(N01.5) Rapidly progressive nephritic syndrome : diffuse mesangiocapillary glomerulonephritis

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103 436 in individuals diagnosis rapidly progressive nephritic syndrome : diffuse mesangiocapillary glomerulonephritis confirmed
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2 185 deaths with diagnosis rapidly progressive nephritic syndrome : diffuse mesangiocapillary glomerulonephritis
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2% mortality rate associated with the disease rapidly progressive nephritic syndrome : diffuse mesangiocapillary glomerulonephritis

Diagnosis rapidly progressive nephritic syndrome : diffuse mesangiocapillary glomerulonephritis is diagnosed Women are 35.75% more likely than Men

33 231

Men receive the diagnosis rapidly progressive nephritic syndrome : diffuse mesangiocapillary glomerulonephritis

937 (2.8 %)

Died from this diagnosis.

100
95
90
85
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75
70
65
60
55
50
45
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25
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15
10
5
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70 205

Women receive the diagnosis rapidly progressive nephritic syndrome : diffuse mesangiocapillary glomerulonephritis

1 248 (1.8 %)

Died from this diagnosis.

Risk Group for the Disease rapidly progressive nephritic syndrome : diffuse mesangiocapillary glomerulonephritis - Men aged 55-59 and Women aged 25-29

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In Men diagnosis is most often set at age 0-89
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Less common in men the disease occurs at Age 90-95+Less common in women the disease occurs at Age 5-9, 90-95+
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In Women diagnosis is most often set at age 0-5, 10-89

Disease Features rapidly progressive nephritic syndrome : diffuse mesangiocapillary glomerulonephritis

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Absence or low individual and public risk
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Rapidly progressive nephritic syndrome : diffuse mesangiocapillary glomerulonephritis - what does this mean

Rapidly progressive nephritic syndrome (rpns) is a type of diffuse mesangiocapillary glomerulonephritis that is characterized by the rapid loss of renal function due to inflammation and scarring of the glomeruli, which are the small filtering units of the kidneys. this inflammation and scarring can lead to proteinuria, hematuria, hypertension, and edema, and can lead to renal failure if not treated.

What happens during the disease - rapidly progressive nephritic syndrome : diffuse mesangiocapillary glomerulonephritis

Rapidly progressive nephritic syndrome is caused by diffuse mesangiocapillary glomerulonephritis, an immune-mediated disease in which antibodies and complement proteins are deposited in the glomerular capillaries, leading to inflammation, scarring, and progressive deterioration of kidney function. this results in a decrease in the glomerular filtration rate and an increase in proteinuria, hematuria, and edema. the rapid progression of the disease can lead to end-stage renal failure if left untreated.

Clinical Pattern

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How does a doctor diagnose

  • Complete Blood Count
  • Urinalysis
  • Creatinine Clearance
  • Creatinine Blood Test
  • Urine Protein/Creatinine Ratio
  • Urine Microscopy
  • Kidney Biopsy
  • Renal Imaging
  • Serum Complement Levels
  • Anti-Neutrophil Cytoplasmic Antibody Test
  • Angiotensin Converting Enzyme Test

Treatment and Medical Assistance

Main Goal: To reduce inflammation and slow the progression of the disease
  • Prescribe corticosteroids to reduce inflammation
  • Prescribe immunosuppressant drugs to prevent further damage to the kidneys
  • Prescribe antibiotics to treat any associated infections
  • Prescribe diuretics to reduce fluid retention
  • Prescribe medications to control blood pressure
  • Prescribe medications to control cholesterol levels
  • Prescribe medications to reduce proteinuria
  • Administer dialysis to remove waste products from the blood
  • Provide nutritional support and advice
  • Refer to a kidney specialist for further evaluation and treatment
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11 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Rapidly progressive nephritic syndrome : diffuse mesangiocapillary glomerulonephritis - Prevention

Rapidly progressive nephritic syndrome is a serious, potentially life-threatening condition, and prevention is key. the best way to prevent diffuse mesangiocapillary glomerulonephritis, the most common form of this syndrome, is to maintain a healthy lifestyle, including regular exercise, a balanced diet, and adequate hydration. additionally, regular check-ups with a healthcare provider and prompt treatment of any underlying medical conditions may help to reduce the risk of this syndrome.