Original Investigations: Dialysis Therapies
Native arteriovenous fistula blood flow and resistance during hemodialysis

https://doi.org/10.1053/ajkd.2003.50032Get rights and content

Abstract

Background: Measurement of vascular access flow (Qa) has been proposed as the ideal method for surveillance of native fistulae. However, debate exists about the influence of blood pressure (mean arterial pressure [MAP]) on Qa during dialysis. Methods: During three consecutive dialysis treatments, 10 patients had paired measurements of Qa and MAP performed at 30, 60, 120, 180, 210, and 240 minutes. Access resistance (AR; in peripheral resistance units, PRUs) was calculated from MAP and Qa values. Results: Overall pooled coefficients of variation (CVs) for MAP, Qa, and AR were 8.4%, 12.3%, and 12.9%, respectively. A significant reduction in Qa and MAP occurred throughout the dialysis treatment (Qa, 104 mL/min; P = 0.008; MAP, 10.4 mm Hg; P = 0.007). Mean percentages of change in Qa for the first third compared with the middle and last thirds of the session were −4.6% ± 11.15% (SD) and −9.6% ± 10.5%, respectively. Thus, Qa varied between 11.4% and −30.6% from baseline during the last hour of dialysis treatments. A stronger correlation between MAP and Qa was seen in radiocephalic (r2 = 0.55; P < 0.0001) compared with brachiocephalic fistulae (r2 = 0.06; P = 0.023). Mean AR was unchanged during the dialysis session (0.23 PRU; P = 0.358). AR for radiocephalic fistulae was significantly greater compared with brachiocephalic fistulae (6.03 ± 3.90 versus 3.00 ± 1.11 PRU; P < 0.0001). Conclusion: Qa could decrease up to 30% from baseline, potentially impairing the ability of Qa to predict impending vascular access failure. AR remained stable during the treatment and may be a more useful measure of vascular access performance as part of an access surveillance program. Am J Kidney Dis 41:132-139. © 2003 by the National Kidney Foundation, Inc.

Section snippets

Study protocol

We prospectively evaluated 10 stable chronic hemodialysis patients. Nine patients usually performed their own dialysis at home. However, their dialysis was currently being performed in the hemodialysis unit at Monash Medical Centre (Melbourne, Australia) because the patients were either retraining on new dialysis machines or undergoing a routine medical assessment. All patients underwent thrice-weekly 4-hour hemodialysis treatments. Each patient was studied during three consecutive dialysis

Results

Basic demographics of study participants are listed in Table 1.

. Basic Demographics of Study Participants

No. of patients10
Age (y)49 ± 13.8
No. of men6
No. of antihypertensives prescribed (per patient)
 07
 11
 22
Access type
 Radiocephalic fistula5
 Brachiocephalic fistula4
 Saphenous vein forearm loop1
Predialysis BP (mm Hg)
 Systolic157 ± 18.5
 Diastolic87 ± 12.3
 MAP96.9 ± 14.1
Interdialytic weight gain (kg)1.4 ± 0.53
Mean age was 48 years, and there were six men and four women in the group. Causes of end-stage

Discussion

The ability of Qa surveillance to predict access thrombosis will depend, in part, on hemodynamic conditions at the time of the test. Because trends in Qa are important in determining the presence of a hemodynamically significant stenosis and heightened risk for thrombosis, variability not just during a given treatment, but also from one treatment to the next is important.15

To quantify this variability, we measured Qa not just at multiple times during one treatment session, but also during three

References (20)

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    The pooled CV for Qa measurements and the regression equation between mean Qa values and their SDs obtained in our study indicate that assay reproducibility accounts for up to 16% of Qa measurement variability, even under standardized conditions in which hemodynamic variability is minimized. Qa variability was lower in our study than that reported for grafts,23 but similar to what others reported in AVFs,4 who found pooled CVs similar to ours for MAP (7.9% versus 8.2%), Qa (9.5% versus 7.9%), and MAP/Qa (11.9% versus 11.2% for Qa/MAP in our study) in hemodynamically stable subjects during the first hour of dialysis. Despite the relatively high variability, Qa measurement shows an excellent diagnostic performance in detecting access dysfunction; this finding is explained partially by the high prevalence of stenosis and thrombosis in our unselected forearm AVF population, a situation that usually ensures good performance, even for tests with less than ideal diagnostic accuracy.

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Address reprint requests to Kevan R. Polkinghorne, FRACP, Department of Nephrology, Monash Medical Centre, 246 Clayton Rd, Clayton, Melbourne, Victoria 3168, Australia. E-mail: [email protected].

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