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EDITORIAL article

Front. Pediatr.

Sec. Pediatric Critical Care

Volume 13 - 2025 | doi: 10.3389/fped.2025.1677006

This article is part of the Research TopicPediatric Respiratory Critical Illness: Etiology, Diagnosis, and TreatmentView all 10 articles

Editorial: Pediatric Respiratory Critical Illness: Etiology, Diagnosis, and Treatment

Provisionally accepted
  • Children‘s Hospital of Chongqing Medical University, Chongqing, China

The final, formatted version of the article will be published soon.

Severe respiratory diseases-including acute respiratory distress syndrome (ARDS), bronchopulmonary dysplasia (BPD), and severe pneumonia-remain leading causes of pediatric morbidity and mortality worldwide. Despite decades of advances, mortality from pediatric ARDS remains high,particularly in patients with sepsis or multi-organ dysfunction (1,2). BPD affects more than 20% of extremely low birth weight infants and contributes to prolonged hospital stays and long-term respiratory complications (3). Globally, pneumonia remains a top cause of death among children under (4). These challenges highlight the urgent need for improved diagnostics, monitoring tools, and targeted therapies. This Research Topic gathers nine original contributions that offer valuable insights into early assessment, physiologic monitoring, clinical management, and rare disease phenotypes in pediatric respiratory critical illness. Qin et al. explored the use of exhaled nitric oxide (FeNO) and tidal breathing parameters to assess airway hyperresponsiveness (AHR) in infants under 3 years of age. Their findings reinforce the predictive value of FeNO >14 ppb and flow-volume ratios in suspected asthma-a significant advance for a difficult-to-test age group. This aligns with recent pediatric studies showing FeNO as a noninvasive surrogate for eosinophilic inflammation and long-term asthma risk (5).Colak et al. introduced renal near-infrared spectroscopy (RrSO₂) as a physiologic marker for extubation failure in ventilated children. A >6.15% drop in RrSO₂ during readiness testing had a sensitivity of 98.4% and specificity of 88.9%, suggesting it may be a reliable adjunct to respiratory monitoring in complex cases. Ge et al. developed a multifactorial prediction model integrating P/F ratio, diaphragm ultrasound indices (DE-RSBI, DTF-RSBI), and Pediatric Critical Illness Score (PCIS). This model significantly outperformed individual variables (AUC = 0.96) in predicting successful weaning. The study supports a shift from single-parameter thresholds to multimodal, data-driven decision tools. Banik et al. evaluated the usability of the Vayu bCPAP system in five neonatal care facilities in Bangladesh. Providers reported strong acceptability and effectiveness in treating respiratory distress syndrome (RDS), highlighting how low-cost, portable innovations can improve neonatal care in resource-limited settings. Li et al. reviewed the role of oxidative stress in the pathogenesis of BPD. Their analysis identified 8-hydroxy-2'-deoxyguanosine (8-OHdG) as a promising biomarker for early detection, adding to a growing body of evidence supporting biomarker-guided neonatal care (5).Duenas-Meza et al. studied sleep-disordered breathing in children with cystic fibrosis at high altitude. They found that total sleep time with oxygen saturation <90% and <85% correlated negatively with FEV₁, reinforcing the importance of polysomnography in evaluating pulmonary function in high-altitude environments. Together, these articles underscore critical advancements in pediatric respiratory critical care: Noninvasive biomarkers such as FeNO and RrSO₂ offer new pathways for early detection and monitoring; Multimodal prediction models outperform traditional approaches in ventilator weaning; Low-cost devices like Vayu bCPAP expand respiratory care access in LMICs; Precision recognition of rare and complex conditions facilitates timely and targeted interventions.

Keywords: Respiratory Insufficiency, Bronchopulmonary Dysplasia, mechanical ventilation, biomarkers, Pediatric intensive care units

Received: 31 Jul 2025; Accepted: 04 Aug 2025.

Copyright: © 2025 Dang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Hongxing Dang, Children‘s Hospital of Chongqing Medical University, Chongqing, China

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