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Atrioventricular septal defect repair with severe pulmonary arterial hypertension: A novel surgical approach using a valved Potts shunt

Bastien Provost, Emmanuelle Fournier, Estibaliz Valdeolmillos, Guy Vaksmann, Emre BelliMarie Lannelongue Hospital. Hôpital Privé de La Louvière.France Journal of Thoracic and Cardiovascular Surgery TechniquesJTCVS Tech 2026; 47: DOI: 10.1016/j.xjtc.2026.102304 AbstractAbstract Not Available CategoryClass I. Pulmonary Hypertension Associated with Congenital Cardiovascular DiseaseSurgical and Catheter-mediated Interventions for Pulmonary Vascular Disease Age Focus: Pediatric Pulmonary Vascular Disease Fresh or […]

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Case Report: Prolonged extracorporeal membrane oxygenation as a deliberate operative adjunct for tracheobronchial reconstruction in a child with invasive aspergillosis

Marcin Łosin, Wojciech Karolak, Romuald Lango, Witold Rzyman, Monika Rosinski, Weronika Lotkowska, Piotr CzaudernaMedical University of Gdansk and University Clinical Center.Poland Frontiers in PediatricsFront Pediatr 2026; 14: DOI: 10.3389/fped.2026.1843892 AbstractWe report the case of a 6-year-old boy with newly diagnosed type 1 diabetes mellitus presenting in diabetic ketoacidosis, who developed a massive acquired tracheo-esophageal fistula (TEF)

Case Report: Prolonged extracorporeal membrane oxygenation as a deliberate operative adjunct for tracheobronchial reconstruction in a child with invasive aspergillosis Read More »

Single-center experience with aortopexy in pediatric tracheomalacia: a case series

Ali Tadayon, Shayan Yousufzai, Mehdi Forooghi, Shahdokht Abooali, Parisa Zare, Hossein Hosseini, Alireza Yousefi, Mostafa Poorkhosravani, Mostafa Moqadas, Omidreza AzhNamazi Hospital and Shiraz University of Medical Sciences.Iran Journal of Cardiothoracic SurgeryJ Cardiothorac Surg 2026; DOI: 10.1186/s13019-026-04415-z AbstractBackground: Tracheomalacia in infants often results from vascular compression and is frequently associated with multiple congenital anomalies. Aortopexy is a well-established

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Disease-related complications and risk factors in hemoglobin H disease in a Thai multicenter registry

Nattiya Teawtrakul, Duantida Songdej, Chattree Hantaweepant, Adisak Tantiworawit, Sasinee Hantrakool, Pornpun Sripornsawan, Pacharapan Surapolchai, Supanun Lauhasurayotin, Kitti Torcharus, Pranee Sutcharitchan, Noppacharn Uaprasert, Krissana Panrong, Napat Laoaroon, Patcharee Komvilaisak, Panachai Silpsamrit, Arunotai Meekaewkunchorn, Bunchoo Pongtanakul, Pimlak Charoenkwan & Red Blood Cell Disorders Study GroupSrinagarind Hospital and Khon Kaen University. Ramathibodi Hospital, Siriraj Hospital and Mahidol University.

Clinical Factors Associated with Ventilator-Free Days in Newborns with Persistent Pulmonary Hypertension of the Newborn: A Retrospective Cohort Study in Thailand

Sirichan Larpnarongchai, Gunlawadee Maneenil, Anucha Thatrimontrichai Supaporn Dissaneevate, Manapat Praditaukrit, Pattima PakhathirathienPrince of Songkla University.Thailand Journal of Clinical MedicineJ Clin Med 2026; 15: DOI: 10.3390/jcm15114377 AbstractBackground/Objectives: Ventilator-free days (VFDs) are a useful composite measure to assess both survival and duration of mechanical ventilation in critically ill patients. This study aimed to determine the factors associated with

Clinical Factors Associated with Ventilator-Free Days in Newborns with Persistent Pulmonary Hypertension of the Newborn: A Retrospective Cohort Study in Thailand Read More »

Contemporary Endothelial Genome Editing Technologies: Towards Precision Genetic Medicine for Vascular Diseases

You-Yang Zhou, Colin E. EvansAnn and Robert H. Lurie Children’s Hospital of Chicago and Northwestern University Feinberg School of Medicine. United States International Journal of Molecular SciencesInt J Mol Sci 2026; 27: DOI: 10.3390/ijms27115100 AbstractEndothelial dysfunction is a key characteristic of many diseases, including atherosclerosis, hypertension, heart failure, stroke, cancer, acute respiratory distress syndrome (ARDS), peripheral

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Evaluation and Management of Genetic Respiratory Disorders Presenting as Hypoxemic Respiratory Failure in the Newborn Infant

Jennifer A. Wambach, F. Sessions Cole, Lawrence M. NogeeWashington University School of Medicine and St. Louis Children’s Hospital. Johns Hopkins University. United States Clinics in PerinatologyClin Perinatol 2026; 53: 381-401DOI: 10.1016/j.clp.2026.03.003 AbstractHypoxemic respiratory failure is a common reason for admission to the neonatal intensive care unit for term and late preterm infants. Some infants have rare

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Management of Hypoxemic Respiratory Failure in the Newborn During Therapeutic Hypothermia

Paulina Hume, Luna Khanal, Satyan Lakshminrusimha, Deepika SankaranUniversity of California, Davis.United States Clinics in PerinatologyClin Perinatol 2026; 53: 317-332DOI: 10.1016/j.clp.2026.02.008 AbstractTherapeutic hypothermia (TH) is the gold standard for the management of hypoxic ischemic encephalopathy (HIE) in newborns. Both hypoxia and TH may contribute to an increase in pulmonary vascular resistance (PVR), resulting in persistent pulmonary hypertension

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Advances in the Management of Persistent Pulmonary Hypertension of the Newborn

Emily Mooers, Satyan Lakshiminrusimha, G. Ganesh KonduriMedical College of Wisconsin and Children’s Wisconsin. University of California and UC Davis Children’s Hospital.United States Clinics in PerinatologyClin Perinatol 2026; 53: 297-316DOI: 10.1016/j.clp.2026.02.003 AbstractThis article details an integrated approach to optimize management strategies for hypoxemic respiratory failure and hemodynamic instability in persistent pulmonary hypertension of the newborn (PPHN). Even

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Respiratory Management for the Infant with Congenital Diaphragmatic Hernia

Michelle J. Yang, Matthew Douglass, Ryan J. Carpenter, Bradley A. YoderUniversity of Utah School of Medicine and Primary Children’s Hospital.United States Clinics in PerinatologyClin Perinatol 2026; 53: 277-295DOI: 10.1016/j.clp.2026.02.002 AbstractCongenital diaphragmatic hernia (CDH) is a complex neonatal condition characterized by pulmonary hypoplasia and pulmonary hypertension, requiring specialized ventilatory management from birth through postoperative care. This article

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