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

Reduced Right Ventricular Size and Function in Adolescents and Adults Born Preterm

Zachary W. Blair, Alvin Chandra, Gregory P. Barton, Nataly Sanchez Solano, Jarett D. Berry, Kara N. GossUniversity of Texas Southwestern Medical Center. Parkland Health. University of Texas Health Tyler. United States Journal of the American Society of EchocardiographyJ Am Soc Echocardiogr 2025; DOI: 10.1016/j.echo.2025.04.007 AbstractBackground: Adults born premature have smaller cardiac chamber sizes, and some develop right […]

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Novel Use of Drug-Coated Balloon Angioplasty to Treat Pulmonary Vein Stenosis

Saloni Agrawal, Kali A. Hopkins, Ali N. Zaidi, Barry LoveMount Sinai Hospital. Mount Sinai Fuster Heart Hospital.United States Journal of the American College of Cardiology Case ReportsJACC Case Rep 2024; 29: DOI: 10.1016/j.jaccas.2024.102613 AbstractPulmonary vein stenosis is challenging to treat due to high rate of recurrence. Multiple interventions exist but are limited by high rates of

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Characteristics and sex differences in bronchopulmonary dysplasia-related pulmonary hypertension

Dansha Zhou, Ting Wang, Yuqin Chen, Yulin Zheng, Yingzhen Zhou, Mingxiang Zhang, Aofeng Liu, Biao Hu, Shuang Fu, Ruixian Wu, Wei Chen, Xiaoli Jiang, Zehui Ye, Yuan Shi, Zhou Fu, Jian WangFirst Affiliated Hospital of Guangzhou Medical University and Guangzhou Medical University. Children’s Hospital of Chongqing Medical University. China BioMedical Central Pulmonary MedicineBMC Pulm Med

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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 »

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

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TGFBI regulates pulmonary vascular remodeling through endothelial-to-mesenchymal transition in pulmonary arterial hypertension

Da Eun Roh, Na Rae Park, Bo Geum Choi, Youra Kang, Jung-Eun Kim, Yeo Hyang KimKyungpook National University, Kyungpook National University Children’s Hospital and Kyungpook National University Hospital. Republic of Korea Biochemical and Biophysical Research CommunicationsBiochem Biophys Res Commun 2025; 751: DOI: 10.1016/j.bbrc.2025.151435 AbstractPulmonary arterial hypertension (PAH) is a progressive disorder characterized by elevated pulmonary artery

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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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Pulmonary hypertension in infancy: a reversible cause

Cassandra Campbell, Kawaljeet Singh, Mark Weems, Panjit PhilipUniversity of Tennessee Health Science Center.United States British Medical Journals Case ReportsBMJ Case Rep 2025; 18:DOI: 10.1136/bcr-2024-263731 AbstractA term, healthy infant presented with respiratory distress and severe pulmonary hypertension (PH). With an unclear aetiology and the intent to decrease right ventricular afterload, pulmonary vasodilators were initiated. Follow-up imaging revealed

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His-Bundle Pacing for Pulmonary Hypertension With Bradycardia in Congenital Heart Disease: A Case Report

Daiji Takeuchi, Takashi Fujii, Tomomi Nishimura, Kei Inai, Morio ShodaTokyo Women’s Medical University.Japan Pacing and Clinical ElectrophysiologyPacing Clin Electrophysiol 2024; DOI: 10.1111/pace.15098 AbstractBradycardia, atrial tachyarrhythmia, heart failure, residual shunts, and pulmonary hypertension (PH) are significant problems after congenital heart disease surgery. We performed His-bundle pacing (HBP) for drug-resistant PH with bradycardia in a woman post-total anomalous

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Late-Onset Noninfectious Pulmonary Complications after Hematopoietic Stem Cell Transplantation

Andrew C. Harris, Kimia Ganjaei, Camila Vilela, Alexander GeyerMemorial Sloan Kettering Cancer Center. Lenox Hill Hospital and Northwell Health. United States Transplantation and Cellular TherapyTransplant Cell Ther 2024; 30: DOI: 10.1016/j.jtct.2024.05.022 AbstractAbstract Not Available CategoryClass V. Pulmonary Hypertension Associated with Hematological, Systemic, Metabolic and Other DisordersReview Articles Concerning Pulmonary Vascular Disease Age Focus: Pediatric Pulmonary Vascular

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