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(P74.9) Transitory metabolic disturbance of newborn, unspecified
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167 466 in individuals diagnosis transitory metabolic disturbance of newborn, unspecified confirmed
Diagnosis transitory metabolic disturbance of newborn, unspecified is diagnosed Men are 7.87% more likely than Women
90 319
Men receive the diagnosis transitory metabolic disturbance of newborn, unspecified
0 (less than 0.1%)Died from this diagnosis.
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77 147
Women receive the diagnosis transitory metabolic disturbance of newborn, unspecified
0 (less than 0.1%)Died from this diagnosis.
Risk Group for the Disease transitory metabolic disturbance of newborn, unspecified - 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 5-95+
In Women diagnosis is most often set at age 0-5
Disease Features transitory metabolic disturbance of newborn, unspecified
Absence or low individual and public risk
Transitory metabolic disturbance of newborn, unspecified - what does this mean
Transitory metabolic disturbance of newborn, unspecified is a condition that is caused by a disruption in the body's metabolism, usually due to a lack of nutrients or a disruption in the body's normal processes. this can cause a range of symptoms such as jaundice, poor feeding, dehydration, and abnormal electrolyte levels. it is usually resolved with supportive care and nutritional supplementation.
What happens during the disease - transitory metabolic disturbance of newborn, unspecified
Transitory metabolic disturbance of newborn, unspecified is a condition in which the newborn experiences a temporary disruption of their normal metabolic processes. this can be caused by a variety of different factors, including genetic predisposition, environmental exposure, and nutritional deficiencies. it can lead to a variety of symptoms, including jaundice, hypoglycemia, and electrolyte imbalances. treatment typically involves providing supportive care, such as intravenous fluids and glucose, and identifying and managing the underlying cause.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Complete physical examination of the newborn
- Blood tests to measure electrolyte levels
- Urine tests to measure electrolyte levels
- EKG to measure heart rate and rhythm
- X-ray to assess bone structure
- CT scan to assess brain structure
- MRI to assess brain structure
- Ultrasound to assess organ structure
- Genetic testing to identify any genetic abnormalities
Treatment and Medical Assistance
Main goal of the treatment: To reduce the severity of the transitory metabolic disturbance of newborn, unspecified.
- Administering fluids and electrolytes to reduce dehydration
- Providing glucose to maintain blood sugar levels
- Administering antibiotics to treat any underlying infection
- Administering vitamins and minerals to reduce the risk of deficiencies
- Monitoring vital signs and oxygen levels
- Providing nutritional support to ensure adequate caloric intake
- Providing respiratory support, if necessary
- Monitoring for any signs of complications
10 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Transitory metabolic disturbance of newborn, unspecified - Prevention
Transitory metabolic disturbance of newborn, unspecified can be prevented by ensuring that pregnant women receive adequate prenatal care, including regular check-ups to monitor the health of the baby and mother, proper nutrition, and avoiding exposure to environmental toxins. additionally, it is important to provide the newborn with appropriate medical care and nutrition after birth.