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Prof. Rai Muhammad Asghar Head of Paediatric Department RMC Rawalpindi
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Acute Post streptococcal Glomerulonephritis
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Sudden onset of Gross hematuria Edema Hypertension Renal insufficiency
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Cause of AGN Post infectious (Gp A B sterp) Vasculitis HS purpura SLE
Microscopic polyarteritis Polyarteritis nodosa IgA nephropathy Antiglomerular basement membrane disease
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Post streptococcal Glomerulonephritis
Triad of Acute nephritic syndrome Evidence of recent strep infection Low C3 level
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ETIOLOGY and EPIDEMIOLOGY
Infection of the throat or skin by nephrogenic strains of group A beta – hemolytic sterptococci Commonly follows streptococcal pharyngitis during cold weather months and sterptococcal skin infections or pyoderma during warm weather
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Pharyngitis Pyoderma Strep type Gp A (12) Gp A (49) Climate Temperature , Cold Hot, tropical Season Wniter & spring Summer & fall Incubation period 1-2 wks 3-6 wks Sex incidence B:G 2:1 Equal
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PATHOLOGY Light microscopy: Enlarged and bloodless glomeruli
Diffuse mesangial proliferation with increase in mesangial matrix Polymorphonuclear leukocytes Crescent farmation and interstitial inflammation
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Immunofluorescene microscopy
Lumpy – Bumpy deposits of immunoglobulin and complement on GBM and in the mesangium Electron Microscopy Electron – dense deposits, or humps are observed on epithelial of the GBM
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PATHOGENESIS Exact mechanism not known
Morphological studies and depression in the serum complement (C3) level strongly suggest immune mediated illness
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CLINICAL MANIFESTATIONS
Age 5-15 year Incubation period: 1-2 weeks after pharyngitis 3-6 weeks after pyoderma Hematuria either asymptomatic microscopic with normal renal function or Gross hematuria (cola colored) with acute renal failure Oliguria Edema Hypertension Hypertensive encephalopathy
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Edema results from salt and water retention and nephrotic syndrome may develop in < 5%
Malaise, lethargy, abdominal or flank pain and fever are non specific features Acute subglottic edema and airway compromise Acute phase resolve within 6-8 weeks, urinary protein excretion and hypertension normalize by 4-6 weeks persistent microscopic hematuria may persist for years
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INVESTIGATIONS Urine R/E Renal function Test Serum electrolytes CXR
Red blood cells Red blood cells cast Proteinuria Leukocytes Renal function Test Serum electrolytes Hyponatermia and hyperkalemia CXR
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Evidence of streptococcal infection
Throat culture Raised ASO titer Streptozyme Test Complement C3 Level Low Complete Blood count Hemoglobin – Low Total and differential count usually within normal limits Retics – Raised ESR- Raised
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Indication for Renal Biopsy
Acute renal failure Nephrotic syndrome Absence of evidence of streptococcal infection Normal complement level Hematuria, Proteinuria, diminished renal function and or a low C3 level persist more than 2 months after onset
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Differential Diagnosis
UTI Nephrotic syndrome CRF Liver disorders Cardiac disease Malabsorption disorder
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Differential Diagnosis
Membrano-proliferative glomerulonephritis IgA nephropathy Systemic lupus erythematosis Henoch-schonlein purpura Hemolytic Uremic Syndrome Infective Endocarditis
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Complication Hypertension Acute renal failure Heart failure
Hyperkalemia Hyperphosphatemia Hypocalcemia Acidosis Seizures Uremia
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Treatment General and Supportive Care Treatment of Complications
Bed Rest Antibiotics (benzyl penicillin x 10 days) Dietary Restriction Treatment of Complications Renal failure Left Ventricular failure Hypertensive
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ARF Protein restriction Fluid & electrolyte balance Acid base balance
Control of infections Control of seizures Anemia
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Heart Failure Bed Rest Prop up O2 inhalation Digitalization Diuretics
ACE inhibitors
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Hypertensive Encephalopathy
Labetalol 0.2 – 1.0mg/kg/dose then 0.25 – 2.0mg/kg/hour Isosorbide dinitrate (Isoket) 5µg/kg/mint Hydralazine 0.15kg/dose Furosemide ( 1-2mg/kg/dose 4-6 hrly) Captopril (0.5-5mg/kg/day 8 hrly)
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Prevention Early systemic antibiotic therapy dose not eliminate the risk Family members of patients with AGN should be cultured for group A beta hemolytic streptococcus and treated if culture positive
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Prognosis Complete recovery in more than 95% cases
Infrequently, the acute phase be severe and lead to glomerular hyalinization and chronic renal insufficiency Recurrences are extremely rare
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Thank You
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