Conditions summary Flashcards
lemon yellow skin fatigue weight loss nocturia GFR 65
G2 stage CKD
treatment of G1-G4 stage CKD (3)
ACE inhibitor
statins
lifestyle - decrease Na, K, PO4, fluid restriction
monitor GFR regularly
treatment of G5 stage CKD (established renal failure)
dialysis/transplant
CKD diagnosis
bone pain
fractures
vascular calcification
CKD mineral bone disease (causing secondary hyperparathyroidism bc calcium turn into calcium phosphate so is actually low)
CKD mineral bone disease treatment
alfacidol (hydroxylated vit D)
phosphate binders eg calcium carbonate
diarrhoea
oliguria (<0.5ml/kg/hour)
creatinine has more than doubled in last 24 hours
pre renal AKI (hypo perfusion)
untreated pre renal AKI (from hypoperfusion)
muddy brown casts of epithelial cells
acute tubular necrosis
treatment of acute tubular necrosis
fluids
bc the cause is untreated hypovolaemia
old person/alcoholic thats collapsed and lay on floor for 2 days before being found
oliguria <0.5ml/kg/hour
‘coca cola urine’
rhabdomyolysis causing renal AKI
AKI with inadequate monitoring (lazy nurses)
arrhythmias
hyperkalaemia
treatment of hyperkalaemia (associated with AKI) (4)
calcium gluconate
insulin dextrose
salbutamol nebulised
dialysis if K>7
proteinuria/haematuria
caused by either drugs (gold, penicillin, NSAIDs) or immune (lupus, ANCA pos vasculitis, good pastures)
glomerulonephritis
treatment of glomerulonephritis generally
ACE inhibitor/ARB
steroids (prednisolone 40-60mg)
glomerulonephritis
1-3 weeks after URTI
glomerular crescents on histology of biopsy
acute rapidly progressive glomerulonephritis
glomerulonephritis
rusty coloured urine after recent URTI/gastroenteritis
mesangial proliferation = haematuria
HSP purpuric skin rash on extensor surfaces
IgA nephropathy
chromosome 16 mutation in adults chronic flank pain palpable kidney hypertension! (with no other cause)
10 years later - hepatic cysts, berrys aneurysm
polycystic kidney disease (PCK) autosomal dominant
treatment of polycystic kidney disease (PCK) (autosomal recessive and dominant)
ACE inhibitor/ARB
tolvaptan
chromosome 6 mutation renal failure with hepatic lesions in a kid hypertension abdo mass renal failure
autosomal recessive polycystic kidney disease (PCK)
sensorineural hearing loss haematuria bulging of lens in eye x linked genetic condition thickened glomerular basement membrane from type IV collagen deposition
alports syndrome
lysosomal storage disease (every where = hence lots of random symptoms)
angiokeratoma (blue dots in umbilical area)
renal failure
Anderson fabrys disease
alports syndrome treatment
ACE inhibitor/ARB
Anderson fabrys disease treatment
fabrysyme enzyme replacement
20 y/o
genetic condition causing decreased kidney size
= polyuria, polydipsia, enuresis (unable to concentrate urine)
medullary cystic kidney
treatment of medullary cystic kidney
transplant (bc young)
genetic condition
renal medulla looks like a sponge from dilation of collecting ducts
medullary sponge kidney
tuberose sclerosis patient
abdo mass
CT scan - lots of fat and blood vessels in kidney
angiomyolipoma (fat/blood vessel filled benign renal tumour)
fluid filled lumps in kidney picked up as an incidental finding on US/CT
asymptomatic, no pain
benign renal cyst