R Cesarone, Claudia Scipione, Valeria Scipione, Umberto Cornelli, Roberto Cotellese, Edmondo Ippolito, Mark Dugall, Morio Hosoi, Marcello Corsi, Beatrice Feragalli, Pietro Bavera
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引用次数: 0

摘要

背景:这项补充剂登记研究的目的是评估 Pycnogenol® 在控制慢性静脉功能不全 (CVI)、糖尿病微血管病变的症状和体征以及微循环参数方面的疗效--针对患有慢性静脉功能不全和微血管病变的糖尿病患者。这些 CVI 患者符合接受医疗程序的条件,因为他们的浅表静脉不通可根据需要通过反复硬化疗法或局部手术进行治疗:方法:在这项登记研究中,只采用了非介入性治疗方法。方法:在这项登记研究中,只使用了非干预性治疗方法,将使用弹性压力和标准治疗方法(SM)与摄入 Pycnogenol®(150 毫克/天)和不使用弹性压力的标准治疗方法(SM)进行了为期 8 周的比较:58名患有CVI的糖尿病患者完成了研究,其中28人补充了Pycnogenol®,30人在对照组。完成 8 周研究的两组基线值相当。8 周后,未观察到任何副作用;依从性最佳,超过 98.5% 的补充剂胶囊被正确使用。对丝袜的耐受性较低(73% 的丝袜全天未完全使用)。没有出现脱袜现象。两组基线静脉压相当。纳入研究时,患者的微循环和临床测量结果相当。8 周后,在皮肤静息通量(RF)、踝关节肿胀率(RAS)、经皮 PO2 和 PCO2 方面,Pycnogenol® 和弹力压迫之间的差异具有显著的统计学意义。与此同时,通过综合症状评分(CSS)、静脉临床严重程度评分(VCSS)和静脉残疾评分(VDS)评估的临床症状在 Pycnogenol® 组明显低于加压组,这表明 Pycnogenol® 与弹性加压相比具有显著的临床效果:这项登记研究证实了Pycnogenol®对糖尿病患者CVI的临床和微循环疗效。这项研究表明,Pycnogenol® 在短期内治疗这种常见的临床症状方面具有重要的辅助性临床作用,并有可能预防溃疡的发生。
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Pycnogenol® relieves chronic venous insufficiency (CVI) in diabetics: a supplement registry study.

Background: The aim of this supplement registry study was to evaluate the efficacy of Pycnogenol® in controlling signs and symptoms of chronic venous insufficiency (CVI), diabetic microangiopathy and microcirculatory parameters - in diabetic patients with CVI and microangiopathy. These CVI patients are eligible for medical procedures as their incompetent superficial veins can be treated with repeated sclerotherapy and or local surgery according to needs.

Methods: During this registry study, only non-interventional managements were used. The effects of the use of elastic compression with standard management (SM) was compared to Pycnogenol® intake (150 mg/day) and SM, without using elastic compression for 8 weeks.

Results: Fifty-eight diabetic patients with CVI completed the study with 28 subjects supplemented with Pycnogenol® and 30 in the control group. The two groups completing 8 weeks were comparable at baseline. After 8 weeks, no side effects were observed; the compliance was optimal with >98.5% of the supplement capsules correctly used. The tolerability to stockings was lower (73% of stockings were not fully used for the whole day). There were no dropouts. Venous pressures were comparable in the two groups at baseline. Microcirculatory and clinical measurements of the patients were comparable at inclusion. After 8 weeks, the differences between Pycnogenol® and elastic compression were statistically significant for skin resting flux (RF), rate of ankle swelling (RAS), transcutaneous PO2 and PCO2 indicating a significant improvement in microcirculatory perfusion with Pycnogenol® in comparison with elastic compression. In parallel, clinical symptoms assessed by the Composite Symptom Score (CSS), the venous Clinical severity Score (VCSS) and the Venous Disability Score (VDS), were significantly lower in the Pycnogenol® group than in the compression group, indicating a significant clinical effect of Pycnogenol® compared to elastic compression (P<0.05). Pycnogenol® showed important antioxidant properties and lowered oxidative stress as seen also in previous studies.

Conclusions: This registry study confirms the clinical and microcirculatory efficacy of Pycnogenol® in CVI in diabetics. The study indicates the significant supplementary, clinical role of Pycnogenol® in the management of this common clinical condition over a short period of time, possibly preventing ulcerations.

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来源期刊
Minerva Surgery
Minerva Surgery SURGERY-
CiteScore
1.90
自引率
7.10%
发文量
320
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