新型口服抗凝剂(Noacs)是否如人们所说的那样安全

F. Kamali
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引用次数: 6

摘要

与华法林相比,NOACs的主要优点是其可预测的药代动力学和临床反应,因此无需常规抗凝监测或监测血浆药物水平,药物相互作用较少,并且不与饮食相互作用。更重要的是,开发和销售NOACS是为了作为固定剂量方案使用,这被认为是比华法林有实质性优势。NOAC的处方数量自推出以来急剧上升,无论是新诊断的需要抗凝治疗的患者,还是现有的华法林抗凝控制不良的患者,都转向了NOAC。与2011年相比,2012年英国达比加群的处方增加了1600%,从约3000人增加到约48000人,2012年利伐沙班的处方约16000人。虽然在RE-LY、ROCKET-AF和ARISTOTLE研究中,NOACs在房颤患者卒中预防的临床效果上与华法林没有劣效性,但这些试验中报告的出血不良反应可能与患者年龄有关,75岁及以上的患者出血发生率更高[3-5]。值得关注的是,鉴于NOACs在房颤治疗中的使用,更多的老年人在试验中没有得到很好的代表,临床经验太短,无法提供使用模式,以优化治疗的益处,并确保治疗可以安全地开处方。尽管noac的处方率自推出以来迅速增长,但对致命出血的担忧已经出现,特别是在老年人中,他们的风险更大。后来,达比加群制造商勃林格殷格翰公司对RE-LY试验数据进行了亚分析,结果显示,两种剂量(110和150毫克)的血浆达比加群浓度各有5倍的变化。进一步的数据分析表明,肾功能是最重要的决定因素
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Are Novel Oral Anticoagulants (Noacs) as Safe as They are Said to Be
The main advantages of NOACs over warfarin are their predictable pharmacokinetics and clinical response thus obviating the need for routine anticoagulation monitoring or monitoring of plasma drug levels, fewer drug interactions and the lack of interaction with diet. More crucially NOACS were developed and marketed to be used as fixed-dose regimens, which is considered to be a substantial advantage over warfarin. Prescription numbers for NOACs have risen sharply since their launch for both newly diagnosed patients requiring initiation of anticoagulant therapy and existing patients on warfarin with poor anticoagulation control being switched to a NOAC, with prescriptions in England for dabigatran in 2012 compared to 2011 increasing 1,600%, from around 3,000 to around 48,000, and prescriptions for rivaroxaban in 2012 being around 16,000 [2]. Whilst non-inferiority of NOACs to warfarin in their clinical effectiveness for stroke prophylaxis in patients with atrial fibrillation in the RE-LY, ROCKET-AF, and ARISTOTLE studies has been established, the bleeding adverse reactions reported in those trials, may be contributed to by patient age, with the noted incidence of bleeding being greater in those aged 75 years and over [3-5]. It is of concern that in view of the use of NOACs in atrial fibrillation the more elderly were not well represented in the trials, and clinical experience is too short to provide models of use which optimise the benefits of therapy and ensure therapy can be safely prescribed. Although prescribing rates for NOACs have grown rapidly since their launch, concerns about fatal bleeds have emerged particularly in elderly people, who are at a greater risk. A later sub-analysis of the RE-LY trial data by the manufacturer of dabigatran, Boehringer Ingleheim, showed that there were 5-fold variations in plasma dabigatran concentration for each of the two doses (110 and 150 mg) that were tested [6]. Further analysis of the data showed that renal function is the most important determinant for
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