Background <p>This study explores vascular access complications in patients established on in-centre nocturnal haemodialysis (INHD) compared to conventional haemodialysis.</p> Methods <p>This was a retrospective cohort study; patients acted as their own control. Data were collected from three centres. Adults established on INHD (intervention) preceded by usual daytime haemodialysis (control) were eligible. Data were collected between 01/01/2009 and 12/31/2021. The data collection period was up to 12&#xa0;months for both control and intervention periods.</p> <p>The primary outcome was a composite of outcomes related to vascular access complications: hospitalisation, intervention, change in vascular access modality, change in dialysis modality and death. The primary outcome was evaluated by time-to-event rate in days using Kaplan–Meier plots. Statistical significance was accepted at a <i>P</i> &lt; 0.05<i>.</i></p> Results <p>One hundred forty-five individuals were included: median age was 52.0&#xa0;years (IQR 36.0–65.0), 71.0% (<i>n</i> = 103) were male, and 57.2% (<i>n</i> = 83) were White.</p> <p>The primary outcome occurred in 24.1% (<i>n</i> = 35) during the intervention and in 25.5% (<i>n</i> = 37) during the control period (<i>P</i> = 0.875). The 12-month vascular access survival probability was 73.4% (95%CI 65.8–81.0%) for the intervention and 70.6% (95%CI 62.4%-78.8%) for the control period.</p> <p>During the intervention period, arteriovenous grafts were associated with lower vascular access survival (<i>P</i> &lt; 0.001). Regular vitamin K antagonist was associated with a lower 12-month vascular access survival for both the intervention (<i>P</i> = 0.044) and the control periods (<i>P</i> &lt; 0.001).</p> Conclusion <p>There does not appear to be an increased risk to vascular access events for INHD compared to daytime haemodialysis. Vascular access type and regular anticoagulation were associated with a reduced vascular access survival probability.</p> Graphical abstract <p></p>

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Exploring vascular access survival in prevalent thrice-weekly in-centre nocturnal haemodialysis patients

  • Katherine L. Hull,
  • Ann Bugeja,
  • Matthew P. M. Graham-Brown,
  • Lindsay Reid,
  • Aiden J. Smith,
  • Brigit C. van Jaarsveld,
  • James O. Burton

摘要

Background

This study explores vascular access complications in patients established on in-centre nocturnal haemodialysis (INHD) compared to conventional haemodialysis.

Methods

This was a retrospective cohort study; patients acted as their own control. Data were collected from three centres. Adults established on INHD (intervention) preceded by usual daytime haemodialysis (control) were eligible. Data were collected between 01/01/2009 and 12/31/2021. The data collection period was up to 12 months for both control and intervention periods.

The primary outcome was a composite of outcomes related to vascular access complications: hospitalisation, intervention, change in vascular access modality, change in dialysis modality and death. The primary outcome was evaluated by time-to-event rate in days using Kaplan–Meier plots. Statistical significance was accepted at a P < 0.05.

Results

One hundred forty-five individuals were included: median age was 52.0 years (IQR 36.0–65.0), 71.0% (n = 103) were male, and 57.2% (n = 83) were White.

The primary outcome occurred in 24.1% (n = 35) during the intervention and in 25.5% (n = 37) during the control period (P = 0.875). The 12-month vascular access survival probability was 73.4% (95%CI 65.8–81.0%) for the intervention and 70.6% (95%CI 62.4%-78.8%) for the control period.

During the intervention period, arteriovenous grafts were associated with lower vascular access survival (P < 0.001). Regular vitamin K antagonist was associated with a lower 12-month vascular access survival for both the intervention (P = 0.044) and the control periods (P < 0.001).

Conclusion

There does not appear to be an increased risk to vascular access events for INHD compared to daytime haemodialysis. Vascular access type and regular anticoagulation were associated with a reduced vascular access survival probability.

Graphical abstract