Two-Year Autism Risk Screening and 3-Year Developmental Outcomes in Very Preterm Infants.


Journal

JAMA pediatrics
ISSN: 2168-6211
Titre abrégé: JAMA Pediatr
Pays: United States
ID NLM: 101589544

Informations de publication

Date de publication:
26 Dec 2023
Historique:
medline: 26 12 2023
pubmed: 26 12 2023
entrez: 26 12 2023
Statut: aheadofprint

Résumé

Use of the Modified Checklist for Autism in Toddlers, Revised With Follow-Up, a 2-stage parent-report autism risk screening tool, has been questioned due to reports of poor sensitivity and specificity. How this measure captures developmental delays for very preterm infants may provide support for continued use in pediatric care settings. To determine whether autism risk screening with the 2-stage parent-report autism risk screening tool at age 2 years is associated with behavioral and developmental outcomes at age 3 in very preterm infants. Neonatal Neurobehavior and Outcomes for Very Preterm Infants was a longitudinal, multisite cohort study. Enrollment occurred April 2014 to June 2016, and analyses were conducted from November 2022 to May 2023. Data were collected across 9 university-affiliated neonatal intensive care units (NICUs). Inclusion criteria were infants born less than 30 weeks' gestational age, a parent who could read and speak English and/or Spanish, and residence within 3 hours of the NICU and follow-up clinic. Prematurity and use of the 2-stage parent-report autism risk screening tool at age 2 years. Outcomes include cognitive, language, motor composites on Bayley Scales for Infant and Toddler Development, third edition (Bayley-III) and internalizing, externalizing, total problems, and pervasive developmental disorder (PDD) subscale on the Child Behavior Checklist (CBCL) at age 3 years. Generalized estimating equations tested associations between the 2-stage parent-report autism risk screening tool and outcomes, adjusting for covariates. A total of 467 children (mean [SD] gestational age, 27.1 [1.8] weeks; 243 male [52%]) were screened with the 2-stage parent-report autism risk screening tool at age 2 years, and outcome data at age 3 years were included in analyses. Mean (SD) maternal age at birth was 29 (6) years. A total of 51 children (10.9%) screened positive on the 2-stage parent-report autism risk screening tool at age 2 years. Children with positive screening results were more likely to have Bayley-III composites of 84 or less on cognitive (adjusted odds ratio [aOR], 4.03; 95% CI, 1.65-9.81), language (aOR, 5.38; 95% CI, 2.43-11.93), and motor (aOR, 4.74; 95% CI, 2.19-10.25) composites and more likely to have CBCL scores of 64 or higher on internalizing (aOR, 4.83; 95% CI, 1.88-12.44), externalizing (aOR, 2.69; 95% CI, 1.09-6.61), and PDD (aOR, 3.77; 95% CI, 1.72-8.28) scales. Results suggest that the 2-stage parent-report autism risk screening tool administered at age 2 years was a meaningful screen for developmental delays in very preterm infants, with serious delays detected at age 3 years.

Identifiants

pubmed: 38147347
pii: 2812810
doi: 10.1001/jamapediatrics.2023.5727
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Coral L Shuster (CL)

The Brown Center for the Study of Children at Risk, Women and Infants Hospital, Providence, Rhode Island.

Stephen J Sheinkopf (SJ)

Thompson Center for Autism and Neurodevelopment, University of Missouri, Columbia.

Elisabeth C McGowan (EC)

The Brown Center for the Study of Children at Risk, Women and Infants Hospital, Providence, Rhode Island.
Brown Alpert Medical School, Providence, Rhode Island.

Julie A Hofheimer (JA)

UNC School of Medicine, Chapel Hill, North Carolina.

T Michael O'Shea (TM)

UNC School of Medicine, Chapel Hill, North Carolina.

Brian S Carter (BS)

Children's Mercy Hospital, Kansas City, Missouri.

Jennifer B Helderman (JB)

Wake Forest School of Medicine, Winston-Salem, North Carolina.

Jennifer Check (J)

Wake Forest School of Medicine, Winston-Salem, North Carolina.

Charles R Neal (CR)

University of Hawaii John A. Burns School of Medicine, Honolulu, Hawaii.

Steven L Pastyrnak (SL)

Spectrum Health-Helen Devos Hospital, Grand Rapids, Michigan.

Lynne M Smith (LM)

Harbor-UCLA Medical Center, Torrance, California.

Cynthia Loncar (C)

Brown Alpert Medical School, Providence, Rhode Island.

Lynne M Dansereau (LM)

The Brown Center for the Study of Children at Risk, Women and Infants Hospital, Providence, Rhode Island.

Sheri A DellaGrotta (SA)

The Brown Center for the Study of Children at Risk, Women and Infants Hospital, Providence, Rhode Island.

Carmen J Marsit (CJ)

Emory University, Atlanta, Georgia.

Barry M Lester (BM)

The Brown Center for the Study of Children at Risk, Women and Infants Hospital, Providence, Rhode Island.
Brown Alpert Medical School, Providence, Rhode Island.

Classifications MeSH