Difference between revisions of "Long QT Syndrome"

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#[http://www.sads.org Sudden Arrhythmia Death Syndrome Foundation]. LQTS patient group.
 
#[http://www.sads.org Sudden Arrhythmia Death Syndrome Foundation]. LQTS patient group.
 
#[http://www.fsm.it/cardmoc/ Inherited Arrhythmias Database]
 
#[http://www.fsm.it/cardmoc/ Inherited Arrhythmias Database]
 +
#Labor der Kardiologie des Herz- und Diabeteszentrum NRW [http://www.kardiogenetik.de kardiogenetik.de]
  
 
==Referenties==
 
==Referenties==

Revision as of 11:19, 30 September 2009

Author(s) J.S.S.G. de Jong, MD
Moderator P.G. Postema, MD
Supervisor
some notes about authorship
A 12 lead ECG of a patient with acquired long QT syndrome. Notice the QT prolongation. The QTc is about 640ms.

The Long QT Syndrome (LQTS) is characterized on the ECG by prolongation of the heart rate corrected QT interval. 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 Long QT syndrome may be divided into two distinct forms: congenital Long QT syndrome and acquired Long QT syndrome. These forms may however

Diagnosis

  • The diagnosis is by maesurement of the heart rate corrected QT interval on the ECG, which can be calculated with the QTc calculator.
  • Sometinmes 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 for 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]

Treatment[5]

  • "Lifestyle modification":
    • No competitive sports in all LQTS patients
    • No swimming in LQT1 patients
    • Avoid nightly noise in LQT2 patients (e.g. no alarm clock)
  • Medication: beta-blockers. 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.
  • ICD implantation in combination with beta-blockers in LQTS patients with previous cardiac arrest or syncope or ventricular tachycardia while on beta-blockers.

Acquired LQTS

Acquired LQTS is most often caused by drugs that prolong the QT interval. Combined with risk factors (see table) the risk of Torsade de Pointes increases.

Common drugs that can cause Torsade de Pointes include:[6]
  • Sotalol
  • Amiodarone
  • Erythromycin
  • Clarithromycin
Less often used drugs include:
  • Cisapride
  • antibiotics: halofantrine, pentamidine, sparfloxacin
  • Anti-emetics: domperidon, droperidol
  • Anti-psychotics: chlorpromazine, haloperidol, mesoridazine, thioridazine, pimozide
  • Methadon
  • Disopyramide
  • Dofetilide
  • Ibutilide
  • Procainamide
  • Quinidine
  • Bepridil
Torsades.org has an extensive list of drugs that can TdP
Concomittant risk factors for medication induced Torsade de Pointes:
  • Female sex
  • Hypokalemia
  • Bradycardia
  • Recent conversion of atrial fibrillation, especially if QT prolonging drugs were used (sotalol, amiodarone)
  • Cardiac decompensation
  • Digoxin treatment
  • High or overdosing or rapid infusion of a QT prolonging drug
  • Pre-existing QT prolongation
  • Congenital long QT syndrome

Congenital LQTS

The three most common forms of LQTS can be recognized by the characteristic ECG abnormalities

:

  • LQT1 'early onset' broad based T wave
  • LQT2 small late T wave
  • LQT3 prolonged QT interval with 'late onset' T wave with a normal configuration

In congenital LQTS the ventricular repolarisation is prolonged. The prevalence is about 1:3000-5000.

More than 10 different types of congenital LQTS have been described. However, only LQTS 1-3 are relatively common.[5]

Type Chromosome Gene Protein Ionchannel Frequency[7] SCD incidence[8] Inheritance ECG characteristics Trigger Eponyme OMIM™ link
LQTS1 11p15 KCNQ1 KvLQT1 Iks ~50% 0.30%/year AD, AR broad base 'early onset' T wave exercise, especially swimming JLN1 if homozygous, LQTS1 if heterozygous 607542
LQTS2 7q35 KCNH2 hERG Ikr 30-40% 0.60%/year AD small late T wave adrenergic triggers, especially nightly noise JLN2 if homozygous, LQTS2 if heterozygous 152427
LQTS3 3p21 SCN5A NA channel 5-10% 0.56%/year AD 'Late onset' T wave with normal configuration 600163
LQTS4 4q25-q27 ANK2 Ankyrin B INa,K <1% AD 106410
LQTS5 21q22.1 KCNE1 minK Iks <1% unknown AD/AR 176261
LQTS6 21q22.1 KCNE2 MiRP1 Ikr <1% unknown AD 603796
LQTS7 = ATS1 17q23 KCNJ2 Kir 2.1 IK1 <1% unknown AD Anderson-Tawil syndrome 600681
LQTS8 = TS1 12p13.3 CACNA1C Cav1.2 ICa-L <1% unknown alternating T waves Timothy syndrome 601005
LQTS9 3p25.3 CAV3 Caveolin 3 INa unknown 601253
LQTS10 11q23.3 SCN4B Nav1.5 b4 1 family unknown 608256
LQTS11 7q21-q22 Akap9 AKAP Iks 1 family unknown 611820
LQTS
Long QT syndrome
JLN
Jervell and Lange-Nielsen syndrome
SCD
Sudden Cardiac Death

Long before the genes involved were known, two syndromes had been described that were associated with a prolonged QT interval on the ECG.

  • Anton Jervell and Fred Lange-Nielsen from Oslo described in 1957 a autosomaal recessive syndrome that was associated with QT interval prolongation, deafness and sudden death: the now called Jervell-Lange-Nielsen syndrome. [1]
  • Romano-Ward syndrome is a long QT syndrome with normal auditory function and autosomal dominant inheritance.
  • In a genotype–phenotype study by Moss et al. that studied type-1 LQTS, it was found that mutations located in the transmembrane portion of the ion channel protein and the degree of ion channel dysfunction caused by the mutations are important independent risk factors influencing the clinical course of this disorder.[9]

External links

  1. Torsades.org has a list of QT prolonging drugs
  2. QTdrugs.org, another list of QT prolonging drugs
  3. Sudden Arrhythmia Death Syndrome Foundation. LQTS patient group.
  4. Inherited Arrhythmias Database
  5. Labor der Kardiologie des Herz- und Diabeteszentrum NRW kardiogenetik.de

Referenties

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  1. Error fetching PMID 13435203: [Lang1957]
  2. Error fetching PMID 17090615: [Hofman]
  3. Error fetching PMID 16949500: [Goldenberg]
  4. Error fetching PMID 16935995: [ACC2006]
  5. Error fetching PMID 14999113: [Roden]
  6. Error fetching PMID 18184962: [Roden]
  7. Error fetching PMID 12736279: [priori]
  8. Error fetching PMID 16230503: [Shah2005]
  9. Error fetching PMID 17470695: [moss]
  10. Error fetching PMID 11136691: [Schwartz2001]

All Medline abstracts: PubMed | HubMed