Validation of a new predictive model to improve risk stratification in bronchopulmonary dysplasia.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
17 01 2020
Historique:
received: 12 07 2019
accepted: 08 12 2019
entrez: 19 1 2020
pubmed: 19 1 2020
medline: 20 11 2020
Statut: epublish

Résumé

We need a better risk stratification system for the increasing number of survivors of extreme prematurity suffering the most severe forms of bronchopulmonary dysplasia (BPD). However, there is still a paucity of studies providing scientific evidence to guide future updates of BPD severity definitions. Our goal was to validate a new predictive model for BPD severity that incorporates respiratory assessments beyond 36 weeks postmenstrual age (PMA). We hypothesized that this approach improves BPD risk assessment, particularly in extremely premature infants. This is a longitudinal cohort of premature infants (≤32 weeks PMA, n = 188; Washington D.C). We performed receiver operating characteristic analysis to define optimal BPD severity levels using the duration of supplementary O2 as predictor and respiratory hospitalization after discharge as outcome. Internal validation included lung X-ray imaging and phenotypical characterization of BPD severity levels. External validation was conducted in an independent longitudinal cohort of premature infants (≤36 weeks PMA, n = 130; Bogota). We found that incorporating the total number of days requiring O2 (without restricting at 36 weeks PMA) improved the prediction of respiratory outcomes according to BPD severity. In addition, we defined a new severity category (level IV) with prolonged exposure to supplemental O2 (≥120 days) that has the highest risk of respiratory hospitalizations after discharge. We confirmed these findings in our validation cohort using ambulatory determination of O2 requirements. In conclusion, a new predictive model for BPD severity that incorporates respiratory assessments beyond 36 weeks improves risk stratification and should be considered when updating current BPD severity definitions.

Identifiants

pubmed: 31953419
doi: 10.1038/s41598-019-56355-5
pii: 10.1038/s41598-019-56355-5
pmc: PMC6969113
doi:

Substances chimiques

Oxygen S88TT14065

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

613

Subventions

Organisme : NHLBI NIH HHS
ID : R41 HL145669
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL141237
Pays : United States
Organisme : NHLBI NIH HHS
ID : R56 HL141237
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI130502
Pays : United States

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Auteurs

Gustavo Nino (G)

Division of Pediatric Pulmonary and Sleep Medicine. Children's National Medical Center, George Washington University, Washington, DC, USA. gnino@childrensnational.org.
Department of Pediatrics, George Washington University, Washington, DC, USA. gnino@childrensnational.org.

Awais Mansoor (A)

Sheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Medical Center, Washington, DC, USA.

Geovanny F Perez (GF)

Division of Pediatric Pulmonary and Sleep Medicine. Children's National Medical Center, George Washington University, Washington, DC, USA.
Department of Pediatrics, George Washington University, Washington, DC, USA.

Maria Arroyo (M)

Division of Pediatric Pulmonary and Sleep Medicine. Children's National Medical Center, George Washington University, Washington, DC, USA.
Department of Pediatrics, George Washington University, Washington, DC, USA.

Xilei Xuchen (X)

Division of Pediatric Pulmonary and Sleep Medicine. Children's National Medical Center, George Washington University, Washington, DC, USA.
Department of Pediatrics, George Washington University, Washington, DC, USA.

Jered Weinstock (J)

Division of Pediatric Pulmonary and Sleep Medicine. Children's National Medical Center, George Washington University, Washington, DC, USA.
Department of Pediatrics, George Washington University, Washington, DC, USA.
Division of Pediatric Pulmonary and Sleep Medicine. Children's National Medical Center, George Washington University, Washington, DC, USA.

Mariam Said (M)

Division of Neonatology. Children's National Medical Center, George Washington University, Washington, DC, USA.
Department of Pediatrics, George Washington University, Washington, DC, USA.

Ranniery Acuña-Cordero (R)

Department of Pediatric Pulmonology, Hospital Militar Central, Department of Pediatrics, School of Medicine, Universidad Militar Nueva Granada, Bogotá, Colombia.

Monica P Sossa-Briceño (MP)

Department of Internal Medicine, School of Medicine, Universidad Nacional de Colombia, Bogotá, Colombia.

Carlos E Rodríguez-Martínez (CE)

Department of Pediatrics, School of Medicine, Universidad Nacional de Colombia, Bogotá, Colombia.
Department of Pediatric Pulmonology and Pediatric Critical Care Medicine, School of Medicine, Universidad El Bosque, Bogota, Colombia.

Marius Linguraru (M)

Sheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Medical Center, Washington, DC, USA.
Department of Pediatrics, George Washington University, Washington, DC, USA.
Department of Radiology, George Washington University, Washington, DC, USA.
Department of Biomedical Engineering, George Washington University, Washington, DC, USA.

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