(D76.2) Haemophagocytic syndrome, infection-associated

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80 032 in individuals diagnosis haemophagocytic syndrome, infection-associated confirmed
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7 898 deaths with diagnosis haemophagocytic syndrome, infection-associated
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10% mortality rate associated with the disease haemophagocytic syndrome, infection-associated

Diagnosis haemophagocytic syndrome, infection-associated is diagnosed Men are 32.15% more likely than Women

52 883

Men receive the diagnosis haemophagocytic syndrome, infection-associated

4 637 (8.8 %)

Died from this diagnosis.

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27 149

Women receive the diagnosis haemophagocytic syndrome, infection-associated

3 261 (12.0 %)

Died from this diagnosis.

Risk Group for the Disease haemophagocytic syndrome, infection-associated - 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 75-79, 85-95+
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In Women diagnosis is most often set at age 0-74, 80-84

Disease Features haemophagocytic syndrome, infection-associated

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Absence or low individual and public risk
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Haemophagocytic syndrome, infection-associated - what does this mean

Haemophagocytic syndrome, infection-associated, is a rare and potentially life-threatening disorder caused by an uncontrolled immune response to an infection. it occurs when the body's immune system overreacts to an infection, leading to increased production of white blood cells and an excessive inflammatory response. this can lead to the destruction of red blood cells, platelets, and other vital components of the immune system, resulting in organ failure and death.

What happens during the disease - haemophagocytic syndrome, infection-associated

Haemophagocytic syndrome, infection-associated is a rare disorder caused by an abnormal immune response to an infection. it is characterized by an overproduction of inflammatory cytokines, which leads to an excessive activation of immune cells, such as macrophages and natural killer cells. this activation leads to the increased production of inflammatory mediators, such as tnf-alpha and interferon-gamma, which trigger the activation of the haemophagocytic cells. as a result, these cells engulf and destroy red blood cells, platelets, and other blood cells, leading to a decrease in the number of circulating blood cells and anemia. additionally, the excessive activation of the immune system can lead to a variety of systemic symptoms, such as fever, fatigue, and organ dysfunction.

Clinical Pattern

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How does a doctor diagnose

  • Complete blood count
  • Liver function tests
  • Serum ferritin
  • Serum triglycerides
  • Serum calcium
  • Serum albumin
  • Serum lactate dehydrogenase
  • Serum creatinine
  • Serum uric acid
  • Serum C-reactive protein
  • Serum interleukin-6
  • Serum fibrinogen
  • Flow cytometry
  • Bone marrow biopsy
  • Chest X-ray
  • Computerized tomography scan
  • Magnetic resonance imaging
  • Viral studies
  • Bacterial cultures
  • Fungal cultures

Treatment and Medical Assistance

Main goal of the treatment: To reduce the inflammation and control the infection associated with Haemophagocytic Syndrome
  • Administering corticosteroids to reduce inflammation
  • Prescribing immunosuppressants to control the immune response
  • Administering antibiotics to treat the underlying infection
  • Prescribing antiviral medications to treat viral infections
  • Providing supportive care such as oxygen therapy, IV fluids, and blood transfusions
  • Providing nutrition support to prevent malnutrition
  • Performing regular blood tests to monitor the patient’s condition
  • Referring the patient to a specialist for further treatment
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14 Days of Hospitalization Required
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Average Time for Outpatient Care Not Established

Haemophagocytic syndrome, infection-associated - Prevention

Haemophagocytic syndrome, infection-associated is a rare but serious condition that can be prevented by adhering to good hygiene practices, such as washing hands regularly and avoiding contact with those who are ill. vaccines for the underlying infections should be kept up to date, and any signs of infection should be treated promptly and aggressively. additionally, early recognition of the signs and symptoms of this condition is important to ensure prompt diagnosis and treatment.