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NEONATAL HEMATOLOGIC
CONDITIONS
Soumya Ranjan Parida
RED BLOOD CELL DISORDER
HEMOGLOBIN LEVEL IN AN INFANT IS
SIGNIFICANTLY INFLUENCED BY THE AMOUNT
PLACENTAL TRANSFUSION
Placental vessels : 75- 125 ml of blood
one – fourth in first 15 secs.
one – half at end of first min.
Anemia(physiologic)
• Term infants – 11.4 +/- 0.9gm/dl
• Preterm : 7 – 10 gm/dl
Bleeding Disorders
HEMORRHAGIC DISEASE
• Vitamin K–dependent clotting factors (II, VII,
IX, and X).
• Bleeding occurs in 0.25–1.7% of newborns
who do not receive vitamin K prophylaxis after
birth, generally in the first 5 days to 6 weeks in
an otherwise well infant.
Hemolytic Disease
Immune
Alloimmune & Autoimmune
Non immune
Membranopathies, enzymopathies,
Hemoglobinopathies
Three Types of HDN( Allo)
• ABO
• “Other” – unexpected immune antibodies
other than anti-D – Jk, K, Fy, S, etc.
• Rh – anti-D alone or may be accompanied by
other Rh antibodies – anti-C, -c, -E or –e.
ABO Hemolytic Disease
• Mother group O, baby A or B
• Group O individuals have anti-A, -B and fetal RBCs
attacked by 2 antibodies
• Occurs in only 3%, is severe in only 1%, and <1:1,000
require exchange transfusion.
“Other” Hemolytic Disease
• Uncommon, occurs in ~0.8% of pregnant women.
• Immune alloantibodies usually due to anti-E, -c, -
Kell, -Kidd or -Duffy.
• Anti-K
– disease ranges from mild to severe
– over half of the cases are caused by multiple blood
transfusions
– is the second most common form of severe HDN
Rh Hemolytic Disease
• Anti-D is the commonest form of severe HDN. The
disease varies from mild to severe.
• Anti-c can range from a mild to severe disease - is the
third most common form of severe HDN
• The prevalence of Rh –ve genotype is zero
in china & Japan
• 0.05ml – 0.1 ml fetal blood – immunisation
• Toxemia, Manual removal of placenta , CS
increases prevalence
Anemia( Iatrogenic)
• Frequent blood sampling
• Removal of 20% of blood volume
• 1500 gm infant – 25 ml blood loss – Anemia
• Approx 10% of blood loss is hidden.
Hemoglobinopathies
• Predominant Hb is HbF(α2γ2)
• Abnormalities of β chain production do not
manifest ( SCD, β thalassemia)
Enzymopathies
Membranopathies
Elliptocytes
Evaluation Of anemia
• Site Of blood sampling
• Capillary Or Venous ??????
• Duplicate Capillary Sampling : Difference 0.8
gm/dl
Capillary > Venous
Difference upto 3.6gm/dl
Found in both term & preterm infants
Persists upto 6wks – 3months
Most marked in premature infants
Leucocyte Disorder
Band cell/ Non segmented neutroplil
Neonatal hematologic conditions

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Neonatal hematologic conditions

  • 2. RED BLOOD CELL DISORDER HEMOGLOBIN LEVEL IN AN INFANT IS SIGNIFICANTLY INFLUENCED BY THE AMOUNT PLACENTAL TRANSFUSION
  • 3. Placental vessels : 75- 125 ml of blood one – fourth in first 15 secs. one – half at end of first min.
  • 4.
  • 5. Anemia(physiologic) • Term infants – 11.4 +/- 0.9gm/dl • Preterm : 7 – 10 gm/dl
  • 6. Bleeding Disorders HEMORRHAGIC DISEASE • Vitamin K–dependent clotting factors (II, VII, IX, and X). • Bleeding occurs in 0.25–1.7% of newborns who do not receive vitamin K prophylaxis after birth, generally in the first 5 days to 6 weeks in an otherwise well infant.
  • 7. Hemolytic Disease Immune Alloimmune & Autoimmune Non immune Membranopathies, enzymopathies, Hemoglobinopathies
  • 8. Three Types of HDN( Allo) • ABO • “Other” – unexpected immune antibodies other than anti-D – Jk, K, Fy, S, etc. • Rh – anti-D alone or may be accompanied by other Rh antibodies – anti-C, -c, -E or –e.
  • 9. ABO Hemolytic Disease • Mother group O, baby A or B • Group O individuals have anti-A, -B and fetal RBCs attacked by 2 antibodies • Occurs in only 3%, is severe in only 1%, and <1:1,000 require exchange transfusion.
  • 10.
  • 11. “Other” Hemolytic Disease • Uncommon, occurs in ~0.8% of pregnant women. • Immune alloantibodies usually due to anti-E, -c, - Kell, -Kidd or -Duffy. • Anti-K – disease ranges from mild to severe – over half of the cases are caused by multiple blood transfusions – is the second most common form of severe HDN
  • 12. Rh Hemolytic Disease • Anti-D is the commonest form of severe HDN. The disease varies from mild to severe. • Anti-c can range from a mild to severe disease - is the third most common form of severe HDN
  • 13. • The prevalence of Rh –ve genotype is zero in china & Japan • 0.05ml – 0.1 ml fetal blood – immunisation • Toxemia, Manual removal of placenta , CS increases prevalence
  • 14. Anemia( Iatrogenic) • Frequent blood sampling • Removal of 20% of blood volume • 1500 gm infant – 25 ml blood loss – Anemia • Approx 10% of blood loss is hidden.
  • 15.
  • 16. Hemoglobinopathies • Predominant Hb is HbF(α2γ2) • Abnormalities of β chain production do not manifest ( SCD, β thalassemia)
  • 20. Evaluation Of anemia • Site Of blood sampling • Capillary Or Venous ??????
  • 21. • Duplicate Capillary Sampling : Difference 0.8 gm/dl Capillary > Venous Difference upto 3.6gm/dl Found in both term & preterm infants Persists upto 6wks – 3months Most marked in premature infants
  • 22.
  • 24. Band cell/ Non segmented neutroplil