Blood and Blood Products Flashcards

1
Q

Define a blood component

A

A blood product manufactured in a local blood centre that is derived from a single donation or a small pool (4-6) of donations
Red cells, platelets, FFP

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2
Q

Define plasma derivative

A

blood product manufactured from a large pool of plasma donations (1000s) using industrial type systems

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3
Q

Priorities for the national blood service

A
  • Min risk to recipients of blood products and to the crown (liability)
  • Responsive to situations e.g. emergencies or potential infection risks
  • Strategic direction and leadership
  • Nationally consistent and accessible service
  • protection of the gift status of blood
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4
Q

CSL Behring Australia

A
  • Plasma fractionator in melbourne
  • Receives plasma from NZBS and manufactures into a range of plasma derivatives for use in NZ
    Products:
  • Factor VIII (Biostate)
  • Factor IX (MonoFIX, ProthrombineX)
  • IV immunoglobulin (Intagram P)
  • Human Albumin solution (Albumex)
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5
Q

Strategies for maintaining a safe blood supply

A

use voluntary non-enumerated donors
Exclusion of potential donors who’s behaviour or lifestyle places them at increased at risk of acquiring recognised blood borne infections
Testing all blood donations for evidence of major blood borne viruses
Use of physical and chemical methods to destroy any pathogens that maybe present

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6
Q

Examples of infections transmissible by blood

  • Viruses
  • Protozoa
  • Bacteria
A
  • Hep, HIV, Epstein- Barr
  • Malaria, toxoplasma gondii
  • Syphyllis, staph and strep, salmonella
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7
Q

Paid donation associated with?

A

Increased risk of blood borne virus transmission

Exploitation of the poor and disadvantaged

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8
Q

The precautionary principle

A

Risk is inherent in the use of blood products, it can never be said that there is absolutely no risk and that it is perfectly safe
Preventative agent should be taken when there is evidence that a potential disease causing agent may be blood borne, even when there is no evidence that recipients have been affected.
If harm can occur it should be assumed that it will occur

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9
Q

Donor eligibility criteria

A
between 16-70
good general health 
able to donate blood every 12 weeks 
- complete health questionarre 
- interview with a registered nurse 
- Hemoglobin check
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10
Q

Donor selection aims to protect

A

The potential recipient
- identify medical and lifestyle factors that might increase the risk to the potential recipient
The Donor
- Identify health problems that might increase risk of complications from donation

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11
Q

In NZ all donations tested for?

A

ABO, Rh(d) type and antibody screen
Hep B surface antigen and nucleic acid test for HBV DNA
HIV 1/2 antibody and nucleic acid test for HIV-1 RNA
HTLV antibody (first time donors only)
Serological test for syphilis

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12
Q

Mian clinical indication

  • Red cells
  • Platelet concentrations
  • FFP
A
  • Improve oxygen delivery to tissues in cases of anaemia or blood loss
  • Management of prevention of bleeding in patients with low platelet counts
  • Correction of abnormal coagulation on patients who are bleeding
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13
Q

Restrictive vs conservative transfusion

A

use associated with at least as good clinical outcome, now check their Hb after giving each unit, to see whether they need another one

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14
Q

Danger of using ‘older’ red cells?

A

One retrospective study of clinical outcomes found increased risk of postoperative complications when patients given blood two weeks or older.
However this study has been debunked
To date all control trials have failed to demonstrate any benefit from using fresh vs older blood

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15
Q

The factors to consider when deciding whether to transfuse red cells

A
Signs and symptoms of hypoxia 
Ongoing blood loss 
Risk of anaemia to patient 
Risk of transfusion 
Hemoglobin, although important shouldn't be the deciding factor
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16
Q

Red cell transfusion, specific factors to consider

A

Patients Cardiopulmonary reserve
- If pulmonary function not normal, consider transfusing at a higher threshold
Volume of blood loss
- clinical assessment should attempt to quantify the volume of blood loss before, during and after surgery, to ensure maintenance of normal blood volume
Oxygen consumption
- Affected by fever, anaesthesia and shivering
- If increased, patients may need more RBC’s
Atherosclerotic disease
- Critical arterial stenosis to major organs, particularly the heart may modify indications may modify indications for the use of red cells

17
Q

Hb levels and transfusion

A

<70g/L lower thresholds acceptable in patients without symptoms and where specific therapy available
70-100g/L appropriate during surgery associated with major blood loss, if there are signs or symptoms of impaired oxygen transport
>80g/L appropriate to control anaemia related symptoms in a patient on a chronic transfusion regime, or during marrow suppressive therapy
>100g/L not likely appropriate

18
Q

Describe platelet concentrations

A

A adult therapeutic dose: pool form 4 donations, or an aphaeresis machine donation
Specific component manufactured for neonatal use
Platelet con’s manufactures only from group O and A donors

19
Q

What is the normal platelet count?

A

150-400x10^9/L

20
Q

Indications for platelet transfusion

A

PROPHYLAXIS
Bone marrow failure
<10^9/L when NO risk factors present
<20x10^9 when fever and other risk factors present

Surgery and other invasive procedures
<50x10^9/L for normal surgery
<100x10^9/L for high risk surgeries e.g. ocular and neuro

Platelet function
may be appropriate in inherited and acquired disorders, platelet count unlikely to be helpful

21
Q

Indications for platelet transfusion

A

Patient bleeding
- When platelet count below trigger level and significant bleeding
Massive haemorrhage/ transfusion
- use confined to patients with low platelet counts and or functional abnormalities, who have significant bleeding from this cause
- May be appropriate when count 50x10^9/l in presence of diffuse microvascular bleeding

22
Q

Describe FFP

A

Plasma from single donation frozen within 6 hours of collection to <20 deg celsius
Vol approx 200ml
Initial dose where indicated 12-15ml/Kg
NZBS currently manufactures all FFP from male apheresis donors
Evidence from clinical audits indicates a significant level of overuse

23
Q

Donor and recipient matches (in terms of blood groups for FFP)

A
Opposite to red cells!!
O from AB, A and B (and O if it was collected but its not)
A from A and AB 
B from B and AB 
AB only from AB
24
Q

Indications for FFP

A

Replacement of single factor deficiencies where specific or combined factor concentrate not available
Immediate reversal of warfarin effect in the presence of potentially life threatening bleeding
Treatment of the multiple coagulation deficiencies associated with acute DIC
Treatment of thrombotic thrombocytopenia purpura
Treatment of inherited deficiencies of coagulation inhibitors in patients undergoing high-risk procedures where a specific factor concentrate not available
In bleeding patients with abnormal coagulation parameters following massive transfusion, cardiac bypass surgery or liver disease

25
Q

FFP not considered appropriate as?

A

volume expander in cases of hypovolemia
Plasma exchange procedures
Treatment of immunodeficiency states

26
Q

How are plasma derivatives manufactured?

A

industrial processes involving large plasma pools
Highly regulated
1-2 viral inactivation steps
good safety profile