Blood Transfusion Flashcards

1
Q

What are the two main grouping systems in blood products?

A

ABO grouping system
Rhesus grouping system

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2
Q

What two main grouping systems need to be known to minimise transfusion reactions?

A

ABO grouping system
* antigens attached to RBC cell surface.
Rhesus grouping system
* rhesus D = most immunogenic, so most likely to precipitate a transfusion reaction.

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3
Q

Describe the ABO Grouping system
1. how are antigens inherited?
2. what antigens and antibodies does each group have?
3. why is understanding the ABO grouping system important?

A
  1. one ABO allele from each parent - A and B alleles are co-dominant
  2. Group A have antigen A and antiB antibodies. Group B have antigen B and antiA antibodies. Group AB have both antigen A and B. and neither antibody. Group O have neither antigen, but have both antiA and antiB antibodies.
  3. Important - have ABO antibodies in plasma.
    * these recognise and attack RBCs that express foreign antigens
    * antibodies develop in first few years of life
    * important in blood transfusion
    * if give incompatible blood group to someone = fatal
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4
Q

What type of immunoglobulins are A and B antibodies?

A

IgM

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5
Q

What blood group is a universal acceptor of blood?
Why are they an acceptor?

A

AB+ve
* can have any donor blood - so A, B, AB, O, Rh+ve or Rh-ve.
* an acceptor as they have no A or B antibodies in plasma and no Rhesus anitbodies.
* because of this - the body can not initiate an immune response to donor blood.

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6
Q

What are the Rh D groups?
list and describe them

A

RhD +ve –> have the Rh D antigen and can recieve both Rh+ and RH- blood
RhD -ve –> lack the Rh D antigen and should only recieve Rh- blood

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7
Q

Why should Rh- patients only receive Rh- blood?

A
  • Anti-D antibody is usually absent in Rh- patients (until they have been exposed to Rh+ erythrocytes).
  • Rh- patients should not be transfused with Rh+ blood as this can cause them to develop anti-D antibodies.
  • This may cause transfusion reactions in the future.
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8
Q

What blood type are universal donors, and why?

A
  • People with blood type O- are universal donors
  • they can donate their blood to anyone.
  • This is because their RBCs have no A, B, or RhD antigens which the recipient’s immune system could attack.
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9
Q

Describe haemolytic disease of the newborn (HDN)

A

1st pregnancy
* Mother is RhD-ve. Her partner is RhD+ve.
* She becomes preggo with fetus who is RhD+ve.
* In childbirth, mother comes into contact with the foetal RhD+ve blood
* Because of this, she makes has RhD sensitisation and makes antibodies to the RhD+ve. She has produced anti-D antibodies which are in her maternal circulation. This is a first exposure - antibodies are IgM so can NOT cross the placenta.
* If the mother becomes pregnant again with a child who is RhD+ve = not good.

2nd pregnancy with child who is RhD+ve
* Mothers anti-D antibodies can cross the placenta during this pregnancy –> foetal circulation containing RhD+ve antigens.
* Maternal anti-D antibodies recognise and destroy foetal Rh+ RBCs.
* Why? This is a second exposure –> anti-D antibodies are IgG which can cross the placenta and cause haemolysis.
* leads to foetal anaemia = HDN.

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10
Q

What happens when you give a RhD-ve patient RhD+ve blood transfusion?
When would this specifically be a problem?

A
  • the patient will make RhD antibodies
  • for the patient - this is not a problem as their blood does not have RhD in - so have nothing to attack

This would be a problem during pregnancy
* anti-D antibodies (made from the intiial blood recieved) can cross the placenta
* cause haemolytic disease of the newborn
* so need to give women blood specific to their RhD status.

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11
Q

What investigations/tests do you need to do before giving a patient blood transfusion?

A
  • Group and save
  • Cross match
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12
Q

What is a group and save blood test?

A
  • aka ABO typing
  • tests the patient’s blood for the presence of A/B antigens, A/B antibodies and Rh typing.
  • The lab will also screen the patient’s blood for atypical antibodies
  • takes ~40mins
  • blood can NOT be issued after this test alone.
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13
Q

What is cross-matching?

