Left ventricular growth after 1 year of haemodialysis does not correlate with arteriovenous access flow: a

Swapnil Hiremath1, Steve P Doucette, Robert Richardson

  • 1Division of Nephrology, Kidney Research Centre, Ottawa Health Research Institute, Ottawa, Ontario, Canada.

Insights

Arteriovenous (AV) access flow in hemodialysis (HD) patients does not correlate with increased left ventricular mass (LVM) or N-terminal pro-brain natriuretic peptide (NT-proBNP) levels after one year. This finding suggests AV access flow is not a primary driver of heart failure risk in HD patients.

Area of Science:

  • Nephrology
  • Cardiology
  • Vascular Access

Background:

  • Congestive heart failure (CHF) is significantly more common in hemodialysis (HD) patients than acute coronary syndrome.
  • The role of arteriovenous (AV) access blood flow in the development of left ventricular mass (LVM) and subsequent CHF risk in HD patients requires clarification.

Purpose of the Study:

  • To investigate whether blood flow through an AV access contributes to increased LVM in HD patients.
  • To assess the relationship between AV access flow and changes in LVM and N-terminal pro-brain natriuretic peptide (NT-proBNP) levels.

Main Methods:

  • A 1-year prospective cohort study involving HD patients at high risk for CHF.
  • Echocardiography and plasma NT-proBNP levels were measured pre- and post-AV access creation.
  • AV access blood flow was measured, and data were analyzed using statistical methods including correlation and regression.

Main Results:

  • One year after AV access creation, LVM increased by 12.2% (P=0.025) and NT-proBNP levels increased by 170% (P=0.02).
  • No significant correlation was found between average AV access blood flow and the increase in LVM or NT-proBNP levels.

Conclusions:

  • In patients undergoing chronic HD, AV access flow does not correlate with increases in LVM or NT-proBNP levels after one year.
  • These findings suggest that AV access flow is not a direct contributor to the observed changes in cardiac structure and biomarkers related to heart failure in this population.
Abstract