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By Dr. Ahmed Azhad
Moderator: Dr. Zubair
2nd July 2012
 Definition
 Anemia – The World Health Organisation
defines anemia as a hemoglobin level < 130
g/L (13g/dL) in men and <120g/L (12g/dL)
in women.
 The critical elements of erythropoesis are
used for the initial classification of anemia.
 EPO production
 Iron availability
 Proliferative capacity of the bone marrow
 Effective maturation of red cell precursors
http://www.oncoprof.net/Generale2000/g09_Chimiotherapie/Complements/g09-gb_comp56.html
 Often found during routine screening
 Acute blood loss – Hb/HCT does not reflect
the volume of blood loss
◦ Mild – No symptoms. Enhanced oxygen delivery by
changes in pH and increased CO2
◦ 10-15% - hypotension and decreased organ
perfusion
◦ >30% - postural hypotension, tachycardia
◦ >40% - hypovolemic shock: confusion, dyspnoea,
diaphoresis
 Acute hemolysis
◦ Intravascular hemolysis: acute back pain, free
hemoglobin in plasma and urine, renal failure
 Moderate anemia
◦ Fatigue
◦ Loss of stamina
◦ Breathlessness
◦ Tachycardia on physical exertion
◦ Symptoms may not appear in young, healthy
patients until hemoglobin is 7-8 g/dL
 Diseases in which patient presents with
anemia
◦ Infections
◦ Rheumatoid Arthritis
◦ Cancer
◦ Lymphoproliferative disorders (CLL, B cell
neoplasm)
 Anemia – a major sign of disease
 Evaluation by History:
◦ Symptoms of known diseases causing anemia:
 Gastric ulceration
 Rheumatoid arthritis
 Renal failure
◦ Duration of symptoms:
 Hemoglobinopathies in longer duration
◦ Treatment history
 Medications for pain, hematinics
◦ Nutritional history
◦ Physical examination
 Build, nourishment
 Signs of disease
 Vitals – fever, tachycardia, blood pressure
 Pallor
 Jaundice
 Lymphadenopathy
 Bone tenderness
 Petechiae
 CVS: Flow murmurs
 RS: Dyspnoea
 Abdomen: Splenomegaly
 Hb, Hematocrit
 RBC count
 MCV (Hct x 10 / RBC x 106) [ 90±8 fl ]
 MCH (Hb x 10 / RBC x 106) [ 30 ± 3 pg ]
 MCHC (MCH/MCV) [ 33 ± 2 % ]
 Reticulocyte count
 Indices vary with age, gender and pregnancy
 WBC count including differential count, neutrophil
segment count
 Platelet count
 Cell size
 Hb content
 Anisocytosis
 Poikilocytosis
 Polychromasia
 Gives clues to
specific disorders
Normal peripheral smear
Severe Iron defeciency
anemia
Anisocytosis (size), Poikilocytosis (shape)
Macrocytosis
Macrocytes, Ovalocytes
Myelofibrosis
Tear drop shaped cells, nucleated cells
Thallassemia
Target cells
Howell-Jolly bodies
Red cell fragmentation
Uremia Spur cells
 A reliable measure of red cell production
 Patient’s reticulocyte is compared with
expected reticulocyte counts
 In established anemia, reticulocyte count of
less than two-three times is an inadequate
marrow response
 Reticulocyte correction needs to be done for
anemia (1)
 And shift cells (2), If polychromatophilic cells are not
seen on the blood smear, the second correction is not
required.

