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2.
Circ Cardiovasc Interv ; 17(8): e014044, 2024 Aug.
Article de Anglais | MEDLINE | ID: mdl-38853741

RÉSUMÉ

BACKGROUND: Surgery or fibrinolysis is the currently available evidence-based treatment for obstructive mechanical valve thrombus. We reported the feasibility and short-term outcomes of percutaneous transcatheter therapy with cerebral embolic protection. Mid- and long-term outcomes remain unknown. METHODS: From 2020 to 2023, 24 patients underwent percutaneous transcatheter release of stuck leaflets with cerebral embolic protection for obstructive mitral mechanical valve thrombus. The indications for the transcatheter therapy were failed fibrinolysis, contraindications for fibrinolysis, not willing for fibrinolysis, or high risk for surgery. The study participants were followed up for a median period of 344.50 (65.00-953.75) days. RESULTS: Technical success was achieved in 91.67% (n=22) of procedures. During the follow-up, 12.50% (n=3) all-cause death, 4.17% (n=1) stroke, and 16.67% (n=4) recurrence were seen. The mean survival time free from death was 1101.48 (95% CI, 929.49-1273.47) days, stroke was 1211.38 (95% CI, 1110.40-1312.35) days, and recurrence was 907.71 (95% CI, 760.20-1055.21) days. CONCLUSIONS: Transcatheter release of the stuck mitral mechanical valve with cerebral embolic protection is an alternative therapy with promising mid-term outcomes where surgery or fibrinolysis is not possible or in failed fibrinolysis subsets.


Sujet(s)
Cathétérisme cardiaque , Dispositifs de protection embolique , Implantation de valve prothétique cardiaque , Prothèse valvulaire cardiaque , Embolie intracrânienne , Valve atrioventriculaire gauche , Humains , Mâle , Femelle , Valve atrioventriculaire gauche/chirurgie , Valve atrioventriculaire gauche/physiopathologie , Valve atrioventriculaire gauche/imagerie diagnostique , Sujet âgé , Embolie intracrânienne/prévention et contrôle , Embolie intracrânienne/étiologie , Embolie intracrânienne/mortalité , Embolie intracrânienne/imagerie diagnostique , Cathétérisme cardiaque/effets indésirables , Cathétérisme cardiaque/instrumentation , Cathétérisme cardiaque/mortalité , Adulte d'âge moyen , Facteurs temps , Facteurs de risque , Implantation de valve prothétique cardiaque/effets indésirables , Implantation de valve prothétique cardiaque/instrumentation , Implantation de valve prothétique cardiaque/mortalité , Résultat thérapeutique , Études rétrospectives , Sujet âgé de 80 ans ou plus , Récidive , Conception de prothèse , Thrombose/prévention et contrôle , Thrombose/étiologie , Thrombose/mortalité , Thrombose/imagerie diagnostique , Études de faisabilité , Défaillance de prothèse , Appréciation des risques
3.
Int J Cardiol ; 353: 22-28, 2022 Apr 15.
Article de Anglais | MEDLINE | ID: mdl-35065155

RÉSUMÉ

BACKGROUND: There are published reports of safety and feasibility of percutaneous coronary intervention (PCI) without contrast, using intravascular ultrasound (IVUS) and coronary physiology guidance in chronic kidney disease population. We prospectively evaluated the safety and feasibility of zero-contrast PCI technique. METHODS: In this prospective study, we hypothesized that PCI is feasible without contrast, using IVUS guidance alone without mandatory coronary physiology to rule out slow-flow or no-flow at the end of PCI in a population at risk of contrast-induced acute kidney injury (CI-AKI). In this study, we included 31 vessels in 27 patients at risk of CI-AKI and assessed the primary outcome of technical success at the end of PCI. Major adverse cardio-cerebro vascular events (MACCE) and percent change in estimated glomerular filtration rate(eGFR) one month after PCI were the secondary outcomes of the study. RESULTS: The primary outcome was met in 87.1%(n = 27) of the procedures. Technical failure was seen in 12.9%(n = 4) of the procedures. None of the patients developed MACCE at one-month follow-up. The median percent change in eGFR at one-month follow-up was -8.19%(-24.40%, +0.92%). There was no newer initiation of renal replacement therapy at one-month follow-up. CONCLUSIONS: Zero-contrast PCI is safe and feasible in selective coronary anatomies with IVUS guidance. Coronary physiology is not mandatory to rule out slow-flow or no-flow at the end of procedure. Contrast may be needed to tide over the crisis during the possible complications, namely slow-flow, geographical miss and intraprocedural thrombus.


Sujet(s)
Atteinte rénale aigüe , Maladie des artères coronaires , Intervention coronarienne percutanée , Atteinte rénale aigüe/induit chimiquement , Atteinte rénale aigüe/diagnostic , Coronarographie/méthodes , Maladie des artères coronaires/imagerie diagnostique , Maladie des artères coronaires/chirurgie , Études de faisabilité , Humains , Intervention coronarienne percutanée/effets indésirables , Intervention coronarienne percutanée/méthodes , Études prospectives , Résultat thérapeutique , Échographie interventionnelle/méthodes
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