Cochrane Summariesbeta

Independent high-quality evidence for health care decision making

Medical adjuvant treatment to increase the patency of arteriovenous fistulae and grafts used for renal dialysis

Osborn G, Escofet X, Da Silva A
Published Online: 
October 8, 2008

People with advanced kidney disease (end-stage renal disease) need dialysis to perform kidney functions. In haemodialysis, blood is filtered through a machine. To allow a large enough passage for blood to flow between the person and the machine, an artery and a vein can be surgically joined (to form an arteriovenous fistula) or an artificial graft (a substitute for a vein) is used to join the artery to the vein. These access points might last for years but can become blocked or infected. The review of trials found that anti-clotting drugs (anti-platelet drugs like aspirin) can keep these dialysis access points clear, at least in the short term. The review authors found ten randomised controlled trials of anti-platelet drugs such as ticlodipine, aspirin, dipyridimole and clopidogrel or anti-thrombotic and other drug treatment used to prevent blockages in the artery and vein access points for dialysis. Three trials of aspirin that involved a total of 173 participants gave an overall result favouring treatment. The follow-up time and the dosage of aspirin (325 mg/once daily; 500 mg/once daily; and 160 mg/once daily) were different in each of the trials. In three trials with a total 312 participants, ticlopidine (250 mg/twice daily) improved patency at one month compared with placebo (OR for loss of patency 0.47, range 0.26 to 0.85). Single trials involving from 16 to 36 participants compared dipyridimole, fish oil (4 g/daily), clopidogrel (75 mg/once daily) or sulfinpyrazone (a uricosuric drug) with placebo. Although the results favoured treatment the trials were small and single trials are insufficient to recommend use. One trial compared low dose warfarin with placebo. A total of 107 patients were followed for 37 months before the trial was terminated early because of major bleeding events in the treatment group. Some of the trials were from the 1970s and 80s. Most had a short follow-up period so that any benefits in the longer term are not clear. Information given on complications of the treatments was limited.

Find the research