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Association between Abnormal Antenatal Doppler Characteristics and Gastrointestinal Outcomes in Preterm Infants

Antenatal Doppler disturbances are associated with fetal hypoxia and may induce a brain-sparing vascular redistribution at the expense of splanchnic circulation, possibly predisposing to gut complications. We aimed to compare several gastrointestinal outcomes among very-low-birthweight (VLBW) preter...

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Autores principales: Martini, Silvia, Annunziata, Mariarosaria, Della Gatta, Anna Nunzia, Aceti, Arianna, Brunetti, Marica, Pilu, Gianluigi, Simonazzi, Giuliana, Corvaglia, Luigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738995/
https://www.ncbi.nlm.nih.gov/pubmed/36501150
http://dx.doi.org/10.3390/nu14235121
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author Martini, Silvia
Annunziata, Mariarosaria
Della Gatta, Anna Nunzia
Aceti, Arianna
Brunetti, Marica
Pilu, Gianluigi
Simonazzi, Giuliana
Corvaglia, Luigi
author_facet Martini, Silvia
Annunziata, Mariarosaria
Della Gatta, Anna Nunzia
Aceti, Arianna
Brunetti, Marica
Pilu, Gianluigi
Simonazzi, Giuliana
Corvaglia, Luigi
author_sort Martini, Silvia
collection PubMed
description Antenatal Doppler disturbances are associated with fetal hypoxia and may induce a brain-sparing vascular redistribution at the expense of splanchnic circulation, possibly predisposing to gut complications. We aimed to compare several gastrointestinal outcomes among very-low-birthweight (VLBW) preterm infants with different antenatal Doppler features. VLBW infants born between 2010–2022 were retrospectively included and stratified into the following clusters based on antenatal Doppler characteristics: normal Doppler (controls); absent or reversed end-diastolic flow in the umbilical artery (UA-AREDF) alone or also in the ductus venosus (UA+DV-AREDF); and abnormal Doppler with or without brain-sparing redistribution. The following outcomes were evaluated: time to reach full enteral feeds (FEF), feeding intolerance (FI), necrotizing enterocolitis (NEC), and spontaneous intestinal perforation (SIP). Overall, 570 infants were included. Infants born following UA+DV-AREDF had significantly higher FI, NEC, and SIP rates and achieved FEF later compared to controls. Increased FI prevalence and a longer time to FEF compared to controls were also observed among UA-AREDF infants and in the presence of brain-sparing redistribution, which also increased NEC rates. Antenatal Doppler abnormalities exacerbate the gastrointestinal risks of preterm infants. Detailed knowledge of Doppler features can aid in identifying those at highest risk of intestinal complications who may benefit from tailored enteral feeding management.
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spelling pubmed-97389952022-12-11 Association between Abnormal Antenatal Doppler Characteristics and Gastrointestinal Outcomes in Preterm Infants Martini, Silvia Annunziata, Mariarosaria Della Gatta, Anna Nunzia Aceti, Arianna Brunetti, Marica Pilu, Gianluigi Simonazzi, Giuliana Corvaglia, Luigi Nutrients Article Antenatal Doppler disturbances are associated with fetal hypoxia and may induce a brain-sparing vascular redistribution at the expense of splanchnic circulation, possibly predisposing to gut complications. We aimed to compare several gastrointestinal outcomes among very-low-birthweight (VLBW) preterm infants with different antenatal Doppler features. VLBW infants born between 2010–2022 were retrospectively included and stratified into the following clusters based on antenatal Doppler characteristics: normal Doppler (controls); absent or reversed end-diastolic flow in the umbilical artery (UA-AREDF) alone or also in the ductus venosus (UA+DV-AREDF); and abnormal Doppler with or without brain-sparing redistribution. The following outcomes were evaluated: time to reach full enteral feeds (FEF), feeding intolerance (FI), necrotizing enterocolitis (NEC), and spontaneous intestinal perforation (SIP). Overall, 570 infants were included. Infants born following UA+DV-AREDF had significantly higher FI, NEC, and SIP rates and achieved FEF later compared to controls. Increased FI prevalence and a longer time to FEF compared to controls were also observed among UA-AREDF infants and in the presence of brain-sparing redistribution, which also increased NEC rates. Antenatal Doppler abnormalities exacerbate the gastrointestinal risks of preterm infants. Detailed knowledge of Doppler features can aid in identifying those at highest risk of intestinal complications who may benefit from tailored enteral feeding management. MDPI 2022-12-02 /pmc/articles/PMC9738995/ /pubmed/36501150 http://dx.doi.org/10.3390/nu14235121 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Martini, Silvia
Annunziata, Mariarosaria
Della Gatta, Anna Nunzia
Aceti, Arianna
Brunetti, Marica
Pilu, Gianluigi
Simonazzi, Giuliana
Corvaglia, Luigi
Association between Abnormal Antenatal Doppler Characteristics and Gastrointestinal Outcomes in Preterm Infants
title Association between Abnormal Antenatal Doppler Characteristics and Gastrointestinal Outcomes in Preterm Infants
title_full Association between Abnormal Antenatal Doppler Characteristics and Gastrointestinal Outcomes in Preterm Infants
title_fullStr Association between Abnormal Antenatal Doppler Characteristics and Gastrointestinal Outcomes in Preterm Infants
title_full_unstemmed Association between Abnormal Antenatal Doppler Characteristics and Gastrointestinal Outcomes in Preterm Infants
title_short Association between Abnormal Antenatal Doppler Characteristics and Gastrointestinal Outcomes in Preterm Infants
title_sort association between abnormal antenatal doppler characteristics and gastrointestinal outcomes in preterm infants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738995/
https://www.ncbi.nlm.nih.gov/pubmed/36501150
http://dx.doi.org/10.3390/nu14235121
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