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    • Case Report
      Open Access

      Lyme carditis presenting with an incessant atrioventricular nodal reentrant tachycardia masking a variable atrioventricular block

      HeartRhythm Case Reports
      Vol. 8Issue 12p829–835Published online: September 16, 2022
      • Jamal A. Anthony
      • David Jordanovski
      • Steven K. Furer
      Cited in Scopus: 0
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        Lyme disease is a common tick-borne illness with a high prevalence in the Northeast region of the United States.1 It is an infection caused by Borrelia burgdorferi, a gram-negative spirochetal bacterium carried by infected ticks such as Ixodes scapularis. They are found outdoors, latched onto blades of grass until they can attach to a host. If not treated early, serious complications can develop. Since Lyme antibodies can take several weeks to develop, false-negatives can arise in about 50% of cases when testing is done too early.
        Lyme carditis presenting with an incessant atrioventricular nodal reentrant tachycardia masking a variable atrioventricular block
      • Case Report
        Open Access

        Leadless atrioventricular synchronous pacing in Eisenmenger syndrome

        HeartRhythm Case Reports
        Vol. 7Issue 8p538–541Published online: May 5, 2021
        • Paul Khairy
        • Blandine Mondésert
        • François-Pierre Mongeon
        • Nancy Poirier
        • Bernard Thibault
        Cited in Scopus: 1
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          Eisenmenger syndrome is at the extreme end of the phenotypic spectrum of pulmonary arterial hypertension associated with congenital heart disease. Over time, a large nonrestrictive left-to-right shunt provokes progressive pulmonary vascular disease that results in the shunt becoming bidirectional or reversing direction (ie, right-to-left). When the need for pacing arises, transvenous leads are generally considered contraindicated owing to a prohibitively high risk of paradoxical thromboembolism.
          Leadless atrioventricular synchronous pacing in Eisenmenger syndrome
        • Case Report
          Open Access

          Cardiac magnetic resonance imaging–negative cardiac sarcoidosis

          HeartRhythm Case Reports
          Vol. 7Issue 3p139–143Published online: December 31, 2020
          • See-Yue Arthur Yung
          • James Chung-Man Ho
          • Maximus C.F. Yeung
          • Carmen Chan
          • Chung-Wah Siu
          Cited in Scopus: 0
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            Sarcoidosis is a multisystem inflammatory granulomatous disease of unknown etiology. Up to 55% of patients with systemic sarcoidosis have documented cardiac involvement.1 Albeit less common, cardiac manifestations can be the first clinical presentation of sarcoidosis. These include conduction disturbances, ventricular arrhythmias, heart failure, and sudden cardiac death, accounting for 13%–25% of sarcoidosis-related death.1 Initial diagnostic workup often requires comprehensive cardiac imaging, including echocardiography, cardiac magnetic resonance imaging (CMR), and 18F-FDG positron emission tomography (PET); nonetheless, the diagnosis of cardiac sarcoidosis remains challenging.
            Cardiac magnetic resonance imaging–negative cardiac sarcoidosis
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