Haem 11 Flashcards

(55 cards)

1
Q

Where is blood from for donation

A

Human source - no synthetics yet (research) - not risk free

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2
Q

When is blood used

A

When no safer alternative

If massive bleeding - if ‘plain fluids’ not sufficient

If anaemic - if iron/ B12/ folate not appropriate

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3
Q

Outline the basis of blood group

A

All have common H antigen:

A has galnac added on
B has gal added on

AB has some with either, O just has H stem

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4
Q

What are antigens determined by

A

Antigens determined by corresponding genes

A gene codes for enzyme which adds N-acetyl galactosamine to common glycoprotein and fucose stem

B gene codes for enzyme which adds galactose

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5
Q

Inheritence of O

A

It is receissive, so must have 2 O groups if you are blood group O

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6
Q

Possible blood group for A

A

AA, or OA

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7
Q

Which antibodies do you have against antigens

A

Person has antibodies against any antigen NOT present on own red cells

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8
Q

What type of antibody is made against the blood cell antigens that you do not have

A

Naturally occurring (nearly from birth) - IgM: it is a ‘complete’ antibody, so:- fully activates complement cascade to cause haemolysis of red cells

(pentameric so it cross links, activates complemet, and causes MAC and punches holes in the red cell membranes, and cytokine storms)

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9
Q

Group A given to group O patient

A

blood group A given to patient who is group O - so has anti-A and anti-B - then antibody/ antigen interaction often fatal

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10
Q

What i shown in tests to determine blood group

A

In laboratory tests, IgM Abs interact with corresponding ag to cause agglutination eg: if patient is group B, he has anti-A antibody in plasma - when add to group A cells - agglutination seen (clump) - shows cells are incompatible

How is ABO blood group determined (slide 9)

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11
Q

Commonest blood group in UK

A

O, A, B and AB

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12
Q

Which antibodies for each blood group

A

A: anti B
B: Anti A
O: Anti A and Anti B
AB: none

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13
Q

What is the Cross match

A

Final check, adding patient’s plasma to the blood you are going to transfuse to ensure it doesnt agglutinate

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14
Q

What types of RH groups

A

RhD is most important

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15
Q

What are the types of RhD groups

A

RhD positive or RhD negative

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16
Q

What are the potential genotypes for RhD positive and RhD negative

A

RhD +ve: DD or Dd

RhD -ve: dd

Most RhD positive in UK

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17
Q

How are antibodies made against RhD in RhD negative people

A

RhD-ve people CAN make anti-D antibodies AFTER they are exposed to the RhD antigen - either by transfusion of RhD positive blood or in women, if they are pregnant with an RhD positive fetus

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18
Q

What type of antibodies made against RhD antigens

A

IgG antibodies

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19
Q

What is the consequence of IgG coating of the RhD antien

A

Not MAC, but complex recognised by spleen, and has membrane pinched out, leading to spherocytes and then are taken out second time around… causes delayed haemolytic transfusion reaction - anaemia; high bilirubin; jaundice etc

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20
Q

Implications of anti-D antibodies (antibodies aginst RhD postiive)

A
  1. Future transfusions
  2. Haemolytic disease of the newborn (HDN)…
    if RhD neg mother has anti-D - and in next pregnancy, fetus is RhD pos - mother’s IgG anti-D antibodies can cross placenta - causes haemolysis of fetal red cells - if severe: hydrops fetalis; death
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21
Q

Why isn’t RhD neg given to RhD positive people

A

no harm to give RhD neg to a pos patient - just wasteful

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22
Q

What blood group can be used for everyone

A

O neg used as emergency blood when patient’s blood group not known (NB only 6-7% of donors are O neg)
….

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23
Q

What other antigens can be present on red cells, do they matter

A

Don’t routinely match blood for all these, eg Rh group -C, c, E, e; others - Kell, Duffy, Kidd, etc

about 8% of patients transfused will form antibody to one or more of these antigens…..

