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Effects of Premature Birth on Neurocognitive Development and Academic
Performance: Longitudinal IEP Review of PT and SGA Student
Alamy, 2015; Beery, Buktenic , 2011; Woodcock-Johnson III Normative Update (NU) Complete
1Ozella Brundidge, 4/3/2017
Neonatal
Hyperbilirubemia and Jaundice
2
Sherman, 2016
Ozella Brundidge, 4/3/2017
Infants born with very low birth weight (≤ 1500 grams), neonatal hyperbilirubinemia, and
bronchopulmonary dysplasia experienced language delay at 3-years of age.
3
Infants born with very low birth weight (≤ 1500
grams), neonatal hyperbilirubinemia, and
bronchopulmonary dysplasia experienced
language delay at 3-years of age.
(Amin, Prinzing, & Myers, 2009)
Birth Weight and Neonatal Complications are Associated with
Language Delays
Ozella Brundidge, 4/3/2017
Bilirubin is Toxic to Brain Cells
Jaundice is defined as maximal indirect serum bilirubin greater than 10 mg/dL
(171 per m/L)
(Usher & McLean, 1969 in Taylor, 2004; Amin, 2004) Ozella Brundidge, 4/3/2017
5
Phototherapy and Exchange Transfusion are
Recommended at a Lower Serum Total Blood (STB)
level. Bilirubin Neurotoxicity may Increase the Risk
of Developing Central Auditory System Damage
Borderline Premature Infants are at Especial Risk of Bilirubin Production-Conjugation Imbalance.
(Can, et al., 2015; Kaplan, Muraca, Vreman, Hammerman, Vilei,
Rubaltelli, & Stevenson, 2005; Kaplan, Bromiker, & Hammerman, 2014)
Borderline Premature Infants (35-36 weeks gestation) are at
Significant Risk of Producing Excess Bilirubin
Hyperbilirubinemia – an imbalance between bilirubin production and excretion out of the body.
Sawyer, 2015, Dec. 6
Ozella Brundidge, 4/3/2017
Late Preterm (34-36 𝟔
𝟕 weeks) Infants
have a 2- to 5-Fold Increased
Risk of Developing
Hyperbilirubemia and Jaundice
(Can, Verim, Baser, & Inan, 2015; Baron, Erickson, Ahronovich, Baker, & Littman, 2011; Adams-Chapman,
2006 in Loftin, et al., 2010; Bhutani & Johnson, 2006 in 2010; Watchko & Maisels, 2003 in Morse, et al., 2009)
6
Late Preterm (34-36 𝟔
𝟕 weeks) Infants have a 2- to 5-Fold Increased Risk of Developing
Hyperbilirubemia and Jaundice
Neonatal Hyperbilirubinemia has a Degenerative Effect on the Auditory System
Ozella Brundidge, 4/3/2017
hyperbilirubinemia has a the neurotoxic effect on
the auditory pathway
7
Hyperbilirubinemia has a Neurotoxic
Effect on the Auditory Pathway that
may lead to Auditory Neuropathy
Spectrum Disorder.
(Can, Verim, Baser, & Inan, 2015; Raveh et al, 2007 in 2015)
Inner Hair Cells Cochlear Cochlear Nerve Auditory Brainstem Primary Auditory Center
Bilirubin Values Varying from 7 to 25 mg/dl may Cause
Auditory Neuropathy/Auditory Dyssynchrony
*Can and colleagues assert that total serum bilirubin levels 20 mg/dl (mean 22.3 1.76 mg/dl) may cause AN/AD in 2% of late
preterms treated with phototherapy, and lower levels may be safe.
Ozella Brundidge, 4/3/2017
Most Cases of Infantile Hyperbilirubinemia (60%) are
Physiological Conditions and Harmless
8
(Rance, 2005 in Can, Verim, Baser, & Inan, 2015)
• Even Short-Term Increases in the Bilirubin Blood
Level can Induce Temporary or Permanent
Changes in Evoked Potentials.
