HSP Flashcards
1
Q
What is HSP?
A
Small vessel vasculitis ( most common vasculitis of childhood)
2
Q
Peak age of HSP
A
2-8yo
3
Q
Common triggers of HSP
A
- ~50% cases have Hx recent URTI
- Others - vax, meds, cold, bites
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
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
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
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
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
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