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Iron Deficiency Anemia 

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  • Chapter 25: Hematology Anemia Microcytic Hypochromic Anemia (MHA) Iron Deficiency Anemia (IDA)
  • Iron Deficiency Anemia 

Iron Deficiency Anemia 

Iron Deficiency Anemia 

on 09 Jan, 2025
  • Date09 Jan, 2025

Storage iron is divided about equally among

  • Reticuloendothelial cells (Spleen, Liver & Bone marrow)
  • Hepatic parenchymal cells 
  • Skeletal muscle 

Storage iron occurs in two forms:

  1. Ferritin
  2. Hemosiderin

 

Important information bullets:

  • Hemosiderin is the main form in RES; Ferritin is the main form in hepatocytes. 
  • In deficiency ferritin form is more easily mobilized and in overload hemosiderin is more increased.
  • About 3-4 mg of iron is present in plasma which is bound to transferrin.
  • Transferrin transports iron from alimentary tract to tissue stores, from stores to bone marrow erythroblasts and from one store to another store.
  • The concentration of transferrin in blood is total iron binding capacity (TIBC).
  • The percentage of transferrin to which iron is attached is called percentage saturation of iron binding protein (transferrin)
  • Serum ferritin concentrations generally correlate well with tissue iron stores. A serum Ferritin level of 12 μg/l or less is diagnostic of iron deficiency. Single best test to confirm IDA.

 

Sites of absorption:

  1. Stomach
  2. Duodenum, Proximal jejunum

 

Dietary iron requirement:

  • Male: 1 mg/day
  • Menstruating female: 2 mg/day
  • Pregnancy: 3 mg/day

 

Serum transferrin receptor:

Directly related to extent of erythroid activity as well as being inversely related to iron supply to cells

 

Serum Iron Profile:

  • Thalassaemia: ALL NORMAL
  • IDA: Only TIBC & soluble transferrin receptor  – increased, all decreased
  • ACD: 
    • Remember: ফেরারী (ferritin)  আসামীরা chronic (ACD) ঘুরে বেড়ায় (বাড়ে)
    • Only serum ferritin increased, all decreased
  • Sideroblastic anemia: NO DECREASED
    • Serum iron; ferritin; transferrin saturation – increased
    • TIBC, soluble transferrin receptor- N

 

Causes of Iron Deficiency 

  • For men or postmenopausal women 
    • Peptic ulcer disease, gastritis, Hookworm infestations, schistosomiasis
    • Occult gastric on colorectal malignancy, IBD, Haemorrhoids
    • Diverticulitis, polyp, angiodysplasia, 
    • Chronic hemoptysis, Hematuria
    • Achlorhydria, Gastric surgery, Coeliac disease
    • Drugs: Aspirin or NSAID use
  • Female of child bearing age 
    • Menstrual blood loss, pregnancy, breast feeding 

 

Increased Demand for Iron
  • Rapid growth in infancy or adolescence 
  • Pregnancy 
  • Erythropoietin therapy 
Increased Iron Loss
  • Chronic blood loss 
  • Acute blood loss 
  • Menses
  • Blood donation 
  • Phlebotomy as treatment for polycythemia vera
Decreased Iron Intake or Absorption
  • Inadequate diet 
  • Malabsorption from disease (sprue, Crohn’s disease) 
  • Malabsorption from surgery (gastrectomy and some forms of bariatric surgery) 
  • Acute or chronic inflammation

 

Investigation

  1. Investigation to confirm diagnosis: CBC, PBF, Iron profile
  2. Investigation to find out cause: eg. stool RE

 

Investigation  Finding 
CBC PBF
  • microcytic hypochromic anemia 

Iron profile

  1. Serum Ferritin
  2. TIBC 
  3. Serum iron
  4. Percent saturation 
  1. low
  2. increased
  3. low
  4. low
Serum soluble transferrin Receptor 
  • elevated in iron deficiency
Bone marrow aspirate/biopsy for iron stain
  • To see iron storage 
UGI endoscopy, colonoscopy
  • To fid out cause

Small gut imaging: 

  • Barium follow through, 
  • MR enterography, 
  • Double balloon/ capsule enteroscopy
  • Anti endomysial ab, 
  • Anti tTG, 
  • Duodenal biopsy
  • to exclude Coeliac disease 
  • Stool RE, OBT, fecal calprotectin 
  • Urine RE, USG KUB, cystoscopy
  • to exclude urinary blood loss
  • Hemoglobin electrophoresis
  • to exclude alternative diagnosis: thalassemia minor 

 

