MLAB 1415- Hematology Keri Brophy-Martinez Chapter 9: Iron Metabolism and Hypochromic Anemias.
MLAB 1415-Hematology Keri Brophy-Martinez Chapter 14: Introduction to Hemolytic Anemias.
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Transcript of MLAB 1415-Hematology Keri Brophy-Martinez Chapter 14: Introduction to Hemolytic Anemias.
![Page 1: MLAB 1415-Hematology Keri Brophy-Martinez Chapter 14: Introduction to Hemolytic Anemias.](https://reader035.fdocuments.us/reader035/viewer/2022081501/56649ec15503460f94bcd2e4/html5/thumbnails/1.jpg)
MLAB 1415-Hematology
Keri Brophy-Martinez
Chapter 14: Introduction to Hemolytic Anemias
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Hemolytic anemia
• Anemia caused by hemolysis of red blood cells– Hemolysis is the destruction of erythrocytes
resulting in the release of hemoglobin
• Results in reduction of normal red cell lifespan.
• Normocytic, normochromic anemia• RBC’s are prematurely destroyed
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Classified by…
• Source of defect causing the hemolysis– Intrinsic/extrinsic• Poikilocyte present
– Schistocytes/Spherocytes
• Mode of onset– Inherited/acquired
• Location of hemolysis– Intravascular/Extravascular
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Lab Features• Reticulocytosis– RPI> 2
• Erythroid hyperplasia of bone marrow• M:E ratio decreased• Peripheral blood– Normochromic,normocytic– Polychromasia– nRBCs
• Tests for heme catabolism abnormal– Unconjugated/conjugated bilirubin– Haptoglobin
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Lab FeaturesIncreased Bone Marrow Production of Erythrocytes
Increased Erythrocyte Destruction
Reticulocytosis (RPI>2) Anemia
Leukocytosis Spherocytes, Schistocytes, Poikilocytes
nRBCs in PB Decreased haptoglobin
Polychromasia Increased bilirubin
Normoblastic erythroid hyperplasia in bone marrow
Increased LDH
M:E decreased Increased urobilinogen
Increased expired CO
Hemoglobinemia*
Hemoglobinuria*
Hemosiderinuria*
*Only with intravascular hemolysis
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Diagnostic Approach to Hemolytic Anemias
Increased RBC ProductionIncreased RBC Destruction
COOMBS (DAT) test
Immune Hemolytic Anemias
Peripheral blood smearRBC Morphology
Lab Investigation
Definitive Diagnosis
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Clinical Findings
• Jaundice• Pallor• Fatigue• Cardiac symptoms• Gallstones• Dark or red urine• Splenomegaly
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Sites of Destruction
• Intravascular– Hemolysis occurs within the circulation– RBC’s are severely damaged
• Extravascular– Hemolysis occurs within the macrophages of the
spleen, liver or bone marrow– More common than intravascular
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Intravascular Destruction
1. RBC is hemolyzed2. Free hgb released into plasma3. Hgb binds to haptoglobin
– If haptoglobin depleted, hemopexin can step in
4. This complex goes to liver 5. Complex converted to bilirubin6. Bilirubin excreted to intestinal
tract
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Terms
1. Hemoglobinemia– Occurs if hemopexin and haptoglobin is depleted.
Free hgb circulates in blood.2. Hemoglobinuria– Occurs if free hgb can not be absorbed by the
liver and kidney3. Hemosiderinuria• Hemosiderin in the urine, sign of filtration of
hemoglobin thru the kidney
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Causes ofIntravascular Hemolysis
Activation of Complement on RBC Membrane
Physical or Mechanical Trauma to the RBC
Toxic Microenvironment of the RBC
Paroxysmal noctural hemoglobinuria
Microangiopathic hemolytic anemia
Bacterial infections
Paroxysmal cold hemoglobinuria
Abnormalities of heart vessels
Plasmodium falciparum infection
Some transfusion reactions Disseminated intravascular coagulation
Venoms
Some autoimmune hemolytic anemias
Thermal injury
Acute drug reaction in G6PD deficiency
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Extravascular Destruction
1. Hgb is degraded within the phagocyte to heme and globina. Phagocyte locations:• Spleen: removes slightly damaged RBCs• Liver: removes severely damaged RBCs• Bone marrow: remove mature precursor cells that are
intrinsically abnormal
2. Heme further degraded to iron, biliverdin and carbon monoxide
3. Biliverdin enters plasma as bilirubin4. Bilirubin binds to albumin, excreted by the liver
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Causes of Extravascular Hemolysis
Origin Anemias
Inherited RBC Defects Thalassemia, Hemoglobinopathies, Enzyme deficiencies, Membrane disorder
Acquired RBC Defects Megaloblastic anemia, Vitamin E deficiency in newborns
Immunohemolytic anemias Autoimmune, Drug induced, Some transfusion reactions
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Source of Defect of RBC
• Intrinsic – Abnormality of the RBC• Membrane• Cell enzymes• Hemoglobin molecule
– Usually hereditary• EXCEPTION: Acquired
– Paroxysymal noctural hemoglobinuria (PNH)
– Site of hemolysis: extravascular
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Source of Defect of RBC
• Extrinsic– Antagonist in cell’s environment causes injury to
the RBC• Antagonistic plasma factors• Traumatic physical cell injury• Immune mediated cell destruction
– RBC is normal– Usually acquired– Site of hemolysis: intra or extravascular
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Referenes
• Harmening, D. M. (2009). Clinical Hematology and Fundamentals of hemostasis (5th ed.). Philadelphia, PA: F.A. Davis Company.
• McKenzie, S. B. (2010). Clinical Laboratory Hematology (2nd ed.). Upper Saddle River, NJ: Pearson Education, Inc..