Pediatric Pulmonary Vascular Disease

Pertussis infection in critically ill infants: meta-analysis and validation of a mortality score

Vladimir L. Cousin, Caroline Caula, Jason Vignot, Raphael Joye, Matthieu Blanc, Clémence Marais, Pierre TissièresAP-HP Paris Saclay University, Bicêtre Hospital. Evelina London Children’s Hospital. Geneva University Hospital. Hospital for Sick Children and University of Toronto. France, United Kingdom, Switzerland and Canada Critical CareCrit Care 2025; 29: DOI: 10.1186/s13054-025-05300-2 AbstractBackground: Despite widespread vaccination programs, pertussis continues circulating within […]

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Physical Activity Measured by Hip-Anchored Accelerometry in Pediatric Pulmonary Hypertension: Association with Disease Severity & Estimation of Minimal Important Differences

Mark-Jan Ploegstra, Rosaria J. Ferreira, Chantal Lokhorst, Eva Gouwy, Suzanne S. J. Schwartz, Marlies G. Haarman, Matthieu Villeneuve, Dimitri Stamatiadis, Johannes M. Douwes, Rolf M. F. BergerBeatrix Children’s Hospital, University Medical Center Groningen andUniversity of Groningen. Actelion Pharmaceuticals.Netherlands and Switzerland ChestChest 2025; DOI: 10.1016/j.chest.2025.01.038 AbstractBackground: Pediatric pulmonary hypertension (PH) is a severe incurable disease with poor prognosis.

Physical Activity Measured by Hip-Anchored Accelerometry in Pediatric Pulmonary Hypertension: Association with Disease Severity & Estimation of Minimal Important Differences Read More »

Response to Inhaled Nitric Oxide and Mortality Among Very Preterm Neonates With Pulmonary Hypertension

Michelle Baczynski, Dany Weisz, Laura Thomas, Stephanie Fevrier, Michael Castaldo, Amuchou Soraisham, Abbas Hyderi, Rula Agarushi, Soume Bhattacharya, Renjini Lalitha, Amneet Sidhu, Muzafar Gani Abdul Wahab, Gabriel Altit, Audrey Hébert, Deepak Louis, Yasser Elsayed, Souvik Mitra, Poorva Deshpande, Ashraf Kharrat, Faith Zhu, Joseph Ting, Eugene Yoon, Prakesh S. Shah, Amish Jain for the Canadian Neonatal

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Corrigendum to “Relationship Between Urine Serotonin and Persistent Pulmonary Hypertension of the Newborn”. J Pediatr 2025; 276:114290

Jamie L. Archambault, Teri L. Hernandez, Eva S. Nozik, Claire Palmer, Mairead Dillon, Ravinder J. Singh, Csaba Galambos, Cassidy A. DelaneyUniversity of Colorado. Mayo Clinic College of Medicine. United States Journal of PediatricsJ Pediatr 2025; DOI: 10.1016/j.jpeds.2025.114462 AbstractAbstract Not Available CategoryClass I. Persistent Pulmonary Hypertension of the NewbornAcquired Patient Factors Associated with Pulmonary Vascular DiseasePotential Biomarkers

Corrigendum to “Relationship Between Urine Serotonin and Persistent Pulmonary Hypertension of the Newborn”. J Pediatr 2025; 276:114290 Read More »

Refractory Chylothorax and Ventricular Hypertrophy Treated with Trametinib in a Patient with Noonan Syndrome: 18-Month Follow-Up

Antonia Pascarella, Giuseppe Limongelli, Alessandro De Falco, Elia Marco Paolo Minale, Giangiacomo Di Nardo, Giovanni Maria Di Marco, Geremia Zito Marinosci, Giorgia Olimpico, Paolo Siani, Daniele De BrasiSantobono-Pausilipon Children’s Hospital. University of Campania “Luigi Vanvitelli” and Monaldi Hospital. University “Federico II”. Italy ChildrenChildren 2024; 11: DOI: 10.3390/children11111342 AbstractRASopathies are a group of genetic syndromes caused by