Investigations for Schistosomiasis 

  • Blood
    1. CBC, ESR – Eosinophilia 
    2. ELISA – positive 

 

  • Urinary system:
    1. Urine dipstick Examination – blood and Albumin
    2. Microscopic examination of centrifuged deposit: eggs
    3. USG of KUB: Bladder wall thickening,  Bladder calcification, Hydronephrosis
    4. cystoscopy: sandy patches, bleeding mucosa, distention of mucosa

 

  • Sigmoidoscopy: Inflammation and bleeding 

 

 

Q. Malignancy that may develop, if this patient remains untreated (IDA)? 

  • Esophageal carcinoma (from Plummer – Vinson syndrome)

 

Management of IDA:

  1. Treatment of underlying cause: stop aspirin/NSAIDs
  2. Correction of iron deficiency.

Iron Preparation:

  • Oral: Ferrous sulfate 200 mg, 3 times daily after meals 3-6 months 
  • Parenteral: Ferric carboxymaltose (Inj. ferisen)

 

Oral Iron Preparations  Parenteral: chance of anaphylaxis 
  1. Ferrous sulfate 
  2. Ferrous fumarate 
  3. Ferrous gluconate 
  4. Polysaccharide iron
  1. Ferric carboxymaltose (maltofer/ferinject), 
  2. Ferric isomaltose 
  3. Iron Dextran
  4. Iron sucrose (defiron)

 

Q. What are the causes of failure to response to oral therapy:

  1. Non compliance
  2. Malabsorption
  3. Continued blood loss
  4. Incorrect diagnosis
  5. Delayed release iron preparation 

 

Q. What investigation will you do to monitor the response to therapy?

  • After 7-10 days 
    • Hb% and 
    • Reticulocyte count  

 

Q. What are the indication for parenteral iron therapy:

  • Malabsorption
  • Chronic gut disease
  • Iability to tolerate 

 

Q. What are the problems with ferrous sulfate

  • Dyspepsia
  • Altered bowel habit
  • Solve: either dose reduction to 200 mg BD, or switch to ferrous gluconate 

 

Calculation of Dosage: (parenteral)

  • The amount of iron needed by an individual patient is calculated by the following formula: (harrisson)

 

Body weight (kg) × 2.3 × (15 – patient’s Hb, g/dL)  + 500 or 1000 mg (for stores)

 

Follow Up:

  • The hemoglobin rise by 1 g/dl per weeks (7– 10 days) 
  • Reticulocytosis within a week
  • If no response of the hematological parameters is observed after 1 to 2 weeks, the original diagnosis should be reconsidered. 

 

 

***                   ***                    ***

 

OSPE: A 32 year-old woman has presented with weakness, dizziness and palpitation with no organomegaly. Study her hematology report and give answer to the following questions:

 

  • Hemoglobin 10.7 g/dl
  • WBC- 5.5 x 109/L
  • Platelets- 220 x 109/L
  • RDW-CV: 24%

 

  • PCV-0.29
  • MCV- 66 fl
  • MCH-20 pg
  • MCHC-24

 

Q. What is your diagnosis?

  • Iron deficiency anemia (2) / microcytic hypochromic anemia (1)

 

Q. Mention her treatment with appropriate formulation, dose and duration.

  • Ferrous sulfate 200 mg, thrice daily after meals at least for three months  after correction 

 

Q. What investigations will you do to monitor the response to therapy?

  • After 7 to 10 days, 
  • Hb% and reticulocyte count

 

Q. If there is inadequate response what are the factors you will consider?

  • Non compliance
  • Continued blood loss
  • Malabsorption
  • Incorrect diagnosis
  • Incorrect drug formulation

 

IDA

 

PBF Finding History
  • Anisocytosis, Poikilocytosis
  • Microcytosis, Hypochromia
  • Pencil cells

CBC:

  • Hb low, Hct low, 
  • MCV, MCH low, 
  • Menorrhagia, pregnancy
  • Upper abdominal pain, relation to food
  • Upper GI bleeding/ hematemesis
  • Aspirin, NSAID intake, H/O peptic ulcer/gastric surgery 
  • Rectal fresh/ altered bleeding
  • Family history of GI malignancy
  • Weight loss, altered bowel habit,  abdominal lamp 
Examination  Investigation
  • Pallor, anemia, 
  • koilonychia, 
  • glossitis, angular stomatitis
  • Iron profile / serum ferritin / serum iron and TIBC
  • Soluble transferrin receptor
  • Hb electrophoresis
  • Stool for RME / OBT
  • Barium meal examination / endoscopy UGIT
  • Barium enema/ Colonoscopy

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