Mahawish Karim M, White Harvey, Feigin Valery, Krishnamurthi Rita
Stroke Physician, Adult Rehabilitation & Health of Older People, Middlemore Hospital, Auckland, Aotearoa New Zealand; Doctoral Student, School of Clinical Sciences, Auckland University of Technology, Auckland, Aotearoa New Zealand.
Director, Coronary Care and Cardiovascular Research, Auckland City Hospital, Green Lane Cardiovascular Service, Auckland, Aotearoa New Zealand.
N Z Med J. 2025 Mar 14;138(1611):102-113. doi: 10.26635/6965.6846.
The predictive risk model CHA2DS2 VASc helps clinicians assess the risk of stroke in patients with atrial fibrillation (AF). Originally developed and validated in predominantly European populations, it may not accurately reflect the stroke risk for diverse ethnic groups; in Aotearoa New Zealand, Māori and Pacific peoples with AF are at higher stroke risk. As part of global efforts to address health inequities, there is growing interest in adapting predictive models to suit local- and ethnic-specific risks better. Our objectives were to determine: 1) if stroke risk from AF varies by ethnic background/race, 2) stroke rates in non-anticoagulated AF cohorts, and 3) model performance of CHA2DS2 VASc across different geographical regions. Finally, we provide an overview of methodological considerations for risk model development.
We searched English language peer-reviewed studies reporting stroke rates in unselected cohorts with AF, published between 1995 and 2024. For stroke risk, we included cohorts with over 5,000 non-anticoagulated patients. The sources of evidence were PubMed, Scopus and EMBASE.
Twenty-seven studies were eligible for inclusion. We found significantly elevated stroke risk in African Americans and Hispanics with AF compared with whites (odds ratio [OR] 1.44 [95% confidence interval (CI) 1.25-1.66] and OR 1.11 [95% CI 1.05-1.18] respectively). In Māori and Pacific peoples with AF, the risk of stroke was higher than in New Zealand Europeans, but this difference was not significant (OR 1.28 [95% CI 0.89-1.82], p=0.18 and OR 1.29 [95% CI 0.93-1.52], p=0.17 respectively). Stroke risk (0.6/100-6.8/100 person-years) and CHA2DS2 VASc performance (c-statistics 0.55-0.8) varied substantially between studies.
We support the local refinement of risk prediction models in line with cardiology society recommendations.
预测风险模型CHA2DS2-VASc有助于临床医生评估心房颤动(AF)患者的中风风险。该模型最初在主要为欧洲人群中开发和验证,可能无法准确反映不同种族群体的中风风险;在新西兰,患有AF的毛利人和太平洋岛民中风风险更高。作为全球解决健康不平等问题努力的一部分,人们越来越有兴趣调整预测模型,以更好地适应当地和特定种族的风险。我们的目标是确定:1)AF导致的中风风险是否因种族背景/种族而异;2)未接受抗凝治疗的AF队列中的中风发生率;3)CHA2DS2-VASc在不同地理区域的模型性能。最后,我们概述了风险模型开发的方法学考虑因素。
我们检索了1995年至2024年期间发表的、报告未选择的AF队列中风发生率的英文同行评审研究。对于中风风险,我们纳入了超过5000名未接受抗凝治疗患者的队列。证据来源为PubMed、Scopus和EMBASE。
27项研究符合纳入标准。我们发现,与白人相比,患有AF的非裔美国人和西班牙裔中风风险显著升高(优势比[OR]分别为1.44[95%置信区间(CI)1.25-1.66]和1.11[95%CI1.05-1.18])。在患有AF的毛利人和太平洋岛民中,中风风险高于新西兰欧洲人,但差异不显著(OR分别为1.28[95%CI0.89-1.82],p=0.18和1.29[95%CI0.93-1.52],p=0.17)。不同研究之间的中风风险(0.6/100-6.8/100人年)和CHA2DS2-VASc性能(c统计量0.55-0.8)差异很大。
我们支持根据心脏病学会的建议对风险预测模型进行本地化优化。