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Biologic versus PTFE hemodialytic vascular accesses: a single-center experience.
Luca Freni, M.D., Assistant1, Claudio Mariani, M.D.1, Alice Basiric̣, M.D.,1, Alberto Settembrini, M.D.,1, Maurizio Gallieni, M.D.2, Piergiorgio Settembrini, Professor of Vascular Surgery1.
1Vascular Surgery, San Carlo Borromeo Hospital, Milano, Italy, 2Nephrology, San Carlo Borromeo Hospital, Milano, Italy.

Objective:
The optimal hemodialytic vascular access still remains the native arteriovenous fistula. If anatomically feasible, it is preferred to the early use of prosthetic material. Native vessels consumption in long-lasting hemodialysis and aging of the population accessing hemodialytic treatment, increase the use of prosthetic grafts. We analyzed our prosthetic accesses series.
Methods:
Data concerning hemodialytic prosthetic accesses created in our institution from 1998/1 to 2011/8 were reviewed. Patency rates were calculated with Kaplan-Meier method.
Results:
On 800 arteriovenous fistulas, 104 (13%) are prosthetic. Follow-up (1998/2-2012/2) is available for 94 (90,3%). Twelve (12.7%) prosthetic grafts were placed as first vascular access. Five (5.3%) early failure were observed. Eighty-nine accesses created in 72 patients (38M; 34F; 70,5 years-old-median age at surgery) allowed hemodialytic treatment, resulting eligible to thorough follow-up: 22 biologic (depopulated bovine ureter - SynerGraft®), 67 PTFE. All grafts were placed in the upper extremities: 46 forearm, 43 arm, (61 left, 28 right).
Cumulative primary patency rates at 12, 36 and 60 months were: 41%, 16% and 3%, respectively; for biologic 60.5%, 16% and not significant (n.s.), respectively; for PTFE 34%, 14% and 4%, respectively.
Cumulative assisted primary patency rates at 12, 36 and 60 months were: 46%, 27% and 12.4%, respectively; for biologic 69.9%, 38.8% and 19.9%, respectively; for PTFE 37%, 23% and 11.4%, respectively.
Cumulative secondary patency rates at 12, 36 and 60 months were: 80%, 61% and 45%, respectively; for biologic 89%, 74% and 44.8%, respectively; for PTFE 76%, 56% and 46%, respectively.
Complications observed were: infection, in 4,5% biologic (1/22) and in 6% PTFE (4/67); aneurysm or false aneurysm, both requiring surgical correction, in 18% biologic (4/22) and in 6% PTFE (4/67); 47 stenosis, in 41% biologic (9/22) and in 28.6% (12/67); 88 thrombosis, in 41% biologic (9/22) and in 52% PTFE (35/67).
Conclusions:
We used both PTFE and SynerGraft®, the latter until available (2008). Since then we have been using PTFE only. Despite its tendency to dilation, we assumed good results with SynerGraft®. However, in our experience, latest PTFE grafts represent a valid and reliable option when native vessels are depleted. An increase in the use of prosthetic grafts is expected. Long-time employment and deterioration of graft material constitute a matter of challenge. Further improvements for long-term performance are desirable.


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