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(P56.9) Hydrops fetalis due to other and unspecified haemolytic disease
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2 250 in individuals diagnosis hydrops fetalis due to other and unspecified haemolytic disease confirmed
2 297 deaths with diagnosis hydrops fetalis due to other and unspecified haemolytic disease
102% mortality rate associated with the disease hydrops fetalis due to other and unspecified haemolytic disease
Diagnosis hydrops fetalis due to other and unspecified haemolytic disease is diagnosed Men are 31.73% more likely than Women
1 482
Men receive the diagnosis hydrops fetalis due to other and unspecified haemolytic disease
1 957 (132.1 %)Died from this diagnosis.
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Women receive the diagnosis hydrops fetalis due to other and unspecified haemolytic disease
340 (44.3 %)Died from this diagnosis.
Risk Group for the Disease hydrops fetalis due to other and unspecified haemolytic disease - Men and Women aged 0
In Men diagnosis is most often set at age 0-1
Less common in men the disease occurs at Age 0-95+Less common in women the disease occurs at Age 0-95+
In Women diagnosis is most often set at age 0-1
Disease Features hydrops fetalis due to other and unspecified haemolytic disease
Absence or low individual and public risk
Hydrops fetalis due to other and unspecified haemolytic disease - what does this mean
Hydrops fetalis due to other and unspecified haemolytic disease is a severe condition in which an unborn baby accumulates fluid in two or more body cavities, such as the abdomen, chest, and/or skin. this is caused by an imbalance between red blood cell production and destruction, resulting in anemia and an accumulation of fluid in the body. this is a life-threatening condition that requires immediate medical attention.
What happens during the disease - hydrops fetalis due to other and unspecified haemolytic disease
Hydrops fetalis due to other and unspecified haemolytic disease is caused by an imbalance between red blood cell production and destruction. this imbalance can be caused by a variety of conditions, including genetic disorders, infections, and autoimmune diseases. in these cases, the body produces more red blood cells than it can destroy, leading to a buildup of fluid in the body and causing symptoms such as edema, anemia, and jaundice.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Complete Blood Count (CBC)
- Blood Smear Examination
- Erythrocyte Sedimentation Rate (ESR)
- Hemoglobin Electrophoresis
- Direct Coombs Test
- Indirect Coombs Test
- Immunoglobulin Levels
- Ultrasound
- Amniocentesis
- Fetal Echocardiography
Treatment and Medical Assistance
Main Goal: Treat the underlying cause of Hydrops fetalis due to other and unspecified haemolytic disease.
- Administer blood transfusions to replace lost red blood cells.
- Prescribe corticosteroids to reduce inflammation.
- Prescribe antibiotics to treat any infections.
- Prescribe anticoagulants to prevent clotting.
- Administer intravenous immunoglobulins to reduce the immune system’s response.
- Prescribe diuretics to reduce swelling.
- Provide nutrition and hydration support.
- Provide supportive care for any organ damage.
- Monitor the baby’s development.
21 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Hydrops fetalis due to other and unspecified haemolytic disease - Prevention
The prevention of hydrops fetalis due to other and unspecified haemolytic disease can be achieved by early detection and treatment of the underlying haemolytic disorder. this includes routine antenatal screening, genetic testing and counselling, and prompt treatment of the underlying condition. additionally, pregnant women should be monitored for signs and symptoms of haemolytic disease, and should be provided with appropriate antenatal care.