nephrology Flashcards

1
Q

what are the functions of the kidney ?

A
waste handling
water handling
salt balance
acid/base control
endocrine - RBC, BP, Vit D
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2
Q

what is nephrotic syndrome ?

A

proteinuria - 3+
hypoalbuminaemia
oedema

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3
Q

what are typical features of nephrotic syndrome ?

A

age 2-5
normal BP
resolving microscopic haematuria
normal renal function

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4
Q

how do you treat nephrotic syndrome ?

A

prednisolone 8 weeks

side effects - check varicella status, pneumococcal vaccination

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5
Q

what causes steroid resistant nephrotic syndrome ?

A

acquired - focal segmental glomerulosclerosis FSGS - podocyte loss, inflammation

congenital - infants

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6
Q

what causes macroscopic haematuria ?

A

GN, post infective GN
IGA

UTI
trauma
stones

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7
Q

what causes microscopic haematuria ?

A

GN, post infection GN
IGA

UTI
trauma
stones

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8
Q

what is nephritic syndrome ?

A

haematuria
proteinuria
reduced GFR - oliguria, fluid overload, hypertension, worsening renal failure

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9
Q

what causes glomerulonephritis ?

A
post infective
HSP/ IgA nephropathy
membranoproliferative GN
Lupus nephritis
ANCA positive vasculitis
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10
Q

what is the usual causative organism of post-infective GN ?

A

group A strep
beta haemolytic

throat 7-10 days
skin 2-4 weeks

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11
Q

how is post infective strep diagnosed ?

A

bacterial culture
positive ASOT
low C3 normalises

self-limiting

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12
Q

how do you treat post-infective GN ?

A

antibiotics
support renal function
diuretics if overload/ hypertension

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13
Q

when is IgA nephropathy seen ?

A

1-2 days after URTI
usually older children/adults
most common glomerulonephritis

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14
Q

what are clinical signs of IgA nephropathy ?

A

recurrent macroscopic/ +/- microscopic haematuria

varying degree of proteinuria

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15
Q

how do you treat IgA nephropathy ?

A

mild - ACEi
moderate to severe - immunosuppression

outcomes variable 25% ESRF by 10 yrs

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16
Q

what are features of Henoch Schonlein purpura IgA related vasculitis ?

A

mandatory palpable purpura

1 of;
abdominal pain
renal involvement
arthritis or arthralgia
biopsy - IgA deposition
17
Q

how do you treat IgA vasculitis ?

A

symptomatic
glucocorticoids may help with GI involvement
immunosuppression
long term hypertension and proteinuria screening

18
Q

how do you manage AKI ?

A

3Ms
monitor - urine output, PEWs, BP, weight
maintain - good hydration
minimise - drugs

19
Q

what are different intrinsic renal problems and what causes them ?

A

glomerular disease - HUS, GN
tubular injury - acute tubular necrosis - hypoperfusion, drugs
interstitial nephritis - NSAIDs, autoimmune

20
Q

what is haemolytic-uraemic syndrome ?

A

typical post diarrhoea
E.coli

pneumococcal infection
drugs

21
Q

what is the triad of haemolytic-uraemic syndrome ?

A

microangiopathic haemolytic anaemia
thrombocytopenia
AKI

22
Q

what are the grades of vesico-ureteric reflux ?

A
1 - ureter only
2 - ureter, pelvis, calyces
3- dilatation ureter
4 - moderate dilatation of ureter
5 - gross dilatation
23
Q

what factors affect progression of CKD ?

A
late referral
hypertension
proteinuria
high intake of protein, phosphate, salt
bone health
acidosis
recurrent UTIs
24
Q

what is Potter’s sequence ?

A
decreased amniotic fluid
pulmonary hypoplasia
fetal compression
bilateral renal agenesis
AR polycycstic kidney disease
25
Q

what is Alport syndrome ?

A

glomerular basement membrane disease
collagen 4 abnormalities
X linked dominant inheritance

26
Q

what is the presentation of Alport syndrome ?

A
heamaturia
proteinuria
hypertension
rena failure in early adult life
deafness
eye changes - lenticonous, macular changes