Transfusions Flashcards

1
Q

What are the main differentials for regenerative anaemia?

A

■ Haemolytic disorders (causes/triggers)
● Infectious (viral, bacterial, parasitic)
● Immune disorders (IMHA, systemic lupus erythematosus, hypothyroidism, immunodeficiencies)
● Drugs (vaccines, sulphonamides, methimazole,
procainamide, cephalosporins, penicillins, propyluracil)
● Oxidants (paracetamol, phenothiazines, vitamin K, methylene blue, methionine, propylene glycol)
● Neoplasia
● Genetic predisposition
■ Haemorrhage

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2
Q

What are the main differentials for non regenerative anaemia?

A

■ Preregenerative anaemias
■■ Anaemia of chronic inflammatory disease
■■ Iron-deficiency anaemia
■■ Bone marrow disorders
■■ Infections (viral, mycoplasma, ehrlichiosis, babesiosis)
■■ Drugs (chemotherapy, immunotherapy)
■■ Myelofibrosis
■■ Myelopthistic disease (neoplasia)
■■ Myelodysplasia
■■ Pure red cell aplasia
■■ Ineffective erythropoiesis (deficiencies in
erythropoietin, vitamin B12, folic acid, globins
or porphyrin)

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3
Q

When should transfusions be performed?

A

No set line - risk v benefit
■ A patient is exhibiting significant clinical signs of
anaemia;
■ An animal has a PCV of less than 10 per cent;
■ An animal’s PCV has fallen rapidly to less than 20
per cent in dogs or 15 per cent in cats.
In patients with a poor or absent bone marrow
response, red cells are unlikely to be replenished in the short term and, hence, earlier transfusion may be indicated in order to prevent further clinical compromise

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4
Q

What is the use of fresh whole blood?

A

Fresh whole blood contains red blood cells, all clotting
factors, plasma proteins and anti-inflammatory proteins, with a small number of platelets. Whole blood can therefore be used in many conditions, including
acute or severe haemorrhage, haemolytic anaemia,
chronic blood loss or non-regenerative anaemia, and
coagulopathies if other blood products are not available. Whole blood must be used within four to six hours of collection to maximise its full range of benefits.

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5
Q

What is the use of stored whole blood?

A

Stored whole blood is fresh whole blood collected into
an appropriate bag (usually one designed and used
in human medicine) that contains an anticoagulant
(eg, citrate phosphate dextrose adenine-1 [CPDA-1]).
Whole blood can be stored in a refrigerator at 1 to 6°C
for up to 28 days. However, after 12 to 24 hours, many
plasma proteins will be degraded, making the product
ineffective in conditions requiring coagulation factors.
As a rule of thumb, 2 ml/kg of whole blood will
raise a recipient’s PCV by 1 per cent or the haemoglobin level by 0·3 g/dl.

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6
Q

What is the use of pRBCs?

A

A unit of canine packed red blood cells is
about 200 to 250 ml and has the same oxygen carrying capacity as one unit of whole blood (450 ml)
As packed red blood cells contain only a
small amount of plasma, they have a minimal effect on
oncotic pressure - may therefore be safer in those prone to volume over load
As a rule of thumb, 2 ml/kg of packed red blood
cells will raise a recipient’s PCV by 2 per cent or the
haemoglobin level by 0·6 g/dl.

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7
Q

When is Fresh Frozen Plasma good?

A
Fresh frozen plasma is generally indicated for animals with inherited and acquired coagulopathies and
in patients with prolonged clotting times undergoing
invasive procedures (eg, liver biopsy). It can be used for
some plasma protein deficiencies (eg, immunoglobulin) and may be useful in providing antiparvovirus
antibodies and immunoglobulins in cases of parvovirus infection, although conclusive evidence is lacking.
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8
Q

What is Frozen plasma?

A

Frozen plasma has lost the action of many clotting factors (V, VIII, von Willebrand factor [vWF]) and plasma proteins, but it still contains vitamin K-dependent
factors (II, VII, IX, X).
Frozen plasma has either been frozen more than six
hours after collection, has been thawed and refrozen,
or has been frozen beyond the recommended maximum storage time (see above). This product can be used in patients with deficiencies of the non-labile
clotting factors (eg, anticoagulant rodenticide toxicity
and some plasma protein deficiencies).

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9
Q

What is cryoprecipitate?

A

Cryoprecipitate is made up of approximately 20 per cent fibrinogen, 50 per cent clotting factor VII and 30 per cent clotting factors VIIIc, XIII and vWF. It is separated from the plasma fraction of blood using a process of controlled thawing and centrifugation. Cryoprecipitate must be stored frozen at –18°C and is stable at this temperature for up to one year. It can be used in patients with inherited clotting factor deficiencies such as haemophilia A and von Willebrand’s disease.

