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

Antithrombotic Therapy Use in Children With Pulmonary Hypertension

Meredith J. O’Neil, Lynn A. Sleeper, Nidhy P. Varghese, Paul J. Critser, Eric D. Austin, Catherine M. Avitabile, Angela Bates, Erika B. Rosenzweig, Carly E. Byrd, Patrick D. Evers, Stephanie S. Handler, Rachel K. Hopper, Emma O. Jackson, Roberta L. Keller, Usha S. Krishnan, Minmin Lu, Jessica Maclean, Raysa Morales‐Demori, Mary P. Mullen, Meredith Riker,

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Evaluation of Pediatric Cardiologists’ Knowledge Levels Regarding Pulmonary Hypertension: Commonly Misunderstood Concepts

Serdar Kula, Gizem Karkin Tozlu, Meliz YudaerGazi University School of Medicine and Gazi University Graduate School of Informatics.Turkey Türk Kardiyoloji Derneği Arşivi (Archives of the Turkish Society of Cardiology)Turk Kardiyol Dern Ars 2026; DOI: 10.5543/tkda.2026.13808 AbstractObjective: This study aimed to identify common misconceptions regarding pulmonary hypertension (PH) among pediatric cardiologists.Method: Before an online educational session

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Case Report: A pediatric case of multifocal Streptococcus intermedius brain abscesses as the initial manifestation of SMAD4-associated juvenile polyposis-hereditary hemorrhagic telangiectasia overlap syndrome

Nala Al-Khatib, Patricia Martin, Katherine Sinchek, Colleen Buhrfiend, Lubov Romantseva, Edith Chernoff, David C. NguyenRush University Medical Center. Ann & Robert H. Lurie Children’s Hospital of Chicago. University of Chicago. United States Frontiers in PediatricsFront Pediatr 2026; 14: DOI: 10.3389/fped.2026.1866003 AbstractHereditary hemorrhagic telangiectasia (HHT) is a rare genetic disease characterized by epistaxis, telangiectasias, and arteriovenous

Case Report: A pediatric case of multifocal Streptococcus intermedius brain abscesses as the initial manifestation of SMAD4-associated juvenile polyposis-hereditary hemorrhagic telangiectasia overlap syndrome Read More »

A Case of Pulmonary Hypertensive Crisis Following Treatment of Retinopathy of Prematurity in an Extremely Preterm Infant

Naofumi Hanyu, Shonosuke Nara, Toshihiro Nakayama, Gaku YamanakaTokyo Medical University.Japan Pediatrics InternationalPediatr Int 2026; 68: DOI: 10.1111/ped.70558 AbstractAbstract Not Available CategoryClass III. Pulmonary Hypertension Associated with Lung DiseaseClass I. Drug-induced and Toxin-induced Pulmonary Hypertension Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Fresh (PHresh). Less than 1-2 years since publication Article Access Free

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Rare Coding Variants in FOXF1 are Associated with Pulmonary Arterial Hypertension

Jose Gomez-Arroyo, Arjan C. Houweling, Alex V. Postma, Tushar Ganjawala, Dennis Dooijes, Harm Jan Bogaard, Jurjan Aman, Rob Zwart, Joseph A. Kizmiller, Gabriëla G. Edel, Aleksey Porollo, Lilian J. Meijboom, Nidhy P. Varghese, Philip Hale, Jason Hong, Na Zhu, Carrie L. Welch, Yufeng Shen, Francis X. McCormack, Micheala A. Aldred, Matthew T. Weirauch, Robbert J.

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Persistent Pulmonary Hypertension of the Newborn: A Practical Review for UK Level 2 Local Neonatal Units

Elnazeer MohamedEast Surrey Hospital.United Kingdom CureusCureus 2026; 18: DOI: 10.7759/cureus.116003 AbstractIn persistent pulmonary hypertension of the newborn (PPHN), pulmonary vascular resistance fails to fall after birth, resulting in right-to-left shunting and hypoxemia out of proportion to the underlying lung disease. Inhaled nitric oxide (iNO) is generally provided by tertiary neonatal intensive care units and neonatal

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Transcatheter Potts Shunt in Pulmonary Arterial Hypertension After Patent Ductus Arteriosus Closure

Zhuoyuan Xu, Yiwei Chen, Xiafeng, Yanjun Sun, Jie Bai, Zhuoming Xu, Lijun Fu, Hao ZhangNational Children’s Medical Center, Shanghai Children’s Medical Center and Shanghai Jiao Tong University School of Medicine. Shanghai Institute of Pediatric Congenital Heart Disease.China Pulmonary CirculationPulm Circ 2026; 16:DOI: 10.1002/pul2.70422 AbstractWe report the case of an 18-year-old female with progressive, end-stage pulmonary

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Neonatal extracorporeal membrane oxygenation in congenital urinary tract obstruction with pulmonary hypoplasia: a case complicated by alveolar capillary dysplasia emphasizing importance of early rapid genetic testing

Ahreen Allana, Syed Talha Ahmed, Tavleen Sandhu, Sadori Khawaja, Keri Drake, Laura Mackay, Abhishek MakkarChildren’s Hospital of Dallas, University of Texas Southwestern.United States Pediatric NephrologyPediatr Nephrol 2026; DOI: 10.1007/s00467-026-07550-w AbstractA late preterm male infant born at 36 weeks and 2 days of gestation with birth weight of 2.5 kg and prenatally diagnosed bilateral hydronephrosis, megaureter,

Neonatal extracorporeal membrane oxygenation in congenital urinary tract obstruction with pulmonary hypoplasia: a case complicated by alveolar capillary dysplasia emphasizing importance of early rapid genetic testing Read More »

Addressing micronutrient deficiencies and vitamin metabolism disorders in pediatric pulmonary hypertension: a strategic proposal for low- and middle-income countries

Mattia Pasquinucci, Marco Scaglione, Sofia Mezzalira, Luisa Bonsembiante, Mariaelena Zaffina, Pietro Pogacnik, Sara Bondanza, Ramona Marini, Maria E. Derchi, Davide MeneghessoSan Bassiano Hospital. Hôpital Universitaire Necker-Enfants Malades. University of Padua.  IRCCS Istituto Giannina Gaslini. Università degli Studi Gugliemo Marconi.Italy and France Frontiers in Cardiovascular MedicineFront Cardiovasc Med 2026; 13: DOI: 10.3389/fcvm.2026.1900356 AbstractBackground: Pediatric pulmonary hypertension

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Portopulmonary hypertension: an integrated approach to diagnosis, risk stratification, and management

Jesús Donate, Susana del Prado, Andrés Tenes, María Jesus del Cerro, Agustín Albillos, Luis TéllezHospital Universitario Ramón y Cajal and Universidad de Alcalá. Spain Annals of HepatologyAnn Hepatol 2026; DOI: 10.1016/j.aohep.2026.102466 AbstractPortopulmonary hypertension (PoPH) is a complex and underrecognized form of pulmonary arterial hypertension arising in the setting of portal hypertension, in which outcomes are

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