Genitourinary System Flashcards
(44 cards)
Renal failure/injury is asymptomatic until ___ % of the nephron is lost
60
Oliguric = \_\_\_\_ ml/day Non-oliguric = \_\_\_ml/day
<400; >400
Prerenal (60%-70%)
⬇️ renal blood flow (hypoxia) Hypovolumia ⬇️ CO (CHF) Sepsis Burns Renal artery stenosis
Renal (intrinsic) injury
Damage to renal parenchyma
Acute tubular necrosis (MCC)
Nephrotoxic drugs (aminoglycosides, antifreeze, contrast)
Myoglobinuria (crush injury)
Postrenal injury
Uriniary tract obstuction (BPH, stone, neoplasm)
FEFNa (fractional excretion of filtered sodium):
___ suggests renal etiology (ATN:filter is broken)
___ suggests prerenal etiology (hypoperfusion)
> 1%; <1%
Muscle relaxants of choice for acute renal failure. Which is contraindicated?
Atracurium, vecuronium, mivacurium;
Sux bc it causes hyperkalemia
What is the most serious problem of uremia? MCC of death?
It inhibits immunity. Sepsis
MC type of stone with nephrolithiasis
Calcium oxalalate
Acute onset, colicky severe flank pain, N/V
Nephrolithiasis
Tx of nephrolithiasis
Hydration, analgesia, lithotripsy, nephrolithotomy, Thiazide diuretics (⬇️ Ca conc in urine)
What is the best test for renal function?
Creatinine clearance. Approximately equals GFR
What test distinguishes prerenal from renal failure?
Fractional excretion of filtered sodium (FEFNa)
⬇️ prerenal, ⬆️ renal
What organism causes glomerulonephritis?
Beta-streptococcal infection (cross reaction of antibodies)
Immune complex mediated
Hematuria, proetinuria, HTN, & edema
Increase Cr
Red cell cast
Glomerulonephritis
Tx for glomerulonephritis
Steroid + immunosuppressant
Proteniuria > 3.5 g/day Edema Na retention HTN Hyperlipoproteinemia Thromboembolic phenomenon & infections
Nephrotic syndrome
Causes of nephrotic syndrome
DM, neoplasia, HIV, preeclampsia
Hemoptysis & hematuria
Cross-reaction of antibodies
Progress to RF
Goodpasture syndrome
Proteinuria
Decrease concentration ability
HTN
Reversible
Interstitial presentation
Have deafness & ocular problems
HTN
RF
Tx ACE inhibitor for some protection
Hereditary nephritis (alport’s syndrome)
Autosomal dominant
Accompanying Berry’s aneurysm -> subarachnoid hemorrhage
Polycystic renal disease
Defects in PCT functions that lead to: Polyuria Metabolic acidosis d/t loss fo HCO3 Skeletal muscle weakness d/t loss of K Dwarfism & osteomalcia d/t loss of phosphorous Vit-D resistant rickets
Fanconi syndrome
Detrusor Muscle
Filling of bladder: Relaxed B2
Emptying of bladder: Contracted M