Blood Transfusions Flashcards

1
Q

Define blood transfusion

A

Intravenous therapy with whole blood or blood products.

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

What are blood products?

A

Blood components

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

What is oxyglobin?

A

Chemically modified haemoglobin of bovine origin.

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

What to transfuse and why?

A

•TRY to establish why you think the dog or cat is anaemic

–Helps determine WHAT you should be transfusing (less so cats)

–E.g. haemorrhage, haemolysis or erythropoietic failure

  • This may not be apparent initially but must be considered in addition to your transfusion plans
  • If the animal is bleeding its demand for and the type of blood products required will be very different
  • Care if not bleeding with products with high oncotic pressures…

–Careful history from the owner will be invaluable for planning appropriately in these cases

•What is the duration of the anaemia, clinical signs associated with

–Short term, medium term or long-term

  • Evidence for reduced oxygen carrying capacity?
  • Replace what is lacking

  • Supports patient whilst investigations are being carried out/treatment is being initiated
  • Aim for a clinical improvement rather than a normal PCV.

–Post-transfusion PCV of 25 to 30% in dogs

20% in cats

  • Remember the benefits of transfusion MUST outweigh the drawbacks
  • Responses to transfusion tend to depend on how quickly they became anaemic
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Name iminent triggers for transfusion

A

–Evidence for circulatory collapse means transfusion is essential

–Rapid drop in PCV to <20% in dogs or <15% in cats (e.g. 10% or more)

–Absolute PCV of 15-20%

•Depends a lot on historical and presenting clinical signs

–If PCV <10-12%, automatic trigger as organ hypoxia is imminent – particularly myocardium

–Signs of specific organ hypoxia – particularly CNS

–Clear evidence for reduced oxygen carrying capacity

•Tachycardia, Tachypnoea, bounding peripheral pulse (water-hammer – rapid rise and fall of pulse)

–(Concern that PCV is likely to fall lower over period of time whereby transfusion would be difficult to organize e.g. Friday afternoon)

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

Why is the transfusion product important?

A
  • Don’t want to give them more than we need
  • The importance relies on our ability to assess suitability of the use of each of the products

–A diagnosis is required to ensure appropriate product choice

•e.g. IMHA, whole blood loss, deficiency in Vit-K dependent clotting factors, hypoproteinaemia and secondary pro-coagulability

–if we only need coagulation factor replacement many of the products are suitable

  • Some contain more than you need – risks?
  • Some may contain less – risks?
  • Identifying the main reason for using the product is important
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What products are available for transfusion?

A

–Products containing everything

•Whole blood products

–Products containing cells

•PRBC, platelet products, (WBC)

–Products containing plasma proteins

•Plasma and its fractions

–Products containing none of the above

•Oxygen carrying solutions

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

What products do we use most frequently and why?

A
  • Fresh whole blood – surgery
  • Packed red blood cells (most commonly used as hemolytic anaemia is common)
  • Fresh frozen plasma – coagulopathy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Discuss fresh whole blood

A

–‘Unadulterated’ blood from a suitable donor

–Should be harvested aseptically into closed collection system

–Single unit is ~450ml

–Must be transfused within 8 hours or must be refrigerated after collection – becomes SWB

–All blood products are present and functional

•Red cells, platelets, WBC, labile and non-labile clotting factors

–Most common agent transfused in private practices

–Most appropriate for animals that are haemorrhaging

  • Coagulopathies
  • Thrombocytopaenia
  • Whole blood loss due to trauma/surgical complications
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Discuss stored whole blood

A

–Fresh whole blood that is not transfused within 8 hours can be stored in fridge (<4°C)

–Storage life of SWB is around 3-5 weeks depending on anticoagulant used

–The major difference cf. FWB is the lack of platelets, white blood cells and labile clotting factors (FV, FVIII and vWF)

•Valuable in haemorrhage due to trauma (less ideal that FWB), vitamin K dependent rodenticide toxicity, coagulopathies due to liver disease (where whole blood is not contraindicated)

–Once transfusion has begun MUST be completed within 4 hours

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

Discuss packed red cells

A

–This is prepared from whole blood by centrifugation

–The whole blood is collected into a system where there is an extra bag for the plasma to be separated

–The red cells are then resuspended in small volume of plasma and nutrient solution

