Paediatric Nephrology Flashcards

1
Q

define UTI

A

urinary tract growing bacteria, with a single bacteria 10 to the power 5 grown on urine culture
(although any growth on suprapubic aspiration = UTI)

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2
Q

categorise UTIs

A

upper UTI = acute pyelonephritis

lower UTI = acute cystitis

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3
Q

what are long term complications of UTIs?

A

kidney scarring, hypertension, CKD

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4
Q

what dipstick results come up in UTI

A

leukocytes and nitrites

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5
Q

infants younger than 3 months should have what if you suspect a UTI?

A

urine microscopy, culture, sensitivities (MCS)

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6
Q

how do you collect urine from an infant?

A

clean catch is best
urine collection pads (risk of contamination) /bag
catheter samples
suprapubic aspiration

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7
Q

most common UTI bug in children?

A

e.coli

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8
Q

which children with UTIs should you admit?

A

children <3 months
systemically unwell children
significant risk factors (one kidney etc)

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9
Q

how would you treat the child <3 months admitted with suspected UTI

A

IV cefuroxime 2-4 days then switch to oral abx

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10
Q

how would you treat a child >3 months who has (uncomplicated, sustemically well):

LUTI?
UUTI?

A

LUTI - 3 days oral abx with trimethoprim

UUTI - 7 days oral abx with cefalexin

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11
Q

what children with UTIs need further investigation (ie imaging)

A

those presenting with atypical UTI

  • non ecoli UTI
  • septicaemia
  • poor urine flow
  • abdo/bladder mass
  • raised creatinine

OR those with recurrent UTIs

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12
Q

name the types of imaging investigations you can do for UTIs and what they are good for and their limitations

A

US KUB - good for obstruction and rare stuff like duplex kidney, horseshoe kidney, single kidney (structural abnormalities) and is non invasive but observer dependent

MCUG - micturating cystourethrogram - BEST FOR VESICOUTERIC REFLUX identification but invasive

DMSA scan - nuclear medicine scan using radio-isotopes - good for seeing renal scarring (e.g due to recurrent UTIs maybe)

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13
Q

what does oedema in a child present as?

A

swelling, pitting oedema, facial puffiness, ascites

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14
Q

what are the causes of oedema in a child?

A

blockages:
- lymph drainage (turners)
- venous drainage (DVT)

lowered oncotic pressure: low albumin/protein

  • nutritional (poor intake)
  • decreased production (liver problems)
  • increased loss (nephrotic syndrome)

salt and water retention
impaired GFR

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15
Q

what is nephrotic syndrome? described the triad

A
  • heavy proteinuria (frothy/foamy urine and confirmed on dip)

causing. ..
- hypoalbuminemia (low albumin in the blood)

causing. ..
- oedema (as low serum albumin leads to fluid retention)

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16
Q

other than a urine dip, what test would you do on the urine sample in suspected nephrotic syndrome and what would you find in a positive result?

A

protein creatinine ratio
normal = <20mg/mmol
in nephrotic syndrome, could be over 1000s

17
Q

what are the three different types of nephrotic syndrome in children?

A

congenital
steroid sensitive
steroid resistant

18
Q

how do you treat most nephrotic syndromes in children? - condition and symptomatic

A

PREDNISOLONE
- high for 4 weeks then lower dose on alternate days for 4 weeks

symptomatic in the meantime:

  • diuretics
  • salt and water intake moderation (dietary mods)
  • pen V - prophylaxis for infection
  • chickenpox and pneumococcal vaccinations
  • DO NOT GIVE live vaccinations (MMR, BCG)
19
Q

What is nephritic syndrome? and how would they typically present?

A

acute inflammation in the kidney, most commonly post -strep glomerular nephritis (2 weeks after ‘tonsillitis’ etc)

Haematuria (LOTS - coco cola coloured urine)
proteinuria (a bit)
impaired GFR
salt and water retention- (hypertension, oedema)

20
Q

management of nephritic syndrome

A

The treatment of primary pathology ranges from watchful waiting, as in postinfectious GN, to treatment with immunosuppressive medication, such as steroids or cyclophosphamide in lupus.

supportive treatment;
fluid balance – measurements of input/output, fluid moderation, diuretics, salt restriction

Correction of other imbalances: potassium, acidosis

Dialysis – uncommon but might need it

Antibiotics

21
Q

causes of nephrotic syndrome

A

idiopathic, though to be immune mediated

or

secondary to another illness: HSP - henoch-schonlein purpura

22
Q

causes of nephritic syndrome

A

IgA nephropathy
Post-streptococcal glomerulonephritis
Hemolytic uremic syndrome
Henoch–Schönlein purpura

23
Q

what is HSP?

A

type of IgA vasculitis

  • Red purpura on the lower limbs and buttocks
  • multisystem involvement: Skin, joints, gut, kidneys
  • Joint pain
  • May have blood in the stool and bad abdo pain: intersussuption/GI bleed
  • Inflamed kidneys – the most dangerous as can lead to CKD : can either give nephrotic or nephritic picture –> can lead to hypertension