• An Increase in Threshold and Wave Latency (I–V)
in Auditory Brainstem Responses (ABR) indicates
that both peripheral and central auditory systems
are sensitive to high bilirubin levels.
Ozella Brundidge, 4/3/2017
Incomplete Maturation of the Bilirubin Conjugating Enzymes in Premature
Infants Increase Risk for Developing Hyperbilirubinemia
(Kaplan, Muraca, Vreman, Hammerman, Vilei, Rubaltelli, Stevenson, 2005; Dennery, 2001 in Kaplan, 2005; American
Academy of Pediatrics, Subcommittee on Neonatal Hyperbilirubinemia. Neonatal jaundice and kernicterus. Pediatrics
2001 in 2005; Morse, Zheng, Tang, & Roth, 2009; Watchko & Maisels, 2003 in Morse, et al., 2009)
Borderline prematurity was previously found to be an
important contributing factor to hyperbilirubinemia,
*UDP-glucuronosyltransferase 1A1 (UGT)
9
placing these neonates at a high risk status for
developing jaundice.
Ozella Brundidge, 4/3/2017
The Current Case Study Student was a High
Risk Neonate born with Complications
Resulting in Incubation Treatment for
Jaundice in the Neonatal Intensive Care Unit
(NICU).
(Case Study Student's (1998, June 3). Individual and family assessment outline-adoption – Part B, Section II. Individual and family
life areas-Background, A. Child to be adopted. Division of Family and Youth Services; Baron, Erickson, Ahronovich, Baker, &
Littman, 2011; Adams-Chapman, 2006 in Loftin, et al., 2010; Bhutani & Johnson, 2006 in 2010)
10
Case Study Student was Born Small for Gestational (SGA) with Neonatal Complications Including
Incubation Treatment for Jaundice in a Neonatal Intensive Care Unit (NICU)
Hyperbilirubin Levels may Lead to Jaundice
(Sherman, 2016)
Ozella Brundidge, 4/3/2017
Odds of Health Complications Decrease with Advancing Gestational
Age through the Late Preterm Period (34-36 𝟔
𝟕 weeks)
0
1
2
3
4
5
6
Respiratory Distress Septis (Hyperbilirubin/Jaudice) Patent Ductus Arteriosus
Rate of Health Problems Associated with Late Preterm Deliveries by
Gestational Age
34 Weeks 35 Weeks 36 Weeks
Figure 1. Rate of respiratory distress, sepsis, and patent ductus arteriosus (PDA) by gestational age (Loftin, Habli, Snyder,
Cormier, Lewis, & DeFranco, 2010, p.14).
Percent(%)
(Current Case Study
Student had
Jaundice)
11Ozella Brundidge, 4/3/2017
End of Neonatal
Hyperbilirubemia/Jaundice
12Ozella Brundidge, 4/3/2017

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Neonatal hyperbilirubemia and jaundice

  • 1. Effects of Premature Birth on Neurocognitive Development and Academic Performance: Longitudinal IEP Review of PT and SGA Student Alamy, 2015; Beery, Buktenic , 2011; Woodcock-Johnson III Normative Update (NU) Complete 1Ozella Brundidge, 4/3/2017
  • 2. Neonatal Hyperbilirubemia and Jaundice 2 Sherman, 2016 Ozella Brundidge, 4/3/2017
  • 3. Infants born with very low birth weight (≤ 1500 grams), neonatal hyperbilirubinemia, and bronchopulmonary dysplasia experienced language delay at 3-years of age. 3 Infants born with very low birth weight (≤ 1500 grams), neonatal hyperbilirubinemia, and bronchopulmonary dysplasia experienced language delay at 3-years of age. (Amin, Prinzing, & Myers, 2009) Birth Weight and Neonatal Complications are Associated with Language Delays Ozella Brundidge, 4/3/2017
