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Gap between guidelines and practice: echocardiography reporting in neonatal pulmonary hypertension

Sophia Gremont, Eveliina Ronkainen, Merja KallioUniversity of Oulu. Oulu University Hospital. Helsinki University Hospital, University of Helsinki.Finland Cardiology in the YoungCardiol Young 2026; DOI: 10.1017/S104795112611292X AbstractObjectives: Targeted neonatal echocardiography is increasingly integrated into neonatal care and plays a crucial role in the evaluation and management of persistent pulmonary hypertension of the newborn. The objective of this study […]

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Pediatric pulmonary hypertension registry: Single-center experience from India

Wadile Santosh, Mishra Arpita, Banpurkar Ashishkumar Moreshwar, Raeen Shahena Parveen, Kulkarni SnehalSri Sathya Sai Sanjeevani Centre for Child Heart Care and Training in Pediatric Cardiac Skills.India Annals of Pediatric CardiologyAnn Pediatr Cardiol 2026; 19: 14-22DOI: 10.4103/apc.apc_181_24 AbstractBackground: Pulmonary hypertension (PH) is a rare and usually irreversible disease, eventually leading to right heart failure (RHF). There are multiple

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Surgical management of complex congenital heart diseases in the context of South-South cooperation: case series

Laurence Carole Ngo Yon, Hermann Nestor Tsague Kengni, Godwin Sharau, Deogratias Nkya, Stella Mongella, Flora Fondjo, Alex Loth, Vivienne Mlawi, Salvatore AgatiUniversity of Yaounde I. Yaounde General Hospital. Jakaya Kikwete Cardiac Institute. Catholic University of Central Africa. San Vincenzo Hospital in Taormina.Cameroon, Tanzania and Italy PanAfrican Medical JournalPan Afr Med J 2026; 53: DOI: 10.11604/pamj.2026.53.21.49748 AbstractComplex

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Antenatally diagnosed severe congenital pulmonary airway malformation requiring life-saving lobectomy in the early neonatal period: A case report

Maroua El Ouaer, Hayet Ben Hamida, Tasnim Frigui, Seifeddine Ben Hammouda, Samia Bel Hssan, Amina Ben SalemUniversity of Monastir. Teaching Hospital of Monastir. Tunisia Radiology Case ReportsRadiol Case Rep 2026; 21: 3039-3045DOI: 10.1016/j.radcr.2026.04.025 AbstractCongenital pulmonary airway malformation (CPAM) ranges from asymptomatic lesions to life-threatening neonatal presentations. Large lesions can lead to severe respiratory failure requiring urgent

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Hepatopulmonary syndrome as presentation of pediatric metabolic dysfunction-associated steatohepatitis

Shruti Sakhuja, Stacey S. Beer, Kalyani R. Patel, Alexiss M. Williams, Nhu Thao Galvan, John A. Goss, Krupa R. MysoreBaylor College of Medicine and Texas Children’s Hospital. United States Journal of Pediatric Gastroenterolgy and Nutrition ReportsJPGN Rep 2026; 7: 362-365DOI: 10.1002/jpr3.70139 AbstractChildhood obesity is rising and leading to serious co-morbidities, among which is metabolic dysfunction-associated steatotic

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Safety of Sildenafil in Premature Infants with Severe Bronchopulmonary Dysplasia (SILDI-SAFE): A Randomized Controlled Trial

Wesley M. Jackson, Henry P. Foote, Nicole Stephenson, Steven M. Kemp, Ryan T. Moore, Christopher R. Nitkin, Dan Stewart, Gloria S. Pryhuber, John T. Berger, Ankita Shukla, Amand England, Stephanie M. Ford, Lance A. Parton, Jennifer F. Check, Mina H. Hanna, Megan Lagoski, Ramesh Krishnan, Kristen T. Leeman, Shilpa Vyas-Read, Mark L. Hudak, Anup C.

Safety of Sildenafil in Premature Infants with Severe Bronchopulmonary Dysplasia (SILDI-SAFE): A Randomized Controlled Trial Read More »

Experience with selexipag in triple therapy for pulmonary arterial hypertension in Chinese children

Meng Li, Yingchun Wang, Xiaoyu Hu, Haizhao Zhao, Weida Lu, Yuan Ji, Xiaopei CuiQilu Hospital and Cheeloo College of Medicine of Shandong University. China BioMedical Central PediatricsBMC Pediatr 2026; DOI: 10.1186/s12887-026-06954-9 AbstractBackground: Selexipag is an orally effective prostacyclin receptor agonist that has been approved for treating pulmonary arterial hypertension (PAH) in adults but is still used off-label

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Transcatheter Interventional Options in Pulmonary Vein Stenosis: When to Stent?

Heidi Van Christopher J. Petit, Oliver M. BarryColumbia University Vagelos College of Physicians and Surgeons and NewYork-Presbyterian Hospital Morgan Stanley Children’s HospitalUnited States Seminars in Thoracic and Cardiovascular Surgery Pediatric Cardiac Surgery AnnualSemin Thorac Cardiovasc Surg Pediatr Card Surg Ann 2026;DOI: 10.1053/j.pcsu.2026.02.007 AbstractPulmonary vein stenosis (PVS) is a rare and aggressive condition in infants and children,

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Successful Completion of High-Risk Neuroblastoma Therapy After Stabilization of Pulmonary Hypertension With Tadalafil

Takuma Sugahara, Hirohito Kubota, Tatsuya Kamitori, Koichi Matsuda, Shiro Baba, Katsutsuga Umeda, Junko TakitaKyoto University.Japan Pediatric InternationalPediatr Int 2026; DOI: 10.1111/ped.70427 AbstractAbstract Not Available CategoryMedical Therapy. Efficacy or Lack of Efficacy Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Fresh (PHresh). Less than 1-2 years since publication Article Access Free PDF File or Full

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Pulmonary Vein Stenosis Medical Therapy: Current and on the Horizon

Mudit Gupta, David B. FrankPerelman School of Medicine at the University of Pennsylvania and Children’s Hospital of PhiladelphiaUnited States Seminars in Thoracic and Cardiovascular Surgery Pediatric Cardiac Surgery AnnualSemin Thorac Cardiovasc Surg Pediatr Card Surg Ann 2026;DOI: 10.1053/j.pcsu.2026.02.006 AbstractPulmonary vein stenosis (PVS) is a severe vascular obstructive lesion historically associated with poor survival. As outcomes have

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