Department of Neurology, University of Alabama at Birmingham, AL 35294-0021, USA.
Am J Kidney Dis. 2010 Nov;56(5):823-31. doi: 10.1053/j.ajkd.2010.05.023. Epub 2010 Aug 14.
In patients with kidney impairment, warfarin, a drug metabolized primarily by the cytochrome P-450 system, is initiated at similar doses and managed similarly as in the general medical population. Unfortunately, few data exist to guide dose adjustment in patients with decreased kidney function. Here, we determine the degree of warfarin dose reduction associated with kidney impairment and make recommendations for warfarin dosing.
Cross-sectional analysis.
SETTING & PARTICIPANTS: Long-term warfarin users followed up at anticoagulation clinics (n = 980); 708 participants from the University of Alabama (UAB) and 272 participants from the University of Chicago (UIC).
No/mild (estimated glomerular filtration rate [eGFR] ≥ 60 mL/min/1.73 m(2)), moderate (eGFR, 30-59 mL/min/1.73 m(2)), and severe (eGFR < 30 mL/min/1.73 m(2)) kidney impairment; CYP2C9 and VKORC1 genotype; age; race; sex; body mass; sociodemographic factors; smoking status; alcohol; vitamin K intake; comorbid conditions (eg, congestive heart failure); and drug interactions (eg, amiodarone and statins).
OUTCOME & MEASUREMENT: Warfarin dose (milligrams per day) was evaluated using linear regression after adjustment for clinical, demographic, and genetic factors.
Prevalences of moderate (31.8% and 27.6%) and severe kidney impairment (8.9% and 6.6%) were similar in the UAB and UIC cohorts. Warfarin dose requirements were significantly lower in patients with moderate and severe kidney impairment compared with those with no/mild kidney impairment in the UAB (P < 0.001) and UIC (P < 0.001) cohorts. Compared with patients with no/mild kidney impairment, patients with moderate kidney impairment required 9.5% lower doses (P < 0.001) and patients with severe kidney impairment required 19% lower doses (P < 0.001).
No measurement of warfarin, serum albumin, vitamin K, and coagulation factors; no evaluation of other markers (eg, cystatin).
Moderate and severe kidney impairment were associated with a reduction in warfarin dose requirements.
在肾功能受损的患者中,华法林主要通过细胞色素 P-450 系统代谢,起始剂量与普通人群相似,管理方法也相似。然而,目前几乎没有数据可以指导肾功能下降患者的剂量调整。本研究旨在确定与肾功能损害相关的华法林剂量减少程度,并提出华法林剂量建议。
横断面分析。
在抗凝门诊接受长期华法林治疗的患者(n=980);其中 708 名来自阿拉巴马大学(UAB),272 名来自芝加哥大学(UIC)。
无/轻度(估算肾小球滤过率[eGFR]≥60mL/min/1.73m2)、中度(eGFR,30-59mL/min/1.73m2)和重度(eGFR<30mL/min/1.73m2)肾功能损害;CYP2C9 和 VKORC1 基因型;年龄;种族;性别;体重;社会人口学因素;吸烟状况;饮酒;维生素 K 摄入量;合并症(如充血性心力衰竭);以及药物相互作用(如胺碘酮和他汀类药物)。
使用线性回归方法,在调整了临床、人口统计学和遗传因素后,评估华法林剂量(毫克/天)。
UAB 和 UIC 队列的中度(31.8%和 27.6%)和重度(8.9%和 6.6%)肾功能损害的患病率相似。与无/轻度肾功能损害的患者相比,UAB(P<0.001)和 UIC(P<0.001)队列中,中度和重度肾功能损害患者的华法林剂量需求明显较低。与无/轻度肾功能损害的患者相比,中度肾功能损害患者的剂量降低了 9.5%(P<0.001),重度肾功能损害患者的剂量降低了 19%(P<0.001)。
未测量华法林、血清白蛋白、维生素 K 和凝血因子;未评估其他标志物(如胱抑素)。
中度和重度肾功能损害与华法林剂量需求减少相关。