  • E.g. SAG-M (Sodium chloride, Adenine, Glucose, Mannitol)
  • Unit volume ~ 250ml

–PCV of this is between 70-80% (depending on starting PCV)

  • Shelf life is between 3-6 weeks depending on preservative used (SAG-M provides up to 6 weeks shelf life)
  • Should be stored to enable air to circulate around units
  • Indications:

–Anaemia due to haemolysis/chronic disease/erythropoietic failure

»Where patients are volume replete

–Can use this in conjunction with colloidal solution in animals needing whole blood if unavailable

  • Saline was historically introduced into the bag or coadministered during transfusion
  • No longer considered necessary
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Discus autologous transfusion

A

–Often overlooked source of recipient matched blood

  • harvest blood ready for later transfusion when anticipating haemorrhage
  • acute cavity haemorrhage due to trauma/coagulopathies

–Caution if there is other organ damage – such as urinary or gall bladder

–Benefits of reducing potential for exposure to allogenic blood, reduces risk of (new) infectious diseases, reduces chance of transfusion reactions, immediate availability (!)

–Scavenging systems are available to harvest the blood however these are not considered essential

•Surgical suction catheters, dialysis catheters or needles can be used as long as sterility is assured

–Cavity blood can be drawn into sterile syringes and driven back into the patient using an in-line filter or placed aseptically into sterile freshly emptied fluid bags delivered via blood giving set, depending on volume

–Survival of the replaced autologous blood is better when transfused using gravity feed

•This is thought at least in part due to increased osmotic fragility from contact with serosal surfaces

–Risks include sepsis and dissemination of neoplasia. The dissemination of neoplasia is a theoretical concern, which may be borne out by immediate survival of the patient.

  • No need to anticoagulate if has been present in body cavity for >1 hour
  • If <1 hour then anticoagulation is recommended (although in cases of coagulopathy this would be of questionable benefit)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Discuss fresh frozen plasma. Indications for use?

A

–This is plasma harvested from fresh whole blood (historically) within 8 hours of collection

•More recent data would suggest ok within 24 hours

–Provides maximal concentrations of all factors

–Dose: 6-10ml/kg every 12hrs (up to 20ml/kg for severe coagulopathy)

–If stored

•Although may be longer……

–Indications for use

–Acquired or inherited coagulopathies

–DIC, pancreatitis (?)

–Liver disease

–Perioperative use for vWD or other inherited coagulopathies

–Once defrosted or after fresh is collected, it should be used within 5 days

–It should NOT be used for albumin replacement or as colloidal therapy due to the volume required to increase the plasma oncotic pressure and albumin concentration

–Recent study has suggested that transfusion of freeze thaw cycled fresh frozen plasma (refrozen within 1 hour of defrosting) is expected to provide the recipient with comparable replacement of hemostatic proteins as FFP that has remained frozen

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

Discuss stored plasma/frozen plasma. Uses?

A

–This is the term used to describe FFP which is >1 year old

–OR FFP that has been thawed or separated from whole blood >8 hours after collection

•However new data would suggest that up to 24 hours is acceptable to prepare FFP

–Some factor activity lost (particularly labile factors)

•However vitamin K dependent factors (II, VII, IX and X) are not labile and so should be functional

–Can use up to 5 years from preparation if stored at

  • Standard unit is ~200ml
  • Dose is ~10-20ml/kg

–Standard approach to transfusion

–Uses –

  • Anticoagulant rodenticide toxicity, Haemophilia B
  • Liver disease, DIC, pancreatitis (?)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Discuss oxyglobin

A

–Currently unavailable!! (prevoiusly Dechra Veterinary Products)

–Cell free bovine polymerised haemoglobin in LRS

•Slows clearance from vasculature

–Stored as deoxyhaemoglobin

–Binds oxygen less tightly that normal RBC-Hb

•This improves dissociation at lower tissue oxygen conc

–Once opened should discard within 24 hours

  • Methaemoglobin develops which is irreversible
  • no preservative – high risk of bacterial growth

–Has significant colloidal influence as well as oxygen carrying capacity

•Low doses therefore are recommended in cats

–No preservative! – bag needs to be used/thrown away

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

Discuss oxyglobin doses

A

–Impact and duration of effect is dose dependent

  • 10ml/kg theoretical PCV increase ~3%, duration 11-23h
  • 30ml/kg theoretical PCV increase ~12%, duration 74-82h

–In dogs

  • dose should not exceed 30ml/kg in given 24 hour period
  • Rate should not exceed 10ml/kg/hr

–In cats

  • Dose should not exceed 10ml/kg in given 24 hour period
  • Rate should not exceed 3ml/kg/hr (0.5-2ml/kg/h)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Where are the uses of oxyglobin and where should we take care?

