Long-Term Outcome of Necrotizing Enterocolitis and Spontaneous Intestinal Perforation.


Journal

Pediatrics
ISSN: 1098-4275
Titre abrégé: Pediatrics
Pays: United States
ID NLM: 0376422

Informations de publication

Date de publication:
01 11 2022
Historique:
accepted: 21 07 2022
pubmed: 7 10 2022
medline: 3 11 2022
entrez: 6 10 2022
Statut: ppublish

Résumé

Necrotizing enterocolitis (NEC) and spontaneous intestinal perforation (SIP) are complications in preterm infants associated with high morbidity, mortality, impaired growth, and neurodevelopmental (ND) outcomes. Few studies have reported growth or ND outcomes of infants born extremely preterm with NEC/SIP beyond early childhood. Here, we compared anthropometric and ND outcomes, at 10 and 15 years, for children with medical NEC, surgical NEC, SIP, and neither NEC nor SIP. Participants from the prospective longitudinal extremely low gestational age newborns study were evaluated at ages 10 and 15 years for anthropometrics, neurocognition, attention-deficit/hyperactivity disorder, epilepsy, and gross motor function. At age 10 years, 889 children were followed-up (medical NEC = 138, surgical NEC = 33, SIP = 29, no NEC/SIP = 689), and 694 children were followed up-at 15 years. Children with medical NEC had similar weight, BMI, height, and head circumference compared with controls at both 10 and 15 years. At 15 years, children with surgical NEC had lower weight z-score (adjusted β: -0.75, 95% confidence interval [CI]: -1.25 to -0.25), lower BMI z-score (adjusted β: -0.55, 95% CI: -1.09 to -0.01), and lower height z-score (adjusted β: -0.65, 95% CI: -1.16 to -0.14). Children with SIP had lower weight and height z-scores at age 10 years when adjusted for sample attrition, but these differences were not significant when adjusted for confounders. We observed no differences in long-term ND outcomes. Surgical NEC- and SIP-associated growth impairment may persist through late childhood. ND outcomes among school-aged children born extremely preterm with any NEC or SIP are no different from children without NEC/SIP.

Identifiants

pubmed: 36200375
pii: 189675
doi: 10.1542/peds.2022-056445
pmc: PMC9647591
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NINDS NIH HHS
ID : U01 NS040069
Pays : United States
Organisme : NIH HHS
ID : UG3 OD023348
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 by the American Academy of Pediatrics.

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Auteurs

Ruben Vaidya (R)

Department of Pediatrics, University of Massachusetts Chan Medical School, Baystate, Springfield, Massachusetts.

Joe X Yi (JX)

Frank Porter Graham Child Development Institute.

T Michael O'Shea (TM)

Departments of Pediatrics.

Elizabeth T Jensen (ET)

Departments of Epidemiology and Prevention, Internal Medicine.

Robert M Joseph (RM)

Department of Anatomy and Neurobiology, Boston University School of Medicine, Boston, Massachusetts.

Jeffrey Shenberger (J)

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

Semsa Gogcu (S)

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

Kathryn Wagner (K)

Department of Pediatrics, University of Massachusetts Chan Medical School, Baystate, Springfield, Massachusetts.
Department of Biostatistics and Epidemiology, University of Massachusetts, Amherst, Massachusetts.

Michael E Msall (ME)

Kennedy Research Center on Intellectual and Neurodevelopmental Disabilities, University of Chicago, Chicago, Illinois.

Amanda L Thompson (AL)

Anthropology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.

Jean A Frazier (JA)

Department of Psychiatry, Eunice Kennedy Shriver Center, University of Massachusetts Chan Medical School, Worcester, Massachusetts.

Rebecca Fry (R)

Institute for Environmental Health Solutions.

Rachana Singh (R)

Department of Pediatrics, Tufts Children's Hospital, Tufts University School of Medicine, Boston, Massachusetts.

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