  • 4. Bilirubin is Toxic to Brain Cells Jaundice is defined as maximal indirect serum bilirubin greater than 10 mg/dL (171 per m/L) (Usher & McLean, 1969 in Taylor, 2004; Amin, 2004) Ozella Brundidge, 4/3/2017
  • 5. 5 Phototherapy and Exchange Transfusion are Recommended at a Lower Serum Total Blood (STB) level. Bilirubin Neurotoxicity may Increase the Risk of Developing Central Auditory System Damage Borderline Premature Infants are at Especial Risk of Bilirubin Production-Conjugation Imbalance. (Can, et al., 2015; Kaplan, Muraca, Vreman, Hammerman, Vilei, Rubaltelli, & Stevenson, 2005; Kaplan, Bromiker, & Hammerman, 2014) Borderline Premature Infants (35-36 weeks gestation) are at Significant Risk of Producing Excess Bilirubin Hyperbilirubinemia – an imbalance between bilirubin production and excretion out of the body. Sawyer, 2015, Dec. 6 Ozella Brundidge, 4/3/2017
  • 6. Late Preterm (34-36 𝟔 𝟕 weeks) Infants have a 2- to 5-Fold Increased Risk of Developing Hyperbilirubemia and Jaundice (Can, Verim, Baser, & Inan, 2015; Baron, Erickson, Ahronovich, Baker, & Littman, 2011; Adams-Chapman, 2006 in Loftin, et al., 2010; Bhutani & Johnson, 2006 in 2010; Watchko & Maisels, 2003 in Morse, et al., 2009) 6 Late Preterm (34-36 𝟔 𝟕 weeks) Infants have a 2- to 5-Fold Increased Risk of Developing Hyperbilirubemia and Jaundice Neonatal Hyperbilirubinemia has a Degenerative Effect on the Auditory System Ozella Brundidge, 4/3/2017
  • 7. hyperbilirubinemia has a the neurotoxic effect on the auditory pathway 7 Hyperbilirubinemia has a Neurotoxic Effect on the Auditory Pathway that may lead to Auditory Neuropathy Spectrum Disorder. (Can, Verim, Baser, & Inan, 2015; Raveh et al, 2007 in 2015) Inner Hair Cells Cochlear Cochlear Nerve Auditory Brainstem Primary Auditory Center Bilirubin Values Varying from 7 to 25 mg/dl may Cause Auditory Neuropathy/Auditory Dyssynchrony *Can and colleagues assert that total serum bilirubin levels 20 mg/dl (mean 22.3 1.76 mg/dl) may cause AN/AD in 2% of late preterms treated with phototherapy, and lower levels may be safe. Ozella Brundidge, 4/3/2017
  • 8. Most Cases of Infantile Hyperbilirubinemia (60%) are Physiological Conditions and Harmless 8 (Rance, 2005 in Can, Verim, Baser, & Inan, 2015) • Even Short-Term Increases in the Bilirubin Blood Level can Induce Temporary or Permanent Changes in Evoked Potentials. • An Increase in Threshold and Wave Latency (I–V) in Auditory Brainstem Responses (ABR) indicates that both peripheral and central auditory systems are sensitive to high bilirubin levels. Ozella Brundidge, 4/3/2017
