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  1. Início
  2. Palavra-chave: Long QT Syndrome
IJCS
Original Article

QT Prolongation Following Premature Ventricular Contractions: A Potential Marker of Concealed Long QT Syndrome

Khatuna Jalabadze et al. Pavle Machavariani Bachuki Tsiklauri Natalia Garuchava … Ia Avaliani Maya Chigogidze

Abstract

Background:

Long QT syndrome (LQTS) predisposes individuals to malignant ventricular arrhythmias and sudden cardiac death; however, diagnosis remains challenging in patients with borderline corrected QT (QTc) values. Premature Ventricular Contractions (PVCs) may unmask concealed abnormalities of ventricular repolarization.

Aim:

To determine whether post-PVC QTc prolongation can differentiate patients with confirmed LQTS, healthy controls, and borderline index cases.

Methods:

In this retrospective study, 24-hour electrocardiography (ECG) recordings from 84 subjects were analyzed, including 10 patients with confirmed LQTS, 72 healthy controls, and 2 index patients with borderline baseline QTc values. QTc intervals before and after PVCs were measured manually and corrected using Bazett’s formula. Between-group differences were evaluated using analysis of covariance (ANCOVA) adjusted for baseline QTc, whereas within-group changes were assessed with paired t-tests. A two-tailed p < 0.05 was considered statistically significant.

Results:

Post-PVC QTc intervals were longer in patients with LQTS than in healthy controls (488 ± 23 ms vs 391 ± 37 ms; adjusted p = 0.066). Overall, PVCs were associated with a mean QTc increase of +15.7 ms (95% CI 7.1–24.3; p = 0.0005), with larger increases observed in LQTS patients (+22.3 ms; p = 0.0019) compared with healthy controls (+10.0 ms; p = 0.0098). The two index patients exhibited marked QTc prolongation, rising from borderline baseline values (360–460 ms) to 540–600 ms (Δ≈165 ms).

Conclusion:

PVC-induced QTc prolongation may help distinguish healthy individuals from patients with overt or borderline LQTS. Whereas healthy controls demonstrated mild physiologic adaptation, patients with confirmed LQTS showed consistent QTc prolongation, and index patients exhibited marked post-PVC increases suggestive of concealed repolarization abnormalities. Assessment of QTc following PVCs may represent a simple bedside approach to improve diagnostic accuracy and risk stratification in LQTS; prospective studies in larger cohorts are warranted to confirm these findings.

  • Cardiac Arrhythmias
  • Long QT Syndrome
  • Ventricular Premature Complexes
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Creative Commons Attribution (CC BY) Creative Commons license
07/09/2026 DOI: 10.36660/ijcs.20250230 Visualizações 3
IJCS
Case Report

Mexiletine in The Treatment of Long QT Syndrome Type 2 in Infants: A Case Report

Jessica Laureano Martins et al. Nicole Sarmento Queiroga Fernanda Calumby Nóbrega Guimarães Guilherme Augusto Teodoro Athayde … Halbiege Léa Silva Quirino da Silva Rogério Braga Andalaft

Introduction

Congenital Long QT Syndrome (LQTS) is one of the main causes of sudden cardiac death (SCD) in the pediatric age group, with a prevalence of approximately one case for every 2,000 newborns. The most prevalent inheritance is dominant, with the typical phenotype associated with cardiac manifestations.

The genetic alteration of LQTS is multigenic, with 17 main genes, and in 80% of the cases, it identifies: KCNQ1 (LQTL1), KCNH2 (LQTL2), and SCN5A (LQTL3). The LQTS type 2 (LQTS2) subtype alters the expression of potassium channels in myocytes, causing electrical instability and ventricular arrhythmias. The most common arrhythmia is Torsades de Pointes (TdP), a type of polymorphic ventricular tachycardia, which can lead to syncope, seizures, and sudden death.

[…]

  • Cardiac Arrhythmias
  • Long QT Syndrome
  • Torsades de Pointes
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Creative Commons Attribution (CC BY) Creative Commons license
10/02/2025 DOI: 10.36660/ijcs.20240099 Visualizações 1
IJCS
Case Report

Aborted Sudden Death Due to Severe Ventricular Arrhythmia in Timothy Syndrome

Erivelton Nascimento et al. Carollina Fernandes Tinoco Camila Diniz Silva Fabiana Ferreira Mitidieri Cortez Renato Kaufman

Abstract

Timothy Syndrome is a rare autosomal dominant multisystem genetic condition. The CACNA1C gene, codifier of the CaV1.2 calcium channel, is affected, resulting in the loss of voltage-dependent calcium channel inactivation. Relevant clinical characteristics: (1) corrected QT interval greater than 480ms; (2) syndactyly. Death often occurs during childhood, and results from ventricular tachyarrhythmias. This study presents the case of a female newborn who suffered a cardiorespiratory arrest, secondary to ventricular arrhythmia. A prolonged QT interval, combined with 2:1 AV block, was also identified, requiring a definitive cardiac pacemaker implant that, during inpatient care, developed pulmonary sepsis, followed by death.

  • Arrhythmias, Cardiac/complications
  • Child
  • Death Sudden
  • Long QT Syndrome
  • Syndactyly/genetics
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Creative Commons Attribution (CC BY) Creative Commons license
30/04/2021 DOI: 10.36660/ijcs.20200061 Visualizações 1

Como citar este artigo

EndNote RIS

Formato de Documento Eletrônico (Vancouver)

Jalabadze K, Machavariani P, Tsiklauri B, Garuchava N, Avaliani I, Chigogidze M. QT Prolongation Following Premature Ventricular Contractions: A Potential Marker of Concealed Long QT Syndrome. International Journal of Cardiovascular Sciences 2026;39:e20250230.

