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A Murine Model of Hemodialysis Access-Related Hand Dysfunction
Published on: May 31, 2022
Hemodialysis vascular access monitoring: current concepts
Michael Allon1, Michelle L Robbin
1Division of Nephrology, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA. mdallon@uab.edu
Insights
Routine screening for arteriovenous graft stenosis with preemptive angioplasty does not reduce graft thrombosis. Future research should focus on pharmacologic interventions to prevent stenosis.
Area of Science:
- Vascular Surgery
- Nephrology
- Interventional Radiology
Background:
- Arteriovenous grafts (AVGs) frequently fail due to thrombosis.
- Stenosis is a common underlying cause of AVG thrombosis.
- Early detection of stenosis via surveillance aims to prevent thrombosis.
Purpose of the Study:
- To evaluate the effectiveness of routine AVG stenosis surveillance with preemptive angioplasty in reducing graft thrombosis.
- To assess the predictive value of current surveillance methods for graft thrombosis.
- To determine if preemptive angioplasty is beneficial in preventing AVG failure.
Main Methods:
- Review of noninvasive surveillance methods for AVG stenosis (clinical monitoring, dialysis venous pressures, flow monitoring, duplex ultrasound).
- Analysis of observational studies and randomized clinical trials comparing surveillance programs with clinical monitoring.
- Evaluation of the impact of preemptive angioplasty on graft thrombosis rates.
Main Results:
- Surveillance tests have high predictive value for stenosis but low predictive value for thrombosis.
- No current surveillance reliably distinguishes stenosed grafts that will clot from those that will remain patent.
- Randomized trials (5 of 6) failed to show a reduction in graft thrombosis with surveillance compared to clinical monitoring.
- Graft thrombosis often occurs despite normal surveillance tests.
- Rapid stenosis recurrence after angioplasty limits the benefit of surveillance programs.
Conclusions:
- Routine surveillance for AVG stenosis with preemptive angioplasty is not recommended for reducing graft thrombosis.
- Current surveillance strategies lead to unnecessary angioplasties and do not reliably prevent thrombosis.
- Future research should explore pharmacologic interventions to prevent AVG stenosis.
Abstract:
Most arteriovenous grafts fail due to irreversible thrombosis, and most clotted grafts have an underlying stenotic lesion. These observations raise the plausible hypothesis that early detection of graft stenosis with preemptive angioplasty will reduce the likelihood of graft thrombosis. A number of noninvasive methods can be used to detect hemodynamically significant graft stenosis with a high positive predictive value. These tests include clinical monitoring, as well as surveillance by static dialysis venous pressures, flow monitoring, or duplex ultrasound. However, these surveillance tests have a much lower positive predictive value for graft thrombosis in the absence of preemptive angioplasty. In other words, none of the currently available surveillance tests can reliably distinguish between stenosed grafts destined to clot, and those that will remain patent without intervention. As a consequence, any program of graft surveillance necessarily results in a substantial proportion of unnecessary angioplasties. Moreover, a substantial proportion of grafts thrombose despite a normal antecedent surveillance test. Numerous observational studies have found an impressive reduction of graft thrombosis after implementation of a stenosis surveillance program. In contrast, 5 of 6 randomized clinical trials failed to show a reduction of graft thrombosis in patients undergoing graft surveillance, as compared with those receiving only clinical monitoring. The lack of benefit of surveillance is largely attributable to the rapid recurrence of stenosis after angioplasty. Thus, routine surveillance for graft stenosis, with preemptive angioplasty, cannot be recommended for reduction of graft thrombosis. Future research should be directed at pharmacologic interventions to prevent graft stenosis.
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