Cerebral perfusion and neurological examination characterise neonatal opioid withdrawal syndrome: a prospective cohort study.


Journal

Archives of disease in childhood. Fetal and neonatal edition
ISSN: 1468-2052
Titre abrégé: Arch Dis Child Fetal Neonatal Ed
Pays: England
ID NLM: 9501297

Informations de publication

Date de publication:
Jul 2022
Historique:
received: 01 04 2021
accepted: 15 10 2021
pubmed: 3 11 2021
medline: 22 6 2022
entrez: 2 11 2021
Statut: ppublish

Résumé

To test the hypothesis that cerebral blood flow (CBF) assessed with arterial spin labelling (ASL) MRI is increased and standardised neurological examination is altered in infants with neonatal opioid withdrawal syndrome (NOWS) compared with those without. Prospective cohort study. Level IV neonatal intensive care unit and outpatient primary care centre. Infants with NOWS receiving pharmacological treatment and unexposed controls matched for gestational age at birth and post-menstrual age at MRI. CBF assessed by ASL on non-sedated 3-Tesla MRI and standardised Hammersmith Neonatal Neurological Examination (HNNE) within 14 days of birth. Thirty infants with NOWS and 31 control infants were enrolled and included in the final analysis. Global CBF across the brain was higher in the NOWS group compared with controls (14.2 mL/100 g/min±5.5 vs 10.7 mL/100 g/min±4.3, mean±SD, Cohen's d=0.72). HNNE total optimality score was lower in the NOWS group compared with controls (25.9±3.6 vs 28.4±2.4, mean±SD, Cohen's d=0.81). A penalised logistic regression model including both CBF and HNNE items discriminated best between the two groups. Increased cerebral perfusion and neurological examination abnormalities characterise infants with NOWS compared with those without intrauterine drug exposure and suggest prenatal substance exposure affects fetal brain development. Identifying neurological and neuroimaging characteristics of infants with NOWS can contribute to understanding mechanisms underlying later outcomes and to designing potential new treatments.

Identifiants

pubmed: 34725106
pii: archdischild-2021-322192
doi: 10.1136/archdischild-2021-322192
doi:

Substances chimiques

Analgesics, Opioid 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

414-420

Informations de copyright

© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: NLM is a consultant for and has equity in Thrive Neuromedical. No funding was obtained from this company and the study is not related to this disclosure. DJJW has equity in Translational MRI that provided the CereFlow software, DJJW was not involved in study design.

Auteurs

Kristen L Benninger (KL)

Department of Pediatrics and Neonatology, Nationwide Children's Hospital, Columbus, Ohio, USA kristen.benninger@nationwidechildrens.org.
Center for Perinatal Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, Ohio, USA.

Jin Peng (J)

Research Information Solutions and Innovation Research & Development, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, Ohio, USA.

Mai-Lan Ho (ML)

Department of Radiology, Nationwide Children's Hospital, Columbus, Ohio, USA.

Julia Newton (J)

Center for Perinatal Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, Ohio, USA.

Danny J J Wang (DJJ)

Stevens Neuroimaging and Informatics Institute, University of Southern California Keck School of Medicine, Los Angeles, California, USA.

Houchun H Hu (HH)

Department of Radiology, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, Ohio, USA.

Ann R Stark (AR)

Department of Neonatology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.

Jerome A Rusin (JA)

Department of Radiology, Nationwide Children's Hospital, Columbus, Ohio, USA.

Nathalie L Maitre (NL)

Pediatrics, Emory University, Atlanta, Georgia, USA.

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