Management Plan for Anemia
The management of anemia should follow a restrictive transfusion strategy, reserving red blood cell transfusions primarily for patients with severe anemia symptoms (hemoglobin <7-8 g/dL) who need rapid hemoglobin improvement. 1
Diagnostic Evaluation
- Assess the type of anemia based on MCV values: microcytic (<80 fL), normocytic (80-100 fL), or macrocytic (>100 fL) 1
- Evaluate iron status in all patients before and during treatment with serum ferritin and transferrin saturation 2
- Check reticulocyte count to determine if anemia is regenerative (>10×10^9/L) or non-regenerative 1
- For normocytic anemia (as in this case with MCV 93.4 fL), evaluate:
- Renal function (creatinine)
- Inflammatory markers (CRP)
- Thyroid function (TSH)
- Vitamin B12 and folate levels 1
Treatment Algorithm
For Mild to Moderate Anemia (Hb 8-10 g/dL):
- Identify and treat underlying cause of anemia 1
- For iron deficiency (ferritin <100 μg/L, transferrin saturation <20%):
For Severe Anemia (Hb <7-8 g/dL) or Symptomatic Patients:
- Consider RBC transfusion using restrictive strategy (Hb threshold <7 g/dL) 1
- Transfuse minimum number of RBC units required to relieve symptoms or return to safe Hb range 1
- Monitor hemoglobin weekly after transfusion until stable 2
For Anemia in Cancer Patients:
- For patients with non-myeloid malignancies receiving chemotherapy:
For Anemia in MDS Patients:
- For symptomatic anemia (Hb <10 g/dL) with serum EPO <500 IU/L:
Special Considerations
- ESA Safety Concerns: ESAs increase risk of death, myocardial infarction, stroke, and venous thromboembolism when targeting Hb >11 g/dL 2
- Cancer Patients: ESAs may shorten overall survival or increase tumor progression risk; use only for anemia from myelosuppressive chemotherapy, not when cure is anticipated 2
- Patient Blood Management: Focus on three pillars:
- Optimizing patient's own red cell mass
- Minimizing blood loss and bleeding
- Evaluating physiological tolerance of anemia 1
Common Pitfalls to Avoid
- Targeting hemoglobin levels >11 g/dL with ESAs, which increases cardiovascular risks 2
- Failing to evaluate iron status before initiating treatment 2
- Using ESAs in cancer patients receiving hormonal agents, biologics, or radiotherapy without concomitant myelosuppressive chemotherapy 2
- Overlooking functional iron deficiency in patients with inflammatory conditions 3
- Increasing ESA dose more frequently than once every 4 weeks 2
Follow-up Recommendations
- Monitor hemoglobin weekly after initiating therapy until stable, then monthly 2
- Evaluate response to iron therapy within 4 weeks 2
- For patients on ESAs who do not respond adequately after 12 weeks, increasing the dose further is unlikely to improve response and may increase risks 2
- Discontinue ESA if responsiveness does not improve 2