Neonatal jaundice
Neonatal jaundice is a yellowish discoloration of the white part of the eyes and skin in a newborn baby due to high bilirubin levels. Other symptoms may include excess sleepiness or poor feeding. Complications may include seizures, cerebral palsy, or kernicterus.
About 60% of full term newborn and 80% of premature babies are jaundice.
Indirect serum bilirubin level = >5mg/dl.
Total = > 12mg/dl At term.
It total bilirubin > 20mg/dl causes bilirubin encephalopathy called as Kernicture.
In many cases there is no specific underlying disorder. In other cases it results from red blood cell breakdown, liver disease, infection, hypothyroidism, or metabolic disorders. A bilirubin level more than 34 μmol/l may be visible. Concerns, in otherwise healthy babies, occur when levels are greater than 308 μmol/L, jaundice is noticed in the first day of life, there is a rapid rise in levels, jaundice lasts more than two weeks, or the baby appears unwell. In those with concerning findings further investigations to determine the underlying cause are recommended.
The need for treatment depends on bilirubin levels, the age of the child, and the underlying cause. Treatments may include more frequent feeding, phototherapy, or exchange transfusions. In those who are born early more aggressive treatment tends to be required. Physiologic jaundice generally lasts less than seven days. The condition affects over half of babies in the first week of life. Of babies that are born early about 80% are affected. Globally over 100,000 late-preterm and term babies die each year as a result of jaundice.
Signs and symptoms
The primary symptom is yellowish discoloration of the white part of the eyes and skin in a newborn baby. Other symptoms may include excess sleepiness or poor feeding.A bilirubin level more than 34 μmol/l may be visible. For the feet to be affected level generally must be over 255 μmol/l.
Complications
Prolonged hyperbilirubinemia can result in chronic bilirubin encephalopathy. Quick and accurate treatment of neonatal jaundice helps to reduce the risk of neonates developing kernicterus.Infants with kernicterus may have a fever or seizures. High pitched crying is an effect of kernicterus.
Exchange transfusions performed to lower high bilirubin levels are an aggressive treatment.
Causes
In newborns, jaundice tends to develop because of two factors—the breakdown of fetal hemoglobin as it is replaced with adult hemoglobin and the relatively immature metabolic pathways of the liver, which are unable to conjugate and so excrete bilirubin as quickly as an adult. This causes an accumulation of bilirubin in the blood, leading to the symptoms of jaundice.If the neonatal jaundice is not resolved with simple phototherapy, other causes such as biliary atresia, Progressive familial intrahepatic cholestasis, bile duct paucity, Alagille syndrome, alpha 1-antitrypsin deficiency, and other pediatric liver diseases should be considered. The evaluation for these will include blood work and a variety of diagnostic tests. Prolonged neonatal jaundice is serious and should be followed up promptly.
Severe neonatal jaundice may indicate the presence of other conditions contributing to the elevated bilirubin levels, of which there are a large variety of possibilities. These should be detected or excluded as part of the differential diagnosis to prevent the development of complications. They can be grouped into the following categories:
Unconjugated
Hemolytic
Intrinsic causes of hemolysis
- Membrane conditions
- *Spherocytosis
- *Hereditary elliptocytosis
- Enzyme conditions
- *Glucose-6-phosphate dehydrogenase deficiency
- *Pyruvate kinase deficiency
- Globin synthesis defect
- *sickle cell disease
- *Alpha-thalassemia, e.g. HbH disease
Extrinsic causes of hemolysis
- Systemic conditions
- *Sepsis
- *Arteriovenous malformation
- Alloimmunity
- *Hemolytic disease of the newborn
- *Rh disease
- *Hemolytic disease of the newborn
- *Hemolytic disease of the newborn
- *Other blood type mismatches causing hemolytic disease of the newborn
Non-hemolytic causes
- Breastfeeding jaundice
- Breast milk jaundice
- Cephalohematoma
- Polycythemia
- Urinary tract infection
- Sepsis
- Hypothyroidism
- Gilbert's syndrome
- Crigler–Najjar syndrome
- High GI obstruction
Conjugated (Direct)
Liver causes
- Infections
- *Sepsis
- *Hepatitis A
- *Hepatitis B
- *TORCH infections
- Metabolic
- *Galactosemia
- *Alpha 1-antitrypsin deficiency, which is commonly missed, and must be considered in DDx
- *Cystic fibrosis
- *Dubin–Johnson syndrome
- *Rotor syndrome
- Drugs
- Total parenteral nutrition
- Idiopathic
Post-liver
- Biliary atresia or bile duct obstruction
- *Alagille syndrome
- *Choledochal cyst
Non-organic causes
Breastfeeding jaundice
"Breastfeeding jaundice" is caused by insufficient breast milk intake, resulting in inadequate quantities of bowel movements to remove bilirubin from the body. This leads to increased enterohepatic circulation, resulting in increased reabsorption of bilirubin from the intestines. Usually occurring in the first week of life, most cases can be ameliorated by frequent breastfeeding sessions of sufficient duration to stimulate adequate milk production.Breast milk jaundice
Whereas breastfeeding jaundice is a mechanical problem, breast milk jaundice is a biochemical occurrence and the higher bilirubin possibly acts as an antioxidant. Breast milk jaundice occurs later in the newborn period, with the bilirubin level usually peaking in the sixth to 14th days of life. This late-onset jaundice may develop in up to one third of healthy breastfed infants.- First, the gut is sterile at birth and normal gut flora takes time to establish. The bacteria in the adult gut convert conjugated bilirubin to stercobilinogen which is then oxidized to stercobilin and excreted in the stool. In the absence of sufficient bacteria, the bilirubin is de-conjugated by brush border β-glucuronidase and reabsorbed. This process of re-absorption is called enterohepatic circulation. It has been suggested that bilirubin uptake in the gut is increased in breast fed babies, possibly as the result of increased levels of epidermal growth factor in breast milk. Breast milk also contains glucoronidase which will increase deconjugation and enterohepatic recirculation of bilirubin.
