Blood Transfusion and Plasma Exchange

Introduction

  • Blood transfusion and plasma exchange are life-saving medical procedures that involve the transfer of blood or blood components from a donor to a recipient.

  • It is widely used in the management of anemia, massive blood loss, hematological disorders, malignancies, coagulation abnormalities, and critical care conditions.

  • With advancements in transfusion medicine, there has been a shift from whole blood transfusion to component therapy.

  • Component therapy allows targeted replacement of deficient blood components, improving efficacy and reducing complications.

  • Modern transfusion practice also includes the use of transfusion filters to prevent infusion of clots and cellular debris.

  • Post-transfusion monitoring is essential for early detection and management of transfusion reactions.

  • Advanced procedures such as therapeutic plasma exchange (TPE) have expanded the role of transfusion medicine in immune-mediated and metabolic disorders.

  • Proper knowledge of transfusion techniques, safety measures, and post-procedure care is vital to ensure patient safety, improve clinical outcomes, and minimize transfusion-related risks.

 


Blood Transfusion


Blood transfusion is the intravenous administration of whole blood or specific blood components such as red blood cells (RBCs), platelets, plasma, or cryoprecipitate to a patient for therapeutic purposes.

Indications of Blood Transfusion

Blood transfusion is indicated in the following conditions:

  • Acute blood loss (trauma, surgery, obstetric hemorrhage)

  • Severe anemia (Hb <7 g/dL or symptomatic anemia)

  • Hematological disorders (thalassemia, aplastic anemia)

  • Bleeding disorders and coagulopathies

  • Thrombocytopenia with active bleeding

  • Burns and shock

  • Liver disease with coagulation factor deficiency


Types of Blood Transfusion

a) Whole Blood Transfusion

  • Contains RBCs, plasma, platelets, and clotting factors

  • Rarely used today

  • Indicated in massive acute blood loss where component separation is unavailable

b) Component Therapy (Preferred Method)

Component Indication
Packed Red Blood Cells (PRBCs) Anemia, blood loss
Platelet Concentrates Thrombocytopenia
Fresh Frozen Plasma (FFP) Coagulation factor deficiency
Cryoprecipitate Hemophilia A, hypofibrinogenemia

 


Pre-Transfusion Compatibility Testing

Before transfusion, the following tests are mandatory:

  • ABO blood grouping

  • Rh typing

  • Antibody screening

  • Cross-matching

  • Infectious disease screening (HIV, HBV, HCV, Syphilis, Malaria)

 


Risks and Complications of Blood Transfusion

  • Acute hemolytic transfusion reaction

  • Febrile non-hemolytic reaction

  • Allergic reactions

  • Transfusion-related acute lung injury (TRALI)

  • Transfusion-associated circulatory overload (TACO)

  • Transmission of infections

  • Iron overload (chronic transfusion)

 


Transfusion Filters


A transfusion filter is a device incorporated into the blood transfusion set that removes clots, cellular debris, fibrin strands, and aggregates from blood or blood components before they enter the patient’s circulation.

Purpose of Transfusion Filters

  • Prevent microembolism

  • Reduce febrile transfusion reactions

  • Prevent infusion of clots and debris

  • Improve patient safety


Types of Transfusion Filters

a) Standard Blood Filters (170–260 µm)

  • Used routinely for whole blood and PRBC transfusion

  • Removes macroaggregates and clots

b) Microaggregate Filters (20–40 µm)

  • Used in massive transfusion

  • Removes platelet-leukocyte aggregates

c) Leukocyte Reduction Filters

  • Removes leukocytes

  • Reduces febrile reactions, CMV transmission, and HLA alloimmunization

d) Specialized Filters

  • Platelet-specific filters

  • Pediatric transfusion filters


Guidelines for Using Transfusion Filters

  • One filter per blood unit

  • Do not flush with dextrose or calcium-containing solutions

  • Maintain aseptic technique

  • Replace clogged filters immediately

 


Post-Transfusion Care


Importance of Post-Transfusion Monitoring

Post-transfusion care is critical for early detection of adverse reactions and ensuring therapeutic efficacy. Many transfusion reactions occur within the first few hours after transfusion.


Immediate Post-Transfusion Care

  • Monitor vital signs (pulse, BP, temperature, respiration)

  • Observe patient for:

    • Fever

    • Chills

    • Rash or itching

    • Dyspnea

    • Chest or back pain

  • Maintain IV access

  • Document transfusion details

 


Delayed Post-Transfusion Monitoring

Delayed reactions may occur days to weeks later:

  • Delayed hemolytic reaction

  • Post-transfusion purpura

  • Transfusion-associated graft-versus-host disease

  • Iron overload

Patients receiving chronic transfusions require:

  • Serum ferritin monitoring

  • Liver and cardiac evaluation

  • Iron chelation therapy if needed

 


Management of Transfusion Reactions

If any reaction is suspected:

  1. Stop transfusion immediately

  2. Maintain IV line with normal saline

  3. Inform blood bank and physician

  4. Send blood bag and patient samples for investigation

  5. Provide symptomatic treatment

 


Therapeutic Plasma Exchange


Therapeutic plasma exchange is an extracorporeal procedure in which plasma containing pathogenic substances is removed from the patient’s blood and replaced with donor plasma or replacement fluids.


