Management of Decreased Hemoglobin and Hematocrit
The management of decreased Hb/Hct depends critically on the clinical context: in acute hemorrhage, transfuse when Hb <7-7.5 g/dL (or <10 g/dL with cardiac disease/symptoms); in chronic kidney disease, initiate erythropoiesis-stimulating agents (ESAs) when Hb <10 g/dL targeting 11-12 g/dL; and in all cases, immediately investigate and correct iron deficiency before considering other interventions. 1
Initial Assessment and Recognition
Critical timing consideration: Hb and Hct values do not fall for several hours after acute hemorrhage, so normal initial values can mask significant ongoing blood loss. 1 Serial measurements are essential—repeated Hb/Hct monitoring increases sensitivity for detecting blood loss in patients with severe injury. 1
Key diagnostic thresholds:
- Anemia is defined as Hb <13 g/dL in adult males and <12 g/dL in adult females 1
- However, visible cyanosis requires at least 5 g/dL of unsaturated hemoglobin, meaning anemia may cause hypoxemia without visible cyanosis 1
Acute Blood Loss Management
Transfusion Thresholds
For acute anemia, transfusion is almost always indicated when Hb <6 g/dL and rarely indicated when Hb >10 g/dL. 1 For intermediate values (6-10 g/dL), base the decision on:
- Rate of ongoing blood loss 1
- Cardiorespiratory reserve 1
- Presence of atherosclerotic disease 1
- Oxygen consumption requirements 1
Special populations requiring higher thresholds:
- Patients with ischemic heart disease, older age, or significant comorbidities should receive transfusion at Hb <7.5 g/dL 1
- Hemodynamic instability warrants immediate transfusion regardless of Hb level 1
Transfusion Strategy
Packed red cell transfusions: Each 400 mL unit should increase Hb by approximately 1.5 g/dL. 1 Transfuse 2-3 units to resolve acute episodes while avoiding volume overload complications. 1
In massive hemorrhage (>40% blood volume loss): Initially restore circulating volume with rapid crystalloid or colloid infusion through large-bore (≥14 gauge) peripheral cannulae before red cell transfusion. 1
Chronic Kidney Disease-Associated Anemia
When to Initiate ESA Therapy
Begin ESA therapy when Hb falls below 10 g/dL in CKD patients. 1 The target Hb range should be 11-12 g/dL, balancing quality of life improvement and transfusion avoidance against the risk of life-threatening adverse events at Hb >13 g/dL. 1
Evidence basis: Hb levels <10 g/dL are associated with increased mortality, worsening left ventricular hypertrophy, and decreased survival in dialysis patients. 1 However, targeting normal Hb levels (>13 g/dL) increases cardiovascular events. 1
Iron Status Requirements Before ESA Initiation
Absolute prerequisites for ESA therapy:
For hemodialysis-dependent CKD: Maintain TSAT >20% and ferritin >200 ng/mL 1
For non-dialysis and peritoneal dialysis CKD: Maintain TSAT >20% and ferritin >100 ng/mL 1
Upper ferritin limit: Insufficient evidence supports IV iron administration when ferritin >500 ng/mL 1
ESA Dosing Strategy
Initial therapy goal: Achieve Hb increase of 1.0-2.0 g/dL per month. 1
Dose adjustment algorithm:
- If Hb does not increase by 2 g/dL over 8 weeks and remains insufficient to avoid transfusion, increase ESA dose by 25% 1
- When Hb approaches 12 g/dL, decrease dose by 25% 1
- If Hb continues rising toward 12 g/dL, temporarily hold ESA until Hb begins decreasing, then restart at 25% below previous dose 1
- Do not increase doses more frequently than once monthly 1
Monitoring frequency: Check Hb at least monthly during ESA therapy 1
Iron Deficiency Management
Diagnostic Approach
Iron deficiency is frequently encountered and requires specific testing beyond mean corpuscular volume (MCV), which is unreliable. 1 Assess serum iron, ferritin, and transferrin levels directly. 1
Functional iron deficiency: This is the principal reason for lack of response to ESA therapy in non-hematologic conditions. 1 Even with adequate ferritin stores, functional deficiency can develop during ESA therapy due to increased erythropoiesis. 1
Iron Replacement
Treat when TSAT <20% with iron supplementation until stores are replete. 1 This can be done safely and may prevent stroke and myocardial ischemia, though data are inconsistent. 1
Parenteral iron administration: Consider when oral iron is ineffective or not tolerated to increase ESA response. 1 In non-dialysis CKD patients intolerant to oral iron, IV iron (ferric carboxymaltose 15 mg/kg up to 750 mg on two occasions separated by ≥7 days) produces greater Hb increases than oral iron. 2
Special Considerations
Hepatitis C Triple Therapy-Induced Anemia
Management hierarchy:
- When Hb decreases to <10 g/dL with clinical symptoms: reduce ribavirin dose 1
- If Hb continues decreasing or symptoms persist: initiate epoetin therapy 1
- For severe anemia (Hb <7.5 g/dL) or hemodynamic instability: transfuse packed red cells 1
EPO resistance indicators: Do not use exogenous EPO when endogenous erythropoietin levels exceed 500 IU/L, as response probability is low. 1
Cyanotic Heart Disease
Secondary erythrocytosis management: Routine phlebotomy is not supported by data. 1 There is no safe hematocrit cutpoint, and symptoms do not correlate with measured Hct. 1
First-line therapy for suspected hyperviscosity: Rehydrate with oral fluids or IV normal saline, evaluate for iron deficiency, and treat if present. 1
Phlebotomy indications (rare): Only after adequate hydration, when Hct remains higher than patient's baseline, symptoms persist, or end-organ damage (myocardial ischemia, stroke) is attributable to hyperviscosity. 1 Always replace with equal volume fluids. 1
Common Pitfalls
Avoid these errors:
- Relying on initial Hb/Hct in acute hemorrhage—values lag behind actual blood loss by hours 1
- Using MCV alone to screen for iron deficiency—direct iron studies are required 1
- Initiating ESA therapy without ensuring adequate iron stores (ferritin >100 ng/mL, TSAT >20%) 1
- Targeting Hb >13 g/dL in CKD patients—this increases cardiovascular events 1
- Routine phlebotomy in secondary erythrocytosis without first addressing hydration and iron status 1