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与注册试验相比,美国心脏病学实际临床实践中阿哌沙班和利伐沙班的处方剂量。

Doses of apixaban and rivaroxaban prescribed in real-world United States cardiology practices compared to registration trials.

作者信息

Nguyen Elaine, White C Michael, Patel Manesh R, Fields Larry E, Peacock W Frank, Crivera Concetta, Coleman Craig I

机构信息

a University of Connecticut/Hartford Hospital Health Outcomes, Policy and Evidence Synthesis Group , Hartford , CT , U.S.A. ;

b Department of Pharmacy Practice , University of Connecticut School of Pharmacy , Storrs , CT , U.S.A. ;

出版信息

Curr Med Res Opin. 2016 Jul;32(7):1277-9. doi: 10.1185/03007995.2016.1170672. Epub 2016 Apr 1.

Abstract

Using an I.M.S. LifeLink dataset (19 September 2014-11 September 2015), we compared U.S. cardiologist prescribing of the reduced dose of apixaban (2.5 mg) or rivaroxaban (15 mg) to utilization in their corresponding nonvalvular atrial fibrillation registration randomized trials. Of all prescriptions written by cardiologists for these agents, 20.8% of apixaban and 21.7% of rivaroxaban prescriptions were for a reduced dose; corresponding to a 4.4-fold (16.1% absolute) increase in the use of reduced dose apixaban and a 3% relative (0.6% absolute) increase in reduced dose rivaroxaban use vs. their respective registration trials. Further research is needed to better understand appropriate dosing of patients with novel anticoagulants.

摘要

利用I.M.S. LifeLink数据集(2014年9月19日至2015年9月11日),我们将美国心脏病专家开具的低剂量阿哌沙班(2.5毫克)或利伐沙班(15毫克)处方与它们在相应的非瓣膜性心房颤动注册随机试验中的使用情况进行了比较。在心脏病专家开具的所有这些药物处方中,20.8%的阿哌沙班处方和21.7%的利伐沙班处方为低剂量;与各自的注册试验相比,低剂量阿哌沙班的使用增加了4.4倍(绝对增加16.1%),低剂量利伐沙班的使用相对增加了3%(绝对增加0.6%)。需要进一步研究以更好地了解新型抗凝剂患者的合适剂量。

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