Management of Low Hematocrit (Anemia)
The management of low hematocrit requires first determining the underlying cause through systematic evaluation of iron studies, MCV classification, and reticulocyte count, followed by targeted treatment of the specific etiology while addressing any severe symptomatic anemia with restrictive transfusion strategies (Hb threshold <7-8 g/dL). 1, 2
Initial Diagnostic Workup
Laboratory Assessment
- Obtain complete blood count with MCV to classify anemia morphologically: microcytic (MCV <80 fL), normocytic (MCV 80-100 fL), or macrocytic (MCV >100 fL) 1, 2
- Measure reticulocyte count to distinguish regenerative (>10×10⁹/L) from non-regenerative anemia 1, 3
- Check serum ferritin (most powerful test for iron deficiency), iron, transferrin saturation (TSAT), and total iron-binding capacity 4
- Screen for coeliac disease in all patients with iron deficiency anemia 4
- For normocytic anemia, evaluate renal function (creatinine), inflammatory markers, thyroid function, vitamin B12, and folate levels 1, 2
Iron Status Interpretation
- Absolute iron deficiency: serum ferritin <100 ng/mL 4, 2
- Functional iron deficiency: TSAT <20% with serum ferritin >100 ng/mL 4, 2
- Anemia of chronic disease typically shows: low iron, low TSAT (mean 15%), elevated ferritin, and low reticulocyte count 5, 6
Etiology-Specific Investigation
Iron Deficiency Anemia in Men and Postmenopausal Women
- All men and postmenopausal women with confirmed iron deficiency anemia require upper gastrointestinal endoscopy with small bowel biopsy AND colonoscopy (or CT colography) to exclude gastrointestinal malignancy 4
- Only advanced gastric cancer or confirmed coeliac disease on upper endoscopy should deter lower GI investigation 4
- In patients aged >50 years, those with marked anemia, or significant family history of colorectal carcinoma, proceed with lower GI investigation even if coeliac disease is identified 4
Premenopausal Women
- Screen for coeliac disease, but reserve upper and lower GI investigations for those with concerning symptoms or risk factors 4
Treatment Algorithm by Severity and Etiology
Severe Symptomatic Anemia (Hb <7-8 g/dL)
- Transfuse red blood cells using restrictive strategy with Hb threshold <7 g/dL in most patients, or <8 g/dL in patients with cardiovascular disease 4, 1, 2
- Transfuse the minimum number of RBC units required to relieve symptoms or return to safe Hb range 1
- In patients with acute MI or known ischemic heart disease, a restrictive transfusion threshold (Hb 7-8 g/dL) does not increase mortality compared to liberal strategies 4
Iron Deficiency Anemia Treatment
- Initiate oral iron supplementation as first-line therapy to correct anemia and replenish body stores 4, 2, 7
- Administer intravenous iron when: oral iron is not tolerated, malabsorption is present (including active inflammatory bowel disease), or rapid repletion is needed 4, 2
- In cancer patients receiving chemotherapy with absolute or functional iron deficiency, use intravenous iron preparations 4
- Continue iron treatment for 2-3 months after correction of anemia to replenish stores 2
Anemia of Chronic Disease
- Treat the underlying inflammatory or chronic condition as primary therapy 2, 5
- Supplement with iron (preferably intravenous in inflammatory conditions), vitamin B12, and folate as indicated by laboratory deficiencies 3, 5
Cancer-Related Anemia (Chemotherapy-Induced)
- Consider erythropoiesis-stimulating agents (ESAs) only if: Hb <10 g/dL, patient is receiving chemotherapy, symptomatic anemia is present, and there is a minimum of 2 additional months of planned chemotherapy 4, 8
- ESA dosing for epoetin alfa: 150 Units/kg subcutaneously 3 times weekly OR 40,000 Units subcutaneously weekly in adults 8
- Target Hb level is 12 g/dL without RBC transfusions; do NOT exceed this target 4, 8
- Reduce ESA dose by 25% if Hb increases >1 g/dL in any 2-week period 8
- Discontinue ESA if no response after 8 weeks of therapy 8
Chronic Kidney Disease
- Initiate treatment when Hb <10 g/dL in dialysis patients 8
- In non-dialysis CKD patients, consider treatment only when Hb <10 g/dL AND the rate of decline indicates likelihood of requiring transfusion 8
- Target Hb should NOT exceed 11 g/dL; higher targets (>11 g/dL) increase risks of death, cardiovascular events, and stroke 8, 9
- Starting dose of epoetin alfa: 50-100 Units/kg 3 times weekly IV or subcutaneously 8
- Monitor Hb weekly until stable, then monthly 8
Critical Warnings and Contraindications
ESA Safety Concerns
- ESAs are contraindicated in patients NOT receiving chemotherapy 4, 8
- ESAs increase risk of death, serious cardiovascular reactions, stroke, and thromboembolism when targeting Hb >11 g/dL 8
- In cancer patients, ESAs may decrease locoregional control and overall survival, particularly in head and neck cancer 8
- Avoid ESAs in patients with uncontrolled hypertension 8
Iron Supplementation Requirements
- Evaluate iron status before and during ESA therapy; most CKD patients require supplemental iron during ESA treatment 8
- Administer supplemental iron when serum ferritin <100 mcg/L or TSAT <20% 8
Monitoring Parameters
- Monitor Hb weekly after initiating therapy or dose adjustments until stable 8
- Do not increase ESA dose more frequently than once every 4 weeks 8
- If Hb does not increase by >1 g/dL after 12 weeks of dose escalation, further increases are unlikely to help and may increase risks 8
Special Populations
Patients with Cardiovascular Disease
- Use restrictive transfusion strategy (Hb threshold 7-8 g/dL) even in patients with chronic cardiovascular disease or acute coronary syndrome 4, 2
- Avoid ESAs in patients with mild to moderate anemia and heart disease due to increased cardiovascular risks 2