Med Flashcards
Radiologic study to evaluate structure, function of KUB
Using radiographs and radiopaque dye
Force fluids after to excrete dye
Intravenous pyelography
Visualization of complete ureter, renal pelvis needed.
Performed during cystoscopy
Carries risk of sepsis, severe UTI
Retrograde pyelography
Evaluates the bladder structure abnormalities, filling.
Cystogram
Rapid series of x rays while voiding
Contradicted in UTI
Voiding cystourethrography
Evaluate bladder, renal function, assess cause of reduced urinary flow, urinary retention or incontinence.
Uroflowmetry, cystometrography
Urodynamic studies
BUN normal range
7-20
GFR normal range
90 or greater
Inflammation in glomeruli believed to be from antigen antibody stimulation in the glomerular membrane which changes the membrane permeability. More common in males
More common in children and young adults.
Proceeded by strep or viral inf
Acute glomerulonephriris/ Bright’s disease
Hematuria and proteinuria is a S/S of
Acute glomerularnephritis/Brights disease
How do you dx acute glomerularnephritis/brights disease
Proteinuria
Elevated ASO titer
Percutaneous renal biopsy
Tx for acute glomerularnephritis/Bright’s disease
Tx SS
Bed rest until BUN decreases and hematuria decreases
Low sodium diet and dec fluids if needed
Diuretics/ antihypertensives/ steroids
i&O and weights
Nursing care for acute glomerularnephritis/ Bright’s disease
Inc urine output and dec wt means patient is improving.
VS monitor BP
Sodium and protein diet restriction
BR
Pt not cured till urine free of protein and RBC for 6 mo
Causes of ____ ____ causes are autoimmune connective tissue disorders (lupus) resulting in scar tissue that replaces nephrons and may progress in renal failure
Slow progressive disease in which there is inflammation of the glomeruli that causes irreversible damage to nephrons
Chronic glomerulonephritis
S/S of ___ ___ may not have SS for years
Anasarca- which is caused by a fluid shift and protein (albumin) is lost in urine.
Ss of renal failure
DX- dec RBC
Azotemia- nitrogenous waste in blood
Protein and casts in urine
Early stages percutaneous kidney bx
TX: symptomatic
Dec edema, and bp
Prevent CHF, correct fluid and electrolyte prob, eliminate UTI
May eventually require dialysis or kidney transplant
Chronic glomerulonephritis
___ ___ ___ inherited as autosomal dominant trait, infantile (rare) and adult forms, formation of multiple bilateral kidney cysts. They cause kidneys to greatly enlarge as cysts accumulate fluids
*hypertension, pain, colic. Hematuria, renal stones
Dx findings:
Abd US, CT, MRI, IVP, labs
Tx- no cure, tx HTN, *avoid all nephrotoxic meds-nsaids/cephalosporins
Surgical removal of kidney, dialysis, transplant
Monitor BP, I&O and labs
Polycystic renal disease