Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/38834
Title: Reduction in Cerebral Oxygenation due to Patent Ductus Arteriosus Is Pronounced in Small-for-Gestational-Age Neonates.
Authors: Baerts W.;Dix L.;Van Bel F.;Lemmers P.;Alderliesten T.;Cohen E.
Institution: (Cohen, Dix, Baerts, Alderliesten, Lemmers, Van Bel) Department of Neonatology, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, Netherlands (Cohen) Ritchie Centre, Hudson Institute of Medical Research, Department of Paediatrics, Monash University, Melbourne, VIC, Australia (Cohen) Ritchie Centre, Hudson Institute of Medical Research, Level 5, Monash Medical Centre, 246 Clayton Road, Clayton, VIC 3168, Australia
Issue Date: 14-Feb-2017
Copyright year: 2017
Publisher: S. Karger AG
Place of publication: Switzerland
Publication information: Neonatology. 111 (2) (pp 126-132), 2017. Date of Publication: 01 Feb 2017.
Journal: Neonatology
Abstract: Background: A haemodynamically significant patent ductus arteriosus (hsPDA) reduces cerebral oxygenation in appropriate-for-gestational-age (AGA) preterm neonates. Reduced cerebral oxygenation has been associated with brain injury. Preterm small-for-gestational-age (SGA) neonates show higher cerebral oxygenation than AGA peers throughout the first postnatal days. To date, no studies have investigated the effect of hsPDA on cerebral oxygenation in preterm SGA neonates. Objective(s): We aimed to assess the effect of hsPDA on cerebral oxygenation in preterm SGA neonates compared to AGA peers. We hypothesised that higher baseline cerebral oxygenation would reduce the impact of hsPDA on cerebral oxygenation in preterm SGA neonates. Method(s): We monitored regional cerebral oxygen saturation (rScO2) with near-infrared spectroscopy and calculated the cerebral fractional tissue oxygen extraction (cFTOE) for 72 h after birth. Retrospective analysis compared 36 preterm SGA neonates (birth weight <10th percentile, 18 with hsPDA) to 36 preterm AGA neonates (birth weight 20th to 80th percentile, 18 with hsPDA). Result(s): In contrast to the other groups, SGA-hsPDA neonates demonstrated a significant fall in rScO2 [69% (SEM 2.5) at 4-8 h to 61% (2.7) at 68-72 h, p < 0.001] with a concurrent rise in cFTOE [0.26 (0.026) at 4-8 h to 0.34 (0.030) at 68-72 h, p < 0.001]. Conclusion(s): Contrary to our hypothesis, hsPDA had a significant negative effect on cerebral oxygenation in preterm SGA neonates. Future studies should explore the potential benefits of early screening and treatment for hsPDA on long-term neurodevelopmental outcome in preterm SGA neonates.Copyright © 2016 S. Karger AG, Basel.
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1159/000448873
PubMed URL: 27756065 [http://www.ncbi.nlm.nih.gov/pubmed/?term=27756065]
ISSN: 1661-7800
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/38834
Type: Article
Type of Clinical Study or Trial: Case series or case report
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