Introduction
-
Blood transfusion is a life-saving medical procedure widely used in anemia, trauma, surgery, obstetric emergencies, hematological disorders, and critical care.
-
Advances in transfusion medicine, such as component therapy, donor screening, and improved laboratory testing, have significantly increased transfusion safety.
-
Despite these advances, blood transfusion is not completely risk-free.
-
Blood is a complex biological product containing red cells, white cells, platelets, plasma proteins, electrolytes, and immunologically active substances.
-
Transfusion of donor blood can trigger immune, infectious, metabolic, and circulatory complications in the recipient.
-
Transfusion reactions may range from mild febrile or allergic reactions to severe life-threatening complications, such as:
-
Acute hemolytic transfusion reaction
-
Transfusion-related acute lung injury (TRALI)
-
Transfusion-associated circulatory overload (TACO)
-
Transfusion-transmitted infections
-
-
A large proportion of transfusion hazards occur due to human and system-related errors, including:
-
Incorrect patient identification
-
Improper blood grouping or cross-matching
-
Inappropriate indication for transfusion
-
Inadequate monitoring during transfusion
-
-
Therefore, prevention of transfusion hazards is a critical component of safe transfusion practice.
-
Prevention requires a multilevel approach, involving:
-
Proper donor selection and screening
-
Strict blood bank protocols
-
Rational clinical decision-making
-
Careful patient monitoring
-
Classification
Transfusion hazards are broadly classified based on time of onset and mechanism:
-
Immediate (Acute) Complications
-
Delayed Complications
-
Infectious Complications
-
Metabolic and Hemodynamic Complications
-
Immunological Complications
-
Complications Related to Massive Transfusion
Immediate (Acute) Transfusion Complications
These occur during transfusion or within 24 hours.
A. Acute Hemolytic Transfusion Reaction (AHTR)
Cause
-
ABO incompatibility (most commonly due to clerical or labeling errors)
-
Preformed IgM antibodies activate complement
Pathophysiology
-
Rapid destruction of donor red cells
-
Release of free hemoglobin
-
Activation of inflammatory mediators
Clinical Features
-
Sudden fever and chills
-
Severe back pain
-
Chest tightness
-
Hypotension
-
Hemoglobinuria
-
Oliguria or anuria
Complications
-
Acute renal failure
-
Disseminated intravascular coagulation (DIC)
-
Shock
-
Death
Management
-
Immediate stoppage of transfusion
-
Maintain urine output
-
Supportive therapy
B. Febrile Non-Hemolytic Transfusion Reaction (FNHTR)
Cause
-
Cytokines released from donor leukocytes
-
Recipient antibodies against donor white cells
Clinical Features
-
Rise in temperature ≥1°C
-
Chills and rigors
-
Headache
Importance
-
Common but usually benign
-
Must be differentiated from hemolysis or sepsis
Prevention
-
Leukoreduced blood components
C. Allergic and Anaphylactic Reactions
Mild Allergic Reaction
-
Caused by plasma proteins
-
Urticaria, itching, flushing
Severe Anaphylaxis
-
Seen in IgA-deficient recipients
-
Bronchospasm
-
Hypotension
-
Angioedema
Management
-
Antihistamines (mild)
-
Epinephrine and airway support (severe)
D. Transfusion-Related Acute Lung Injury (TRALI)
Cause
-
Donor anti-HLA or anti-neutrophil antibodies
Onset
-
Within 6 hours of transfusion
Features
-
Acute respiratory distress
-
Hypoxemia
-
Non-cardiogenic pulmonary edema
Significance
-
Leading cause of transfusion-related mortality
E. Transfusion-Associated Circulatory Overload (TACO)
Cause
-
Rapid or excessive volume transfusion
High-Risk Groups
-
Elderly
-
Pediatric patients
-
Cardiac or renal disease
Features
-
Dyspnea
-
Raised JVP
-
Pulmonary edema
-
Hypertension
Delayed Transfusion Complications
These occur days to weeks after transfusion.
A. Delayed Hemolytic Transfusion Reaction
Cause
-
Secondary immune response to minor RBC antigens
Features
-
Mild anemia
-
Jaundice
-
Fall in hemoglobin
B. Alloimmunization
Definition
-
Formation of antibodies against donor antigens
Clinical Importance
-
Makes future transfusions difficult
-
Increases risk of hemolytic reactions
Common in
-
Thalassemia
-
Sickle cell disease
C. Transfusion-Associated Graft Versus Host Disease (TA-GVHD)
Mechanism
-
Viable donor T lymphocytes attack recipient tissues
Symptoms
-
Fever
-
Skin rash
-
Diarrhea
-
Pancytopenia
Mortality
-
Very high (>90%)
Prevention
-
Irradiated blood products
Infectious Complications of Blood Transfusion
Despite screening, window period infections can occur.
