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在心房颤动患者中使用低剂量直接口服因子 Xa 抑制剂的超适应证用法:临床证据综述。

Off-label use of reduced dose direct oral factor Xa inhibitors in subjects with atrial fibrillation: a review of clinical evidence.

机构信息

Section of Geriatrics, Department of Medical Sciences, Università di Torino, A.O.U. Città della Salute e della Scienza, Molinette, Corso Bramante 88, 10126 Turin, Italy.

Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Via Giuseppe Balzaretti 9, 20133 Milan, Italy.

出版信息

Eur Heart J Cardiovasc Pharmacother. 2021 Jul 23;7(4):334-345. doi: 10.1093/ehjcvp/pvaa103.

Abstract

In real-world clinical practice, underdosing, i.e. off-label use of reduced doses (RDs), of oral factor Xa inhibitors (oFXaIs) is quite common in stroke prevention in non-valvular atrial fibrillation, possibly reflecting the hope to increase safety without reducing efficacy in selected patients. To assess whether this strategy is associated with some clinical benefit, we used a physician-centred approach to evaluate whether current evidence supports the hypothesis that a substantial proportion of underdosing may be voluntary rather than casual, whether and to what extent oFXaIs' dose rather than patients' characteristics are associated with bleeding events, and which are the safety and efficacy clinical implications of oFXaIs' underdosing. Our review found consistent evidence that underdosing is often an intentional strategy; however, available studies do not demonstrate a sizeable net clinical benefit of using off-label RD oFXaIs.

摘要

在真实的临床实践中,在非瓣膜性心房颤动的卒中预防中,口服 Xa 因子抑制剂(oFXaIs)的剂量不足(即标签外使用降低剂量,RD)相当常见,这可能反映了在某些选定的患者中,增加安全性而不降低疗效的希望。为了评估这种策略是否与某些临床获益相关,我们采用了以医生为中心的方法,评估当前的证据是否支持以下假设,即大量的剂量不足可能是自愿的而不是偶然的,oFXaIs 的剂量而不是患者的特征与出血事件相关,以及 oFXaIs 剂量不足的安全性和疗效的临床意义是什么。我们的综述发现了一致的证据,表明剂量不足通常是一种有意的策略;然而,现有研究并未证明使用标签外 RD oFXaIs 的净临床获益显著。

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