Pathogenesis and Management of Indirect Hyperbilirubinemia in Preterm Neonates Less Than 35 Weeks: Moving Toward a

Anish Pillai1, Aakash Pandita2, Horacio Osiovich1

  • 1Department of Pediatrics, Division of Neonatology, British Columbia Women's Hospital and Health Center, University of British Columbia, Vancouver, Canada.

Neoreviews
|May 3, 2020
PubMed

Insights

Managing indirect hyperbilirubinemia in premature infants requires specific guidelines. This review proposes standardized treatment charts for early phototherapy to prevent bilirubin-induced neurologic dysfunction (BIND) and reduce exchange transfusions.

Area of Science:

  • Neonatology
  • Pediatric Neurology
  • Bilirubin Metabolism

Background:

  • Premature infants face higher risks of indirect hyperbilirubinemia and bilirubin-induced neurologic dysfunction (BIND) compared to term infants.
  • Existing guidelines for neonatal hyperbilirubinemia management are insufficient for preterm populations, leading to clinical practice variations.
  • Preterm infants are more susceptible to BIND at lower bilirubin levels due to metabolic immaturity.

Purpose of the Study:

  • To review the epidemiology and pathophysiology of BIND in preterm neonates.
  • To propose a standardized management approach for indirect hyperbilirubinemia in preterm infants.
  • To introduce pragmatic treatment charts for phototherapy initiation, escalation, and cessation.

Main Methods:

  • Literature review on BIND in preterm neonates.
  • Development of evidence-based treatment charts for indirect hyperbilirubinemia management.
  • Analysis of phototherapy's role in preventing BIND and minimizing exchange transfusions.

Main Results:

  • Proposed treatment charts recommend early phototherapy for preterm neonates to prevent BIND.
  • The charts aim to reduce exposure to high irradiance levels and minimize exchange transfusions.
  • Standardized charts include parameters for stopping phototherapy and escalating its intensity.

Conclusions:

  • A standardized approach to managing indirect hyperbilirubinemia is crucial for preterm infants.
  • Early phototherapy, guided by proposed charts, can prevent BIND and reduce interventions.
  • Standardized management facilitates future research and quality improvement in phototherapy use for preterm neonates.

Related Concept Videos

Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
130
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test01:22

Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test

In clinical practice, the direct measurement of hepatic blood flow to evaluate liver function presents significant challenges due to the intricate and specialized nature of the necessary techniques. Consequently, healthcare professionals often rely on empirical estimates derived from thorough patient examinations and liver function tests to gauge liver health. Among the tools at their disposal, the Child–Pugh and MELD scoring systems stand out for their ability to categorize and assess...
120
Pharmacokinetics in Pediatric Patients: Drug Distribution01:17

Pharmacokinetics in Pediatric Patients: Drug Distribution

Drug distribution in the pediatric population exhibits unique challenges and considerations due to the physiological differences between children, particularly neonates and infants, and adults. A crucial aspect of pediatric pharmacology is understanding how these differences impact the pharmacokinetics of various drugs, necessitating age-specific dosing strategies to ensure efficacy and safety.Neonates and infants have a higher total body water content, ~75%–90% of their body weight,...
194
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption01:23

Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption

Understanding the physiological differences in the pediatric population is crucial for effective pharmacotherapy. Neonates, infants, and children exhibit significant variations in gastric pH, gastric emptying time, intestinal transit time, and biliary function. These variations profoundly affect oral drug absorption, necessitating a nuanced approach to pediatric dosing.Neonates present with a unique physiological profile, having a gastric pH greater than 4 and faster and more irregular gastric...
170
Pharmacokinetics in Pediatric Patients: Drug Excretion01:26

Pharmacokinetics in Pediatric Patients: Drug Excretion

In pediatric medicine, understanding the renal function and drug elimination nuances is crucial for administering safe and effective treatments. Newborns, in particular, display markedly slower renal functions than adults, profoundly affecting how drugs are cleared from their bodies. This slower drug clearance requires clinicians to extend the dosing intervals for many medications to prevent drug accumulation and toxicity while ensuring therapeutic efficacy.One key area where these adjustments...
148
Diseases of the Liver and Gallbladder01:26

Diseases of the Liver and Gallbladder

Liver and gallbladder diseases are a significant health concern, with prominent conditions including cirrhosis, hepatitis, non-alcoholic fatty liver disease (NAFLD), and gallstones. Jaundice is a common manifestation of liver and biliary disease.
Cirrhosis is characterized by the scarring of hepatic lobules in the liver, which are replaced by fibrous tissue, affecting the liver's normal functioning. NAFLD, on the other hand, is caused by an excessive build-up of fat in the liver, not...
1.7K