Key result
The Nordic Atrial Fibrillation and Stroke Study is an ongoing prospective observational trial designed to evaluate the occurrence of occult atrial fibrillation using a 12-month insertable cardiac monitor in patients with cryptogenic stroke or TIA.
Why the study?
More studies are needed to identify factors that help select cryptogenic stroke or TIA patients most likely to have AF detected with prolonged monitoring, and to assess the clinical relevance of short-term AF.
Does prolonged rhythm monitoring with an insertable cardiac monitor detect occult atrial fibrillation in patients with cryptogenic stroke or TIA?
Observational
Yes
Does prolonged rhythm monitoring with an insertable cardiac monitor detect occult atrial fibrillation in patients with cryptogenic stroke or TIA?
The NOR-FIB study is designed to evaluate the occurrence of occult atrial fibrillation using 12-month insertable cardiac monitoring in patients with cryptogenic stroke or TIA.
Identifying high-risk features may refine ICM selection after cryptogenic stroke; leaves open prospective validation before guiding practice.
PURPOSE: Paroxysmal atrial fibrillation is often suspected as a probable cause of cryptogenic stroke. Continuous long-term ECG monitoring using insertable cardiac monitors is a clinically effective technique to screen for atrial fibrillation and superior to conventional follow-up in cryptogenic stroke. However, more studies are needed to identify factors which can help selecting patients with the highest possibility of detecting atrial fibrillation with prolonged rhythm monitoring. The clinical relevance of short-term atrial fibrillation, the need for medical intervention and the evaluation as to whether intervention results in improved clinical outcomes should be assessed. METHOD: The Nordic Atrial Fibrillation and Stroke Study is an international, multicentre, prospective, observational trial evaluating the occurrence of occult atrial fibrillation in cryptogenic stroke and transient ischaemic attack. Patients with cryptogenic stroke or transient ischaemic attack from the Nordic countries are included and will have the Reveal LINQ® Insertable cardiac monitor system implanted for 12 months for atrial fibrillation detection. Biomarkers which can be used as predictors for atrial fibrillation and may identify patients, who could derive the most clinical benefit from the detection of atrial fibrillation by prolonged monitoring, are being studied. CONCLUSION: -VASc score, incidence of recurrent stroke or transient ischaemic attack, use of anticoagulation and antiarrhythmic drugs, and quality of life measurements. The clinical follow-up period is 12 months. The study started in 2017 and the completion is expected at the end of 2020.
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Ratajczak‐Tretel et al. (2019) conducted an observational in Cryptogenic stroke and transient ischaemic attack. Reveal LINQ Insertable cardiac monitor system was evaluated on Occurrence of occult atrial fibrillation. The Nordic Atrial Fibrillation and Stroke Study is an ongoing prospective observational trial designed to evaluate the occurrence of occult atrial fibrillation using a 12-month insertable cardiac monitor in patients with cryptogenic stroke or TIA.
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