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Heart Rhythm Case Reports
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    • December 2022 - January 2023Remove December 2022 - January 2023 filter
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    • Case Report4

    Author

    • Calvert, Peter1
    • Choudhury, Moinuddin1
    • Davis, Megan1
    • de Groot, Natasja MS1
    • Fujiu, Katsuhito1
    • Gupta, Dhiraj1
    • Hasumi, Eriko1
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    • Ramdat Misier, Nawin L1
    • Snowdon, Richard1
    • Srivathsan, Komandoor1
    • Taverne, Yannick JHJ1
    • van Leeuwen, Wouter J1
    • van Schie, Mathijs S1

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    • HeartRhythm Case Reports4

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    • Ablation1
    • Anomalous coronary artery1
    • Atrial fibrillation1
    • Autoimmune disease1
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    • Electroanatomic mapping1
    • Electrocardiogram1
    • Epicardial mapping1
    • Moderator band1
    • Outflow tract1
    • Pacemaker lead1
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    • Radiofrequency ablation1
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    • Case Report
      Open Access

      Multiple recurrent episodes of pacemaker-associated postcardiac injury syndrome

      HeartRhythm Case Reports
      In Press Corrected Proof
      Published online: January 24, 2023
      • Eriko Hasumi
      • Katsuhito Fujiu
      • Issei Komuro
      Cited in Scopus: 0
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        Postcardiac injury syndrome (PCIS) is an autoimmune disease that causes damage to the pericardium, myocardium, and pleura after myocardial infarction, cardiac surgery, or trauma. Although most cases are benign, anti-inflammatory agents may be used to treat PCIS. Rarely, PCIS may become refractory or recur after anti-inflammatory treatment.1 In such cases, long-term oral corticosteroids are usually prescribed2; however, the optimal duration of administration remains unclear. We report a patient who experienced multiple recurrent episodes of pacemaker lead–related PCIS that were treated with oral prednisone and pericardial drainage.
        Multiple recurrent episodes of pacemaker-associated postcardiac injury syndrome
      • Case Report
        Open Access

        Idiopathic premature ventricular contraction–triggered ventricular fibrillation: Subcutaneous implantable cardioverter-defibrillator (S-ICD) template matched ablation in the absence of inducible clinical premature ventricular contraction

        HeartRhythm Case Reports
        In Press Corrected Proof
        Published online: January 15, 2023
        • Sudeepthi Reddy Mekala
        • Megan Davis
        • Komandoor Srivathsan
        Cited in Scopus: 0
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          Idiopathic ventricular fibrillation is diagnosed in patients who have survived sudden cardiac arrest from ventricular fibrillation (VF) without identifiable structural heart disease.1 It is the main cause of unexplained sudden cardiac death, particularly in young patients under the age of 35.2 An implantable cardioverter-defibrillator (ICD) is usually recommended for the secondary prevention of sudden cardiac death. VF ablation is recommended for clinical VF recurrence and for reducing the number of ICD shocks.
          Idiopathic premature ventricular contraction–triggered ventricular fibrillation: Subcutaneous implantable cardioverter-defibrillator (S-ICD) template matched ablation in the absence of inducible clinical premature ventricular contraction
        • Case Report
          Open Access

          An unexpected finding by epicardial mapping: Atrial fibrillation in a 14-month-old patient with short QT syndrome

          HeartRhythm Case Reports
          In Press Corrected Proof
          Published online: December 31, 2022
          • Mathijs S. van Schie
          • Nawin L. Ramdat Misier
          • Wouter J. van Leeuwen
          • Yannick J.H.J. Taverne
          • Natasja M.S. de Groot
          Cited in Scopus: 0
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            Short QT syndrome (SQTS) is a very rare channelopathy accompanied by familial clustering and sudden cardiac death.1 It has an estimated prevalence ranging from 0.02% up to 2% in the adult population, but only 0.05% among pediatric patients.2–6 To date, 9 mutations in 6 different genes have been identified, including KCNH2, KCNQ1, KCNJ1, CACNA1C, CACNB2, and CACNA2D1. In pediatric patients, SQTS is characterized by shortening of the corrected QT interval (QTcB <316 ms, J-Tpeak cB <181 ms, and the presence of early repolarization) on the surface electrocardiogram (ECG).
            An unexpected finding by epicardial mapping: Atrial fibrillation in a 14-month-old patient with short QT syndrome
          • Case Report
            Open Access

            Right ventricular outflow tract ablation close to an anomalous right coronary artery: When imaging meets electrophysiology

            HeartRhythm Case Reports
            In Press Corrected Proof
            Published online: December 28, 2022
            • Peter Calvert
            • Moinuddin Choudhury
            • Afshin Khalatbari
            • Richard Snowdon
            • Dhiraj Gupta
            • Simon Modi
            • and others
            Cited in Scopus: 0
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            • Video
            Catheter ablation is a commonly undertaken and highly effective treatment for symptomatic right ventricular outflow tract (RVOT) ventricular ectopy / ventricular tachycardia (VT).1 Despite the high chance of cure with ablation, caution is required to avoid collateral injury to coronary arteries in certain well-described locations. Anomalous coronary arteries are rare2 and may have an unfamiliar path involving the outflow tracts, posing a significantly increased risk with ablation. The approach to outflow tract ablation in a patient with an anomalous coronary artery has not been previously reported.
            Right ventricular outflow tract ablation close to an anomalous right coronary artery: When imaging meets electrophysiology
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