The assessment of P-wave dispersion and myocardial repolarization parameters in patients with chronic kidney disease

Korhan Kollu1, Lutfullah Altintepe2, Cevdet Duran3

  • 1a The Department of Internal Medicine , Konya Health Application and Research Center, University of Health Sciences , Konya , Turkey.

Renal Failure
|December 30, 2017
PubMed

Insights

Patients with chronic kidney disease (CKD) stages 3-5 not on renal replacement therapy exhibit increased indicators of cardiac arrhythmia, including p-wave dispersion and QTc dispersion. These findings highlight potential risks for sudden cardiac events in this population.

Area of Science:

  • Cardiology
  • Nephrology
  • Clinical Electrophysiology

Background:

  • Chronic kidney disease (CKD) is associated with a higher risk of sudden cardiac death and arrhythmias.
  • Identifying specific electrocardiographic markers can aid in risk stratification for CKD patients.

Purpose of the Study:

  • To evaluate key arrhythmia indicators: p-wave dispersion (P-WD), QTc dispersion, Tp-e interval, and Tp-e/QT ratio.
  • To assess these markers in patients with stages 3-5 CKD who are not yet on renal replacement therapy (RRT).

Main Methods:

  • A cohort of 133 patients with stages 3-5 CKD (no RRT) and 32 healthy controls were studied.
  • Electrocardiograms were used to measure P-WD, QTc dispersion, and Tp-e interval.
  • The Tp-e/QT ratio was calculated for all participants.

Main Results:

  • Patients with CKD showed significantly higher P-WD (p < .001) and QTc dispersion (p < .001) compared to controls.
  • Elevated Tp-e maximum (p < .001), Tp-e minimum (p < .001), and Tp-e/QTc ratio (p = .001) were observed in the CKD group.
  • No significant differences were found in QTc-max or Tp-e interval between groups.

Conclusions:

  • Patients with stages 3-5 CKD not on RRT demonstrate increased P-WD and QTc dispersion.
  • The study suggests that these electrophysiological changes may contribute to the heightened arrhythmia risk in non-dialyzed CKD patients.
Abstract

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