 Premature release of recticulocytes are due to
EPO stimulation
 Severe chronic hemolytic anemia – RPI
increases upto six to sevenfold. Confirms
appropriate response to EPO, normal
functioning marrow and iron availability
 If reticulocyte production index < 2, suggests
a defect in marrow proliferation or maturation
 Serum Iron: 50–150 µg/dL
 TIBC: 300–360 μg/dL
 Serum ferritin (also an acute phase reactant)
◦ 15-20 µg/dL – Lack of Iron stores
◦ Women: ~30 µg/dL
◦ Men: ~ 100 µg/dL
◦ 200 µg/dL – adequate iron stores
 Serum Transferrin saturation: 25-50%
 Marrow aspirate
◦ M/E ratio
◦ Cell morphology
◦ Iron stain
 Marrow biopsy
◦ Cellularity
◦ Morphology
 Required in patients with normal iron status
with hypoproliferative anemia
 Can be used to diagnose primary bone
marrow diseases: myelofibrosis, infiltrative
diseases
Hematocrit Production
Index
Reticulocytes (incl.
corrections)
Marrow M:E
ratio
45 1.0 1 3:1
35 2.0-3.0 4.8%/3.8/2.5 2:1 – 1:1
25 3.0-5.0 14%/8/4.0 1:1 – 1:2
15 3.0-5.0 30%/10/4.0 1:1 – 1:2
 Can be stained to confirm iron status (ferritin
/ hemosiderin).
 Other laboratory tests maybe indicated
depending on the type of anemia.
Normal Iron Stain
http://www.rightdiagnosis.com/phil/html/iron-deficiency-anemia/2657.html
 75% of all anemias
 Absolute or relative bone marrow failure
 Causes:
◦ Mild to moderate iron defeciency
◦ Inflammation
◦ Marrow damage
◦ Ineffective EPO production (impaired renal function,
IL-1, hypothyroidism, diabetes mellitus, myeloma)
◦ Normocytic normochromic, occasionally microcytic
hypochromic
 Investigations:
◦ S. Iron
◦ TIBC
◦ RFT
◦ TFT
◦ Bone Marrow biopsy/aspiration
◦ Serum Ferritin
◦ Iron stain of bone marrow
 Anemia of chronic inflammation:
◦ S. Iron: Low
◦ TIBC: normal or low
◦ Transferrin saturation: Low
◦ S. Ferritin: Normal – High
 Iron defeciency anemia
◦ S. Iron: Low
◦ TIBC: High
◦ Transferrin: Low
◦ S. Ferritin: Low
 Leukemia and lymphoma, marrow aplasia
◦ Peripheral smear
◦ Bone marrow biopsy
Bone marrow biopsy in Acute Leukemia
http://wikidoc.org/index.php/Bone_marrow_examination
 Features:
◦ Anemia with low reticulocyte count
◦ Macro or microcytosis on smear
◦ Abnormal red-cell indices
 Two categories:
◦ Macrocytic – nuclear abnormalities
◦ Microcytic – cytoplasmic abnormalities
 Ineffective erthropoeisis due to destruction in
marrow
 Bone marrow shows erythroid hyperplasia
 Nuclear maturation disorders:
◦ Folate or Vitamin B12 defeciency, drug damage
(methotrexate), myelodysplasia
◦ Alcohol causes macrocytosis with variable degree of
anemia due to folate defeciency
 Cytoplasmic maturation disorders:
◦ Severe iron defeciency, thallassaemias
 Iron defeciency: Low reticulocyte
index, microcytosis, Serum Iron profile can be used to
differentiate from thallassaemias
 Myelodysplasia:
◦ Macro or microcytosis
◦ Iron ring in mitochondria
◦ Sideroblasts on marrow stain
◦ Iron studies can help differentiate from other
conditions
 Red cell production indices > 2.5 or normal
 Polychromatophilic macrocytes on smear
 Red cells indices: Normocytic to Macrocytic
due to increased reticulocytes
 Acute blood loss: Not associated with
increased reticulocyte production because of
time required for EPO production
 Subacute blood loss: Moderate reticulocytosis
 Chronic blood loss: Iron defeciency with
increased red cell production
 Least common form of anemia
 High reticulocyte count – marrow able to sustain
erythropoesis with efficient recycling of iron in
case of extravascular hemolysis
 Intravascular hemolysis – Paroxysmal nocturnal
hemoglobinuria – Loss of iron may limit marrow
response
 Hemoglobinopathies like sickle cell
disease/thallassemias present a mixed picture
and may have a high reticulocyte count which is
low compared to marrow hyperplasia.
