Newborn electrocardiography as a screening method for long-QT syndrome
Prolongation of the QT interval is the cause of about 10% cases of sudden infant death syndrome (SIDS) innewborns but it is also responsible for about 5% of sudden deaths in adults. LQTS is associated with life threateningarrhythmias such us torsade de pointes ventricular tachycardia or ventricular...
| Autores: | , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2015 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:10230/26953 |
| Acceso en línea: | http://hdl.handle.net/10230/26953 http://dx.doi.org/10.4172/2155-9880.1000370 |
| Access Level: | acceso abierto |
| Palabra clave: | Mort sobtada Neonatologia Infants nadons |
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Newborn electrocardiography as a screening method for long-QT syndromeTorres Andrés, FrancescHernández Castellano, María del CristoGarcía Álvarez, JuanaMartí-Almor, JulioGarcía Algar, OscarMort sobtadaNeonatologiaInfants nadonsProlongation of the QT interval is the cause of about 10% cases of sudden infant death syndrome (SIDS) innewborns but it is also responsible for about 5% of sudden deaths in adults. LQTS is associated with life threateningarrhythmias such us torsade de pointes ventricular tachycardia or ventricular fibrillation (VF) leading to suddendeath.Congenital causes (channelopathies) of LQTS are associated to mutations with different hereditary patternaccording affected gene but it has been proven that several drugs and electrolytic alterations can significantlyincrease the QT interval. However, the cost-effectiveness of neonatal electrocardiographic (EKG) screening hasbeen questioned and despite studies made in newborns there is still no consensus about the best moment to makeand electrocardiographic screening.Previous studies demonstrate that newborns with QTc values over 470 msec often normalize by themselves inthe first month of life. However in some cases these values remain high after first months of life. These cases aremore frequently in determinate ethnics (Maghreb, Morocco and India-Pakistan). These races could be linked tocardiac electrical alterations with a hereditary pattern of variable penetrance. An EKG performed in the first month oflife will allow the early identification of still asymptomatic infants with LQTS and also infants with some correctablecongenital heart defects (CHD) not recognized by routine neonatal examinations. Appropriate therapy will preventunnecessary deaths in infants, children, and young adults. At the light of this literature review we could assess thatneonatal electrocardiographic screening is highly cost-effective and it may permit the early identification of infants atrisk for SIDS.OMICS International 201620162015info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttp://hdl.handle.net/10230/26953http://dx.doi.org/10.4172/2155-9880.1000370reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésJournal of Clinical and Experimental Cardiology. 2015;6:370©2015 Torres F. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use,distribution, and reproduction in any medium, provided the original author and source are credited.info:eu-repo/semantics/openAccessoai:recercat.cat:10230/269532026-05-29T05:05:01Z |
| dc.title.none.fl_str_mv |
Newborn electrocardiography as a screening method for long-QT syndrome |
| title |
Newborn electrocardiography as a screening method for long-QT syndrome |
| spellingShingle |
Newborn electrocardiography as a screening method for long-QT syndrome Torres Andrés, Francesc Mort sobtada Neonatologia Infants nadons |
| title_short |
Newborn electrocardiography as a screening method for long-QT syndrome |
| title_full |
Newborn electrocardiography as a screening method for long-QT syndrome |
| title_fullStr |
Newborn electrocardiography as a screening method for long-QT syndrome |
| title_full_unstemmed |
Newborn electrocardiography as a screening method for long-QT syndrome |
| title_sort |
Newborn electrocardiography as a screening method for long-QT syndrome |
| dc.creator.none.fl_str_mv |
Torres Andrés, Francesc Hernández Castellano, María del Cristo García Álvarez, Juana Martí-Almor, Julio García Algar, Oscar |
| author |
Torres Andrés, Francesc |
| author_facet |
Torres Andrés, Francesc Hernández Castellano, María del Cristo García Álvarez, Juana Martí-Almor, Julio García Algar, Oscar |
| author_role |
author |
| author2 |
Hernández Castellano, María del Cristo García Álvarez, Juana Martí-Almor, Julio García Algar, Oscar |
| author2_role |
author author author author |
| dc.subject.none.fl_str_mv |
Mort sobtada Neonatologia Infants nadons |
| topic |
Mort sobtada Neonatologia Infants nadons |
| description |
Prolongation of the QT interval is the cause of about 10% cases of sudden infant death syndrome (SIDS) innewborns but it is also responsible for about 5% of sudden deaths in adults. LQTS is associated with life threateningarrhythmias such us torsade de pointes ventricular tachycardia or ventricular fibrillation (VF) leading to suddendeath.Congenital causes (channelopathies) of LQTS are associated to mutations with different hereditary patternaccording affected gene but it has been proven that several drugs and electrolytic alterations can significantlyincrease the QT interval. However, the cost-effectiveness of neonatal electrocardiographic (EKG) screening hasbeen questioned and despite studies made in newborns there is still no consensus about the best moment to makeand electrocardiographic screening.Previous studies demonstrate that newborns with QTc values over 470 msec often normalize by themselves inthe first month of life. However in some cases these values remain high after first months of life. These cases aremore frequently in determinate ethnics (Maghreb, Morocco and India-Pakistan). These races could be linked tocardiac electrical alterations with a hereditary pattern of variable penetrance. An EKG performed in the first month oflife will allow the early identification of still asymptomatic infants with LQTS and also infants with some correctablecongenital heart defects (CHD) not recognized by routine neonatal examinations. Appropriate therapy will preventunnecessary deaths in infants, children, and young adults. At the light of this literature review we could assess thatneonatal electrocardiographic screening is highly cost-effective and it may permit the early identification of infants atrisk for SIDS. |
| publishDate |
2015 |
| dc.date.none.fl_str_mv |
2015 2016 2016 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/10230/26953 http://dx.doi.org/10.4172/2155-9880.1000370 |
| url |
http://hdl.handle.net/10230/26953 http://dx.doi.org/10.4172/2155-9880.1000370 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Journal of Clinical and Experimental Cardiology. 2015;6:370 |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf application/pdf |
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OMICS International |
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OMICS International |
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reponame:Recercat. Dipósit de la Recerca de Catalunya instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Recercat. Dipósit de la Recerca de Catalunya |
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