blood transfusion n Flashcards

1
Q

wwhat are the major ABO blood groups *

A

A - AA/AO

B - BB/BO

AB - AB

O - OO (recessive)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

where do you get blood from

A

human source - no synthetics yet - human source so not risk free

it is a scarce resource, 1 donor gives 1 pint - max every 2-4 months - we need 9000 units of blood/day in uk and cant stockpile it because blood shelf life is only 5 weeks

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

when do we use blood

A

when there is no safer alternative eg if massive bleeding (1L) plain fluids will not be sufficient

if anaemic - iron/B12/folate alone is not appropriate - if you can replace any of these directly then this is better because they can malke up the rest themselves

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

describe ABO blood groups *

A

this is the most important opf all blood groups - people die if you get it wrong

A and B antigens on red cells are formed by adding onee or other sugar residue onto a common glycoprotein and fucose stem on a red cell membrane

n-acetylgalactosamine is added to A

galactose residue is added to B

all red cells have H antigen - this is the common antigen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

consequences of ABO groups *

A

if you dont have the antigens the body recognises them as foreign and makes antibodies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

how are the blood groups made *

A

they are controlled by genetics

A gene codes for enzyme that adds N-acetyl galatosamine to common glucoprotein and fucose stem

B codes for enzyme that attches galactose stem

A and B genes are codominant

O gene is recessive - codes for nothing, noting is added to H

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

describe the formation of Ab against te ABO groups, and the siggnificnace of the type of Ab *

A

Ab against the antigen not present in blood

they are made from birth - because from birth you are exposed to bacteria that make proteins similar to A and B - body makes Ab against these that then attack ABO antigens

they are IgM Ab - complete Ab so fully activates complemet to the membrane attack complex - make holes in the red cell membrane = release of Hb and BR = jaundic e- induces cytokine storm - reduction in BP = shock

in lab tests - Igm Abs interact with ag to form agglutins - agglutination is seen as clumping and shows the blood types are incompatable

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

which blood group can give to anybody *

A

O

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what blood group cna get blood from anybody *

A

AB - no Ab

when we transfuse it is only the red cells that is transfused not the plasma so teh Ab in donated blood doesnt matter

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

describe how you test for ABO blood groups *

A

take patient blood sample with plasma and cells

centrifuge so cells are at bottom - but cells in bottom of well

ABO group test with known anti-A and anti-B

anti-a soln is blue to avoid error, anti-b is yellow

if there is a clump - those red cells have the matching antigens ie a antigens with anti-a

test your plasma to see what ab are present

select donor with the right grroup - ie have the same antigens

cross match - mix bit of patient’s serum with donor red cells- there should be no reaction - if there is agglutination blood is incompatible

this is all automated

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what are the RH blood groups *

A

RhD is most important - most immunogenic after ABO

have RhD positive or negative

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what are the genes for RhD

A

D - codes for D antigen on the red cell surface membrane

d - codes for no antigen - recessive

dd = no D antigen = D -ve 15%

DD/Dd = D +ve 85%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

describe the formation of anti-D Ab *

A

made by people wo are D -ve

have to have 1st exposure eg pregnancy or transfusion - when fine

on 2nd exposure the Ab detect this and cause effects

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

describe the anti-D Ab and which groups make them *

A

IgG

D +ve have antigens - cant make the ab

-ve - dont have the ag so if exposed - make the ab = problems on second exposure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what are the impilcations of anti-D ab *

A

patients with anti-d ab must have d - ve blood - otherwise ab attack transfused blood = delayed haemolysis (5-10 days after transfusion) dont activate the whole complement pathway - only as far as CD3 = anaemia - plasma Hb causes renal failure , high BR = jaundice

in pregnancy - if RhD -ve mother and RhD +ve father - if foetus is RhD - IgG Ab cross placenta give mother 1st exposure (fetomaternal leakage of red cells across the placenta occurs at delivery, silent bleeds are not uncommon during late pregnancy) - if 2nd preg is RhD +ve - IgG from mother pass through placenta and destroy red cell in foetus - anaemia - in pregnancy the rise in BR can be taklen out by placenta, or cross the BBB = brain damage causes hyperextension of the arms, legs and neck and death (BR stain the brain columns) - if anaemia severe die in pregnancy becuase not enough O2 transportation so eart work faster = HR

