نتایج جستجو برای: ecg abnormalities

تعداد نتایج: 124780  

Journal: :Thorax 1977
D Siegler

Previous reports have documented the occurrence of reversible electrocardiographic changes including right axis deviation, P pulmonale, right bundle-branch block, and ST-segment and T-wave abnormalities in patients with acute attacks of asthma. In a further systematic study, the electrocardiographs of 63 patients admitted with severe acute asthma have been evaluated. The most consistent change ...

Journal: :Chest 1988
L Bodin J J Rouby P Viars

Fifty five patients suffering from blunt chest trauma were studied to assess the diagnosis of myocardial contusion using thallium 201 myocardial scintigraphy. Thirty-eight patients had consistent scintigraphic defects and were considered to have a myocardial contusion. All patients with scintigraphic defects had paroxysmal arrhythmias and/or ECG abnormalities. Of 38 patients, 32 had localized S...

Journal: :CJEM 2012
Venkatesh Thiruganasambandamoorthy Erik P Hess Ekaterina Turko My-Linh Tran George A Wells Ian G Stiell

BACKGROUND Previous studies have indicated that the suboptimal performance of the San Francisco Syncope Rule (SFSR) is likely due to the misclassification of the "abnormal electrocardiogram (ECG)" variable. We sought to identify specific emergency department (ED) ECG and cardiac monitor abnormalities that better predict cardiac outcomes within 30 days in adult ED syncope patients. METHODS Thi...

2016
Laura Geraldino-Pardilla Yevgeniya Gartshteyn Paloma Piña Marina Cerrone Jon T Giles Afshin Zartoshti Joan M Bathon Anca D Askanase

OBJECTIVES Cardiovascular disease (CVD) is a leading cause of death in systemic lupus erythematosus (SLE) and in rheumatoid arthritis (RA). Although only explored in one study, ECG non-specific ST-T abnormalities, in addition to corrected QT-interval (QTc) prolongation, were recently reported in an SLE inception cohort. Importantly, these ECG abnormalities are known predictors of CVD mortality ...

2012
Mieke CE Hermans Catharina G Faber Sebastiaan CAM Bekkers Christine EM de Die-Smulders Monique M Gerrits Ingemar SJ Merkies Gabriel Snoep Yigal M Pinto Simon Schalla

BACKGROUND Myotonic dystrophy type 1 (MD1) is a neuromuscular disorder with potential involvement of the heart and increased risk of sudden death. Considering the importance of cardiomyopathy as a predictor of prognosis, we aimed to systematically evaluate and describe structural and functional cardiac alterations in patients with MD1. METHODS Eighty MD1 patients underwent physical examinatio...

Journal: :archives of cardiovascular imaging 0
arash gholoobi preventive cardiovascular care research center, imam reza hospital, faculty of medicine, mashhad university of medical sciences, mashhad, ir iran; preventive cardiovascular care research center, imam reza hospital, faculty of medicine, mashhad university of medical sciences, p. o. box: 9137913316, mashhad, ir iran. tel/fax: +98-5138544504

discussion the reason is that we assess the relative and not absolute differences of the tracer uptake in this imaging modality. there may be other findings on mpi images which could help us overcome this pitfall, including detecting wall motion abnormalities, lung uptake of the tracer, or transient ischemic dilation. another important issue is the ecg changes during exercise stress testing, wh...

2014
Axel Josefsson Michael Fu Einar Björnsson Evangelos Kalaitzakis

BACKGROUND Although cardiovascular disease is thouht to be common in cirrhosis, there are no systematic investigations on the prevalence of electrocardiographic (ECG) abnormalities in these patients and data on the occurrence of post-transplant cardiac events in comparison with the general population are lacking. We aimed to study the prevalence and predictors of ECG abnormalities in patients w...

A Ramazanpour H Babaei

LEOPARD syndrome is an autosomal dominant hereditary disease, which is characterized with cutaneous pigmented patches, electrocardiographic changes, ocular hypertelorism, retarded growth, pulmonic stenosis, genital abnormalities and congenital deafness. The gene of this disease have high penetrance but expression is varied and incomplete forms may be seen. We report a 23 year-old woman wi...

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