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Retrospective cohort study of the efficacy and safety of dabigatran: real-life dabigatran use including very low-dose 75 mg twice daily administration

机译:回顾性队列研究达比茄菌的疗效和安全性:现实生活达比河用途,包括非常低剂量75毫克每日施用

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摘要

Abstract Background Dabigatran is a direct thrombin inhibitor and an anticoagulant that is prescribed to prevent ischemic stroke and systemic embolism in non-valvular atrial fibrillation. Dabigatran (150 mg twice daily) is non-inferior to warfarin for the prevention of stroke and systemic embolism. A dose reduction to 110 mg twice daily should be considered for patients with decreased renal function, elderly patients, and those with a history of gastrointestinal bleeding. A small number of patients are prescribed 75 mg twice daily; however, excessive dose reduction below that indicated on the package insert may decrease the effectiveness of dabigatran. In this study, we investigated the incidence of thromboembolic events and hemorrhagic complications in patients receiving different doses of dabigatran, including patients receiving the very low-dose of 75 mg twice daily. Methods Five hospitals in Meguro and Setagaya areas of Tokyo were included in this study. The subjects were patients receiving dabigatran in the hospitals from March 2011 to February 2014. Thromboembolic events (stroke, systemic embolism, and transient cerebral ischemic attack) and hemorrhagic complications occurring before December 2014 were retrospectively evaluated. Results A total of 701 subjects received dabigatran during the study period: 187 patients (26.7%) received 150 mg twice daily (normal dose), 488 patients (69.6%) received 110 mg twice daily (low-dose), and 26 patients (3.7%) received 75 mg twice daily (very low-dose). Thromboembolism occurred in 4 (2.1%), 11 (2.3%), and 3 patients (11.5%), in the normal dose, low-dose, and very low-dose groups, respectively. The odds ratio of the 75 mg dose to the 150 and 110 mg doses was 5.73 (95% CI, 1.55–21.2; p = 0.009), and the incidence with the 75 mg dose was higher than that with the other doses. Although the number of events was limited, it should be noted that 3 patients in the very low-dose group had thromboembolic events. Conclusions The results suggest that sufficient anticoagulation efficacy may not be maintained when the dabigatran dose is excessively reduced to 75 mg twice daily.
机译:摘要背景Dabigatran是直接凝血酶抑制剂和抗凝血剂,其规定,以防止非瓣膜心房颤动中的缺血性卒中和全身栓塞。 Dabigatran(每天两次)是非逊素的预防下划线和全身性栓塞。对于肾功能下降,老年患者和胃肠道出血史的患者,应考虑每天两次降至110毫克。少数患者每天两次规定75毫克;然而,在包装插入件上指示的过度剂量减少可能降低达比税兰的有效性。在这项研究中,我们研究了接受不同剂量的Dabigatran的患者的血栓栓塞事件和出血并发症的发病率,包括每天两次接受75毫克的低剂量的患者。方法本研究中纳入了梅戈罗和东京的塞塔亚塔山区的五家医院。该受试者是2011年3月至2014年3月在医院接受Dabigatran的患者。回顾性评估2014年12月之前发生的血栓栓塞事件(中风,全身栓塞和瞬态脑缺血性发作)和出血性并发症。结果共有701名受试者在研究期间接受Dabigatran:187名患者(26.7%)每日两次(正常剂量),488名患者(69.6%)每日每日210毫克(低剂量)和26名患者( 3.7%)每天两次收到75毫克(非常低剂量)。血栓栓塞分别发生在4例(2.1%),11(2.3%)和3名患者(11.5%),正常剂量,低剂量和非常低剂量基团中发生。 75mg剂量为150和110mg剂量的差距为5.73(95%CI,1.55-21.2; p = 0.009),并且75mg剂量的发病率高于其他剂量。虽然事件的数量有限,但应该注意,非常低剂量组中的3例患者患有血栓栓塞事件。结论结果表明,当Dabigatran剂量过于每天两次降至75mg时,可能不会保持足够的抗凝功效。

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