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

how can you avoid problems with blood groups *

A

want to avoid D -ve people making D ab - avoid D antigen exposure

transfuse blood of same RH group - if giv e-ve to D+ve no problem - just wasteful as -ve is rare

O negative blood used when emergancy - universal donor

can give anti-d injections to prevent sensitisation - when there is spillage of blood eg in child birth, the anti d coats the babies red cells and takes them out of the circulation before mothers immune system can mount a response - only work if small blood mixing eg pregnancy - not if give whole transfusion

17
Q

what are other red cell groups - other than RhD and ABO *

A

Rh C c R e, Kell, Duffy, Kidd etc

RhC and Kell can harm foetus

18
Q

how do you test for the blood groups *

A

antibody screen - blood incubated with 2/3 blood donors that have all the clinically important antigens - if -ve any ABO and D matched donors are ok

if postive ab present needs to be identified against a large panal of red cells - donor packs that dont have ag corresponding to ab in pts blood are needed other wise delayed haematolysis can occur and be severe

19
Q

if 2 people - O positive and AB positive have child - possible blood groups of child *

A

A positive

B positivee

20
Q

if a pt is B positive whic could kill them:

A positive

O positive

B negative

A

A positive - they have B ag so have anti-A ab

21
Q

describe how a blood sample is split up *

A

1 pint blood collected into bag with anticoagulant

dont give all blood - just parts

whole bag is centrifuged - red cells go to bottom, platelets and white cells in middle (white cells die quickly) and plasma at the top

each layer is squeezed into satellite bags and cut free - this is a closed system to avoid contamination - heat sealed so bacteria cant get in

22
Q

why do you give parts of blood, not all of it *

A

more efficient - less waste as people dont need all the parts

some componeents degenerate quickly of stored as whole blood

if gave everything = too much fluid = heart work harder - can cause HF

23
Q

what are the different uses for plasma *

A

fresh frozen plasma (FFP) - contains the coagulation factors - ave to freeze in 6hrs to preserve the coag factors

cyroprecipitate - FFP thawed in fridge -separates into cyroppte and liquid - cyroppte contains fibrinogen and factor 1 and 8

plasma for fractionation (this is not from UK) - pools of thousands of donors - fractionalise for loads of components eg albumin, factor 8, ig, anti-d

24
Q

describe te red cell product *

A

1 unit from 1 donor - packed cells

shelf life 5wks stored at 4degrees C

give through ‘blood giving set’ - has filter to remove clumps and debris from white cells and fibrinogens

can freeze but not efficient because need to add glycerol to stop ice crystals forming - lose 1/3 cells. relyed on for rare blood gps/abs

25
Q

describe FFP product *

A

1 unit from 1 donor 300ml

stored at -30 degrees within 6hrs to preserve coag factors

self life 3yrs

thaw 20-30minutes before use - cook proteins if try to speed it up

if dont need anymore can last in fridge not much longer than an hour

need 3 units at a time for an adult

contain clotting factors, ig, albumin, water and electrolytes

dose 12-15ml/kg - usually 3units

need to use te same ABO group - has the ab - could cause a bit of haemolysis - not going to kill you so dont have to do cross test

26
Q

when would you use FFP *

A

in bleeding, or abnormal APTT or PT (coag test results) - monitor clinically (see if bleeding stopping) and by coagulation tests

reverses warfarin eg for urgent surgery if PCC (prothrombin complex concentrate) not available which includes factor 2, 7, 9, 10 - if possible just replace what need, not entire plasma - more concentrated so work faster

