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neonatal jaundice
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Description
Neonatal Jaundice: A Common Condition in Newborns
Neonatal jaundice, also known as infant jaundice, is a common condition that affects many newborn babies. It is characterized by a yellow discoloration of the skin and eyes, caused by an excess of bilirubin in the blood.
Causes and Risk Factors
Jaundice occurs when a baby's liver is not mature enough to process bilirubin, a yellow pigment produced during the breakdown of old red blood cells. This can happen in babies born before 38 weeks' gestation (preterm babies) and some breast-fed babies [1]. Other risk factors include:
- Preterm birth: Babies born before 38 weeks are more likely to develop jaundice.
- Breast-feeding: Some breast-fed babies may have higher levels of bilirubin, increasing the risk of jaundice.
- Liver immaturity: Newborn livers are not fully developed and may struggle to process bilirubin.
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Additional Characteristics
- neonatal jaundice
- preterm birth
- breast-feeding
- liver immaturity
Signs and Symptoms
What are the signs and symptoms of neonatal jaundice?
Neonatal jaundice, also known as infant jaundice, is a common condition in newborns characterized by yellowing of the skin and eyes. The main sign of jaundice is the yellowing of your baby's skin, which can be seen best in natural lighting. It usually appears first on the face before spreading across the body.
Common symptoms:
- Yellow tinge to the skin, usually appearing first on the face and scalp
- Yellow tinge to the white parts of the eyes (sclera)
- Difficulty feeding the baby
- Yellowing of the skin below the knee
- Yellowing of the skin becoming more intense in color
Important note:
Jaundice during the first 24 hours after birth, or yellowing of the palms of the hands and soles of the feet, is a medical emergency. If this happens, doctors will perform blood tests to identify and treat the problem.
Causes and treatment:
Neonatal jaundice can be caused by various factors, including physiological jaundice (which usually resolves on its own), breast milk jaundice, or other underlying conditions. Treatment may involve monitoring bilirubin levels, phototherapy, or in severe cases, hospitalization for further evaluation and treatment.
References:
- [1] Yellowing of the skin and the whites of the eyes — the main sign of infant jaundice — usually appears between the second and fourth day after birth. To check for infant jaundice, press gently on your baby's forehead or nose.
- [3] The first sign of jaundice is the yellowing of a baby’s skin and eyes, which may start in the face before spreading across the body.
- [4] Symptoms of jaundice in babies · a yellow tinge to the skin, usually appearing first on the face and scalp · a yellow tinge to the white parts of the eyes (sclera) ...
- [5] May 5, 2022 — Symptoms of neonatal jaundice · Yellow skin below the knee · Yellow skin becoming more intense in colour · Difficulty feeding the baby · Difficulty ...
- [6] Jan 24, 2023 — Jaundice causes a yellow color of the skin. It usually begins on the face and then moves down to the chest, belly area, legs, and soles of the ...
- [8] Sep 26, 2024 — Jaundice is the medical term for a yellow-tinged coloring of the skin or mucous membranes (such as the thin inner lining of the eyes and mouth).
- [10] Yellowing of the skin and the whites of the eyes — the main sign of infant jaundice — usually appears between the second and fourth day after birth. To check for infant jaundice, press gently on your baby's forehead or nose.
- [12] Neonatal jaundice is a clinical manifestation of elevated total serum bilirubin, termed neonatal hyperbilirubinemia, which results from bilirubin that is deposited into an infant's skin. The characteristic features of neonatal jaundice include yellowish skin, sclerae, and mucous membranes.
- [14] Jaundice is the yellow color seen in the skin of many newborns. Jaundice happens when a chemical called bilirubin builds up in the baby’s blood. During pregnancy, the mother’s liver removes bilirubin for the baby, but after birth the baby’s liver must remove the bilirubin.
- [15] Jaundice during the first 24 hours after birth, or yellowing of the palms of the hands and soles of the feet, is a medical emergency. If this happens, doctors will perform blood tests in order to identify and treat the problem.
Additional Symptoms
- Yellow tinge to the skin, usually appearing first on the face and scalp
- Yellow tinge to the white parts of the eyes (sclera)
- Difficulty feeding the baby
- Yellowing of the skin below the knee
- Yellowing of the skin becoming more intense in color
Diagnostic Tests
Diagnostic Tests for Neonatal Jaundice
Neonatal jaundice, also known as hyperbilirubinemia, can be diagnosed through various tests that measure the level of bilirubin in a newborn's blood. The following are some common diagnostic tests used to diagnose neonatal jaundice:
- Total Serum Bilirubin (TSB) test: This is considered the gold standard test for diagnosing neonatal jaundice and is essential for definitive diagnosis of severe hyperbilirubinaemia and treatment decisions [15]. It measures the total level of bilirubin in the blood.
- Transcutaneous Bilirubin (TcB) test: This non-invasive test uses a device to measure the reflection of light through the skin to estimate the bilirubin level [3].
- Direct and Indirect Bilirubin levels: A blood test can determine if the bilirubin is bound with or without glucose, which helps in identifying the cause of jaundice [8].
- Coombs' Test: This test is used to detect "foreign" antibodies that are already adhered to the infant's red blood cells (RBCs), a potential cause of hemolytic disease [10].
Other Tests
In some cases, additional tests may be ordered to rule out other conditions or to determine the underlying cause of jaundice. These include:
- Blood type and Rh determination: This test is used to check if the mother's blood type matches the baby's blood type, which can help identify potential causes of hemolytic disease [4].
