transfusion

1. Transfusion Medicine:
Types, Indications and
Complications
David Harford
Hematology/Oncology

2. History of Transfusions
• Blood transfused in humans since mid-
1600’s
• 1828 – First successful transfusion
• 1900 – Landsteiner described ABO groups
• 1916 – First use of blood storage
• 1939 – Levine described the Rh factor

3. Transfusion Overview
• Integral part of medical treatment
• Most often used in Hematology/Oncology, but
other specialties as well (surgery, ICU, etc)
• Objectives
– Blood components
– Indications for transfusion
– Safe delivery
– Complications

4. Blood Components
• Prepared from Whole blood collection or apheresis
• Whole blood is separated by differential centrifugation
– Red Blood Cells (RBC’s)
– Platelets
– Plasma
• Cryoprecipitate
• Others
• Others include Plasma proteins—IVIg, Coagulation
Factors, albumin, Anti-D, Growth Factors, Colloid volume
expanders
• Apheresis may also used to collect blood components

5. Differential Centrifugation
First Centrifugation
Whole Blood
Main Bag
Satellite Bag
1
Satellite Bag
2
RBC’s
Platelet-rich
Plasma
First
Closed System

6. Differential Centrifugation
Second Centrifugation
Platelet-rich
Plasma
RBC’s
Platelet
Concentrate
RBC’s
Plasma
Second

7. Whole Blood
• Storage
– 4° for up to 35 days
• Indications
– Massive Blood Loss/Trauma/Exchange Transfusion
• Considerations
– Use filter as platelets and coagulation factors will not
be active after 3-5 days
– Donor and recipient must be ABO identical

8. RBC Concentrate
• Storage
– 4° for up to 42 days, can be frozen
• Indications
– Many indications—ie anemia, hypoxia, etc.
• Considerations
– Recipient must not have antibodies to donor RBC’s
(note: patients can develop antibodies over time)
– Usual dose 10 cc/kg (will increase Hgb by 2.5 gm/dl)
– Usually transfuse over 2-4 hours (slower for chronic
anemia

9. Platelets
• Storage
– Up to 5 days at 20-24°
• Indications
– Thrombocytopenia, Plt <15,000
– Bleeding and Plt <50,000
– Invasive procedure and Plt <50,000
• Considerations
– Contain Leukocytes and cytokines
– 1 unit/10 kg of body weight increases Plt count by 50,000
– Donor and Recipient must be ABO identical

10. Plasma and FFP
• Contents—Coagulation Factors (1 unit/ml)
• Storage
– FFP--12 months at –18 degrees or colder
• Indications
– Coagulation Factor deficiency, fibrinogen replacement, DIC, liver
disease, exchange transfusion, massive transfusion
• Considerations
– Plasma should be recipient RBC ABO compatible
– In children, should also be Rh compatible
– Account for time to thaw
– Usual dose is 20 cc/kg to raise coagulation factors approx 20%

11. Cryoprecipitate
• Description
– Precipitate formed/collected when FFP is thawed at 4°
• Storage
– After collection, refrozen and stored up to 1 year at -18°
• Indication
– Fibrinogen deficiency or dysfibrinogenemia
– vonWillebrands Disease
– Factor VIII or XIII deficiency
– DIC (not used alone)
• Considerations
– ABO compatible preferred (but not limiting)
– Usual dose is 1 unit/5-10 kg of recipient body weight

12. Granulocyte Transfusions
• Prepared at the time for immediate transfusion (no
storage available)
• Indications – severe neutropenia assoc with
infection that has failed antibiotic therapy, and
recovery of BM is expected
• Donor is given G-CSF and steroids or Hetastarch
• Complications
– Severe allergic reactions
– Can irradiate granulocytes for GVHD prevention

13. Leukocyte Reduction Filters
• Used for prevention of transfusion reactions
• Filter used with RBC’s, Platelets, FFP,
Cryoprecipitate
• Other plasma proteins (albumin, colloid
expanders, factors, etc.) do not need filters—
NEVER use filters with stem cell/bone marrow
infusions
• May reduce RBC’s by 5-10%
• Does not prevent Graft Verses Host Disease
(GVHD)