A. Viral Infections
-
HIV
-
Hepatitis B
-
Hepatitis C
-
HTLV
B. Bacterial Contamination
Most Common With
-
Platelet concentrates (stored at room temperature)
Features
-
High fever
-
Hypotension
-
Septic shock
C. Parasitic Infections
-
Malaria
-
Babesiosis
-
Trypanosomiasis
Metabolic Complications
A. Citrate Toxicity
-
Citrate binds calcium
-
Leads to hypocalcemia
Features
-
Tingling
-
Tetany
-
Arrhythmias
B. Hyperkalemia
-
Potassium leaks from stored RBCs
-
Risk in neonates and massive transfusions
C. Hypothermia
-
Rapid transfusion of cold blood
-
Causes arrhythmias and coagulopathy
Complications of Massive Blood Transfusion
Definition
-
Replacement of one blood volume within 24 hours
Complications
-
Dilutional coagulopathy
-
Thrombocytopenia
-
Metabolic acidosis
-
Electrolyte imbalance
Iron Overload
Cause
-
Repeated transfusions
Organ Damage
-
Liver (cirrhosis)
-
Heart (cardiomyopathy)
-
Endocrine glands (diabetes, hypogonadism)
Prevention of Transfusion Hazards
1. Prevention at the Donor Level
A. Proper Donor Selection
-
Detailed medical history and physical examination
-
Exclusion of donors with:
-
Recent infections
-
High-risk behavior
-
Chronic diseases
-
-
Ensures safety for both donor and recipient
B. Mandatory Screening of Donor Blood
Each donated unit must be tested for:
-
HIV 1 & 2
-
Hepatitis B (HBsAg)
-
Hepatitis C
-
Syphilis
-
Malaria
Nucleic Acid Testing (NAT) further reduces the window period and risk of transfusion-transmitted infections.
2. Prevention at the Blood Bank Level
A. Proper Blood Grouping and Cross-Matching
-
Accurate ABO and Rh typing
-
Antibody screening
-
Compatibility testing between donor and recipient
Most fatal transfusion reactions occur due to clerical errors, not lab errors.
B. Component Therapy Instead of Whole Blood
-
Use only the required component:
-
Packed RBCs
-
Platelets
-
Fresh Frozen Plasma (FFP)
-
-
Reduces volume overload and unnecessary exposure
C. Leukoreduction
-
Removal of donor leukocytes
-
Prevents:
-
Febrile non-hemolytic reactions
-
CMV transmission
-
HLA alloimmunization
-
D. Irradiation of Blood Products
-
Inactivates donor lymphocytes
-
Prevents Transfusion-Associated Graft-Versus-Host Disease (TA-GVHD)
-
Indicated in:
-
Immunocompromised patients
-
Neonates
-
Bone marrow transplant recipients
-
E. Proper Storage and Handling
-
Maintain correct temperature:
-
RBCs: 2–6°C
-
Platelets: 20–24°C with agitation
-
-
Avoid expired or improperly stored units
-
Prevent bacterial contamination
3. Prevention at the Patient Level
A. Strict Patient Identification
-
Verify:
-
Patient name
-
Hospital ID
-
Blood group
-
-
Match with blood unit label and compatibility report
This is the most critical step in preventing acute hemolytic reactions.
B. Rational Indication for Transfusion
-
Transfuse only when clearly indicated
-
Avoid unnecessary transfusions
-
Follow restrictive transfusion thresholds when possible
C. Informed Consent
-
Explain:
-
Benefits
-
Risks
-
Alternatives
-
-
Obtain written consent prior to transfusion
4. Prevention During Transfusion
A. Proper Administration
-
Use standard transfusion sets with filters
-
Do not add drugs to blood
-
Start transfusion slowly (first 15 minutes critical)
B. Close Monitoring of Patient
-
Monitor:
-
Pulse
-
Blood pressure
-
Temperature
-
Respiratory rate
-
-
Especially during initial 15–30 minutes
C. Early Recognition of Adverse Reactions
Stop transfusion immediately if:
-
Fever or chills
-
Breathlessness
-
Chest or back pain
-
Rash or itching
-
Hypotension
5. Prevention of Metabolic and Volume-Related Hazards
A. Prevention of TACO
-
Slow transfusion rate
-
Use diuretics in high-risk patients
-
Avoid unnecessary volume
B. Prevention of Citrate Toxicity
-
Monitor calcium levels
-
Calcium supplementation during massive transfusion
C. Prevention of Hyperkalemia
-
Use fresh blood in neonates
-
Monitor electrolytes in massive transfusion
D. Prevention of Hypothermia
-
Use blood warmers during rapid transfusion
6. Post-Transfusion Prevention Measures
A. Post-Transfusion Monitoring
-
Observe patient for delayed reactions
-
Monitor hemoglobin and vital signs
B. Documentation and Reporting
-
Document transfusion details
-
Report adverse reactions to:
-
Blood bank
-
Hospital transfusion committee
-
C. Hemovigilance Programs
-
Continuous monitoring of transfusion safety
-
Helps identify system errors and improve practices
7. Institutional and Policy-Level Prevention
-
-
Standard operating procedures (SOPs)
-
Regular staff training
-
Transfusion audits
-
National hemovigilance systems
-