GU/Nephrology 6% Flashcards
Proximal convoluted tubules (resorb/secrete) ____
What medication work here?
Resorb All organic nutrients (glucose, AA) Bicarb Na, Cl 75-90% of H2O
Acetazolamide
Mannitol
Thin Descending Limb of Loop of Henle (resorbs/secretes) ___
Resorbs
H20 passively
Impermeable to Na and solutes
Thick Ascending Limb of Loop of Henle (resorbs/secretes) ___
What medication work here?
Resorbs
Actively Na+, K+, Cl-
Indirectly resorbs Mg+ and Ca+
Loop diuretics –> inhibit water, Na, K, Cl cotransport
Early distal convoluted tubule (resorbs/secretes) ____
Other functions?
What medication work here?
SECRETES
Organic acids, toxins, drugs
K+, H+
Dilutes urine by actively resorbing Na+ and Cl-
Thiazide diuretics –> impairs urinary dilution
____ determine final osmolarity of urine via ____
What medication work here?
Distal collecting tubules
Via Aldosterone, ADH
K-sparing diuretics: inhibit aldosterone mediated Na/H2O absorption –> hyperkalemia, metabolic acidosis
Nephrotic syndrome is characterized by ___ (4)
Proteinuria
Hypoalbuminemia
Hyperlipidemia
Edema
80% of nephrotic syndrome in children =
Microscopy findings:
Tx:
Minimal change disease
Loss of foot processes of podocytes
Loss of negative charge of glomerular basement membrane
Tx: Prednisone
Sclerosis(fibrosis) within glomerulus
Seen in ___
Tx:
Focal segmental glomerulosclerosis
Seen in HTN in blacks
Tx: steroids
Thickened glomerular basement membrane
Caused by:
Membranous Nephropathy
Caused by SLE, viral hepatitis, malaria, drugs (Pencillamine)
D/t immune complex deposition
MC cause of nephrotic syndrome in adults
Diabetes mellitus
Gold standard of dx of nephrotic syndrome
Urinalysis shows:
24 hrs urine protein collection > 3.5 g/d
Oval fat bodies “maltese cross shaped”
Acute glomerulonephritis is characterized by (4)
HTN
Hematuria (RBC casts)
Dependent edema (proteinuria)
Azotemia (build up of nitrogen waste in blood)
All of the following are causes of Acute glomerulonephritis EXCEPT: A. IgA Nephropathy (Berger's dz) B. Goodpasture's syndrome C. Post infectious D. Membranousproliferative GN E. Vasculitis
TRICK QUESTION. All are causes of AGN.
IgA Nephropathy (a.k.a. ____)
T/F: MC cause of AGN in children worldwide
When does it usually occur? Why?
Dx?
Tx?
Berger’s dz
False. MC cause of AGN in ADULTS worldwide
Young men within days after URI or GI infection d/t IgA overproduction
Dx: IgA depositis in mesangium w/ immunostaining
Tx: ACE-I + Corticosteroids
Post infectious AGN occurs MC after ____
Presentation:
Dx:
Tx:
Group A Beta-hemolytic Strep (can occur after any infection)
Skin/pharyngeal infection
2-14 y/o boys w/ puffy eyelids, facial edema, cola colored/dark urine
Dx: Increased antistreptolysin (ASO) titers
Low serum complement (C3)
Tx: supportive, abx
Rapidly progressive glomerulonephritis (RPGN) is (good/bad) prognosis
Bx findings?
Tx?
bad prognosis –> rapid progression to ESRD
Cresent formation d/t fibrin and plasma protein deposition
Tx: steroids + cyclophosphamide
+ Anti-GBM antibodies seen in ____
Results in ___
Often occurs ____
Dx:
Tx:
Goodpasture’s syndrome
Kidney failure and HEMOPTYSIS (d/t ab against type 4 collagen of GBM in kidney and lung alveoli)
Often occurs after URI
Dx: Linear IgG deposits
Tx: High dose steroid immunosuppression + Cyclophosphamide + plasmapharesis
Vasculitis AGN is characterized by ___
2 types:
lack of immune deposits, + ANCA ab
Microscopic polyangiitis = vasculitis of small renal vessels –> + P-ANCA
Granulomatosis w/ polyangiitis (Wegener’s) = necrotizing vasculitis –> + C-ANCA
Gold standard dx of AGN
renal bx
Urinalysis: RBC casts, high specific gravity > 1.020osm
WBC casts are pathognomonic for ___
Other clinical features?
acute tubulointerstitial nephritis (AIN)
EOSINOPHILIA
fever
maculopapular rash
arthralgia
4 causes of intrinsic AKI
MC type?
Acute Tubular Necrosis (ATN) = MC type of intrinsic AKI
Acute tubulointerstitial nephritis (AIN)
Glomerular (AGN)
Vascular
Medication that may cause Acute Tubular Necrosis
Aminoglycosides
Inflammatory or allergic response in interstitium, sparing glomeruli and blood vessels =
Commonly caused by ____
Acute tubulointerstitial nephritis (AIN)
PCN, NSAIDs, Sulfa drugs
All of the following are features of ATN EXCEPT:
A. Epithelial cell casts and muddy brown casts
B. High specific gravity
C. Hypokalemia
D. High phosphate
B, C
LOW specific gravity
HYPERkalemia
Narrow waxy casts seen in ___
Broad waxy casts seen in ___
Chronic ATN/Glomerlonephritis
End stage renal disease
ATN or Prerenal? Low specific gravity Creatinine rapidly improves w/ IVF BUN:Cr > 20:1 UNA > 40 , FeNa > 2% Cr increases at 0.3-0.5 mg/dL/day
Low specific gravity: ATN
Creatinine rapidly improves w/ IVF: Prerenal
Creatinine does NOT improve w/ IVF = ATN
BUN:Cr > 20:1 = Prerenal
BUN:Cr 10-15:1 = ATN
UNA > 40 , FeNa > 2% = ATN
Cr increases at 0.3-0.5 mg/dL/day = ATN
Cr increases slower than 0.3 mg/dL/day = prerenal
Causes of HYPERphosphatemia
Associated Ca, Phosphate and PTH levels of each?
Renal failure (MC) : dec. Ca, inc. phosphate, inc. PTH
Primary hypoparathyroidism: dec. Ca, inc. phosphate, dec. PTH
Vit D intoxication: inc. Ca, inc. phosphate, dec. PTH
Causes of HYPOphosphatemia
Primary HYPERparathyroidism Excessive IV glucose, Tx for DKA Refeeding syndrome in ETOHics Respiratory alkalosis Vit D deficiency (dec Ca and dec phosphate)
Polycystic Kidney Dz = autosomal (dominant/recessive) d/o d/t mutation of ____ gene(s).
Characterized by ___
Extrarenal manifestations:
AD
PKD1, PKD2
formation and enlargement of kidney cysts in other organs (LIVER, spleen, pancreas)
Vasopressin stimulates cystogenesis –> ESRD
Cerebral “berry” aneurysms**
Mitral valve prolapse **
Chronic kidney disease staging
Normal GFR =
0 = at risk; normal GFR and urine 1 = kidney damage w/ normal GFR (>90) 2 = GFR 89-60 3 = GFR 59-30 4 = GFR 29-15 5 = GRF < 15
Normal GFR = 120-130