Long-term outcome in children after Henoch-Schonlein purpura nephritis

Clin Pediatr (Phila). 2007 Jul;46(6):505-11. doi: 10.1177/0009922806298896.

Abstract

This study investigated predictors of renal survival in children with Henoch-Schönlein purpura glomerulonephritis. Records of patients with Henoch-Schönlein purpura glomerulonephritis evaluated at our center, from 1953-1990, were reviewed. Data were abstracted from records of patients seen within 5 years. Others were mailed a questionnaire or contacted by telephone. Primary outcome measures were renal survival and presence of urinary abnormalities or hypertension. Of the 65 eligible patients with Henoch Schönlein purpura glomerulonephritis, follow-up data was obtainable for 81.5%. The median follow-up was 20 years. At last follow-up, 66% of patients had normal renal function and urinalyses, and 21% had progressed to end-stage renal disease. The only factor associated with the development of end-stage renal disease was the use of cytotoxic agents. There are no features at initial presentation that identify children at risk of disease progression. Close follow-up of all children with Henoch Schönlein purpura glomerulonephritis is warranted.

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Disease Progression
  • Female
  • Glomerulonephritis / etiology*
  • Glomerulonephritis / mortality
  • Glomerulonephritis / therapy
  • Humans
  • IgA Vasculitis / complications*
  • Infant
  • Kaplan-Meier Estimate
  • Kidney Failure, Chronic / diagnosis
  • Kidney Failure, Chronic / etiology*
  • Kidney Failure, Chronic / mortality
  • Longitudinal Studies
  • Male
  • Prognosis
  • Risk Factors
  • Time Factors
  • Treatment Outcome