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10
Q

What is cryosupernatant?

A

Cryosupernatant is the plasma that remains following
separation of the cryoprecipitate as described above.
It is a source of all coagulation and plasma proteins,
except for clotting factors VII, VIIIc and XIII, fibrinogen and vWF. When stored at –18°C, it is stable for one
year. Cryosupernatant can be used for the treatment of
most clotting factor deficiencies, except haemophilia A
and von Willebrand’s disease, and can also be used for plasma protein deficiencies.

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11
Q

What is oxyglobin?

A

sterile haemoglobin based oxygen-carrying solution made from bovine haemoglobin.
It is only licensed in dogs with anaemia, but its use in cats has been reported.
potent colloid and must therefore be used with caution in patients with cardiorespiratory or central nervous system diseases, or those with oliguric renal failure. Oxyglobin should also be used with care in cats due to the risks of volume overload and possible pulmonary bed vasoconstriction.
Following administration, Oxyglobin causes discoloration of the mucous membranes, sclera and urine, making clinical assessment difficult. It also interferes with some biochemical analysers.
Most gone within a week of use

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12
Q

Outline canine blood types

** whelping should be considered a whelping event**

A

eight different blood groups have been recognised in the dog, with the major and most immunogenic being DEA 1.1 for which dogs can be either positive or negative.
The others include DEA 1.2, DEA 3, DEA 4, DEA 5, DEA 7 and a new antigen in dalmatians called DAL.
DEA 1.1 is the most common blood type in dogs and, although naturally occurring antibodies to DEA 1.1 are rare, the determination of DEA 1.1 antigen is strongly recommended as this antigen is highly immunogenic and will result in antibody formation.
The antigen to DEA.1.1 is not naturally occuring so should be fine for the first transufsion, sensitisation takes 2-4 days. Naturally occurring antibodies against DEA 7 are present in 15 per cent of dogs, but DEA 7 antigen is rare. These antibodies may be responsible for
the occasional mild reactions following first transfusions.

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13
Q

Outline feline blood types

A

Cats have three main blood types (on the AB system),
which are type A, B or AB. The antigens associated with these types are highly immunogenic and type B cats have high levels of naturally occurring antibodies. This means that fatal transfusions can occur with even tiny volumes of incompatible blood (Callan and Giger 1994).
Although type AB cats have no naturally occurring
antibody, they posses both A and B antigens and donor blood from these animals can therefore cause a significant reaction in recipients, as their cells are susceptible to destruction by antibodies in the donor plasma.
Type A cats possess only low titres of anti-B antibodies and so the transfusion of incompatible blood to
type A cats only results in a mild reaction with minimal
clinical signs

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14
Q

How much blood can an animal donate?

A

Dogs and cats can donate 10 per cent of their total
blood volume with no adverse effect (blood volume =
66 ml/kg in cats and 90 ml/kg in dogs [Turnwald and
Pichler 1985]). Collection of 20 per cent of blood volume should not result in clinically significant anaemia provided the donor has a normal PCV at collection, although it can produce hypovolaemia in the short term.
Collection of >20 per cent of blood volume can produce hypovolaemia of sufficient magnitude to compromise health

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15
Q

What do you normally collect canine blood in?

A

human blood collection bag which contains enough
acid citrate dextrose (ACD) or citrate phosphate dextrose (CPD) anticoagulant for approximately 500 ml
of blood.

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16
Q

Outline fluid therapy for cats donating blood

A

The usual donation volume for cats is 11 ml/kg; for most cats, it may be useful to administer intravenous saline to maintain normovolaemia. An acceptable fluid therapy protocol is to give 90 ml of saline subcutaneously immediately before donation, and to infuse 60 to 90 ml saline over 15 to 20 minutes starting half way through a donation (this equates to two to four times the volume collected).

17
Q

What do you collect feline blood into?

A

Blood from cats should therefore routinely be collected into a 50 ml syringe attached to a butterfly needle or catheter.
Although heparin can be added to the syringe, ACD or CPD are preferred since the blood can then be stored for up to four weeks after collection provided it is kept refrigerated. The syringe should contain 1·3 ml ACD or CPD (withdrawn from a human blood collection bag) per 10 ml of blood to be collected.

18
Q

What should you not mix blood with?

A

Blood should not be administered concurrently (ie, through the same catheter) with intravenous fluids containing calcium or glucose, or with lactated Ringer’s solution (eg, Hartmann’s solution). No medications or solutions other than 0·9 per cent sodium chloride or species-specific plasma should be added or
infused through the same tubing as blood products.

19
Q

What non-immune reactions can occur with transfusions?

A
Mechanical or thermal haemolysis
Circulatory overload
Hypocalcaemia (including citrate toxicity)
Dilutional coagulopathy
Pulmonary microembolism
Hypercalcaemia
Infectious disease
Vomiting
Hypothermia
Air embolism
Bacteraemia/infectious disease
20
Q

What immune reactions can occur with transfusions?

