Renal Flashcards

1
Q

rise in creatinine AKI definition

A

25 mml/L in 48 hrs
over 50% in 7 days

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2
Q

rise in creatinine in past 48 hrs for diagnosis of AKI

A

25 microcol/L

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3
Q

rise in creatinine over past 7 days for diagnosis of AKI

A

over 50%

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4
Q

urine output for diagnosis of AKI

A

less than 0.5ml/kg/hr over minimum 6 hrs

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5
Q

renal causes of AKI

A

acute tubular necrosis
glomerulonpehritis
acute interstitial nephritis
haemolytic uraemic syndrome
rhabdomyolysis

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6
Q

pre renal causes of AKI

A

dehydration
shock eg sepsis, acute blood loss
heart failure

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7
Q

most common renal intrinsic cause of AKI

A

acute tubular necrosis

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8
Q

what cells are damaged in acute tubular necrosis

A

epithelial cells of renal tubules

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9
Q

medications that cause AKI

A

NSAIDs
gentamicin
diuretics
ACEi

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10
Q

how do ACEi affect the kidneys

A

they are reno protective

they are stopped in AKI as they reduce the filtration pressure, but are given to protect the kidneys in htn, diabetes, CKD

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11
Q

complications of AKI

A

fluid overload- pulmonary oedema
hyperkalemia
metabolic acidosis
uraemia

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12
Q

how is proteinuria quantified

A

urine albumin:creatinine

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13
Q

eGFR for diagosis of CKD

A

<60 ml/min for 3 months

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14
Q

urine albumin:creatinine for diagnosis of CKD

A

> 30 mg/mmol for 3 months

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15
Q

what medications help slow the progression of CKD

A

ACEi
SGLT-2 inhibitors

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16
Q

what medication are all patients with CKD put on

A

atorvastatin 20 mg

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17
Q

what happens to phosphate in CKD

what advice is given

A

rises

low phosphate diet and phosphate binders

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18
Q

what should be corrected before giving erythropoietin in CKD

A

iron deficiency

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19
Q

describe what happens in renal bone disease

A

calcium is low as the kidneys cant metabolise vitamin D into calcitriol

this causes a rise in PTH and activates osteoclasts, so calcium can be released from bones

when this is done with inadequate calcium supply, osteomalacia occurs

osteosclerosis also occur as osteoblasts match osteoclast activity, but without sufficient calcium this leads to unmineralised bone

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20
Q

pneumonic for indications for dialysis

A

AEIOU

acidosis
electrolyte imbalance
intoxication
oedema
uraemia

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21
Q

how might long term haemodialysis be carried out

A

tunnelled cuffed catheter
ateriovenous fistula

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22
Q

where is a tunnelled cuff catheter inserted

A

subclavian or jugular vein

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23
Q

how might you identify a ateriovenous fistula

A

aneurysm
palpable thrill
machinery murmur

24
Q

what is steal syndrome

A

when the portion of the lim distal to an AV fistula doesnt receive enough blood leading to ischaemia

25
Q

what does peritoneal dialysis occur through

A

a tenckhoff catheter

26
Q

2 types of dialysis

A

haemo
peritoneal

27
Q

most common AV fistula

A

radiocephalic

28
Q

where is a donor kidney implanted

A

in the iliac fossa

29
Q

what scar is seen in kidney transplant

A

hockey stick

30
Q

tacrolimus side effect

A

tremor

31
Q

cyclosporine side effect

A

gum hypertrophy

32
Q

what is given after kidney transplant to prevent acute rejection

A

basiliximab

33
Q

complications of immunosupression in kidney transplant

A

due to steroids:
cushings
diabetes

NHL
skin cancer
tremor (tacrolimus)
gum hypertrophy (cyclosporine)

34
Q

nephritic syndrome features

A

heamaturia
oliguria
fluid retention

35
Q

nephrotic syndrome triad

A

proteinuria
hypoalbuminaemia
oedema

36
Q

what happens to cholesterol in nephrotic syndrome

A

rises

37
Q

most common cause of nephrotic syndrome in children

A

minimal change disease

38
Q

how is minimal change disease mx

A

steroids

39
Q

causes of nephrotic syndrome

A

minimal change disease
membranous glomerulonephropathy
FSGS
membranoprolifertive glomerulonephritis
HSP

40
Q

nephrotic syndrome inflammation occurs where

A

basement membrane

41
Q

histology of IgA deposits and mesangial proliferation suggests

A

Bergers disease

42
Q

other name for bergers disease

A

IgA nephropathy

43
Q

histology of IgG and complement deposits on the basement membrane suggests

A

membranous nephropathy

44
Q

histology of immune complex deposits and mesangial proliferation suggests

A

membranoproliferative glomerulonephritis

45
Q

how long after infection does post strep glomerulonephritis occur

A

1-3 weeks

46
Q

what is goodpastures syndrome

A

where there are anti glomerular basement membrane antibodies

47
Q

goodpasture syndrome sx

A

acute kidney failure and haemoptysis

48
Q

patient presents with AKI and haemoptysis

how do you reach a diagnosis

A

test for autoantibodies

anti GBM= goodpastures syndrome
p-ANCA= microscopic polyangiitis
c-ANCA= granulomatosis with polyangiitis

49
Q

what are MPO antibodies

A

p ANCA

50
Q

what are PR3 antibodies

A

c ANCA

51
Q

p ANCA, AKI and haemoptysis diagnosis

A

microscopic polyangitis

52
Q

c ANCA, AKI and haemoptysis diagnosis

A

granulomatosis with polyangiitis

53
Q
A
54
Q

what are microscopic polyangiitis and granulomatosis with polyangiitis

A

vasculitis

they can present with AKI and haemoptysis

the first is assoc w p ANCA
the second is assoc w c ANCA

55
Q

how are nephrotic/nephritic syndromes definetively diagnosed

A

kidney biopsy

56
Q
A