Kidney Disorders Flashcards

1
Q

define polycystic kidney disease (PKD)

A

an autosomal dominant disease characterised by cystic dilation of renal tubular epithelium

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2
Q

causes of PKD

A
PKD1 mutation (polycystin-1) on chromosome 16 (85%)
PKD2 mutation (polycystin-2) on chromosome 4
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3
Q

risk factors of PKD

A

FH of PKD
FH of intracranial aneurysm
PMH of hypertension

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4
Q

clinical features of PKD

A

flank/suprapubic and lower back pain
bilateral kidney enlargement
polyuria, dysuria and urinary urgency

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5
Q

external manifestation features of PKD

A

intracranial berry aneurysm
mitral valve prolapse
colonic diverticular
extrarenal cysts

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6
Q

investigations of PKD

A

urine dip + M,C&S
bloods (FBC, U+E, CRP and lipids)
renal US
CT abdomen and pelvic

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7
Q

common investigation findings in PKD

A

proteinuria + haematuria ⬆️ urea, creatinine and cholesterol in bloods
⬇️ eGFR
bilateral cysts and kidney enlargement on imaging

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8
Q

medical management of PKD

A

vasopressin receptor antagonist (tolvaptan)
ACE inhibitor or ARB (ramipril or losartan)
paracetamol

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9
Q

conservative management of PKD

A

regular monitoring of bloods and cyst progression

avoiding contact sport

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10
Q

define nephrotic syndrome

A

a clinical syndrome characterised by a triad of:

  • proteinuria (>3g/day)
  • hypoalbuminaemia
  • oedema
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11
Q

pathophysiology of nephrotic syndrome

A

arise secondary to increased permeability of serum protein through a damaged basement membrane in renal glomerulus

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12
Q

causes of nephrotic syndrome

A

systemic (DM, SLE)
minimal change disease
drugs (gold or penicillamine)

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13
Q

clinical features of nephrotic

A

weight gain
loss of appetite
nausea + vomiting
frothy urine

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14
Q

signs of nephrotic syndrome

A

periorbital + peripheral oedema

mild hypertension

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15
Q

investigations of nephrotic syndrome

A

bloods (FBC, U+Es, RFTs, LFTs, autoatnibodies, serum cholesterol, glucose)
urine dipstick
renal US + biopsy

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16
Q

management of nephrotic syndrome

A

high dose steroids
anticoagulants
diuretics
ACE inhibitors

17
Q

complications of nephrotic syndrome

A

infection
venous thromboembolism
hyperlipidaemia

18
Q

define chronic kidney disease (CKD)

A

a gradual irreversible decline in kidney function defined by either a decreased GFR or kidney damage markers

19
Q

describe the requirements of a CKD diagnosis

A

decreased GFR (<60) for >3mnths
histological or structural kidney abnormalities
electrolye abnormalities
albuminuria

20
Q

risk factors of CKD

A
CVD 
proteinuria
AKI 
hypertension 
diabetes 
smoking 
chronic NSAID use
21
Q

clinical features of advanced CKD

A
weight loss/anorexia 
nausea + vomiting 
fatigue and weakness 
pruritus 
muscle cramps
dyspnoea
22
Q

signs of CKD

A

skin pigmentation
pallor
peripheral oedema
pleural effusion

23
Q

investigations of CKD

A

bloods (FBC, U+Es, creatinine, serology autoantibodies)
urine dipstick
ECG
renal US + biopsy

24
Q

define stage I of CKD

A

> 90ml/min GFR with demonstratable kidney damage

25
Q

define stage II of CKD

A

60-89ml/min GFR with demonstrable kidney damage, proteinuria or raised albumin/creatinine

26
Q

define stage III of CKD

A

30-59ml/min GFR

27
Q

define stage IV of CKD

A

15-30ml/min GFR

28
Q

define stage V of CKD

A

< 15ml/min GFR

29
Q

complications of CKD

A
CVD 
renal osteodystrophy
fluid (oedema)
hypertension 
electrolyte disturbance 
anaemia 
leg restlessness 
sensory neuropathy
30
Q

management of anaemia in CKD

A

subcutaneous erythropoietin injections

31
Q

management of oedema in CKD

A

reduce fluid and salt intake

diuretics (e.g. furosemide)

32
Q

management of hypocalcaemia and hypophosphataemia in CKD

A

restrict dietary potassium

prescribe sevelamer and alfacalcidol

33
Q

additional management of CKD

A

stop nephrotoxic drugs
start antihypertensives
refer for parathryoidectomy if PTH >28mmol/L