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Approach to Anemia
Hb < 13 M ; < 12 F
Pathophysiology
↓ O2 delivery-
Fatigue, DOE, S/S Hyperdynamic state (Bounding pulse)
palpitation
Severe cases - Lethargy, confusion, CCF, Angina, Arrhythmia,
AMI
Vol depletion –
Easy fatigability, Lassitude, Muscle cramps
Postural dizziness, lethargy, syncope, ↓ BP, Shock, Death
Normal peripheral blood smear
High power view of a normal peripheral blood smear. Several platelets (black arrows) and a normal
lymphocyte (blue arrow) can also be seen. The red cells are of relatively uniform size and shape.
The diameter of the normal red cell should approximate that of the nucleus of the small
lymphocyte; central pallor (red arrow) should equal one-third of its diameter.
Causes – Kinetic approach → ↓ RBC production
↑ RBC destruction
Morphologic approach
↓ Effective RBC production
1.Lack of nutrients B12, Fe
2.Marrow disorders→
-- ↓RBC precursors – AA, Pure RBC aplasia, Marrow
infiltration
-- Marrow supression – Drugs, chemo, irradiation
3.Low level of Trophic hormones- EPO
4. Infection, inflammation or malignant disorder
↓ availability of Iron ↓absorption from GIT
↓ release of Iron from macrophages
↓ Level of EPO
5. Ineffective erythropoiesis – Megaloblastic, α and β Thal,
MDS, Sideroblastic anemia
↑ Destruction of circulating RBC
Inherited Hemolytic anemia – Hereditary Spherocytosis, SCD,
Thal major
Acquired Hemolytic anemia- Autoimmune Coombs positive
HA, TTP, Malaria,
Enlarged spleen – Hypersplenism, PNH
Morphologic approach
Macrocytic – MCV > 100ft
Folate, B12 deficiency
Drugs – Zidovidine, Hyroxyurea
MDS, Acute Leukemia
Alcohol Liver Disease
Microcytic MCV < 80 ft
↓ Iron availability
Inflammation,
↓ cu
Acquired – Lead, sideroblastic
↓ Globin prodn – Thal , Hbpathies
Microcytic hypochromic red cells in iron deficiency anemia
Peripheral smear at two different magnifications from a patient with iron deficiency shows small (microcytic) red
cells with a thin rim of pink hemoglobin (hypochromic); occasional "pencil" shaped cells are also present. Normal
red cells are similar in size to the nucleus of a small lymphocyte (arrow) and central pallor should equal about one-
third of its diameter; thus, many hypochromic and microcytic cells are present in this smear.
Normocytic – MCV 80 to100 ft
Systemic disorders
CKD
Cardio renal syndrome
Cancer Associated
IDA - ↓ Ferritin, ↑ TIBC, ↓ S iron
α or β Thal minor – Minimum anaemia, F/H Negative
splenomegaly
PS shows - Microcytic Hypochromic, Target, Tear Drop,
Basophil Stippling
↑ RBC count, Iron stores Normal or ↑ , Hb A2 ↑
Inflammation - ↓ Fe, ↓ TIBC, Ferritin – N
Beta thalassemia trait
Peripheral smear from a patient with beta thalassemia trait. The field shows numerous hypochromic and microcytic
red cells (thin arrows), some of which are also target cells (blue arrows).
Teardrop-shaped red blood cells (dacrocytes)
This peripheral smear from a patient with bone marrow fibrosis shows numerous teardrop-shaped red cells
Evaluation – Is patient bleeding now or past
Evidence of ↑ RBC destn (Intra /
Extra Vasc)
Is bone marrow suppressed
Is patient Iron deficient
Deficient in Folate or Vit B12
History
Recent loss of appetite, Weight loss, fever, night
sweats ,
Tarry stool
Drugs Aspirin, NSAID
H/o Transfusion, liver disease
Physical Examination
↑ HR, ↑ RR, Fever, Postural ↓ BP
Jaundice, Pallor (palm, nail bed, face, conjunctiva)
LN, Hepatosplenomegaly
Bone(Sternum) tender – (Infilt- CML, MM)
Laboratory
RBC indices –
MCV 80- 100; > 115 – B12/FA
MCH 27.5-33.2 ; ↓ IDA
Thal:↑Macrocytosis
MCHC 31-33 ↓ like MCV, MCH:
↑ cong / Acq Spherocytosis
Reticulocytes
↑ - Hemolysis / Blood loss
↓ - Reduced marrow ; ↓ Response to anaemia
↓ Retic count + Pancytopenia – AA
↓ Retic count + Normal WBC, Platelets – Pure RBC
aplasia
WBC
↓ TLC – AA, Marrow suppression, Hypersplenism ↓
B12
↑ TLC- Infection, Inflammation, Carcinoma
DLC - ↑ Polymorphs- Infect
↓ Abs Lymphocytes - HIV / Following steroid
Peripheral smear
Hypersegmented neutrophils-
> 5% with 5 lobes or >1 Polymorph with > 6 Lobes
Megaloblastic blood picture
Peripheral blood smear showing a hypersegmented neutrophil (seven lobes) and macroovalocytes, a pattern that
can be seen with cobalamin or folate deficiency.
