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Leadless pacing in patients undergoing transvenous lead extraction due to infection: A small step in a long journey

  • Arwa Younis
    Affiliations
    Cardiac Electrophysiology and Pacing Section, Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio
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  • Bruce L. Wilkoff
    Correspondence
    Address reprint requests and correspondence: Dr Bruce L. Wilkoff, Department of Cardiovascular Medicine, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, 9500 Euclid Avenue, Desk J2-2, Cleveland, OH 44195.
    Affiliations
    Cardiac Electrophysiology and Pacing Section, Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio
    Search for articles by this author
Published:February 27, 2023DOI:https://doi.org/10.1016/j.hrthm.2023.02.021
      Improvement in technology and expansion of indications have led to a progressive increase in the implantation of cardiovascular implantable electrical devices (CIED). This trend is accompanied by a rise in CIED-related complications, particularly device-related infections (DRIs), which are associated with a significant impact on patient prognosis and health care–associated costs.
      • Voigt A.
      • Shalaby A.
      • Saba S.
      Rising rates of cardiac rhythm management device infections in the United States: 1996 through 2003.
      ,
      • Diemberger I.
      • Segreti L.
      • Rinaldi C.A.
      • et al.
      on behalf of the ELECTRa Investigators. Transvenous lead extraction in patients with cardiac implantable device: the impact of systemic and local infection on clinical outcomes—An ESC-EHRA ELECTRa (European Lead Extraction Controlled) Registry Substudy.
      In the case of DRI, current guidelines give a class I indication to complete system removal using a transvenous lead extraction (TLE) approach.
      • Kusumoto F.M.
      • Schoenfeld M.H.
      • Wilkoff B.L.
      • et al.
      2017 HRS expert consensus statement on cardiovascular implantable electronic device lead management and extraction.
      Until recent years, most of the focus of the management of DRI was related to the TLE procedure itself. Physicians, researchers, and industry all have invested tremendous resources into improving periprocedural outcomes, aiming to increase the success rate as well as to decrease the complexity of the procedure. In addition, efforts were made to reduce the rate of DRI and implantation complications.
      • Tarakji K.G.
      • Mittal S.
      • Kennergren C.
      • et al.
      Antibacterial envelope to prevent cardiac implantable device infection.
      However, little has been done to optimize the postprocedural course following TLE, especially in DRI patients. Recent literature has shown that, although the timing of TLE and the periprocedural outcomes are of significant relevance for prognosis, postprocedure mortality remains several times higher than procedure-related mortality, reaching 30% at 1 year post-TLE in DRI patients.
      • Narui R.
      • Nakajima I.
      • Norton C.
      • et al.
      Risk factors for repeat infection and mortality after extraction of infected cardiovascular implantable electronic devices.
      • Lee J.Z.
      • Tan M.C.
      • Karikalan S.
      • et al.
      Causes of early mortality after transvenous lead removal.
      • Younis A.
      • Beinart R.
      • Nehoray N.
      • et al.
      Characterization of a previously unrecognized clinical phenomenon: delayed shock after cardiac implantable electronic device extraction.
      This information has a significant impact on post-TLE management, including reimplantation strategies. The timing of reimplantation becomes even more challenging in patients who are pacing dependent, those with cardiac resynchronization therapy (CRT), and those with secondary prevention defibrillators with increased risk of ventricular tachyarrhythmias and sudden cardiac death. In the setting of DRI, the optimal timing of CIED reimplantation for these patients after successful TLE currently is unknown.
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