Patent ductus arteriosus (also non-hemodynamically significant) correlates with poor outcomes in very low birth weight infants. A multicenter cohort study.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 18 09 2023
accepted: 24 06 2024
medline: 9 7 2024
pubmed: 9 7 2024
entrez: 9 7 2024
Statut: epublish

Résumé

To standardize the diagnosis of patent ductus arteriosus (PDA) and report its association with adverse neonatal outcomes in very low birth weight infants (VLBW, birth weight < 1500 g). A multicenter prospective observational study was conducted in Emilia Romagna from March 2018 to October 2019. The association between ultrasound grading of PDA and adverse neonatal outcomes was evaluated after correction for gestational age. A diagnosis of hemodynamically significant PDA (hsPDA) was established when the PDA diameter was ≥ 1.6 mm at the pulmonary end with growing or pulsatile flow pattern, and at least 2 of 3 indexes of pulmonary overcirculation and/or systemic hypoperfusion were present. 218 VLBW infants were included. Among infants treated for PDA closure in the first postnatal week, up to 40% did not have hsPDA on ultrasound, but experienced clinical worsening. The risk of death was 15 times higher among neonates with non-hemodynamically significant PDA (non-hsPDA) compared to neonates with no PDA. In contrast, the risk of death was similar between neonates with hsPDA and neonates with no PDA. The occurrence of BPD was 6-fold higher among neonates with hsPDA, with no apparent beneficial role of early treatment for PDA closure. The risk of IVH (grade ≥ 3) and ROP (grade ≥ 3) increased by 8.7-fold and 18-fold, respectively, when both systemic hypoperfusion and pulmonary overcirculation were present in hsPDA. The increased risk of mortality in neonates with non-hsPDA underscores the potential inadequacy of criteria for defining hsPDA within the first 3 postnatal days (as they may be adversely affected by other clinically severe factors, i.e. persistent pulmonary hypertension and mechanical ventilation). Parameters such as length, diameter, and morphology may serve as more suitable ultrasound indicators during this period, to be combined with clinical data for individualized management. Additionally, BPD, IVH (grade ≥ 3) and ROP (grade ≥ 3) are associated with hsPDA. The existence of an optimal timeframe for closing PDA to minimize these adverse neonatal outcomes remains uncertain.

Identifiants

pubmed: 38980835
doi: 10.1371/journal.pone.0306769
pii: PONE-D-23-29459
doi:

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0306769

Informations de copyright

Copyright: © 2024 Chesi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Elena Chesi (E)

Neonatal Intensive Care Unit, Department of Obstetrics and Pediatrics, IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Katia Rossi (K)

Neonatal Intensive Care Unit, Women's and Children's Health Department, University Hospital of Modena, Modena, Italy.

Gina Ancora (G)

Neonatal Intensive Care Unit, Infermi Hospital, Rimini, Italy.

Cecilia Baraldi (C)

Neonatal Intensive Care Unit, Women's and Children's Health Department, University Hospital of Modena, Modena, Italy.

Mara Corradi (M)

Neonatal Intensive Care Unit, Women's and Children's Health Department, AOUP, University of Parma, Parma, Italy.

Francesco Di Dio (F)

Neonatal Intensive Care Unit, Department of Obstetrics and Pediatrics, IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Giorgia Di Fazzio (G)

Neonatal Intensive Care Unit, ARNAS Garibaldi Hospital, Catania, Italy.

Silvia Galletti (S)

Neonatal Intensive Care Unit, Women's and Children's Health Department, University Hospital Sant'Orsola-Malpighi, Bologna, Italy.

Giovanna Mescoli (G)

Neonatal Intensive Care Unit, Women's and Children's Health Department, Maggiore University Hospital, Bologna, Italy.

Irene Papa (I)

Neonatal Intensive Care Unit, Infermi Hospital, Rimini, Italy.

Agostina Solinas (A)

Neonatal Intensive Care Unit, University Hospital S.Anna, Ferrara, Italy.

Luca Braglia (L)

Biostatistician IRCCS of Reggio Emilia, Italy.

Antonella Di Caprio (A)

School of Pediatrics Residency, University of Modena and Reggio Emilia, Modena, Italy.

Riccardo Cuoghi Costantini (R)

Department of Medical and Surgical Sciences for Mother, Child and Adult, University of Modena and Reggio Emilia, Modena, Italy.

Francesca Miselli (F)

Neonatal Intensive Care Unit, Women's and Children's Health Department, University Hospital of Modena, Modena, Italy.
PhD Program in Clinical and Experimental Medicine, University of Modena and Reggio Emilia, Modena, Italy.

Alberto Berardi (A)

Neonatal Intensive Care Unit, Women's and Children's Health Department, University Hospital of Modena, Modena, Italy.

Giancarlo Gargano (G)

Neonatal Intensive Care Unit, Department of Obstetrics and Pediatrics, IRCCS di Reggio Emilia, Reggio Emilia, Italy.

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