Duration of Neonatal Antibiotic Exposure in Preterm Infants in Association with Health and Developmental Outcomes in Early Childhood

Over 90% of preterm neonates are, often empirically, exposed to antibiotics as a potentially life-saving measure against sepsis. Long-term outcome in association with antibiotic exposure (NABE) has insufficiently been studied after preterm birth. We investigated the association of NABE-duration with...

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Main Authors: Nancy Deianova, Nanne K. de Boer, Hafsa Aoulad Ahajan, Cilla Verbeek, Cornelieke S. H. Aarnoudse-Moens, Aleid G. Leemhuis, Mirjam M. van Weissenbruch, Anton H. van Kaam, Daniel C. Vijbrief, Chris V. Hulzebos, Astrid Giezen, Veerle Cossey, Willem P. de Boode, Wouter J. de Jonge, Marc A. Benninga, Hendrik J. Niemarkt, Tim G. J. de Meij
Format: Article
Language:English
Published: MDPI AG 2023-05-01
Series:Antibiotics
Subjects:
Online Access:https://www.mdpi.com/2079-6382/12/6/967
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author Nancy Deianova
Nanne K. de Boer
Hafsa Aoulad Ahajan
Cilla Verbeek
Cornelieke S. H. Aarnoudse-Moens
Aleid G. Leemhuis
Mirjam M. van Weissenbruch
Anton H. van Kaam
Daniel C. Vijbrief
Chris V. Hulzebos
Astrid Giezen
Veerle Cossey
Willem P. de Boode
Wouter J. de Jonge
Marc A. Benninga
Hendrik J. Niemarkt
Tim G. J. de Meij
author_facet Nancy Deianova
Nanne K. de Boer
Hafsa Aoulad Ahajan
Cilla Verbeek
Cornelieke S. H. Aarnoudse-Moens
Aleid G. Leemhuis
Mirjam M. van Weissenbruch
Anton H. van Kaam
Daniel C. Vijbrief
Chris V. Hulzebos
Astrid Giezen
Veerle Cossey
Willem P. de Boode
Wouter J. de Jonge
Marc A. Benninga
Hendrik J. Niemarkt
Tim G. J. de Meij
author_sort Nancy Deianova
collection DOAJ
description Over 90% of preterm neonates are, often empirically, exposed to antibiotics as a potentially life-saving measure against sepsis. Long-term outcome in association with antibiotic exposure (NABE) has insufficiently been studied after preterm birth. We investigated the association of NABE-duration with early-childhood developmental and health outcomes in preterm-born children and additionally assessed the impact of GA on outcomes. Preterm children (GA < 30 weeks) participating in a multicenter cohort study were approached for follow-up. General expert-reviewed health questionnaires on respiratory, atopic and gastrointestinal symptoms were sent to parents of children > 24 months’ corrected age (CA). Growth and developmental assessments (Bayley Scales of Infant and Toddler Development (BSID) III) were part of standard care assessment at 24 months’ CA. Uni- and multivariate regressions were performed with NABE (per 5 days) and GA (per week) as independent variables. Odds ratios (OR) for health outcomes were adjusted (aOR) for confounders, where appropriate. Of 1079 infants whose parents were approached, 347 (32%) responded at a mean age of 4.6 years (SD 0.9). In children with NABE (97%), NABE duration decreased by 1.6 days (<i>p</i> < 0.001) per week of gestation. Below-average gross-motor development (BSID-III gross-motor score < 8) was associated with duration of NABE (aOR = 1.28; <i>p</i> = 0.04). The aOR for constipation was 0.81 (<i>p</i> = 0.04) per gestational week. Growth was inversely correlated with GA. Respiratory and atopic symptoms were not associated with NABE, nor GA. We observed that prolonged NABE after preterm birth was associated with below-average gross-motor development at 24 months’ CA, while a low GA was associated with lower weight and stature Z-scores and higher odds for constipation.