THAT’S ALL FOR TODAY…….
Hemolysis – Retic, Abnormal shape, ↑ LDH, ↑ Indirect
Bilirubin, ↓ Heptoglobin
↑ LDH, ↓ Hepto- 90% specific for diagnosis; NLDH + > 25
Hepto 92% sens to rule out
Intravasc Hemolysis – Plasma, Urine Hb, Urinary
hemosidrin PNH
Marrow - ↑Retic – Erythroid Hyperplasia
↓Retic Erythroid Hyperplasia Ineffective
erylhropoiesis
Indication – Pancytopenia, blast cells → AA,
MDS, Marrow replacement
Myeloprolifn
Hemolytic – Intra / Extra corpuscular defect
Intravasc – Direct trauma – March Hguria
Sheer stress – Mech Heart Valve
Heat – Thermal burn
Complement induced lysis Parox cold Hburia
Osmotic – Hypotonic soln
Bact toxin , ↑ Cu
Approach- Rapid onset pallor
Jaundice - ↑ Indurest Bilirubin
Pigmentory gall stone
Splenomegaly, spherocytosis
↑ LDH, ↓ Heploglobin
Coomb +, ↑ Retic

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Approach to anemia

  • 1. Approach to Anemia Hb < 13 M ; < 12 F
  • 2.
  • 3. Pathophysiology ↓ O2 delivery- Fatigue, DOE, S/S Hyperdynamic state (Bounding pulse) palpitation Severe cases - Lethargy, confusion, CCF, Angina, Arrhythmia, AMI Vol depletion – Easy fatigability, Lassitude, Muscle cramps Postural dizziness, lethargy, syncope, ↓ BP, Shock, Death
  • 4. Normal peripheral blood smear High power view of a normal peripheral blood smear. Several platelets (black arrows) and a normal lymphocyte (blue arrow) can also be seen. The red cells are of relatively uniform size and shape. The diameter of the normal red cell should approximate that of the nucleus of the small lymphocyte; central pallor (red arrow) should equal one-third of its diameter.
  • 5. Causes – Kinetic approach → ↓ RBC production ↑ RBC destruction Morphologic approach
  • 6. ↓ Effective RBC production 1.Lack of nutrients B12, Fe 2.Marrow disorders→ -- ↓RBC precursors – AA, Pure RBC aplasia, Marrow infiltration -- Marrow supression – Drugs, chemo, irradiation 3.Low level of Trophic hormones- EPO
  • 7. 4. Infection, inflammation or malignant disorder ↓ availability of Iron ↓absorption from GIT ↓ release of Iron from macrophages ↓ Level of EPO 5. Ineffective erythropoiesis – Megaloblastic, α and β Thal, MDS, Sideroblastic anemia
  • 8. ↑ Destruction of circulating RBC Inherited Hemolytic anemia – Hereditary Spherocytosis, SCD, Thal major Acquired Hemolytic anemia- Autoimmune Coombs positive HA, TTP, Malaria, Enlarged spleen – Hypersplenism, PNH
  • 9. Morphologic approach Macrocytic – MCV > 100ft Folate, B12 deficiency Drugs – Zidovidine, Hyroxyurea MDS, Acute Leukemia Alcohol Liver Disease
  • 10. Microcytic MCV < 80 ft ↓ Iron availability Inflammation, ↓ cu Acquired – Lead, sideroblastic ↓ Globin prodn – Thal , Hbpathies
  • 11. Microcytic hypochromic red cells in iron deficiency anemia Peripheral smear at two different magnifications from a patient with iron deficiency shows small (microcytic) red cells with a thin rim of pink hemoglobin (hypochromic); occasional "pencil" shaped cells are also present. Normal red cells are similar in size to the nucleus of a small lymphocyte (arrow) and central pallor should equal about one- third of its diameter; thus, many hypochromic and microcytic cells are present in this smear.
