Wearable Holter cardiac monitoring for 30 days detected atrial fibrillation in 17.1% of patients with embolic stroke of undetermined source.
Cohort (n=352)
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Does 30-day wearable Holter monitoring improve the detection of occult atrial fibrillation in patients with embolic stroke of undetermined source?
30-day wearable Holter monitoring detects occult atrial fibrillation in 17.1% of patients with embolic stroke of undetermined source, particularly in older patients with larger left atria and excessive supraventricular ectopy.
BACKGROUND: Hidden atrial fibrillation (AF) is considered a major contributor to embolic strokes of undetermined source (ESUS). Prolonged cardiac monitoring is effective for detecting AF, especially when started soon after stroke onset. METHODS: This prospective multicentre study evaluated the rate of AF detection in ESUS patients under real-world clinical conditions using wearable Holter cardiac monitoring for 30 days. RESULTS: A total of 352 patients were included. The mean age was 67.8 years, and 46% were women. The AF detection rate was 17.1%, with a mean episode duration of 401.7min. Compared with patients without AF, those with AF were older (72.2 vs 67.0 years; mean difference, 5.16 years; 95% CI, 2.24-8.09; p=0.0012), had a higher frequency of large vessel occlusion (35.9% vs 17.0%; OR, 2.66; 95% CI, 1.40-5.05; p=0.002), showed larger left atrial diameter (40.4 vs 38.1mm; mean difference, 2.25mm; 95% CI, 0.56-3.95; p=0.013), and more often had excessive supraventricular ectopic activity on 24-hour Holter monitoring (37.5% vs 20.5%; OR, 2.33; 95% CI, 1.26-4.32; p=0.006). Notably, 73.3% of AF cases were detected during monitoring initiated within the first 6 months after stroke onset. CONCLUSIONS: These findings support the potential clinical utility of 30-day prolonged cardiac monitoring to detect AF in ESUS patients, highlighting its value in etiological stroke assessment in real-world clinical practice, with greater efficacy during the first 30 days, but also in cases where monitoring is initiated months after the event.
Chacón et al. (Fri,) realizaron una cohorte en accidente cerebrovascular embólico de origen indeterminado (ESUS) (n=352). Se evaluó el monitoreo cardíaco Holter portátil en la tasa de detección de fibrilación auricular. El monitoreo cardíaco Holter portátil durante 30 días detectó fibrilación auricular en el 17.1% de los pacientes con accidente cerebrovascular embólico de origen indeterminado.