Paediatrics Renal and Urology - Liam Flashcards

1
Q

UTI

  • treatment
A
  • <3
    • IV antibiotics (ceftriaxone) and full septic screen
  • >3
    • Oral antibiotics (trimethoprim/nitrofurantoin/cefalexin/amoxicillin)
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2
Q

Vesico-ureteric reflex:

  • pathology
A

Urine flows from bladder back into ureters

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3
Q

Vesico-ureteric reflux

  • diagnosis
A

Micturating cystourethrogram (MCUG)

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4
Q

Nephrotic syndrome

  • pathology
A

Basement membrane permeable to protein (proteinuria)

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5
Q

Nephrotic syndrome

  • classic triad
A

Low serum albumin

High urine protein

Oedema

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6
Q

Nephrotis syndrome

  • causes
A

Minimal change disease

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7
Q

Minimal change disease

  • pharmacological treatment
A

Corticosteroids (predinisolone)

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8
Q

Nephritic syndrome

  • pathology
A

Inflammation within nephrons causing HAEMATURIA

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9
Q

Nephritic syndrome

  • causes
A

Post-streptococcal glomerulonephritis

IgA nephropathy (Burgers disease)

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10
Q

What organism preceds post-streptococcal glomerulonephritis

A

B-haemolytic strep (strep pyogenes in tonsillitis)

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11
Q

Post-strep glomerulonephritis

  • treatment
A

Supportive

Antihypertensive medication and diuretics

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12
Q

IgA nephropathy

  • pathology
A

Releated to Henoch-Schonlein Purpura which is IgA vasculitis

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13
Q

IgA nephropathy

  • age
A

Teenangers and young adults

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14
Q

IgA nephropathy

  • treatment
A

Supportive treat and immunosuppresants (steroids)

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15
Q

Haemolytic uraemic syndrome

  • pathology
A

Thrombosis within small vessels throughout body

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16
Q

Haemolytic uraemic syndrome

  • classic triad
A

Haemolytic anaemia

Acute kidney injury

Thrombocytopenia

17
Q

Haemolytic uraemic syndrome

  • organism that preceeds
A

E-coli

18
Q

Haemolytic uraemic syndrome

  • treatment
A

Medical emergency

Supportive management

Maybe renal dialysis

19
Q

Polycystic kidney disease

  • cause
A
  • genetic
  • 2 types - autosommal dominant and autosommal ressesive
20
Q

Polycystic kidney disease

  • features
A

Cystic enlargement of renal collecting ducts

Oligohydramnios, pulmonary hypoplasia and Potter syndrome

Congenital liver fibrosis

21
Q

Hydrospadias

  • pathology
A

Urethral meatus displaces, normal further towards bottom of glans