  • 12. Normocytic – MCV 80 to100 ft Systemic disorders CKD Cardio renal syndrome Cancer Associated
  • 13. IDA - ↓ Ferritin, ↑ TIBC, ↓ S iron α or β Thal minor – Minimum anaemia, F/H Negative splenomegaly PS shows - Microcytic Hypochromic, Target, Tear Drop, Basophil Stippling ↑ RBC count, Iron stores Normal or ↑ , Hb A2 ↑ Inflammation - ↓ Fe, ↓ TIBC, Ferritin – N
  • 14. Beta thalassemia trait Peripheral smear from a patient with beta thalassemia trait. The field shows numerous hypochromic and microcytic red cells (thin arrows), some of which are also target cells (blue arrows).
  • 15. Teardrop-shaped red blood cells (dacrocytes) This peripheral smear from a patient with bone marrow fibrosis shows numerous teardrop-shaped red cells
  • 16.
  • 17. Evaluation – Is patient bleeding now or past Evidence of ↑ RBC destn (Intra / Extra Vasc) Is bone marrow suppressed Is patient Iron deficient Deficient in Folate or Vit B12
  • 18. History Recent loss of appetite, Weight loss, fever, night sweats , Tarry stool Drugs Aspirin, NSAID H/o Transfusion, liver disease
  • 19. Physical Examination ↑ HR, ↑ RR, Fever, Postural ↓ BP Jaundice, Pallor (palm, nail bed, face, conjunctiva) LN, Hepatosplenomegaly Bone(Sternum) tender – (Infilt- CML, MM)
  • 20. Laboratory RBC indices – MCV 80- 100; > 115 – B12/FA MCH 27.5-33.2 ; ↓ IDA Thal:↑Macrocytosis MCHC 31-33 ↓ like MCV, MCH: ↑ cong / Acq Spherocytosis
  • 21. Reticulocytes ↑ - Hemolysis / Blood loss ↓ - Reduced marrow ; ↓ Response to anaemia ↓ Retic count + Pancytopenia – AA ↓ Retic count + Normal WBC, Platelets – Pure RBC aplasia
  • 22. WBC ↓ TLC – AA, Marrow suppression, Hypersplenism ↓ B12 ↑ TLC- Infection, Inflammation, Carcinoma DLC - ↑ Polymorphs- Infect ↓ Abs Lymphocytes - HIV / Following steroid
  • 23. Peripheral smear Hypersegmented neutrophils- > 5% with 5 lobes or >1 Polymorph with > 6 Lobes
  • 24. Megaloblastic blood picture Peripheral blood smear showing a hypersegmented neutrophil (seven lobes) and macroovalocytes, a pattern that can be seen with cobalamin or folate deficiency.
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  • 31. THAT’S ALL FOR TODAY…….
  • 32.
  • 33. Hemolysis – Retic, Abnormal shape, ↑ LDH, ↑ Indirect Bilirubin, ↓ Heptoglobin ↑ LDH, ↓ Hepto- 90% specific for diagnosis; NLDH + > 25 Hepto 92% sens to rule out Intravasc Hemolysis – Plasma, Urine Hb, Urinary hemosidrin PNH
  • 34. Marrow - ↑Retic – Erythroid Hyperplasia ↓Retic Erythroid Hyperplasia Ineffective erylhropoiesis Indication – Pancytopenia, blast cells → AA, MDS, Marrow replacement Myeloprolifn
  • 35. Hemolytic – Intra / Extra corpuscular defect Intravasc – Direct trauma – March Hguria Sheer stress – Mech Heart Valve Heat – Thermal burn Complement induced lysis Parox cold Hburia Osmotic – Hypotonic soln Bact toxin , ↑ Cu
  • 36. Approach- Rapid onset pallor Jaundice - ↑ Indurest Bilirubin Pigmentory gall stone Splenomegaly, spherocytosis ↑ LDH, ↓ Heploglobin Coomb +, ↑ Retic