A
  • involves mixing the donor’s blood with the recipient’s blood to detect any immune reaction.
  • takes ~40mins to do this after an initial 40mins to G+S
  • if no immune reaction = donor blood CAN be issued and transfused into patient.
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14
Q

In blood transfusion…

What is electronic issue (EI)?

A

Leeds Teaching Hospital website:
* Electronic Issue is the process whereby blood is issued to a patient without crossmatching thus creating a large time saving for urgent and theatre cases. For EI to be applied, certain strict criteria must be met.

NHS website:

  • Electronic issue (EI) is the selection and issue of red cell units where compatibility is determined by the Laboratory Information Management System (LIMS) without serological testing (serological crossmatch) of donor cells against patient plasma.
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15
Q

What is the Coombs’ test?
Describe direct and indirect Coombs’ test

A

Detects presence of antibodies against RBCs.
Direct:
* mix patient blood with coombs’ reagent
* coombs’ reagent binds to specific immunoglobulins on RBCs
* positive result = RBCs clump together (agglutinate)

Indirect:
* used in cross matching and to detect anti-D igG.
* Donor’s RBCs and Coombs’ reagent is combined with the patient’s isolated plasma
* positive result = if agglutination occurs. i.e. patient has antibodies against the antigens in donor’s RBCs.

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16
Q

Explain how to take and label blood samples and request blood components for transfusion

A

Check patient details
* Using 3 points of identification to check you are with the correct patient (name, DOB and patient number).

Consent
* Consent the patient appropriately – many transfusion request forms will now have a script on them, which you should read to the patient. A consent form (as you would use for consent for any procedure) is completed.

Labelling
* Labelling the bottle at the bedside (pre-printed stickers for blood transfusion are usually not allowed in many countries, including the UK)

Request transfusion
* Completing the transfusion request form at the bedside. Before you put the blood bottle into the request bag, check with the patient that they are happy you have labelled things correctly.

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17
Q

What is Hb concentration threshold for patients needing blood cell transfusion?

A

Current NICE guidelines recommend a restrictive haemoglobin concentration threshold of 70 g/L for those who need red blood cell transfusions (without any major haemorrhage or acute coronary syndrome) and a haemoglobin concentration target of 70-90 g/L after transfusion

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18
Q

How is blood safely stored?

A
  • RBC are stored between 2-6 degrees and can be kept for up to 35 days
  • Platelets are kept at 22 degrees and are only kept for 5 days. Note: Moving shelves which stop them sticking together
  • Plasma and cryo are frozen and stored in freezers for up to one year

from Sas

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19
Q

How are blood products safely administered?
* what needs to be done to blood before administration?
* how should they be prescribed if more than one unit is needed?
* what observations are required?
* what cannula is used? and why?

A

Blood must be warmed to prevent hypothermia and prevent haemolysis.

If a patient requires more than one unit of blood, each unit must be prescribed individually.
Whilst the patient is receiving the transfusion, there are specific observations timings that should be carried out:

  • Before the transfusion starts.
  • 15-20 minutes after it has started.
  • At 1 hour.
  • At completion.

Blood products should only be administered through a 18G or 16G cannula, otherwise the cells haemolyse due to sheering forces in the narrow tube.

NICE guidelines suggest single unit red blood cell transfusions for the surgical patient who does not have active bleeding, reassessing the patient after each transfusion.

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20
Q

What are blood donors screened for?

A
  • Syphillis
  • Hep B
  • HIV
  • HepC
  • HepE
  • Human T-lymphotropic virus
  • Malaria
  • T-cruzi - Trypanosoma cruzi
  • West Nile Virus
  • Cutomegalovirus (CMV)
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21
Q

How are blood donors recruited?

A

Volunteers
This Is Amazing - NHS Blood donation campagn = celebrate donors and urge others to join/volunteer.

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22
Q

What are the different types of blood products that can be transfused?

