What are the initial steps and treatment options for managing severe anaemia?

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Last updated: November 26, 2025View editorial policy

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Management of Severe Anaemia

For severe anaemia, immediately transfuse packed red blood cells to achieve a target hemoglobin of 7-8 g/dL in stable patients, while simultaneously investigating the underlying cause and correcting iron deficiency with intravenous iron therapy. 1, 2

Immediate Transfusion Strategy

Transfuse 2-3 units of packed red blood cells immediately for patients with hemoglobin <7 g/dL or those with severe symptoms at any hemoglobin level. 1, 2 Each unit increases hemoglobin by approximately 1 g/dL. 2

Transfusion Thresholds by Clinical Context

  • Stable, non-cardiac patients: Target Hb 7-8 g/dL as the initial goal 3, 1, 4
  • Patients with cardiovascular disease or acute coronary syndrome: Consider higher threshold (>8 g/dL) due to increased risk of cardiac events with restrictive strategies 1, 2
  • Septic shock patients: Maintain restrictive threshold of Hb <7 g/dL, as no mortality benefit exists with higher targets 1
  • Hemodynamically unstable patients: Transfuse regardless of absolute hemoglobin value based on symptoms 2

Transfusion Technique

Administer single units sequentially rather than multiple units simultaneously, reassessing hemoglobin after each unit. 1 This minimizes transfusion-related complications. Check hemoglobin 1 hour post-transfusion to confirm response, then monitor daily until stable. 2

Provide continuous cardiac monitoring during transfusion and watch for signs of transfusion reactions or volume overload. 1, 2

Concurrent Diagnostic Workup

Do not delay transfusion while awaiting diagnostic results—treatment and diagnosis must proceed simultaneously. 2

Essential Initial Tests

  • Complete blood count with reticulocyte count: Reticulocyte count >10 × 10⁹/L indicates regenerative anaemia 1
  • Peripheral blood smear: Look for schistocytes (hemolysis/TTP), malaria parasites, or other morphologic abnormalities 3, 1
  • Hemolysis markers: LDH, indirect bilirubin, haptoglobin levels 1
  • Iron studies: Serum ferritin, transferrin saturation (TSAT), assess for absolute (ferritin <100 ng/mL) or functional iron deficiency (TSAT <20% with ferritin >100 ng/mL) 3
  • Direct antiglobulin test (Coombs): If hemolysis suspected 1
  • Liver function tests and coagulation panel (PT/INR) 1

Additional Considerations

  • Rule out malaria in patients with fever, anaemia, and thrombocytopenia, especially with travel history—severe malaria requires IV artesunate 1
  • Pregnancy test in women of childbearing age 1
  • Consider platelet transfusion if platelet count <50,000/µL with active bleeding or planned procedures 1

Iron Therapy

Administer intravenous iron for both absolute and functional iron deficiency—oral iron has limited efficacy in severe anaemia. 3, 5, 6

Dosing Strategy

  • Absolute iron deficiency (ferritin <100 ng/mL): Give 1000 mg IV iron as single or multiple doses according to product labeling 3
  • Functional iron deficiency (TSAT <20%, ferritin >100 ng/mL): Give 1000 mg IV iron, particularly if considering erythropoiesis-stimulating agents 3
  • Timing with chemotherapy: Administer IV iron before or after (not same day) cardiotoxic chemotherapy 3

Erythropoiesis-Stimulating Agents (ESAs)

ESAs are NOT appropriate for acute severe anaemia management due to slow onset of action—reserve for chronic anaemia after stabilization. 2, 7

When ESAs May Be Considered (After Acute Phase)

  • Cancer patients on chemotherapy: Only if Hb ≤11 g/dL, receiving myelosuppressive chemotherapy with ≥2 months planned, and not curable intent 3, 7
  • Chronic kidney disease: After stabilization, targeting lowest dose to reduce transfusion need 7
  • Dosing: Epoetin alfa 40,000 units weekly or 150 units/kg three times weekly 3, 7

Critical ESA Warnings

Never target hemoglobin >11 g/dL with ESAs—this increases mortality, myocardial infarction, stroke, and thromboembolism risk. 7 ESAs also increase tumor progression risk in cancer patients. 7

Supportive Measures

  • Supplemental oxygen: For respiratory distress with continuous oxygen saturation monitoring 1
  • Urinary catheter: Monitor hourly urine output (target >30 mL/h) 1
  • Folic acid supplementation: 1 mg daily 3
  • Reduce phlebotomy: Minimize diagnostic blood draws (mean daily volume in critical care is 40-80 mL) 3, 1

Common Pitfalls to Avoid

  • Do not wait for complete workup before transfusing—symptoms and hemoglobin level together guide immediate transfusion decisions 2
  • Do not use ESAs for acute management—they take weeks to work and are contraindicated in acute severe anaemia 2, 7
  • Do not transfuse to Hb >10 g/dL in stable patients—liberal strategies increase transfusion requirements without improving outcomes 3, 1
  • Do not use oral iron in severe anaemia—IV iron is required for adequate repletion 3, 5
  • Do not overlook functional iron deficiency—even with normal/high ferritin, TSAT <20% indicates need for IV iron 3

Special Population: Immune Checkpoint Inhibitor-Related Anaemia

If severe anaemia develops in patients on immune checkpoint inhibitors (Grade 3-4):

  • Permanently discontinue checkpoint inhibitor 3
  • Hematology consultation immediately 3
  • Prednisone 1-2 mg/kg/day (IV if Grade 4 or rapid development) 3
  • Transfuse per guidelines above, coordinating with blood bank team 3
  • Monitor hemoglobin weekly until steroid taper complete 3

References

Guideline

Management of Hemolytic Anemia in the Inpatient Setting

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Severe Anemia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Anaemia of Chronic Disease: An In-Depth Review.

Medical principles and practice : international journal of the Kuwait University, Health Science Centre, 2017

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.

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