A

–Uses

•Anaemia and circulatory collapse

–Care with volume replete patients

–Particularly useful where rapid (temporary) oxygen provision is required

–Due to the heavy colour of the product this influences some clinical pathology parameters

•Colorimetric assays are affected

–Biochemistry and optical coagulation methods

–Haematology parameters are less affected

–However those machines directly measuring Hb will also measure the oxyglobin

–Care with repeated administration due to antibody development

•However these do not seem to influence oxygen carriage

18
Q

Do we have a feline blood bank?

A

–At present there is no repository for feline blood or blood products in the UK

•Problem with storage of feline blood is absence of true closed collection system

–This may change over the next few years

  • Available in the USA
  • However in UK major problem is with collection methods and ethics associated with this

–Until then whole blood should be obtained from practice based donor schemes

–Human albumin has been used with some success in hypoalbuminaemic cats and caveats are the same as that seen in dogs

19
Q

How much blood do you transfuse? Dogs/cats?

A

•This has had recent scrutiny however previous equations suggested

–Dogs for donor PCV of around 45%

–2ml/kg will raise the recipients PCV by around 1%

–Cats for donor PCV of around 37%

–3ml/kg will raise the recipients PCV by 1%

•Recent publication (Short et al 2012) suggested best formulae for Dogs

–Volume to be transfused = recipients blood volume (BW in kg x 90ml) x [(desired PCV – recipient PCV)/donor PCV]

–Volume to be transfused = 1.5ml x desired PCV rise x BW in kg

•In cats reasonable formulae would be:

–Volume of whole blood (ml) = desired PCV rise (%) x BW in kg x 2

20
Q

What is an older formula to decide how much to transfuse?

A

–Volume to be transfused (ml) = BW of recipient (kg) x average blood volume (ml/kg) for species in question* x [required PCV – current PCV]/donor PCV

–* dogs 85ml/kg, cats 60ml/kg

–For PRC rule of thumb:

•2ml PRC/kg BW raises PCV by 2%

21
Q

What rate should I transfuse the blood?

A

–Depends on circulatory status

•It is possible to use blood as a colloid and as a shock/replacement fluid and deliver as rapidly as possible

–Risks of calcium chelation and hypocalcaemia, influence on clotting cascade and platelet function/activation

–If animals cannot tolerate the required volume in 4 hours then this should be aliquoted and refrigerated for no longer than 24 hours

–Longer the blood is out the more the blood has a chance of septic – must put in in 4 hours

–Dogs

  • Usually 0.25ml/kg/h for 10-20 minutes followed by 0.5ml/kg/h for 10-20 minutes
  • If no reactions are observed then increase rate to between 5-10ml/kg/h to deliver blood within 4 hours

–Cats

•Usually 1-3ml/h for the first 10-20 minutes, if all ok then can increase rate to 5-10ml/kg/h if circulation status appropriate

22
Q

How should the blood product be transfused?

A
  • Important that LRS (hartmanns) is not co-administered with blood or blood products as this can lead to clotting or haemolysis
  • Historically need to use supplementary fluid when using packed red cells to reduce viscosity

–This can be added directly to the bag or run in separately

–More recently concentration of blood in PRC means this is no longer considered necessary by some

•What about chlorpheniramine prior to starting the transfusion

–The evidence that this is essential to reduce the incidence of acute reactions is lacking

–Increases comfort level of clinician (perhaps survival?)!

•Cephalic or jugular vein (intraosseous)

•Filtered giving set

–removes microthrombi and other cells fragments

•Infusion pump or standard giving set?

