Long QT Syndrome
Einstein Health Glossary
ICD 10 - I45.8
ICD 10 - I45.8
It is a genetic disorder characterized by an abnormal prolongation of a measurement on the electrocardiogram called the QT interval. It results from abnormalities in the potassium or sodium channels of the heart and can lead to severe arrhythmias in young and otherwise healthy individuals.
The disease is caused by genetic alterations in certain ion channels (structures that control the flow of electrical currents across cell membranes) of the heart.
Often, it causes no symptoms, but it can lead to fainting and, in more severe cases, cardiac arrest.
Diagnosis is based on clinical features and electrocardiogram findings. Genetic testing may be necessary in some cases.
Treatment may involve medications or the implantation of a defibrillator.
In some forms of the disease, intense physical exercise should be avoided. Caution is also needed with the use of certain medications (antiarrhythmics, antiemetics, antidepressants, antibiotics) that can trigger episodes of tachycardia in these patients.
By Einstein Editorial Board