Kernicterus in Newborn Babies

Kernicterus is a serious medical condition affecting the brain that can potentially result if infant jaundice is not managed properly and treated after childbirth.

Kernicterus is a rare type of infant brain damage that can result from excessive levels of bilirubin in the brain caused by untreated cases of jaundice. Bilirubin is a bi-product substance naturally produced in the body during the disposal of old red blood cells. When levels of bilirubin in the blood become too high, however, it can be toxic – a condition referred to as hyperbilirubinemia. Jaundice occurs when hyperbilirubinemia progresses beyond a moderate level. The excessive accumulation of bilirubin caused by jaundice can eventually damage the brain and nervous system.

Newborn babies are particularly susceptible to jaundice because their livers are not fully developed. The underdeveloped liver of a newborn can quickly become overworked. This causes bilirubin levels to increase and result in jaundice. Jaundice in newborns is a very common condition. About 60% of newborns will experience some degree of jaundice during the first few weeks of life.

Infant jaundice is typically pretty harmless and short-lived. When the baby is exposed to regular sunlight, jaundice typically goes away quickly. In some cases, however, infant jaundice does not go away easily. Then you may have a serious concern. If a case of infant jaundice becomes very severe and is not properly managed or treated, the excessive bilirubin levels in the baby’s blood can cause a particular type of infant brain damage known as kernicterus.

Stage I Symptoms

• Jaundice : severe and/or prolonged infant jaundice is the root cause of kernicterus, so anytime a newborn has a particularly serious case of infant jaundice that does not clear up on its own it can be a symptom of kernicterus.
• Poor Feeding : newborns with early-stage kernicterus will often demonstrate significant difficulties with feeding, latching on, and sucking (with both breast and bottle feeding).
• Hypotonia : hypotonia (often called “floppy baby syndrome”) is a condition characterized by extreme lack of muscle tone. Babies with hypotonia may feel floppy, like a rag-doll when picked up.
• Chronic Fatigue : abnormal levels of lethargy or apparent fatigue in a newborn (e.g., lack of intense crying, not getting up at night to feed, etc.) can be early symptoms of kernicterus.

Stage II Symptoms

• Seizures : as the neurologic damage of kernicterus advances, babies may experience sudden, uncontrolled infant seizures.
• Head Bulge : babies with kernicterus may develop a noticeable bulge in the “soft spots” or fontanel areas of the head.

Stage III Symptoms

• Increased Seizures : as kernicterus reaches the most advanced stages, a baby’s seizures will often increase in both frequency and intensity.
• Hearing Loss : a common symptom of advanced kernicterus is extensive high-frequency hearing loss. This is sometimes difficult to identify in newborn infants.
• Stiffness : in early stages, kernicterus may cause hypotonia (floppy baby syndrome). In the late stages, however, the condition will often result in excessive muscle stiffness and problems with movement and body control.

When bilirubin is initially created from red blood cell breakdown it is in the unconjugated form. Unconjugated bilirubin is toxic because it is not water-soluble and it will build up in the body’s tissues. The liver filters unconjugated bilirubin out of the bloodstream and converts into conjugated bilirubin. Conjugated bilirubin from the liver is water-soluble. This means it can be removed from the body through urine.

When many babies are first born, their livers are often unable to efficiently filter and convert unconjugated bilirubin into conjugated bilirubin fast enough to keep up with production. This invariably causes a backlog of unconjugated bilirubin in the bloodstream of many newborn babies which leads to infant jaundice.

Infant jaundice is usually short-lived as the baby’s liver is quickly able to get caught up with bilirubin conversion. For some babies, however, the conversion and disposal of bilirubin by the liver does not get back on pace. As a result, the child’s jaundice becomes more severe. If not properly managed and treated this can cause kernicterus where unconjugated bilirubin in the blood to infiltrates and damages brain tissue. There are factors that put a baby at increased risk of severe jaundice and kernicterus:

• Premature Birth : the liver is one of the last organs to develop during gestation. So when a baby is born before week 37 their liver will be less efficient at bilirubin conversion and will take longer to get caught up.
• Poor Feeding : feeding problems can prolong infant jaundice because frequent stools and urination help accelerate bilirubin disposal.
• Genetic Predisposition : babies with a family history of severe infant jaundice (i.e. siblings or parents who had serious jaundice as an infant) are at increased risk.
• Maternal Blood Type : research has found that mothers with type O or Rh-negative blood types are more prone to have babies with high bilirubin levels.

