Blood Transfusion-Associated Complications: Prevention and Management
Immediate Life-Threatening Complications
The two most critical acute complications requiring immediate recognition are Transfusion-Associated Circulatory Overload (TACO) and Transfusion-Related Acute Lung Injury (TRALI), both presenting with respiratory distress within hours of transfusion but requiring opposite management strategies. 1
TACO (Transfusion-Associated Circulatory Overload)
- Now the leading cause of transfusion-related mortality, occurring during or up to 12 hours post-transfusion 1
- Presents with acute respiratory compromise, pulmonary edema, cardiovascular changes (hypertension, tachycardia), and evidence of fluid overload 1
- High-risk patients: age >70 years, non-bleeding patients, heart failure, renal failure, hypoalbuminemia 1
- Management: Immediate cessation of transfusion, diuretic therapy, oxygen support 1
- Prevention: Body weight-based dosing, slow transfusion rates, close monitoring of vital signs and fluid balance 1
TRALI (Transfusion-Related Acute Lung Injury)
- Presents with non-cardiogenic pulmonary edema 1-6 hours after transfusion 1, 2
- Key features: hypoxemia, fever, dyspnea, fluid in endotracheal tube 1
- Caused by donor leukocyte antibodies (HLA class I, II, or granulocyte-specific) interacting with recipient neutrophils 1
- Management: Immediate cessation of transfusion, critical care supportive measures, oxygen therapy—avoid diuretics (ineffective and potentially harmful) 1, 2
- Prevention: Male-only plasma donors (multiparous women have significantly higher anti-HLA antibodies), screening donors for leukocyte antibodies 1
Critical distinction: TACO requires diuretics; TRALI is worsened by diuretics. 1, 2
Acute Hemolytic Transfusion Reactions
Stop transfusion immediately at first sign of any suspected reaction—this single intervention prevents progression to severe morbidity or mortality. 1, 2
Clinical Presentation
- Hypotension, tachycardia, hemoglobinuria, microvascular bleeding 2
- Back pain, chest tightness, fever (may be masked under general anesthesia) 1, 2
- Most reactions occur within the first minute of infusion 1
Immediate Management Protocol
- Stop transfusion immediately and maintain IV access with normal saline 1, 2
- Administer 100% high-flow oxygen 2
- Monitor vital signs every 5-15 minutes (heart rate, blood pressure, temperature, respiratory rate, oxygen saturation) 1, 2
- Aggressive fluid resuscitation with normal saline or lactated Ringer's to maintain MAP >65-70 mmHg 2
- Double-check patient identification and blood component compatibility for clerical errors 2
Essential Laboratory Workup
- Complete blood count, direct antiglobulin test (Coombs), repeat crossmatch 1, 2
- PT, aPTT, Clauss fibrinogen 1, 2
- Visual inspection of plasma for hemolysis 1, 2
- Urine analysis for hemoglobinuria 2
- Blood cultures if bacterial contamination suspected 2
Allergic and Anaphylactic Reactions
Mild-Moderate Allergic Reactions
- Urticaria, rash, pruritus without respiratory or hemodynamic compromise 1
- Management: Stop transfusion, administer antihistamines, consider hydrocortisone 100-500 mg IV and famotidine 20 mg IV 1
- Prevention for future transfusions: Consider washed blood products 3
Anaphylaxis
- Hypotension with bronchospasm, urticaria, or cardiovascular collapse 2
- Management:
- Send mast cell tryptase levels at three time points if anaphylaxis suspected 2
Bacterial Contamination
- Fever with hypotension within 6 hours, particularly with platelet transfusion (highest risk due to room temperature storage) 2
- Management: Immediate blood cultures from patient and blood bag, broad-spectrum antibiotics 2, 3
- Can present similarly to TACO and TRALI—maintain high index of suspicion 1
Alloimmunization and Delayed Hemolytic Reactions
For patients with sickle cell disease or history of multiple transfusions, prophylactic extended antigen matching (Rh C, E, c, e and K) significantly reduces alloimmunization risk. 4
High-Risk Patients Requiring Immunosuppression
- Patients with alloantibodies for whom antigen-negative blood is unavailable 4
- History of multiple or life-threatening delayed hemolytic transfusion reactions 4
- Recommended therapy: IVIg, steroids, and/or rituximab before transfusion in acute need situations 4