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spelling doaj.art-e3bd6e38236d484fb1e37eefad9d15812023-11-18T09:00:11ZengMDPI AGAntibiotics2079-63822023-05-0112696710.3390/antibiotics12060967Duration of Neonatal Antibiotic Exposure in Preterm Infants in Association with Health and Developmental Outcomes in Early ChildhoodNancy Deianova0Nanne K. de Boer1Hafsa Aoulad Ahajan2Cilla Verbeek3Cornelieke S. H. Aarnoudse-Moens4Aleid G. Leemhuis5Mirjam M. van Weissenbruch6Anton H. van Kaam7Daniel C. Vijbrief8Chris V. Hulzebos9Astrid Giezen10Veerle Cossey11Willem P. de Boode12Wouter J. de Jonge13Marc A. Benninga14Hendrik J. Niemarkt15Tim G. J. de Meij16Department of Pediatric Gastroenterology, Emma Children’s Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, 1105 AZ Amsterdam, The NetherlandsDepartment of Gastroenterology and Hepatology, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam University Medical Centre, Vrije Universiteit Amsterdam, 1105 AZ Amsterdam, The NetherlandsDepartment of Pediatric Gastroenterology, Emma Children’s Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, 1105 AZ Amsterdam, The NetherlandsDepartment of Pediatric Gastroenterology, Emma Children’s Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, 1105 AZ Amsterdam, The NetherlandsDepartment of Neonatology, Emma Children’s Hospital, Amsterdam Reproduction and Development Research Institute, 1105 AZ Amsterdam, The NetherlandsDepartment of Neonatology, Emma Children’s Hospital, Amsterdam Reproduction and Development Research Institute, 1105 AZ Amsterdam, The NetherlandsDepartment of Neonatology, Emma Children’s Hospital, Amsterdam Reproduction and Development Research Institute, 1105 AZ Amsterdam, The NetherlandsDepartment of Neonatology, Emma Children’s Hospital, Amsterdam Reproduction and Development Research Institute, 1105 AZ Amsterdam, The NetherlandsDepartment of Neonatology, University Medical Center Utrecht, Wilhelmina Children’s Hospital, 3584 CX Utrecht, The NetherlandsDepartment of Neonatology, Beatrix Children’s Hospital, University Medical Center Groningen, 9713 GZ Groningen, The NetherlandsDepartment of Neonatology, Isala Hospital, Amalia Children’s Center, 8025 AB Zwolle, The NetherlandsDepartment of Neonatology, University Hospitals Leuven, 3000 Leuven, BelgiumDepartment of Neonatology, Radboud University Medical Center, Radboud Institute for Health Sciences, Amalia Children’s Hospital, 6525 XZ Nijmegen, The NetherlandsTytgat Institute for Liver and Intestinal Research, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The NetherlandsDepartment of Pediatric Gastroenterology, Emma Children’s Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, 1105 AZ Amsterdam, The NetherlandsDepartment of Neonatology, Máxima Medical Center, 5504 DB Veldhoven, The NetherlandsDepartment of Pediatric Gastroenterology, Emma Children’s Hospital, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam UMC, 1105 AZ Amsterdam, The NetherlandsOver 90% of preterm neonates are, often empirically, exposed to antibiotics as a potentially life-saving measure against sepsis. Long-term outcome in association with antibiotic exposure (NABE) has insufficiently been studied after preterm birth. We investigated the association of NABE-duration with early-childhood developmental and health outcomes in preterm-born children and additionally assessed the impact of GA on outcomes. Preterm children (GA < 30 weeks) participating in a multicenter cohort study were approached for follow-up. General expert-reviewed health questionnaires on respiratory, atopic and gastrointestinal symptoms were sent to parents of children > 24 months’ corrected age (CA). Growth and developmental assessments (Bayley Scales of Infant and Toddler Development (BSID) III) were part of standard care assessment at 24 months’ CA. Uni- and multivariate regressions were performed with NABE (per 5 days) and GA (per week) as independent variables. Odds ratios (OR) for health outcomes were adjusted (aOR) for confounders, where appropriate. Of 1079 infants whose parents were approached, 347 (32%) responded at a mean age of 4.6 years (SD 0.9). In children with NABE (97%), NABE duration decreased by 1.6 days (<i>p</i> < 0.001) per week of gestation. Below-average gross-motor development (BSID-III gross-motor score < 8) was associated with duration of NABE (aOR = 1.28; <i>p</i> = 0.04). The aOR for constipation was 0.81 (<i>p</i> = 0.04) per gestational week. Growth was inversely correlated with GA. Respiratory and atopic symptoms were not associated with NABE, nor GA. We observed that prolonged NABE after preterm birth was associated with below-average gross-motor development at 24 months’ CA, while a low GA was associated with lower weight and stature Z-scores and higher odds for constipation.https://www.mdpi.com/2079-6382/12/6/967neonatal antibiotic exposurepretermpsychomotor developmentatopypediatric constipationgrowth
spellingShingle Nancy Deianova
Nanne K. de Boer
Hafsa Aoulad Ahajan
Cilla Verbeek
Cornelieke S. H. Aarnoudse-Moens
Aleid G. Leemhuis
Mirjam M. van Weissenbruch
Anton H. van Kaam
Daniel C. Vijbrief
Chris V. Hulzebos
Astrid Giezen
Veerle Cossey
Willem P. de Boode
Wouter J. de Jonge
Marc A. Benninga
Hendrik J. Niemarkt
Tim G. J. de Meij
Duration of Neonatal Antibiotic Exposure in Preterm Infants in Association with Health and Developmental Outcomes in Early Childhood
Antibiotics
neonatal antibiotic exposure
preterm
psychomotor development
atopy
pediatric constipation
growth
title Duration of Neonatal Antibiotic Exposure in Preterm Infants in Association with Health and Developmental Outcomes in Early Childhood
title_full Duration of Neonatal Antibiotic Exposure in Preterm Infants in Association with Health and Developmental Outcomes in Early Childhood
title_fullStr Duration of Neonatal Antibiotic Exposure in Preterm Infants in Association with Health and Developmental Outcomes in Early Childhood
title_full_unstemmed Duration of Neonatal Antibiotic Exposure in Preterm Infants in Association with Health and Developmental Outcomes in Early Childhood
title_short Duration of Neonatal Antibiotic Exposure in Preterm Infants in Association with Health and Developmental Outcomes in Early Childhood
title_sort duration of neonatal antibiotic exposure in preterm infants in association with health and developmental outcomes in early childhood
topic neonatal antibiotic exposure
preterm
psychomotor development
atopy
pediatric constipation
growth
url https://www.mdpi.com/2079-6382/12/6/967
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