It is important….
Once have formed antibody must use corresponding antigen negative blood; or else risk of delayed haemolytic reaction (can be severe)

24
Q

What is done to avoid the delayed haemolysis associated with these other antibodues

A

as well as testing their ABO and RhD group BEFORE each transfusion episode, test patient’s blood sample for red cell antibodies

you need to do a new one each time

25
Questions on slide 16
Cannot be AB or O
26
Components of blood How much is collected from each donor Why is blood not kept as whole blood Why is red cells + plasma not given to patients needing RBC What layers appear after centrifugation of blood
1 unit (‘pint’) blood collected into a bag containing anticoagulant Whole blood not given: - more efficient, less waste - some components degenerate if stored as whole blood Red cells – concentrated, as plasma removed; also avoids fluid overloading patients Split one unit of blood by centrifuging whole bag (red cells bottom, platelets + leukocytes middle (=buffy coat), plasma top) then squeeze each layer into satellite bags and cut free (closed system)
27
What can whole blood be used to make
1. Red cells 2. Platelets 3. Plasma
28
Why would you use cryoprecipitate
it's fibrinogen rich
29
What can you do with plasma
-into fresh frozen plasma (FFP) or cryopreciptate, or plasma for fractionation, in which you pool thousands...
30
What can plasma for fractionation be used for
Can take out albumin, factor VIII, IX immunoglobulins, anti-D etc.
31
Shelf life of the red cells
Shelf life 5 weeks; stored at 4oC (fridge) 1 unit from 1 donor - ‘packed cells’ (fluid plasma removed)
32
How are red cells given
Give through a ‘blood giving set’ - has filter to remove clumps/debris
33
What are frozen red cells needed for
for rare groups/ antibodies - poor recovery on thawing, rare... but you lose some red blood cells
34
Fresh frozen plasma how much from each donor
1 unit from 1 donor (300ml) can get small packs for children
35
How is FFP stores and shelf life
Stored at -30oC (frozen within 6h of donation to preserve coag factors) Must thaw approx 20-30 mins before use (if too hot, proteins cook)
36
What dose of FFP needed
Dose 12-15ml/kg = usually 3 units
37
What is needed to match FFP
Need to know blood group - no x-match, just choose same group (as contains ABO antibodies from donor, which could cause a bit of haemolysis with receipient cells
38
When is FFP needed
1. If bleeding + abnormal coag test results (PT, APTT) - Monitor response - clinically and by coag tests 2. Reversal of warfarin (anticoagulant) eg for urgent surgery (if PCC not available= Prothrombin complex concentrate, also known as factor IX complex, is a medication made up of blood clotting factors II, IX, and X. Some versions also contain factor VII. It is used to treat and prevent bleeding in hemophilia B if pure factor IX is not available.. ) 3. Other conditions occasionally
39
Cryoprecipitate storage
Same as FFP - store at -30oC for 2 yrs
40
Standard cryoprecipitate dose
Standard dose = from 10 donors (can split into 5 in each pack and give two bags)
41
Important feature of cryoprecipitate
Contains fibrinogen and factor VIII
42
Indication for cryoprecipiate
If massive bleeding and fibrinogen very low | Rarely hypofibrinogenaemia
43
How many donors needed for a pool of platelets
4 donors or from 1 donor by apheresis (cell separator machine)
44
Shelf life of platelets
Shelf life 5 days only - (risk of bacterial infection)
45
What info is needed for platelet
Blood group: No cross-match, just choose same group (as platelets have low levels of ABO antigens on, so wrong group platelets would be destroyed quickly) - and can cause RhD sensitisation, as some red cell contamination
46
Indications for platelets
Mostly haematology patients with bone marrow failure (if platelets <10 x 109/L) Massive bleeding or acute DIC If very low platelets and patient needs surgery If for cardiac bypass and patient on anti-platelet drugs
47
How much plateltet is needed usually
1 pool
48
Which cotting factors affected by warfarin
2, 7, 9 and 10
49
How does fractionated plasma work
Fractionated (like oil)
50
What can be gleaned from fractionated plasma ..
Factor VIII and IX, | Immunoglobulins and albumin
51
When is factor VIII and IX needed from fractionated products
For haemophilia A and B respectively (males) Factor VIII for von Willebrand’s disease Heat treated - viral inactivation Recombinant factor VIII or IX alternatives increasingly used, but expensive
52
When are immunoglobulins needed from fractionated products
IM: Specific - tetanus; anti-D; rabies IM: Normal globulin - broad mix in population (eg: HAV) IVIg – pre-op in patients with ITP or AIHA
53
When is albumin needed and at what dose
4.5% Useful in burns, plasma exchanges, etc Probably overused (not indicated in malnutrition) 20% (salt poor) For certain severe liver and kidney conditions only
54
WHat does cross matching involve
X-match: patient’s serum mixed with donor red cells - should not react
55
WHat proportion of people have RhD negative and which proportion RhD positive blood
85% of people are RhD positive; 15% are RhD negative