 Acute: specific patterns like autoimmune
hemolysis, glutathione reductase.
 Inherited hemolytic anemias: have a lifelong
history of typical of disease process
 Chronic hemolytic diseases like hereditary
spherocytosis may present with complication
of increased red cell destruction (bilrubin
gallstones, splenomegaly).
 Susceptible to aplastic crises
 Differential diagnosis of acute or chronic
hemolysis requires careful investigation of
family history and specialised laboratory tests
like hemoglobin electrophoresis or screening
for red cell enzymes.
 Acquired defects in red cell survival – may
requires testing of indirect antiglobulin test,
cold agglutinin titres to detect hemolytic
antibodies or complement mediated
destruction.
 Mild to moderate anemia: Treatment once
specific diagnosis in made
 Acute causes may require treatment before
diagnosis is made.
 Some causes of anemia are multifactoral and
it is important to check iron status before and
during treatment.
 43yrs / F, k/c/o Beta Thal Carrier
 Generalised weakness x 7 days
 Hb – 6.4g% (17/6)
 7.0/26.4% on admission, 7 days later after
starting Mumfer
 Tot RBC: 4.42 x 106 cells/mm3
 MCV – 60 fl [78-98]
 MCH – 16pg [27-32]
 MCHC 27% [31-34]
 TLC: 8000cells/cumm, N46 L44 M7 E2.1 B0.1
 Plt: 289,000/cumm
 RBC: Microcytic Hypochromic with many
ovalocytes, few dacryocytes and schistocytes
 WBC: normal maturation
 Platelets: adequate in number
 Parasites: not seen
 Corrected Retic count = 4 x 9/12 = 3
 Harrison’s Principles of Internal Medicine,
18th Edition
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Approach to anaemia .pdf

  • 1. By Dr. Ahmed Azhad Moderator: Dr. Zubair 2nd July 2012
  • 3.  Anemia – The World Health Organisation defines anemia as a hemoglobin level < 130 g/L (13g/dL) in men and <120g/L (12g/dL) in women.  The critical elements of erythropoesis are used for the initial classification of anemia.
  • 4.
  • 5.  EPO production  Iron availability  Proliferative capacity of the bone marrow  Effective maturation of red cell precursors http://www.oncoprof.net/Generale2000/g09_Chimiotherapie/Complements/g09-gb_comp56.html
  • 6.  Often found during routine screening  Acute blood loss – Hb/HCT does not reflect the volume of blood loss ◦ Mild – No symptoms. Enhanced oxygen delivery by changes in pH and increased CO2 ◦ 10-15% - hypotension and decreased organ perfusion ◦ >30% - postural hypotension, tachycardia ◦ >40% - hypovolemic shock: confusion, dyspnoea, diaphoresis
  • 7.  Acute hemolysis ◦ Intravascular hemolysis: acute back pain, free hemoglobin in plasma and urine, renal failure  Moderate anemia ◦ Fatigue ◦ Loss of stamina ◦ Breathlessness ◦ Tachycardia on physical exertion ◦ Symptoms may not appear in young, healthy patients until hemoglobin is 7-8 g/dL
  • 8.  Diseases in which patient presents with anemia ◦ Infections ◦ Rheumatoid Arthritis ◦ Cancer ◦ Lymphoproliferative disorders (CLL, B cell neoplasm)  Anemia – a major sign of disease
  • 9.  Evaluation by History: ◦ Symptoms of known diseases causing anemia:  Gastric ulceration  Rheumatoid arthritis  Renal failure ◦ Duration of symptoms:  Hemoglobinopathies in longer duration ◦ Treatment history  Medications for pain, hematinics ◦ Nutritional history
  • 10. ◦ Physical examination  Build, nourishment  Signs of disease  Vitals – fever, tachycardia, blood pressure  Pallor  Jaundice  Lymphadenopathy  Bone tenderness  Petechiae  CVS: Flow murmurs  RS: Dyspnoea  Abdomen: Splenomegaly
