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一种促静脉回流药物的临床药理活性评估。应用于500毫克达弗隆的研究。

Evaluation of the clinical pharmacological activity of a phlebotonic agent. Application to the study of Daflon 500 mg.

作者信息

Duchene Marullaz P, Amiel M, Barbe R

机构信息

Faculty of Medicine, Clermont Ferrand, Lyon Bron, France.

出版信息

Int Angiol. 1988 Apr-Jun;7(2 Suppl):25-32.

PMID:3053940
Abstract

Provided certain methodological precautions are observed, mercury strain gauge venous occlusion plethysmography represents one of the best available function tests in phlebology to evaluate the efficacy of a phlebotonic agent. All physiological and environmental parameters liable to affect venous tone must be determined and controlled before and during the procedure, which is to be carried out in controlled and fully reproducible conditions. Intra and inter-observed reproducibility of results must be checked regularly in each laboratory. The objective character of the parameters assessed (Hmax, delta Vmax, T50, T2p...) does not spare the need for randomized, crossover or comparative, double-blind placebo-controlled trials, as plethysmographic results may show wide variations from one subject to another, and even from one moment to another, in chronic venous insufficiency, depending on the subject's environment and occupation. Furthermore, knowledge of treatment by the observer may affect the validity of the results. Taking into account all of these methodological pre-requisites, the phlebotonic activity of a single dose of Daflon 500 mg in lower limb chronic venous insufficiency was assessed in placebo-controlled clinical pharmacological studies. The following characteristics emerged: (1) significant improvement of venous capacitance, distensibility, and emptying times, as from the 2nd hour following Daflon 500 mg administration; (2) dose-response relationship, with an optimal dose of 2 tablets per day; (3) rapid onset and long duration of action; (4) significant hemodynamic effect on the venous system, whatever the type of venous insufficiency: organic, functional or gestational.

摘要

只要遵循某些方法学上的预防措施,汞应变计静脉阻塞体积描记法就是静脉病学中评估静脉活性药物疗效的最佳功能测试方法之一。在该操作之前及过程中,所有可能影响静脉张力的生理和环境参数都必须确定并加以控制,且该操作应在可控且完全可重复的条件下进行。每个实验室都必须定期检查结果在内部和不同观测者之间的可重复性。所评估参数(Hmax、delta Vmax、T50、T2p……)的客观特性并不能免除进行随机、交叉或对比、双盲安慰剂对照试验的必要性,因为在慢性静脉功能不全中,体积描记结果可能因受试者不同,甚至同一受试者在不同时刻而有很大差异,这取决于受试者的环境和职业。此外,观察者对治疗的了解可能会影响结果的有效性。考虑到所有这些方法学前提条件,在安慰剂对照的临床药理学研究中评估了单剂量500毫克达芙通在下肢慢性静脉功能不全中的静脉活性。出现了以下特征:(1)自服用500毫克达芙通后第2小时起,静脉容量、扩张性和排空时间有显著改善;(2)剂量反应关系,最佳剂量为每日2片;(3)起效迅速且作用持续时间长;(4)无论静脉功能不全的类型是器质性、功能性还是妊娠性,对静脉系统均有显著的血流动力学效应。

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