Catecholaminergic polymorphic ventricular tachycardia: Difference between revisions

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{{SI}}
{{Infobox medical condition
| name            = Catecholaminergic polymorphic ventricular tachycardia
| image          = [[File:ECG000033_(CardioNetworks_ECGpedia).jpg|left|thumb|ECG showing polymorphic ventricular tachycardia]]
| caption        = ECG showing polymorphic ventricular tachycardia
| field          = [[Cardiology]]
| symptoms        = [[Palpitations]], [[syncope]], [[sudden cardiac arrest]]
| onset          = Childhood or adolescence
| duration        = Episodic
| causes          = Genetic mutations in [[RYR2]] or [[CASQ2]]
| risks          = [[Exercise]], [[emotional stress]]
| diagnosis      = [[Electrocardiogram]], [[genetic testing]]
| differential    = [[Long QT syndrome]], [[Brugada syndrome]]
| treatment      = [[Beta blockers]], [[implantable cardioverter-defibrillator]]
| prognosis      = Variable, risk of sudden cardiac death
| frequency      = Rare
}}
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) is an [[inherited cardiac disorder]] characterized by an abnormal heart rhythm known as [[ventricular tachycardia]], which arises in response to physical activity or acute emotional stress. It is considered a [[rare genetic condition]] that can lead to [[syncope]] (fainting), [[cardiac arrest]], or even [[sudden cardiac death]] in young individuals with structurally normal hearts.
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) is an [[inherited cardiac disorder]] characterized by an abnormal heart rhythm known as [[ventricular tachycardia]], which arises in response to physical activity or acute emotional stress. It is considered a [[rare genetic condition]] that can lead to [[syncope]] (fainting), [[cardiac arrest]], or even [[sudden cardiac death]] in young individuals with structurally normal hearts.
[[File:Lead II rhythm ventricular tachycardia Vtach VT (cropped).JPG|Lead II rhythm ventricular tachycardia Vtach VT|500px|right|frameless]]
[[File:Lead II rhythm ventricular tachycardia Vtach VT (cropped).JPG|Lead II rhythm ventricular tachycardia Vtach VT|500px|right|frameless]]
=== Pathophysiology ===
=== Pathophysiology ===
CPVT is primarily caused by mutations in genes that encode proteins responsible for calcium regulation within the [[cardiac myocyte]]. The most commonly implicated genes are the [[RYR2]], which encodes the ryanodine receptor, and [[CASQ2]], which encodes calsequestrin. These mutations lead to an abnormal calcium release from the [[sarcoplasmic reticulum]], causing the heart muscle cells to contract inappropriately.
CPVT is primarily caused by mutations in genes that encode proteins responsible for calcium regulation within the [[cardiac myocyte]]. The most commonly implicated genes are the [[RYR2]], which encodes the ryanodine receptor, and [[CASQ2]], which encodes calsequestrin. These mutations lead to an abnormal calcium release from the [[sarcoplasmic reticulum]], causing the heart muscle cells to contract inappropriately.
=== Symptoms and Diagnosis ===
=== Symptoms and Diagnosis ===
Individuals with CPVT may experience symptoms such as [[dizziness]], [[palpitations]], [[syncope]], or [[seizures]], typically triggered by physical or emotional stress. In some cases, the first manifestation of the disorder can be [[sudden cardiac death]]. Diagnosis is based on the clinical history, family history, genetic testing, and the characteristic findings on [[exercise stress testing]] or [[Holter monitoring]], where exercise or stress can provoke the characteristic [[bidirectional ventricular tachycardia]] or [[ventricular fibrillation]].
Individuals with CPVT may experience symptoms such as [[dizziness]], [[palpitations]], [[syncope]], or [[seizures]], typically triggered by physical or emotional stress. In some cases, the first manifestation of the disorder can be [[sudden cardiac death]]. Diagnosis is based on the clinical history, family history, genetic testing, and the characteristic findings on [[exercise stress testing]] or [[Holter monitoring]], where exercise or stress can provoke the characteristic [[bidirectional ventricular tachycardia]] or [[ventricular fibrillation]].
=== Treatment and Management ===
=== Treatment and Management ===
Management strategies for CPVT aim to prevent the occurrence of arrhythmias and include:
Management strategies for CPVT aim to prevent the occurrence of arrhythmias and include:
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* [[Implantable Cardioverter Defibrillator (ICD)]]: Recommended for high-risk patients or those who have experienced a cardiac arrest.
* [[Implantable Cardioverter Defibrillator (ICD)]]: Recommended for high-risk patients or those who have experienced a cardiac arrest.
* Lifestyle modification: Includes avoidance of competitive sports and situations that can lead to emotional stress.
* Lifestyle modification: Includes avoidance of competitive sports and situations that can lead to emotional stress.
=== Prognosis ===
=== Prognosis ===
The prognosis for individuals with CPVT who are not treated is poor due to the risk of recurrent arrhythmias and sudden cardiac death. However, with appropriate diagnosis, genetic counseling, and treatment, many patients can lead a normal life.
The prognosis for individuals with CPVT who are not treated is poor due to the risk of recurrent arrhythmias and sudden cardiac death. However, with appropriate diagnosis, genetic counseling, and treatment, many patients can lead a normal life.
== Glossary of Terms ==
== Glossary of Terms ==
* '''[[Adrenergically mediated arrhythmias]]''' - Abnormal heart rhythms triggered by the body's adrenaline response.
* '''[[Adrenergically mediated arrhythmias]]''' - Abnormal heart rhythms triggered by the body's adrenaline response.

