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Embolic stroke of undetermined source (ESUS) accounts for approximately 25% of all ischemic strokes, with patent foramen ovale (PFO) considered a major mechanism behind ESUS. When specific anatomic criteria are met, transcatheter PFO occlusion is regarded as the gold standard for secondary stroke prevention.
However, previous studies have shown that percutaneous PFO closure may increase the risk of new-onset atrial fibrillation and atrial flutter (AF), arrhythmias that elevate the risk of embolic stroke. This raises concerns about performing PFO closure. Indeed, the most common clinically significant complication after catheter-based PFO closure is AF. Available data indicates that AF typically occurs in the early period following occluder implantation, with peak incidence around the 14th day post-closure, followed by a decline after the 45th day. Although AF is considered the most frequent adverse complication after percutaneous PFO occlusion, its incidence remains relatively low, ranging from 3% to 7.4%, depending on the method used for arrhythmia screening, though this remains unclear.
In this study, investigators will prospectively monitor patients who have experienced ESUS and are indicated for PFO closure. They will be screened for the occurrence of AF following percutaneous PFO closure using a 3-week ECG Holter monitor (from day 7 to day 28 post-closure) and again 1 week (one year post-closure) after the procedure. The study aims to determine the true incidence of new-onset AF following catheter-based PFO occlusion and to identify the risk factors associated with its development.
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| Measure | Description | Time Frame |
|---|---|---|
| New onset of atrial fibrillation after percutaneous patent foramen ovale closure - Na Homolce Hospital | The primary endpoint - Number of participants with at least 1 episode of atrial arrythmia (atrial fibrillation, atrial flutter, atrial tachycardia), defined as any episode of atrial fibrillation, atrial flutter, or atrial tachycardia lasting ≥ 30 seconds recorded on external cardiac monitor (ECG-Holter) during follow-up. | 2025-2028 |
| Measure | Description | Time Frame |
|---|---|---|
| Time to first episode of atrial arrythmia (atrial fibrillation, atrial flutter, atrial tachycardia) . | 2025-2028 | |
| Number of participants with new stroke or transient ischemic attack during follow up. | 2025-2028 |
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Inclusion Criteria:
Exclusion Criteria:
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The study will include patients who have experienced ischemic stroke attributed to patent foramen ovale and for whom percutaneous closure has been recommended.
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Nemocnice na Homolce | Recruiting | Prague | 15030 | Czechia |
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| ID | Term |
|---|---|
| D002318 | Cardiovascular Diseases |
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| Risk factor at baseline. | Age - in years (at time of the procedure). | 2025-2028 |
| Risk factor at baseline. | Weight - in kilograms | 2025-2028 |
| Risk factor at baseline. | Height - in centimetres | 2025-2028 |
| Risk factor at baseline. | Body mass index (BMI) - in kg/m2 | 2025-2028 |
| Risk factor at baseline. | Sex - male/female | 2025-2028 |
| Risk factor at baseline. | CHA₂DS₂-VASc Score for Atrial Fibrillation Stroke Risk | 2025-2028 |
| Risk factor at baseline. | Risk of Paradoxical Embolism (RoPE) Score - - in points (0-10) | 2025-2028 |
| Risk factor at baseline. | Number of participants with atrial hypertension | 2025-2028 |
| Risk factor at baseline. | Number of participants with Diabetes mellitus | 2025-2028 |
| Risk factor at baseline. | Number of participants with antidiabetic oral drugs | 2025-2028 |
| Risk factor at baseline. | Number of participants taking insulin | 2025-2028 |
| Risk factor at baseline. | Number of participants with hypercholesterolemia | 2025-2028 |
| Risk factor at baseline. | Number of participants actively smoking | 2025-2028 |
| Risk factor at baseline. | Number of participants formerly smoking | 2025-2028 |
| Risk factor at baseline. | Number of participants with peripheral embolism | 2025-2028 |
| Risk factor at baseline. | Number of participants with deep vein thrombosis | 2025-2028 |
| Risk factor at baseline. | Number of participants with coronary artery disease | 2025-2028 |
| Risk factor at baseline. | Left Atrial Volume Index in echocardiography - ml/m2 | 2025-2028 |
| Risk factor at baseline. | Right Atrial Volume Index in echocardiography - ml/m2 or right atrial width/lenght in apical 4 chamber view in mm | 2025-2028 |
| Risk factor at baseline. | Left ventricle ejection fraction in % | 2025-2028 |
| Risk factor at baseline. | Left ventricle end-diastolic diameter - in mm | 2025-2028 |
| Risk factor at baseline. | Number of participants with presence of atrial septal aneurysm (assessed on preclosure echocardiography) defined as a septum mobility ≥10 mm from midline | 2025-2028 |
| Risk factor at baseline. | Presence of right to left shunt on pre-closure echocardiography - Small shunt referred to the appearance of 3 to 10 microbubbles, mild shunt referred to the appearance of 11 to 20 microbubbles, and severe shunt referred to the appearance of >20 microbubbles in the left atrium within 3 cardiac cycles after opacification of the right atrium | 2025-2028 |
| Risk factor at baseline. | Length of patent foramen ovale (PFO) canal - measured on transoesophageal echocardiography during the procedure in millimetres | 2025-2028 |
| Risk factor at baseline. | Height of patent foramen ovale (PFO) canal - measured on transoesophageal echocardiography during the procedure in millimetres, defined as the distance between the septum primum and septum secundum at maximum opening | 2025-2028 |
| Risk factor at baseline. | Invasive pressure measurement in right and left atrium - during the patent foramen ovale (PFO) closure procedure in mmHg | 2025-2028 |
| Risk factor at baseline. | Type and size of occluder | 2025-2028 |
| Nemocnice na Homolce | Recruiting | Prague | 15030 | Czechia |
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