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NEONATAL ANAEMIA
NEONATAL ANAEMIA
Outline
 Definition
 Normal values
 Erythropoiesis
 Pathophysiological classification.
DEFINITION
 A reduction in red cell volume or hemoglobin
concentration below range of values occurring in
healthy newborn with respect to gestational age.
 Is there a cut off? Depends on
 Post natal age of neonate
 Birth weight
 Site of sampling (capillary vs. venous)
 Term infant at birth, venous sample 14-20g/dl..
Average 17g/dl
 Few clinical disturbances occur till Hb 7-8g/dl ??
2/8/2024
Normal Hb Levels
What shall we say then,
 cord blood levels <13g/dl in term & premature (<36 wks
gestation) should be interpreted as abnormal
 In very premature infants < 26wks gestation, values as
low as 12g/dl may be acceptable
 If anemia is confirmed, a prompt and careful search for
the cause should be initiated.
2/8/2024
Development of
erythropoiesis
 Hematopoiesis in embryo and fetus
 Hepatic -chief site 3-6mo in utero
 Myeloid – takes over 6 mo
 First cells produced in embryo are red cells
2/8/2024
Erthropoiesis after birth
 In the bone marrow
 Rate of Hb synthesis and red cell production
dramatically decreases(nadir 2nd wk, then increase to
max at 3/12 2ml packed cells/day
 Sudden decrease is initiated by equal sudden increase in
tissue [oxygen ]at birth
 At birth 55-95% is HbF , thereafter HbA more
2/8/2024
2/8/2024
Control of Erythropoiesis
 Erythropoiesis is controlled by a negative feedback loop
involving erythropoietin (EPO) .
 ↓ RBC mass - ↑ EPO which drives erythropoiesis to ↑RBC
mass which in turn reduces EPO production
2/8/2024
Pathophysiological
classiffication
1. Anemia due to blood loss(hemorrhage)
2. Anemia due to increased destruction of RBCs
(hemolysis)
3. Anemia due to decreased red cell production
2/8/2024
Blood loss
 Prenatal or at birth
 Laboratory sampling
 Occult hemorrhage before birth-fetal to maternal
hemorrhage, twin to twin transfusion.
 Obstetric accidents-umbilical cord rupture in
precipitous labour, unusually short, entangled around
neck, traction with forceps, arterial aneurysm. APH
 Inadvertent incision during CS
2/8/2024
TWIN TO TWIN TRANSFUSION
2/8/2024
ct
 Internal hemorrhage
 Traumatic delivery-subdural, sub arachnoid,
cephalohematoma, subaponeurotic
 Breech delivery-adrenals, kidney, spleen , retroperitoneal,
liver
 Intraventricular (50% of those <1500),SAH
 Bleeding disorders acquired or congenital
 Less cmn causes-maternal antiepileptic use, fetal
adenovirus, CMV ix, hemangiomas of GIT
2/8/2024
phlebotomy
 Repeated phlebotomy, confirmed major cause of
anaemia
 It hastens onset/worsens severity
2/8/2024
Hemolysis
 Immune mediated-most common cause of neonatal
hemolysis; Rhesus incompatibility, ABO, Minor blood
group incompatibility, maternal infantile AIHA, drug
induced penicillamine, α-methyl dopa.
 Infection –bacterial sepsis,TORCHES, Malaria,
adenovirus.
 Hereditary red cell membrane defects hereditary
spherosocytosis
 Hereditary enzymopathies G6PD, pyruvate kinase def.
 Hereditary hemoglobinopathies α –thal, γ-thal.
2/8/2024
Decreased erythropoiesis
 Congenital infection-rubella,CMV,adenovirus,parvovirus
 Congenital dyserythropoietic anaemia, anemia, early
jaundice,hepatosplenomegally
 Congenital leukemia,down syndrome, osteoporosis
2/8/2024
Physiologic anaemia of
prematurity
 The Hb of normal term infants usually decreases over
first few weeks of life (physiologic anaemia of
infancy).nadir 11-12g/dl, 8-12wks.
 Physiologic process , asymptomatic, requires no
treatment.
 Preterms have an exaggerated decrease (physiologic
anaemia of preterms). nadir 7-8g/dl, 4-8wks,more
immature, lower nadir.
2/8/2024
2/8/2024
 The physiological phenomenon is due to:-
 Increase in tissue oxygenation at birth (placenta to lungs)
 Rapid body growth
 Shortened rbc lifespan 80d vs 120d
 Low blood erythropoietin due inadequate production and bunted
EPO response to decreasing Hb.
 Decrease in hematopoietic activity.