  • 9. Incomplete Maturation of the Bilirubin Conjugating Enzymes in Premature Infants Increase Risk for Developing Hyperbilirubinemia (Kaplan, Muraca, Vreman, Hammerman, Vilei, Rubaltelli, Stevenson, 2005; Dennery, 2001 in Kaplan, 2005; American Academy of Pediatrics, Subcommittee on Neonatal Hyperbilirubinemia. Neonatal jaundice and kernicterus. Pediatrics 2001 in 2005; Morse, Zheng, Tang, & Roth, 2009; Watchko & Maisels, 2003 in Morse, et al., 2009) Borderline prematurity was previously found to be an important contributing factor to hyperbilirubinemia, *UDP-glucuronosyltransferase 1A1 (UGT) 9 placing these neonates at a high risk status for developing jaundice. Ozella Brundidge, 4/3/2017
  • 10. The Current Case Study Student was a High Risk Neonate born with Complications Resulting in Incubation Treatment for Jaundice in the Neonatal Intensive Care Unit (NICU). (Case Study Student's (1998, June 3). Individual and family assessment outline-adoption – Part B, Section II. Individual and family life areas-Background, A. Child to be adopted. Division of Family and Youth Services; Baron, Erickson, Ahronovich, Baker, & Littman, 2011; Adams-Chapman, 2006 in Loftin, et al., 2010; Bhutani & Johnson, 2006 in 2010) 10 Case Study Student was Born Small for Gestational (SGA) with Neonatal Complications Including Incubation Treatment for Jaundice in a Neonatal Intensive Care Unit (NICU) Hyperbilirubin Levels may Lead to Jaundice (Sherman, 2016) Ozella Brundidge, 4/3/2017
  • 11. Odds of Health Complications Decrease with Advancing Gestational Age through the Late Preterm Period (34-36 𝟔 𝟕 weeks) 0 1 2 3 4 5 6 Respiratory Distress Septis (Hyperbilirubin/Jaudice) Patent Ductus Arteriosus Rate of Health Problems Associated with Late Preterm Deliveries by Gestational Age 34 Weeks 35 Weeks 36 Weeks Figure 1. Rate of respiratory distress, sepsis, and patent ductus arteriosus (PDA) by gestational age (Loftin, Habli, Snyder, Cormier, Lewis, & DeFranco, 2010, p.14). Percent(%) (Current Case Study Student had Jaundice) 11Ozella Brundidge, 4/3/2017

Editor's Notes

  1. Alamy (2015). African American boy writing in a classroom in Washington DC. Retrieved from http://www.alamy.com/stock-photo-african-american-boy-writing-in-a-classroom-in-washington-dc-34085287.html Woodcock-Johnson® III Normative Update (NU) Complete (2015). http://www.riverpub.com/products/wjIIIComplete/ Beery-Buktenica Developmental Test of Visual-Motor Integration, 6th Edition (BEERY™ VMI 6) 2010 | Beery, Keith E., Buktenica, Norman A., and Beery, Natasha A. http://www.pearsonassess.ca/en/programs/00/62/35/p006235.html?prodCategory=ot-motor-visual-motor Bender Visual-Motor Gestalt Test, Second Edition (Bender-Gestalt II) Lauretta Bender, MD, the American Orthopsychiatric Association, Inc., Revised by Scott L. Decker, PhD, Gary G. Brannigan http://www.pearsonclinical.com/psychology/products/100000190/bender-visual-motor-gestalt-test-second-edition-bender-gestalt-ii.html
  2. Sherman, M. (2016). Jaundice: causes the baby’s skin and eyes to look slightly yellow. Slideplayer.com. Retrieved from http://slideplayer.com/slide/8000082/
  3. Amin, S. B. (2004). Clinical assessment of bilirubin-induced neurotoxicity in premature infants. Semen Perinatology, 2004(28), 340-347.
