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Inherited long QT syndrome

Overview of attention for article published in Herzschrittmachertherapie + Elektrophysiologie, September 2012
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Title
Inherited long QT syndrome
Published in
Herzschrittmachertherapie + Elektrophysiologie, September 2012
DOI 10.1007/s00399-012-0232-8
Pubmed ID
Authors

Sven Zumhagen, Birgit Stallmeyer, Corinna Friedrich, Lars Eckardt, Guiscard Seebohm, Eric Schulze-Bahr

Abstract

Inherited long QT syndrome (LQTS) is characterized by a prolonged ventricular repolarization (QTc interval) and symptoms (syncope, sudden cardiac arrest) due to polymorphic ventricular arrhythmias. As of today, 13 different cardiac ion channel genes have been associated with congenital LQTS. The most common ones are due to KCNQ1 (LQT-1), KCNH2 (LQT-2), and SCN5A (LQT-3) gene mutations and account for up to 75 % of cases. Typical clinical findings are an increased QT interval on the surface electrocardiogram, specifically altered T wave morphologies, polymorphic ventricular arrhythmias, or an indicative family history. Recently, in the HRS/EHRA expert consensus statement, comprehensive genetic testing of major LQTS genes was recommended for index patients for whom there is a strong clinical suspicion of LQTS. Overall, antiadrenergic therapy, in particular β-receptor blockers, has been the mainstay of therapy and has significantly reduced cardiac events. For high-risk patients, an implantable cardioverter defibrillator (ICD) is recommended. Importantly, lifestyle modification and avoidance of arrhythmia triggers are additional important approaches.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 29 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 29 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 17%
Student > Ph. D. Student 5 17%
Student > Bachelor 4 14%
Student > Master 4 14%
Student > Postgraduate 3 10%
Other 4 14%
Unknown 4 14%
Readers by discipline Count As %
Medicine and Dentistry 15 52%
Agricultural and Biological Sciences 7 24%
Biochemistry, Genetics and Molecular Biology 1 3%
Neuroscience 1 3%
Chemistry 1 3%
Other 0 0%
Unknown 4 14%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 17 October 2012.
All research outputs
#16,049,105
of 23,815,455 outputs
Outputs from Herzschrittmachertherapie + Elektrophysiologie
#74
of 155 outputs
Outputs of similar age
#109,421
of 172,351 outputs
Outputs of similar age from Herzschrittmachertherapie + Elektrophysiologie
#2
of 2 outputs
Altmetric has tracked 23,815,455 research outputs across all sources so far. This one is in the 22nd percentile – i.e., 22% of other outputs scored the same or lower than it.
So far Altmetric has tracked 155 research outputs from this source. They receive a mean Attention Score of 3.7. This one is in the 41st percentile – i.e., 41% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 172,351 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 26th percentile – i.e., 26% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 2 others from the same source and published within six weeks on either side of this one.