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t in both (EF-TPVR 0.0% [n=0 of 8] vs. SPVR 4.3% [n=1 of 43]; p=1.00; 30days). EF-TPVR may be an alternative for patients with pulmonic insufficiency and enlarged RVOTs ineligible for other therapies. EF-TPVR may be an alternative for patients with pulmonic insufficiency and enlarged RVOTs ineligible for other therapies. The aim of this study was to investigate the effect of management on the risk for recurrent events among patients with cryptogenic ischemic stroke or transient ischemic attack. The combination of patent foramen ovale (PFO