14. RBC Transfusions
Preparations
• Type
– Typing of RBC’s for ABO and Rh are determined for
both donor and recipient
• Screen
– Screen RBC’s for atypical antibodies
– Approx 1-2% of patients have antibodies
• Crossmatch
– Donor cells and recipient serum are mixed and
evaluated for agglutination

15. RBC Transfusions
Administration
• Dose
– Usual dose of 10 cc/kg infused over 2-4 hours
– Maximum dose 15-20 cc/kg can be given to hemodynamically
stable patient
• Procedure
– May need Premedication (Tylenol and/or Benadryl)
– Filter use—routinely leukodepleted
– Monitoring—VS q 15 minutes, clinical status
– Do NOT mix with medications
• Complications
– Rapid infusion may result in Pulmonary edema
– Transfusion Reaction

16. Platelet Transfusions
Preparations
• ABO antigens are present on platelets
– ABO compatible platelets are ideal
– This is not limiting if Platelets indicated and type
specific not available
• Rh antigens are not present on platelets
– Note: a few RBC’s in Platelet unit may sensitize the
Rh- patient

17. Platelet Transfusions
Administration
• Dose
– May be given as single units or as apheresis units
– Usual dose is approx 4 units/m2—in children using 1-2
apheresis units is ideal
– 1 apheresis unit contains 6-8 Plt units (packs) from a
single donor
• Procedure
– Should be administered over 20-40 minutes
– Filter use
– Premedicate if hx of Transfusion Reaction
• Complications—Transfusion Reaction

18. Transfusion Complications
• Acute Transfusion Reactions (ATR’s)
• Chronic Transfusion Reactions
• Transfusion related infections

19. Acute Transfusion Reactions
• Hemolytic Reactions (AHTR)
• Febrile Reactions (FNHTR)
• Allergic Reactions
• TRALI
• Coagulopathy with Massive transfusions
• Bacteremia

20. Frequency of Transfusion Reactions
Adverse Effect Frequency Comments
Acute Hemolytic Rxn 1 in 25,000 Red cells only
Anaphylactic hypotensive 1 in 150,000 Including IgA
Febrile Nonhemolytic 1 in 200 Common
Allergic 1 in 1,000 Common
Delayed Hemolytic 1 in 2,500 Red cells only
RBC alloimmunization 1 in 100 Red cells only
WBC/Plt
alloimmunization
1 in 10 WBC and Plt only

21. Acute Hemolytic Transfusion
Reactions (AHTR)
• Occurs when incompatible RBC’s are transfused into a
recipient who has pre-formed antibodies (usually ABO or
Rh)
• Antibodies activate the complement system, causing
intravascular hemolysis
• Symptoms occur within minutes of starting the transfusion
• This hemolytic reaction can occur with as little as 1-2 cc of
RBC’s
• Labeling error is most common problem
• Can be fatal

22. Symptoms of AHTR
• High fever/chills
• Hypotension
• Back/abdominal pain
• Oliguria
• Dyspnea
• Dark urine
• Pallor

23. What to do?
If an AHTR occurs
• STOP TRANSFUSION
• ABC’s
• Maintain IV access and run IVF (NS or LR)
• Monitor and maintain BP/pulse
• Give diuretic
• Obtain blood and urine for transfusion reaction
workup
• Send remaining blood back to Blood Bank

24. Blood Bank Work-up of AHTR
• Check paperwork to assure no errors
• Check plasma for hemoglobin
• DAT
• Repeat crossmatch
• Repeat Blood group typing
• Blood culture

25. Labs found with AHTR
• Hemoglobinemia
• Hemoglobinuria
• Positive DAT
• Hyperbilirubinemia
• Abnormal DIC panel

26. Monitoring in AHTR
• Monitor patient clinical status and vital
signs
• Monitor renal status (BUN, creatinine)
• Monitor coagulation status (DIC panel–
PT/PTT, fibrinogen, D-dimer/FDP, Plt,
Antithrombin-III)
• Monitor for signs of hemolysis (LDH, bili,
haptoglobin)

