Document Detail


Short QT interval in clinical practice.
MedLine Citation:
PMID:  20667544     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The last ten years have seen a growing interest in clinical scenarios, where a short QT interval may play a role, especially because of an increased risk of sudden cardiac death in some situations. One such entity is Short QT Syndrome, which has emerged as a rare, but very malignant disease, in particular when the QT interval is very short. A short QT interval has also been noticed in some patients with other arrhythmic syndromes such as Idiopathic Ventricular Fibrillation, Brugade Syndrome and Early Repolarization Syndrome, but the role of a short QT interval in these settings is so far not known. Hypercalcemia often leads to shortening of the QT interval, but there are no data in humans to suggest an increased risk of sudden cardiac death in this setting. In addition, a shorter-than-usual QT interval has been reported in patients with Chronic Fatigue Syndrome and in response to atropine, catecholamine and Hyperthermia. When a short QT interval is encountered in daily clinical practice, these various scenarios needs to be considered, but it is still not possible to come up with clear guidelines for how to work up and risk stratify such individuals. Genetic testing is only useful in very few and the value of an electrophysiologic study, Holter monitoring or stress testing to assess QT adaptation to heart rate and T wave morphology analysis may all be helpful, but not well-established, tests in this setting.
Authors:
Preben Bjerregaard; Hari Nallapaneni; Ihor Gussak
Related Documents :
19400534 - A case of brugada syndrome in a 63 y/o man with chest pain.
17399644 - Novel scn5a mutation (q55x) associated with age-dependent expression of brugada syndrom...
19365654 - Short qt syndrome in a pediatric patient.
8225664 - Syncope and long qt syndrome with an initially normal qt interval.
18672144 - Multiple endocrine neoplasia syndromes.
11801894 - 22q11.2 deletion syndrome: digeorge, velocardiofacial, and conotruncal anomaly face syn...
Publication Detail:
Type:  Journal Article; Review     Date:  2010-07-27
Journal Detail:
Title:  Journal of electrocardiology     Volume:  43     ISSN:  1532-8430     ISO Abbreviation:  J Electrocardiol     Publication Date:    2010 Sep-Oct
Date Detail:
Created Date:  2010-08-23     Completed Date:  2011-01-11     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0153605     Medline TA:  J Electrocardiol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  390-5     Citation Subset:  IM    
Copyright Information:
Published by Elsevier Inc.
Affiliation:
Division of Cardiology, VA Medical Center and Washington University in St. Louis, St. Louis, MO 63106, USA. preben.bjerregaard@va.gov
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Arrhythmias, Cardiac / complications,  diagnosis*,  genetics,  physiopathology
Death, Sudden, Cardiac / etiology
Electrocardiography
Electrophysiologic Techniques, Cardiac
Genetic Testing
Humans
Risk Assessment
Risk Factors

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Self-assembly of polyoxometalate-azure A multilayer films and their photocatalytic properties for de...
Next Document:  Dynamic properties of selected repolarization descriptors.