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

Inhaled Nitric Oxide Treatment of Early Pulmonary Hypertension to Reduce the Risk of Death or Bronchopulmonary Dysplasia in Infants Born Extremely Preterm: A Masked Randomized Controlled Trial

Hussnain Mirza, Jorge Garcia, Matthew Zussman, Rajan Wadhawan, Julie Pepe, William OhAdvent Health for Children.United States Journal of PediatricsJ Pediatr 2024; DOI: 10.1016/j.jpeds.2024.114427 AbstractObjective: To determine whether inhaled nitric oxide (iNO) treatment of early pulmonary hypertension (PH) would decrease the risk of death or bronchopulmonary dysplasia (BPD) among infants born extremely preterm.Study design: This was a single-center, masked, […]

Inhaled Nitric Oxide Treatment of Early Pulmonary Hypertension to Reduce the Risk of Death or Bronchopulmonary Dysplasia in Infants Born Extremely Preterm: A Masked Randomized Controlled Trial Read More »

THBS1 mediates hypoxia driven EndMT in pulmonary hypertension

Bingming Peng, Yingzhen Zhou, Xingmeng Fu, Li Chen, Zhengxia Pan, Qijian Yi, Tengteng Zhao, Zhou Fu, Ting WangChildren’s Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders and Ministry of Education Key Laboratory of Child Development and Disorders. University of California, San Diego.China and United States Pulmonary CirculationPulm Circ 2024;

THBS1 mediates hypoxia driven EndMT in pulmonary hypertension Read More »

T follicular helper cell is essential for M2 macrophage polarization and pulmonary vascular remodeling in hypoxia-induced pulmonary hypertension

Cheng Li, Pingping Liu, Hao Zhu, Huan Yang, Jun Zha, Huiling Yao, Shaoze Zhang, Jin Huang, Guang Li, Gang Jiang, Yongliang Jiang, Aiguo DaiHunan Provincial People’s Hospital and First Affiliated Hospital of Hunan Normal University. Hunan Children’s Hospital. Changsha Central Hospital and University of South China. Hunan University of Chinese Medicine. China Respiratory ResearchRespir Res

T follicular helper cell is essential for M2 macrophage polarization and pulmonary vascular remodeling in hypoxia-induced pulmonary hypertension Read More »

Extracorporeal membrane oxygenation as bridge to transplant in severe pulmonary hypertension

Sophie Kruszona, Khalil Aburahma, Philipp Wand, Nunzio D. de Manna, Murat Avsar, Dmitry Bobylev, Carsten Müller, Julia Carlens, Alexander Weymann, Nicolas Schwerk, Tobias Welte, Bin Liu, Arjang Ruhparwar, Christian Kuehn, Jawad Salman, Mark Greer, Fabio IusHannover Medical School.Germany European Journal of Cardiothoracic SurgeryEur J Cardiothorac Surg 2024; DOI: 10.1093/ejcts/ezae420 AbstractObjectives: Severe pulmonary hypertension is the leading lung

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Management and Follow-Up of a Cohort of Neonates With Meconium Aspiration Syndrome Before and After the Revision of the 2015 Neonatal Resuscitation Program

Inês Silva Costa, Jose Alarcão, Ana Rodrigues Silva, Raquel HenriquesUnidade Local de Saúde (ULS) de Viseu Dão-Lafões. Unidade Local de Saúde (ULS) de Coimbra.Portugal CureusCureus 2024; 16: DOI: 10.7759/cureus.72894 AbstractIntroduction: Meconium aspiration syndrome (MAS) is a respiratory condition associated with high morbimortality. Standards of care changed over the years addressing its specificities, aiming to decrease poor respiratory

Management and Follow-Up of a Cohort of Neonates With Meconium Aspiration Syndrome Before and After the Revision of the 2015 Neonatal Resuscitation Program Read More »

Survival comparison in adults with congenital systemic to pulmonary shunt and borderline elevated pulmonary vascular resistance versus Eisenmenger syndrome

