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Acute Nephritic Syndrome

Epidemiology
Incidence

Risk Factors Alcoholism

Description
Acute nephritic syndrome is a term that covers kidney diseases of a variety of aetiologies, which lead to active glomerulonephritis. May be due to infection (mostly with group A ß-haemolytic streptococci), auto-immune disease (particularly systemic lupus erythematosus), drug-induced (gold, penicillamine), or idiopathic2.

Presentation
Symptoms Variable: symptoms are generally non-specific and may be absent.

Signs

  • Haematuria, often with dysmorphic RBCs
  • Urine sediment containing RBC casts
  • Proteinuria
  • Peripheral oedema

Differential Diagnosis

Investigations

  • Urinalysis
  • 24-h urine
  • Renal biopsy

Associated Diseases
Systemic lupus erythematosus

Management
Patients with known or suspected acute nephritic syndrome should generally be managed by a renal specialist.

Non-Drug Plasmapheresis

Drugs Acute nephritic syndrome due to auto-immune causes can be treated with steroids (iv methlprednisolone 0.5–1 g per day for 3 days, followed by daily oral prednisolone 1mg/kg per day) or cyclophosphamide (1–2 mg/kg per day)3. Otherwise, treatment is generally supportive rather than specific.

Surgical Renal transplantation.

Complications

Prognosis
Prognosis is variable and depends on aetiology.

References Used

  1. Hedger N, Stevens J, Drey N, et al; Incidence and outcome of pauci-immune rapidly progressive glomerulonephritis in Wessex, UK: a 10-year retrospective study.;Nephrol Dial Transplant 2000 Oct;15(10):1593-9.[abstract] Full text 
  2. Couser WG; Glomerulonephritis.;Lancet 1999 May 1;353(9163):1509-15.[abstract]
  3. Glomerulo-nephritis. Singapore: Ministry of Health; 2001 Practice guidelines from Singapore

Last issued 30 Aug 2006















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