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Dataset results
32 results for “patent foramen ovale closure”
Residual Shunt After Patent Foramen Ovale Device Closure in Patients With Cryptogenic Stroke
ClinicalTrials.gov study NCT03416426. IPD Sharing: NO. Countries: 1. Publications: 0.
Patent Foramen Ovale Closure in Migraine
ClinicalTrials.gov study NCT06192173. IPD Sharing: NO. Countries: 1. Publications: 0.
Evaluation of the Efficacy and Safety of a Simplified Procedure for the Percutaneous Closure of the Patent Foramen Ovale
ClinicalTrials.gov study NCT03828825. IPD Sharing: Not stated. Countries: 1. Publications: 0.
New Onset of Arrhythmia After Patent Foramen Ovale (PFO) Closure
ClinicalTrials.gov study NCT06983613. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Swartz Sheath With Angioplasty Guidewire-Assisted Technique for Patent Foramen Ovale Closure (STAGE-PFO)
ClinicalTrials.gov study NCT06793969. IPD Sharing: Not stated. Countries: 1. Publications: 0.
The Effect of Device Closure of Patent Foramen Ovale in Elderly Patients With Crytogenic Stoke/TCI
ClinicalTrials.gov study NCT01018355. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Discontinuation of Antithrombotic Treatment Following Patent Foramen Ovale Closure in Young Patients With Cryptogenic Stroke
ClinicalTrials.gov study NCT04475510. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Patent Foramen Ovale Closure Reduce in SCUBA-divers
ClinicalTrials.gov study NCT03997084. IPD Sharing: NO. Countries: 0. Publications: 0.
Clinical Performance of the Gore Septal Occluder in Patent Foramen Ovale Closure in Different Septal Anatomies: 1-Year Results from a Single-Center Experience
Open the record for dataset details and reuse information.
Mechanisms of ineffective patent foramen ovale closure using the percutaneous suture-mediated NobleStitch system.
<p>Zannoni J, Popolo Rubbio A, Tusa MB, Corciu AI, Casenghi M, Cannone G, Barletta M, Stefanini E, Mantovani V, Gorla R, Brambilla N, Testa L, Bedogni F, De Marco F. Mechanisms of ineffective patent foramen ovale closure using the percutaneous suture-mediated NobleStitch system. EuroIntervention. 2022 May 15;18(1):68-70. doi: 10.4244/EIJ-D-21-01021. PMID: 35403602.</p> <p>Introduction Percutaneous suture-mediated patent foramen ovale (PFO) closure with the “device-less” NobleStitch system (HeartStitch) has been employed in clinical practice as an effective and safe alternative to traditional device closure123. In previous studies, recurrence of a residual atrial right-to-left shunt (RLS) during follow-up was estimated at almost 20%123. In any case, specific mechanisms of failure have not been systematically described and they still remain unknown. The aim of the study was to describe the mechanisms of failure after NobleStitch from a prospective single-centre cohort.</p>
Mechanisms of ineffective patent foramen ovale closure using the percutaneous suture-mediated NobleStitch system
<p>Zannoni J, Popolo Rubbio A, Tusa MB, Corciu AI, Casenghi M, Cannone G, Barletta M, Stefanini E, Mantovani V, Gorla R, Brambilla N, Testa L, Bedogni F, De Marco F. Mechanisms of ineffective patent foramen ovale closure using the percutaneous suture-mediated NobleStitch system. EuroIntervention. 2022 May 15;18(1):68-70. doi: 10.4244/EIJ-D-21-01021. PMID: 35403602; PMCID: PMC9903156.</p> <p> </p>
raw dataset related to the article "Patent foramen ovale closure with the Occlutech Figulla Flex II device: A long-term (up to 10-years) follow-up"
<p><strong>Abstract</strong></p> <p><strong>Background.</strong> Percutaneous closure represents the first line of treatment In patients with cryptogenic stroke and documented patent foramen ovale (PFO). Scarce data report the long-term outcomes of patients undergoing PFO closure with the Figulla Flex II device (Occlutech, Germany).</p> <p><strong>Methods</strong>. Consecutive patients undergoing PFO closure with a Figulla Flex II device at a single, high-volume Institution were included. Baseline clinical and procedural features were collected and patients were followed up for up to 10 years. The device's long-term safety was assessed, as well as mortality, recurrent cerebrovascular events, new-onset atrial fibrillation (AF) and residual shunt.</p> <p><strong>Results.</strong> Overall, 442 patients were included. The main indication for PFO closure was cryptogenic stroke/transitory ischemic attack (65.5%), followed by migraine (21.7%), silent lesions at MRI (10.8%), and decompression disease (2.0%). Atrial septal aneurysm was present in 20.8% of cases, Eustachian valve in 9.0%, Chiari network in 19.9%. The most frequently implanted device was the 23/25 mm (49.5% of cases). One procedural failure due to device embolization; in-hospital complications occurred in 15 cases (3.4%; 4 minor access site complications, 11 transient supraventricular tachycardias (SVT)/AF). After a follow-up of 9.2 years, 2 patients suffered recurrent TIA (with no residual R-L shunt detected). A moderate or severe residual shunt was observed in 3 patients after discharge. </p> <p><strong>Conclusions</strong>. Figulla Flex II devices for PFO closure are associated with high procedural success and low incidence of adverse events even at long-term follow-up.</p>
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