appoach to anemia 07

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    Anemiay Definition: Low Hemoglobin concentration.

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    Reference ranges for Hbs at different ages

    Age group Hb range (g/dl)

    Newborn (< 1 week) 14 22

    6 months old 11 14

    Children (1 16 years) 11 15

    Adults

    Men

    Women

    13 16

    12 - 14

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    Anaemia

    Clinical grading (Adults)

    Mild (Hb > 10 g/dl) Asymptomatic

    Moderate (Hb 7 10 g/dl) Pallor, lethargyDyspnoea, vertigo

    headache

    Severe (Hb < 7 g/dl) Tachycardia

    hypotension

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    Mechanisms of anaemia

    1. Decreased productiony Ineffective erythropoiesis

    y Deficiency of B12/folate

    y Abnormal synthesis of haemoglobin (thalassaemia)

    y Decreased effective erythropoiesisy Aplastic anaemia/marrow failure

    2. Increased blood lossy Gastrointestinal bleeding

    3. Increased destructiony haemolysis

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    Classification of anaemia

    1. Morphologicaly Based on red cell indices and blood film

    y Hypochromic microcytic anaemia (MCVq, MCHq)

    y Normochromic normocytic anaemia (MCV N, MCH N)y Normochromic macrocytic anaemia (MCVo, MCH N)

    2. Pathophysiological

    y Based on causes of anaemiay Iron deficiency anaemia

    y Megaloblastic anaemia

    y Haemolytic anaemia

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    Classification of anaemia

    y MCV mean corpuscular volume (fl)

    y MCH mean corpuscular Hb (pg)

    MCV (80 100 fl) Normocytic

    MCV (< 80 fl) Microcytic

    MCV (>100 f l) Macrocytic

    MCH (27 - 32 pg) Normochromic

    MCH (< 27 pg) Hypochromic

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    History Takingy Any blood loss

    y Melena, epigastric painy Menorrhagiay

    Hemoptysisy Per rectal bleed

    y Family hx of blood transfusiony Traditional meds/ drugs ingestiony Bleeding tendency, recurrent fever, infectionsy A

    utoimmune ds oral ulcer, hair loss, photosensitivityy Dietary intakey Sx of anemia lethargy, reduced effort tolerance, angina,

    dyspnea, giddiness, syncope, palpitation, LOW, LOA

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    Physical Examinationy Conjunctiva pallory Jaundicey Angular stomatitis

    y Glossitisy Gum hypertrophyy Thalassemic facies (frontal bossing, malar prominence)y Bruisingy Lymphadenopathy

    y Koilonychiay Leukonychiay Cachexiay Hepatosplenomegalyy Propioceptive loss prenicious anemia

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    I

    nvestigationsy First step to diagnosis: look at MCV!!!

    y Microcytic anemia

    y Iron deficiency anemia

    y Thalassemia

    y Anemia of chronic disease

    y

    Sideroblastic anemia

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    y Macrocytic anemia

    y Folate deficiency

    y B12 deficiencyy Hypothyroidism

    y Chronic liver disease

    y Alcohol excess

    y Reticulocytosis eg with hemolysisy Myelodysplastic syndrome

    y Cytotoxic drugs

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    y Normocytic anemia

    y Acute blood loss

    y Anemia of chronic diseasey Bone marrow failure

    y Pregnancy

    y Hypothyroidism (can be macrocytic too)

    y Hemolysis (can be macrocytic too)

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    Microcytic anemiay Serum Iron, TIBC, ferritin

    y PBF

    y Stool occult bloody Stool ova and cyst

    y Endoscopy (if hx, PE suggestive)

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    yLow Iron, Low TIBCy Anemia of chronic disease

    y Low Iron, High TIBC

    y Iron deficiencyy Causes: blood loss, malabsorption (Celiac ds), low

    intake, hookworm

    y Stool occult blood, ova & cyst, endoscopy

    y Normal Iron, TIBC, ferritin

    y Hb electrophoresis Thalassemia

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    Macrocytic Anemiay PBF

    y B12 level

    y Folate levely LFT, GGT

    y T4, TSH

    y Retic count

    y Bone marrow biopsy if cause not revealed by abovetests

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    y B12 deficiency

    y Dietary e.g vegans

    y Malabsorptiony Lack of intrinsic factor (pernicious anemia) Schilling test,

    anti-parietal cell Ab

    y Post gastrectomy

    y Ilieum resection

    y Chrons disease

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    y Folate deficiency

    y Dietary poverty

    y

    Pregnancyy Malabsorption - Celiac disease

    y Drugs phenytoin, MTX, sodium valproate

    ** never treat without folate in low B12 state, amyprecipitate subacute combined degeneration of cord

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    Hemolytic Anemiay Causes:

    y Acquired

    y Immune mediated drug induced,

    AIHA

    y Isoimmune transfusion reaction

    y Infection - malaria

    y Hereditary

    y Enzyme defect: G6PD deficiency, pyruvate kinase deficiency

    y Membrane defect: hereditary spherocytosis, sickle cell disease,Thalassemia

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    y Clues

    y Anemia normocytic

    y

    Jaundicey Dark colored urine hemoglobinuria

    y Hepatosplenomegaly

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    Investigations (as appropriate)y FBC

    y Retic count

    y LDH

    y LFT

    y Bilirubins (direct, indirect)

    y UFEME

    y Coombs test direct

    y

    BFMPy G6PD level

    y Hb electrophoresis

    y Plasma haptoglobin