A

Red cell transfusion
Platelet transfusion
Cryoprecipitate
Fresh frozen plasma
Prothrombin complex concentrate

Note: when a donor gives blood, it is separated into these different parts.

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23
Q

What are the indications for red cell transfusion? (aka packed red cells = red blood cells)

A

Indications
* Acute blood loss
* Chronic anaemia, where the Hb ≤ 70g/L (or ≤ 80g/L in those with cardiovascular disease) or symptomatic anaemia

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24
Q

For packed red cells (red cell transfusion), what duration is it administered over?

A

2-4 hours. It must be completed within 4 hours of coming out of the store

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25
Q

After giving 1 unit of blood, how much will patient’s Hb increase by?

A

10 g/L

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26
Q

Why would a patient given red blood cells need a new G+S to be done?

A
  • Patients given red blood cells may produce autoantibodies to donor surface antigens (of which there are many, other than ABO and RhD).
  • Because of this, before any future transfusions, a new G&S will need to be sent (unless the last G&S was sent and processed within around 3 days of the most recent transfusion).
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27
Q

What are the indications for platelet transfusion?

A
  • Haemorrhagic shock in a trauma patient
  • Profound thrombocytopenia (< 20 x 10^9/L; normal range 150 – 400)
  • Bleeding with thrombocytopenia
  • Pre-operative platelet level < 50 x 10^9/L
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28
Q

What duration is a platelets transfusion administered over?

A

30 minutes

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29
Q

After giving 1 adult theraputic dose of platelets, how much should platelet levels increase by?

A

20-40 x 10^9 /L

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30
Q

What is major constituent of FFP?

A

Clotting factors

31
Q

What are indications for FFP?

A
  • Disseminated Intravascular Coagulation (DIC)
  • Any haemorrhage secondary to liver disease
  • All massive haemorrhages (commonly given after the 2nd unit of packed red cells)
32
Q

What duration is a FFP transfusion administered over?

A

30 mins

33
Q

What are major constituents of cryoprecipitate?

A

Fibrinogen, von Willebrands Factor (vWF), Factor VIII and fibronectin

34
Q

What are indications of cryoprecipitate?

A
  • DIC with fibrinogen < 1g/L
  • von Willebrands Disease
  • Massive haemorrhage
35
Q

What duration should cryoprecipitate be administered over?

A

STAT!!!

36
Q

What are major constituents of prothrombin complex concentrate (PPC)?

A

Vitamin K dependent coagulation factors

37
Q

What are the indications for prothrombin complex concentrate (PPC)?

A
  • Rapid warfarin reversal in major or life-threatening bleeding (including intracranial bleeding)
  • Reversal of anticoagulation prior to urgent surgery
  • Patients who refuse blood products and are bleeding
38
Q

What duration should prothrombin complex concentrate (PPC) be administered over?

A

STAT!!!

39
Q

Who requires CMV-negative blood products?
and why?

A

CMV negative blood should be given to:
* women during pregnancy
* intra-uterine transfusions
* to neonates (up to 28 days).

Why? Cytomegalovirus is a common congenital infection that may lead to sensorineural deafness and cerebral palsy.

(and relation to paeds - SCID needs CMV-ve irradiated blood products)

40
Q
  1. What are irradiated blood products?
  2. Why are they required?
  3. What groups of people should recieve them?
A
  1. Blood that is treated with low dose radiation to stop lymphocytes(WBC) in donated blood from harming patients with weak immune system
  2. required to reduce the risk of transfusion associated graft-versus-host-disease in at risk populations. This occurs when the donor WBCs attack the patients tissues
  3. Groups:
    * Those receiving blood from first or second-degree family members
    * Patients with Hodgkin’s Lymphoma
    * Recent haematpoietic stem cell(HSC) transplants
    * After Anti-Thymocyte Globulin (ATG) or Alemtuzumab therapy
    * Those receiving purine analogues (e.g. fludarabine) as chemotherapy
    * Intra-uterine transfusions
    * SCID
41
Q

What is the management for massive blood loss?

