Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
1994-4-5
pubmed:abstractText
Arrhythmogenic right ventricular dysplasia (ARVD) may result in sudden death of young and sometimes athletic individuals, while if properly treated it is associated with a good prognosis. It is probably more widespread than currently thought. Comparison of the electrocardiograms of 43 ARVD patients with those of 44 normal individuals provided a new criterion enabling identification of the disease. Measurement of a QRS interval longer than 110 ms in sinus rhythm in lead V1 in an individual with an apparently normal heart enabled identification of the disease with a sensitivity of 55 p. cent and specificity of 100 p. cent if used alone, and a sensitivity of 60 p. cent if used in combination with a prolongation of QRS in lead V3 to greater than 110 ms, but with a specificity of 82 p. cent. After elimination of appearances of right bundle branch block, sensitivity was 50 p. cent for V1. This parameter studied in a hospital population should be validated in minor forms before leading to compulsory ECGs for individuals in high-risk occupations (athletes, public vehicle drivers, etc.).
pubmed:language
fre
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0003-3928
pubmed:author
pubmed:issnType
Print
pubmed:volume
42
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
399-405
pubmed:dateRevised
2009-11-11
pubmed:meshHeading
pubmed:year
1993
pubmed:articleTitle
[Duration of QRS complexes in arrhythmogenic right ventricular dysplasia. A new non-invasive diagnostic marker].
pubmed:affiliation
Service de Rythmologie et de Stimulation Cardiqque, Hôpital Jean-Rostand, Ivry-sur-Seine.
pubmed:publicationType
Journal Article, English Abstract