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

The results of atrial flow regulator implantation in pulmonary arterial hypertension patients with severe heart failure despite maximal medical therapy

Grzegorz Kopeć, Aleksander Araszkiewicz, Wojciech Magoń, Jakub Stępniewski, Sylwia Sławek-Szmyt, Magdalena Janus, Ilona Skoczylas, Zbigniew Gąsior, Łukasz Wilczek, Monika Komar, Andrzej Gackowski, Anna Sabiniewicz, Marek Grygier, Piotr Podolec, Robert SabiniewiczJagiellonian University Medical College and John Paul II Hospital in Krakow. University of Medical Sciences. Medical University of Silesia. Medical University of Gdansk.Poland Kardiologia PolskaKardiol Pol […]

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Cardiopulmonary physiological effects of diuretic therapy in preterm infants with chronic pulmonary hypertension

Faith Zhu, Daniel Ibarra Rios, Sebastien Joye, Michelle Baczynski, Danielle Rios, Regan E. Giesinger, Patrick J. McNamara, Amish JainMount Sinai Hospital and University of Toronto. Hospital Infantil de México Federico Gómez. Lausanne University Hospital. University of Iowa.Canada, Mexico, Switzerland and United States Journal of PerinatologyJ Perinatol 2023DOI: 10.1038/s41372-023-01742-0 AbstractObjective: Using targeted neonatal echocardiography (TNE) to examine cardiopulmonary

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Risk factors of transient tachypnea of the newborn developing into pulmonary hypertension of the newborn: a case-control study

Gunlawadee Maneenil, Waricha Janjindamai, Supaporn Dissaneevate, Anucha ThatrimontrichaiPrince of Songkla UniversityThailand Asian BiomedicineAsian Biomed 2023; 16: 310-315DOI: 10.2478/abm-2022-0034 AbstractBackground: Transient tachypnea of the newborn (TTN) is the consequence of delayed resorption of lung fluid. When TTN develops, the infant may develop severe hypoxemia and progress to persistent pulmonary hypertension of the newborn (PPHN).Objectives: To examine factors associated with

Risk factors of transient tachypnea of the newborn developing into pulmonary hypertension of the newborn: a case-control study Read More »

Three-Dimensional, Right Ventricular Surface Strain Computation From Three Dimensional Echocardiographic Images From Patients With Pediatric Pulmonary Hypertension

Priyamvada Kundu, Michal Schafer, Lisa Le, Thomas Thomas, Pei-Ne Jone, Kendall HunterChildren’s Hospital Colorado. Ann and Robert H. Lurie Children’s Hospital of Chicago.United States Journal of Biomechanical EngineeringJ Biomech Eng 2023; DOI: 10.1115/1.4063121 AbstractBackground: Right Ventricular (RV) dysfunction is routinely assessed with echocardiographic-derived global longitudinal strain (GLS). GLS is measured from a two-dimensional echo (2DE) image and

Three-Dimensional, Right Ventricular Surface Strain Computation From Three Dimensional Echocardiographic Images From Patients With Pediatric Pulmonary Hypertension Read More »

Association between immediate oxygenation response and survival in preterm infants receiving rescue inhaled nitric oxide therapy for hypoxemia from pulmonary hypertension: A systematic review and meta-analysis

Michelle Baczynski, Bonny Jasani, Charmaine De Castro, Carlo Dani, Nimish V. Subhedar, Praveen Chandrasekharan, Satvan Lakshminrusimha, Patrick J. McNamara, Adrianne R. Bishchoff, Amish JainMount Sinai Hospital. Hospital for Sick Children. Careggi University Hospital of Florence and University of Florence. Liverpool Women’s Hospital. University at Buffalo. UC Davis Children’s Hospital. University of Iowa. Canada, Italy, United

Association between immediate oxygenation response and survival in preterm infants receiving rescue inhaled nitric oxide therapy for hypoxemia from pulmonary hypertension: A systematic review and meta-analysis Read More »

Meconium aspiration syndrome: a comprehensive review

Ahmed Osman, Cecilie Halling, Mary Crume, Hayat Al Tabosh, Namrita Odackal, Molly K. BallThe Ohio State University and Nationwide Children’s Hospital. United States Journal of PerinatologyJ Perinatol 2023; DOI: 10.1038/s41372-023-01708-2 AbstractMeconium aspiration syndrome (MAS) is a complex respiratory disease that continues to be associated with significant morbidities and mortality. The pathophysiological mechanisms of MAS include airway

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Fenfluramine in the treatment of Dravet syndrome: Results of a third randomized, placebo-controlled clinical trial

Joseph Sullivan, Lieven Lagae, J. Helen Cross, Orrin Devinsky, Renzo Guerrini, Kelly G. Knupp, Linda Laux, Marina Nikanorova, Tilman Polster, Dinesh Talwar, Berten Ceulemans, Rima Nabbout, Gail M. Farfel, Bradley S. Galer, Arnaold R. Gammaitoni, Michael Lock, Anupam Agarwal, Ingrid E. Scheffer, The FAiRE DS Study GroupUniversity of California San Francisco. University of Leuven. Great

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Intra-amniotic sildenafil treatment improves lung blood flow and pulmonary hypertension in congenital diaphragmatic hernia rats

Shiho Yoshida, Alexander M. Kreger, George K. Gittes UPMC Children’s Hospital of Pittsburgh and University of Pittsburgh School of Medicine.United States Frontiers in Bioengineering and BiotechnologyFront Bioeng Biotechnol 2023; DOI: 10.3389/fbioe.2023.1195623 AbstractPulmonary hypertension associated with congenital diaphragmatic hernia (CDH) is a critical factor in determining prognosis. We propose that intra-amniotic sildenafil administration is an effective prenatal therapy for

Intra-amniotic sildenafil treatment improves lung blood flow and pulmonary hypertension in congenital diaphragmatic hernia rats Read More »

Measurement of Physical Activity by Actigraphy in Infants and Young Children with Pulmonary Arterial Hypertension

Catherine M. Avitabile, Delphine Yung, Stephanie Handler, Rachel K. Hopper, Jeff Fineman, Grace Freire, Nidhy Varghese, Mary Mullen, Usha S. Krishnan, Eric Austin, Lori Silveira, D. Dunbar IvyChildren’s Hospital of Philadelphia and University of Pennsylvania Perelman School of Medicine. University of Washington School of Medicine. Medical College of Wisconsin. Stanford University School of Medicine. University

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Recent Advances in Pediatric Pulmonary Hypertension: Implications for Diagnosis and Treatment

Rachel T. Sullivan, J. Usha Raj, Eric D. AustinVanderbilt University Medical Center and Monroe Carrell Jr Children’s Hospital. University of Illinois at Chicago.United States Clinical TherapyClin Ther 2023; DOI: 10.1016/j.clinthera.2023.07.001 AbstractPurpose: Pediatric pulmonary hypertension (PH) is a condition characterized by elevated pulmonary arterial pressure, which has the potential to be life-limiting. The etiology of pediatric PH varies.

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