The good news is that newborn jaundice is something that can be very effectively treated. The first level of treatment for jaundice involves phototherapy (or light therapy) in which the baby is exposed to natural sunlight or a special artificial light. Light exposure accelerates the filtration and conversion of bilirubin inside the body. A second level of treatment for infant jaundice can involve blood exchange transfusions. This involves the removal of some of the baby’s blood and replacement with donor blood.

Medical Literature and Studies on Kernicterus

Grossman, M. R., et al. (2022). Questioning Our Approach to Hyperbilirubinemia. Hospital Pediatrics, 12(4), e137-e139. (This article recommended that the American Academy of Pediatrics make updates on its recommendations for hyperbilirubinemia management and kernicterus prevention. It reported that more recent data showed that kernicterus occurred at higher bilirubin levels than previously thought.)

Khan, A., & Kim, T.Y. (2022). Neonatal hyperbilirubinemia: recommendations for diagnosis and management in the emergency department. Pediatric Emergency Medicine Practice, 19(1), 1-24. (This article looked at diagnosis and treatment recommendations for neonatal hyperbilirubinemia.)

Lai, N. M., et al. (2021). The Association between Serum Bilirubin and Kernicterus Spectrum Disorder: A Systematic Review and Meta-Analysis. Neonatology, 118, 654-664. (This study looked at total serum bilirubin’s association with kernicterus spectrum disorder. The research found that TSB was associated with KSB patients who have certain risk factors. However, they found no clear association between TSB and ASB in the overall neonatal population. The researchers concluded that there was insufficient evidence on TSB’s prognostic value for adverse neurodevelopmental outcomes in the general neonatal populace.)

Oh, K. S., et al. (2021). Neonatal acute liver failure with pulmonary yellow hyaline membrane and kernicterus. Autopsy and Case Reports, 11. (This case study looked at an 8-day-old newborn who suffered from neonatal acute liver failure. She initially suffered lethargy, jaundice, and poor oral intake. The girl developed multi-organ failure. The researchers reported that her autopsy revealed liver necrosis, yellow hyaline membrane disease, and kernicterus. They concluded that NALF required timely recognition and specific treatment approaches. They also reported that toxic bilirubin accumulation in the lungs could cause hypoxia and hepatic ischemia.)

Vidavalur, R. & Devapatla, S. (2021). Trends in hospitalizations of newborns with hyperbilirubinemia and kernicterus in United States: an epidemiological study. The Journal of Maternal-Fetal & Neonatal Medicine, 1-6. (This article looked at the population trends involving hyperbilirubinemia, kernicterus, phototherapy treatments, intravenous immunoglobulin therapy, and exchange transfusion between the years 1997 and 2012. The researchers found that the proportion of newborns diagnosed with hyperbilirubinemia increased while the kernicterus, exchange transfusion, phototherapy, and intravenous immunoglobulin therapy rates decreased.)

Donneborg, M.L., et al. (2020). Extreme neonatal hyperbilirubinemia and kernicterus spectrum disorder in Denmark during the years 2000–2015. Journal of Perinatology 40(2), 194-202. (This study identified ABO hemolytic disease of the newborn as the main kernicterus cause. They concluded that a systematic approach to neonatal jaundice and the surveillance of kernicterus and neonatal hyperbilirubinemia were necessary.)

Alkén, J., et al. (2019). Rates of extreme neonatal hyperbilirubinemia and kernicterus in children and adherence to national guidelines for screening, diagnosis, and treatment in Sweden. JAMA network open 2(3), e190858-e190858. (This study looked at newborn hyperbilirubinemia and kernicterus rates and concluded that many hyperbilirubinemia-related brain damage cases could be avoided if healthcare providers followed the right medical practices.)

McCarthy, M.E., et al. (2019). Newborn metabolic profile associated with hyperbilirubinemia with and without kernicterus. Clinical and translational science 12(1), 28-38. (This study concluded that healthcare providers should consider a newborn’s metabolic profile when investigating hyperbilirubinemia causes and risks.)

Rennie, J.M., et al. (2019). Learning from claims: Hyperbilirubinaemia and kernicterus. Archives of Disease in Childhood-Fetal and Neonatal Edition, 104(2), F202-F204. (This study found that infants with kernicterus typically had an underlying condition.)

Wennberg, R.P., et al. (2017). Maternal Empowerment-An Underutilized Strategy to Prevent Kernicterus? Current Pediatric Reviews, 13(3), 210-219. (This study concluded that informing parents on identifying jaundice and kernicterus empowers them to intervene when health care providers fail to do this.)