Between January 1996 and arch 1997, 49 HDS
® grafts were implanted in 47 patients (male/female; 25/24, average age of 59 years old) who were diagnosed that autologous fistula construction was impossible to create.
The causes of renal failure were diabetes mellitus in 21 and chronic lomeruloephritis in 11. The mean duration of hemodialysis at the time of implantation was 3.7 years, and the mean number of previous vascular access procedures was 2.4. Forty-two grafts were implanted in the proximal upper arm, 3 in the forearm, 3 in the distal upper arm, and 1 between the brachial artery and the axillry vein. The mean interval between surgery and the first use was 8.5 days and 39 of 43 grafts (90%) were cannulated within 14 days. The hemostasis after cessation of cannulation was able to be done within 15 minutes in all cases. Thirteen complications occurred in 12 grafts. Thrombosis was the most common complication (9), and 4 thrombosed grafts were salvaged. Other complications included infection (2), seroma (1), raft exposure (1).
Five patients died during the course of the study, but none of the deaths were related to the graft. The overall primary, i. e., without any treatments, and secondary, i. e., necessary for treatments patency rates were 85%, 87% at 6 months, and 77%, 83% at 12 months, respectively. The patency rate of HDS
® graft is superior to that of conventional ePTFE graft.
We conclude that the HDS
® graft is well to tolerable for an earlier use after creation and the long-term patency rate is superior to that with conventional ePTFE graft.
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