Professional Documents
Culture Documents
ANEMIA IN CHILDHOOD
Irwin, 2001
Hermiston,Mentzer, 2002
Anemia
• Reduction in the hemoglobin concentration,
hematocrit, or number of RBC per cubic
milimeter.
• WHO criteria:
Age Hb below (g/dL) Ht below
(%)
6 mos-5 yrs 11 33
12 – 18 yrs 12 36
Normal Erythropoiesis
Erythroid marrow maturation
RBC precursor maturation proceeds through a series of morphologically distinct stages. Identifiable populations in
this maturation sequence include pronormoblast; basophilic, polychromatic and orthochromatic normoblasts; and
the marrow reticulocytes. With development, there is a progressive reduction in cell size, a shrinkage of the cell’s
nucleus, a loss of cellular mitochondria and RNA, and a dramatic increase in hemoglobin. Specific red blood cell
disorders can be identified from disruption in this normal maturation sequence.
Etiology of anemia
Clinical approach to diagnosis
Hermiston,Mentzer 2003
….clinical approach to diagnosis (2)
Signs and symptoms vs
diseases
Diseases Pallor Bleeding Organomegaly
IDA + - -
Acute hemolytic anemia + - -/+
Aplastic anemia + + -
Hemorrhage anemia +/++ + -
Chronic hemolytic anemia/thal + - +
Acute leukemia + + -/+
Hypersplenisme + + +
Liver disease + + -/+
Metastatic tumor + -/+ -/+
Chronic infection + - -
Initial evaluation
Wintrobe’s 2007
Laboratory
Refining the differential diagnosis of anemia:
Use of the
CBC
RBC indices (MCV,MCH,MCHC, RDW)
Reticulocyte count
Blood smear
History and physical examination
Irwin 2001
Rossbach 2005
Wintrobe’s 2007
microcytic anemia....
IDA:
• Peak prevalence: late infancy, early childhood,
adolescence
• Etiology: rapid body growth, low levels of dietary iron,
menstrual blood loss (females)
• Th/ trial of oral iron initial diagnostic test evaluation :
▫ Response (+)
Reticulocyte count ↑ in 5-10 days
Hb ↑ by 1 g/dl/month
▫ Response (-)
Poor compliance, poor absorption, incorrect diagnosis, etiology
still persist
microcytic anemia......
absent present
increased
low normal
Medication
Liver/thyroid disease
Hemolysis
Hemorrhage idiopathic
deficiency
Hyperslenisme No Aplastic
anemia BMA
Wintrobe’s 2007
Management approach
• Depend on the underlying disease
• Emergency: Hb ≤ 5 g/dl give PRC transfusion 5
ml/kg/BW/X, then 10-15 ml/kg BW/X
• The rules: ∆ Hb X BW X 4
• Transfusion are given in multiple small volumes,
separated by several hours