What is Neonatal Cholestasis?
Neonatal cholestasis occurs in a newborn baby or within 3 months of birth. This disease is defined as conjugated hyperbilirubinemia. It occurs due to reduced excretion or bile formation. Both situations can lead to many disorders in the baby. One such disorder is known as biliary atresia.
In this article, we will discuss the symptoms of this disease, along with the major causes and treatments. Keep reading to uncover every detail about neonatal Cholestasis.
Symptoms of Neonatal Cholestasis
The initial symptoms of cholestasis are yellow skin and eyes, which means jaundice. Liver diseases are not the primary cause of newborn jaundice, but in this case, liver disease is the underlying cause of jaundice.
Following that, you will be able to notice symptoms like:
- Fatigue
- poor feeding
- difficulty gaining weight
- Itchiness
Here's a list of things that you need to keep an eye on for a newborn baby
- Along with having jaundice, your baby might have pale stools and dark-coloured urine.
- In addition to having jaundice, your baby might have other abnormal conditions in the body. Abnormalities can be spotted in the skeleton, the heart, the eyes, the skin, and the spleen.
Causes of Neonatal Cholestasis
There are two types of causes for neonatal cholestasis: extrahepatic causes and intrahepatic causes.
Extrahepatic causes
Biliary atresia is the most common extrahepatic disorder. In most cases, biliary atresia is visible in babies many weeks after birth. The reason for that could be the inflammation of extrahepatic and intrahepatic bile ducts.
Infants with cystic fibrosis are more likely to experience inspissated bile duct syndrome, which is also a potential contributor to extrahepatic newborn cholestasis.
Intrahepatic causes
Intrahepatic causes are mostly metabolic/genetic, toxic, infectious, or alloimmune.
Viral, bacterial, or parasitic infections in newborn babies under parenteral nutrition can lead to cholestasis.
Transplacental transit of maternal IgG causes a complement-mediated membrane assault complex, which damages the foetal liver, resulting in gestational alloimmune liver disease.
Metabolic causes of neonatal cholestasis include a lot of inborn metabolic errors, which include:
- galactosemia, tyrosinemia
- alpha-1 antitrypsin deficiency
- disorders of lipid metabolism
- bile acid defects
- mitochondrial disorders
- fatty acid oxidation defects.
In addition to that, there are also genetic defects, which include:
- Alagille syndrome
- cystic fibrosis
- arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome
The major source of toxic causes is prolonged parenteral feeding given to newborns with small bowel syndrome or extremely premature neonates.
When to see a doctor
Neonatal cholestasis is a medical emergency. Hence, rapid diagnosis is essential. Before 4-6 weeks of age, biliary atresia must be detected and diagnosed, and a Kasai portoenterostomy should be provided. Many of the illnesses, except for biliary atresia, are curable and need a thorough evaluation.
Treatment for Neonatal Cholestasis
Here is a list of treatments that will be undertaken if your child is suffering from Neonatal Cholestasis:
First and most importantly, your child will be given special formulas, specific medications, or vitamin supplements, depending particularly on the problem.
Doctors generally suggest low-fat foods for newborn babies with cholestasis because these types of foods cause less diarrhoea.
Babies with cholestasis have difficulty absorbing certain vitamins. Thus, high dosages of vitamins A, D, E, and K, sometimes known as fat-soluble vitamins, are suggested by doctors.
Infants may develop itchiness due to cholestasis. Thus, a lot of different medications to control itchiness are suggested by doctors.
Conclusion
In conclusion, Neonatal Cholestasis is a complex and potentially serious medical condition. It can be effectively treated with medications and dietary changes. However, it is important to seek medical help right away if you suspect that your baby may have the disease.
Request an appointment at Apollo Cradle, Hyderabad - Kondapur. Call 1860-500-4424 to book an appointment.
Primary sclerosing cholangitis (PSC) and primary biliary cirrhosis (PBC) are two of the most frequent forms of cholestatic liver disease (PSC).
Biochemically, cholestasis is characterized by an increase in serum alkaline phosphatase. Jaundice is a clinical manifestation of bilirubinostasis, which is caused histologically by the retention of bilirubin in the hepatocytes, bile canaliculi, or bile ducts.
Usually, two weeks after birth, it goes away. However, newborn cholestasis (NC), which is indicated by conjugated hyperbilirubinemia, is never innocuous and always points to a serious underlying disease.
An uncommon disorder called cholestasis affects roughly 1 in every 2,500 newborn babies. Cholestasis in babies may be a hereditary disorder. Any child may be affected by this illness, irrespective of his/her age.
Treatments
- Anaemia In Newborn
- Anemia in newborn
- Chronic Lung Disease
- Congenital Diaphramatic Hernia
- High-risk Newborns
- Hypoglycemia/Hyperglycemia
- Inborn Errors Of Metabolism
- Intracranial Haemorrhage
- Meconium Aspiration Syndrome
- Neonatal Cholestasis
- Neonatal Jaundice
- Neonatal Seizures
- Neonatal Sepsis
- Neonatal Stroke
- Perinatal Asphyxia
- Persistent Pulmonary Hypertension Of The Newborn
- Premature Baby
- Pulmonary Air Leaks
- Pulmonary Haemorrhage
- Respiratory Distress Syndrome
- Retinopathy Of Prematurity