- Direct Antiglobulin Test (DAT): This test is used to detect antibodies against RBCs, which can be a cause of jaundice [11].
Visual Examination
A physical examination by a healthcare provider can also help diagnose neonatal jaundice. The provider will check for signs of jaundice, such as yellowing of the skin and sclera, and measure the bilirubin level using a transcutaneous bilirubinometer [2].
It's essential to note that not all cases of neonatal jaundice require diagnostic testing. In some cases, a healthcare provider may diagnose jaundice based on clinical examination alone.
References:
[1] Context result 3 [2] Context result 1 [3] Context result 15 [4] Context result 4 [5] Context result 10 [6] Context result 11 [7] Context result 8 [8] Context result 12
Additional Diagnostic Tests
- Direct Antiglobulin Test (DAT)
- Total Serum Bilirubin (TSB) test
- Transcutaneous Bilirubin (TcB) test
- Direct and Indirect Bilirubin levels
- Coombs' Test
- Blood type and Rh determination
Treatment
Pharmacological Interventions for Neonatal Jaundice
Neonatal jaundice, a common condition in newborns, can be treated with various pharmacological interventions. While phototherapy remains the most common treatment, several drugs have been studied and used to manage this condition.
- Metalloporphyrins: These compounds have shown promise in inhibiting heme catabolism and bilirubin production, making them a novel pharmacological intervention for neonatal jaundice [2].
- Phenobarbitone: This medication has been studied as a potential treatment for neonatal jaundice, although its use is not without risks [12].
- Intravenous immunoglobulins: These have also been explored as a possible treatment option for neonatal jaundice, although more research is needed to fully understand their efficacy and safety [12].
Important Considerations
When treating neonatal jaundice with pharmacological interventions, it's essential to consider the potential risks associated with these treatments. Some medications can increase the entry of bilirubin into the brain, leading to kernicterus or other complications.
- Avoid sulfonamides and certain antibiotics: These drugs can contribute to hemolytic jaundice in newborns [15].
- Be cautious with glucose-6-phosphate dehydrogenase (G6PD) deficiency: Certain medications, such as vitamin K3 and K4, sulfonamides, and furfural, should be avoided in G6PD-deficient infants to prevent hemolytic jaundice [15].
Current Guidelines
The American Academy of Pediatrics (AAP) has revised its guidelines for the treatment of neonatal jaundice, emphasizing the importance of phototherapy as a first-line treatment. However, pharmacological interventions may still be necessary in certain cases.
- Phototherapy remains the most common treatment: This approach is effective in reducing bilirubin levels and preventing complications [6, 7, 8].
- Pharmacological treatment should be individualized: The choice of medication will depend on the severity of jaundice, the infant's overall health, and other factors [12].
In summary, while phototherapy remains the primary treatment for neonatal jaundice, pharmacological interventions such as metalloporphyrins, phenobarbitone, and intravenous immunoglobulins may be used in specific cases. It's essential to carefully consider the potential risks and benefits of these treatments and to follow current guidelines and recommendations from reputable medical organizations.
Differential Diagnosis
Differential Diagnosis of Neonatal Jaundice
Neonatal jaundice, also known as neonatal hyperbilirubinemia, is a clinical manifestation of elevated total serum bilirubin (TSB) in infants. The differential diagnosis of neonatal jaundice is extensive and can be broadly divided into pre-hepatic, hepatic, and post-hepatic causes.
Pre-hepatic Causes
- Physiologic hyperbilirubinemia: a normal condition that occurs in newborns due to the breakdown of red blood cells.
- Breastfeeding jaundice: a condition that occurs when breastfed infants do not receive enough milk or have difficulty digesting lactose.
- Breast milk jaundice: a rare condition caused by certain compounds in breast milk that can increase bilirubin levels.
Hepatic Causes
- Hemolysis associated with blood group incompatibility between mother and baby
- Liver disease, such as biliary atresia or cirrhosis
Post-hepatic Causes
- Cholestasis: a condition where bile flow is blocked, leading to an accumulation of bilirubin in the blood.
Other Causes
- Infections, such as sepsis or pneumonia
- Metabolic disorders, such as galactosemia or hereditary fructose intolerance
It's essential to note that the differential diagnosis of neonatal jaundice can be complex and requires a structured approach to investigation. The most important investigation is to determine whether the infant has liver disease or benign jaundice.
References
- [1] Neonatal Jaundice Differential Diagnoses. Updated: Dec 27, 2017 Author: Thor WR Hansen, MD, PhD, MHA, FAAP; Chief Editor: Muhammad Aslam, MD
- [2] The differential diagnosis of neonatal hyperbilirubinemia is broad. Table 3 lists the most common causes.
- [3] In general, the differential diagnoses of jaundice in infancy follow those of adults and can broadly be divided into pre-hepatic, hepatic, and post-hepatic causes.
Note: The above information is based on the search results provided and may not be an exhaustive list of all possible causes of neonatal jaundice.
Additional Differential Diagnoses
- Other Causes
- Pre-hepatic Causes
- Hepatic Causes
- Post-hepatic Causes
- Alagille syndrome
Additional Information
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- A pigmentation disease characterized by a high level of bilirubin in the blood, causing a yellowing of the skin and other tissues of a newborn infant.
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