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Neonatal Hyperbilirubinemia in 35 Weeks: Neonatal Policy & Procedures Manual Policy Group Approved By: Date Effective
Neonatal Hyperbilirubinemia in 35 Weeks: Neonatal Policy & Procedures Manual Policy Group Approved By: Date Effective
Purpose To identify and treat neonates at risk for hyperbilirubinemia and to prevent and reduce the
incidence of neonatal hyperbilirubinemia encephalopathy and kernicterus.
Policy • All infants 32 weeks to less than 35 weeks gestation will have TcB (Transcutaneous
Statement Bilirubin) or SB (serum bilirubin) measured in the first 72 hours of life.
• Infants less than 32 weeks gestation will have SB done before 36 hours of life. This may
be timed with the Newborn Metabolic Screen.
• Infants with visible jaundice in the first 24 hours will have a TcB or SB done within 2
hours.
• TcB levels that suggest treatment is needed, are confirmed with a SB level before
treatment is started.
• Decisions for further screening or treatment will be made based on National Institute for
Health & Clinical Excellence (NICE) treatment threshold guidelines for gestational age.
• Information will be given to parents regarding jaundice, screening for jaundice, and
treatment information as applicable (phototherapy / exchange transfusion).
Applicability This policy applies to Covenant Health employees, members of the medical and midwifery
staff, students, volunteers and other persons acting on behalf of or in conjunction with
Covenant Health (including contracted services providers as necessary).
Assessment 1. All newborns less than 35 weeks will be monitored for the development of
hyperbilirubinemia by physical assessment for the presence of jaundice every 6 hours
for the first week of life. This includes the evaluation of jaundice when the forehead skin
is blanched with digital pressure.
Assessment 3. SB results will be plotted on a gestational age specific treatment threshold graph to
determine the risk of progression of severe hyperbilirubinemia and recommendation for
treatment.
4. Infants visibly jaundiced within the first 24 hours of life will have a systemic assessment
including evaluation of maternal & infant blood group, DAT, and CBC with peripheral
smear.
Treatment Phototherapy
The efficacy of phototherapy depends on the dose of phototherapy administered. The
dose is dependent on the spectrum of light emitted by the unit, spectral irradiance, and
spectral power (average irradiance across the surface area). Efficacy also depends on
cause of jaundice with less power to lower SB if the cause is related to hemolysis or if
cholestasis is present.
Phototherapy will be started at the SB level indicated on the gestational age specific graph
based on the infant’s age in hours.
Intensive phototherapy provides coverage over as much body surface as possible with light
intensity at least 30µW/cm2 / nm. To maximize phototherapy intensity, the distance
between the light and patient should be minimized subject to manufacturer’s
recommendations for halogen phototherapy. Surface area receiving phototherapy can be
maximized by using a fibre-optic blanket phototherapy unit. More than one spot
phototherapy light may be used if the light area does not cover the anterior surface area of
the patient.
May change to conventional phototherapy use if SB greater than 50 micromol/L less than
threshold for exchange.
Hyperbilirubinemia in Less Than 35 Weeks Date Approved Policy Group Page 3 of 8
September, 2015 Integument
Treatment Discontinuing phototherapy depends on the age at which phototherapy was initiated and
the cause of the hyperbilirubinemia. For infants who are readmitted after their birth
hospitalization with hyperbilirubinemia not related to an identified pathology, phototherapy
may be discontinued when the SB falls below 240µmol/L.
Exchange Transfusions
Decision for an exchange transfusion will be based on the SB level indicated on the
gestational age specific graph based on the infant’s age in hours or if signs of acute
bilirubin encephalopathy are present (hypertonia, arching, retrocollis, opisthotonus, fever,
high pitched cry).
Performed only by trained personnel in neonatal intensive care units with full monitoring
and resuscitation capabilities
Double-volume exchange transfusions are preferred.
Arterial-venous exchange transfusions preferred to venous exchange transfusion
Do not routinely administer calcium during exchange transfusion.
Continue intensive phototherapy during exchange transfusion
References Evidence Update Advisory Group NICE (2012) Neonatal jaundice: Evidence Update March
2012.A summary of selected new evidence relevant to NICE clinical guideline 98 ‘Neonatal
jaundice’ (2010). National Institute for Clinical Evidence: Manchester U.K.
National Collaborating Centre for Women’s and Children’s Health Commissioned by the
National Institute for Health and Clinical Excellence (May 2010). Neonatal Jaundice. Royal
College of Obstetricians and Gynaecologists: London.
Hyperbilirubinemia in Less Than 35 Weeks Date Approved Policy Group Page 5 of 8
September, 2015 Integument
NEONATAL JAUNDICE – Investigation Pathway Care for babies < 35 weeks gestation
No Yes
No Yes
Signing
Original Signed
September, 2015
_________________________ ____________________
GAIL CAMERON DATE
SENIOR DIRECTOR, OPERATIONS
MATERNAL, NEONATAL & CHILD HEALTH PROGRAMS
COVENANT HEALTH
GREY NUNS & MISERCORDIA HOSPITALS