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Jaundice in Infants – Indirect

Jaundice in Infants – Indirect: Excerpt from In A Page: Pediatric Signs and Symptoms

Jaundice is the presence of a yellow hue of the skin, sclerae, or mucous membranes due to elevation of serum bilirubin; it usually becomes apparent at a total serum bilirubin level of 5 mg/dL. It is present in approximately 60% of term infants and 80% of premature infants during the first week of life. Although the indirect form is neurotoxic, differentiating the nonpolar, lipid-soluble, indirect form from the potentially more serious polar, water-soluble direct form represents the most important first step.

Differential Diagnosis

    • Icterus neonatorum (physiologic jaundice)
      –The most common form of indirect jaundice in infants under 14 days of age
      –Caused by increased bilirubin production with transient limited conjugation abilities
    • Breast-feeding jaundice
      –Occurs in first week of life in 13% of breast-fed infants
      –Secondary to poor volume intake
    • Breast-milk jaundice
      –Occurs in about 2% of breast-fed infants after day 7 of life
      –Secondary to glucuronidase in breast milk
    • Hematologic: Hemolysis increases bili load
      –Rh incompatability
      –ABO incompatability
      –Glucose-6-phosphate dehydrogenase (G6PD) deficiency
      –Pyruvate kinase deficiency
      –Hereditary spherocytosis
      –Elliptocytosis
      –Thalassemia
      –Polycythemia
  • Extravascular blood
    –Cephalohematoma
    –Trauma
    –Swallowed maternal blood
  • Endocrinologic
    –Hypothyroidism
    –Maternal diabetes
  • Sepsis
  • Metabolic
    –Crigler-Najjar I
    –Crigler-Najjar II (Arias syndrome)
    –Crigler-Najjar III
  • Cardiopulmonary
    –Congestive heart failure
    –Patent ductus arteriosus
    –Portal vein thrombosis
  • Anatomic
    –Pyloric stenosis
    –Duodenal atresia/stenosis
    –Duodenal web
  • Drugs
    –Oxytocin
    –Sulfonamides
    –Ceftriaxone
    –Chuen-Lin
  • Lucey-Driscoll syndrome

Workup and Diagnosis

  • History
    –Prenatal/perinatal: Pregnancy complications, gestational age, maternal blood type/Rh, drug use, infections, delivery method, delivery intervention, birth weight, newborn screen results, previous miscarriages
    –HPI: Onset of jaundice, feeding tolerance, appropriate weight gain, trauma, evidence of bleeding/bruising, urine output, stool output/diarrhea, emesis, lethargy, drug exposure
    –Diet history: Breast- and/or formula-fed, length of time on each breast, latch strength
    –Family history: Bleeding disorders, perinatal deaths, endocrinopathies
    • Physical exam
      –Weight, overall appearance, level of jaundice, fontanelle size, cranial abnormalities, scleral icteris, mucous membranes, cardiac murmurs, hepatosplenomegaly, bruising, bleeding, reflexes, tone, seizures
    • Labs: Fractionated bilirubin (total, indirect, direct), CBC with smear, reticulocyte count
    • Hemolysis: Blood type/Rh, Coombs, hemoglobin electrophoresis
    • Thyroid function tests (check state newborn screen)
    • Limited value of imaging unless looking for obstruction or bleeding
    • Hearing evaluation if kernicterus likely

    Treatment

      • Treatment options vary based on level of bilirubin, age of presentation, and cause
        –Goal is prevent levels high enough to cause kernicterus
      • Phototherapy involves the use of photon energy to change the structure of bilirubin and permit excretion without glucuronidation
        –Decisions for use are age-based
        –Considered when serum level above 14 mg/dL
    • Exchange transfusion should be considered with serum levels above 25 mg/dL
    • IVF or breast-feed more frequently to increase volume
    • Correct endocrine abnormality
    • Improve perfusion if cardiac problem
    • Correct anatomic abnormality
    • Consider enteral binding agents
      –Cholestyramine, charcoal, calcium phosphate
    • Crigler-Najjar: Phenobarbital, may need liver transplantation

Book Source Details

  • Book Title: In A Page: Pediatric Signs and Symptoms
  • Author(s): Jonathan E. Teitelbaum, Kathleen O. Deantonis, Scott Kahan
  • Year of Publication: 2007
  • Copyright Details: In A Page: Pediatric Signs and Symptoms, Copyright © 2007 Lippincott Williams & Wilkins.

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Medical Books Excerpts
  • ASCITES
  • "Algorithmic Diagnosis of Symptoms and Signs" (2003)
  • JAUNDICE
  • "Algorithmic Diagnosis of Symptoms and Signs" (2003)
  • Ascites
  • "In A Page: Pediatric Signs and Symptoms" (2007)
  • JAUNDICE
  • "Differential Diagnosis in Primary Care" (2007)
  • Jaundice
  • "Handbook of Signs & Symptoms (Third Edition)" (2006)
  • Ascites
  • "A Pocket Manual of Differential Diagnosis" (1999)
  • Jaundice
  • "A Pocket Manual of Differential Diagnosis" (1999)
  • Hepatomegaly
  • "Professional Guide to Signs & Symptoms (Fifth Edition)" (2006)
  • Ascites
  • "The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter" (2000)
  • Hepatomegaly
  • "The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter" (2000)
  • Jaundice
  • "The 10-Minute Diagnosis Manual: Symptoms and Signs in the Time-Limited Encounter" (2000)
  • Jaundice
  • "Field Guide to Bedside Diagnosis" (2007)
  • Hepatomegaly
  • "Signs & Symptoms: A 2-in-1 Reference for Nurses" (2007)
  • Jaundice
  • "Signs & Symptoms: A 2-in-1 Reference for Nurses" (2007)
  • Hepatomegaly
  • "The Diagnostic Approach to Symptoms and Signs in Pediatrics" (2006)
  • Jaundice
  • "The Diagnostic Approach to Symptoms and Signs in Pediatrics" (2006)
  • JAUNDICE
  • "Differential Diagnosis in Primary Care" (2007)
 

Copyright notice for book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.




More About This Book:
Title: In A Page: Pediatric Signs and Symptoms
Authors: Jonathan E. Teitelbaum, Kathleen O. Deantonis, Scott Kahan
Publisher: Lippincott Williams & Wilkins
Copyright: 2007
ISBN: 1-4051-0427-9

 » Next page: HEPATOMEGALY (Differential Diagnosis in Primary Care)

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