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Mechanical tricuspid valve replacement in hypoplastic left heart syndrome: An institutional experience

OBJECTIVE: Atrioventricular valvar regurgitation in patients with single ventricles is associated with worse outcomes. Valve repair or replacement has been undertaken in an attempt to reduce mortality and morbidity. Current data on valve replacement in single ventricle patients are limited and deriv...

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Autores principales: Hoda, Mehar, Jaquiss, Robert Douglas Benjamin, James, Lorraine, Thankavel, Poonam Punjwani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9510852/
https://www.ncbi.nlm.nih.gov/pubmed/36172450
http://dx.doi.org/10.1016/j.xjon.2022.06.015
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author Hoda, Mehar
Jaquiss, Robert Douglas Benjamin
James, Lorraine
Thankavel, Poonam Punjwani
author_facet Hoda, Mehar
Jaquiss, Robert Douglas Benjamin
James, Lorraine
Thankavel, Poonam Punjwani
author_sort Hoda, Mehar
collection PubMed
description OBJECTIVE: Atrioventricular valvar regurgitation in patients with single ventricles is associated with worse outcomes. Valve repair or replacement has been undertaken in an attempt to reduce mortality and morbidity. Current data on valve replacement in single ventricle patients are limited and derived from heterogenous populations. We describe our experience with repair and replacement of the tricuspid valve in children undergoing single ventricle palliation for hypoplastic left heart syndrome. METHODS: We included 27 patients with hypoplastic left heart syndrome with at least moderate tricuspid regurgitation who underwent valve intervention between 2007 and 2021 at our institution; charts were retrospectively reviewed for data. RESULTS: Eleven patients (73% male) underwent valve replacement (median age, 3 years). Preoperative ventricular systolic function was normal in 10 patients (91%). Median follow-up postoperatively was 4 years with no early mortality, 1 (9%) late mortality, and 1 heart transplant (9%). Morbidity consisted of complete heart block in 1 patient (9%), with no important hemorrhagic or thrombotic events. Among survivors of replacement (n = 9), ventricular function was preserved in all (n = 8) who had normal function preoperatively and improved in the remaining patient. Sixteen patients underwent valve repair (median age, 4 months) with no early mortality, 8 (50%) midterm mortalities, and 2 heart transplants (12%). CONCLUSIONS: Tricuspid valve replacement is a feasible option in hypoplastic left heart syndrome with significant tricuspid regurgitation, with favorable outcomes in the intermediate follow-up. When undertaken in the setting of normal function, ventricular function may be preserved in up to 80% of patients. Long-term follow-up is needed.
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spelling pubmed-95108522022-09-27 Mechanical tricuspid valve replacement in hypoplastic left heart syndrome: An institutional experience Hoda, Mehar Jaquiss, Robert Douglas Benjamin James, Lorraine Thankavel, Poonam Punjwani JTCVS Open Congenital: Tricuspid Valve OBJECTIVE: Atrioventricular valvar regurgitation in patients with single ventricles is associated with worse outcomes. Valve repair or replacement has been undertaken in an attempt to reduce mortality and morbidity. Current data on valve replacement in single ventricle patients are limited and derived from heterogenous populations. We describe our experience with repair and replacement of the tricuspid valve in children undergoing single ventricle palliation for hypoplastic left heart syndrome. METHODS: We included 27 patients with hypoplastic left heart syndrome with at least moderate tricuspid regurgitation who underwent valve intervention between 2007 and 2021 at our institution; charts were retrospectively reviewed for data. RESULTS: Eleven patients (73% male) underwent valve replacement (median age, 3 years). Preoperative ventricular systolic function was normal in 10 patients (91%). Median follow-up postoperatively was 4 years with no early mortality, 1 (9%) late mortality, and 1 heart transplant (9%). Morbidity consisted of complete heart block in 1 patient (9%), with no important hemorrhagic or thrombotic events. Among survivors of replacement (n = 9), ventricular function was preserved in all (n = 8) who had normal function preoperatively and improved in the remaining patient. Sixteen patients underwent valve repair (median age, 4 months) with no early mortality, 8 (50%) midterm mortalities, and 2 heart transplants (12%). CONCLUSIONS: Tricuspid valve replacement is a feasible option in hypoplastic left heart syndrome with significant tricuspid regurgitation, with favorable outcomes in the intermediate follow-up. When undertaken in the setting of normal function, ventricular function may be preserved in up to 80% of patients. Long-term follow-up is needed. Elsevier 2022-06-25 /pmc/articles/PMC9510852/ /pubmed/36172450 http://dx.doi.org/10.1016/j.xjon.2022.06.015 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Congenital: Tricuspid Valve
Hoda, Mehar
Jaquiss, Robert Douglas Benjamin
James, Lorraine
Thankavel, Poonam Punjwani
Mechanical tricuspid valve replacement in hypoplastic left heart syndrome: An institutional experience
title Mechanical tricuspid valve replacement in hypoplastic left heart syndrome: An institutional experience
title_full Mechanical tricuspid valve replacement in hypoplastic left heart syndrome: An institutional experience
title_fullStr Mechanical tricuspid valve replacement in hypoplastic left heart syndrome: An institutional experience
title_full_unstemmed Mechanical tricuspid valve replacement in hypoplastic left heart syndrome: An institutional experience
title_short Mechanical tricuspid valve replacement in hypoplastic left heart syndrome: An institutional experience
title_sort mechanical tricuspid valve replacement in hypoplastic left heart syndrome: an institutional experience
topic Congenital: Tricuspid Valve
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9510852/
https://www.ncbi.nlm.nih.gov/pubmed/36172450
http://dx.doi.org/10.1016/j.xjon.2022.06.015
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