Principle of Therapeutic Plasma Exchange

  • Blood is withdrawn from the patient

  • Plasma is separated from cellular components

  • Plasma containing autoantibodies, immune complexes, or toxins is discarded

  • Cellular components are returned with replacement fluid


Indications of Therapeutic Plasma Exchange

Neurological Disorders

  • Guillain-Barré syndrome

  • Myasthenia gravis

  • Chronic inflammatory demyelinating polyneuropathy

Hematological Disorders

  • Thrombotic thrombocytopenic purpura (TTP)

  • Hyperviscosity syndrome

  • Cryoglobulinemia

Renal and Autoimmune Diseases

  • Rapidly progressive glomerulonephritis

  • Lupus nephritis

  • Goodpasture syndrome

Metabolic and Toxic Conditions

  • Familial hypercholesterolemia

  • Certain drug or toxin removal


Replacement Fluids Used

  • Fresh frozen plasma

  • Albumin solution

  • Normal saline (limited use)

Choice depends on disease indication and coagulation status.


Complications of Therapeutic Plasma Exchange

  • Hypotension

  • Electrolyte imbalance

  • Bleeding due to coagulation factor loss

  • Allergic reactions

  • Infection risk due to central venous access


Advantages of Therapeutic Plasma Exchange

  • Rapid removal of pathogenic substances

  • Life-saving in acute immune-mediated disorders

  • Improves response to immunosuppressive therapy

 


Role of Laboratory and Blood Bank Services


Laboratory services are central to safe transfusion practices:

  • Donor screening and selection

  • Component preparation and storage

  • Compatibility testing

  • Transfusion reaction investigation

  • Quality control and hemovigilance

Strict adherence to transfusion protocols significantly reduces morbidity and mortality.


MCQs


1. Blood transfusion is defined as:
A. Oral administration of blood
B. Transfer of blood from patient to donor
C. Transfer of blood or blood components from donor to recipient
D. Exchange of plasma only

Answer: C


2. The most commonly used form of transfusion today is:
A. Whole blood
B. Plasma only
C. Component therapy
D. Autologous transfusion

Answer: C


3. Packed red blood cells (PRBCs) are mainly indicated for:
A. Coagulation disorders
B. Thrombocytopenia
C. Anemia
D. Hypoproteinemia

Answer: C


4. Fresh frozen plasma is used primarily to treat:
A. Anemia
B. Platelet deficiency
C. Coagulation factor deficiency
D. Iron overload

Answer: C


5. Which blood component is rich in fibrinogen?
A. PRBCs
B. Platelets
C. Cryoprecipitate
D. Whole blood

Answer: C


6. The minimum hemoglobin level commonly considered for transfusion in stable patients is:
A. 10 g/dL
B. 9 g/dL
C. 7 g/dL
D. 12 g/dL

Answer: C


7. Cross-matching is done to detect:
A. Blood group
B. Rh factor
C. Antibody-antigen incompatibility
D. Platelet count

Answer: C


8. Which infection is mandatorily screened before blood transfusion?
A. Tuberculosis
B. HIV
C. Dengue
D. Typhoid

Answer: B


9. Acute hemolytic transfusion reaction is most commonly due to:
A. Platelet incompatibility
B. ABO incompatibility
C. Leukocyte reaction
D. Volume overload

Answer: B


10. The safest route for blood transfusion is:
A. Intramuscular
B. Subcutaneous
C. Intravenous
D. Intra-arterial

Answer: C


Transfusion Filters – MCQs

11. The main function of a transfusion filter is to remove:
A. Viruses
B. Bacteria
C. Clots and debris
D. Plasma proteins

Answer: C


12. The pore size of a standard blood transfusion filter is:
A. 5–10 µm
B. 20–40 µm
C. 170–260 µm
D. 500 µm

Answer: C


13. Microaggregate filters are mainly used during:
A. Platelet transfusion
B. Massive transfusion
C. Plasma exchange
D. Pediatric transfusion

Answer: B


14. Leukocyte reduction filters help reduce:
A. Hemolysis
B. Iron overload
C. Febrile reactions
D. Bleeding risk

Answer: C


15. One transfusion filter should be used for:
A. Multiple patients
B. One blood unit
C. One hospital shift
D. One donor

Answer: B


16. Which solution should NOT be used to flush transfusion filters?
A. Normal saline
B. Dextrose
C. Sterile saline
D. Isotonic saline

Answer: B


17. Transfusion filters are mandatory for transfusion of:
A. Oral iron
B. Blood components
C. IV fluids
D. Medications

Answer: B


Post-Transfusion Care – MCQs

18. The most critical period for transfusion reactions is:
A. After 24 hours
B. First 15–30 minutes
C. After 7 days
D. After 1 month

Answer: B


19. Which vital sign must be monitored during transfusion?
A. Pulse
B. Blood pressure
C. Temperature
D. All of the above

Answer: D


20. The first step when a transfusion reaction is suspected is to:
A. Give antihistamines
B. Slow the transfusion
C. Stop the transfusion
D. Change IV line