–majority of studies in humans suggest storage of blood is major influence on administration haemolysis

–Rate or volume administered does not seem to influence integrity (slow vs. fast)

•Aim to complete transfusion within 4 hours

–This prevents contamination of blood products

•It is important not to actively warm the blood before transfusion

–This damage cells

–Increases risks of bacterial growth

–(although you should warm plasma)

–DO NOT FREEZE blood

  • In dogs a standard blood unit is infused via a blood giving set which contains a filter to remove clots and other large fragments
  • In cats and smaller dogs where syringe collection has been used this is best administered via a syringe driver and in-line paediatric filter
23
Q

What are blood groups?

A
  • The presence of naturally occuring antibodies to blood group antigens determines the nature and frequency of any reaction
  • Dogs have very few naturally occurring antibodies to major blood groups

–Low risk of transfusion reaction

•Cats frequently have naturally occurring antibodies to major blood groups

–Increases risk of transfusion reaction

•Rare to blood transfuse cat – must tell them it might kill them – theyd have to be dying anyway (best to refer if poss to type them)

24
Q

Whata re the main blood groups in dogs?

A

–There are >10 blood group systems

•Dog erythrocyte antigen (DEA)

–There are 6 of these 1.1,1.2, (1.3), 3, 4, 5 and 7

–Alternate – 1, 3, 4, 5 and 7

  • Dal
  • Kai
25
Q

How do we avoid transfusion reactions?

A
  • Blood typing
  • Cross matching

–Assesses blood compatibility between the donor and recipient

•Major cross-match detects if the recipient’s serum contains any antibodies against the donor’s RBCs.

Minor cross-match detects if the donor’s serum contains any antibodies against the recipient’s RBCs

26
Q

Discuss first transfusions in dogs

A

–Most dogs can receive their first transfusions safely, the donor blood should be DEA 1.1 negative (though less crucial cf. cats)

  • Antibodies to DEA 1.1 are responsible for acute reactions in dogs – most ok for the first transfusion
  • Give negative to everyone
  • +ve to +ve

–Around 30% of dogs may carry naturally occurring anti-DEA antibodies and thus the risk of transfusing untyped dog blood to untyped dogs should be considered.

  • This is most important for anti-DEA 1.1 antibodies however the naturally occurring rate is low (but theoretically remains a risk)
  • The occurrence of acute reactions are low for some of the less significant antigens (such as DEA 3, 5 and 7). These are more commonly associated with delayed reactions

–Should really cross match or at least type before first transfusion in dogs

27
Q

Discuss the ideal transfusion in a dog after the first one

A

•DEA 1.1 negative dogs receiving positive blood will form antibodies against the DEA 1.1 antigen.

–Care with a second transfusion

•Ideally

–Thus second transfusion (after 4-5 days) MUST be cross-matched

–Typing under these circumstances is less important

–NB minor mismatches become more significant over tim

•DEA 1.1 positive dogs can receive either DEA 1.1 positive or negative blood.

28
Q

Discuss transfusion in cats. Risks and groups

A

•Much greater risk in cats than dogs of peracute and fatal transfusion reactions – make owners aware

–Never transfuse cats that have not been typed

•If you do it is a coin toss whether your effort will kill or cure

–Types AB, A and B (Mik and many others probably)

  • Various reports prevalence of feline blood groups
  • As a rule type B is considered less common
  • In UK data (Forcada et al 2007) reported ~2/3 of DSH were type A
  • Some pedigree cats are almost invariably type A

–Siamese and derivative breeds

•Some pedigree cats have high incidence of type B

–BSH, Rex’s and Ragdolls

29
Q

Discus which feline blood transfusions can be given

A

•High incidence of anti-A antibodies in type B cats leads to peracute reaction in any recipient with an A antigen (either type A or AB)

–This can happen with minimal volume delivered

  • AB donate to either A or AB animals, not B animals
  • AB can receive from A or AB, anti-B antibodies in type A cats means minor reaction could occur but risk is low
  • Rule of thumb only give B blood to B cats, not AB due to anti-A antibodies in type B cats
  • Mik group is responsible for some reactions in cats that have been typed for A and B

–The Mik antigen is occasionally deleted in some type A cats

–Alloantibodies to the Mik Ag in these cats can lead to transfusion reactions when these are used as transfusion donors

30
Q

What happens if we give type B cats type A?

