Does This Patient Need Prescription Oral Iron Supplementation?
Yes, this patient absolutely requires iron supplementation immediately—the laboratory findings demonstrate severe microcytic anemia with markedly elevated RDW (20.9%), which is pathognomonic for iron deficiency anemia requiring urgent treatment. 1
Diagnostic Confirmation
The laboratory values definitively establish iron deficiency anemia:
- Hemoglobin 7.6 g/dL represents severe anemia requiring prompt intervention 1
- MCV 66 fL with RDW 20.9% is the classic pattern distinguishing iron deficiency from thalassemia trait (which would show normal RDW ≤14.0%) 1, 2
- The combination of low MCV with high RDW (>14.0%) strongly indicates iron deficiency anemia rather than genetic causes 1, 2
While serum ferritin would be the definitive confirmatory test (with <15 μg/L indicating absent iron stores and <45 μg/L optimal for diagnosis), the clinical picture is sufficiently clear to initiate treatment 1
Treatment Protocol
First-line treatment is oral iron supplementation with ferrous sulfate 200 mg three times daily for at least three months after correction of anemia to replenish iron stores. 1
Alternative formulations if ferrous sulfate is not tolerated:
Expected response:
- Hemoglobin should rise ≥10 g/L (≥1 g/dL) within 2 weeks if iron deficiency is the cause 1
- Hemoglobin should increase by at least 2 g/dL within 4 weeks 1
Critical Investigation Required
This patient requires urgent investigation for the source of iron loss, as severe iron deficiency in adults always warrants evaluation for occult bleeding: 1
- Adult men with Hb <110 g/L or non-menstruating women with Hb <100 g/L warrant fast-track gastrointestinal referral 1
- If the patient is female of childbearing age, assess for heavy menstrual bleeding (most common cause in premenopausal women) 1
- Gastrointestinal blood loss is found in 60-70% of patients with iron deficiency anemia referred for endoscopy 3
- Consider celiac disease screening, H. pylori infection, or autoimmune atrophic gastritis if malabsorption suspected 1
Monitoring Plan
- Check hemoglobin concentration and red cell indices at 2 weeks to confirm response 1
- Continue monitoring at three-monthly intervals for one year, then after a further year 1
- Provide additional oral iron if hemoglobin or MCV falls below normal 1
- Monitor serum ferritin and transferrin saturation to assess iron store repletion 1
When to Consider Intravenous Iron
If the patient fails to respond to oral iron therapy within 2-4 weeks, consider: 1
- Non-compliance with oral regimen
- Ongoing blood loss exceeding replacement capacity
- Malabsorption (celiac disease, inflammatory bowel disease, H. pylori, atrophic gastritis)
- True intolerance to oral preparations
In these cases, switch to intravenous iron (iron sucrose or iron gluconate) with expected hemoglobin increase of at least 2 g/dL within 4 weeks 1
Common Pitfalls to Avoid
- Do not assume all microcytic anemia is iron deficiency: While this patient's elevated RDW confirms iron deficiency, thalassemia trait and anemia of chronic disease must be differentiated in other cases to avoid unnecessary iron therapy 1
- Do not overlook combined deficiencies: Iron deficiency can coexist with B12 or folate deficiency 1
- Do not stop iron therapy prematurely: Continue for at least 3 months after hemoglobin correction to replenish iron stores 1
- Ferritin can be falsely elevated by inflammation: In the presence of inflammation, ferritin up to 100 μg/L may still be consistent with iron deficiency 1
Rare Genetic Considerations (Unlikely in This Case)
Given the patient's age and presentation, genetic disorders of iron metabolism (IRIDA, SLC11A2 defects) are extremely unlikely but should be considered only if: 4
- Failure to respond to both oral and intravenous iron
- Family history of refractory anemia
- Low-to-normal ferritin with remarkably low transferrin saturation
- Extreme microcytosis (MCV <60 fL) from early childhood