Fresh (PHresh). Less than 1-2 years since publication

Fetal left pulmonary artery-to-left atrial fistula with aplasia of the left lung: successful postnatal transcatheter closure

Bilgehan Betül Biçer, Hayrettin Hakan Aykan, Tevfik Karagöz, Ercan TutarHacettepe University and a Private Clinic.Turkey Cardiology in the YoungCardiol Young 2025; DOI: 10.1017/S1047951125001714 AbstractIntroduction: In the presence of fetal cardiomegaly, when there is no cardiac malformation or dysfunction, systemic or pulmonary arteriovenous malformations that may cause volume loading should be sought. We aimed to present a fetus […]

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A large pulmonary arteriovenous malformation in an adolescent girl – timely diagnosis and treatment: a case report

Shilpa Krishnapura Lakshiminarayana, Bangalore Srinivas Pranathi, Dhanalakshmi Kumble, Mallesh Kariyappa, Usha Mk SastryVani Vilas Hospital and Bangalore Medical College and Research Institute. Sri Jayadeva Institute of Cardiovascular Sciences and Research.India Paediatrics and International Child HealthPaediatr Int Child Health 2025; DOI: 10.1080/20469047.2025.2515723 AbstractPulmonary arteriovenous malformation (PAVM) is a rare, pathological, intrapulmonary, right-to-left shunt resulting from abnormal communication

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Pediatric Pulmonary Arteriovenous Malformations in Patients with Hereditary Hemorrhagic Telangiectasia: Screening, Diagnosis, and Management

Claire S. Kaufman, Minh Anh Nguyen, Amy Bezold, Mark S. ChesnuttOregon Health and Science University. United States Journal of Clinical MedicineJ Clin Med 2025; 14: DOI: 10.3390/jcm14113739 AbstractPulmonary arteriovenous malformations (PAVMs) are abnormal communications between a pulmonary artery and pulmonary vein that bypass the capillary bed, resulting in right-to-left shunting. The majority of PAVMs are associated

Pediatric Pulmonary Arteriovenous Malformations in Patients with Hereditary Hemorrhagic Telangiectasia: Screening, Diagnosis, and Management Read More »

Ten-Year Experience with Pediatric Pulmonary Vein Interventions: Adverse Events and Institutional Strategies for Safety

Daijo Takajo, Paul J. Critser, Amr Matoq, Sarosh P. Batlivala, Shabana Shahanavaz, Russel HirschCincinnati Children’s Hospital Medical Center. University of Cincinnati College of Medicine. United States Pediatric CardiologyPediatr Cardiol 2025; DOI: 10.1007/s00246-025-03955-w AbstractPulmonary vein stenosis (PVS) in pediatric patients is associated with significant morbidity and requires repeated transcatheter interventions to maintain pulmonary vein patency. While these

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The effectiveness of pulmonary hypertension screening in infants born preterm

Stephanie Vachon, Rajiv Devanagondi, Andrew Dylag, Hongyue Wang, Gloria PryhuberUniversity of Rochester Medical Center. University of Iowa Stead Family Department of Pediatrics. United States Early Human DevelopmentEarly Hum Dev 2025; DOI: 10.1016/j.earlhumdev.2025.106342 AbstractObjective: To determine if pulmonary hypertension (PH) screening in at-risk infants born preterm reduces morbidity and/or NICU length of stay.Study design: This single-center retrospective cohort chart

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c-Myc promotes metabolic reprogramming in pulmonary hypertension via the stimulation of glutaminolysis and the reductive tricarboxylic acid cycle

Manivannan Yegambaram, Xutong Sun, Qing Lu, Alejandro Garcia Flores, Marina Zemskova, Jamie Soto, Adam Rauckhorst, Emin Maltepe, Ting Wang, Jeffrey R. Fineman, Stephen M. BlackHerbert Wertheim College of Medicine and Florida International University. University of California San Francisco. United States Redox BiologyRedox Biol 2025; DOI: 10.1016/j.redox.2025.103765 AbstractEndothelial cell (EC) dysfunction is key in initiating and progressing

c-Myc promotes metabolic reprogramming in pulmonary hypertension via the stimulation of glutaminolysis and the reductive tricarboxylic acid cycle Read More »

Mitochondrial cardiomyopathies: navigating through different clinical and management pictures between adult and paediatric forms

Rachele Adorisio, Nicoletta Cantarutti, Barbara Siri, Elisa Bellettini, Gessica Ingrasciotta, Erica Mencarelli, Francesca Graziani, Rosa Lillo, Sara Di Marzio, Corrado Di Mambro, Fabrizio Drago, Antonio Amodeo, Diego MartinelliBambino Gesù Children’s Hospital. University of Turin. Fondazione Policlinico Universitario A. Gemelli.Italy Frontiers in Cardiovascular MedicineFront Cardiovasc Med 2025; 12: DOI: 10.3389/fcvm.2025.1621096 AbstractMitochondrial diseases (MD) represent a group of

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Indications for pediatric lung transplantation in 2025: A new era

Nicholas Avdimiretz, Don Hayes, Melinda Solomon, Nicolaus Schwerk, Christian BendenBritish Columbia Children’s Hospital and University of British Columbia. Cincinnati Children’s Hospital Medical Center and University of Cincinnati College of Medicine. Hospital for Sick Children and University of Toronto. Hannover Medical School. Boston Children’s Hospital and Harvard Medical School. University of Zurich.Canada, United States, Germany and

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Giant Omphalocele: Systematic Review of Pulmonary Complications and Implications for Neonatal Care

Joana Peixoto, Joana Neto, Susana Pissarra, Inês Azevedo, Henrique Soares, Gustavo RochaUniversidade do Porto. Centro Hospitalar Universitário de São João. Portugal European Journal of Pediatric SurgeryEur J Pediatr Surg 2025; DOI: 10.1055/a-2649-0781 AbstractThe primary objectives were to know the prevalences of pulmonary hypoplasia (PH), persistent pulmonary hypertension of the newborn (PPHN), and mortality in newborn infants

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Enhancing Drug Development for Paediatric Pulmonary Hypertension-An Integrative Perspective

Steven H. Abman, Sylvia M. Nikkho, Rolf M. F. Berger, Maria Jesus del Cerro, Eric D. Austin, Maurice Beghetti, Dunbar Ivy, Megan Griffiths, Anne Hilgendorff, Steven H. Kawut, Usha S. Krishnan, Mary P. Mullen, Shahin Moledina, Bernard Thébaud, Norman StockbridgeUniversity of Colorado School of Medicine and Children’s Hospital Colorado. Bayer AG. Beatrix Children’s Hospital, University

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