Potential overdiagnosis of long QT syndrome using exercise stress and QT stand testing in children and adolescents with a low probability of disease.


Journal

Journal of cardiovascular electrophysiology
ISSN: 1540-8167
Titre abrégé: J Cardiovasc Electrophysiol
Pays: United States
ID NLM: 9010756

Informations de publication

Date de publication:
02 2021
Historique:
received: 24 05 2020
revised: 07 12 2020
accepted: 22 12 2020
pubmed: 1 1 2021
medline: 10 8 2021
entrez: 31 12 2020
Statut: ppublish

Résumé

Long QT syndrome (LQTS) is a dangerous arrhythmia disorder that often presents in childhood and adolescence. The exercise stress test (EST) and QT-stand test may unmask QT interval prolongation at key heart rate transition points in LQTS, but their utility in children is debated. To determine if the QT-stand test or EST can differentiate children with a low probability of LQTS from those with confirmed LQTS. This retrospective study compares the corrected QT intervals (QTc) of children (<19 years) during the QT-stand test and EST. Patients were divided into three groups for comparison: confirmed LQTS (n = 14), low probability of LQTS (n = 14), and a control population (n = 9). Using the Bazett formula, confirmed LQTS patients had longer QTc intervals than controls when supine, standing, and at 3-4 min of recovery (p ≤ .01). Patients with a low probability of LQTS had longer QTc duration upon standing (p = .018) and at 1 min of recovery (p = .016) versus controls. There were no significant QTc differences at any transition point between low probability and confirmed LQTS. Using the Fridericia formula, differences in QTc between low probability and confirmed LQTS were also absent at the transition points examined, except at 1 min into exercise, where low probability patients had shorter QTc intervals (437 vs. 460 ms, p = .029). The diagnostic utility of the QT stand test and EST remains unclear in pediatric LQTS. The formula used for heart rate correction may influence accuracy, and dynamic T-U wave morphology changes may confound interpretation in low probability situations.

Sections du résumé

BACKGROUND
Long QT syndrome (LQTS) is a dangerous arrhythmia disorder that often presents in childhood and adolescence. The exercise stress test (EST) and QT-stand test may unmask QT interval prolongation at key heart rate transition points in LQTS, but their utility in children is debated.
OBJECTIVE
To determine if the QT-stand test or EST can differentiate children with a low probability of LQTS from those with confirmed LQTS.
METHODS
This retrospective study compares the corrected QT intervals (QTc) of children (<19 years) during the QT-stand test and EST. Patients were divided into three groups for comparison: confirmed LQTS (n = 14), low probability of LQTS (n = 14), and a control population (n = 9).
RESULTS
Using the Bazett formula, confirmed LQTS patients had longer QTc intervals than controls when supine, standing, and at 3-4 min of recovery (p ≤ .01). Patients with a low probability of LQTS had longer QTc duration upon standing (p = .018) and at 1 min of recovery (p = .016) versus controls. There were no significant QTc differences at any transition point between low probability and confirmed LQTS. Using the Fridericia formula, differences in QTc between low probability and confirmed LQTS were also absent at the transition points examined, except at 1 min into exercise, where low probability patients had shorter QTc intervals (437 vs. 460 ms, p = .029).
CONCLUSION
The diagnostic utility of the QT stand test and EST remains unclear in pediatric LQTS. The formula used for heart rate correction may influence accuracy, and dynamic T-U wave morphology changes may confound interpretation in low probability situations.

Identifiants

pubmed: 33382510
doi: 10.1111/jce.14865
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

500-506

Informations de copyright

© 2020 Wiley Periodicals LLC.

Références

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Auteurs

Thomas M Roston (TM)

Department of Pediatrics, Division of Cardiology, British Columbia Children's Hospital and The University of British Columbia, Vancouver, Canada.
Department of Medicine, Division of Cardiology, The University of British Columbia, Vancouver, Canada.

Astrid M De Souza (AM)

Department of Pediatrics, Division of Cardiology, British Columbia Children's Hospital and The University of British Columbia, Vancouver, Canada.

Hilary V Romans (HV)

Department of Pediatrics, Division of Cardiology, British Columbia Children's Hospital and The University of British Columbia, Vancouver, Canada.

Sonia Franciosi (S)

Department of Pediatrics, Division of Cardiology, British Columbia Children's Hospital and The University of British Columbia, Vancouver, Canada.

Kathryn R Armstrong (KR)

Department of Pediatrics, Division of Cardiology, British Columbia Children's Hospital and The University of British Columbia, Vancouver, Canada.

Shubhayan Sanatani (S)

Department of Pediatrics, Division of Cardiology, British Columbia Children's Hospital and The University of British Columbia, Vancouver, Canada.

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