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慢性静脉功能不全的新兴药理学干预措施:疗效、安全性及治疗进展的全面系统评价与荟萃分析

Emerging Pharmacological Interventions for Chronic Venous Insufficiency: A Comprehensive Systematic Review and Meta-Analysis of Efficacy, Safety, and Therapeutic Advances.

作者信息

Miguel Camila Botelho, Andrade Ranielly de Souza, Mazurek Laise, Martins-de-Abreu Melissa Carvalho, Miguel-Neto Jamil, Barbosa Aurélio de Melo, Silva Glicélia Pereira, Góes-Neto Aristóteles, Soares Siomar de Castro, Lazo-Chica Javier Emilio, Rodrigues Wellington Francisco

机构信息

Multidisciplinary Laboratory of Scientific Evidence, University Center of Mineiros (Unifimes), Mineiros 75833-130, GO, Brazil.

Postgraduate Program in Tropical Medicine and Infectious Diseases, Federal University of the Triângulo Mineiro-UFTM, Uberaba 38025-180, MG, Brazil.

出版信息

Pharmaceutics. 2025 Jan 3;17(1):59. doi: 10.3390/pharmaceutics17010059.

Abstract

Chronic Venous Insufficiency (CVI) is a progressive vascular condition characterized by venous hypertension and chronic inflammation, leading to significant clinical and socioeconomic impacts. This study aimed to evaluate the efficacy and safety of emerging pharmacological interventions for CVI, focusing on clinical outcomes such as pain, edema, cutaneous blood flow, and quality of life. Eligible interventions comprised new vasoprotective drugs, such as hydroxyethylrutoside, Pycnogenol, aminaphthone, coumarin + troxerutin, and Venoruton, compared to the standard therapy of diosmin and hesperidin. : Hydroxyethylrutoside and Pycnogenol showed significant benefits in pain reduction and resting flux improvement, with mean differences of 38 (95% CI: 10.56-65.44) and 25.30 (95% CI: 18.73-31.87), respectively. Improvements in edema and quality of life were less consistent. Substantial heterogeneity was observed (I = 100%, < 0.001). Conclusions: Hydroxyethylrutoside and Pycnogenol emerge as promising alternatives for managing CVI. However, limitations such as high heterogeneity, small sample sizes, and methodological inconsistencies highlight the need for more robust and standardized clinical trials. This study underscores the importance of personalized and cost-effective strategies, particularly in resource-limited settings.

摘要

慢性静脉功能不全(CVI)是一种进行性血管疾病,其特征为静脉高压和慢性炎症,会导致重大的临床和社会经济影响。本研究旨在评估针对CVI的新型药物干预措施的疗效和安全性,重点关注疼痛、水肿、皮肤血流量和生活质量等临床结局。符合条件的干预措施包括新型血管保护药物,如羟乙基芦丁、碧萝芷、氨基萘酮、香豆素+曲克芦丁和维脑路通,与地奥司明和橙皮苷的标准疗法进行比较。羟乙基芦丁和碧萝芷在减轻疼痛和改善静息血流量方面显示出显著益处,平均差异分别为38(95%CI:10.56 - 65.44)和25.30(95%CI:18.73 - 31.87)。水肿和生活质量的改善不太一致。观察到存在显著异质性(I = 100%,P < 0.001)。结论:羟乙基芦丁和碧萝芷成为管理CVI的有前景的替代方案。然而,诸如高异质性、小样本量和方法学不一致等局限性突出表明需要更有力和标准化的临床试验。本研究强调了个性化和具有成本效益策略的重要性,尤其是在资源有限的环境中。

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