Active Circulating Blood Volume During Hemodialysis: A Bench Model.

Intradialytic hypotension due to excessive fluid removal is a common complication of hemodialysis. A bench model was constructed to evaluate quantification of active circulating blood volume (ACBV). The model included a central pump representing the heart and compartments to represent the central and peripheral circulation. A blood oxygenator was used to simulate lung volume and two containers represented fast and slow circulation compartments. A separate dialysis circuit with a blood pump and two ultrasound flow-dilution probes was incorporated. Vascular access was simulated with both a shunt (fistula or graft) and a central venous catheter. Hypertonic saline (5%) was circulated in the system. A bolus of isotonic saline was introduced in the dialysis circuit, which dispersed through the physiologic model. ACBV was measured by comparing the baseline dilution curve to the curve as it returned to the probes. To evaluate the sensitivity of this technique, we investigated changing cardiac output, central venous volume, shunt flow, vascular access type, and HD pump flow. Overall percentage error (mean ± SD) across all tests (n = 15 conditions, each in triplicate) was 2.6% ± 7.4%. This study demonstrates the ability to accurately measure ACBV on the bench.

Theory and in vitro validation of a new extracorporeal arteriovenous loop approach for hemodynamic assessment in pediatric and neonatal intensive care unit patients.

OBJECTIVES: No simple method exists for repeatedly measuring cardiac output in intensive care pediatric and neonatal patients. The purpose of this study is to present the theory and examine the in vitro accuracy of a new ultrasound dilution cardiac output measurement technology in which an extracorporeal arteriovenous tubing loop is inserted between existing arterial and venous catheters. DESIGN: Laboratory experiments. SETTING: Research laboratory. SUBJECTS: None. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: In vitro validations of cardiac output, central blood volume, total end-diastolic volume, and active circulation volume were performed in a model mimicking pediatric (children 2-10 kg) and neonatal (0.5-3 kg) flows and volumes against flows and volumes measured volumetrically. Reusable sensors were clamped onto the arterial and venous limbs of the arteriovenous loop. A peristaltic pump was used to circulate liquid at 6-12 mL/min from the artery to the vein through the arteriovenous loop. Body temperature injections of isotonic saline (0.3-10 mL) were performed. In the pediatric setting, the absolute difference between cardiac output measured by dilution and cardiac output measured volumetrically was 3.97% +/- 2.97% (range 212-1200 mL/min); for central blood volume the difference was 4.59% +/- 3.14% (range 59-315 mL); for total end-diastolic volume the difference was 4.10% +/- 3.08% (range 24-211 mL); and for active circulation volume the difference was 3.30% +/- 3.07% (range 247-645 mL). In the neonatal setting the difference for cardiac output was 4.40% +/- 4.09% (range 106-370 mL/min); for central blood volume the difference was 4.90% +/- 3.69% (range 50-62 mL); and for active circulation volume the difference was 5.39% +/- 4.42% (range 104-247 mL). CONCLUSIONS: In vitro validation confirmed the ability of the ultrasound dilution technology to accurately measure small flows and volumes required for hemodynamic assessments in small pediatric and neonatal patients. Clinical studies are in progress to assess the reliability of this technology under different clinical situations.

Determining lung water volume in stable hemodialysis patients.

Lung water (LW) reflects the water content of the lung interstitium. Because hemodialysis patients have expanded total body water (TBW) they may also have increased LW. Hypertonic saline promotes a flux of water from lung to blood, which is measured by ultrasound flow probes on hemodialysis tubing. The volume of flux is an indirect measure of LW. Our purpose was to determine the feasibility and reproducibility of LW derived with ultrasound velocity dilution, to determine the effect of ultrafiltration on LW in stable hemodialysis patients, and to compare changes in LW with fluid compartment shifts using bioimpedance. Lung water, cardiac output, total body water, and extracellular and intracellular fluid volumes were measured in 24 stable hemodialysis patients at the beginning of hemodialysis and after ultrafiltration. The LW values at the beginning of hemodialysis (298.8 +/- 90.2 ml or 3.67 +/- 1.47 ml/kg) fell during hemodialysis (250.8 +/- 55.8 ml or 3.12 +/- 0.96 ml/kg; p < 0.05), as did TBW and extracellular fluid volumes (p < 0.001). Cardiac output, cardiac index, and central blood volume also decreased significantly with ultrafiltration (p < 0.005, p < 0.005, and p < 0.01, respectively). Results showed that stable hemodialysis patients have higher specific LW values (3.67 ml/kg) than the normal population (2 ml/kg) and ultrafiltration produces a significant decline in LW values.

