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==References==
==References==
{{reflist|2}}
{{reflist|2}}
[[Category:Cardiology]]
[[Category:Electrophysiology]]
[[Category:Channelopathy]]
[[Category:Genetic disorders]]
[[Category:Syndromes]]

Revision as of 02:25, 21 September 2012

Long QT Syndrome Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]

Overview

Electrocardiogram

The diagnosis of LQTS is not easy since 2.5% of the healthy population have prolonged QT interval, and 10% of LQTS patients have a normal QT interval. A commonly used criterion to diagnose LQTS is the LQTS "diagnostic score". Its based on several criteria giving points to each. With 4 or more points the probability is high for LQTS, and with 1 or less point the probability is low. Two or 3 points indicates intermediate probability.

  • QTc (Defined as QT interval / square root of RR interval)
    • >= 480 msec - 3 points
    • 460-470 msec - 2 points
    • 450 msec and male gender - 1 point
  • Torsades de Pointes ventricular tachycardia - 2 points
  • T wave alternans - 1 point
  • Notched T wave in at least 3 leads - 1 point
  • Low heart rate for age (children) - 0.5 points
  • Syncope (one cannot receive points both for syncope and Torsades de pointes)
  • With stress - 2 points
  • Without stress - 1 point
  • Congenital deafness - 0.5 points
  • Family history (the same family member cannot be counted for LQTS and sudden death)
  • Other family members with definite LQTS - 1 point
  • Sudden death in immediate family (members before the age 30) - 0.5 points

References