Results 41 to 50 of about 24,399 (268)

Platypnea Orthodeoxia Syndrome Secondary to Intracardiac Shunt Following Orthotopic Liver Transplantation

open access: yesJournal of Investigative Medicine High Impact Case Reports, 2020
Platypnea orthodeoxia syndrome (POS) occurs when an upright position results in acute-onset hypoxemia and is relieved with recumbency. POS can be due to intracardiac shunting, intrapulmonary shunting, ventilation-perfusion mismatch, or a combination of ...
Sophia R. Larson MD   +2 more
doaj   +1 more source

Prenatal ultrasonographic characteristics and prognosis of isolated redundant foramen ovale flap

open access: yesGynecology and Obstetrics Clinical Medicine, 2022
Objective: To analyze the prenatal ultrasonographic characteristics and prognosis of the isolated redundant foramen ovale flap (RFOF). Methods: From January 2014 to December 2021, we collected data on fetal echocardiography analyses and perinatal ...
Yuntao Li   +4 more
doaj   +1 more source

Critical congenital heart disease screening by pulse oximetry in a neonatal intensive care unit. [PDF]

open access: yes, 2014
ObjectiveCritical congenital heart disease (CCHD) screening is effective in asymptomatic late preterm and term newborn infants with a low false-positive rate (0.035%).
Carrion, V   +3 more
core   +2 more sources

Giant aneurysm of the atrial septum associated with premature closure of foramen ovale

open access: yesCardiovascular Ultrasound, 2005
Premature closure or restriction of foramen ovale (PCFO) is a rare congenital anomaly that can lead to a wide spectrum of cardiac malformations. This spectrum of secondary malformations appears to depend on the gestational timing of closure of the ...
Romaguera Rita L   +2 more
doaj   +1 more source

Paradoxical Embolism After a Traffic Accident: A Rare Case of Thrombus Entrapped in a Patent Foramen Ovale

open access: yesİstanbul Medical Journal, 2021
Paradoxical embolism is the passage of a thrombus formed in the venous system through shunts in the lung or heart into the systemic circulation. The most common intracardiac shunt is a patent foramen ovale (PFO). Since the transition of a thrombus formed
Şerif Ahmet Kandemir   +3 more
doaj   +1 more source

Endocardial fibroelastosis [PDF]

open access: yes, 1967
This is an article delivered at a meeting of the British Medical Association (Malta Branch) on the 7th March 1967. During the eleven-year period 1955-66 eight cases of endocardial fibroelastosis were diagnosed or confirmed at autopsy.
Captur, Victor   +2 more
core   +1 more source

Platypnea-orthodeoxia due to osteoporosis and severe kyphosis: a rare cause for dyspnea and hypoxemia

open access: yesHeart International, 2011
Platypnea orthodeoxia is a rare disorder characterised by dyspnea and arterial desaturation, exacerbated by the upright position and relieved when the subject is recumbent.
Gerian C. Groenefeld, Claudius Teupe
doaj   +1 more source

Evaluation of critical congenital heart defects screening using pulse oximetry in the neonatal intensive care unit. [PDF]

open access: yes, 2017
ObjectiveTo evaluate the implementation of early screening for critical congenital heart defects (CCHDs) in the neonatal intensive care unit (NICU) and potential exclusion of sub-populations from universal screening.Study designProspective evaluation of ...
Allen, D   +20 more
core   +2 more sources

Platypnea-Orthodeoxia Syndrome With Normal Right Heart Pressures in an Octogenarian

open access: yesJACC: Case Reports, 2020
We describe a case of platypnea-orthodeoxia syndrome in an 88-year-old man who presented with progressive dyspnea. Right-to-left shunting through a patent foramen ovale (PFO) was seen in the setting of normal right-sided heart pressures.
Marcin Kuzma, MD   +2 more
doaj   +1 more source

Patent foramen ovale and thromboembolic complications [PDF]

open access: yes, 2010
The foramen ovale, an atrial septal defect which is essential in the fetal circulation, remains patent through adulthood in approximately 25% of the general population and so it represents the most common persistent abnormality of fetal origin.
Barbaro, G   +6 more
core   +1 more source

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