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Evaluation of Dosing Practices of Rivaroxaban and Dabigatran

机译:利伐沙班和达比加群的给药实践评价

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摘要

Background: Anticoagulation is standard practice for the prevention and treatment of thromboembolic events. Two of the newer agents, rivaroxaban (Xarelto) and dabigatran (Pradaxa) are being utilized frequently in the inpatient and outpatient settings. Prescribers may not appreciate the need for dose reduction in the setting of renal insufficiency. Objective: The objective of this study was to evaluate whether rivaroxaban and dabigatran were dosed according to recommendations in the package insert for patients with renal insufficiency. Methods: Eligible patients were those >I8 years of age who received rivaroxaban or dabigatran as an inpatient or had a prescription filled from the outpatient pharmacy. The use of the Cockcroft-Gault equation was utilized to calculate creatinine clearance to evaluate whether patients had appropriate manufacturer recommended dose reductions based on their renal function. Results: There were very few patients (8 of 355, or 2.3%) who should have received a reduced dose when creatinine clearance was calculated utilizing actual body weight. In those patients with renal insufficiency, 3 of 6 (50.0%) patients receiving rivaroxaban and I of 2 (50%) patients receiving dabigatran were appropriately dosed. When ideal body weight was substituted for creatinine clearance calculation, there were 15 patients receiving rivaroxaban and 10 patients receiving dabigatran who fell below the creatinine clearance threshold for dose reduction. Conclusions: Based on this evaluation, very few patients required a dose reduction due to renal insufficiency. It is important for clinicians to always monitor renal function when utilizing these medications to optimize the benefits of the new oral anticoagulants while limiting potential deleterious effects. Furthermore, it is necessary to ensure that actual body weight is being utilized for creatinine clearance calculations with the new oral anticoagulants and not to base dosing on estimated glomerular filtration rate or other calculated creatinine clearance as this could lead to inappropriate dose reductions.
机译:背景:抗凝是预防和治疗血栓栓塞事件的标准做法。两种较新的药物,利伐沙班(Xarelto)和达比加群(Pradaxa)在住院和门诊患者中经常使用。处方者可能不了解在肾功能不全的情况下需要减少剂量。目的:本研究的目的是评估是否根据肾功能不全患者的包装说明书中的剂量服用利伐沙班和达比加群。方法:符合条件的患者是> I8岁且接受利伐沙班或达比加群住院治疗或由门诊药房开出处方的患者。使用Cockcroft-Gault方程来计算肌酐清除率,以评估患者是否根据其肾功能适当降低了制造商建议的剂量。结果:当根据实际体重计算肌酐清除率时,很少有患者应减少剂量(355例中的8例,占2.3%)。在那些肾功能不全的患者中,接受利伐沙班治疗的6名患者中有3名(50.0%)和接受达比加群治疗的2名患者中有I(50%)接受了适当剂量。当用理想体重代替肌酐清除率计算时,有15例接受利伐沙班的患者和10例接受达比加群的患者均降至降低肌酐清除率阈值以下。结论:基于该评估,由于肾功能不全,很少有患者需要降低剂量。对于临床医生而言,在使用这些药物以优化新型口服抗凝药的益处同时限制潜在有害作用的同时,始终监测肾功能非常重要。此外,有必要确保使用新的口服抗凝剂将实际体重用于肌酐清除率的计算,并且不要以估计的肾小球滤过率或其他计算得出的肌酐清除率为基础给药,因为这可能导致剂量减少不当。

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