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Effect of sodium glucose cotransporter 2 inhibitors on atrial tachy-arrhythmia burden in patients with cardiac implantable electronic devices.
Younis, Arwa; Arous, Tania; Klempfner, Robert; Kharsa, Adnan; McNitt, Scott; Schleede, Susan; Polonski, Bronislava; Abdallah, Zeinab; Buttar, Ruppinder; Bodurian, Christopher; Tabaja, Chadi; Yavin, Hagai D; Shamroz, Farooq; Wazni, Oussama M; Wittlin, Steven D; Aktas, Mehmet; Goldenberg, Ilan.
Afiliação
  • Younis A; Department of Medicine, Division of Cardiology, Clinical Cardiovascular Research Center, University of Rochester Medical Center, Rochester, New York, USA.
  • Arous T; Department of Cardiology, Clinical Electrophysiology, Cleveland Clinic, Cleveland, Ohio, USA.
  • Klempfner R; Department of Medicine, Division of Endocrine-Metabolism, University of Rochester Medical Center, Rochester, New York, USA.
  • Kharsa A; Leviev Heart Center, Sheba Medical Center, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • McNitt S; Department of Internal Medicine, Rochester General Hospital, Rochester, New York, USA.
  • Schleede S; Department of Medicine, Division of Cardiology, Clinical Cardiovascular Research Center, University of Rochester Medical Center, Rochester, New York, USA.
  • Polonski B; Department of Medicine, Division of Cardiology, Clinical Cardiovascular Research Center, University of Rochester Medical Center, Rochester, New York, USA.
  • Abdallah Z; Department of Medicine, Division of Cardiology, Clinical Cardiovascular Research Center, University of Rochester Medical Center, Rochester, New York, USA.
  • Buttar R; Department of Medicine, Division of Cardiology, Clinical Cardiovascular Research Center, University of Rochester Medical Center, Rochester, New York, USA.
  • Bodurian C; Department of Internal Medicine, Rochester General Hospital, Rochester, New York, USA.
  • Tabaja C; Department of Medicine, Division of Cardiology, Clinical Cardiovascular Research Center, University of Rochester Medical Center, Rochester, New York, USA.
  • Yavin HD; Department of Cardiology, Clinical Electrophysiology, Cleveland Clinic, Cleveland, Ohio, USA.
  • Shamroz F; Department of Cardiology, Clinical Electrophysiology, Cleveland Clinic, Cleveland, Ohio, USA.
  • Wazni OM; Department of Medicine, Division of Cardiology, Clinical Cardiovascular Research Center, University of Rochester Medical Center, Rochester, New York, USA.
  • Wittlin SD; Department of Cardiology, Clinical Electrophysiology, Cleveland Clinic, Cleveland, Ohio, USA.
  • Aktas M; Department of Medicine, Division of Endocrine-Metabolism, University of Rochester Medical Center, Rochester, New York, USA.
  • Goldenberg I; Department of Medicine, Division of Cardiology, Clinical Cardiovascular Research Center, University of Rochester Medical Center, Rochester, New York, USA.
J Cardiovasc Electrophysiol ; 34(8): 1595-1604, 2023 08.
Article em En | MEDLINE | ID: mdl-37453072
ABSTRACT

INTRODUCTION:

Use of sodium glucose cotransporter 2 inhibitors (SGLT2i) was associated with a reduction in atrial fibrillation hospitalizations. Therefore, we aim to evaluate the effects of SGLT2i on atrial tachy-arrhythmias (ATA) in patients with cardiac implantable electronic devices (CIEDs).

METHODS:

All 13 888 consecutive patients implanted with a CIED in two tertiary medical centers were enrolled. Treatment with SGLT2i was assessed as a time dependent variable. The primary endpoint was the total number of ATA. Secondary endpoints included total number of ventricular tachy-arrhythmias (VTA), ATA and VTA, and death. All events were independently adjudicated blinded to the treatment. Multivariable propensity score modeling was performed.

RESULTS:

During a total follow-up of 24 442 patient years there were 62 725 ATA and 10 324 VTA events. Use of SGLT2i (N = 696) was independently associated with a significant 22% reduction in the risk of ATA (hazard ratio [HR] = 0.78 [95% confidence interval {CI} = 0.70-0.87]; p < .001); 22% reduction in the risk of ATA/VTA (HR = 0.78 [95% CI = 0.71-0.85]; p < .001); and with a 35% reduction in the risk of all-cause mortality (HR = 0.65 [95% CI = 0.45-0.92]; p = .015), but was not significantly associated with VTA risk (HR = 0.92 [95% CI = 0.80-1.06]; p = .26). SGLT2i were associated with a lower ATA burden in heart failure (HF) patients but not among diabetes patients (HF HR = 0.68, 95% CI = 0.58-0.80, p < .001 vs. Diabetes HR = 0.95, 95% CI = 0.86-1.05, p = .29; p < .001 for interaction between SGLT2i indication and ATA burden).

CONCLUSION:

Our real world findings suggest that in CIED HF patients, those with SGLT2i had a pronounced reduction in ATA burden and all-cause mortality when compared with those not on SGLT2i.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Diabetes Mellitus Tipo 2 / Inibidores do Transportador 2 de Sódio-Glicose / Insuficiência Cardíaca Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: J Cardiovasc Electrophysiol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Diabetes Mellitus Tipo 2 / Inibidores do Transportador 2 de Sódio-Glicose / Insuficiência Cardíaca Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: J Cardiovasc Electrophysiol Ano de publicação: 2023 Tipo de documento: Article