Answer: C


21. Febrile non-hemolytic transfusion reaction is commonly due to:
A. RBC destruction
B. Leukocyte cytokines
C. Plasma proteins
D. Platelet deficiency

Answer: B


22. Which is a delayed transfusion reaction?
A. Anaphylaxis
B. TRALI
C. Delayed hemolytic reaction
D. Hypotension

Answer: C


23. Iron overload is seen mainly in:
A. Single transfusion
B. Plasma transfusion
C. Chronic transfusion patients
D. Platelet transfusion

Answer: C


24. Transfusion-associated circulatory overload (TACO) occurs due to:
A. Infection
B. Excess volume
C. Hemolysis
D. Allergy

Answer: B


25. After stopping transfusion due to reaction, IV line should be kept open with:
A. Dextrose
B. Ringer lactate
C. Normal saline
D. Blood

Answer: C


Therapeutic Plasma Exchange (TPE) – MCQs

26. Therapeutic plasma exchange involves removal of:
A. RBCs only
B. Platelets only
C. Plasma
D. Whole blood

Answer: C


27. TPE is also known as:
A. Hemodialysis
B. Plasmapheresis
C. Hemofiltration
D. Ultrafiltration

Answer: B


28. The main purpose of TPE is to remove:
A. Electrolytes
B. Pathogenic antibodies
C. Oxygen
D. Red cells

Answer: B


29. TPE is the treatment of choice for:
A. Iron deficiency anemia
B. Thrombotic thrombocytopenic purpura
C. Hemophilia
D. Leukemia

Answer: B


30. Guillain-Barré syndrome is treated by:
A. Whole blood transfusion
B. Platelet transfusion
C. Therapeutic plasma exchange
D. Cryoprecipitate

Answer: C


31. Replacement fluid commonly used in TPE is:
A. Whole blood
B. Packed RBCs
C. Albumin
D. Platelets

Answer: C


32. Which condition is NOT an indication for TPE?
A. Myasthenia gravis
B. TTP
C. Iron deficiency anemia
D. Hyperviscosity syndrome

Answer: C


33. A common complication of TPE is:
A. Hypertension
B. Hypotension
C. Polycythemia
D. Hyperglycemia

Answer: B


34. Loss of coagulation factors during TPE may cause:
A. Thrombosis
B. Bleeding
C. Infection
D. Fever

Answer: B


35. Central venous access is often required for:
A. Platelet transfusion
B. Plasma exchange
C. IM injection
D. Oral therapy

Answer: B


Mixed / Applied MCQs

36. TRALI stands for:
A. Transfusion-Related Acute Lung Injury
B. Transfusion-Related Allergic Lung Infection
C. Transfusion-Related Arterial Lung Ischemia
D. Transfusion-Related Autoimmune Lung Injury

Answer: A


37. Which blood component should be ABO compatible?
A. PRBCs
B. Platelets
C. Plasma
D. All of the above

Answer: D


38. CMV transmission risk is reduced by:
A. Plasma exchange
B. Leukocyte-reduced blood
C. Whole blood
D. Iron chelation

Answer: B


39. The best blood component for hypofibrinogenemia is:
A. PRBC
B. FFP
C. Cryoprecipitate
D. Platelets

Answer: C


40. Post-transfusion purpura is due to:
A. Platelet antibodies
B. RBC antibodies
C. Plasma proteins
D. Iron toxicity

Answer: A


41. The safest IV fluid compatible with blood transfusion is:
A. Dextrose
B. Ringer lactate
C. Normal saline
D. DNS

Answer: C


42. Which reaction presents with fever and chills without hemolysis?
A. Allergic reaction
B. Febrile non-hemolytic reaction
C. Acute hemolytic reaction
D. TRALI

Answer: B


43. The aim of component therapy is to:
A. Reduce blood usage
B. Target specific deficiency
C. Increase transfusion reactions
D. Delay treatment

Answer: B


44. Therapeutic plasma exchange is most useful in:
A. Infectious diseases
B. Immune-mediated diseases
C. Nutritional anemia
D. Trauma

Answer: B


45. Which blood component has the longest shelf life?
A. Platelets
B. PRBCs
C. Plasma (frozen)
D. Whole blood

Answer: C


46. Platelets should be transfused using:
A. No filter
B. Standard blood filter
C. Microaggregate filter only
D. Dialysis filter

Answer: B


47. Iron chelation therapy is required in:
A. Acute transfusion
B. Platelet transfusion
C. Chronic transfusion patients
D. Plasma exchange

Answer: C


48. The primary goal of post-transfusion care is to:
A. Increase Hb rapidly
B. Detect adverse reactions early
C. Reduce blood cost
D. Improve storage

Answer: B


49. Blood transfusion reactions should always be:
A. Ignored
B. Documented and reported
C. Treated at home
D. Delayed

Answer: B


50. Therapeutic plasma exchange mainly removes substances present in:
A. RBCs
B. Platelets
C. Plasma
D. Bone marrow

Answer: C