ASN's Mission

To create a world without kidney diseases, the ASN Alliance for Kidney Health elevates care by educating and informing, driving breakthroughs and innovation, and advocating for policies that create transformative changes in kidney medicine throughout the world.

learn more

Contact ASN

1401 H St, NW, Ste 900, Washington, DC 20005

email@asn-online.org

202-640-4660

The Latest on X

Kidney Week

Abstract: FR-PO776

Which Test Is Best for Detecting Stenosis and Predicting Thrombosis in Arteriovenous Graft? A Diagnostic Accuracy Comparative Study

Session Information

Category: Dialysis

  • 603 Hemodialysis: Vascular Access

Authors

  • Tessitore, Nicola, AOUI Verona, Nephrology Unit, Verona, Italy
  • Pessolano, Giuseppina, AOUI Verona, Nephrology Unit, Verona, Italy
  • Lipari, Giovanni, AOUI Verona, Surgery Dpt, Verona, Italy
  • Mansueto, Giancarlo, AOUI Verona, Diagnostics & Public Health Dpt, Verona, Italy
  • Bedogna, Valeria, AOUI Verona, Nephrology Unit, Verona, Italy
  • Contro, Alberto, AOUI Verona, Diagnostics & Public Health Dpt, Verona, Italy
  • Poli, Albino, AOUI Verona, Diagnostics & Public Health Dpt, Verona, Italy
  • Lupo, Antonio, AOUI Verona, Nephrology Unit, Verona, Italy
Background

Guidelines recommend regular screening of grafts for significant >50% stenosis (St) by surveillance (access blood flow[Qa], static venous pressure ratio[sVPR] or Duplex Ultrasound [D]) and state that there is insufficient evidence to prefer one tool over another due to the lack of studies comparing vis-a-vis all of the options

Methods

To identify optimal criteria for St detection and elective repair, we compared in 52 PTFE grafts the Area under Receiver Operator Curve (AUC[95%CI]), sensitivity (SE) & false positive rate (FPR) of clinical monitoring (M), Qa by ultrasound dilution (QaU), sVPR, & D to detect >50% St (StD) and measure Qa (QaD) for >50% St at angiography (StA) and incipient thrombosis (within 4-mo).

Results

Prevalence of StA was 52%. M could not detect StA (AUC 0.60[0.45-0.76]), while all surveillance tools had a similarly significant accuracy for StA: StD (AUC 0.91[0.79-0.97]; SE 85%, FPR 4%), QaU (AUC 0.89[0.77-0.96]; Qa<1300 ml/min: SE 78%, FPR 8%), sVPR (AUC 0.78[0.65-0.89]; sVPR>0.7: SE 89%, FPR 40%), QaD (AUC 0.73[0.59-0.84]; Qa<1300 ml/min: SE 76%, FPR 48%).
31 thromboses occurred during the follow-up. Only QaU (AUC 0.75[0.64-0.84], p<0.001; QaU<1200: SE 68%, FPR 29%), QaD (AUC 0.67[0.53-0.80], p<0.03; QaD<1300: SE 87%, FPR 57%) & StA (AUC 0.61[0.50-0.72], p<0.05; SE 73%, FPR 47%) were equally significant predictors of thrombosis, though their AUC was similar to StD (AUC 0.60[0.46-0.72]) & sVPR (AUC 0.59[0.47-0.70]). At Cox’s multivariate analysis (in a model including StA or StD, QaU or QaD, sVPR, M & acute symptomatic Hypotension during the follow-up) the only significant & independent predictors of incipient thrombosis were Hypotension (with a 4-fold [95%CI:2-18] increased risk, p=0.001), QaU or QaD (with a 20% [95% CI:10-40] greater risk for each 100 ml/min drop in Qa, p<0.01). At univariate analysis, the risk of thrombosis increased significantly at QaU<1200 ml/min (RR 3.7 [95%CI:1.7-8.7], p<0.001) or QaD<1300 ml/min (RR 4.1 [95%CI:0.9-37.1], p<0.05).

Conclusion

Our comparative study suggests that in graft an effective screening program should be based on Qa surveillance (QaU or QaD) & the risk of thrombosis may be contained by avoiding acute hypotension & electively repairing St at a QaU<1200 ml/min or QaD<1300 ml/min.