Arrhythmia: Long QT syndrome (Complete) Flashcards
What is long QT syndrome?
Inherited or aquired condition characterised by delayed repolarisation of the ventricles resulting in a prolonged QT interval
What can long QT syndrome progress to?
Ventricular tacchycardia and then sudden cardiac death
What are 2 congenital causes of a prolonged QT interval?
Jervell-Lange-Nielsen syndrome (includes deafness and is due to an abnormal potassium channel)
Romano-Ward syndrome (no deafness)
List drugs which can cause a prolonged QT interval (8)
Antiarrhythmics: e.g. amiodarone, sotalol (beta-blocker), class 1A antiarrhythmics
TCAs and SSRIs (especially citalopram)
Methadone (opiod)
Chloroquine (antimalarial)
Terfenadine (antihistamine)
Macrolide ABs (e.g. erythromycin)
Anti-psychotics (e.g. Haloperidol)
Ondanestron (anti-emetic for chemotherapy)
What are non congenital/drug related causes of a prolonged QT interval? (8)
Hypocalcaemia
Hypokalaemia
Hypomagnasaemia
Acute MI
Myocarditis
Hypothermia
SAH
What are some of the main presentations of long QT syndrome? (5)
Depends on the type of long QT syndrome:
Long QT1: Exertional syncope (e.g. often occurs when swimming)
Long QT2: Syncope during emotional stress, exercise or auditory stimuli.
Long QT3: Events occur at night or at rest
May be picked up on ECG
Sudden cardiac death (common cause in young people)
What are the main investigations for long QT syndrome? (4)
Bedside: ECG (would show signs prolonged QT intervals)
Bloods:
U&Es: Serum pottasium
serum magnesium
serum calcium (can cause long QT syndrome)
What is the management plan for patients with long QT syndrome?
Conservative/lifestyle:
Avoid drugs which can cause QT syndrome
Avoid strenous exercise
Pharmacological:
Beta-blockers (AVOID SOLTALOL)
Surgical: Implantable cardioverter defibrilators (in severe cases)