27
Q

would you use ffp to replace vol loss *

A

no wouldnt use human products for this - too much risk of contamination or rejection

28
Q

describe cyroppte product *

A

ffp thawed at 4-8 degrees over night - residue remains containing factor 8 and fibrinogen

store at -30degrees for 3yrs

standard does is from 10 donors - 5 in a pack

29
Q

when would you use cyroppte *

A

if massive bleeding and fibrinogen very low and all clottong factors used up - trauma

hypofibrinogenaemia - rare inherited condition

treatment of DIC with other blood components

30
Q

describe platelet product *

A

1 pool from 4 donors = standard adult dose, or from 1 donor using apheresis

store at 22 degrees - room temp otherwise reduced function - constantly agitated otherwise platelets clump

shelf life - 7 days only - otherwise risk of bacterial infection

need to know blood group - platelets have low densitiy abo antigens so if gove wrong gp the pt wont die - but the ab wouldd destroy the platelets quicker than normal. also goive plasma with platelets so the platelets can function - donors antigens will destroy some of the patients blood no cross match, just choose same gp - need to know if it is better to haemolyse a bit of pts blood or reduce lifespan of donated platelets for that individual. also can cause RhD sensitisation by blood cell contamination

31
Q

wat is apheresis *

A

cell separating machine - takes platelets and returns everything else to donor

have to do it for 2hours

more expensive

can make 2/3 samples

32
Q

when would you use platelets *

A

mostly haematological platelets with bone marrow failure or from chemo - ie low platelets

massive bleeding or acute DIC - all platelets have been used up

if already ave low platelets and pt needs surgery

if on cardiac bypass adn pt on anti-platelet drug - machine destroys platelets

1 pool is usually enough - rarely need more

dont overuse platelets and FFP otherwise casue transfusion reactions unnecessarily

33
Q

if platelet count is normal and PT and APTT are prolongued what does pt need *

A

FFP - containing all coag factors because both APTT and PT are down

34
Q

what does pt need if PT and APTT and fibrinogen are down *

A

FFP and cyroppte

will not be enoughh fibrinogen in ffp

35
Q

describe fractionated products *

A

get factor 8 and 9 (recombinant is used in preference to fractioned) - for haemophilia A and B, factor 8 for vwd - heat treated to inactivate virus

intermediate purity factor 9 is now turned into prothrombin complex concentrate is original fraction of factor 9 but also has factors 2 7 and 10 - anbtidote for warfarin

immunoglobulins - IM specific (eg tetanus, anti-D and rabies - cant fractionate these so need apheresis after donor has been infected), IM normlal globins - broad mix in pop eg HAV, IVIg - pre-operation in patients with ITP or AIHA

albumin - 4.5% - for burns, plasma exchange when lose water and proteins, probably overused.20% - for certain severe kidney and liver diseases only

36
Q

how do you keep the blood safe *

A

prevent transmission of drugs, infection or disease

test for indications - cant pick up early infection:

hep b - BsAg, PCR

hep c - anti-hcv pcr

hiv - anti-hiv, pcr

htlv - anti-hilv (endemic in some parts of the world, can cause acute leukaemia/neurdegenrative disease

sphylis - TPHA - spirochete

hep E - PCR (from pig food chain)

some for CMV

question for risk behaviour - exclude groups which as a group have risk for >1% of something that would double transmission of infection

use voluntary unpayed donors

37
Q

describe prion disease and what is done as a precaution now *

A

vCJD

can be transmitted by blood transfusion

4 cases where people recieved blood from people who died from vCJD - 3 of recipients developed it too and 1 had it but died of other causes

as precaution all products pooled to make fraction come from usa

all blood componenets hhave white cells filtered out - vCJD needs white cells

38
Q

potential side effects of blood and plasma transfusions *

A

RH sensitivity

infection

haemolysis = shock

39
Q

example of donors who are excluded to protec themself *

A

people with heart problems