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1-CBC Interpretation

This document provides guidance on interpreting complete blood count (CBC) results. It discusses how to safely interpret a CBC by looking at hemoglobin, white blood cell, and platelet counts initially. It then provides details on classifying and diagnosing various types of anemia based on mean corpuscular volume. Other sections cover approaches to thrombocytopenia, thrombocytosis, neutropenia, leukopenia, and pancytopenia. Case studies are presented to demonstrate CBC interpretation for conditions like iron deficiency anemia, thalassemia, kidney disease, B12 deficiency, and polycythemia.
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0% found this document useful (0 votes)
111 views10 pages

1-CBC Interpretation

This document provides guidance on interpreting complete blood count (CBC) results. It discusses how to safely interpret a CBC by looking at hemoglobin, white blood cell, and platelet counts initially. It then provides details on classifying and diagnosing various types of anemia based on mean corpuscular volume. Other sections cover approaches to thrombocytopenia, thrombocytosis, neutropenia, leukopenia, and pancytopenia. Case studies are presented to demonstrate CBC interpretation for conditions like iron deficiency anemia, thalassemia, kidney disease, B12 deficiency, and polycythemia.
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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CBC interpretation

CBC interpretation objectives

 Safe CBC interpretation

 Approach to Anemia

 Diagnosis and highlight about polycythemia

 Diagnosis and highlight about thrombocytopenia

 Diagnosis and highlight about Thrombocytosis

 Diagnosis and highlight about neutropenia and leukopenia.

 Diagnosis and highlight about Pancytopenia

 The major components of CBC are:

1-Hb2-WBC3-plateltes

If all major components are normal, then it is very less likely you miss a serious disease.

 Safe CBC interpretation:


1- look at Hb>>if low >> look at other major components (WBCs and Platelets) to not miss a
bone marrow disease.
2- if there is no striking abnormality of WBC and platelet then check MCV to classify the anemia
into microcytic, normocytic or macrocytic.
3- some references recommend to check reticulocyte before MCV to not miss hemolytic anemia
but not practical.
Anemia
 Anemia Classification based on MCV:

 Helpful parameters to diagnose the underlying cause of anemia


 Size of red blood cells (MCV): (small/ normal/ big)
 Abnormal cells on microscopic examination (like blast cells in leukemia)
 Status of leukocytes and platelets (bone marrow function)
 Reticulocyte count (ability of marrow to respond to anemia)>> can help in hemolytic
anemia (if high) and in marrow suppression (if low).
 Evidence of destruction(hemolysis) >> (elevated LDH and indirect bilirubin)

o Microcytic anemia

 features might help in distinguishing between IDA and Thalassemia

feature IDA Thalassemia


RBC Low, Low normal High, High normal
MCV Mild to moderate low Very low (< 70)
(most likely above 70)
RDW Mostly High Mostly normal
Mentzer index: MCV/RBC > 13 < 13
IDA treatment

NOTE: Consider upper and lower GI endoscopy for any males (esp. elderly) and postmenopausal
women to R/O GI malignancy

 How much Hb increment is excepted with treatment?


-Around 2 to 4 g/dLevery three weeks.
(if Hb increased in slower rate >> check for ongoing bleeding??
 How long the treatment course is expected?
-Oral Fe TID (or less if not tolerated)
(around 6 weeks to correct anemia; and 6 months to replete Fe stores)

 Case: A 25 year- old lady, presented with 2 months H/O dizziness and fatigue

WBC .........................7. 0 4 – 11 x10.e9/L


RBC ......................... 3.7 L 4.2 – 5.5 x10.e12/L
HGB ........................ 90 L 120 – 160 g/L
HCT ......................... 28 L 42 – 52 %
MCV ....................... 73 L 80 – 94 fl
MCH .................. ......23.6 L 27 – 32 pg
MCHC ................. ... 320 320 – 360 g/L
RDW .................. ......15.8 H 11.5 – 14.5 %
PLT .................. ....... 330 140 – 450 x10.e9/L

Interpretation: Hypochromic microcytic anemia, Most likely: IDA

NOTE: Generally, The Hb threshold for blood transfusion for asymptomatic patient is <70 g/L
- - - - - - - - - - - - - - - - - - - -
 Case: A 29 years old female came for premarital checkup:

WBC .........................7. 0 4 – 11 x10.e9/L


RBC ......................... 5.3 L 4.2 – 5.5 x10.e12/L
HGB ........................ 101 L 120 – 160 g/L
HCT ......................... 40 L 42 – 52 %
MCV ....................... 62 L 80 – 94 fl
MCH .................. ......25.3 L 27 – 32 pg
MCHC ................. ... 320 320 – 360 g/L
RDW .................. ......14.1 11.5 – 14.5 %
PLT .................. ....... 339 140 – 450 x10.e9/L

interpretation: Hypochromic microcytic anemia, Most likely: Thalassemia


-What you will order to confirm Dx?
Hemoglobin electrophoresis (HE).

