Abstract
Introduction: A brachiobasilic arteriovenous fistula (BB-AVF) can
provide access for haemodialysis in patients who are not eligible for a
more superficial fistula. However, it is unclear whether one or two
stage BB-AVF is the best option for patients.
Aim: To systematically assess the difference between both procedures in terms of access maturation, patency and postoperative
complications.
Methods: Online search for randomised controlled trials (RCTs) and
observational studies that compared the one-stage versus the twostage technique for creating a BB-AVF.
Results: Eight studies were included (849 patients with 859 fistulas),
366 created using a one stage technique, while 493 in a two stage
approach. There was no statistically significant difference between the
two groups in the rate of successful maturation (pooled risk
ratio = 0.95 [0.82, 1.11], P = 0.53). Similarly, the incidence of
postoperative haematoma (pooled risk ratio = 0.73 [0.34, 1.58],
P = 0.43), wound infection (pooled risk ratio = 0.77 [0.35, 1.68],
P = 0.51) and steal syndrome (pooled risk ratio = 0.65 [0.27, 1.53],
P = 0.32) were statistically comparable.
Conclusion: Although more studies seem to favour the 2-stage
BVT approach, evidence in the literature is not sufficient to draw a final conclusion as the difference between the 1-stage and the
2-stage approaches for creation of a BB-AVF is not statistically
significant in terms of the overall maturation rate and postoperative
complications. Patency rates (primary, assisted primary and secondary) were comparable in the majority of studies. Large
randomised properly conducted trials with superior methodology
and adequate sub-group analysis are needed before making a final
recommendation
| Original language | English (Ireland) |
|---|---|
| Title of host publication | Sylvester OHalloran Meeting 2015 |
| Publication status | Published - 1 Mar 2015 |
Authors (Note for portal: view the doc link for the full list of authors)
- Authors
- Bashar, K; Healy, D; Elsheikh, S; Browne, LD; Walsh, MT; Clarke-Moloney, M; Burke, PE; Kavanagh, EG; Walsh SR