Predicting atrial fibrillation after cryptogenic stroke via a clinical risk score-a prospective observational study

被引:21
|
作者
Kneihsl, Markus [1 ]
Bisping, Egbert [2 ]
Scherr, Daniel [2 ]
Mangge, Harald [3 ]
Fandler-Hoefler, Simon [1 ]
Colonna, Isabella [1 ]
Haidegger, Melanie [1 ]
Eppinger, Sebastian [1 ]
Hofer, Edith [1 ,4 ]
Fazekas, Franz [1 ]
Enzinger, Christian [1 ,5 ]
Gattringer, Thomas [1 ,5 ]
机构
[1] Med Univ Graz, Dept Neurol, Auenbruggerpl 22, A-8036 Graz, Austria
[2] Med Univ Graz, Dept Internal Med, Div Cardiol, Graz, Austria
[3] Med Univ Graz, Clin Inst Med & Chem Lab Diagnost, Graz, Austria
[4] Med Univ Graz, Inst Med Informat Stat & Documentat, Graz, Austria
[5] Med Univ Graz, Dept Radiol, Div Neuroradiol Vasc & Intervent Radiol, Graz, Austria
关键词
atrial fibrillation; biomarker; cryptogenic stroke; NT-proBNP; risk score; INSERTABLE CARDIAC MONITORS; PREVENTION; THERAPY;
D O I
10.1111/ene.15102
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and purpose Atrial fibrillation (AF) often remains undiagnosed in cryptogenic stroke (CS), mostly because of limited availability of cardiac long-term rhythm monitoring. There is an unmet need for a pre-selection of CS patients benefitting from such work-up. A clinical risk score was therefore developed for the prediction of AF after CS and its performance was evaluated over 1 year of follow-up. Methods Our proposed risk score ranges from 0 to 16 points and comprises variables known to be associated with occult AF in CS patients including age, N-terminal pro-brain natriuretic peptide, electrocardiographic and echocardiographic features (supraventricular premature beats, atrial runs, atrial enlargement, left ventricular ejection fraction) and brain imaging markers (multi-territory/prior cortical infarction). All CS patients admitted to our Stroke Unit between March 2018 and August 2019 were prospectively followed for AF detection over 1 year after discharge. Results During the 1-year follow-up, 24 (16%) out of 150 CS patients with AF (detected via electrocardiogram controls, n = 18; loop recorder monitoring, n = 6) were diagnosed. Our predefined AF Risk Score (cutoff >= 4 points; highest Youden's index) had a sensitivity of 92% and a specificity of 67% for 1-year prediction of AF. Notably, only two CS patients with <4 score points were diagnosed with AF later on (negative predictive value 98%). Conclusions A clinical risk score for 1-year prediction of AF in CS with high sensitivity, reasonable specificity and excellent negative predictive value is presented. Generalizability of our score needs to be tested in external cohorts with continuous cardiac rhythm monitoring.
引用
收藏
页码:149 / 157
页数:9
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