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Transcatheter Closing Atrial Septal Defect in a Child With Hereditary Spherocytosis
A 3-year-old girl was admitted to our hospital for the correction of atrial septal defect (ASD). Open heart operation with cardiopulmonary bypass is dangerous because the patient also had hereditary spherocytosis, which put her at risk for hemolytic anemia. Therefore, percutaneous transcatheter clos...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929411/ https://www.ncbi.nlm.nih.gov/pubmed/31921720 http://dx.doi.org/10.3389/fped.2019.00506 |
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author | Ji, Zhixian Liu, Na Du, Zhanhui Luo, Gang Bing, Zhen Xing, Quansheng Pan, Silin |
author_facet | Ji, Zhixian Liu, Na Du, Zhanhui Luo, Gang Bing, Zhen Xing, Quansheng Pan, Silin |
author_sort | Ji, Zhixian |
collection | PubMed |
description | A 3-year-old girl was admitted to our hospital for the correction of atrial septal defect (ASD). Open heart operation with cardiopulmonary bypass is dangerous because the patient also had hereditary spherocytosis, which put her at risk for hemolytic anemia. Therefore, percutaneous transcatheter closure for ASD was chosen and performed successfully, which avoided the erythrocyte damage caused by cardiopulmonary bypass. This is the first time such a case has been reported, and we present an alternative approach for ASD with hereditary spherocytosis. |
format | Online Article Text |
id | pubmed-6929411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69294112020-01-09 Transcatheter Closing Atrial Septal Defect in a Child With Hereditary Spherocytosis Ji, Zhixian Liu, Na Du, Zhanhui Luo, Gang Bing, Zhen Xing, Quansheng Pan, Silin Front Pediatr Pediatrics A 3-year-old girl was admitted to our hospital for the correction of atrial septal defect (ASD). Open heart operation with cardiopulmonary bypass is dangerous because the patient also had hereditary spherocytosis, which put her at risk for hemolytic anemia. Therefore, percutaneous transcatheter closure for ASD was chosen and performed successfully, which avoided the erythrocyte damage caused by cardiopulmonary bypass. This is the first time such a case has been reported, and we present an alternative approach for ASD with hereditary spherocytosis. Frontiers Media S.A. 2019-12-17 /pmc/articles/PMC6929411/ /pubmed/31921720 http://dx.doi.org/10.3389/fped.2019.00506 Text en Copyright © 2019 Ji, Liu, Du, Luo, Bing, Xing and Pan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pediatrics Ji, Zhixian Liu, Na Du, Zhanhui Luo, Gang Bing, Zhen Xing, Quansheng Pan, Silin Transcatheter Closing Atrial Septal Defect in a Child With Hereditary Spherocytosis |
title | Transcatheter Closing Atrial Septal Defect in a Child With Hereditary Spherocytosis |
title_full | Transcatheter Closing Atrial Septal Defect in a Child With Hereditary Spherocytosis |
title_fullStr | Transcatheter Closing Atrial Septal Defect in a Child With Hereditary Spherocytosis |
title_full_unstemmed | Transcatheter Closing Atrial Septal Defect in a Child With Hereditary Spherocytosis |
title_short | Transcatheter Closing Atrial Septal Defect in a Child With Hereditary Spherocytosis |
title_sort | transcatheter closing atrial septal defect in a child with hereditary spherocytosis |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929411/ https://www.ncbi.nlm.nih.gov/pubmed/31921720 http://dx.doi.org/10.3389/fped.2019.00506 |
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