Prediction of bronchopulmonary dysplasia in very preterm infants: competitive risk model nomogram

UDC.coleccionInvestigaciónes_ES
UDC.grupoInvEnfermería e Coidados da Saúde (INIBIC)es_ES
UDC.institutoCentroINIBIC - Instituto de Investigacións Biomédicas de A Coruñaes_ES
UDC.journalTitleFrontiers in Pediatricses_ES
UDC.volume12es_ES
dc.contributor.authorSucasas Alonso, Andrea
dc.contributor.authorPértega-Díaz, Sonia
dc.contributor.authorBalboa-Barreiro, Vanesa
dc.contributor.authorGarcía-Muñoz Rodrigo, Fermín
dc.contributor.authorÁvila-Álvarez, Alejandro
dc.date.accessioned2024-04-02T08:12:20Z
dc.date.available2024-04-02T08:12:20Z
dc.date.issued2024-02-20
dc.description.abstract[Abstract] Objective: To develop predictive clinical models of bronchopulmonary dysplasia (BPD) through competing risk analysis. Methods: Retrospective observational cohort study, including preterm newborns ≤32 weeks gestational age, conducted between January 1, 2013 and September 30, 2022 in a third-level Neonatal Intensive Care Unit in Spain. A prediction study was carried out using competing risk models, where the event of interest was BPD and the competing event was death. A multivariate competing risk model was developed separately for each postnatal day (days 1, 3, 7 and 14). Nomograms to predict BPD risk were developed from the coefficients of the final models and internally validated. Results: A total of 306 patients were included in the study, of which 73 (23.9%) developed BPD and 29 (9.5%) died. On day 1, the model with the greatest predictive capacity was that including birth weight, days since rupture of membranes, and surfactant requirement (area under the receiver operating characteristic (ROC) curve (AUC), 0.896; 95% CI, 0.792–0.999). On day 3, the final predictive model was based on the variables birth weight, surfactant requirement, and Fraction of Inspired Oxygen (FiO2) (AUC, 0.891; 95% CI, 0.792–0.989). Conclusions: Competing risk analysis allowed accurate prediction of BPD, avoiding the potential bias resulting from the exclusion of deceased newborns or the use of combined outcomes. The resulting models are based on clinical variables measured at bedside during the first 3 days of life, can be easily implemented in clinical practice, and can enable earlier identification of patients at high risk of BPD.es_ES
dc.description.sponsorshipinfo:eu-repo/grantAgreement/ISCIII/Programa Estatal de Generación de Conocimiento y Fortalecimiento del Sistema Español de I+D+I/PI21%2F01601/ES/HAPLOGRUPOS DE ADN MITOCONDRIAL Y NIVELES DE ADN MITOCONDRIAL CIRCULANTES EN PACIENTES GRANDES PREMATUROS CON DISPLASIA BRONCOPULMONARes_ES
dc.identifier.citationSucasas-Alonso A, Pértega-Díaz S, Balboa-Barreiro V, García-Muñoz Rodrigo F, Ávila-Álvarez A. Prediction of bronchopulmonary dysplasia in very preterm infants: competitive risk model nomogram. Front Pediatr. 2024. 12:1335891.es_ES
dc.identifier.issn2296-2360
dc.identifier.urihttp://hdl.handle.net/2183/36035
dc.language.isoenges_ES
dc.publisherFrontierses_ES
dc.relation.urihttps://doi.org/10.3389/fped.2024.1335891es_ES
dc.rightsCreative Commons Attribution Licence 4.0 International (CC-BY 4.0)es_ES
dc.rights.accessRightsopen accesses_ES
dc.subjectBronchopulmonary dysplasiaes_ES
dc.subjectPredictiones_ES
dc.subjectDeathes_ES
dc.subjectMechanical ventilationes_ES
dc.subjectPretermes_ES
dc.titlePrediction of bronchopulmonary dysplasia in very preterm infants: competitive risk model nomogrames_ES
dc.typejournal articlees_ES
dspace.entity.typePublication
relation.isAuthorOfPublication81bb68c9-ac97-4c16-987d-9469586d17ee
relation.isAuthorOfPublication.latestForDiscovery81bb68c9-ac97-4c16-987d-9469586d17ee

Files

Original bundle

Now showing 1 - 2 of 2
Loading...
Thumbnail Image
Name:
SucasasA_PredictionB_2024.pdf
Size:
4.34 MB
Format:
Adobe Portable Document Format
Description:
Loading...
Thumbnail Image
Name:
SucasasA_PredictionB_2024_Suppl.pdf
Size:
381.99 KB
Format:
Adobe Portable Document Format
Description:
Supplementary material