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Functional cardiac MRI in preterm and term newborns

OBJECTIVE: To use cardiac MRI techniques to assess ventricular function and systemic perfusion in preterm and term newborns, to compare techniques to echocardiographic methods, and to obtain initial reference data. DESIGN: Observational magnetic resonance and echocardiographic imaging study. SETTING...

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Autores principales: Groves, Alan M, Chiesa, Gaia, Durighel, Giuliana, Goldring, Stephen T, Fitzpatrick, Julie A, Uribe, Sergio, Razavi, Reza, Hajnal, Jo V, Edwards, A David
Formato: Texto
Lenguaje:English
Publicado: BMJ Group 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3093932/
https://www.ncbi.nlm.nih.gov/pubmed/20971721
http://dx.doi.org/10.1136/adc.2010.189142
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author Groves, Alan M
Chiesa, Gaia
Durighel, Giuliana
Goldring, Stephen T
Fitzpatrick, Julie A
Uribe, Sergio
Razavi, Reza
Hajnal, Jo V
Edwards, A David
author_facet Groves, Alan M
Chiesa, Gaia
Durighel, Giuliana
Goldring, Stephen T
Fitzpatrick, Julie A
Uribe, Sergio
Razavi, Reza
Hajnal, Jo V
Edwards, A David
author_sort Groves, Alan M
collection PubMed
description OBJECTIVE: To use cardiac MRI techniques to assess ventricular function and systemic perfusion in preterm and term newborns, to compare techniques to echocardiographic methods, and to obtain initial reference data. DESIGN: Observational magnetic resonance and echocardiographic imaging study. SETTING: Neonatal Unit, Queen Charlotte's and Chelsea Hospital, London, UK. PATIENTS: 108 newborn infants with median birth weight 1627 (580–4140) g, gestation 32 (25–42) weeks. RESULTS: Mean (SD) flow volumes assessed by phase contrast (PC) imaging in 28 stable infants were left ventricular output (LVO) 222 (46), right ventricular output (RVO) 219 (47), superior vena cava (SVC) 95 (27) and descending aorta (DAo) 126 (32) ml/kg/min, with flow being higher at lower gestational age. Limits of agreement for repeated PC assessment of flow were LVO ±50.2, RVO ±55.5, SVC ±20.9 and DAo ±26.2 ml/kg/min. Mean (SD) LVO in 75 stable infants from three-dimensional models were 245 (47) ml/kg/min, with limits of agreement ±58.3 ml/kg/min. Limits of agreement for repeated echocardiographic assessment of LVO were ±108.9 ml/kg/min. CONCLUSIONS: Detailed magnetic resonance assessments of cardiac function and systemic perfusion are feasible in newborn infants, and provide more complete data with greater reproducibility than existing echocardiographic methods. Functional cardiac MRI could prove to be a useful research technique to study small numbers of newborn infants in specialist centres; providing insights into the pathophysiology of circulatory failure; acting as an outcome measure in clinical trials of inotropic intervention and so guiding clinical practice in the wider neonatal community.
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spelling pubmed-30939322011-05-20 Functional cardiac MRI in preterm and term newborns Groves, Alan M Chiesa, Gaia Durighel, Giuliana Goldring, Stephen T Fitzpatrick, Julie A Uribe, Sergio Razavi, Reza Hajnal, Jo V Edwards, A David Arch Dis Child Fetal Neonatal Ed Original Articles OBJECTIVE: To use cardiac MRI techniques to assess ventricular function and systemic perfusion in preterm and term newborns, to compare techniques to echocardiographic methods, and to obtain initial reference data. DESIGN: Observational magnetic resonance and echocardiographic imaging study. SETTING: Neonatal Unit, Queen Charlotte's and Chelsea Hospital, London, UK. PATIENTS: 108 newborn infants with median birth weight 1627 (580–4140) g, gestation 32 (25–42) weeks. RESULTS: Mean (SD) flow volumes assessed by phase contrast (PC) imaging in 28 stable infants were left ventricular output (LVO) 222 (46), right ventricular output (RVO) 219 (47), superior vena cava (SVC) 95 (27) and descending aorta (DAo) 126 (32) ml/kg/min, with flow being higher at lower gestational age. Limits of agreement for repeated PC assessment of flow were LVO ±50.2, RVO ±55.5, SVC ±20.9 and DAo ±26.2 ml/kg/min. Mean (SD) LVO in 75 stable infants from three-dimensional models were 245 (47) ml/kg/min, with limits of agreement ±58.3 ml/kg/min. Limits of agreement for repeated echocardiographic assessment of LVO were ±108.9 ml/kg/min. CONCLUSIONS: Detailed magnetic resonance assessments of cardiac function and systemic perfusion are feasible in newborn infants, and provide more complete data with greater reproducibility than existing echocardiographic methods. Functional cardiac MRI could prove to be a useful research technique to study small numbers of newborn infants in specialist centres; providing insights into the pathophysiology of circulatory failure; acting as an outcome measure in clinical trials of inotropic intervention and so guiding clinical practice in the wider neonatal community. BMJ Group 2010-10-21 /pmc/articles/PMC3093932/ /pubmed/20971721 http://dx.doi.org/10.1136/adc.2010.189142 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Original Articles
Groves, Alan M
Chiesa, Gaia
Durighel, Giuliana
Goldring, Stephen T
Fitzpatrick, Julie A
Uribe, Sergio
Razavi, Reza
Hajnal, Jo V
Edwards, A David
Functional cardiac MRI in preterm and term newborns
title Functional cardiac MRI in preterm and term newborns
title_full Functional cardiac MRI in preterm and term newborns
title_fullStr Functional cardiac MRI in preterm and term newborns
title_full_unstemmed Functional cardiac MRI in preterm and term newborns
title_short Functional cardiac MRI in preterm and term newborns
title_sort functional cardiac mri in preterm and term newborns
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3093932/
https://www.ncbi.nlm.nih.gov/pubmed/20971721
http://dx.doi.org/10.1136/adc.2010.189142
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