  • 11.  Hb, Hematocrit  RBC count  MCV (Hct x 10 / RBC x 106) [ 90±8 fl ]  MCH (Hb x 10 / RBC x 106) [ 30 ± 3 pg ]  MCHC (MCH/MCV) [ 33 ± 2 % ]  Reticulocyte count  Indices vary with age, gender and pregnancy  WBC count including differential count, neutrophil segment count  Platelet count
  • 12.  Cell size  Hb content  Anisocytosis  Poikilocytosis  Polychromasia  Gives clues to specific disorders Normal peripheral smear
  • 13. Severe Iron defeciency anemia Anisocytosis (size), Poikilocytosis (shape) Macrocytosis Macrocytes, Ovalocytes Myelofibrosis Tear drop shaped cells, nucleated cells Thallassemia Target cells
  • 14. Howell-Jolly bodies Red cell fragmentation Uremia Spur cells
  • 15.  A reliable measure of red cell production  Patient’s reticulocyte is compared with expected reticulocyte counts  In established anemia, reticulocyte count of less than two-three times is an inadequate marrow response  Reticulocyte correction needs to be done for anemia (1)  And shift cells (2), If polychromatophilic cells are not seen on the blood smear, the second correction is not required.
  • 16.
  • 17.  Premature release of recticulocytes are due to EPO stimulation  Severe chronic hemolytic anemia – RPI increases upto six to sevenfold. Confirms appropriate response to EPO, normal functioning marrow and iron availability  If reticulocyte production index < 2, suggests a defect in marrow proliferation or maturation
  • 18.  Serum Iron: 50–150 µg/dL  TIBC: 300–360 μg/dL  Serum ferritin (also an acute phase reactant) ◦ 15-20 µg/dL – Lack of Iron stores ◦ Women: ~30 µg/dL ◦ Men: ~ 100 µg/dL ◦ 200 µg/dL – adequate iron stores  Serum Transferrin saturation: 25-50%
  • 19.  Marrow aspirate ◦ M/E ratio ◦ Cell morphology ◦ Iron stain  Marrow biopsy ◦ Cellularity ◦ Morphology
  • 20.  Required in patients with normal iron status with hypoproliferative anemia  Can be used to diagnose primary bone marrow diseases: myelofibrosis, infiltrative diseases Hematocrit Production Index Reticulocytes (incl. corrections) Marrow M:E ratio 45 1.0 1 3:1 35 2.0-3.0 4.8%/3.8/2.5 2:1 – 1:1 25 3.0-5.0 14%/8/4.0 1:1 – 1:2 15 3.0-5.0 30%/10/4.0 1:1 – 1:2
  • 21.  Can be stained to confirm iron status (ferritin / hemosiderin).  Other laboratory tests maybe indicated depending on the type of anemia. Normal Iron Stain http://www.rightdiagnosis.com/phil/html/iron-deficiency-anemia/2657.html
  • 22.
  • 23.  75% of all anemias  Absolute or relative bone marrow failure  Causes: ◦ Mild to moderate iron defeciency ◦ Inflammation ◦ Marrow damage ◦ Ineffective EPO production (impaired renal function, IL-1, hypothyroidism, diabetes mellitus, myeloma) ◦ Normocytic normochromic, occasionally microcytic hypochromic
  • 24.  Investigations: ◦ S. Iron ◦ TIBC ◦ RFT ◦ TFT ◦ Bone Marrow biopsy/aspiration ◦ Serum Ferritin ◦ Iron stain of bone marrow
  • 25.  Anemia of chronic inflammation: ◦ S. Iron: Low ◦ TIBC: normal or low ◦ Transferrin saturation: Low ◦ S. Ferritin: Normal – High  Iron defeciency anemia ◦ S. Iron: Low ◦ TIBC: High ◦ Transferrin: Low ◦ S. Ferritin: Low
  • 26.  Leukemia and lymphoma, marrow aplasia ◦ Peripheral smear ◦ Bone marrow biopsy Bone marrow biopsy in Acute Leukemia http://wikidoc.org/index.php/Bone_marrow_examination
  • 27.