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NEONATAL ANAEMIA_114358.pptx

  • 2. Outline  Definition  Normal values  Erythropoiesis  Pathophysiological classification.
  • 3. DEFINITION  A reduction in red cell volume or hemoglobin concentration below range of values occurring in healthy newborn with respect to gestational age.  Is there a cut off? Depends on  Post natal age of neonate  Birth weight  Site of sampling (capillary vs. venous)  Term infant at birth, venous sample 14-20g/dl.. Average 17g/dl  Few clinical disturbances occur till Hb 7-8g/dl ?? 2/8/2024
  • 4. Normal Hb Levels What shall we say then,  cord blood levels <13g/dl in term & premature (<36 wks gestation) should be interpreted as abnormal  In very premature infants < 26wks gestation, values as low as 12g/dl may be acceptable  If anemia is confirmed, a prompt and careful search for the cause should be initiated. 2/8/2024
  • 5. Development of erythropoiesis  Hematopoiesis in embryo and fetus  Hepatic -chief site 3-6mo in utero  Myeloid – takes over 6 mo  First cells produced in embryo are red cells 2/8/2024
  • 6. Erthropoiesis after birth  In the bone marrow  Rate of Hb synthesis and red cell production dramatically decreases(nadir 2nd wk, then increase to max at 3/12 2ml packed cells/day  Sudden decrease is initiated by equal sudden increase in tissue [oxygen ]at birth  At birth 55-95% is HbF , thereafter HbA more 2/8/2024
  • 8. Control of Erythropoiesis  Erythropoiesis is controlled by a negative feedback loop involving erythropoietin (EPO) .  ↓ RBC mass - ↑ EPO which drives erythropoiesis to ↑RBC mass which in turn reduces EPO production 2/8/2024
  • 9. Pathophysiological classiffication 1. Anemia due to blood loss(hemorrhage) 2. Anemia due to increased destruction of RBCs (hemolysis) 3. Anemia due to decreased red cell production 2/8/2024
  • 10. Blood loss  Prenatal or at birth  Laboratory sampling  Occult hemorrhage before birth-fetal to maternal hemorrhage, twin to twin transfusion.  Obstetric accidents-umbilical cord rupture in precipitous labour, unusually short, entangled around neck, traction with forceps, arterial aneurysm. APH  Inadvertent incision during CS 2/8/2024
  • 11. TWIN TO TWIN TRANSFUSION 2/8/2024
  • 12. ct  Internal hemorrhage  Traumatic delivery-subdural, sub arachnoid, cephalohematoma, subaponeurotic  Breech delivery-adrenals, kidney, spleen , retroperitoneal, liver  Intraventricular (50% of those <1500),SAH  Bleeding disorders acquired or congenital  Less cmn causes-maternal antiepileptic use, fetal adenovirus, CMV ix, hemangiomas of GIT 2/8/2024
  • 13. phlebotomy  Repeated phlebotomy, confirmed major cause of anaemia  It hastens onset/worsens severity 2/8/2024
  • 14. Hemolysis  Immune mediated-most common cause of neonatal hemolysis; Rhesus incompatibility, ABO, Minor blood group incompatibility, maternal infantile AIHA, drug induced penicillamine, α-methyl dopa.  Infection –bacterial sepsis,TORCHES, Malaria, adenovirus.  Hereditary red cell membrane defects hereditary spherosocytosis  Hereditary enzymopathies G6PD, pyruvate kinase def.  Hereditary hemoglobinopathies α –thal, γ-thal. 2/8/2024
  • 15. Decreased erythropoiesis  Congenital infection-rubella,CMV,adenovirus,parvovirus  Congenital dyserythropoietic anaemia, anemia, early jaundice,hepatosplenomegally  Congenital leukemia,down syndrome, osteoporosis 2/8/2024
  • 16. Physiologic anaemia of prematurity  The Hb of normal term infants usually decreases over first few weeks of life (physiologic anaemia of infancy).nadir 11-12g/dl, 8-12wks.  Physiologic process , asymptomatic, requires no treatment.  Preterms have an exaggerated decrease (physiologic anaemia of preterms). nadir 7-8g/dl, 4-8wks,more immature, lower nadir. 2/8/2024
  • 17. 2/8/2024  The physiological phenomenon is due to:-  Increase in tissue oxygenation at birth (placenta to lungs)  Rapid body growth  Shortened rbc lifespan 80d vs 120d  Low blood erythropoietin due inadequate production and bunted EPO response to decreasing Hb.  Decrease in hematopoietic activity.

Editor's Notes

  1. Preterms 1-2g/dl lower Site of sampling will see later.
  2. HbA production starts in utero, after 34-36 week the % of HbA increases while HbF reduces. At birth the proportions of HbF to HbA are 53-95% What are the advantages of HbF over A : it has higher affinity for oxygen, thus gives the developing fetus better access to maternal oxygen.
  3. HbF decreases after birth by approx 3%/week to <2 to 3 % by 6 mo.. Hereditary persistence of fetal hb, thal B..can be 100% HbF, SCD max 20% Item 6 switch delayed in infants of DM mothers, Brochopulm dysplasia, those with inability to metabolise propionic acid
  4. The expected correlation between EPO and oxygen delivery (eg Hb, venous oxyen tension) can be detected in premature infants providing evidence that the feedback loop exists
  5. Velamentous placenta-umbilical vessels attach to the fetal membranes between chorion and amnion. No protection with whartons jelly, liable to rupture
  6. Sub aponeurotic bogginess from front to occiput, for each increase in HC beyond expected 35mls of blood.
  7. Several cases of homozygous SCD have been seen clinically in neonates, a B chain, HBS usually <20%. A thal causing anaemia in newborn invariably is homozygous a thall(microcytosis), HbBarts gamma tetramer.
  8. Mention En passant.. Diamond blackfan syndrome-microcephaly,eye anomalies,web neck,thumb deformities;bifid or triphallangeal thumb, cleft palate
  9. After birth EPO levels decreases to almost zero