1. Is the patient anemic?
- Hgb < 12 g/dL, Hct < 37% in females, Hgb < 14 g/dL, Hct < 42% in males
2. Is this anemia acute or chronic?
3. Is this dilutional anemia?(hematocrit)
4. What is the size of the RBC? (MCV)
5. Is body appropriately responding? (reticulocyte count)
6. What does the peripheral blood smear show?
MCV < 80
(hypochromic)
|
normocytic (normochromic)
low reticulocytes
|
normocytic
high reticulocytes
|
MCV > 100
|
Fe deficiency
Anemia of chronic disease (ACD)
|
chronic liver disease
thalassemia trait
liver disease
megaloblastic
marrow failure (pancytopenia)
myelodysplasia
leukemia
alcohol
myeloma
hypothyroidism
mets
infection
|
blood loss
hemolysis
|
lead overload
renal failure (uremia)
B12 lack
sideroblastic
endocrine (thyroid)
folate lack
ACD
hematinic lack
drugs
|
- Fe deficiency - ↓ ferritin, ↑ TIBC
- < 15 confirms, 15 - 25 suggests, 25 - 100 not helpful, > 100 rules out
- Anemia of chronic disease (ACD)
- associated with inflammation (RA, infection, carcinoma)
- ↓ TIBC (Fe not transferred to developing RBCs)
- Thalassemia
- target cells, serum electrophoresis (↑ HbgA2)
- Lead poisoning - ↑ serum Pb
- Sideroblastic - ↑ in cellular iron uptake
- ↑ ferritin, ring sideroblasts
- megaloblastic anemia - hypersegmented polymorphonucleocytes(PMNs)
- defects in DNA synthesis that lead to hematologic abnormalities
- ↓ folate or ↓ vit B12
- drugs: methotrexate, azathioprine (Imuran - immunosuppressant)
- myelodysplasia
- dimorphic smear (micro/macrocytosis)
- Hemolysis
- hypersplenism, drugs, sepsis, autoimmune
- cell morphology (from peripheral smear) is crucial: see below
- ↑ LDH, ↑ bilirubin, ↑ serum Hbg, ↓ haptoglobin (Hgb scavenger), + Coombs
- bone marrow failure
- pancytopenia (↓ WBC, ↓ plt)
- BM aspirate (cell morphology), BM biopsy (structure)
- Increased
- iron deficiency
- duel deficiency (fe, folate)
- pernicious anemia
- liver disease
- AIHA
- normal: biconcave
- spherocyte - immune hemolytic anemia
- schistocytes - MAHA: DIC, vasculitis, prosthetic heart valves, HUS/TTP
- sickle cell - sickle cell disorders
- target cell - liver disease, thalassemia, Fe deficiency
- teardrop cell - myelofibrosis
- rouleaux formation - aggregates of RBC resembling stacks of coins
- paraprotein (multiple myeloma)
- nuclei (immature RBC)
- serious medical disease
- severe anemia, leukemia, bone marrow metastases
- Heinz bodies (denatured hemoglobin)
- Howell-Jolly bodies
- post-splenectomy, hyposplenism
- basophilic stippling (blue granulations of variable size and number, aggregation of ribosomes)
- lead intoxication, thalassemia