Eckman Mark H, Singer Daniel E, Rosand Jonathan, Greenberg Steven M
Division of General Internal Medicine and the Center for Clinical Effectiveness, University of Cincinnati, Cincinnati, OH 45267-0535, USA.
Circ Cardiovasc Qual Outcomes. 2011 Jan 1;4(1):14-21. doi: 10.1161/CIRCOUTCOMES.110.958108. Epub 2010 Dec 7.
The rate of ischemic stroke associated with traditional risk factors for patients with atrial fibrillation has declined over the past 2 decades. Furthermore, new and potentially safer anticoagulants are on the horizon. Thus, the balance between risk factors for stroke and benefit of anticoagulation may be shifting.
The Markov state transition decision model was used to analyze the CHADS(2) score, above which anticoagulation is preferred, first using the stroke rate predicted for the CHADS(2) derivation cohort, and then using the stroke rate from the more contemporary AnTicoagulation and Risk Factors In Atrial Fibrillation cohort for any CHADS(2) score. The base case was a 69-year-old man with atrial fibrillation. Interventions included oral anticoagulant therapy with warfarin or a hypothetical "new and safer" anticoagulant (based on dabigatran), no antithrombotic therapy, or aspirin. Warfarin is preferred above a stroke rate of 1.7% per year, whereas aspirin is preferred at lower rates of stroke. Anticoagulation with warfarin is preferred even for a score of 0 using the higher rates of the older CHADS(2) derivation cohort. Using more contemporary and lower estimates of stroke risk raises the threshold for use of warfarin to a CHADS(2) score ≥2. However, anticoagulation with a "new, safer" agent, modeled on the results of the Randomized Evaluation of Long-Term Anticoagulation Therapy trial of dabigatran, leads to a lowering of the threshold for anticoagulation to a stroke rate of 0.9% per year.
Use of a more contemporary estimate of stroke risk shifts the "tipping point," such that anticoagulation is preferred at a higher CHADS(2) score, reducing the number of patients for whom anticoagulation is recommended. The introduction of "new, safer" agents, however, would shift the tipping point in the opposite direction.
在过去20年里,与房颤患者传统危险因素相关的缺血性卒中发生率有所下降。此外,新型且可能更安全的抗凝药物即将问世。因此,卒中危险因素与抗凝治疗获益之间的平衡可能正在发生变化。
采用马尔可夫状态转移决策模型分析CHADS(2)评分(高于该评分时抗凝治疗更为可取),首先使用CHADS(2)推导队列预测的卒中发生率,然后针对任何CHADS(2)评分使用来自更现代的房颤抗凝与危险因素(AnTicoagulation and Risk Factors In Atrial Fibrillation)队列的卒中发生率。基础病例为一名69岁的房颤男性。干预措施包括使用华法林或一种假设的“新型且更安全”的抗凝药物(基于达比加群)进行口服抗凝治疗、不进行抗栓治疗或使用阿司匹林。每年卒中发生率高于1.7%时,华法林更为可取,而卒中发生率较低时,阿司匹林更为可取。即使使用较旧的CHADS(2)推导队列的较高发生率,对于CHADS(2)评分为0的患者,华法林抗凝治疗仍更为可取。使用更现代且更低的卒中风险估计值会将使用华法林的阈值提高到CHADS(2)评分≥2。然而,以达比加群长期抗凝治疗随机评估试验的结果为模型的“新型、更安全”药物抗凝治疗会将抗凝阈值降低至每年0.9%的卒中发生率。
使用更现代的卒中风险估计值会改变“临界点”,使得在更高的CHADS(2)评分时抗凝治疗更为可取,从而减少推荐进行抗凝治疗的患者数量。然而,“新型、更安全”药物的引入会使临界点向相反方向移动。