Catecholaminergic Polymorphic Ventricular Tachycardia: Difference between revisions

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|mainauthor= [[user:Pgpostema|P.G. Postema, MD]]
|mainauthor= [[user:Drj|J.S.S.G. de Jong, MD]]
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|coauthor= [[user:Drj|J.S.S.G. de Jong, MD]]
|coauthor= [[user:Pgpostema|P.G. Postema, MD]]
|moderator= [[user:Pgpostema|P.G. Postema, MD]]
|moderator= [[user:Pgpostema|P.G. Postema, MD]]
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[[File:ECG000032.jpg|thumb|300px|right|The ECG of a patient with CPVT in rest is normal]]
[[File:ECG000033.jpg|thumb|300px|right|The ECG of the same patient with CPVT during exercise. Asterisks mark polymorphic ventricular beats.]]
'''Catecholaminergic Polymorphic Ventricular Tachycardia''' is a congenital disease that leads to exercise induced [[Ventricular Arrhythmias|ventricular arrhythmias]] and / or syncope and carries an increased risk of sudden death.


Catecholaminerge Polymorfe [[Ritmestoornissen#Ventrikeltachycardie|Ventriculaire Tachycardie]] is een erfelijke aandoening, die zich uit als inspanningsgeboden of door stress uitgelokte ventriculaire ritmestoornissen, [[syncope]] of plotse dood.
'''Characteristics of CPVT:'''
*The mean onset of arrhythmias is 7-9 years
*Absence of structural cardiac abnormalities
*Normal resting ECG
*Syncope during physical activity or emotional stress


De ritmestoornissen treden meestal al in de kinderleeftijd op, maar kunnen zich ook pas in de volwassen leeftijd manifesteren.
'''Diagnosis'''
*The diagnosis is based on the patient's clinical history (dizziness or syncope induced by exercise or emotional stress and a family history containing syncope or sudden death in young relatives related to similar triggers) and reproducible ventricular arrhythmias during [[Exercise Testing|exercise testing]]. The complexity of these arrhythmias often increases with increasing work load, starting with [[Ventricular Premature Beats]], and ending with bidirectional [[Ventricular Tachycardia|ventricular tachycardia]] to [[Ventricular Tachycardia|polymorphic ventricular tachycardia]].
*Two genes have been linked to CPVT. Both lead to a defect in intracellular calcium metabolism:
** the hRyR2 gene, coding for the cardiac ryanodine receptor: ([[w:OMIM|OMIM™]] link {{OMIM2|180902}}) (50-55 % of patients)
** the CASQ2 gene, coding for the calsequestrine protein: ([[w:OMIM|OMIM™]] link {{OMIM2|114251}}) (1-2 % of patients)


De ventriculaire ritmestoornissen treden alleen op in situaties waarbij [[:w:catecholamine|catecholamines]] (zoals adrenaline) vrijkomen zoals fysieke inspanning en / of bij emotionele stress.
'''Treatment'''<cite>sumitomo</cite>
In rust zijn er aan het ECG geen afwijkingen te zien.
* Beta-blockers
Er zijn afwijkingen op 2 genen bekend die CPVT kunnen veroorzaken (een gen dat codeert voor de cardiale ryanodine receptor hRyR2 ([[w:OMIM|OMIM&trade;]] link {{OMIM2|180902}})  en een gen dat codeert vor het eiwit calsequestrine CASQ2 ([[w:OMIM|OMIM&trade;]] link {{OMIM2|114251}}). Beide genen spelen een rol in de calciumhuishouding van hartcellen. De calciumconcentratie in de cellen is daardoor verhoogd.
* [[ICD|ICD (Internal Cardioverter Defibrillator)]] implantation combined with beta-blockers in CPVT patients who survived a cardiac arrest or patients with syncope and/or documented sustained [[Ventricular Tachycardia|ventricular tachycardia]] despite beta-blocker therapy.<cite>ACC2006</cite>
* Surgical left cardiac sympathetic denervation in selected patients whose symptoms and/or ventricular arrhythmias are not controlled by pharmacologic therapy <cite>Wilde</cite><cite>Collura</cite>
* Avoid competitive and other strenuous exercise


De prevalentie van CPVT is nog onbekend. De man/vrouw verhouding is 1.
===References===
 
===Behandeling===
De behandeling:<cite>ACC2006</cite>
* Beta-blokkers
* [[w:nl:Internal_Cardiac_Defibrillator|ICD]] implantatie in combinatie met beta-blokkers bij patiënten die een hartstilstand hebben overleefd
 
===Externe Links===
*[http://www.cardiogenetica.nl Cardiogenetica.nl]
 
===Referenties===
<biblio>
<biblio>
#ACC2006 pmid=16935995
#ACC2006 pmid=16935995
#sumitomo pmid=12482795
#Wilde pmid=18463378
#Collura pmid=19467503
</biblio>
</biblio>
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