首页> 外文期刊>Journal of Pharmaceutical Health Care and Sciences >Inappropriate direct oral anticoagulant dosing in atrial fibrillation patients is associated with prescriptions for outpatients rather than inpatients: a single-center retrospective cohort study
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Inappropriate direct oral anticoagulant dosing in atrial fibrillation patients is associated with prescriptions for outpatients rather than inpatients: a single-center retrospective cohort study

机译:在心房颤动患者中不适当的直接口服抗凝血剂量与门诊患者的处方相关,而不是住院患者:单中心回顾性队列研究

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Background: Inappropriate dosing of direct oral anticoagulants (DOACs) has been associated with clinical safety and efficacy; however, little is known about clinical data associated with an inappropriate DOAC dosing in Japan. In addition, there is no report in which the appropriateness of DOAC dosing between prescription for inpatients and for outpatients was examined. In this study, we aimed to investigate the prevalence and factors associated in the inappropriate dosing of DOACs in patients with atrial fibrillation (AF). Methods: The retrospective cohort study was conducted at a single Japanese university hospital. Both inpatients and outpatients, who were diagnosed with AF and for whom treatment with either dabigatran, rivaroxaban, apixaban, or edoxaban was initiated between April 1, 2014 and March 31, 2018, were enrolled in the study. Appropriateness of DOAC dosing was assessed according to the manufacturer’s labeling recommendations (dose reduction criteria) of each DOAC. Inappropriate reduced dose, namely, underdosing, was defined as prescription of a reduced dose of DOAC despite the patient not meeting the dose reduction criteria. Inappropriate standard dose, namely, overdosing, was defined as prescription of a standard dose of DOAC despite the patient meeting the dose reduction criteria. Inappropriate DOAC dosing was defined as a deviation of the recommended dose (both underdosing and overdosing). Results: A total of 316 patients (dabigatran, 28; rivaroxaban, 107; apixaban, 116; and edoxaban, 65) were included, with a median (interquartile range) age of 75 (66–81) years and 62.3% male. DOACs were prescribed at an appropriate standard dose in 39.2% of patients, an appropriate reduced dose in 36.7%, an inappropriate standard dose in 2.5%, and an inappropriate reduced dose in 19.3%. Multivariate analysis revealed that the inappropriate dosing of DOACs was significantly associated with prescriptions for outpatients (vs. inpatients; odds ratio [OR] 2.87, 95% confidence interval [CI] 1.53–5.62, p 0.001) and those with higher HAS-BLED scores (OR 1.87, 95% CI 1.42– 2.51, p 0.001).Conclusions: Our results demonstrated that the inappropriate dosing of DOACs occurred in approximately 20% of AF patients, and was more frequent in outpatients (vs. inpatients) and in those with a higher risk of bleeding. It is recommended that pharmacists play a greater role in assisting in the prescription process to help physicians make better decisions.
机译:背景:直接口服抗凝血剂(Doacs)的不当剂量与临床安全和疗效有关;然而,关于与日本的不适当的DoAC给药相关的临床资料,很少熟知。此外,还没有报道,研究了在其中检查住院患者处方和门诊患者处方之间的DOAC给药的适当性。在这项研究中,我们旨在探讨在心房颤动(AF)患者的不恰当剂量的Doacs中相关的患病率和因素。方法:在一家日本大学医院进行回顾性队列研究。在2014年4月1日至2018年4月1日期间,在2018年4月1日期间启动了患有AF和Dab and and Dabigatran,Rivaroxaban,Apixaban或Edoxaban的病例和门诊病人。根据制造商的标签推荐(剂量还原标准)评估DoAC给药的适当性。尽管患者不符合剂量还原标准,但不当减少剂量减少剂量,所以被定义为减少剂量的Doac剂量。尽管患者会达到剂量还原标准,但仍被定义为过量的标准剂量,即过量,被定义为Doac的标准剂量的处方。不恰当的DoAC给药被定义为推荐剂量的偏差(减少和过量)。结果:共有316名患者(Dabigatran,28; Rivaroxaban,107; Apixaban,116;和Edoxaban,65),中位数(四分位数)年龄为75(66-81)岁和62.3%的男性。在39.2%的患者中,DOACS在适当的标准剂量,适当减少的剂量为36.7%,不适当的标准剂量为2.5%,4.3%的剂量减少。多变量分析显示,DOAC的不适当的剂量与门诊病例的处方有显着相关(与住院患者;差距[或] 2.87,95%置信区间[CI] 1.53-5.62,P <0.001)和具有更高的患者分数(或1.87,95%CI 1.42- 2.51,P <0.001)。结论:我们的结果表明,在约20%的AF患者中发生了不恰当的Doac剂量,并且在门外(与住院患者的患者中更频繁)患有较高风险的人。建议药剂师在协助处方过程中发挥更大的作用,以帮助医生做出更好的决定。

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