(M30.0) Polyarteritis nodosa

More details coming soon

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186 013 in individuals diagnosis polyarteritis nodosa confirmed
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4 451 deaths with diagnosis polyarteritis nodosa
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2% mortality rate associated with the disease polyarteritis nodosa

Diagnosis polyarteritis nodosa is diagnosed Men are 2.88% more likely than Women

95 684

Men receive the diagnosis polyarteritis nodosa

2 438 (2.5 %)

Died from this diagnosis.

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90 329

Women receive the diagnosis polyarteritis nodosa

2 013 (2.2 %)

Died from this diagnosis.

Risk Group for the Disease polyarteritis nodosa - Men and Women aged 0-5

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In Men diagnosis is most often set at age 0-94
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Less common in men the disease occurs at Age 95+Less common in women the disease occurs at Age 95+
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In Women diagnosis is most often set at age 0-94

Disease Features polyarteritis nodosa

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Absence or low individual and public risk
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Polyarteritis nodosa - what does this mean

Polyarteritis nodosa is an inflammatory disease of the medium and small arteries that is caused by an autoimmune reaction. it is characterized by inflammation of the walls of the arteries, leading to narrowing and obstruction of the vessels, resulting in tissue ischemia and organ damage. symptoms may include abdominal pain, fever, weight loss, rash, and kidney failure.

What happens during the disease - polyarteritis nodosa

Polyarteritis nodosa is an autoimmune disorder caused by an abnormal immune response to an infection or other environmental trigger. it results in inflammation of the walls of medium-sized and small arteries, leading to ischemia and tissue damage. this inflammation is caused by the body's production of autoantibodies, which attack the walls of the arteries, leading to the formation of granulomas and necrosis. the resulting damage to the arteries can lead to organ dysfunction, tissue death, and other life-threatening complications.

Clinical Pattern

More details coming soon

How does a doctor diagnose

  • Physical examination
  • Blood tests
  • Urinalysis
  • Imaging studies (X-ray, MRI, CT scan)
  • Angiography
  • Biopsy

Treatment and Medical Assistance

Main goal of the treatment: Reduce inflammation in the body and reduce the risk of organ damage.
  • Prescription of corticosteroids and/or immunosuppressants
  • Plasmapheresis (plasma exchange)
  • Intravenous immunoglobulin therapy
  • Antibiotic therapy for infections
  • Surgery to remove affected blood vessels
  • Physical therapy to improve mobility
  • Pain management
  • Nutritional support
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16 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Polyarteritis nodosa - Prevention

Polyarteritis nodosa can be prevented by avoiding contact with people who are infected, practicing good hygiene, and maintaining a healthy lifestyle with proper nutrition and regular exercise. vaccines are also available for some types of infections that can lead to polyarteritis nodosa.