Access flow measurement during surveillance and percutaneous transluminal angioplasty intervention.

The introduction of routine access flow measurement methodology has enabled accurate identification of problematic accesses and provided a means for follow-up evaluation. These methods have uncovered, in some cases, that interventions are either immediately unsuccessful or that they fail within 3 months to maintain flow above preintervention levels. The purpose of this article is to analyze the main problems that occur at each step in the loop of flow surveillance-intervention-follow-up and to provide suggestions for improving outcomes. Analysis of published access flow data suggests that the main problems lie in the areas of inadequate analysis of flow surveillance data, lack of objective technology for quantifying intervention effectiveness, and lack of follow-up flow measurements in the hemodialysis (HD) unit after the intervention. The following three recommendations may improve surveillance outcomes: 1). using a reliable access flow technology combined with analysis of all hemodynamic data (including mean arterial pressure) before referring patients for angiography to decrease surveillance false positives; 2). performing intra-access blood flow measurement during angioplasty, which may improve outcomes by giving warning of errors before the patient leaves the intervention suite. Success achieved in restoring flow as measured during the intervention usually predicts good immediate outcomes in the HD unit; 3). measuring access flows during the next week after angioplasty. If the results are unsatisfactory, the patient should be further evaluated to avoid a potential thrombotic event.

Relationship between vascular access flow and hemodynamically significant stenoses in arteriovenous grafts.

BACKGROUND: Vascular access dysfunction is a major source of hemodialysis patient morbidity. The NKF K/DOQI Guidelines promote access flow monitoring as the most preferred access surveillance method and have established access flow thresholds for fistulography: an absolute threshold of 600 ml/min and a dynamic threshold of flow less than 1000 ml/min that has decreased by more than 25% over 4 months. The Guidelines apply universally to accesses of different types, sizes, locations, and initial flow rates. METHODS: This article studies the application of access flow guidelines with human experimental data, animal experimental data, and a mathematical model of the arteriovenous graft system. RESULTS AND CONCLUSIONS: Analysis of experimental data and the mathematical model shows that a 20 to 30% and greater decrease in graft flow generally suggests the appearance of hemodynamically significant stenosis as defined by flow criteria. The model suggests that not all 50 to 60% stenoses may be hemodynamically significant or the most flow limiting. The mathematical model also suggests that positive predictive value of access surveillance may be increased for high-flow upper arm grafts by increasing the dynamic K/DOQI threshold from 1000 ml/min to 1200 ml/min.

Use of a catheter-based system to measure blood flow in hemodialysis grafts during angioplasty procedures.

PURPOSE: The goals of this investigation were to evaluate the accuracy and reliability of the Angioflow meter system with use of in vitro and in vivo methods and to compare it to the standard Transonics HD01 system in a clinical setting. MATERIALS AND METHODS: The Angioflow meter system consists of a 6-F endovascular catheter and a laptop computer containing proprietary software for this application. Bench-top testing with use of a flow model was performed to determine the accuracy of the Angioflow meter system. Initial in vivo studies were performed with use of an animal model to assess the endovascular performance of the Angioflow meter system. Subsequently, a human clinical trial was performed to compare the Angioflow meter to the standard Transonics HD01 system. Twenty-five patients with dysfunctional (<600 mL/min) hemodialysis grafts were referred for fistulography and angioplasty. Intragraft blood flow measurements were obtained before and after angioplasty with use of both the Angioflow meter system and the Transonics HD01 system. A comparison of the two systems was performed. RESULTS: Bench-top testing and animal studies demonstrated an excellent (r =.98) correlation between the measurements of the Angioflow meter and volumetric flow measurements. In the clinical trial, there was reasonable correlation (r =.72) between the blood flow measurements obtained with use of the Angioflow meter and Transonics HD01 system. The reproducibility of consecutive measurements with the Angioflow meter was excellent (r =.98). The mean increase in intragraft blood flow after angioplasty was 320 mL/min. CONCLUSION: The Angioflow meter is an accurate and reliable endovascular device for measuring intragraft blood flow during interventional procedures. Use of this catheter-based system should prove beneficial for quantifying the success of endovascular interventions, the assessment of arterial inflow, and identification of inconspicuous lesions.