Difference between revisions of "LQTS"

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(Clinical diagnosis)
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The three most common forms of LQTS can be recognized by the characteristic clinical features and ECG abnormalities.
The three most common forms of LQTS can be recognized by the characteristic clinical features and ECG abnormalities.
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Revision as of 19:01, 31 October 2012

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The Long QT Syndrome (LQTS) refers to a condition in which there is an abnormally long QT interval on the ECG. This was first recognized by Dr. Jervell and Dr. Lange-Nielsen in 1957. They described 4 children with a long QT interval which was accompanied by hearing deficits, sudden cardiac death and an autosomal recessive inheritance. [1]

The LQTS may be divided into two distinct forms: congenital LQTS and acquired LQTS. These forms may however overlap when QT prolongation due to medication occurs in a patient with congenital LQTS.



File:De-Formule QTc.png
Formula for heart rate corrected QT interval (Bazett’s formula)
  • The diagnosis is by measurement of the heart rate corrected QT interval on the ECG, which can be calculated with the QTc calculator.
  • Sometimes the QT interval can be difficult to assess. Read the guidelines for measurement of difficult QT interval.
  • A QTc of > 500ms in patients with Long QT Syndrome is associated with an increased risk of torsade de pointes and sudden death. [2]
  • In patients suspected of LQTS (e.g. family members of known LQTS patients) a QTc > 430ms makes it likely that a LQTS gene defect is present.[3]
  • Because the QTc can change with age, it is best to take the ECG with the longest QTc interval for risk stratification. [4]

Physical examination

Patients can present with symptoms of arrhythmias:

  • Fast or slow heart beat
  • Skipping beats
  • Weakness, lightheadedness, dizziness, syncope
  • Chest pain
  • Shortness of breath
  • Paleness
  • Sweating

Acquired LQTS

Acquired LQTS is most often caused by drugs that prolong the QT interval; combined with risk factors the risk of Torsade de Pointes is likely to increase.

Notorious QT prolonging drugs: [5]

  1. Amiodarone
  2. Azithromycin
  3. Chloroquine
  4. Chlorpromazine
  5. Citalopram
  6. Claritromycin
  7. Disopyramide
  8. Dofetilide
  9. Erythromycin
  10. Flecainide
  11. Halofantrine
  12. Haloperidol
  13. Procainamide
  14. Quinidine
  15. Sotalol

Concomittant risk factors for medication induced torsade de pointes:

  1. Female sex
  2. Hypokalemia
  3. Bradycardia
  4. Recent conversion of atrial fibrillation, especially if QT prolonging drugs were used (sotalol, amiodarone)
  5. Cardiac decompensation
  6. Digoxin treatment
  7. High or overdosing or rapid infusion of a QT prolonging drug
  8. Pre-existing QT prolongation
  9. Congenital QT syndrome

Congenital LQTS

The prevalence of congenital LQTS is about 1:3000-5000. More than 10 different types of congenital LQTS have been described. However, only LQTS 1-3 are relatively common. [6]

The three most common forms of LQTS can be recognized by the characteristic clinical features and ECG abnormalities.

Gene/current KCNQ1/IKs KCNH2/IKr SCN5A/INa
B-blokker efficacy ++++ + ±
ECG Early onset

broad based T wave

Small late T wave Late onset

T wave with normal configuration

Arrhythmogenic triggers Exercise, especially swimming Adrenergic triggers, especially nightly noise Rest
Number of mutation carriers with events at age <40 25% 50% 50%
SCD incidence 0,30% / year 0,60% / year 0,56% / year
Eponyme If condition is homozygous:

Jervell and Lange-Nielsen syndrome 1

If condition is homozygous:

Jervell and Lange-Nielsen syndrome 2

Before the genes involved were known, some syndromes associated with a prolonged QT interval on the ECG had been described earlier:

  • Anton Jervell and Fred Lange-Nielsen [1] from Oslo described in 1957 an autosomaal recessive syndrome that was associated with QT interval prolongation, deafness and sudden death: the now called Jervell-Lange-Nielsen syndrome.
  • Romano-Ward syndrome is a long QT syndrome with normal auditory function and autosomal dominant inheritance.
  • Andersen-Tawil syndrome was described in 1994 by Tawil et al. and was associated with potassium-sensitive periodic paralysis, ventricular ectopy and dysmorphic features (short stature, low-set ears, hypoplastic mandible, clinodactyly and scoliosis). It later appeared to be associated with a mutation in the KCNJ2 gene (LQTS type 7).
  • Timothy syndrome is a LQTS syndrome (with frequently alternating T-waves) with webbing of fingers and toes, congenital heart disease, immune deficiency, intermittent hypoglycaemia, cognitive abnormalities and autism. It appeared to be caused by mutations in the CACNA1C gene (LQTS type 8).

Clinical diagnosis

Diagnosis of LQTS is established by prolongation of the QTc interval in the absence of specific conditions known to lengthen it (for example QT-prolonging drugs) and/or molecular genetic testing of genes associated with LQTS.

Diagnostic criteria by Schwartz et al.
Findings Points
ECG QTc: >480 ms



>480 during






Torsade de pointes

T-wave alternans

Notched T-wave in 3 leads

Low heart rate for age (<2nd percentile for age)





Syncope: With stress

Without stress



Clinical history Congenital deafness

Family members with definite LQTS



Family history Unexplained sudden cardiac death before age 30 0.5
Total score =1 Low probability; 1.5-3 Intermediate probability; =3.5 High probability
Various triggers for cardiac events have been identified among the different genotypes.

