Renal Flashcards

1
Q

Acute Interstitial Nephritis features

A

fever, rash, arthralgia
eosinophilia
mild renal impairment
hypertension

white cell casts, sterile pyuria

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2
Q

Acute Interstitial Nephritis Causes

A

drugs: (the most common cause, particularly antibiotics)
penicillin
rifampicin
NSAIDs
allopurinol
furosemide

systemic disease: SLE, sarcoidosis, and Sjogren’s syndrome

infection: Hanta virus , staphylococci

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3
Q

Lithium in AKI

A

stop due to increased risk of toxicity

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4
Q

AKI definition

A

↑ creatinine > 26µmol/L in 48 hours
↑ creatinine > 50% in 7 days
↓ urine output < 0.5ml/kg/hr for more than 6 hours

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5
Q

peritonitis secondary to peritoneal dialysis;
most common cause

A

staph epidermis

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6
Q

peritonitis secondary to peritoneal dialysis; treatment

A

vancomycin (or teicoplanin) + ceftazidime added to dialysis fluid
OR
vancomycin added to dialysis fluid + ciprofloxacin by mouth

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7
Q

feature suggestive CKD over AKI

A

hypocalcaemia

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8
Q

ADPKD Tx to slow progression

A

Tolvaptan

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9
Q

Dialysis disequilibrium syndrome

A

rare complication of haemodialysis
It is caused by cerebral oedema, but the exact mechanism is unclear

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10
Q

ADPKD features

A

hypertension
recurrent UTIs
flank pain
haematuria
palpable kidneys
renal impairment
renal stones

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11
Q

ADPKD extra renal features

A

liver cysts (70% - the commonest extra-renal manifestation): may cause hepatomegaly

berry aneurysms (8%): rupture can cause subarachnoid haemorrhage

cardiovascular system: mitral valve prolapse, mitral/tricuspid incompetence, aortic root dilation, aortic dissection

cysts in other organs: pancreas, spleen; very rarely: thyroid, oesophagus, ovary

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12
Q

diabetes insipidus: plasma/urine osmolality

A

high plasma osmolality, low urine osmolality

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13
Q

why is nephrotic syndrome associated with a hypercoagulable state

A

due to loss of antithrombin III via the kidneys

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14
Q

ADPKD Ix

A

Abdominal USS

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15
Q

Urine dip AKI

A

Pre-renal- n/a
intrinsic renal (tubules/glomerulus) - protein (maybe blood)
post-renal- blood

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16
Q

causes of polyuria

A

Common (>1 in 10):
diuretics, caffeine & alcohol
diabetes mellitus
lithium
heart failure

less common:
hypercalcaemia
hyperthyroidism
chronic renal failure
primary polydipsia
hypokalaemia
Diabetes insipidus

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17
Q

negative fluid balance features

A

tachycardia
Hypotension
Oliguria
Sunken eyes and reduced skin turgor

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18
Q

renal transplant acute graft failure

A

usually asymptomatic and is picked up by a rising creatinine, pyuria and proteinuria
happens within 6 months

19
Q

HUS triad

A

acute kidney injury
microangiopathic haemolytic anaemia
thrombocytopenia

20
Q

haematuria and acute urinary retention Tx

A

bladder irrigation via a 3-way urethral catheter

21
Q

myoglobulinuria causes renal failure by

A

tubular cell necrosis

22
Q

central DI treatment

A

desmopressin- vasopressin receptor agonist

23
Q

pre-renal vs renal urinary sodium and urine osmolality

A

pre-renal: urine osmolality high, urine sodium low
renal: urine osmolality low, urine sodium high

24
Q

AKI after initiation of ACEi

A

fibromuscular dysplasia in young patients
atherosclerosis of renal arteries in older patients

25
fibromuscular dysplasia MR angiography finsings
string of beads appearance of renal arteries
26
haemolytic uraemic syndrome
AKI MAHA- fragmented red blood cells (schistocystes) Thrombocytopenia (decreased plt)
27
enlarged kidneys on USS
diabetic nephropathy ADPKD amyloidosis HIV-associated nephropathy
28
maintenance fluid rate
30ml/kg/24hour
29
solid organ transplant- most common infection and treatment
CMV ganciclovir
30
hyaline casts seen on urine microscopy
loop diuretics
31
HSP symptoms
palpable purpura over Lower limbs, arthritis/arthralgia, abdominal pain, renal disease
32
nephrotic syndrome triad
proteinuria hypoalbuminaemia oedema
33
nephritic syndrome triad
haematuria hypertension proteinuria oedema
34
causes of nephritic syndrome
renal causes: - membranoproliferative glomerulonephritis - IgA nephropathy - Crescentic/ rapidly progressive nephritis (Goodpastures, ANCA vasculitis) systemic causes: - post-strep glomerulonephritis - hepatitis C - IgA vasculitis
35
causes of nephrotic syndrome
minimal change disease membranous glomerulonephritis focal segmental glomerulosclerosis
36
nephrotic syndrome complications
thromboembolism --> DVT, renal vein thrombosis (sudden drop in renal function) hyperlipidaemia --> ACS, stroke CKD infection hypocalcaemia
37
Salicylate poisoning (aspirin)
- raised anion gap metabolic acidosis--> respiratory alkalosis nausea, vomiting, tinnitus and headache Tx = sodium bicarbonate
38
renal biopsy will show a thickened basement membrane on light microscopy and sub-epithelial spikes on silver staining.
Membranous nephropathy
39
membranous nephropathy causes
primary- anti-phospholipase A2 antibodies malignancy- prostate, lung, lymphoma leukaemia infections- Hep B, malaria, syphylis drugs- gold, penicillamine, NSAIDs AI - SLE< thyroiditis, rheumatoid
40
proteinuric CKD Tx
SGLT-2 inhibitor
41
metabolic acidosis with normal anion gap
Hyperchloraemia Renal tubular acidosis Addison's disease Diarrhoea
42
CKD stages
stage 1- >90 stage 2- 60-90 stage 3a 45-59 stage 3b- 30-44 stage 4- 15-29 stage 5- <15 N.B. only diagnose stage 1 or 2 if supportive evidence to accompany eGFR
43
uraemia
encephalopathy or pericarditis
44
NSAIDs should be stopped in AKI except
aspirin at cardio-protective dose