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Management and outcomes of acute post-streptococcal glomerulonephritis in children
1Faculty of Medicine, University of Malaya, Kuala Lumpur 50603, Malaysia. leotungong@gmail.com.
Insights
Acute post-streptococcal glomerulonephritis (APSGN) is a common childhood kidney disease, often following throat infections. While typically self-limiting with supportive care, severe cases may show poor outcomes.
Area of Science:
- Pediatric Nephrology
- Infectious Diseases
- Immunology
Background:
- Acute post-streptococcal glomerulonephritis (APSGN) is a leading cause of acute kidney injury in children, particularly in resource-limited regions.
- It arises from an immune-mediated response to streptococcal antigens, often following pharyngitis.
Purpose of the Study:
- To review the epidemiology, pathogenesis, clinical presentation, management, and prognosis of APSGN in children.
- To identify predictors of disease severity and poor outcomes.
Main Methods:
- Literature review of APSGN, focusing on pediatric cases.
- Analysis of clinical features, diagnostic markers, and treatment strategies.
- Identification of prognostic indicators such as renal biopsy findings and presenting renal function.
Main Results:
- APSGN presents with varied renal syndromes, including nephritic, nephrotic, or rapidly progressive forms, and can be subclinical.
- Management is primarily supportive, addressing fluid overload, hypertension, and renal function.
- Indicators of severity include decreased complement levels, elevated C-reactive protein, hypoalbuminemia, crescent formation on biopsy, and initial renal insufficiency.
Conclusions:
- APSGN is generally a self-limiting condition with a favorable prognosis for most children.
- However, certain factors like crescentic glomerulonephritis and impaired renal function at presentation predict a higher risk of persistent kidney issues.
Abstract:
Acute post-streptococcal glomerulonephritis (APSGN) is the major cause of acute glomerulonephritis among children, especially in low- and middle-income countries. APSGN commonly occurs following pharyngitis due to the activation of antibodies and complements proteins against streptococcal antigens through the immune-complex-mediated mechanism. APSGN can be presented as acute nephritic syndrome, nephrotic syndrome, and rapidly progressive glomerulonephritis, or it may be subclinical. The management of APSGN is mainly supportive in nature with fluid restriction, anti-hypertensives, diuretics, and renal replacement therapy with dialysis, when necessary, as the disease is self-limiting. Congestive heart failure, pulmonary edema, and severe hypertension-induced encephalopathy might occur during the acute phase of APSGN due to hypervolemia. APSGN generally has a favorable prognosis with only a small percentage of patients with persistent urinary abnormalities, persistent hypertension, and chronic kidney disease after the acute episode of APSGN. Decreased complement levels, increased C-reactive protein, and hypoalbuminemia are associated with disease severity. Crescent formations on renal biopsy and renal insufficiency on presentation may be the predictors of disease severity and poor outcomes in APSGN in children.
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