Refractory Chylothorax and Ventricular Hypertrophy Treated with Trametinib in a Patient with Noonan Syndrome: 18-Month Follow-Up Read More »

Detection of pulmonary hypertension in preterm infants with bronchopulmonary dysplasia using oxygen saturation data

Pravitha Ramanand, Premananda Indic, Samuel J. Gentle, Namasivayam AmbalavananUniversity of Texas at Tyler. University of Alabama at Birmingham.United States Pediatric ResearchPediatr Res 2025; DOI: 10.1038/s41390-025-03891-8 AbstractBackground: Pulmonary hypertension (PH) complicates the clinical course of bronchopulmonary dysplasia (BPD) in preterm infants, increasing risk of mortality and other morbidities. Early detection of PH may provide the clinical opportunity for

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Infants With a Congenital Diaphragmatic Hernia Had Favourable Pulmonary Hypertension Outcomes at 1 Year of Age

Alice Dirick, Marilyne Levy, Kelly Mellul, Maxime Coignard, Naziha Khen-Dunlop, Alexandre Lapillonne Julien Stirnemann, Elsa Kermorvant-DucheminNecker-Enfants Malades Hospital. France Acta PediatricaActa Pediatr 2025; DOI: 10.1111/apa.70019 AbstractAim: Pulmonary hypertension is frequent in neonates with a congenital diaphragmatic hernia, but long-term data have been scarce. Our aim was to examine its prevalence, evolution and management and identify factors associated

Infants With a Congenital Diaphragmatic Hernia Had Favourable Pulmonary Hypertension Outcomes at 1 Year of Age Read More »

Continuous positive airway pressure versus conventional oxygen therapy in meconium aspiration syndrome: a randomized controlled trial

Arifa Mustaqeem, Anita Yadav, Jogender Kumar, Pradeep DebataVardhman Mahavir Medical College and Safdarjung Hospital. Post Graduate Institute of Medical Education and Research. India Journal of Tropical PediatricsJ Trop Pediatr 2025; 71: DOI: 10.1093/tropej/fmaf002 AbstractNeonates with meconium aspiration syndrome (MAS) frequently require respiratory support. However, the initial mode of respiratory support in these patients remains unclear. We

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MiR-25-3p regulates pulmonary arteriovenous malformation after Glenn procedure in patients with univentricular heart via the PHLPP2-HIF-1α axis

Junpei Kawamura, Munekazu Yamakuchi, Kentaro Ueno, Teruto Hashiguchi, Yasuhiro OkamotoKagoshima University. Japan Scientific ReportsSci Rep 2025; 15: DOI: 10.1038/s41598-025-88840-5 AbstractThe detailed mechanism of pulmonary arteriovenous malformations after Glenn surgery (G-PAVMs) in cyanotic congenital heart disease (CHD) remains unclear. Microarray in situ hybridization was performed to assess the miRNA (miRNA) profiles of serum from pediatric patients (0-6

MiR-25-3p regulates pulmonary arteriovenous malformation after Glenn procedure in patients with univentricular heart via the PHLPP2-HIF-1α axis Read More »

Unusual presentation of anomalous origin of the right pulmonary artery from the ascending aorta: case report

Mohamed Elhudairy, Naif Alkhushi, Osman Al‑Radi, Khadijah Maghrabi, Gaser AbdelmohsenKing Abdul-Aziz University. Kasr Al Ainy School of Medicine and Cairo University.Saudi Arabia and Egypt Egypt Heart JournalEgypt Heart J 2025; 77: DOI: 10.1186/s43044-025-00614-6 AbstractBackground: Anomalous origin of the right pulmonary artery (AORPA) from the ascending aorta is a rare congenital anomaly, representing approximately 0.12% of all congenital

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