Filed (PHiled). Greater than 1-2 years since publication

Impact of the COVID-19 pandemic on chronic disease management and patient reported outcomes in patients with pulmonary hypertension: The Pulmonary Hypertension Association Registry

Megan Mayer, David B. Badesch, Kelly H. Nielsen, Steven Kawut, Todd Bull, John J. Ryan, Jeffrey Sager, Sula Mazimba, Anna Hemnes, James Klinger, James Runo, John W. McConnell, Teresa DeMarco, Murali M. Chakinala, Delphine Yung, Jean Elwing, Adolfo Kaplan, Rahul Argula, Raymond Pomponio, Ryan Peterson, Peter HountrasUniversity of Colorado. University of Pennsylvania. University of Utah. […]

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Pulmonary Hypertension in Chronic Lung Diseases: What Role Do Radiologists Play?

Adele Valentini, Paola Franchi, Giuseppe Cicchetti, Gaia Messana, Greta Chiffi, CeciliaStrappa, Lucio Calandriello, Annemiliadel Ciello, Alessandra Farchione, Lorenzo Preda, Anna Rita LariciFondazione IRCCS Policlinico San Matteo. G. Mazzini Hospital. Fondazione Policlinico Universitario. University of Pavia. Università Cattolica del Sacro Cuore. Italy DiagnosticsDiagnostics 2023; 13: DOI: 10.3390/diagnostics13091607 AbstractPulmonary hypertension (PH) is a pathophysiological disorder, defined by a

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Prenatal MRI assessment of mediastinal shift angle as a feasible and effective risk stratification tool in isolated right-sided congenital diaphragmatic hernia

Wen Ding, Yuanyuan Gu, Kaiyu Wang, Huiying Wu, Xiachun Zhang, Rui Zhang, Hongying Wang, Li Huang, Junjian Lv, Bo Xia, Wei Zhong, Qiuming He, Longlong HouGuangzhou Women and Children’s Medical Center and Guangzhou Medical University. China European RadiologyEur Radiol 2023; DOI: 10.1007/s00330-023-10178-1 AbstractObjectives: To develop a mediastinal shift angle (MSA) measurement method applicable to right-sided congenital diaphragmatic

Prenatal MRI assessment of mediastinal shift angle as a feasible and effective risk stratification tool in isolated right-sided congenital diaphragmatic hernia Read More »

NT-proBNP Is a Predictor of Mortality in Adults with Pulmonary Arterial Hypertension Associated with Congenital Heart Disease

Susanne J. Maurer, Veronika Habdank, Jürgen Hörer, Peter Ewert, Oktay TutarelGerman Heart Centre Munich and Technical University of Munich. Ludwig-Maximilians Universität.Germany Journal of Clinical MedicineJ Clin Med 2023; 12DOI: 10.3390/jcm12093101 AbstractBackground: About 5-10% of adults with congenital heart disease (ACHD) will develop pulmonary arterial hypertension (PAH), which is associated with significant mortality. Studies on risk factors for

NT-proBNP Is a Predictor of Mortality in Adults with Pulmonary Arterial Hypertension Associated with Congenital Heart Disease Read More »

Short-time mortality and severe complications of very premature infants-a multicenter retrospective cohort study from Jiangsu Province during 2019-2021

Ya Pan, Huaiyan Wang, Yan Xu, Xiaohua Zhang, Xiaoqing Chen, Xueting Liu, Songlin Liu, Yan Gao, Weiwei Hou, Zhaojun Pan, Xinping Wu, Mei Xue, Mingfu Wu, Huimin Ju, Weimin Wu, Shuping HanWomen’s Hospital of Nanjing Medical University and Nanjing Maternity and Child Health Care Hospital. Changzhou Maternity and Child Health Care Hospital. Affiliated Hospital of

Short-time mortality and severe complications of very premature infants-a multicenter retrospective cohort study from Jiangsu Province during 2019-2021 Read More »

Cardiac Magnetic Resonance Derived Left Ventricular Eccentricity Index and Right Ventricular Mass Measurements Predict Outcome in Children with Pulmonary Arterial Hypertension

Meindina G. Haarman, Iris Coenraad, Quint A. J. Hagdorn, Hans L. Hillege, Tineke P. Willems, Rolf M. F. Berger, Johannes M. DouwesBeatrix Children’s Hospital and University Medical Center Groningen. Netherlands ChildrenChildren 2023; 10DOI: 10.3390/children10040756 AbstractPulmonary arterial hypertension (PAH) is associated with increased right ventricular (RV) afterload, affecting RV remodeling and RV performance, a major determinant of

Cardiac Magnetic Resonance Derived Left Ventricular Eccentricity Index and Right Ventricular Mass Measurements Predict Outcome in Children with Pulmonary Arterial Hypertension Read More »

Sex-Specific Differences in Congenital Diaphragmatic Hernia Mortality

Shelby R. Sferra, Matthew Guo, Andres J. Gonzalez-Salazar, Annalise B. Penikis, Abigail J. Engwall-Gill, Ashley Ebanks, Matthew T. Harting, Joseph M. Collaco, Shaun M. Kunisaki, CDH Study GroupJohns Hopkins University School of Medicine. University of Texas McGovern Medical School and Children’s Memorial Hermann Hospital. United States Journal of PediatricsJ Pediatr 2023; 259DOI: 10.1016/j.jpeds.2023.113481 AbstractObjective: To compare disease

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Pulmonary hypertension- a novel phenotypic hypothesis of Kabuki syndrome: a case report and literature review

Xiao‑xian Deng, Bo‑wen Jin, Shan‑shan Li, Hong‑mei Zhou, Qun‑shan Shen, Yun‑yan LiWuhan Asia Heart Hospital. China BioMed Central PediatricsBMC Pediatr 2023; 23: DOI: 10.1186/s12887-023-04273-x AbstractBackground: Pediatric pulmonary hypertension (PH) is a serious and rare disease that is often derived from genetic mutations. Kabuki syndrome (KS) is a chromosomal abnormality disease that has its origin in the mutation

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Fatal Association of Eisenmenger Syndrome and Severe Preeclampsia

Said Benlamkaddem, Fatima Bouyermane, Djoudline Doughmi, Mohamed Adnane Berdai, Mustapha HarandouHassan II University Hospital. Sidi Mohamed Ben Abdellah University. Morocco CureusCureus 2023; 15DOI: 10.7759/cureus.37836 AbstractEisenmenger syndrome (ES) is the end stage of pulmonary arterial hypertension (PAH) associated with congenital heart disease (CHD), which can occur in patients with large, unrepaired cardiac shunts (ventricular septal defects (VSD),

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Growing up with Idiopathic Pulmonary Arterial Hypertension: An Arduous Journey

Tanguy Dutilleux, Nesrine Farhat, Ruth Heying, Marie-Christine Seghaye, Maurice BeghettiUniversity Hospital Aachen. Centre Hospitalier Universitaire de Liège. University Hospital Leuven. Children’s University Hospital Geneva.Germany, Belgium and Switzerland Pediatric ReportsPediatr Rep 2023; 15: 301-310DOI: 10.3390/pediatric15020026 AbstractIdiopathic pulmonary arterial hypertension (IPAH) is an uncommon and severe disease. We report the case of a 7-year-old boy investigated for cardiac

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