application) Complications of vascular access in patients treated with chronic hemodialysis are a major source of morbidity. Currently, polytetrafluoroethylene (PTFE) grafts are the most prevalent form of vascular access for hemodialysis in the United States. The most frequent complication of these grafts is thrombosis. Consequences include further access procedures, missed dialysis treatments, and temporary vascular access devices. The costs of maintaining vascular access are approximately one billion dollars a year. In a small study, dipyridamole was shown to decrease the incidence of thrombosis in new PTFE grafts. The objective of this proposal is to determine if the use of dipyridamole is efficacious in decreasing the need for intervention and in prolonging PTFE graft survival in patients undergoing chronic hemodialysis. This will be a prospective, randomized, double blinded trial involving five Clinical Centers. The entrance criteria include patients with a functioning (prevalent) or new (incident) PTFE graft with an access flow of >800 ml/min. One hundred twenty five chronic hemodialysis patients from this center will undergo randomization to receive dipyridamole 75 mg TID or placebo TID. If the graft flow (measured monthly) decreases to <800 ml/min and there is >25 percent decrease in flow compared to baseline, patients will undergo diagnostic fistulography. If a significant lesion is found (as defined by strict criteria), the patients will undergo a radiological or surgical intervention. The primary outcome will be the time from initiation of drug until the first intervention for thrombosis or declining access flow rates. The first secondary outcome will be the time from initiation of drug until the graft is irreversibly lost due to thrombosis. The other secondary outcome will be the number of radiological and surgical interventions required to maintain graft patency normalized to patient-year follow-up. If dipyridamole beneficially affects these outcomes, use of the drug in hemodialysis patients with PTFE grafts should decrease patient morbidity and lower healthcare costs.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project--Cooperative Agreements (U01)
Project #
1U01DK058978-01
Application #
6291247
Study Section
Special Emphasis Panel (ZDK1-GRB-2 (O2))
Program Officer
Kusek, John W
Project Start
2002-04-15
Project End
2006-02-28
Budget Start
2002-04-15
Budget End
2003-02-28
Support Year
1
Fiscal Year
2002
Total Cost
$299,996
Indirect Cost
Name
Washington University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
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Zheng, Sijie; de Las Fuentes, Lisa; Bierhals, Andrew et al. (2009) Relation of serum fetuin-A levels to coronary artery calcium in African-American patients on chronic hemodialysis. Am J Cardiol 103:46-9
Dixon, Bradley S; Beck, Gerald J; Vazquez, Miguel A et al. (2009) Effect of dipyridamole plus aspirin on hemodialysis graft patency. N Engl J Med 360:2191-201
Dember, Laura M; Beck, Gerald J; Allon, Michael et al. (2008) Effect of clopidogrel on early failure of arteriovenous fistulas for hemodialysis: a randomized controlled trial. JAMA 299:2164-71
Dixon, Bradley S; Beck, Gerald J; Dember, Laura M et al. (2005) Design of the Dialysis Access Consortium (DAC) Aggrenox Prevention Of Access Stenosis Trial. Clin Trials 2:400-12
Dember, Laura M; Kaufman, James S; Beck, Gerald J et al. (2005) Design of the Dialysis Access Consortium (DAC) Clopidogrel Prevention of Early AV Fistula Thrombosis Trial. Clin Trials 2:413-22