A

Acute haemolytic transfusion reaction
Delayed haemolytic transfusion reaction
Anaphylactic reaction
Pyrexia

21
Q

What can happen to type B cats receiving type A blood?

A

Massive intravascular haemolysis of type A (donor) cells occurs due to the presence of a high titre of naturally occurring anti-A antibodies. This early reaction can be fatal, which is why unmatched blood should never be used for feline blood transfusions

22
Q

What happens to type A cats receiving type B blood?

A

Although type A cats often have weak anti-B alloantibodies, transfused type B (donor) cells can have a mean half-life of as little as two days. The haemolysis that occurs is extravascular and clinical signs are therefore much milder. The main clinical significance is that PCV will fall to pretransfusion levels within days of
the transfusion

23
Q

What occurs in acute haemolytic reactions?

A

depression, recumbency, cardiac arrhythmia, apnoea, seizures or clinical signs of shock. Patients may urinate, defecate, salivate and cats may vocalise, after which animals can become tachycardic and tachypnoeic for a prolonged period of time. Haemoglobinaemia and haemoglobinuria can occur within hours of transfusion but are only clinically apparent after large volumes of blood have been transfused, and hepatic and renal excretion mechanisms are overwhelmed. The rapid destruction of transfused red blood cells also results in a dramatic fall in recipient PCV

24
Q

What occurs in delayed haemolytic transfusion reactions?

A

delayed haemolysis may be subclinical or mild, and
may even be missed if the underlying disease process
involves ongoing haemolysis (eg, immune-mediated
haemolytic anaemia or sepsis). Transfused red blood
cells are removed one to three weeks after transfusion
and the course of delayed haemolysis is usually benign and requires no immediate treatment, although the longer term benefits of the transfusion will be lost. In cats, these reactions are associated with the induction of antibodies to red blood cell antigens other than the
AB group or the induction of anti-B antibodies in type
A cats without naturally occurring alloantibodies. In
dogs, delayed haemolytic reactions occur in association with the induction of DEA 1.1 and DEA 1.2 antibodies by a first or previous transfusion. Due to the absence or low titres of these antibodies at the time of first transfusion, the risk of a delayed reaction can often not be predicted by cross-matching techniques.

25
Q

What is pre transfusion haemolysis?

A

Haemolysis can occur during the storage of whole
blood, particularly if the blood is subjected to overheating or freezing or has become contaminated with microbes (Harrell and Kristensen 1995). The concurrent administration of blood and hypotonic solutions via the same catheter can also result in red blood cell lysis through osmotic ‘cell bursting’.

26
Q

Outline acute hypersensitivity reactions

A

Allergic reactions to transfused allergens are often
associated with plasma transfusions, but can occur
during the transfusion of whole blood and blood products A reaction usually occurs within 45 minutes of the start of the transfusion and, in severe cases, can result in cardiopulmonary arrest. Any evidence of anaphylaxis (eg, urticaria, pruritus, erythema, anxiety, facial swelling, vomiting or dyspnoea) warrants discontinuation of the transfusion and treatment for an anaphylactic reaction (using corticosteroids, antihistamines, oxygen, as required, and adrenaline in severe cases).

27
Q

What is transfusion related pyrexia?

A

pyrexia is the most common transfusion reaction and is characterised by an increase in body temperature of 1°C or more within four hours of a transfusion
usually occurs within 30 minutes of the start
of the transfusion and may continue for up to eight
hours. Clinical signs are usually mild, but may include
vomiting and tremors. The pyrexia may be related
to bacterial contamination of transfused blood or an
acute reaction caused by antibodies to platelets, white
blood cells or plasma proteins that were not detected by blood typing or cross-matching. The blood bag should be evaluated for evidence of bacterial contamination and the patient examined for evidence of haemolysis. However, non-infectious, non-haemolytic pyrexia is the most common form of pyrexia seen and this is usually transient and does not require treatment.

28
Q

What factors can affect testing for blood type

A

If agglutination +ve - therefore need to wash (mix with saline and centrifuge several times) before testing
Low PVC (fewer RBCs to stick together and less antigen)
Recent transfusion
Occasionally DEA 1.2 can lead to false +ve

29
Q

What are the feline blood types?

A

A (most common), AB (rare), B (variable in different breeds)
Also the MIK antigen - no test for this, although should be identified in cross matchin
Cats (unlike dogs) can have naturally occuring allo antibodies after 2m of age, therefore can get a fatal transfusion first time

30
Q

Which blood types can AB cats receive?

A

A can be given to AB (ideally pRBCs)

Not really B

31
Q

Outline xenotransfusion

A

Short lived - half life of approx 4 days

Stop gap only