Do you what GFR is?
How is GFR used to measure kidney disease severity?
GFR stands for Glomerular Filtration Rate. GFR is an important measure of kidney function. The purpose
of the kidneys is to filter and help remove excess waste products and water from the blood. The glomeruli are the filtering elements inside the kidney. Glomeruli are tiny organelles that contain tightly wrapped blood vessels called capillaries. These capillaries filter blood of waste products as the blood passes through the glomeruli.
Diseased kidneys have fewer functioning glomeruli. In some kidney diseases, the kidneys become scarred and shrunken and therefore there are fewer working filtering glomeruli.
GFR is measured by a formula, which requires knowing several key pieces of data. Some of this data includes the patient's age, race, gender and blood (serum) creatinine level.
Creatinine is a breakdown product of muscle. Patients with higher muscle mass (men, African Americans) can be expected to have a higher normal serum creatinine level.
Low GFR indicates a decreased ability of the kidneys to clear the blood of waste products. Kidney disease is classified by Stages 1 to 5, with 5 meaning very low GFR often requiring dialysis treatments.
Zasuwa G, Frinak S, Besarab A, Peterson E, Yee J.
Division of Nephrology and Hypertension, Department of Internal Medicine, Henry Ford Hospital, Detroit, Michigan.
Although monitoring of vascular accesses by physical examination is nearly as sensitive as surveillance measurements by vascular access pressure when performed by examiners, the frequency of examinations is limited by time.
We developed intravascular access pressure surveillance as a surrogate to physical examination. Using real-time data from hemodialysis machines, we derived intravascular access pressure ratios for each dialytic procedure. An automated, noninvasive surveillance algorithm that generated a "warning" list of patients at risk for thrombosis was formulated.
We hypothesized that this algorithm would reduce access thrombosis frequency. We designed a study comparing thrombosis rates during a baseline 6-month interval to three subsequent 6-month periods of active surveillance.
Referrals for interventions during this 18-month period were based on persistently abnormal elevated vascular access pressure ratio tests (VAPRT) >0.55.
Thrombosis rates declined progressively for arteriovenous grafts (AVG) during the intervention period compared with the baseline period.
Arteriovenous fistula (AVF) thrombosis rates decreased during postintervention months 13-18 during employment of the VAPRT.
We conclude that use of VAPRT can reduce thrombosis rates in vascular accesses, and the magnitude of the effect is larger and more consistent in arteriovenous grafts (AVGs) than autologous AVFs.
Hemodialysis | Kidney Disease | Dialysis Resources and Educational Materials
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