Neonatal hypoglycemia
| Neonatal hypoglycemia | |
|---|---|
| Synonyms | Low blood sugar in newborns |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Jitteriness, lethargy, poor feeding, seizures |
| Complications | Neurological damage, developmental delay |
| Onset | Within the first few days of life |
| Duration | Variable, depending on cause and treatment |
| Types | N/A |
| Causes | Premature birth, maternal diabetes, intrauterine growth restriction, birth asphyxia |
| Risks | Preterm infants, infants of diabetic mothers, small for gestational age |
| Diagnosis | Blood glucose testing |
| Differential diagnosis | Sepsis, inborn errors of metabolism, endocrine disorders |
| Prevention | Monitoring at-risk infants, early feeding |
| Treatment | Intravenous glucose, breastfeeding, formula feeding |
| Medication | N/A |
| Prognosis | Good with prompt treatment |
| Frequency | Common in at-risk populations |
| Deaths | N/A |
Neonatal hypoglycemia is a condition that occurs in newborns, typically within the first few days of life, where the blood sugar level is significantly lower than the normal range. This condition can lead to serious health problems if not promptly diagnosed and treated.
Causes
Neonatal hypoglycemia can be caused by several factors, including:
Symptoms
The symptoms of neonatal hypoglycemia can vary and may include:
Diagnosis
The diagnosis of neonatal hypoglycemia is typically made through a blood test that measures the baby's blood sugar level.
Treatment
The treatment for neonatal hypoglycemia usually involves providing the baby with a source of glucose. This can be done through feeding, intravenous glucose, or medications.
See also
References
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