Latest revision as of 21:20, 4 April 2025

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD medical weight loss NYC and sleep center NYC

Catecholaminergic polymorphic ventricular tachycardia
ECG showing polymorphic ventricular tachycardia
Synonyms N/A
Pronounce N/A
Specialty N/A
Symptoms Palpitations, syncope, sudden cardiac arrest
Complications N/A
Onset Childhood or adolescence
Duration Episodic
Types N/A
Causes Genetic mutations in RYR2 or CASQ2
Risks Exercise, emotional stress
Diagnosis Electrocardiogram, genetic testing
Differential diagnosis Long QT syndrome, Brugada syndrome
Prevention N/A
Treatment Beta blockers, implantable cardioverter-defibrillator
Medication N/A
Prognosis Variable, risk of sudden cardiac death
Frequency Rare
Deaths N/A


Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) is an inherited cardiac disorder characterized by an abnormal heart rhythm known as ventricular tachycardia, which arises in response to physical activity or acute emotional stress. It is considered a rare genetic condition that can lead to syncope (fainting), cardiac arrest, or even sudden cardiac death in young individuals with structurally normal hearts.

Lead II rhythm ventricular tachycardia Vtach VT
Lead II rhythm ventricular tachycardia Vtach VT

Pathophysiology[edit]

CPVT is primarily caused by mutations in genes that encode proteins responsible for calcium regulation within the cardiac myocyte. The most commonly implicated genes are the RYR2, which encodes the ryanodine receptor, and CASQ2, which encodes calsequestrin. These mutations lead to an abnormal calcium release from the sarcoplasmic reticulum, causing the heart muscle cells to contract inappropriately.

Symptoms and Diagnosis[edit]

Individuals with CPVT may experience symptoms such as dizziness, palpitations, syncope, or seizures, typically triggered by physical or emotional stress. In some cases, the first manifestation of the disorder can be sudden cardiac death. Diagnosis is based on the clinical history, family history, genetic testing, and the characteristic findings on exercise stress testing or Holter monitoring, where exercise or stress can provoke the characteristic bidirectional ventricular tachycardia or ventricular fibrillation.

Treatment and Management[edit]

Management strategies for CPVT aim to prevent the occurrence of arrhythmias and include:

Prognosis[edit]

The prognosis for individuals with CPVT who are not treated is poor due to the risk of recurrent arrhythmias and sudden cardiac death. However, with appropriate diagnosis, genetic counseling, and treatment, many patients can lead a normal life.

Glossary of Terms[edit]



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