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BPD Following Preterm Birth: A Model for Chronic Lung Disease and a Substrate for ARDS in Childhood
Journal article   Open access   Peer reviewed

BPD Following Preterm Birth: A Model for Chronic Lung Disease and a Substrate for ARDS in Childhood

Anita Bhandari, Christopher Carroll and Vineet Bhandari
Frontiers in pediatrics, v 4, pp 60-60
15 Jun 2016
PMID: 27379219
url
https://doi.org/10.3389/fped.2016.00060View
Published, Version of Record (VoR)CC BY V4.0 Open

Abstract

Life Sciences & Biomedicine Pediatrics Science & Technology
It has been suggested that pediatric acute respiratory distress syndrome (PARDS) may be a different entity, vis-a-vis adult acute respiratory distress syndrome (ARDS), based on its epidemiology and outcomes. A more pediatric-specific definition of PARDS to include the subgroup of patients with underlying lung (and heart) disease has been proposed. Epidemiological data suggest that up to 13% of the children with ARDS have a history of prematurity and/or underlying chronic lung disease. However, the specific contribution of bronchopulmonary dysplasia (BPD), the most common chronic lung disease in infants, to the development of PARDS is not known. BPD leads to damaged lungs with long-term consequences secondary to disordered growth and immune function. These damaged lungs could potentially act as a substrate, which given the appropriate noxious stimuli, can predispose a child to PARDS. Interestingly, similar biomarkers [KL-6, interleukin (IL)-6, IL-8, sICAM-1, angiopoietin-2, and matrix metalloproteinase-8 and -9] of pulmonary injury have been associated both with BPD and ARDS. Recognition of a unique pattern of clinical symptomatology and/or outcomes of PARDS, if present, could potentially be useful for investigating targeted therapeutic interventions.

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Collaboration types
Domestic collaboration
Web of Science research areas
Pediatrics
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