A Diagnosis that Escapes Our Attention: Short QT Syndrome

Authors

  • Semiha Terlemez Gazi Üniversitesi Tıp Fakültesi
  • Emine Çil
  • Serdar Kula
  • Ayşe Deniz Oğuz
  • Fatma Sedef Tunaoğlu

Abstract

Short QT sydrome (SQT) is one of the rarely seen arythmia causes related to sudden cardiac death. An important part of the patients are diagnosed during the examination due to cardiac arrest. Therefore, diagnosing asymptomatic patients is lifesaving. In this case report, we presented a five-year old asymptomatic female patient how to put the SQT diagnosis. There was no complaint of the patient who had been directed to pediatric cardiology polyclinic due to murmur. In her electrocardiography (EKG), QTc duration was determined in lower limits. However, when the patient’s family history was examined in a detailed way, suspicious deaths were recognized. In the patient’s 24-hour holter EKG; SQT was diagnosed by establishing average QTc duration as 340 ms together with sharp, narrow T waves. Satolol treatment was initiated to the patient. To diagnose asymptomatic SQT patients, a decent family history must be obtained. Spot EKG is insufficient to rule out the diagnosis. All patients with suspicious death histories in their familieis must be directed to pediatric cardiologists.

References

Gussak I, Brugada P, Brugada J, et al. Idiopathic short QT interval: a new clinical syndrome? Cardiology 2000;94:99 –102.

Extramiana F, Antzelevitch C. Amplified transmural dispersion of repolarization as the basis for arrhythmogenesis in a canine ventricular-wedge model of short-QT syndrome. Circulation. 2004;110:3661–6.

Schimpf R, Wolpert C, Gaita F, et al. Short QT syndrome. Cardiovasc Res. 2005;67:357–66.

Bjerregaard P, Collier JL, Gussak I. Upper limit of QT/QTc intervals in the short QT syndrome. Review of the world-wide short QT syndrome population and 3 new USA families. Heart Rhythm 2008;5:S91.

Gallagher M, Magliano G, Yap YG, et al. Distribution and prognostic significance of QT intervals in the lowest half centile in 12,012 apparently healthy persons. Am J Cardiol 2006;98:933–5.

Gollob MH, Redpath CJ, Roberts JD. The short QT syndrome:proposed diagnostic criteria. J Am Coll Cardiol 2011;57:802–12.

Giustetto C, Schimpf R, Mazzanti A, Scrocco C, Maury P, Anttonen O, Probst V, Blanc JJ, Sbragia P, Dalmasso P, Borggrefe M, Gaita F.Long-term follow-up of patients with short QT syndrome.J Am Coll Cardiol. 2011 2;58:587-95.

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Published

19.06.2018

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