A
  • Massive intravascular haemolysis of type A donor blood
  • Can occur following administration of very small volumes of mismatched blood
  • Occurs rapidly
  • May be fatal!!
31
Q

What happens with type A cats receiving type b?

A
  • Extravascular haemolysis = milder clinical signs
  • Low half-life of RBCs (2 days +)
  • PCV will fall to pre-transfusion levels within days of the transfusion
  • Can mimic ongoing haemolysis in cats with IMHA or haemorrhage
32
Q

How do we monitor in a transfusion?

A

–Crucial for identifying early reactions

–Routinely monitor TPR, respiratory effort, CRT and membrane colour every 5 minutes for the first half an hour during which time the rates have changed from 0.25ml/kg to 5-10ml/kg.

•Rate may also depend on volume status of patient…

–This can then be reduced to every 15-30 minutes until completion should all be proceeding well

–If changes in parameters are noted then reduce the rate and review whether these continue to change

•Some suggest a >1°C is a reaction

–This is somewhat contingent on the circulatory status of the patient however

–PCV should be obtained an hour or so after, this ensures some volume redistribution occurs making the PCV more accurate

–Acute haemolytic reactions are due to pre-formed antibodies (IgG usually)

•Directed against RBC (also WBC and platelets)

–These lead to acute intravascular haemolysis

•More common in cats than dogs

–Dogs risk increases with increasing numbers of transfusions

  • If suspect acute reaction stop immediately
  • Signs – hyperthermia, tachycardia, dyspnoea, tremors, vomiting, collapse, haemoglobinaemia/uria
  • Can lead to DIC and RIP (more common in cats)
33
Q

What is acuute non-haemolytic reactions due to?

A

Often bacterial contamination

34
Q

What are the types of reactions which can occur. Discuss, signs causes etc.

A

–Non-haemolytic reactions can occur (IgE and mast cell mediated)

  • Can be rate dependent
  • Various signs but more consistent with anaphylaxis

–Urticaria, respiratory signs (dyspnoea), vomiting

–Stop and provide anti-HA if not done so already and possibly glucocorticoids

–May be severe enough to require circulatory support

–Non-haemolytic non-hypersensitive reactions can also be seen

–Suspected to be due to platelet or WBCs

–Febrile patient for no obvious reason for up to a day

•Pre-sampling leukoreduction filters reduce the incidence of these

35
Q

How can we minimise the risk of non-immunological reactions?

A

–Handle and store blood bags carefully

–Use a filtered giving set for administration

–Administer transfusion at an appropriate rate for the patient’s condition

–Monitor recipient closely during 1st 30 min of transfusion

–Consider initial slow flow rate (0.5 ml/kg/h) during first 30 min of transfusion

36
Q

What are the clinical signs of transfusion reactions

A

Acute (<24hrs of administration)

  • Pyrexia
  • Depression
  • Dyspnoea, tachypnoea or coughing
  • Tachycardia or bradycardia
  • Vomiting
  • Vocalisation (cats)
  • Urticaria (especially dogs)
  • Erythema or pruritus
  • Tremors or seizures
  • Shock
  • Cardiopulmonary arrest

Delayed (>24 hrs after administration)

  • Fever
  • Anorexia
  • Jaundice
  • Often subclinical
37
Q

What shoudl we do if we suspect a transfusion reaction?

A

–Clinical exam

  • cardiorespiratory system
  • temperature
  • haemoglobinaemia or haemoglobinuria

–Supportive treatment as indicated

  • e.g. fluids, corticosteroids, oxygen, antihistamines, adrenaline, diuretics

–Check blood typing or cross-matching

–Check blood bag for evidence of lysis

38
Q

What are the blood groups in horses?

A

•There are 7 blood group systems

–A, C, D, K, P, Q, U

–Aa, Qa, and Ca are the most immunogenic blood groups

•These are important for transfusion reactions

–standard breeds have low prevalence of Aa and Qa and are often used as donors.

–A test kit for Ca is now available

–Use greyhounds – great PCV

39
Q

Who are the ideal horse donors?

A

Geldings

40
Q

What are the most immunogenic blood groups?

A

Aa, Qa, and Ca

41
Q

Discuss donors in cows?

A
  • Choose healthy donor who is easy to handle and not heavily pregnant.
  • Cross matching unnecessary as transfusion reactions after a single administration of blood are rare and mild.