A

see pic

42
Q

Summarise blood products you would give in a code red major haemorrhage

A

Thought was a good summary of deck so far

43
Q

What are alternatives to blood transfusion?

A
  • tranexamic acid - helps prevent and treat bleeding. SE = N, V and diarrhoea
  • iron treatments - tablets usually.
  • EPO - helps body make more RBC. SE = HTN, skin reaction, headaches, bone pain, flu symptoms
  • rFVIIa - Novoseven - a blood clotting factor that helps blood clot when body’s own clotting factors aren’t working. SE = MI, Stroke.
44
Q

In patients who do not want a blood transfusion, how can we conserve their blood supply?

e.g. Jehovas witness

A
  • Medications - tranexamic acid, iron treatments, EPO, rFVIIa factor
  • Transfusion alternative - e.g. cell salvage
45
Q

Describe cell salvage

an alternative to blood transfusion

A

Intraoperative = collect blood that is lost and give it back to patients
Autologous blood transfusion = blood colecting using suction, anticoagulant is added to stop it clotting. RBC are washed, filtered and returned via cannula after operation.

46
Q

What are some complications of blood transfusion?
general, transfusion-specific, other, delayed

A

General:
* Clotting abnormalities
* Electrolyte abnormalities - hypocalcaemia, hyperkalaemia
* Hypothermia

Transfusion specific complications:
* acute haemolytic reaction
* transfusion associated circulation overload - TACO
* transfusion related acute lung injury - TRALI

Other:
* mild allergic reaction
* non-haemolytic febrile reactions
* anaphylaxis
* infective/bacterial shock

Delayed transfusion reactions:
* infection
* Graft vs Host disease
* iron overload

complic = more likely with increased vol of blood

47
Q

Group complications of blood transfusions into immunological and non-immunological

A

Immunological:
 ABO mismatch
 Delayed haemolytic transfusion reactions
 Transfusion-related acute lung injury (TRALI)
 Anaphylaxis
 Non-haemolytic febrile transfusion reactions
Non-Immunological:
 Transfusion-associated circulatory overload (TACO)
 Transmission of infection

48
Q

How does acute haemolytic transfusion reaction present?

Also called ABO mismatch/incompatibility?

A

Begin minutes after transfusion has started
* urticaria
* hypotension
* fever
* may have haemoglobinuria (due to rapid haemolysis)
* abdominal pain

49
Q

What would blood tests show in a pt with acute haemolytic reaction (ABO incompatibility)?
-Hb?
-haptoglobin?
-LDH and bilirubin?

A
  • reduced Hb
  • a low serum haptoglobin
  • high LDH and bilirubin
50
Q

What investigation will confirm Dx of acute haemolytic reaction?

A

positive Direct Antiglobulin Test (DAT) will confirm the diagnosis.
akak Coombes

51
Q

How is acute haemolytic reaction managed?

A
  • Stop transfusion
  • begin supportive measures
  • fluid resus
  • oxygen
  • treat any DIC
  • seek specialist advice for further management
52
Q

What is pathophysiology of acute haemolytic transfusion reaction?

A
  • results from a mismatch of blood group (ABO) which causes massive intravascular haemolysis.
  • This is usually the result of red blood cell destruction by IgM-type antibodies.
  • human error - have given incorrect blood type.
53
Q

What are complications of having acute haemolytic transfusion reaction?

A

DIC
Renal failure

54
Q

What are delayed haemolytic transfusion reaction (DHTR)?
Include: cause? when do they happen? features?

A

Cause? Delayed haemolytic reactions are caused by antibodies to antigens such as Rhesus or Kidd. Rare - usually in pts who have developed abodies from past transfusion or pregnancy.

When? (can be anytime after 24hours after transfusion) can occur between 3 to 14 days after the transfusion

Features? sudden drop in haemoglobin level, fever, jaundice and haemoglobinuria.

55
Q

How is delayed haemolytic transfusion reaction managed?

A
  • usually no treatment
  • if symptomatic (severe anaemia, renal failure), may need IVIg, or EPO.
56
Q

What is Transfusion-related acute lung injury (TRALI)?

