Results 41 to 50 of about 25,126 (264)

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

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

Left atrial anomalous muscular band as incidental finding during video-assisted mitral surgery [PDF]

open access: yes, 2018
Congenital fibromuscular bands have been described inleft ventricle or right atrium and have been diagnosed by echocardiography and CT scan. The first report of anomalous band in the left atrium was described in 1897 by Rollestone (1).
Baldascino, Francesco   +6 more
core   +1 more source

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

Stroke and migraine is there a possible comorbidity? [PDF]

open access: yes, 2016
The association between migraine and stroke is still a dilemma for neurologists. Migraine is associated with an increased stroke risk and it is considered an independent risk factor for ischaemic stroke in a particular subgroup of patients.
Del Balzo, Francesca   +7 more
core   +2 more sources

Local DRLs and automated risk estimation in paediatric interventional cardiology [PDF]

open access: yes, 2019
Introduction : Cardiac catheterization procedures result in high radiation doses and often multiple procedures are necessary for congenital heart disease patients. However, diagnostic reference levels (DRL) remain scarce.
Bacher, Klaus   +5 more
core   +2 more sources

Nationwide Hospitalization Trends in Adult Congenital Heart Disease Across 2003–2012

open access: yesJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2016
BackgroundWe aimed to assess trends in hospitalization, outcomes, and resource utilization among patients admitted with adult congenital heart disease (ACHD). Methods and ResultsWe used the 2003–2012 US Nationwide Inpatient Sample for this study.
Shikhar Agarwal, Karan Sud, Venu Menon
doaj   +1 more source

Proposed neural crest involvement in concomitant bifid xiphoid process and atrial septal defect: A case study and review of literature

open access: yesTranslational Research in Anatomy, 2022
Background: The sternum and the heart are derived from the mesodermal germ layer; abnormalities in their development and differentiation can result in sternal and cardiac defects, including bony malformations and septal defects, respectively.
Adam Pasquinelly   +3 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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