Nephrology & GU - UTI/ Nephrotic Syndrome Flashcards
Describe HSP?
HSP is a characteristic
- skin rash
- arthralgia
- periarticular oedema
- abdominal pain
- glomerulonephritis
When does HSP commonly occur?
twice as common in boys
between the ages of 3 and 10
How do children with HSP present?
- fever
- rash (maculopapular and purpuric) is obvious and distributed over buttocks, extensor surfaces of the arms and legs
- joint pain (knees and ankles)
- colicky abdo pain
- renal involvement w? micro/macroscopic hameaturia
What are the investigations for HSP?
Urinalysis FBC, ESR, creatinine, serum IgA, autoantibody screen Abdo USS (for obstruction) Barium enema (confirm obstruction) Testicular USS (check for torsion) Renal biopsy (if persistent nephrotic syndrome)
How is HSP managed?
self limiting
supportive treatment
NSAIDS for joint pain can be used with caution
Steroids for nephropathy
Follow up for 6 months or longer if renal involvement
What are the long term complications of HSP?
Nephrotic syndrome/renal disease so children with renal involvement should be followed up for at least a year
less than 1% of patients with HSP progress to end stage renal failure
What are the triad of symptoms in nephrotic syndrome?
proteinuria
low plasma albumin
oedema
What are the clinical signs of nephrotic syndrome?
periorbital oedema (earliest sign)
scrotal or vuval, leg or ankle oedema
ascites
breathlessness due to pleural effusions and adobe distention
What is the most common type of nephrotic syndrome?
steroid sensitive nephrotic syndrome
- proteinuria resolves with corticosteroid therapy
usually precipitated by an URTI
What are the investigations for a child presenting with nephrotic syndrome?
urine dipstick FBC, ESR, U&E’s, creatinine, albumin, complement, ASO titre/anti-DNAse B titre throat swab urine culture urinary sodium concentration hepatitis B/C screen malaria screen if travel abroa
What is the management for steroid sensitive nephrotic syndrome?
oral corticosteroids
after 4 weeks reduce the does
usually takes 1 days for urine to become free of protein
What is the prognosis of nephrotic syndrome?
1/3 resolves
1/3 infrequently relapses
1/3 frequently relapses
What are the other types of nephrotic syndrome?
steroid resistant nephrotic syndrome (refer to nephrologist)
congenital nephrotic syndrome (presents in first 3 weeks of life, high mortality)
What are the atypical features of HSP which prompt consideration of second line treatment/renal biopsy?
<1 year and >10 years hypertensive elevated creatinine macroscopic haematuria failed to respond to steroids after 4-8 weeks
How common are UTIs?
3-7% of girls and 1-2% of boys will have a UTI before age of 6
~30% recur within a year
Up to 50% have a structural abnormality