Jantaras Sengsim, Chodchanok Vijarnsorn, Prakul Chanthong, Paweena Chungsomprasong, Supaluck Kanjanauthai, Ploy Thammasate, Thita Pacharapakornpong, Nalin Chaiwangyen, Densiri Bositthipichet, Jarupim Soongswang, Teerapong Tocharoenchok, Ekarat Nitiyarom, Kriangkrai Tantiwongkosri, Thaworn Subtaweesin, Kritvikrom DurongpisitkulSiriraj Hospital and Mahidol University.Thailand Scientific ReportsSci Rep 2024; 14: DOI: 10.1038/s41598-024-81834-9 AbstractPulmonary arterial hypertension (PAH) associated with congenital heart disease (PAH-CHD) is a consequence of unrepaired

Survival comparison in adults with congenital systemic to pulmonary shunt and borderline elevated pulmonary vascular resistance versus Eisenmenger syndrome Read More »

Isolated Left Subclavian Artery, Multiple Ventricular Septal Defects, and Pulmonary Hypertension in a Child: A Case Report

Mohammad Reza Khalilian, Manouchehr Hekmat, Saeed Sadr, Abdolhossein Tavallai-Zavvareh, Tahmineh TahouriMofid Children’s Hospital, Shahid Firoozabadi Hospital, Shahid Modarres Educational Hospital and Shahid Beheshti University of Medical Sciences. Iran Canadian Journal of Cardiology Pediatric and Congenital Heart DiseaseCJC Pediatr Congenit Heart Dis 2024; 3: 221-224DOI: 10.1016/j.cjcpc.2024.07.001 AbstractAbstract not available CategoryClass I. Pulmonary Hypertension Associated with Congenital Cardiovascular

Isolated Left Subclavian Artery, Multiple Ventricular Septal Defects, and Pulmonary Hypertension in a Child: A Case Report Read More »

Bioinformatic Analysis and Molecular Docking Identify Isorhamnetin Is a Candidate Compound in the Treatment of Pulmonary Artery Hypertension

Chen Shao, Wei Xia, Yang LiuSecond People’s Hospital of Lianyungang. Qilu Medical University. China Anatolgy Journal of CardiologyAnatol J Cardiol 2024;DOI: 10.14744/AnatolJCardiol.2024.4723 AbstractBackground: The current study aims to identify the key pathways and potential therapeutic targets for pulmonary arterial hypertension (PAH) and to further evaluate the anti-PAH effects of isorhamnetin.Methods: The dataset of gene expression profiling for PAH

Bioinformatic Analysis and Molecular Docking Identify Isorhamnetin Is a Candidate Compound in the Treatment of Pulmonary Artery Hypertension Read More »

Pulmonary hypertension in preterm neonates with bronchopulmonary dysplasia: a meta-analysis

Dwayne Mascarenhas, Marwa Al-Balushi, Aida Al-Sabahi, Dany E. Weisz, Amish Jain, Bonny JasaniHospital for Sick Children and University of Toronto. Sunnybrook Health Sciences Centre. Mount Sinai Hospital. Canada Archive of Disease in Children Fetal and Neonatal EditionArch Dis Child Fetal Neonatal Ed 2024; DOI: 10.1136/archdischild-2024-327547 AbstractContext: Knowledge gaps exist on the incidence and risk factors for developing

Pulmonary hypertension in preterm neonates with bronchopulmonary dysplasia: a meta-analysis Read More »

SOX17 – Associated Pulmonary Hypertension in Children: A Distinct Developmental and Clinical Syndrome

Mary P. Mullen, D. Dunbar Ivy, Nidhy P. Varghese, Abbey J. Winant, Nahir Cortes-Santiago, Sara O. Vargas, Diego Porres, Nicola Maschietto, Paul J. Critser, Russel Hirsch, Catherine M. Avitabile, Rachel K. Hopper, Benkamin S. Frank, Ryan D. Coleman, Pankaj B. Agrawal, Jill A. Madden, Amy E. Roberts, Shane L. Collins, J. Usha Raj, Eric D.

SOX17 – Associated Pulmonary Hypertension in Children: A Distinct Developmental and Clinical Syndrome Read More »

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