Treatment Options for Anemia
The treatment of anemia should be tailored to the underlying cause, with iron supplementation being the first-line therapy for iron deficiency anemia, erythropoiesis-stimulating agents for anemia related to chronic kidney disease or chemotherapy, and vitamin supplementation for deficiency-related anemias.
Initial Evaluation
Before initiating treatment, a thorough diagnostic workup is essential:
- Complete blood count with RDW and reticulocyte count
- Iron studies (serum iron, ferritin, transferrin saturation)
- Vitamin B12 and folate levels
- Inflammatory markers (CRP, ESR)
- Peripheral blood smear review
- Additional testing based on clinical suspicion:
- Hemoglobin electrophoresis for suspected thalassemia
- Serum haptoglobin, LDH, and bilirubin to rule out hemolysis
- Bone marrow examination in selected cases
Treatment Algorithm by Anemia Type
1. Iron Deficiency Anemia
First-line: Oral iron supplementation
- Ferrous sulfate 325 mg (65 mg elemental iron) three times daily
- Continue for 3 months after hemoglobin normalization to replenish stores 1
- Take between meals with vitamin C to enhance absorption
For poor response, intolerance, or malabsorption:
- Intravenous iron formulations (iron sucrose, ferric carboxymaltose)
- Reserved for severe anemia (Hb <7 g/dL) or symptomatic patients 1
2. Vitamin Deficiency Anemias
B12 Deficiency:
- For pernicious anemia: Intramuscular vitamin B12 100 mcg daily for 6-7 days, then alternate days for 7 doses, then every 3-4 days for 2-3 weeks, followed by 100 mcg monthly for life 2
- For normal intestinal absorption: Oral B12 supplementation after initial parenteral treatment
Folate Deficiency:
- Oral folic acid 1-5 mg daily until resolution
3. Anemia of Chronic Disease/Inflammation
- Primary approach: Treat underlying condition 1
- For persistent anemia:
4. Chemotherapy-Induced Anemia
For Hb <10 g/dL:
For Hb between 10-12 g/dL:
- Clinical judgment should guide whether to use ESAs or wait until Hb falls closer to 10 g/dL 3
5. Genetic Disorders of Iron Metabolism or Heme Synthesis
- SLC11A2 defects: Oral iron supplementation, EPO, and/or erythrocyte transfusions 3
- STEAP3 defects: Erythrocyte transfusions with EPO; iron chelation for systemic iron loading 3
- SLC25A38 defects: Hematopoietic stem cell transplantation; symptomatic treatment with transfusions and chelation 3
- ALAS2 defects (XLSA): Pyridoxine trial (50-200 mg/day); manage both anemia and iron overload 3
6. Severe Symptomatic Anemia
- RBC transfusion considerations:
Special Considerations
Anemia in Cancer Patients
- Before using ESAs, rule out other causes of anemia 3
- ESAs are indicated for chemotherapy-induced anemia, not for patients receiving hormonal agents, biologics, or radiotherapy alone 5
- ESAs are not indicated when the anticipated outcome of chemotherapy is cure 5
- Monitor for thromboembolism risk, especially in patients with prior history, recent surgery, or prolonged immobilization 3
Anemia in Inflammatory Bowel Disease
- Often multifactorial and may require combination therapy 1
- IV iron preferred over oral in active inflammation 1
Pediatric Considerations
- Screen high-risk infants for anemia between 9-12 months, 6 months later, and annually from ages 2-5 years 3
- For iron deficiency anemia in children, prescribe 3 mg/kg/day of iron drops between meals 3
- Recheck hemoglobin after 4 weeks of treatment; an increase of ≥1 g/dL confirms iron deficiency 3
Common Pitfalls to Avoid
- Failure to identify the underlying cause before initiating treatment
- Overlooking iron deficiency in inflammatory states (ferritin may appear normal)
- Inappropriate use of ESAs in patients with cancer when transfusion is more appropriate
- Inadequate duration of iron therapy (should continue for 3 months after hemoglobin normalizes)
- Neglecting to monitor for iron overload in patients receiving chronic transfusions or iron therapy
- Assuming oral iron is effective in all cases (IV iron may be necessary with inflammation or malabsorption)
By systematically identifying the underlying cause and applying evidence-based treatment strategies, most forms of anemia can be effectively managed to improve patient outcomes, reduce morbidity, and enhance quality of life.