-What do you expect in HE?


If HB A2 is > 3.5 >>> B-Thalassaemia Minor
If HB A2 is normal >>> alpha Thalassaemia Minor

o Normocytic anemia
DDxof normocytic anemia:
 Anemia of chronic inflammation or disease like:
1. Chronic kidney disease
2. autoimmune disorders
3. chronic infection
4. malignancy.
5. Combined Macrocytic and microcytic anemia in the same time.

Case : A 44 years old gentleman k\c of CKD , c.o generalized weakness:


WBC .........................8.5 4 – 11 x10.e9/L
RBC ......................... 5.1 L 4.2 – 5.5 x10.e12/L
HGB ........................ 107 L 120 – 160 g/L
HCT ......................... 41 L 42 – 52 %
MCV ....................... 88 80 – 94 fl
MCH .................. ......29 27 – 32 pg
MCHC ................. ... 340 320 – 360 g/L
RDW .................. ......14.1 11.5 – 14.5 %
PLT .................. ....... 339 140 – 450 x10.e9/L

Creatinine :……………188 H 53-106 μmol/L


Urea :……………………..7 2.5 to 7.1 mmol/L
eGFR: 34 mL/min/1.73 m2

interpretation: normocytic normochromic anemia, Most likely: secondary to chronic kidney


disease
o MACROCYTIC ANEMIAS

 Megaloblastic :
• Vitamin B12 deficiency
• Folate deficiency
 Non-megaloblastic:
• Liver disease, Myelodysplastic syndrome, Increased reticulocyte count ,
Alcoholism >>> :BM suppression &macrocytosis independent of folate/B12 deficiency.or
liver cirrhosis

Case: 38 years old gentleman post gastric bypass, c.o fatigue

WBC .........................6.5 4 – 11 x10.e9/L


RBC ......................... 5.3 4.2 – 5.5 x10.e12/L
HGB ........................ 109 L 120 – 160 g/L
HCT ......................... 41 L 42 – 52 %
MCV ....................... 99 H 80 – 94 fl
MCH .................. ......42 H 27 – 32 pg
MCHC ................. ... 340 320 – 360 g/L
RDW .................. ......14.1 11.5 – 14.5 %
PLT .................. ....... 339 140 – 450 x10.e9/L

Interpretation: Macrocytic hyperchromic anemia, could be secondary to Vit b12 deficiency

 What you will order for this patient?


Vit b12 and folate level.
Hemolytic anemia:
hemolytic anemia is suspected in a patient with chronic or new onset anemia with
reticulocytosis and not due to another obvious cause.

Case: 17 years old girl, c.o yellowish discoloration of skin and dark urine.
CBC
WBC ....... ..10.5 4 – 11 x10.e9/L
RBC .......... 4.9 4.2 – 5.5 x10.e12/L
HGB ........ 92 L 120 – 160 g/L
HCT ............ 36 L 42 – 52 %
MCV .......... 86 80 – 94 fl
MCH ............29 27 – 32 pg
MCHC ........ 352 320 – 360 g/L
RDW ..........14.3 11.5 – 14.5 %
PLT ............ 223 140 – 450 x10.e9/L

LFT:

Total bilirubin …………………..… 48 H (3- 17 umol/L)


Direct bilirubin ...................... 4 (0 – 5 umol/L)
Total protein ……………….. 73 (60-80 g/L)
Albumin ……………………………….38 (35-50 g/L)
Alkaline phosphatase …………...55 (50-136u/L)
Alanine aminotransferase ……40 (20-65 u/L)
Aspartate aminotransferase ...22 (10-31 u/L)
G.G. Transferase ………………….40 (5-55 u/L)
Interpretation: anemia (normocytic) associated with high indirect bilirubin.
What you will order?
Reticulocyte>> excepted to be high > 4%, LDH expected to be high and Haptoglobin expected to
be low.

Main DDx of high indirect bilirubin:


Blood Hemolysis,Gilbert's syndrome and Crigler–Najjarsyndrome( mainly in neonate).