- Shared decision-making between hematologist and transfusion medicine specialist is critical 4
Transfusion-Associated Graft-Versus-Host Disease (TA-GVHD)
Rare but usually fatal complication prevented by pretransfusion gamma irradiation (minimum 25 Gy) of blood products. 4
Mandatory Irradiation Indications
- Autologous and allogeneic stem-cell transplant recipients 4
- Blood products from partially matched family members 4
- Severe immunosuppression: Hodgkin's lymphoma, fludarabine/purine nucleoside analogs, antithymocyte globulin, alemtuzumab 4
- Note: Leukocyte depletion alone does NOT prevent TA-GVHD 4
Complications in Specific Surgical Populations
Brain Tumor Surgery
- Transfusion associated with increased risk of major/minor postoperative complications, infections, blood clots, renal failure, cardiovascular events, prolonged hospital length of stay 4
- Restrictive threshold <8 g/dL is safe, but liberal threshold (8-10 g/dL) may be indicated based on clinical judgment for symptomatic anemia or ongoing bleeding 4
- Tranexamic acid perioperatively decreases transfusion rates without increased seizures or thromboembolism 4
Subarachnoid Hemorrhage
- Liberal transfusion threshold of 10.0 g/dL recommended (higher than general critical care) 4
- Benefits of reducing cerebral ischemia and anemia may outweigh transfusion-associated complication risks 4
- Transfusion associated with increased vasospasm rates (particularly blood stored >14 days), infection, cardiovascular complications 4
- Use autologous blood <14 days old when available to minimize vasospasm 4
Monitoring Requirements
Vital signs must be checked at minimum: pre-transfusion, 15 minutes after starting, at completion, and 15 minutes post-transfusion. 1
Signs Requiring Immediate Action
- Tachycardia >110 beats/min 1
- Rash or urticaria 1
- Breathlessness or respiratory distress 1
- Back pain or chest tightness 1
- Temperature change, hypotension 1, 2
Critical Pitfalls to Avoid
- Never restart transfusion even if symptoms improve—reaction may worsen with continued exposure 2
- Do not assume isolated hypotension is benign—general anesthesia and critical illness mask early signs of serious reactions 2
- Do not give diuretics empirically—contraindicated in anaphylaxis, hypovolemic states, and TRALI 2
- Do not use albumin in trauma patients—trend toward higher mortality in trauma subgroup 2
- Avoid over-expansion in trauma—excessive fluid may exacerbate portal pressure, impair clot formation, increase bleeding 2
Documentation and Reporting
- 100% traceability is a legal requirement—document all transfusions in patient record 1
- Contact transfusion laboratory immediately to report any reaction and initiate investigation 1
- Notify patient's general practitioner (removes them from donor pool) 1
- Report to blood bank—TRALI is underdiagnosed and underreported despite being leading cause of transfusion-related mortality 1
- Inform patients they received blood products before discharge 1
Special Considerations for Pregnant Women
- Continuous fetal monitoring essential during suspected transfusion reaction 3
- Consider amniotic fluid embolism in differential diagnosis of fever and hypotension post-transfusion 3
- Obstetric consultation required; consider delivery if maternal condition deteriorates or fetal distress develops 3
- Same immediate management principles apply: stop transfusion, maintain IV access, supportive care 3
Prevention Strategies Summary
The best prevention is avoiding unnecessary transfusions and maintaining a restrictive transfusion strategy. 4, 5
- Preoperative evaluation: review medical records, check for congenital/acquired blood disorders, previous drug exposures (e.g., aprotinin causing allergic reactions on re-exposure) 4
- Discontinue anticoagulation therapy sufficiently in advance (clopidogrel ~1 week, warfarin several days) 4
- Use electronic transfusion management systems rather than manual checking 1
- Positive patient identification with four core identifiers on wristband 1
- Visually inspect blood components for leakage, discoloration, clots, or clumps before administration 1
- Transfuse single units in non-hemorrhaging patients and reassess before additional units 1