Abstract

Rapidly progressive glomerulonephritis (RPGN), characterized by a rapid development of nephritis with loss of kidney function in days or weeks, is typically associated histologically, with crescents in most glomeruli; and is a challenging problem, particularly in low resource settings. RPGN is a diagnostic and therapeutic emergency requiring prompt evaluation and treatment to prevent poor outcomes. Histopathologically, RPGN consists of four major categories, anti-glomerular basement membrane (GBM) disease, immune complex mediated, pauci-immune disorders and idiopathic /overlap disorders. Clinical manifestations include gross hematuria, proteinuria, oliguria, hypertension and edema. Diagnostic evaluation, including renal function tests, electrolytes, urinalysis/microscopy and serology including (anti GBM antibody, antineutrophil cytoplasmic antibody (ANCA)) starts simultaneously with management. An urgent renal biopsy is required to allow specific pathologic diagnosis as well as to assess disease activity and chronicity to guide specific treatment.The current guidelines for management of pediatric RPGN are adopted from adult experience and consist of induction and maintenance therapy. Aggressive combination immunosuppression has markedly improved outcomes, however, nephrotic syndrome, severe acute kidney injury requiring dialysis, presence of fibrous crescents and chronicity are predictors of poor renal survival. RPGN associated post infectious glomerulonephritis (PIGN) usually has good prognosis in children without immunosuppression whereas immune-complex-mediated GN and lupus nephritis (LN) are associated with poor prognosis with development of end stage kidney disease (ESKD) in more than 50% and 30% respectively.Given the need for prompt diagnosis and urgent treatment to avoid devastating outcomes, we conducted a review of the latest evidence in RPGN management to help formulate clinical practice guidance for children in our setting.Information sources and search strategy: The search strategy was performed in the digital databases of PubMed, Cochrane Library, google scholar, from their inception dates to December 2020. Three investigators independently performed a systematic search using the following search terms “Rapidly progressive glomerulonephritis” “children” “crescentic glomerulonephritis” “management” at the same time, backtracking search for references of related literature.

Highlights

  • Rapidly progressive glomerulonephritis in childrenSUMMARY Rapidly progressive glomerulonephritis (RPGN), characterized by a rapid development of nephritis with loss of kidney function in days or weeks, is typically associated histologically, with crescents in most glomeruli; and is a challenging problem, in low resource settings

  • An Indian study showed a higher prevalence of pauci immune (PI) mediated Rapidly progressive glomerulonephritis (RPGN) compared to immune complex (IC) (71.7% vs 28.3%)[9] raising the concern that PI is an important cause of RPGN in children.[10]

  • The most appropriate classification of RPGN is based on histopathology and on the presence, localization, and characteristics of immune deposits on immunofluorescence (IF) staining and is divided into three major categories; Type-I: Linear antibody (IgG) deposition disorders: Antiglomerular basement membrane (GBM) disease, Type-II: GN caused by deposition of immune complexes (i.e., in IgA nephropathy (IgAN), lupus nephritis (LN), post infectious glomerulonephritis (PIGN), Henoch Schonlein Purpura nephritis (HSPN)) and Type-III: Pauci-immune GN

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Summary

Rapidly progressive glomerulonephritis in children

SUMMARY Rapidly progressive glomerulonephritis (RPGN), characterized by a rapid development of nephritis with loss of kidney function in days or weeks, is typically associated histologically, with crescents in most glomeruli; and is a challenging problem, in low resource settings. RPGN is a diagnostic and therapeutic emergency requiring prompt evaluation and treatment to prevent poor outcomes. RPGN associated post infectious glomerulonephritis (PIGN) usually has good prognosis in children without immunosuppression whereas immune-complex-mediated GN and lupus nephritis (LN) are associated with poor prognosis with development of end stage kidney disease (ESKD) in more than 50% and 30% respectively. Given the need for prompt diagnosis and urgent treatment to avoid devastating outcomes, we conducted a review of the latest evidence in RPGN management to help formulate clinical practice guidance for children in our setting.

BACKGROUND
ETIOLOGY OF RAPIDLY PROGRESSIVE GLOMERULONEPHRITIS
PATHOGENESIS OF CRESCENTIC GLOMERULONEPHRITIS
Glomerulonephritis in children
CLINICAL MANIFESTATIONS OF RPGN
LABORATORY EVALUATION IN A CHILD WITH RPGN
Varies with biopsy findings
MANAGEMENT OF CHILDREN WITH RPGN
MAINTENANCE OF REMISSION
TREATMENT OF FAILED INDUCTION
TREATMENT OF RELAPSING DISEASE
OUTCOME OF RPGN
Findings
CONCLUSION
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