Class 1. Pulmonary Hypertension Associated with Congenital Cardiovascular Disease

Timely PAH Identification in Adults With Repaired Congenital Heart Disease? The ACHD-QuERI Registry Insights

Michael J. Landzberg, Curt J. Daniels, Paul Forfia, Vallerie V. McLaughlin, Karimah S. Bell Lynum, Mona Selej, Alexander R. OpotowskyHarvard Medical School, Brigham and Women’s Hospital and Boston Children’s Hospital. Ohio State University College of Medicine and Nationwide Children’s Hospital. Temple University Hospital. University of Michigan Medical Center. Actelion Pharmaceuticals US, Inc. Cincinnati Children’s Hospital […]

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Survival and Risk Factors for Mortality in Infants With Congenital Heart Disease in South Korea

Jue Seong Lee, Jehe Kwon, Hannah Cho, Ju Sun Heo, Kee Soo Ha, Gi Young Jang, O Kyu Noh, Jun Eun ParkKorea University Medical Center and Korea University College of Medicine. University of Oxford. Ajou University School of Medicine. Republic of Korea In VivoIn Vivo 2024; 38: 1984-1992DOI: 10.21873/invivo.13655 AbstractBackground/aim: The survival of patients with congenital heart

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Raghib Syndrome and Pulmonary Arterial Hypertension in a Pediatric Patient: Case Report and Literature Review

Liliana Gozar, Maria Oana Săsăran, Marius Cătălin Cosma, Daniela Toma, Andreea Georgiana Nan, Horea Gozar“George Emil Palade” University of Medicine, Pharmacy, Sciences and Technology. Emergency Institute for Cardiovascular Diseases and Transplantation. Clinical County Hospital Mureș. Romania Journal of Clinical MedicineJ Clin Med 2024; 13: DOI: 10.3390/jcm13123623 AbstractBackground: Raghib syndrome is a rare malformation complex consisting of the

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Identifying Key Biomarkers in Pediatric Pulmonary Hypertension: An Investigative Approach

Farida Mindubayeva, Lyudmila Akhmaltdinova, Mariya Ospanova, Bibigul Tukbekova, Zhanat Bolatbekuly, Yuliya Niyazova, Yelena Salikhova, Olga Avdienko, Meruert AkhmetovaKaraganda Medical University. Multiprofile Hospital No. 2 of Karaganda.Kazakhstan ChildrenChildren 2024; DOI: 10.3390/children11060737 AbstractThis study assesses the utility of early biomarkers-5-hydroxyindoleacetic acid (5-HIAA) and insulin-like growth factor 1 (IGF-1)-for diagnosing and monitoring pulmonary hypertension (PH) in children with congenital

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Embolization treatment of right pulmonary artery agenisis with patent ductus arteriosus causing pulmonary hypertension and hemoptysis: a case report and literature review

Fan Wei, Chang Yaowen, Wang WenhuiFirst Clinical Medical College of Lanzhou University and First Hospital of Lanzhou University.China Journal of Cardiothoracic SurgeryJ Cardiothorac Surg 2024; 19: DOI: 10.1186/s13019-024-02883-9 AbstractAs the pediatric patient with right pulmonary artery agenesis (PAA) matured, she progressively presented symptoms of pulmonary hypertension and hemoptysis. There is limited clinical literature on this condition,

Embolization treatment of right pulmonary artery agenisis with patent ductus arteriosus causing pulmonary hypertension and hemoptysis: a case report and literature review Read More »

Erosion of Pulmonary Artery Banding into the Cardiovascular System: A First Case Report

Manouchehr Hekmat, Hamid Ghaderi, Zahra Ansari Aval, Seyedeh Adeleh Mirjafari, Mandana HekmatShahid Beheshti University of Medical Sciences. Ali-Asghar Children’s Hospital and Iran University of Medical Sciences.Iran ARYA AtherosclerosisARYA Ateroscler 2023; 19: 63-68 DOI: 10.48305/arya.2023.31062.2714 AbstractThere have been very rare reports on the migration of foreign bodies that are left or implanted in the body, and so

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Right ventricular fibrosis in adults with uncorrected secundum atrial septal defect and pulmonary hypertension: a cardiovascular magnetic resonance study with late gadolinium enhancement, native T1 and extracellular volume

Fatwiadi Apulita Ginting Munte, Elen Elen,Olfi Lelya, Estu Rudiktyo, Radityo Prakoso, Oktavia LilyasarUniversity of Indonesia. Indonesia Frontiers in Cardiovascular MedicineFront Cardiovasc Med 2024; DOI: 10.3389/fcvm.2024.1395382 AbstractIntroduction: Right ventricular (RV) fibrosis represents both adaptive and maladaptive responses to the overloaded RV condition. Its role in pulmonary hypertension (PH) associated with secundum atrial septal defect (ASD), which is the

Right ventricular fibrosis in adults with uncorrected secundum atrial septal defect and pulmonary hypertension: a cardiovascular magnetic resonance study with late gadolinium enhancement, native T1 and extracellular volume Read More »

Impact of Portal Flow on the Prognosis of Children With Congenital Portosystemic Shunt: A Multicentric Observation Study in Japan

Hajime Uchida, Masato Shinkai, Hiroomi Okuyama, Takehisa Ueno, Mikihiro Inoue, Toshihiro Yasui, Eiso Hiyama, Sho Kurihara, Yasunasru, Sakuma, Yukihiro Sanada, Akinobu, Taketomi, Shohei Honda, Motoshi Wada, Ryo Ando, Jun Fujishiro, Mariko Yoshida, Yohei Yamada, Hiroo Uchida, Takahisa Tainaka, Mureo Kasahara, Japanese Society of Pediatric Splenology PortalvenologyNational Center for Child Health and Development. Kanagawa Children’s Medical

Impact of Portal Flow on the Prognosis of Children With Congenital Portosystemic Shunt: A Multicentric Observation Study in Japan Read More »

The multisystem nature of isomerism: left isomerism complicated by Abernethy malformation and portopulmonary hypertension

Megan L. Ringle, Rohit Loomba, John C. Dykes, Danyal Khan, David Schidlow, Gil WernovskyLucile Packard Children’s Hospital and Stanford University School of Medicine. Advocate Children’s Hospital and Chicago Medical School. Nicklaus Children’s Hospital. Boston Children’s Hospital and Harvard Medical School. Children’s National Hospital.United States Cardiology in the YoungCardiol Young 2021; 31: 532-540DOI: 10.1017/S1047951121000809 AbstractIsomerism, also referred

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An Infant with High-Output Heart Failure and Pulmonary Hypertension Resulting from a Giant Cutaneous Hemangioma

Andrew A. Lawson, Wayne H. Franklin, Nicolas F. M. Porta, Alan Nugent, Amanda HauckAnn & Robert H. Lurie Children’s Hospital of Chicago and Northwestern University Feinberg School of Medicine. Loyola University Stritch School of Medicine.United States Pediatric CardiologyPediatr Cardiol 2024; DOI: 10.1007/s00246-024-03528-3 AbstractWe present the clinical course of an 8-month-old infant with a giant cutaneous hemangioma

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