Formato de Documento Eletrônico (ABNT)

Jalabadze, Khatuna; Machavariani, Pavle; Tsiklauri, Bachuki; Garuchava, Natalia; Avaliani, Ia; Chigogidze, Maya. QT Prolongation Following Premature Ventricular Contractions: A Potential Marker of Concealed Long QT Syndrome. International Journal of Cardiovascular Sciences, v. 39, e20250230, set. 2026.

Formato de Documento Eletrônico (APA)

Jalabadze, K., Machavariani, P., Tsiklauri, B., Garuchava, N., Avaliani, I., & Chigogidze, M. (2026). QT Prolongation Following Premature Ventricular Contractions: A Potential Marker of Concealed Long QT Syndrome. International Journal of Cardiovascular Sciences, 39, e20250230.

Formato de Documento Eletrônico (ISO)

Jalabadze, Khatuna and Machavariani, Pavle and Tsiklauri, Bachuki and Garuchava, Natalia and Avaliani, Ia and Chigogidze, Maya. QT Prolongation Following Premature Ventricular Contractions: A Potential Marker of Concealed Long QT Syndrome. International Journal of Cardiovascular Sciences [online]. 2026, vol. 39, [citado 2026-10-14], e20250230. Disponível em: <https://journals.cardiol.br/article/qt-prolongation-following-premature-ventricular-contractions-a-potential-marker-of-concealed-long-qt-syndrome-2/>. ISSN 2359-4802

EndNote RIS

Formato de Documento Eletrônico (Vancouver)

Martins JL, Queiroga NS, Guimarães FCN, Athayde GAT, Silva HLQ, Andalaft RB. Mexiletine in The Treatment of Long QT Syndrome Type 2 in Infants: A Case Report. International Journal of Cardiovascular Sciences 2025;38:e20240099.

Formato de Documento Eletrônico (ABNT)

Martins, Jessica Laureano; Queiroga, Nicole Sarmento; Guimarães, Fernanda Calumby Nóbrega; Athayde, Guilherme Augusto Teodoro; Silva, Halbiege Léa Quirino da; Andalaft, Rogério Braga. Mexiletine in The Treatment of Long QT Syndrome Type 2 in Infants: A Case Report. International Journal of Cardiovascular Sciences, v. 38, e20240099, fev. 2025.

Formato de Documento Eletrônico (APA)

Martins, J. L., Queiroga, N. S., Guimarães, F. C. N., Athayde, G. A. T., Silva, H. L. Q. , & Andalaft, R. B. (2025). Mexiletine in The Treatment of Long QT Syndrome Type 2 in Infants: A Case Report. International Journal of Cardiovascular Sciences, 38, e20240099.

Formato de Documento Eletrônico (ISO)

Martins, Jessica Laureano and Queiroga, Nicole Sarmento and Guimarães, Fernanda Calumby Nóbrega and Athayde, Guilherme Augusto Teodoro and Silva, Halbiege Léa Quirino da and Andalaft, Rogério Braga. Mexiletine in The Treatment of Long QT Syndrome Type 2 in Infants: A Case Report. International Journal of Cardiovascular Sciences [online]. 2025, vol. 38, [citado 2026-10-14], e20240099. Disponível em: <https://journals.cardiol.br/article/mexiletine-in-the-treatment-of-long-qt-syndrome-type-2-in-infants-a-case-report-2/>. ISSN 2359-4802

EndNote RIS

Formato de Documento Eletrônico (Vancouver)

Nascimento E, Tinoco CF, Silva CD, Cortez FFM, Kaufman R. Aborted Sudden Death Due to Severe Ventricular Arrhythmia in Timothy Syndrome. International Journal of Cardiovascular Sciences 2021;34(6):743-6.

Formato de Documento Eletrônico (ABNT)

Nascimento, Erivelton; Tinoco, Carollina Fernandes; Silva, Camila Diniz; Cortez, Fabiana Ferreira Mitidieri; Kaufman, Renato. Aborted Sudden Death Due to Severe Ventricular Arrhythmia in Timothy Syndrome. International Journal of Cardiovascular Sciences, v. 34, n. 6, p. 743-746, abr. 2021.

Formato de Documento Eletrônico (APA)

Nascimento, E., Tinoco, C. F., Silva, C. D., Cortez, F. F. M., & Kaufman, R. (2021). Aborted Sudden Death Due to Severe Ventricular Arrhythmia in Timothy Syndrome. International Journal of Cardiovascular Sciences, 34(6), 743-746.

Formato de Documento Eletrônico (ISO)

Nascimento, Erivelton and Tinoco, Carollina Fernandes and Silva, Camila Diniz and Cortez, Fabiana Ferreira Mitidieri and Kaufman, Renato. Aborted Sudden Death Due to Severe Ventricular Arrhythmia in Timothy Syndrome. International Journal of Cardiovascular Sciences [online]. 2021, vol. 34, n. 6, [citado 2026-10-14], pp. 743-746. Disponível em: <https://journals.cardiol.br/article/aborted-sudden-death-due-to-severe-ventricular-arrhythmia-in-timothy-syndrome-2/>. ISSN 2359-4802

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