Hilkens Nina A, Algra Ale, Greving Jacoba P
From the Julius Center for Health Sciences and Primary Care (N.A.H., A.A., J.P.G.) and Department of Neurology and Neurosurgery, Brain Center Rudolf Magnus (A.A.), University Medical Center Utrecht, Utrecht University, the Netherlands.
Stroke. 2017 Nov;48(11):3142-3144. doi: 10.1161/STROKEAHA.117.019183. Epub 2017 Sep 20.
Performance of risk scores for major bleeding in patients with atrial fibrillation and a previous transient ischemic attack or ischemic stroke is not well established. We aimed to validate risk scores for major bleeding in patients with atrial fibrillation treated with oral anticoagulants after cerebral ischemia and explore the net benefit of oral anticoagulants among bleeding risk categories.
We analyzed 3623 patients with a history of transient ischemic attack or stroke included in the RE-LY trial (Randomized Evaluation of Long-Term Anticoagulation Therapy). We assessed performance of HEMORRHAGES (hepatic or renal disease, ethanol abuse, malignancy, older age, reduced platelet count or function, hypertension [uncontrolled], anemia, genetic factors, excessive fall risk, and stroke), Shireman, HAS-BLED (hypertension, abnormal renal/liver function, stroke, bleeding history or predisposition, labile international normalized ratio, elderly, drugs/alcohol concomitantly), ATRIA (Anticoagulation and Risk Factors in Atrial Fibrillation), and ORBIT scores (older age, reduced haemoglobin/haematocrit/history of anaemia, bleeding history, insufficient kidney function, and treatment with antiplatelet) with C statistics and calibration plots. Net benefit of oral anticoagulants was explored by comparing risk reduction in ischemic stroke with risk increase in major bleedings on warfarin.
During 6922 person-years of follow-up, 266 patients experienced a major bleed (3.8 per 100 person-years). C statistics ranged from 0.62 (Shireman) to 0.67 (ATRIA). Calibration was poor for ATRIA and moderate for other models. The reduction in recurrent ischemic strokes on warfarin was larger than the increase in major bleeding risk, irrespective of bleeding risk category.
Performance of prediction models for major bleeding in patients with cerebral ischemia and atrial fibrillation is modest but comparable with performance in patients with only atrial fibrillation. Bleeding risk scores cannot guide treatment decisions for oral anticoagulants but may still be useful to identify modifiable risk factors for bleeding. Clinical usefulness may be best for ORBIT, which is based on a limited number of easily obtainable variables and showed reasonable performance.
心房颤动且既往有短暂性脑缺血发作或缺血性卒中患者的大出血风险评分表现尚未明确。我们旨在验证脑缺血后接受口服抗凝剂治疗的心房颤动患者大出血的风险评分,并探讨口服抗凝剂在不同出血风险类别中的净获益情况。
我们分析了RE-LY试验(长期抗凝治疗随机评估)中纳入的3623例有短暂性脑缺血发作或卒中病史的患者。我们使用C统计量和校准图评估了HEMORRHAGES(肝脏或肾脏疾病、乙醇滥用、恶性肿瘤、老年、血小板计数或功能降低、高血压[未控制]、贫血、遗传因素、跌倒风险增加和卒中)、Shireman、HAS-BLED(高血压、肾/肝功能异常、卒中、出血史或易感性、国际标准化比值不稳定、老年、药物/酒精合用)、ATRIA(心房颤动抗凝与危险因素)和ORBIT评分(老年、血红蛋白/血细胞比容降低/贫血病史、出血史、肾功能不全和抗血小板治疗)。通过比较华法林治疗缺血性卒中的风险降低与大出血风险增加情况,探讨口服抗凝剂的净获益。
在6922人年的随访期间,266例患者发生大出血(每100人年3.8例)。C统计量范围为0.62(Shireman)至0.67(ATRIA)。ATRIA的校准较差,其他模型的校准中等。无论出血风险类别如何,华法林治疗复发性缺血性卒中的降低幅度均大于大出血风险的增加幅度。
脑缺血和心房颤动患者大出血预测模型表现一般,但与仅患有心房颤动的患者相当。出血风险评分不能指导口服抗凝剂的治疗决策,但仍可能有助于识别可改变的出血危险因素。基于有限数量的易于获得的变量且表现合理的ORBIT可能具有最佳临床实用性。