Pediatric Pulmonary Vascular Disease

Extracorporeal Membrane Oxygenation with Bi-Caval Dual-Lumen Catheter in a Neonate with Persistent Pulmonary Hypertension and Interventricular Septal Hypertrophy

Sachin Dangi, Anup Thakur, Neelam Kler, Raja JoshiSir Ganga Ram Hospital.India Indian Journal of PediatricsInd J Pediatr 2024; DOI: 10.1007/s12098-024-05299-4 AbstractAbstract Not Available CategoryClass I. Persistent Pulmonary Hypertension of the NewbornSurgical and Catheter-mediated Interventions for Pulmonary Vascular Disease Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Fresh (PHresh). Less than 1-2 years since publication […]

Extracorporeal Membrane Oxygenation with Bi-Caval Dual-Lumen Catheter in a Neonate with Persistent Pulmonary Hypertension and Interventricular Septal Hypertrophy Read More »

Incidence and severity of pertussis among hospitalized infants, Sarawak, Malaysia, 2015-2021

Anand Mohan, Yee-Yen Tan, Rohaidah Hashim, David Chun-Ern Ng, Veronica Huey-Shin Wong, Da-Wei Liew, Su-Lin Chien, Lee-See Tan, Peter Sie-Teck Lau, Thilagam Rajandran,Yuwana Podin, Mong-How OoiBintulu Hospital, Hospital Tuanku Ja’afar and Ministry of Health Malaysia. Institute for Medical Research. Universiti Malaysia Sarawak.Malaysia Journal of Infection in Developing CountriesJ Infect Dev Ctries 2024; 18: 1394-1403DOI: 10.3855/jidc.18837 AbstractIntroduction: A

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Association of Prenatal Congenital Lung Malformation Volume Ratio to Postnatal Computed Tomography Characteristics

Ashley Elisabeth Montgomery, Sarah Elizabeth Peiffer, John Randall Santa Cruz, Pamela Ketwaroo, Timothey Chen-An Lee, Sundeep Govind Keswani, Alice KingBaylor College of Medicine and Texas Children’s Hospital.United States Journal of Surgical ResearchJ Surg Res 2024; 302: 755-764DOI: 10.1016/j.jss.2024.07.118 AbstractIntroduction: Congenital lung malformations (CLMs) are diverse and readily diagnosed on prenatal ultrasound. Postnatal computed tomography (CT) characteristics, including

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The ten-year evaluation of clinical characteristics in congenital lung anomaly in pediatrics; a retrospective study in North of Iran

Narges Lashkarbolouk, Mahdi Mazandarani, Ali Ahani Azari, Somayeh Ghorbani, Lobat ShahkaTaleghani Pediatric Hospital and Golestan University of Medical Sciences. Tehran University of Medical Sciences. Iran BioMedical Central PediatricsBMC Pediatr 2024; 24: DOI: 10.1186/s12887-024-04911-y AbstractIntroduction: Congenital lung anomalies (CLA) are a group of anomalies, including congenital cystic adenomatoid malformation (CCAM), bronchopulmonary sequestrations (BPS), congenital lobar emphysema (CLE), and bronchogenic cysts (BC). The prevalence

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ASXL1-related Bohring-Optiz Syndrome complicated by Persistent Neonatal Pulmonary Hypertension and Abnormal Alveoli Formation

Makoto Arioka, Shinji Nakamura, Katsufumi Nishioka, Kota Inoue, Yasuhiro Nakao, Yumi Miyai, Hirosuke Morita, Kosuke Koyano, Toshiki Takenouchi, Saneyuki Yasuda, Yoichi Chiba, Takashi Iwase, Masaki Ueno, Takashi KusakaKagawa University Hospital and Kagawa University. Keio University School of Medicine.Japan European Journal of Medical GeneticsEur J Med Genet 2024; DOI: 10.1016/j.ejmg.2024.104978 AbstractBohring-Opitz syndrome (BOS) is a rare disease

ASXL1-related Bohring-Optiz Syndrome complicated by Persistent Neonatal Pulmonary Hypertension and Abnormal Alveoli Formation Read More »

Barriers to and facilitators of physical activity in pediatric pulmonary hypertension

Catherine M. Avitabile, Caroline O’Brien, Divya Dureja, Dana Albizem, Jena Mota, Melissa Xanthopoulos, Babette S. Zemel, Peter F. CronholmChildren’s Hospital of Philadelphia, University of Pennsylvania Perelman School of Medicine and University of Pennsylvania.United States Pulmonary CirculationPulm Circ 2024; 14: DOI: 10.1002/pul2.70000 AbstractTherapeutic exercise has not been widely adopted in pediatric pulmonary hypertension (PH), despite adult data

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Cardiac Comorbidity and Exercise Intolerance in Bilateral Lung Transplant Recipients Followed at a Pediatric Center

Christina M. Mangano, Levent Midyat, Dawn Freiberger, Kimberlee Gauvreau, Debra Boyer, Gary Visner, Ming Hui ChenBoston Children’s Hospital and Harvard Medical School. University of Pittsburgh School of Medicine and Children’s Hospital of Pittsburgh. Nationwide Children’s Hospital and Ohio State University College of Medicine. United States Pediatric CardiologyPediatr Cardiol 2024; DOI: 10.1007/s00246-024-03674-8 AbstractReduced exercise capacity is common

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Vasopressin induced hyponatremia in infants <3 months of age in the neonatal intensive care unit

Kavita Patel, Sharon Thomson, Meera Vijayan, Marjorie Makoni, Peter N. Johnson, Katy Stephens, Stephen B. Neely, Jamie L. MillerUniversity Health, San Antonio. Oklahoma Children’s Hospital at Oklahoma University Health, University of Oklahoma College of Medicine and University of Oklahoma College of Pharmacy. Lucile Packard Children’s Hospital. United States Frontiers in PediatricsFront Pediatr 2024; 12DOI: 10.3389/fped.2024.1465785 AbstractObjectives: Vasopressin

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Echocardiographic evaluation of myocardial dysfunction in term neonates with perinatal asphyxia

Javaria Rasheed, Muhammad Khalid, Iram Nawaz, Barera MaryamNishtar Medical University Hospital. Bakhtawar Amin Medical & Dental College. Pakistan Pakistan Journal of Medical SciencesPak J Med Sci 2024; 40: 2107-2111DOI: 10.12669/pjms.40.9.9501 AbstractBackground and Objective: One third of the neonatal deaths worldwide are attributed to perinatal asphyxia. We aimed to determine the prevalence and determinants of cardiac dysfunction, through

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Utility of urinary NT-proBNP in congenital diaphragmatic hernia: a prospective pilot study

Srirupa Hari Gopal, Kelly Frances Martinek, Candice Vacher, Judith Becker, Nighy P. Varghese, Betul Yilmaz Furtun, Joseph L. Hagan, Sharada H. Gowda, Mohan Pammi, Sridevi Devaraj, Caraciolo J. FernandesBaylor College of Medicine.United States Pediatric ResearchPediatr Res 2024; DOI: 10.1038/s41390-024-03600-x AbstractBackground: Echocardiography is the reference standard for diagnosing pulmonary hypertension (PH) and cardiac dysfunction (CD) in congenital diaphragmatic

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