  • 28.  Features: ◦ Anemia with low reticulocyte count ◦ Macro or microcytosis on smear ◦ Abnormal red-cell indices  Two categories: ◦ Macrocytic – nuclear abnormalities ◦ Microcytic – cytoplasmic abnormalities  Ineffective erthropoeisis due to destruction in marrow  Bone marrow shows erythroid hyperplasia
  • 29.  Nuclear maturation disorders: ◦ Folate or Vitamin B12 defeciency, drug damage (methotrexate), myelodysplasia ◦ Alcohol causes macrocytosis with variable degree of anemia due to folate defeciency  Cytoplasmic maturation disorders: ◦ Severe iron defeciency, thallassaemias  Iron defeciency: Low reticulocyte index, microcytosis, Serum Iron profile can be used to differentiate from thallassaemias
  • 30.  Myelodysplasia: ◦ Macro or microcytosis ◦ Iron ring in mitochondria ◦ Sideroblasts on marrow stain ◦ Iron studies can help differentiate from other conditions
  • 31.
  • 32.  Red cell production indices > 2.5 or normal  Polychromatophilic macrocytes on smear  Red cells indices: Normocytic to Macrocytic due to increased reticulocytes  Acute blood loss: Not associated with increased reticulocyte production because of time required for EPO production  Subacute blood loss: Moderate reticulocytosis  Chronic blood loss: Iron defeciency with increased red cell production
  • 33.  Least common form of anemia  High reticulocyte count – marrow able to sustain erythropoesis with efficient recycling of iron in case of extravascular hemolysis  Intravascular hemolysis – Paroxysmal nocturnal hemoglobinuria – Loss of iron may limit marrow response  Hemoglobinopathies like sickle cell disease/thallassemias present a mixed picture and may have a high reticulocyte count which is low compared to marrow hyperplasia.
  • 34.  Acute: specific patterns like autoimmune hemolysis, glutathione reductase.  Inherited hemolytic anemias: have a lifelong history of typical of disease process  Chronic hemolytic diseases like hereditary spherocytosis may present with complication of increased red cell destruction (bilrubin gallstones, splenomegaly).  Susceptible to aplastic crises
  • 35.  Differential diagnosis of acute or chronic hemolysis requires careful investigation of family history and specialised laboratory tests like hemoglobin electrophoresis or screening for red cell enzymes.  Acquired defects in red cell survival – may requires testing of indirect antiglobulin test, cold agglutinin titres to detect hemolytic antibodies or complement mediated destruction.
  • 36.  Mild to moderate anemia: Treatment once specific diagnosis in made  Acute causes may require treatment before diagnosis is made.  Some causes of anemia are multifactoral and it is important to check iron status before and during treatment.
  • 37.  43yrs / F, k/c/o Beta Thal Carrier  Generalised weakness x 7 days  Hb – 6.4g% (17/6)  7.0/26.4% on admission, 7 days later after starting Mumfer  Tot RBC: 4.42 x 106 cells/mm3  MCV – 60 fl [78-98]  MCH – 16pg [27-32]  MCHC 27% [31-34]  TLC: 8000cells/cumm, N46 L44 M7 E2.1 B0.1  Plt: 289,000/cumm
  • 38.  RBC: Microcytic Hypochromic with many ovalocytes, few dacryocytes and schistocytes  WBC: normal maturation  Platelets: adequate in number  Parasites: not seen  Corrected Retic count = 4 x 9/12 = 3
  • 39.  Harrison’s Principles of Internal Medicine, 18th Edition