HSP Flashcards

1
Q

What is HSP?

A

Small vessel vasculitis ( most common vasculitis of childhood)

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2
Q

Peak age of HSP

A

2-8yo

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3
Q

Common triggers of HSP

A
  • ~50% cases have Hx recent URTI

- Others - vax, meds, cold, bites

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4
Q

Natural history of HSP

A
  • Most self-limiting
  • Clinical features take weeks to develop
  • resolution in 4 weeks (rash last, but arthralgia/abdo pain only few days)
  • Most renal complications occur within 2-6 months
  • 25-35% cases recur within 4 months - subsequent episodes usually lighter and quicker
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5
Q

Clinical features of HSP

A
  • Arthritis/arthralgia (50-75%), often of lower joints
  • Abdo pain (50%), signs of peritonism
  • Renal involvement (25-50%): haematuria/proteinuria/hypertension
  • Purpura: gravity dependent - lower limbs and buttocks
  • Swelling: feet, hands, scrotum
  • Respiratory distress
  • Neuro: change in mental status/focal signs
  • Blood in stool/haematuria
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6
Q

Complications of HSP

A
  • Renal
  • Most common complication is intussussception
  • Others – GI haemorrhage, bowel ischaemia, necrosis or perforation, protein-losing enteropathy and pancreatitis
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7
Q

Investigations for HSP

A
  • If classic HSP, only urinalysis needed
  • If there is hypertension, macroscopic haematuria or significant proteinuria, send urine for formal microscopy and protein-creatinine ratio , and bloods for UEC and albumin
  • AXR for intussusception
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8
Q

Management of HSP

A
  • Oedema: bed rest + elevation
  • Pain:
    • Mild pain: reg paracetamol +/- NSAIDs (careful with renal impairment)
    • Steroids for mod-severe arthralgia/abdo pain
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9
Q

What is important following resolution of HSP?

A
  • Close F/U needed to identify renal involvement (remember, can be asymptomatic for a long time)
    • Weekly for the first month after disease onset

If there is no significant renal involvement plus normal urinalysis at 12 months, no further follow-up is required

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