What are the next steps in managing microcytic anemia in an 18-year-old with a Hemoglobin (Hb) of 10.9 g/dL, Mean Corpuscular Volume (MCV) of 75 fL, Mean Corpuscular Hemoglobin (MCH) of 23.3 pg, and Mean Corpuscular Hemoglobin Concentration (MCHC) of 31.1 g/dL?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: October 27, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Management of Microcytic Anemia in an 18-Year-Old

The next step in managing this 18-year-old patient with microcytic anemia (Hb 10.9 g/dL, MCV 75 fL, MCH 23.3 pg, MCHC 31.1 g/dL) should be serum ferritin testing to confirm iron deficiency, followed by oral iron supplementation with ferrous sulfate 200 mg three times daily if iron deficiency is confirmed. 1, 2

Diagnostic Evaluation

Initial Laboratory Testing

  • Serum ferritin is the most specific test for iron deficiency, with levels <15 μg/L indicating absent iron stores and <30 μg/L indicating low body iron stores 1
  • A ferritin cut-off of 45 μg/L provides optimal sensitivity and specificity for iron deficiency in clinical practice 1
  • Transferrin saturation (TSAT) should be evaluated as it is more sensitive for detecting iron deficiency than hemoglobin concentration alone 1
  • The combination of low MCV with elevated RDW (>14.0%) strongly suggests iron deficiency anemia, while low MCV with normal RDW (≤14.0%) suggests thalassemia minor 1, 3

Additional Testing to Consider

  • If serum ferritin is normal or elevated, further evaluation should include total iron-binding capacity, serum iron level, and possibly hemoglobin electrophoresis to differentiate between other causes of microcytic anemia 3
  • In patients with unexplained microcytic anemia despite normal iron studies, consider genetic disorders of iron metabolism or heme synthesis 4, 1

Treatment Algorithm

First-Line Treatment

  • For confirmed iron deficiency anemia, start oral iron supplementation with ferrous sulfate 200 mg three times daily (equivalent to 65 mg elemental iron per tablet) 1, 2, 5
  • Continue treatment for at least three months after correction of anemia to replenish iron stores 1, 2
  • Alternative formulations include ferrous gluconate and ferrous fumarate if ferrous sulfate is not tolerated 1
  • Adding ascorbic acid can enhance iron absorption 1

Monitoring Response

  • A good response to iron therapy is defined as a hemoglobin rise ≥10 g/L within a 2-week timeframe, which confirms iron deficiency 1, 2
  • Monitor hemoglobin concentration and red cell indices at three-monthly intervals for one year and then after a further year 1
  • Provide additional oral iron if hemoglobin or MCV falls below normal 1

For Non-Responders

  • For patients who fail to respond to oral iron therapy, consider:
    • Intravenous iron if there is malabsorption 1, 2
    • Evaluation for other causes of microcytic anemia including thalassemia traits 2, 3
    • Testing for genetic disorders of iron metabolism or heme synthesis 4, 2

Investigation of Underlying Cause

  • In men and post-menopausal women, iron deficiency anemia is most commonly caused by gastrointestinal blood loss or malabsorption 4

  • In an 18-year-old, common causes to investigate include:

    • Menstrual blood loss if female 4
    • Gastrointestinal blood loss 4, 3
    • Poor dietary intake 4
    • Malabsorption (including celiac disease) 4, 1
    • NSAID use 4
  • If iron deficiency is confirmed, further investigation may be warranted to identify the underlying cause 6, 3

  • For gastrointestinal blood loss, upper and lower gastrointestinal endoscopy may be necessary depending on risk factors and severity 4

Special Considerations

  • Avoid overlooking combined deficiencies, such as iron deficiency coexisting with B12 or folate deficiency 1, 7
  • Consider thalassemia trait in patients with microcytosis who do not respond to iron therapy, especially if RDW is normal 1, 3
  • Genetic testing should be considered in patients with refractory microcytic anemia despite adequate iron supplementation 1
  • Family screening may be recommended if genetic disorders affecting iron metabolism are diagnosed 1

References

Guideline

Management of Microcytic Anemia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Microcytic Hypochromic Anemia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Evaluation of microcytosis.

American family physician, 2010

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Microcytic anemia.

American family physician, 1997

Research

Laboratory evaluation of anemia.

The Western journal of medicine, 1987

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.