Division of Cardiology, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada; Electrophysiology Service at the Montreal Heart Institute and the Department of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Division of Cardiology, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Can J Cardiol. 2018 Aug;34(8):1010-1018. doi: 10.1016/j.cjca.2018.04.019. Epub 2018 Apr 25.
Non-vitamin K antagonist oral anticoagulants (NOACs) require renal dose adjustment. The most common estimates of renal function in clinical practice are derived from estimated glomerular filtration rate (eGFR; Modified Diet in Renal Disease [MDRD] or the Chronic Kidney Disease Epidemiology Collaboration [CKD-EPI]). However, the landmark stroke prevention trials and product monographs recommend the use of the Cockcroft-Gault creatinine clearance equation (eCrCl) for drug eligibility and dose adjustment. We sought to evaluate the agreement in NOAC dosing between these 3 equations in a large population of patients with atrial fibrillation and moderate chronic kidney disease.
We identified 831 patients with non-dialysis-dependent chronic kidney disease and atrial fibrillation (CHADS-VASc 3.9). For each patient, eCrCl, MDRD eGFR, and CKD-EPI eGFR were prospectively calculated. Eligibility criteria for NOAC medications were evaluated by comparing the eGFR as estimated by MDRD or CKD-EPI equation with the eCrCl as estimated by Cockcroft-Gault, with the latter regarded as the "gold standard."
The use of eGFR resulted in significant misclassification with respect to NOAC dosing. Compared with eCrCl, the MDRD eGFR and CKD-EPI eGFR misclassified 36.2% and 35.8% of patients, respectively. The misclassification resulted in undertreatment (eg, inappropriate dose reduction; 26.9% MDRD, 28.8% CKD-EPI), and to a lesser extent overtreatment (eg, inappropriate use of standard dose; 9.3% MDRD, 7.0% CKD-EPI).
MDRD and CKD-EPI eGFR fail to correctly identify a significant proportion of patients who require NOAC dose adjustment, limiting their clinical utility. Cockcroft-Gault eCrCl should be calculated for all patients in whom a NOAC is being prescribed.
非维生素 K 拮抗剂口服抗凝剂(NOACs)需要根据肾功能进行剂量调整。在临床实践中,最常用的肾功能估计值来自估算肾小球滤过率(eGFR;改良肾脏病饮食法 [MDRD] 或慢性肾脏病流行病学合作研究 [CKD-EPI])。然而,具有里程碑意义的卒中预防试验和药品说明书建议使用 Cockcroft-Gault 肌酐清除率方程(eCrCl)来确定药物的适应证和调整剂量。我们旨在评估在伴有中度慢性肾脏病的房颤患者中,这 3 种方程在 NOAC 剂量调整方面的一致性。
我们纳入了 831 名非透析依赖的慢性肾脏病合并房颤(CHA2DS2-VASc 评分 3.9 分)患者。对每位患者,前瞻性计算 Cockcroft-Gault 肌酐清除率(eCrCl)、MDRD eGFR 和 CKD-EPI eGFR。通过比较 MDRD 或 CKD-EPI 方程估算的 eGFR 与 Cockcroft-Gault 估算的 eCrCl,评估 NOAC 药物的适应证,后者被视为“金标准”。
eGFR 的应用导致了与 NOAC 剂量相关的显著错误分类。与 eCrCl 相比,MDRD eGFR 和 CKD-EPI eGFR 分别错误分类了 36.2%和 35.8%的患者。这种错误分类导致剂量不足(例如,不合适的剂量减少;MDRD 为 26.9%,CKD-EPI 为 28.8%),且在一定程度上导致剂量过度(例如,不合适地使用标准剂量;MDRD 为 9.3%,CKD-EPI 为 7.0%)。
MDRD 和 CKD-EPI eGFR 未能正确识别出需要进行 NOAC 剂量调整的相当一部分患者,限制了其临床应用。对于所有需要处方 NOAC 的患者,都应计算 Cockcroft-Gault eCrCl。