Glomerular Kidney Diseases : Nephritic versus Nephrotic Kidney Disorders
The glomerulus is kidney structure which consists of a a cluster or tuft of small blood vessels called capillaries.
These glomerular capillaries are an important part of the filtering process of the blood to produce urine.
Kidney diseases that involve the glomerulus are divided into two main categories,
Nephritic versus Nephrotic kidney diseases. Both types of kidney disease result in too much protein being lost, or 'spilled' into the urine, resulting in proteinuria.
Nephritic syndrome
hypertension, microscopic hematuria (blood visible in urine under the microscope but not necessarily visible with the naked eye)
red blood cell casts in the urine
proteinuria (often <2 g/d in adults)
Nephrotic syndrome
proteinuria >3.5 g/d in adults and >40 mg/kg in children (this will appear as 3+ on urine protein dipstick)
edema, which is the accumulation of salt water that the kidneys have not excreted; the fluid initially accumulates in the legs
low serum albumin, the major serum protein
elevated serum cholesterol, which is produced by the liver in response to proteinuria
New Feature from Hemodialysis.com: Hemodialysis or Chronic Kidney Disease Abstract of the Week
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.
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