Impact of Kidney Function on the Survival of Patients with Chagas Cardiomyopathy and Implantable Cardioverter

Fernanda Pinheiro Martin Tapioca1,2,3, Luiz Carlos Santana Passos3,4, Caio Cafezeiro4

  • 1Nephrology Department, Ana Nery Hospital, Salvador 40301-155, Brazil.

PubMed

Insights

Kidney function impairment did not independently predict mortality in Chagas cardiomyopathy patients receiving implantable cardioverter defibrillators (ICDs) or cardiac resynchronization therapy with a defibrillator (CRT-D). This suggests ICDs/CRT-Ds may be suitable for these patients, even with moderate kidney issues.

Area of Science:

  • Cardiology
  • Nephrology
  • Medical Devices

Background:

  • Impaired kidney function is a known mortality risk in implantable cardioverter defibrillator (ICD) recipients.
  • Patients with Chagas cardiomyopathy (CC) are underrepresented in landmark ICD and cardiac resynchronization therapy with a defibrillator (CRT-D) studies.
  • The impact of kidney dysfunction on mortality in CC patients with ICDs/CRT-Ds is not well-established.

Purpose of the Study:

  • To investigate whether impaired kidney function independently predicts mortality in patients with Chagas cardiomyopathy (CC) undergoing ICD or CRT-D implantation.
  • To compare the prognostic value of kidney dysfunction in CC patients with findings from other cardiomyopathies.

Main Methods:

  • Prospective follow-up of 343 patients with CC and left ventricular ejection fraction (LVEF) ≤40% after ICD or CRT-D implantation.
  • Primary outcome: survival rate during follow-up.
  • Cox regression analysis to identify predictors of mortality, including estimated glomerular filtration rate (eGFR), adjusted for clinical variables.

Main Results:

  • Overall mortality occurred in 32.9% of participants over a median follow-up of 777 days.
  • Estimated glomerular filtration rate (eGFR) was significantly associated with survival in univariate analysis (p=0.007) but not in the multivariate model (p=0.138).
  • Multivariate analysis adjusted for age, gender, atrial fibrillation, BMI, and medications did not identify eGFR as an independent predictor of mortality.

Conclusions:

  • Impaired eGFR is not an independent predictor of mortality in Chagas cardiomyopathy patients receiving ICDs or CRT-Ds.
  • Distinct pathophysiological mechanisms in CC may explain why impaired kidney function does not carry the same mortality risk as in other cardiomyopathies.
  • Clinicians can consider recommending cardiac implantable electronic devices (CIEDs) for CC patients with moderate kidney dysfunction, pending further research on advanced chronic kidney disease outcomes.

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