Abstract

In hemodialysis patients, a native arteriovenous fistula (AVF) is the preferred form of permanent vascular access. Despite recent improvements, vascular access dysfunction remains an important cause of morbidity in these patients. In this prospective observational cohort study, we evaluated potential risk factors for native AVF dysfunction. We included 68 patients with chronic renal disease stage 5 eligible for AVF construction at the Department of General and Vascular Surgery, Central Clinical Hospital Ministry of Internal Affairs, Warsaw, Poland. Patient characteristics and biochemical parameters associated with increased risk for AVF failure were identified using Cox proportional hazards models. Vessel biopsies were analyzed for inflammatory cells and potential associations with biochemical parameters. In multivariable analysis, independent predictors of AVF dysfunction were the number of white blood cells (hazard ratio [HR] 1.67; 95% confidence interval [CI] 1.24 to 2.25; p<0.001), monocyte number (HR 0.02; 95% CI 0.00 to 0.21; p = 0.001), and red blood cell distribution width (RDW) (HR 1.44; 95% CI 1.17 to 1.78; p<0.001). RDW was the only significant factor in receiver operating characteristic curve analysis (area under the curve 0.644; CI 0.51 to 0.76; p = 0.046). RDW>16.2% was associated with a significantly reduced AVF patency frequency 24 months after surgery. Immunohistochemical analysis revealed CD45-positive cells in the artery/vein of 39% of patients and CD68-positive cells in 37%. Patients with CD68-positive cells in the vessels had significantly higher white blood cell count. We conclude that RDW, a readily available laboratory value, is a novel prognostic marker for AVF failure. Further studies are warranted to establish the mechanistic link between high RDW and AVF failure.

Highlights

  • In hemodialysis patients, a native arteriovenous fistula (AVF) is the preferred form of permanent vascular access [1]

  • AVF dysfunction remains a major cause of morbidity in hemodialysis patients and leads to significant health care costs

  • This prospective study showed that white blood cell count (WBC), monocyte count, and red blood cell distribution width (RDW) are significant independent predictors of AVF dysfunction

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Summary

Introduction

A native arteriovenous fistula (AVF) is the preferred form of permanent vascular access [1]. Patients with end-stage renal disease have a bleeding diathesis caused by a reduced number of platelets and alterations in platelet adhesion and aggregation These patients are predisposed to thrombosis due to impaired endothelial function and elevations in PAI-1, homocysteine, and von Willebrand factor [12]. Serum C reactive protein (CRP) levels greater than 0.8 mg/dl conferred an 16.6 times increased risk for vascular access thrombosis in patients with native AVF [13]. Numerous risk factors and correlates to AVF dysfunction have been identified, they do not explain all cases of vascular access thrombosis. In this prospective cohort study, we evaluated the predictive value of numerous biochemical factors, assessed at the time of surgery, for AVF failure

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