The prolonged QT interval can cause torsade de pointes, which is usually self-terminating, thus causing a cardiac syncopal event. The mean age of onset of symptoms (syncope or sudden death) is 12 years and earlier onset is usually associated with more severe form of the disease. In LQTS type 1, cardiac symptoms are often precipitated by exercise; especially swimming is notorious for life-threatening cardiac events. In LQTS type 2, arrhythmogenic triggers are adrenergic; especially nightly noise (such as the morning alarm clock or nightly thunderlightening) is known to cause life-threatening cardiac events. On the other hand, in LQTS type 3, QT prolongation and possibly subsequent torsade de pointes is precipitated by bradycardia.

ECG tests

Various ECG patterns can be recognized among the different genotypes

ECGs can be difficult because there is a considerable overlap between the QT interval of affected and unaffected individuals.

  • The resting ECG is neither completely sensitive nor specific for the diagnosis of LQTS. The diagnostic criteria for the resting ECG are shown in the list of diagnostic criteria by Schwartz. Besides a prolonged QTc, the T-wave can have different patterns among the different genotypes.
  • Holter recordings appear to be of minimal clinical utility from a diagnostic and prognostic prospective in evaluating LQTS
  • The exercise ECG (X-ECG) commonly shows failure of the QT to shorten normally, thereby prolonging the corrected QT interval, and many individuals develop characteristic T-wave abnormalities.
  • A brisk-standing test ECG, where the QT-interval is measured after abrupt standing with subsequent heart rate acceleration. There appears to be a form of QT-stretching and QT-stunning as demonstrated by Viskin et al. and Adler et al.
  • Epinephrine infusion is a provocative test that increases the sensitivity of the ECG findings
  • Adenosine infusion is a test provoking transient bradycardia followed by sinus tachycardia and therefore triggers QT changes that can distinguish patients with LQTS from healthy controls

Genetic diagnosis

Today, 13 LQTS genes associated with LQTS have been identified. Most commonly, KCNQ1, KCNH2 and SCN5A, which are associated with LQTS type 1, type 2 and type 3 respectively, are found. Other, less frequently involved genes are displayed the table below.

LQTS type Gene Protein (Ionchannel) OMIM-link
Type 1 KCNQ1 KVLQT1 (IKs) 607542
Type 2 KCNH2 HERG (IKr) 613688
Type 3 SCN5A Sodium channel (INa) 603830
Type 4 ANK2 Ankyrin B (INa, K) 600919
Type 5 KCNE1 minK (IKs) 176261
Type 6 KCNE2 MiRP1 (IKr) 613693
Type 7 KCNJ2 Kir 2.1 (IK1) 170390
Type 8 CACNA1C Cav1.2 (ICa-L) 601005
Type 9 CAV3 Caveolin-3 601253
Type 10 SCN4B Sodium channel (INa) 608256
Type 11 AKAP9 A-Kinase anchor 9 (IKs) 604001
Type 12 SNTA1 Syntrophin (INa) 601017
Type 13 KCNJ5 Kir3.4 (IK) 600734

There is an important genotype-phenotype relationship on severity of the disease. In genotype–phenotype studies in the Rochester LQTS registry it was shown that in both LQTS type 1 and type 2, mutation locations and the degree of ion channel dysfunction caused by the mutations are important independent risk factors influencing the clinical course of this disorder.

Risk Stratification

Gene-specific differences of the natural history of LQTS have also been demonstrated and allow genotype-based risk stratification. Indeed, QT interval duration, gender and genotype (including mutation location and degree of ion channel dysfunction) are significantly associated with the outcome, with a QTc interval >500ms, and a LQT2 or LQT3 genotype determining the worst prognosis. Gender differently modulates the outcome according to the underlying genetic defect: the LQT3 males and LQT2 females are the highest risk subgroups. Risk stratification is best done by an expert cardio-genetics cardiologist.

Treatment [6]

Lifestyle modification

  • No competitive sports in all LQTS patients
  • Avoid QT-prolonging drugs in all LQTS patients
  • No swimming in LQT1 patients
  • Avoid nightly noise in LQT2 patients (e.g. no alarm clock)

Medication/Other therapies

  • Beta-blockers are the cornerstone of therapy in LQTS. Beta-blockers even reduce the risk of sudden death in patients in whom a genetic defect has been found, but no QT prolongation is visible on the ECG and probably even in LQTS3 patients with bradycardia-associated cardiac events
  • ICD implantation in combination with beta-blockers in LQTS patients with previous cardiac arrest, cardiac syncope or ventricular tachycardia while on beta-blockers. Symptomatic patients with LQTS type 3 can only be treated with an ICD with pacing possibilities, since their arrhythmic episodes are bradycardia-associated.
  • Cardiac sympathetic denervation (LCSD) should be considered in the setting of beta-blocker breakthroughs, intolerance to pharmacotherapy and history of appropriate ICD therapies. Surgically, LCSD involves the resection of the lower half of the left stellate ganglion and the left-sided sympathetic chain at the level of T2, T3 and T4.


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All Medline abstracts: PubMed | HubMed