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Physiological-Based Cord Clamping and Early Oxygenation in Newborns With Transposition of the Great Arteries: A Quality Improvement Study Protocol

Jesse A. Weeda, Arjan B. te Pas, Zsuzsanna Nagy, Gábor H. Kovács, Miklós Szabó, Gergo} Leipold, Nariae Baik-Schneditz, Bernhard Schwaberger, Christian Heiring, Emma Louise Malchau Carlsen, Monique C. Haak, Nico A. Blom, Stuart B. Hooper, Janneke Dekker, Roel L.F. van der PalenWillem-Alexander Children’s Hospital and Leiden University Medical Center. Semmelweis University. Gottsegen National Cardiovascular Centre. […]

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Early Detection of Isolated Transient Right Ventricular Hypertrophy in a Term Neonate: the Neonatologist’s Role

Evgeniya Babacheva, Evangelia Giannousiou, Maria Florou, Apostolia Stampouli, Maria Lithoxopoulou, Christos TsakalidisAristotle University of Thessaloniki and “Papageorgiou” Hospital.Greece MaedicaMaedica 2026; 21: 539-542DOI: 10.26574/maedica.2026.21.2.539 AbstractRight ventricular hypertrophy (RVH) is a rare finding in the neonatal age. Multiple pathological conditions are associated with the development of RVH, such as metabolic diseases, hereditary disorders and premature closure of the

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Bronchiectasis in Inborn Errors of Immunity: Prevalence, Predictors, and Cardiopulmonary Complications in a Genetically Characterized Cohort

Diana Marangu-Boore, Katherine Myint-Hpu, Esther Kang, Luigi D. Notarangelo, Ottavia M. DelmonteNational Institutes of Health. University of Nairobi. United States and Kenya Journal of Clinical ImmunologyJ Clin Immunol 2026; DOI: 10.1007/s10875-026-02044-8 AbstractPurpose: Bronchiectasis poses a serious but incompletely defined burden in patients with inborn errors of immunity (IEI). We determined its prevalence, independent predictors, and cardiopulmonary complications

Bronchiectasis in Inborn Errors of Immunity: Prevalence, Predictors, and Cardiopulmonary Complications in a Genetically Characterized Cohort Read More »

Preliminary Report of a Nationwide Prospective Cohort of Congenital Diaphragmatic Hernia in Korea

Jiyoon Jeong, Byong Sop Lee, Hoseon Eun, Seung Han Shin, So Yoon Ahn, Shin Yun Byun, Eun Song Song, on behalf of the Korean Congenital Diaphragmatic Hernia CohortAsan Medical Center and University of Ulsan College of Medicine. Severance Hospital and Yonsei University College of Medicine. Seoul National University Hospital and Seoul National University College of

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Whole blood and tissue miRNA expression profiles in children with congenital heart disease-associated pulmonary arterial hypertension

Halis Yilmaz, Deniz Elcik, Aydin Tuncay, Ozge Pamukcu, Serpil Taheri, Fatma Sena Topcu, Ismail Duzgun, Nazmi Narin, Ecmel Mehmetbeyoglu Duman, Begum Er, Gökmen ZararsizErciyes University School of Medicine and Erciyes University.Turkey Scientific ReportsSci Rep 2026; DOI: 10.1038/s41598-026-61056-x AbstractPulmonary arterial hypertension (PAH) is a major complication of congenital heart disease (CHD) with left-to-right shunts. Early identification of

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Perinatal survival and long-term neurodevelopmental outcomes of congenital chylothorax

Hideyuki Hawaka, Tomoyuki Shimokaze, Jun Shibasaki, Hiromi Nagase, Tomoko Saito, Hiroshi Ishikawa, Katsuaki ToyoshimaKanagawa Children’s Medical Center. Hiroshima City Hiroshima Citizens Hospital. Japan Pediatric ResearchPediatr Res 2026; DOI: 10.1038/s41390-026-05271-2 AbstractBackground: Congenital chylothorax carries a poor prognosis, particularly with delivery at <32 weeks. Survival outcomes under consistent management prioritizing pregnancy prolongation despite worsening hydrops, as well as long-term

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Inhibition of thrombospondin-1 signaling prevents experimental bronchopulmonary dysplasia

Chantal Gaudet, Kathrine L. Daniel, Sophie Holcik, Ali Hamraghani, Behzad Yeganeh, Robert P JankovChildren’s Hospital of Eastern Ontario. University of Ottawa. Canada American Journal of Physiology Lung Cellular and Molecular PhysiologyAm J Physiol Lung Cell Mol Physiol 2026; DOI: 10.1152/ajplung.00090.2026 AbstractBronchopulmonary dysplasia (BPD) is a neonatal lung injury characterized by inflammation, and alveolar and vascular hypoplasia

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Perioperative anesthetic management in pediatric heart transplantation: a single-center descriptive study involving 27 patients

Ya-fei Cheng, Cong-li Meng, Yi-ru Wang, Lin Chen, Ya-qun Ma, Wen-zhi Guo, Hang GuoSeventh Medical Center to Chinese PLA General Hospital. Southern Medical University.China Frontiers in PediatricsFront Pediatr 2026; 14: DOI: 10.3389/fped.2026.1842135 AbstractBackground: Orthotopic heart transplantation is the standard treatment for pediatric end-stage heart disease. Due to the wide age range and high physiological heterogeneity among pediatric

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Repair of Sinus Venosus Atrial Septal Defect in 2 Patients With Severe Pulmonary Arterial Hypertension

Ryo Sakuma, Gareth Morgan, Elizabeth Yeung, Benjamin S. Frank, Charles Simpkin, Dunbar IvyUniversity of Colorado School of Medicine.United States Pulmonary CirculationPulm Circ 2026; 16: DOI: 10.1002/pul2.70285 AbstractPretreatment with targeted pulmonary arterial hypertension (PAH) therapy in adults with unrepaired atrial septal defects (ASDs) has been increasingly reported as a means to improve pulmonary hemodynamics and expand candidacy

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JCS/JPCPHS 2025 Guideline on Pulmonary Hypertension and Pulmonary Embolism/Deep Vein Thrombosis

Yuichi Tamura, Kenya Kusunose, Yugo Yamashita, Teiji Akagi, Masanori Atsukawa, Yoshihiro Fukumoto, Ayumi Goda, Shinya Goto, Masaru Hatano, Masataka Ikeda, Keiichi Ishida, Masaharu Kataoka, Masataka Kuwana, Hiromi Matsubara, Makoto Mo, Tetsutaro Nagaoka, Takeshi Ogo, Yoshinori Okada, Seiichiro Sakao, Hirofumi Sawada, Toshiro Shinke, Nobuhiro Tanabe, Norikazu Yamada, Hiroyuki Yamagishi, Shingo Yano, Kohtaro Abe, Shiro Adachi, Kazuya

JCS/JPCPHS 2025 Guideline on Pulmonary Hypertension and Pulmonary Embolism/Deep Vein Thrombosis Read More »

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