Necrotizing enterocolitis in haemolytic disease of the newborn: a retrospective cohort study.


Journal

Vox sanguinis
ISSN: 1423-0410
Titre abrégé: Vox Sang
Pays: England
ID NLM: 0413606

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 02 07 2019
revised: 13 10 2019
accepted: 16 10 2019
pubmed: 21 12 2019
medline: 7 7 2020
entrez: 21 12 2019
Statut: ppublish

Résumé

Necrotizing enterocolitis (NEC) is a common and often severe gastrointestinal emergency in newborn infants. While usually affecting (very) premature infants, an association between NEC and haemolytic disease of the foetus and newborn (HDFN) has been suggested. HDFN may be an additional risk factor to develop NEC. The objective of this study was to evaluate the occurrence of NEC in infants affected with moderate to severe HDFN in a large single centre cohort as compared to a broad population of infants without HDFN. Retrospective cohort study of medical records of neonates with and without HDFN, with a gestational age at birth ≥30 weeks and ≤38 weeks, and admitted to the Leiden University Medical Center between January 2000 and December 2016. A total of 3284 patient records of infants born in the study period were reviewed and 317 cases of HDFN were identified. The incidence of NEC was significantly higher among infants with HDFN compared to infants without HDFN: 4/317 affected infants (1·3%) vs. 11/2967 affected infants (0·4%, relative risk 3·40, 95% confidence interval: 1·09-10·63). We observed a higher incidence of NEC in an overall late preterm to near term population of infants with moderate to severe HDFN, compared to infants born without HDFN. The clinician taking care of an HDFN-affected infant should be cautious of this higher risk.

Sections du résumé

BACKGROUND AND OBJECTIVES OBJECTIVE
Necrotizing enterocolitis (NEC) is a common and often severe gastrointestinal emergency in newborn infants. While usually affecting (very) premature infants, an association between NEC and haemolytic disease of the foetus and newborn (HDFN) has been suggested. HDFN may be an additional risk factor to develop NEC. The objective of this study was to evaluate the occurrence of NEC in infants affected with moderate to severe HDFN in a large single centre cohort as compared to a broad population of infants without HDFN.
MATERIALS AND METHODS METHODS
Retrospective cohort study of medical records of neonates with and without HDFN, with a gestational age at birth ≥30 weeks and ≤38 weeks, and admitted to the Leiden University Medical Center between January 2000 and December 2016.
RESULTS RESULTS
A total of 3284 patient records of infants born in the study period were reviewed and 317 cases of HDFN were identified. The incidence of NEC was significantly higher among infants with HDFN compared to infants without HDFN: 4/317 affected infants (1·3%) vs. 11/2967 affected infants (0·4%, relative risk 3·40, 95% confidence interval: 1·09-10·63).
CONCLUSIONS CONCLUSIONS
We observed a higher incidence of NEC in an overall late preterm to near term population of infants with moderate to severe HDFN, compared to infants born without HDFN. The clinician taking care of an HDFN-affected infant should be cautious of this higher risk.

Identifiants

pubmed: 31858620
doi: 10.1111/vox.12862
pmc: PMC7028041
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

196-201

Informations de copyright

© 2019 The Authors. Vox Sanguinis published by John Wiley & Sons Ltd on behalf of International Society of Blood Transfusion.

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Auteurs

Isabelle M C Ree (IMC)

Department of Pediatrics, Division of Neonatology, Leiden University Medical Center, Leiden, The Netherlands.
Center for Clinical Transfusion Research, Sanquin, Leiden, The Netherlands.

Anne M de Grauw (AM)

Department of Pediatrics, Division of Neonatology, Leiden University Medical Center, Leiden, The Netherlands.

Vincent Bekker (V)

Department of Pediatrics, Division of Neonatology, Leiden University Medical Center, Leiden, The Netherlands.

Masja de Haas (M)

Center for Clinical Transfusion Research, Sanquin, Leiden, The Netherlands.
Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands.
Department of Immunohematology Diagnostics, Sanquin, Amsterdam, The Netherlands.

Arjan B Te Pas (AB)

Department of Pediatrics, Division of Neonatology, Leiden University Medical Center, Leiden, The Netherlands.

Dick Oepkes (D)

Department of Obstetrics, Division of Fetal Medicine, Leiden University Medical Center, Leiden, The Netherlands.

Annemieke J M Middeldorp (AJM)

Department of Obstetrics, Division of Fetal Medicine, Leiden University Medical Center, Leiden, The Netherlands.

Enrico Lopriore (E)

Department of Pediatrics, Division of Neonatology, Leiden University Medical Center, Leiden, The Netherlands.

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