Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Usama Kanaan"'
Autor:
Shilpa Vyas-Read, Usama Kanaan, Prabhu Shankar, Jane Stremming, Curtis Travers, David P. Carlton, Anne Fitzpatrick
Publikováno v:
BMC Pediatrics, Vol 17, Iss 1, Pp 1-12 (2017)
Abstract Background Approximately 8–23% of premature infants develop pulmonary hypertension (PH), and this diagnosis confers a higher possibility of mortality. As a result, professional societies recommend PH screening in premature infants. However
Externí odkaz:
https://doaj.org/article/228275047714417a8fe6e05363961908
Autor:
Usama Kanaan, Nidhy P. Varghese, Ryan D. Coleman, Jeryl Huckaby, Patricia Lawrence, Lynda O. Jorgensen, Kathleen Miller-Reed, Ronald W. Day, George B. Mallory, David D. Ivy
Publikováno v:
Pulmonary Circulation, Vol 9 (2019)
Pulmonary arterial hypertension is a progressive, incurable disease that occurs in adults and children alike. Therapeutic options for children are limited and infrequently described, including newer agents such as treprostinil, an oral prostanoid. He
Externí odkaz:
https://doaj.org/article/f1bc8cd380ba483cb081508c16082353
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2018)
Between 4 and 16% of extremely premature infants have late pulmonary hypertension (PH) (onset >30 days of life), and infants with PH have a higher risk of tracheostomy and death. Atrial septal defects (ASD) increase pulmonary blood flow and may promo
Externí odkaz:
https://doaj.org/article/176fb8969618454a8b4e025094559bd5
Autor:
Ololade Akintoye, Bhavesh Patel, Ritu Sachdeva, Kumiyo Matsuo, Danish Vaiyani, Usama Kanaan, Curtis Travers, Michael Kelleman, Christopher J Petit
Publikováno v:
American Heart Journal. 236:69-79
OBJECTIVE While the surgical stages of single ventricle (SV) palliation serve to separate pulmonary venous and systemic venous return, and to volume-unload the SV, staged palliation also results in transition from parallel to series circulation, incr
Autor:
Soham Dasgupta, Dennis Dong Hwan Kim, Ritu Sachdeva, Robert N. Vincent, Usama Kanaan, Erika L. Bettermann, Christopher J. Petit, Holly Bauser-Heaton, Michael Kelleman
Publikováno v:
Cardiology in the Young. 31:1595-1607
Background:Although cardiac catheterisation (cath) is the diagnostic test for pulmonary hypertension, it is an invasive procedure. Echocardiography (echo) is commonly used for the non-invasive diagnosis of pulmonary hypertension but maybe limited by
Autor:
Laura A. Downey, Holly Bauser-Heaton, Usama Kanaan, Danish Vaiyani, Christopher J. Petit, Michael Kelleman
Publikováno v:
Pediatric Cardiology. 42:736-742
Pulmonary hypertension (PH) can lead to progressive heart failure with high morbidity and mortality. Cardiac catheterization (CC) is the gold standard for diagnosis and response to vasodilatory medications. The invasive nature of CC and associated an
Autor:
D. Dunbar Ivy, Ryan D. Coleman, Jeryl Huckaby, Usama Kanaan, Nidhy Varghese, Patricia Lawrence, George B. Mallory, Kathleen Miller-Reed, Lynda O Jorgensen, Ronald W. Day
Publikováno v:
Pulmonary Circulation, Vol 9 (2019)
Pulmonary Circulation
Pulmonary Circulation
Pulmonary arterial hypertension is a progressive, incurable disease that occurs in adults and children alike. Therapeutic options for children are limited and infrequently described, including newer agents such as treprostinil, an oral prostanoid. He
Publikováno v:
Journal of Perinatology. 38:148-153
Assess the effect of increasing pulse oximetry targets on incidence of pulmonary hypertension in very low birthweight premature infants.Retrospective cohort study comparing pulmonary hypertension incidence among three cohorts of premature infants exp
Publikováno v:
Paediatric Respiratory Reviews. 23:27-32
Summary Objectives Preterm infants with bronchopulmonary dysplasia (BPD) are at increased risk for development of Pulmonary Hypertension (PHT). We performed a systematic review and meta-analysis to identify risk factors for development of PHT in infa
Autor:
Adeline Vanderver, Zachary Cross, Laura Adang, Abigail Collins, Stephanie Keller, Guy Helman, Dawn M. Simon, Ahmed Gilani, Asako Takanohashi, David B. Frank, Brian D. Hanna, Csaba Galambos, Nicole Ulrick, Usama Kanaan, Omar Sherbini
While pulmonary hypertension (PH) is a potentially life threatening complication of many inflammatory conditions, an association between Aicardi Goutières syndrome (AGS), a rare genetic cause of interferon (IFN) overproduction, and the development o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01e874008041dca4894a594ef94e0643
https://europepmc.org/articles/PMC6880931/
https://europepmc.org/articles/PMC6880931/