- Second, the breast-milk of some women contains a metabolite of progesterone called 3-alpha-20-beta pregnanediol. This substance inhibits the action of the enzyme uridine diphosphoglucuronic acid glucuronyl transferase responsible for conjugation and subsequent excretion of bilirubin. In the newborn liver, activity of glucuronyl transferase is only at 0.1-1% of adult levels, so conjugation of bilirubin is already reduced. Further inhibition of bilirubin conjugation leads to increased levels of bilirubin in the blood. However, these results have not been supported by subsequent studies.
- Third, an enzyme in breast milk called lipoprotein lipase produces increased concentration of nonesterified free fatty acids that inhibit hepatic glucuronyl transferase, which again leads to decreased conjugation and subsequent excretion of bilirubin.
Physiological jaundice
- Phase one
- Term infants - jaundice lasts for about 10 days with a rapid rise of serum bilirubin up to 204 μmol/l.
- Preterm infants - jaundice lasts for about two weeks, with a rapid rise of serum bilirubin up to 255 μmol/l.
- Phase two - bilirubin levels decline to about 34 μmol/l for two weeks, eventually mimicking adult values.
- Preterm infants - phase two can last more than one month.
- Exclusively breastfed infants - phase two can last more than one month.
- Relatively low activity of the enzyme glucuronosyltransferase which normally converts unconjugated bilirubin to conjugated bilirubin that can be excreted into the gastrointestinal tract. Before birth, this enzyme is actively down-regulated, since bilirubin needs to remain unconjugated in order to cross the placenta to avoid being accumulated in the fetus. After birth, it takes some time for this enzyme to gain function.
- Shorter life span of fetal red blood cells, being approximately 80 to 90 days in a full term infant, compared to 100 to 120 days in adults.
- Relatively low conversion of bilirubin to urobilinogen by the intestinal flora, resulting in relatively high absorption of bilirubin back into the circulation.
Diagnosis
Transcutaneous bilirubinometer
This is hand held, portable and rechargeable but expensive. When pressure is applied to the photoprobe, a xenon tube generates a strobe light, and this light passes through the subcutaneous tissue. The reflected light returns through the second fiber optic bundle to the spectrophotometric module. The intensity of the yellow color in this light, after correcting for the hemoglobin, is measured and instantly displayed in arbitrary units.Pathological jaundice
Any of the following features suggests pathological jaundice:- Clinical jaundice appearing in the first 24 hours or greater than 14 days of life.
- Increases in the level of total bilirubin by more than 8.5 μmol/l per hour or 5 mg/dL per 24 hours.
- Total bilirubin more than 331.5 μmol/l .
- Direct bilirubin more than 34 μmol/l.
Treatment
The bilirubin levels for initiative of phototherapy varies depends on the age and health status of the newborn. However, any newborn with a total serum bilirubin greater than 359 μmol/l should receive phototherapy.Phototherapy
Babies with neonatal jaundice may be treated with colored light called phototherapy, which works by changing trans-bilirubin into the water-soluble cis-bilirubin isomer.The phototherapy involved is not ultraviolet light therapy but rather a specific frequency of blue light. The light can be applied with overhead lamps, which means that the baby's eyes need to be covered, or with a device called a biliblanket, which sits under the baby's clothing close to its skin.
The use of phototherapy was first discovered, accidentally, at Rochford Hospital in Essex, England, when a nurse, Sister Jean Ward, noticed that babies exposed to sunlight had reduced jaundice, and a pathologist, Dr. Perryman, who noticed that a vial of blood left in the sun had turned green. Drs Cremer, Richards and Dobbs put together these observations, leading to a landmark randomized clinical trial which was published in Pediatrics in 1968; it took another ten years for the practice to become established.
Massage therapy could be useful in addition to phototherapy in order to reduce the phototherapy duration. However, it does not appear to reduce the requirement for phototherapy in the treatment of neonatal jaundice.
There is currently no reliable evidence about whether home-based or hospital-based phototherapy is more effective for full term infants with jaundice.