Ebrahim I, Bryer A, Cohen K, Mouton J P, Msemburi W, Blockman M
Division of Clinical Pharmacology, Groote Schuur Hospital and Faculty of Health Sciences, University of Cape Town, South Africa.
S Afr Med J. 2018 May 25;108(6):490-494. doi: 10.7196/SAMJ.2018.v108i6.13062.
Warfarin is the most commonly used anticoagulant for both primary and secondary prevention of thromboembolism. For anticoagulation efficacy, the international normalised ratio (INR) needs to be within the therapeutic range for at least 65% of time on warfarin.
To describe INR control in patients on long-term warfarin and identified predictors of good INR control at two dedicated warfarin follow-up clinics in Cape Town, South Africa (SA).
We reviewed clinical records of patients in care at the INR clinics at Mitchell's Plain Community Health Centre and Groote Schuur Hospital. We included patients who had been on warfarin therapy for at least 27 months and excluded patients with <6 months of INR monitoring data or a >70-day gap between INR tests in the calculation period, and if >25% of follow-up time was at an alternative site. The time in therapeutic range (TTR) over 180 days using the Rosendaal method was calculated, and we categorised INR control as good if the TTR was ≥65%. We constructed a multivariate logistic regression model to identify associations with good INR control.
We included 363 patients, with a median age of 55 years (interquartile range (IQR) 44 - 64), of whom 65.6% were women. The most common indications for warfarin were valvular heart disease (45.7%) and atrial fibrillation (25.1%). The mean TTR was 47%, with only 91/363 patients having good INR control. In a multivariate model adjusted for age, sex, clinic and target INR, patients aged ≥55 years were more likely to have good INR control than younger patients (adjusted odds ratio 1.69, 95% confidence interval 1.03 - 2.79). Poorly controlled patients had more frequent INR monitoring than those with good INR control, with a median of 8 INRs (IQR 6 - 10) v. 6 INRs (IQR 5 - 8) in the 180-day period (p<0.0001).
Only 25.1% of patients in our study achieved good INR control, despite regular INR monitoring. There is an urgent need to improve anticoagulation control of patients receiving warfarin in SA. Validated dosing algorithms are required, and access to lower warfarin dosage formulations may optimise individual dose titration. Advocacy for these formulations is advised.
华法林是用于血栓栓塞一级和二级预防最常用的抗凝剂。为达到抗凝效果,国际标准化比值(INR)在服用华法林期间需至少65%的时间处于治疗范围内。
描述南非开普敦两家专门的华法林随访诊所中接受长期华法林治疗患者的INR控制情况,并确定INR良好控制的预测因素。
我们回顾了米切尔平原社区卫生中心和格罗特舒尔医院INR诊所患者的临床记录。纳入接受华法林治疗至少27个月的患者,排除在计算期内INR监测数据少于6个月或INR检测间隔超过70天的患者,以及随访时间超过25%在其他地点的患者。使用罗森达尔法计算180天内处于治疗范围的时间(TTR),若TTR≥65%,则将INR控制分类为良好。我们构建了多变量逻辑回归模型以确定与INR良好控制的关联。
我们纳入了363例患者,中位年龄55岁(四分位间距(IQR)44 - 64),其中65.6%为女性。华法林最常见的适应证是心脏瓣膜病(45.7%)和心房颤动(25.1%)。平均TTR为47%,仅有91/363例患者INR控制良好。在根据年龄、性别、诊所和目标INR进行校正的多变量模型中,年龄≥55岁的患者比年轻患者更有可能INR控制良好(校正比值比1.69,95%置信区间1.03 - 2.79)。控制不佳的患者比INR控制良好的患者更频繁地进行INR监测,在180天期间的中位数分别为8次INR检测(IQR 6 - 10)和6次INR检测(IQR 5 - 8)(p<0.0001)。
尽管定期进行INR监测,但我们研究中只有25.1%的患者INR控制良好。南非迫切需要改善接受华法林治疗患者的抗凝控制。需要经过验证的给药算法,并且使用较低剂量的华法林制剂可能会优化个体剂量滴定。建议推广这些制剂。