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Silence of the Limbs: Pharmacological Symptomatic Treatment of Intermittent Claudication

机译:四肢沉默:间歇性跛行的药物对症治疗

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Several oral "vasoactive" drugs claim to increase walking capacity in patients with intermittent claudication (IC). Naftidrofuryl, cilostazol, buflomedil, and pentoxifylline are the most studied molecules. Although spanning several decades, several studies underlying these claims were not properly designed, underpowered or showed clinically doubtful outcomes. The evidence for these "vasoactive" drugs has always been received with scepticism, creating the need for systematic reviews and meta-analyses. This brief review discusses the benefit-risk assessment of vasoactive drugs, by applying a systematic review to evaluate randomized, placebo-controlled trials.Oral naftidrofuryl and cilostazol have an acceptable safety profile as well as sustained evidence (documented by Cochrane analyses) of increased walking capacity. Subsequently, these drugs entered recommendations for peripheral arterial disease (PAD). In contrast, buflomedil and pentoxifylline have limited and/or doubtful evidence to increase walking capacity. Moreover, there were safety concerns about the narrow therapeutic range of buflomedil. Most other "vasoactive" drugs were either inappropriately or insufficiently tested or showed no significant if not negative effects on IC. "Vasoactive" drugs are no substitutes for lifestyle or exercise therapy but are adjuvant treatment to the well-appreciated triad of cardiovascular prevention (antiplatelet agents, statins and ACE-inhibitors), of which statins in their own right have documented claims to significantly increase walking capacity."Vasoactive" drugs may have a place in the pharmacological management of symptomatic PAD in addition to the basic cardiovascular pharmacotherapy, when revascularization is not indicated, when exercise therapy is not feasible or when there is still insufficient benefit.
机译:几种口服“血管活性”药物声称可以增加间歇性跛行 (IC) 患者的行走能力。萘呋喃、西洛他唑、丁氟洛地尔和己酮可可碱是研究最多的分子。尽管跨越了几十年,但这些说法背后的几项研究设计不当,力度不足或显示出临床上可疑的结果。这些“血管活性”药物的证据一直受到怀疑,因此需要进行系统评价和荟萃分析。这篇简短的综述通过应用系统评价来评估随机安慰剂对照试验,讨论了血管活性药物的获益风险评估。口服萘呋喃和西洛他唑具有可接受的安全性,以及增加步行能力的持续证据(由 Cochrane 分析记录)。随后,这些药物进入了外周动脉疾病(PAD)的建议。相比之下,丁氟美地尔和己酮可可碱增加步行能力的证据有限和/或值得怀疑。此外,布氟洛地尔的治疗范围狭窄也存在安全问题。大多数其他“血管活性”药物要么不适当,要么测试不充分,或者对IC没有显著的负面影响。“血管活性”药物不能替代生活方式或运动疗法,而是广为人知的心血管预防三联征(抗血小板药物、他汀类药物和ACE抑制剂)的辅助治疗,其中他汀类药物本身已被证明可以显着提高步行能力。除了基本的心血管药物治疗外,血管活性药物可能在症状性PAD的药理学管理中占有一席之地,当血运重建没有指征时,当运动治疗不可行时或当仍然没有足够的益处时。

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