Management of Anemia in Congestive Heart Failure
Intravenous iron supplementation is the primary treatment for heart failure patients with iron deficiency (ferritin <100 μg/L or ferritin 100-300 μg/L with transferrin saturation <20%), regardless of whether anemia is present, as it improves exercise capacity, quality of life, and reduces hospitalizations. 1, 2
Initial Evaluation
Evaluate all heart failure patients for anemia, as it affects 25-40% of this population and independently predicts mortality, reduced exercise capacity, and poor quality of life. 1, 2
Diagnostic workup should include:
- Complete blood count to assess hemoglobin (anemia defined as <12 g/dL in women, <13 g/dL in men per WHO criteria) 1, 2
- Serum iron, ferritin, and transferrin saturation to identify iron deficiency 2
- Vitamin B12, folate, TSH, creatinine, and CRP to exclude other causes 2
Iron deficiency is defined as:
Treatment Algorithm
For Iron Deficiency (With or Without Anemia)
Administer intravenous iron as first-line therapy. 1, 2 The FAIR-HF and CONFIRM-HF trials demonstrated significant improvements in NYHA functional class, 6-minute walk test, and quality of life with IV iron. 1, 2
Dosing for iron deficiency anemia (ferric carboxymaltose):
- Patients ≥50 kg: 750 mg IV in two doses separated by at least 7 days (total 1,500 mg per course) 3
- Patients <50 kg: 15 mg/kg IV in two doses separated by at least 7 days 3
Dosing for iron deficiency in heart failure (to improve exercise capacity):
- Weight <70 kg with Hb <10 g/dL: 1,000 mg on Day 1, then 500 mg at Week 6 3
- Weight ≥70 kg with Hb <10 g/dL: 1,000 mg on Day 1, then 1,000 mg at Week 6 3
- Maintenance: 500 mg at 12,24, and 36 weeks if ferritin <100 ng/mL or ferritin 100-300 ng/mL with transferrin saturation <20% 3
Do not use oral iron supplementation in heart failure patients, as it has poor absorption and cannot adequately replenish iron stores. 2
For Anemia Without Iron Deficiency
Use a restrictive transfusion strategy with a hemoglobin threshold of 7-8 g/dL in hospitalized patients with coronary heart disease. 1 Liberal transfusion strategies (higher hemoglobin thresholds) provide no benefit and may cause harm including transfusion-related acute lung injury and worsening heart failure. 1
What NOT to Do
Do not use erythropoiesis-stimulating agents (ESAs) such as erythropoietin or darbepoetin. 1 The largest randomized trial (n=2,278) demonstrated no benefit and significantly increased thromboembolic events and strokes. 1 This is a strong recommendation based on moderate-quality evidence showing harms outweigh any potential benefits. 1
Expected Timeline of Improvement
Patients receiving IV iron can expect:
- 4 weeks: Initial improvements in shortness of breath, exercise capacity, and quality of life; approximately 50% report feeling "much or moderately improved" 2, 4
- 12 weeks: More robust functional capacity improvements with continued increases in 6-minute walk test distance 4
- 24 weeks: Peak therapeutic benefit with sustained improvements in NYHA class, quality of life, and fatigue scores 4
- 52 weeks: Treatment effects remain sustained throughout one year 4
Monitoring and Follow-Up
Monitor patients for at least 30 minutes after IV iron administration for hypersensitivity reactions, which occur in approximately 1.5% of patients. 3 Only administer when personnel and therapies for treating anaphylaxis are immediately available. 3
Re-evaluate iron status at 3 months after initial correction to determine if additional supplementation is needed. 4 Regular monitoring every 3 months for at least one year is recommended to detect recurrent iron deficiency. 2, 5
Re-treat with IV iron when:
Check serum phosphate levels in patients requiring repeat courses of IV iron, especially if administered within 3 months, as hypophosphatemia can occur. 3
Common Pitfalls
Avoid extravasation during IV iron administration, as brown discoloration at the site may be long-lasting. 3 If extravasation occurs, discontinue administration at that site immediately. 3
Do not assume anemia correction alone will improve hard outcomes. While IV iron improves surrogate endpoints (exercise capacity, quality of life, NYHA class), controlled trials have been underpowered to detect mortality reduction. 1 However, the consistent improvements in functional status and hospitalizations justify treatment. 1, 2
Recurrence of iron deficiency is common without maintenance therapy, so ongoing surveillance is essential. 5 Post-treatment ferritin levels >400 μg/L better prevent recurrence within 1-5 years. 5