Abstract: FR-PO522
Far Infrared Radiation Does Not Improve Time to Cannulation in Newly Placed Arteriovenous Fistulas in Patients on Hemodialysis
Session Information
- Dialysis Vascular Access
October 25, 2024 | Location: Exhibit Hall, Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Dialysis
- 803 Dialysis: Vascular Access
Authors
- Lindhard, Kristine, Herlev Hospital, Herlev, Hovedstaden, Denmark
- Hansen, Henrik Post, Herlev Hospital, Herlev, Hovedstaden, Denmark
- Gliese, Kirstine Moeller, Sjaellands Universitetshospital Roskilde, Roskilde, Sjaelland, Denmark
- Hansen, Emilie Klara, Herlev Hospital, Herlev, Hovedstaden, Denmark
- Hommel, Kristine, Holbaek Sygehus, Holbaek, Sjaelland, Denmark
- Jensen, Boye, Syddansk Universitet, Odense, Syddanmark, Denmark
- Liem, Ylian Serina, Rigshospitalet, Kobenhavn, Denmark
- Pedersen, Brian Lindegaard, Rigshospitalet, Kobenhavn, Denmark
- Pourarsalan, Mahshid, Nordsjaellands Hospital, Hillerod, Denmark
- Rix, Marianne, Rigshospitalet, Kobenhavn, Denmark
- Heaf, James, Sjaellands Universitetshospital Roskilde, Roskilde, Sjaelland, Denmark
- Hansen, Ditte, Herlev Hospital, Herlev, Hovedstaden, Denmark
Background
There is a need to improve arteriovenous fistula (AVF) maturation and decrease the number of central venous catheter days in patients on hemodialysis (HD). Far infrared radiation (FIR) is a treatment modality, which may improve AVF maturation and patency. The present trial examined FIR's effect on AVF maturation
Methods
A randomized, controlled, open-label clinical trial was performed. Patients were randomized to receive FIR treatment (FIR) or no FIR (control). After AVF placement, the FIR group received FIR on their AVF for 40 minutes at every HD treatment for one year. The primary outcome was the difference in time to cannulation, defined as the number of days from AVF placement to the first HD treatment with two functioning dialysis needles in the AVF. The difference was explored in a Kaplan-Meier analysis censored for thrombosed AVFs, death, loss to follow-up, and change of renal replacement therapy. Hazard ratios (HR) were determined by Cox regression analyses and adjusted for age, sex, diabetes, cardiovascular disease, albumin, type of AVF, size of AVF in mm at placement, and peroperativ flow.
Results
In total, 91 patients were randomized to FIR (n=46) or control (n=45). There were no differences in baseline characteristics between groups. No significant difference in time to cannulation with median days of 68 days [52;109.5] in the FIR group and 68 days [56.5;85] in the control group (p=0.8) was seen. The HR for chance of cannulation was 0.71; (95% confidence interval (CI), 0.43-1.18, p=0.19) in the FIR group compared to the control group. HR after adjustment for clinical variables was 0.68 (95% CI 0.40-1.15, p=0.12) in the FIR group compared to the control group. The number of thrombosed AVFs before cannulation was 9 in the FIR group and 4 in the control group (p=0.23)
Conclusion
FIR does not improve time to cannulation in newly placed AVFs in patients on hemodialysis. However, the influence of FIR on clinical maturation, the long-term risk of thrombosis, and the number of interventions in the AVFs are yet to be explored.
Funding
- Private Foundation Support