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Short QT syndrome diagnostic criteria

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Secondary causes of a short QT interval such as drugs and electrolyte disturbances should be ruled out before embarking on an evaluation as to whether the patient has one of the short QT syndrome variants. Recent diagnostic criteria have been published out of the Arrhythmia Research Laboratory at the University of Ottawa Heart Institute from Drs. Michael H Gollob and Jason D Roberts.[1]

The Short QT Syndrome diagnostic criteria is based on a point system as follows:

  • QTc in milliseconds
<370 = 1 point
<350 = 2 points
<330 = 3 points
  • J point – T peak interval in milliseconds
<120 = 1 point
  • Clinical History
Sudden cardiac arrest = 2 points
Polymorphic VT or VF = 2 points
Unexplained syncope = 1 point
Atrial fibrillation = 1 point
  • Family History
1st or 2nd degree relative with SQTS = 2 points
1st or 2nd degree relative with sudden death = 1 point
Sudden infant death syndrome = 1 point
  • Genotype
Genotype positive = 2 points
Mutation of undetermined significance in a culprit gene = 1 point

The points are summed and interpreted as follows:

  • > or equal to 4 points: High-probability of SQTS
  • 3 Points: Intermediate probability of SQTS
  • 2 points or less: Low probability of SQTS

References

  1. Gollob M, Redpath C, Roberts J. (2011). “The Short QT syndrome: Proposed Diagnostic Criteria”. J Am Coll Cardiol. 57 (7): 802–812. doi:10.1016/j.jacc.2010.09.048. PMID 21310316.

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