Class 3. Pulmonary Hypertension Associated with Lung Hypoplasia

Innovative Fetal Therapy for a Giant Congenital Pulmonary Airway Malformation with Hydrops

Denise B. Klinkner, Thomas Atwell, Ayssa Teles Abrao Trad, Matthew R. Callstrom, Mohamed Yasir Qureshi, Ellen Bendel Stenzel, Mauro Schenone, Rodrigo RuanoMayo Clinic. University of Miami.United States Fetal Diagnosis and TherapyFetal Diagn Ther 2022; 49: 250-255DOI: 10.1159/000521690 AbstractIntroduction: Congenital pulmonary airway malformations (CPAMs) complicated by hydrops portend significant morbidity and mortality, with fetal survival estimates less than […]

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Identification of SOX2 Interacting Proteins in the Developing Mouse Lung With Potential Implications for Congenital Diaphragmatic Hernia

Kim A. A. Schilders, Gabriëla G. Edel, Evelien Eenjes, Bianca Oresta, Judith Birkhoff, Anne Boerema-de Munck, Marjon Buscop-van Kempen, Panagiotis Liakopoulos, Petros Kolovos, Jeroen A. A. Demmers, Raymond Poot, Rene M. H. Wijnen, Dick Tibboel and Robbert J. RottierErasmus Medical Center and Sophia Children’s Hospital. Democritus University of Thrace. Netherlands and Greece Frontiers in PediatricsFront

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Expected small left heart size in the presence of congenital diaphragmatic hernia: Fetal values and Z-scores for infants confirmed to have no heart disease postnatally

Anita J. Moon-Grady, Francesca A. Byrne, Leslie A. Lusk, Roberta L. KellerUniversity of California San Francisco and Benioff Children’s Hospital.United States Frontiers in PediatricsFront Pediatr 2022; DOI: 10.3389/fped.2022.1083370 AbstractObjectives: In fetuses with left-sided congenital diaphragmatic hernia (CDH), left heart structures may appear small, but usually normalize after birth in the absence of structural cardiac anomalies. To decrease

Expected small left heart size in the presence of congenital diaphragmatic hernia: Fetal values and Z-scores for infants confirmed to have no heart disease postnatally Read More »

Echocardiographic measures of ventricular-vascular interactions in congenital diaphragmatic hernia

Sanjeev Aggarwal, Christina Shanti, Prashant Agarwal, Joseph Lelli, Girija NatarajanCentral Michigan University and Children’s Hospital of Michigan.United States Early Human DevelopmentEarly Hum Dev 2022; 165: DOI: 10.1016/j.earlhumdev.2021.105534 AbstractObjective: To evaluate the utility of echocardiographic measures of ventricular-vascular interactions in predicting death or ECMO in congenital diaphragmatic hernia (CDH).Design: In this single center retrospective study, early (<48 hour age)

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Morbidity in children after fetoscopic endoluminal tracheal occlusion for severe congenital diaphragmatic hernia: Results from a multidisciplinary clinic

Shelby R. Sferra, Melanie K. Nies, Jena L. Miller, Alejandro V. Garcia, Erica I. Hodgman, Annalise B. Penikis, Abigail J. Engwall-Gill, Vera Joanna Burton, Jessica L. Rice, Peter J. Mogayzel, Ahmet A. Baschat, Shaun M. KunisakiJohns Hopkins University School of Medicine. United States Journal of Pediatric SurgeryJ Pediatr Surg 2023; 58: 14-19DOI: 10.1016/j.jpedsurg.2022.09.042 AbstractBackground: Although fetoscopic endoluminal

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Long-term outcomes of congenital diaphragmatic hernia: A single institution experience

Claire D. Gerall, Latoya A. Stewart, Jessica Price, Sandra Kabagambe, Shelby R. Sferra, Rebecca Hernan, Julie Khlevner, Usha S. Krishnan, Alive De, Gudrun Aspelund, Vincent P. DuronColumbia University Vagelos College of Physicians and Surgeons and NewYork-Presbyterian Morgan Stanley Children’s Hospital.United States Journal of Pediatric SurgeryJ Pediatr Surg 2022; 57: 563-569DOI: 10.1016/j.jpedsurg.2021.06.007 AbstractBackground/purpose: As survival rates for patients

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Quantitative cardiopulmonary magnetic resonance imaging in neonatal congenital diaphragmatic hernia

Jean A. Tkach, Nara S. Higano, Michael D. Taylor, Ryan A. Moore, Monir Hossain, Guixia Huang, David R. Spielberg, Sean B. Fain, Paul S. Kingma, Jason C. WoodsCincinnati Children’s Hospital Medical Center and University of Cincinnati College of Medicine. Texas Children’s Hospital. University of Iowa. University of Wisconsin.United States Pediatric RadiologyPediatr Radiol 2022; 52: 2306-2318DOI: 10.1007/s00247-022-05384-w

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Mediastinal shift angle (MSA) measurement with MRI: a simple and effective tool for prenatal risk stratification in fetuses with congenital diaphragmatic hernia

Wen Ding, Yuanyuan Gu, Huiying Wu, Haiyu Wang, Xiaochun Zhang, Hongying Wang, Li Huang, Rui Zhang, Qiugming He, Wei Zhong, Junjian Lv, Bo Xia, Guanglan Zhang, Shanshan MeiGuangzhou Medical University and Guangzhou Women and Children’s Medical Center. China European RadiologyEur Radiol 2023; 33: 1668-1676DOI: 10.1007/s00330-022-09142-2 AbstractObjectives: To investigate the predictive value of mediastinal shift angle (MSA) in

Mediastinal shift angle (MSA) measurement with MRI: a simple and effective tool for prenatal risk stratification in fetuses with congenital diaphragmatic hernia Read More »

Surgical and Cardiac Catheterization Outcomes of Scimitar Syndrome Patients: A Three Decade Single-Center Experience

Emma Seymour, George Mallory, Raysa Morales-DemoriBaylor College of Medicine and Texas Children’s Hospital.United States Pediatric CardiologyPediatr Cardiol 2023; 44: 579-586DOI: 10.1007/s00246-022-02965-2 AbstractScimitar syndrome (SS) is a rare congenital condition which includes partial anomalous pulmonary venous return (PAPVR) and a variable degree of pulmonary hypoplasia. We describe the clinical features, therapeutic approach and outcomes of patients who

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Characterisation of paediatric pulmonary hypertensive vascular disease from the PPHNet Registry

Steven H. Abman, Mary P. Mullen, Lynn A. Sleeper, Eric D. Austin, Erika B. Rosenzweig, John P. Kinsella, D. Dunbar Ivy, Rachel K. Hopper, J. Usha Raj, Jeffrey Fineman, Roberta L. Keller, Angela Bates, Usha S. Krishnan, Catherine M. Avitabile, Alexander Davidson, Marc D. Natter, Kenneth D. MandlPediatric Pulmonary Hypertension NetworkUnited States and Canada European Respiratory JournalEur Respir J 2021; DOI: 10.1183/13993003.03337-2020 ExtractBackground: There are limited data about the range of diseases, natural history, age-appropriate end-points and optimal care for children with pulmonary hypertension (PH), including the need for developing

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