  4. Sawyer, T. L. (December 6, 2015). Phototherapy for jaundice periprocedural care. Medscape. http://img.medscapestatic.com/pi/meds/ckb/20/26020tn.jpg Kaplan, M., Bromiker, R., & Hammerman, C. (2014). Hyperbilirubinemia, hemolysis, and increased bilirubin neurotoxicity. Seminars in Perinatology, 38(2014), 429-437. http://dx.doi.org/10.1053/j.semperi.2014.08.006 Hemolysis is a major risk factor for the development of hyperbilirubinemia, but is it also a potentiator of bilirubin neurotoxicity? Categorizing hemolytic conditions as “neuro-toxicity risk factors” implies an increased risk of brain damage at equivalent concentrations of Serum total bilirubin (STB) in an infant whose hyperbilirubinemia is the result of hemolytic disease compared with non-hemolyticetiologies. This is the reason why phototherapy and exchange transfusion are recommended at a lower STB level when any of the neurotoxicity risk factors are present.11,12 A hemolytic cause of jaundice is likely if the predischarge STB or TcB level is in the high-risk zone on the hour-specific bilirubin nomogram13 or if jaundice is observed in the first 24hours
  5. Bilirubin values varying from 7 to 25 mg/dl were reported to cause auditory neuropathy/auditory dyssynchrony (AN/AD) (Raveh et al, 2007 in Can, et al., 2015). Watchko JF, Maisels MJ. Jaundice in low birthweight infants: Pathobiology and outcome. Arch Dis Child Fetal Neonatal Ed., 2003;88(6):F455–F458
  6. Auditory neuropathy, also known as auditory dyssynchrony (AN/AD) or auditory neuropathy spectrum disorder (ANSD), comprises a spectrum of problems that may affect any part of the auditory pathway, from the inner hair cells to the auditory brainstem. Patients with this disorder have difficulty with language decoding and speech perception out of proportion to their hearing loss (Can, et al., 2015).
  7. Early detection of hearing impairment around six months of age has been found to be of crucial importance in regard to higher expressive and receptive language development, higher general development, and lifelong improvement in social status (Yoshinaga-Itano et al, 1998).
  8. Hyperbilirubinemia Late-preterm infants have a higher incidence of prolonged physiologic jaundice and thus remain vulnerable for brain damage from jaundice for longer periods compared with term infants (Gartner & Herschel, 2001 in Raju, Higgins, Stark, & Leveno, 2006; Watchko & Maisels, 2003 in 2006). If these infants are assumed to be the same as term infants, they may be discharged early with inadequate evaluation of jaundice, and plans for follow-up. Thus, the late-preterm infants may be at higher risk for bilirubin-induced brain injury (2003 in 2006). Raju and colleagues suggested conducting studies related to prevention and treatment of hyperbilirubinemia and develop strategies to prevent and treat bilirubin-induced brain injury. Since the case study student was not released from the hospital before developing jaundice, bilirubin-induced caused brain Raju, T. N., Higgins, R. D., Stark, A R., & Leveno, K. J. (2006). Optimizing care and outcome for late-preter (near-term) infants: A summary of the workshop sponsored by the national institute of child health and human development. Pediatrics, 2006(118), 1207-1214. doi: 10.1542/peds.2006-0018 3. Gartner LM, Herschel M. Jaundice and breastfeeding. Pediatr Clin North Am. 2001;48:389–399 6. Watchko JF, Maisels MJ. Jaundice in low birthweight infants: pathobiology and outcome. Arch Dis Child Fetal Neonatal Ed. 2003;88:F455–F458 Watchko JF, Maisels MJ. Jaundice in low birthweight infants: Pathobiology and outcome. Arch Dis Child Fetal Neonatal Ed., 2003;88(6):F455–F458 activity of the bilirubin conjugating enzyme, UDP-glucuronosyltransferase 1A1 (UGT), has been shown to increase in concert with gestational age.15 I Incomplete maturation of the bilirubin conjugating enzyme* in premature infants was believed to place neonates at a high risk for developing hyperbilirubinemia. *UDP-glucuronosyltransferase 1A1 (UGT) Kaplan, M., Muraca, M., Vreman, H. J., Hammerman, C., Vilei, M. T., Rubaltelli, F. F., Stevenson, D. K. (2005). Neonatal bilirubin production-conjugation imbalance: Effect of glucose-6-phosphate dehydrogenase deficiency and borderline prematurity. Arch Dis Child Fetal Neonatal Ed 2005;90:F123–F127. doi: 10.1136/adc.2004.058313 M Kaplan, M Muraca*, H J Vreman, C Hammerman, M T Vilei, F F Rubaltelli, D K Stevenson
  9. Habli,