Zobrazeno 1 - 10
of 4 600
pro vyhledávání: '"Congenital heart defect"'
Autor:
Fonthip Naiyananon, Supaporn Dissaneevate, Anucha Thatrimontrichai, Waricha Janjindamai, Gunlawadee Maneenil, Manapat Praditaukrit, Supaporn Roymanee, Voravit Chittithavorn, Alan Geater
Publikováno v:
Pediatrics and Neonatology, Vol 65, Iss 5, Pp 464-468 (2024)
Background: Neonates with critical congenital heart disease of the ductal-dependent pulmonary circulation type (CCHD-DDPC) require prostaglandin E1 (PGE1) to maintain oxygen saturation until surgery. However, the factors contributing to the maintenan
Externí odkaz:
https://doaj.org/article/eca6025f22094396808033c70b9fc2b9
Autor:
Hojjat Mortezaeian, Ata Firouzi, Pouya Ebrahimi, Mohsen Anafje, Peyman Bashghareh, Phuoc Doung, Shakeel Qureshi
Publikováno v:
International Journal of Emergency Medicine, Vol 17, Iss 1, Pp 1-8 (2024)
Abstract Background Percutaneous pulmonary valve implantation (PPVI) is a recognized alternative treatment to surgery for patients with dysfunctional right ventricular outflow tracts. Patient selection is essential to avoid serious complications from
Externí odkaz:
https://doaj.org/article/69ec98ae71064095b2879ea5b785e433
Publikováno v:
Studia Medyczne, Vol 40, Iss 2, Pp 201-207 (2024)
Externí odkaz:
https://doaj.org/article/8e9c2900bc54447893d9fc57d6d2aea0
Autor:
Kira Mascho, Svetlana A. Yatsenko, Cecilia W. Lo, Xinxiu Xu, Jennifer Johnson, Lindsey R. Helvaty, Stephanie Burns Wechsler, Chaya N. Murali, Seema R. Lalani, Vidu Garg, Jennelle C. Hodge, Kim L. McBride, Stephanie M. Ware, Jiuann-Huey Ivy Lin
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Introduction5p deletion syndrome, also called Cri-du-chat syndrome 5p is a rare genetic syndrome with reports up to 36% of patients are associated with congenital heart defects. We investigated the association between left outflow tract obstruction a
Externí odkaz:
https://doaj.org/article/2ea28b86dde34d79982956d3247450a9
Autor:
L. Lily Rosenthal, Tabea Katharina Spickermann, Sarah Marie Ulrich, Robert Dalla Pozza, Heinrich Netz, Nikolaus A. Haas, René Schramm, Michael Schmoeckel, Christian Hagl, Jürgen Hörer, Sebastian Michel, Carola Grinninger
Publikováno v:
Frontiers in Transplantation, Vol 3 (2024)
IntroductionThe aim of this study was to analyze the results after pediatric heart transplantation (pHTx) at our single center differentiating between ABO-incompatible (ABOi) and -compatible (ABOc) procedures.Methods and patientsWe retrospectively an
Externí odkaz:
https://doaj.org/article/dc08b7359c6d4a6182394e9183c12e46
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
ObjectiveTo better understand the experience of parents with neonates with congenital heart diseases (CHD) admitted to a neonatal intensive care unit (NICU) in order to identify challenges faced by parents and discover support strategies helpful in p
Externí odkaz:
https://doaj.org/article/5dbd0feebc674a5d8a389026e1d3a64b
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-7 (2024)
Abstract The main objective of this study was to investigate the incidence and characteristics of electrocardiographic abnormalities in patients with microtia, and to explore cardiac maldevelopment associated with microtia. This retrospective study a
Externí odkaz:
https://doaj.org/article/f2ad90bf50f148919659879a868a596d
Publikováno v:
Kardiyovasküler Tıp E Dergisi/E Journal of Cardiovascular Medicine, Vol 12, Iss 1, Pp 7-11 (2024)
Objectives: Early extubation applications after pediatric congenital heart surgery have increased in recent years because of the positive results of these studies. It remains controversial whether early extubation should be performed in the operating
Externí odkaz:
https://doaj.org/article/bccefdb0b1554eb3823c97c023742674
Autor:
Filippos‐Paschalis Rorris, Meletios Kanakis, George Samanidis, Alexandros Tsoutsinos, Achilleas Lioulias, Dimitrios Bobos
Publikováno v:
Clinical Case Reports, Vol 12, Iss 8, Pp n/a-n/a (2024)
Key Clinical Message Anomalous origin of right pulmonary artery from the ascending aorta is a rare congenital heart malformation that results in early infant mortality. These patients are at risk for the early development of significant pulmonary hyp
Externí odkaz:
https://doaj.org/article/423911bb4b934eb2902ed708c5435dd2
Autor:
Leila Bigdelu, MD, Ossama Maadarani, MD, Ali Azari, MD, Ali Heidari-Bakavoli, MD, Zouheir Bitar, MD
Publikováno v:
JACC: Case Reports, Vol 29, Iss 13, Pp 102398- (2024)
Double connection of partial anomalous pulmonary venous return is a very rare congenital anomaly where at least one pulmonary vein, but not all, drains into the left atrium and systemic venous circulation with subsequent left to right shunt.
Externí odkaz:
https://doaj.org/article/6ff6b5b197f14f7cb667cd5b627db40f