27. Febrile Nonhemolytic Transfusion
Reactions (FNHTR)
• Definition--Rise in patient temperature >1°C
(associated with transfusion without other fever
precipitating factors)
• Occurs with approx 1% of PRBC transfusions and
approx 20% of Plt transfusions
• FNHTR caused by alloantibodies directed against
HLA antigens
• Need to evaluate for AHTR and infection

28. What to do?
If an FNHTR occurs
• STOP TRANSFUSION
• Use of Antipyretics—responds to Tylenol
• Use of Corticosteroids for severe reactions
• Use of Narcotics for shaking chills
• Future considerations
– May prevent reaction with leukocyte filter
– Use single donor platelets
– Use fresh platelets
– Washed RBC’s or platelets

29. Washed Blood Products
• PRBC’s or platelets washed with saline
• Removes all but traces of plasma (>98%)
• Indicated to prevent recurrent or severe reactions
• Washed RBC’s must be used within 24 hours
• RBC dose may be decreased by 10-20% by
washing
• Does not prevent GVHD

30. Allergic Nonhemolytic Transfusion
Reactions
• Etiology
– May be due to plasma proteins or blood
preservative/anticoagulant
– Best characterized with IgA given to an IgA deficient
patients with anti-IgA antibodies
• Presents with urticaria and wheezing
• Treatment
– Mild reactions—Can be continued after Benadryl
– Severe reactions—Must STOP transfusion and may
require steroids or epinephrine
• Prevention—Premedication (Antihistamines)

31. TRALI
Transfusion Related Acute Lung Injury
• Clinical syndrome similar to ARDS
• Occurs 1-6 hours after receiving plasma-
containing blood products
• Caused by WBC antibodies present in donor
blood that result in pulmonary leukostasis
• Treatment is supportive
• High mortality

32. Massive Transfusions
• Coagulopathy may occur after transfusion
of massive amounts of blood
(trauma/surgery)
• Coagulopathy is caused by failure to replace
plasma
• See electrolyte abnormalities
– Due to citrate binding of Calcium
– Also due to breakdown of stored RBC’s

33. Bacterial Contamination
• More common and more severe with
platelet transfusion (platelets are stored at
room temperature)
• Organisms
– Platelets—Gram (+) organisms, ie Staph/Strep
– RBC’s—Yersinia, enterobacter
• Risk increases as blood products age (use
fresh products for immunocompromised)

34. Chronic Transfusion Reactions
• Alloimmunization
• Transfusion Associated Graft Verses Host
Disease (GVHD)
• Iron Overload
• Transfusion Transmitted Infection

35. Alloimmunization
• Can occur with erythrocytes or platelets
• Erythrocytes
– Antigen disparity of minor antigens (Kell, Duffy, Kidd)
– Minor antigens D, K, E seen in Sickle patients
• Platelets
– Usually due to HLA antigens
– May reduce alloimmunization by leukoreduction (since
WBC’s present the HLA antigens)

36. Transfusion Associated GVHD
• Mainly seen in infants, BMT patients, SCID
• Etiology—Results from engraftment of
donor lymphocytes of an immunocompetent
donor into an immunocompromised host
• Symptoms—Diarrhea, skin rash,
pancytopenia
• Usually fatal—no treatment
• Prevention—Irradiation of donor cells

37. Transfusion Associated Infections
• Hepatitis C
• Hepatitis B
• HIV
• CMV
– CMV can be diminished by leukoreduction,
which is indicated for immunocompromised
patients

38. Prevention
Leukocyte
Depletion
Filter
Gamma
Irradiation
CMV
Negative
Single Donor
Platelets
(Apheresis)
Febrile Transfusion
Reactions X1 X
Alloimmunization
X X
CMV
?2 X
Transfusion Related
GVHD X
1 In PRBC transfusion
2 Leukocyte Reduction by filtration may be an alternative to CMV-negative blood

39. Summary
• Blood Components
– Indications
– Considerations
• Preparation and Administration of blood
products
• Acute and chronic transfusion reactions

40. Transfusion Reaction Summary
• AHTR can be fatal
• Stop the Transfusion
• Monitor for symptoms and complete evaluation
• FNHTR is a diagnosis of exclusion
• TRALI (ARDS-like reaction)
• Chronic Transfusion reactions
• Prevention methods – using filters, irradiation and
premedication