Nephrology Flashcards

1
Q

5 kidney functions

A
waste handling - urea and creatinine 
water handling 
salt balance 
acid base control - HCO3
Endocrine - bp,bone, activate vit D, erythropoeitin
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2
Q

3 parts of glomerular filtration barrier

A

fenestrated endothelium
GBM
podocytes
(mesangial cells)

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3
Q

proteinuria signifies…

A

glomerular injury

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4
Q

What is nephrotic syndrome?

A

nephrotic range proteinuria
hypoalbuminaemia
oedema

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5
Q

nephrotic syndrome in terms of starlings forces

A

oncotic vs hydrostatic

lose protein which keeps water in

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6
Q

typical presentation of nephrotic syndrome

A
swollen face and legs
gastroenteritis 10 days prior
periorbital and pitting oedema
ascites 
frothy urine
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7
Q

testing for proteinuria

A

dipstix - >3
protein creatinine ration
24 hour urine collection

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8
Q

patient diagnosis of nephrotic syndrome

A

oedema
proteinuria
bloods - low albumin

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9
Q

Nephrotic syndrome types

A

MINIMAL CHANGE

FSGC/MPGN

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10
Q

typical features of minimal change disease

A

age 2-5 years
normal blood pressure
resolving microscopic haematuria
normal renal function

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11
Q

atypical features of minimal change disease

A

autoimmune
abnormal renal function
steroid resistant

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12
Q

When to consider renal biopsy with MCD

A

atypical features

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13
Q

Treating nephrotic syndrome

A

prednisolone for 8 weeks

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14
Q

side effects from glucocorticoids

A

cushings syndrome

BEHAVIOUR

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15
Q

Pathogenesis of nephrotic syndrome

A

interaction between lymphocytes and podocytes

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16
Q

Outcome of nephrotic syndrome

A

95% remission in 2-4 weeks
80% relapse
immunosuppression

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17
Q

steroid resistant nephrotic syndrome

A

acquired = FSGS

congenital

18
Q

persistent haematuria and proteinuria =

A

glomerular disease

19
Q

Nephritic syndrome presentation

A
haematuria and proteinuria 
reduced GFR - oliguria
fluid overload - high JVP, oedema 
hypertension 
AKI
20
Q

Causes of nephritic syndrome

A

post infectious
IgA nephropathy
lupus nephritis
membranoproliferative

21
Q

diagnosing nephritic syndrome

A

Renal USS
ASOT, throat swab, low complement
immune disease - ANCA -ve

22
Q

Usual cause of PIGN

A

beta haemolytic group A strep

throat or skin infection

23
Q

Treating PIGN

A

antibiotic

diuretics

24
Q

IgA nephropathy presentation

A
1-2 days after URTI 
older children and adults 
recurrent macroscopic haematuria 
chronic microscopic haematuria 
varying proteinuria
25
Diagnosing IgA nephropathy
confirmation biopsy normal complement negative autoimmune
26
treating IgA nephropathy
mild disease - proteinuria with ACEI | mod-severe = immunosuppression
27
mandatory clinical diagnosis for IgA related vasculitis (HSP)
palpable purpura
28
4 of the other criteria for HSP
abdominal pain renal involvement arthritis/arthralgia biopsy - IgA deposition
29
Treating IgA vasculitis
symptomatic - joints, gut immunosuppression glucocorticoids hypertension and proteinuria screening
30
AKI
Anuria/oliguria (<0.5ml/kg/hr) hypertension with fluid overload rapid rise in creatinine more than 1.5 times normal
31
HUS
post diarrhoea - bloody vero/shiga toxin E coli 0157
32
HUS triad
microangiopathic haemolytic anaemia thrombocytopenia AKI
33
AKI long term consequences
Blood pressure proteinuria monitoring evolution to CKD
34
CKD causes - paeds
reflux nephropathy PKD Dysplasia glomerulonephritis
35
UTI definition
clinical signs plus bacteria from MSSU
36
obtaining urine specimen
MSSU collection pads? suprapubic aspiration catheter
37
diagnosing UTI
dipstix - leucocytes, nitrites microscopy = pyuria, bacteria culture
38
imaging renal tract
USS MAG3 and micturating CUG = reflux DMSA - scar
39
treating UTI
3 days oral antibiotic - lower 7-10 days if upper prevent = fluids, hygiene
40
Factors affecting progression of CKD
``` hypertension proteinuria acidosis bone health high intake of salt ```
41
Blood pressure
doppler sphigmanometer oscillometry ABPM
42
Treating metabolic bone disease
phosphate binders activated vitamin D low phosphate diet