A
  • Non-cardiogenic pulmonary oedema thought to be secondary to increased vascular permeability caused by host neutrophils that become activated by substances in donated blood
57
Q

How does TRALI present?

A

Develop within 6hours of transfusion
* sudden onset dyspnoea
* severe hypoxaemia.
* fevere
* hypotension
* CXR shows pulmonary infiltrates

58
Q

How is TRALI managed?

A
  • Stop transfusion
  • high flow oxygen
  • supportive care - e.g. fluids
  • urgent CXR
59
Q

Pathophysiology of anaphylaxis to blood transfusion?

A

Can be caused by patients with IgA deficiency who have anti-IgA antibodies.
* antibodies react to proteins in the blood transfused.
* pt sensitised to allergen –> then re-exposed to allergen in donor blood –> release of IgE
* causes bronchospasm –> life threatening

60
Q

How does anaphylaxis to blood transfusion present?

A

Develops minutes - hours after transfusion
* Hypotension
* dyspnoea
* wheezing
* angiodema
* itchy rash
* vomiting

61
Q

How is anaphylaxis to blood transfusion managed?

A
  • Stop transfusion
  • treat like anaphylaxis - IM adrenaline 0.5-1mg. Repeat every 10mins until improvement.
  • ABC support - oxygen, fluids.
  • Nebulised salbutamol if required.
  • can add steriods –> then antihistamines (if needed)
62
Q

Pathophysiology of non-haemolytic febrile transfusion reaction to blood transfusion?

A

thought to be caused by antibodies reacting with white cell fragments in the blood product and cytokines that have leaked from the blood cell during storage

63
Q

How does non-haemolytic febrile transfusion reaction present?
How is it managed?

A
  • fever during blood transfusion
  • chills
  • no features of haemolysis

Management:
* slow or stop transfusion
* anti-pyretic - paracetamol
* monitor
* (antihistamine - not mentioned in all resources)

64
Q

What is pathophysiology of Transfusion-associated circulatory overload (TACO) ?

A
  • Excessive rate of transfusion
  • Pt has pre-existing heart failure

A common problem in patients who are already overloaded - e.g. heart failure

65
Q

How does Transfusion-associated circulatory overload (TACO) present?

A

Pulmonary oedema, hypertension

66
Q

How is Transfusion-associated circulatory overload (TACO) immediately managed?

How can it be prevented?

A
  • Slow or stop transfusion
  • urgent chest xr
  • intravenous loop diuretic (e.g. furosemide)
  • oxygen

How can it be prevented?
* Patients at risk of overload can be prescribed 20mg furosemide prophylactically during transfusion.

67
Q

Describe transmission of infection in blood transfusion

A
  • There is a theoretical risk of developing any of Hepatitis B, Hepatitis C, HIV, syphilis, malaria, or vCJD with any blood transfusion.
  • less of a concern due to screening of blood donors
68
Q
  1. How does infective/bacterial shock to blood transfusion present?
  2. What is your management for this?
A
  1. hypotension without clinical signs of anaphylaxis
  2. stop transfusion, perform resus basic measures. Then:
    * take blood cultures
    * start IV abx
    * seek immediate senior help
69
Q

What is main difference between TACO and TRALI?

A

TRALI = pt is hypotensive, also have a fever
TACO = pt is hypertensive

70
Q

Before each unit of blood, you should?
(5 things - on a blood transfusion bedside checklist)

A

Note - for 3 on right side of pic= ask for 3 points of ID - name, DOB, S number

71
Q

The transfusion of packed red cells has been shown to increase serum levels of what electrolyte?

passmed

A

Potassium - when you transfuse packed red cells, it can increase potassium levels = causing hyperkalaemia. The risk is higher with large volume transfusions and with old blood.

A pt with an ECG will have associated changes.

72
Q

AR possible blood transfusion reactions

Mnemonic = Got a bad unit

A
73
Q

Compare and contrast TACO and TRALI

A

from blood transfusion slides