Some Causes of hemolytic anemia :


Sickle cell anemia
G6PD
Thalassemia
Drugs
Autoimmune diseases
Polycythemia:

Polycythemia is a laboratory finding in which there is an increased number of red blood


cells (RBC), along with an accompanying increase in the concentration of hemoglobin in
the peripheral blood.

 It could be primary (polycythemia vera) or secondary (in response to hypoxia)

Case: 37 years old lady c.o headache and plethora of face.


WBC .........................17.6 H4 – 11 x10.e9/L
RBC ......................... 7.2 H 4.2 – 5.5 x10.e12/L
HGB ........................ 19.3 H120 – 160 g/L
HCT ......................... 59 L 42 – 52 %
MCV ....................... 91 80 – 94 fl
MCH .................. ......30 27 – 32 pg
MCHC ................. ... 340 320 – 360 g/L
RDW .................. ......14.1 11.5 – 14.5 %
PLT .................. ....... 339 140 – 450 x10.e9/L

 What is the most important test to approach polycythemia?


-erythropoietin
 Low erythropoietin >> most likely primary polycythemia (polycythemia Vera)
 High erythropoietin >> most likely secondary polycythemia (smoking, COPD, high
altitude congestive heart failure ..)
Polycythemia Vera sometimes combined with high WBC and/or platelet.
Thrombocytosis:

Case: A 48 years old lady c.o leg redness and hotness (cellulitis)

WBC .........................6.5 4 – 11 x10.e9/L


RBC ......................... 5.3 4.2 – 5.5 x10.e12/L
HGB ........................ 132 120 – 160 g/L
HCT ......................... 45 42 – 52 %
MCV ....................... 88 80 – 94 fl
MCH .................. ......31 27 – 32 pg
MCHC ................. ... 340 320 – 360 g/L
RDW .................. ......14.1 11.5 – 14.5 %
PLT .................. ....... 521 H140 – 450 x10.e9/L

Interpretation: Thrombocytosis, Most likely reactive based on Hx

 patients with elevated platelet counts, the initial diagnostic question is whether their
thrombocytosis is
1. reactive phenomenon (infection, post-surgery or Trauma..)
or
2. a marker for the presence of a hematologic disorder (chronic myeloproliferative
neoplasms...).

Thrombocytopenia
WBC .........................9.2 4 – 11 x10.e9/L
RBC ......................... 5.1 4.2 – 5.5 x10.e12/L
HGB ........................ 14.2 120 – 160 g/L
HCT ......................... 46 42 – 52 %
MCV ....................... 91 80 – 94 fl
MCH .................. ......30 27 – 32 pg
MCHC ................. ... 340 320 – 360 g/L
RDW .................. ......14.1 11.5 – 14.5 %
PLT .................. ....... 92 L140 – 450 x10.e9/L

 Thrombocytopenia (ie, platelet count <150,000/microL [150 x 109/L])


 Severe spontaneous bleeding is most likely with platelet counts <20,000 to 30,000/microL,
especially below 10,000/microL.
 Surgical bleeding generally may be a concern with platelet counts <50,000/microL
 DDx is wide and including bone marrow malignancy.
Leukopenia and neutropenia:

Case: A 17 y old gentleman k/c of AML on chemotherapy c.o Fever

 We classify neutropenia based on NEU# (Absolute NeutrophilCount) not NEU% (Neutrophil


percentage)
 Leukopenia = low WBCs
 Neutropenia = low absolute neutrophils count (ANC)
 Leukopenia Neutropenia
 Febrile Neutropenia is a medical emergency
 Neutropenia classification is based on Absolute Neutrophil count (ANC)
 Mild < 1.5 K/uL ( 1500 cells / MicroL)
 Moderate <1.0 K/uL (1000 cells / MicroL)
 Sever < 0.5 K/uL ( 500 cells / MicroL)
Pancytopenia:

Case: 19 years old lady c.o weakness

WBC ............2.8 L 4 – 11 x10.e9/L


RBC ........... 3.2 4.2 – 5.5 x10.e12/L
HGB ............. 92L 120 – 160 g/L
HCT ............ 36 L 42 – 52 %
MCV .......... 86 80 – 94 fl
MCH ........... 29 27 – 32 pg
MCHC ........ 352 320 – 360 g/L
RDW ........ 14.3 11.5 – 14.5 %
PLT ............ 76 L140 – 450 x10.e9/L

 What are the common causes pancytopenia?


 Bone marrow malignancy
 Viral infection
 Drug induced
 Autoimmune disease

Usually a careful management is warranted in such case.

Good luck

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