Your browser is out-of-date!

Update your browser to view this website correctly. Update my browser now

×

InFocus

Blood transfusions

It is essential to monitor patients throughout the procedure to ensure any sign of adverse transfusion reaction is caught early on

When selecting blood products to use, it is worth noting the existence of component therapy to deliver targeted blood components, possibly through the UK-based not-for-profit charity Pet Blood Bank UK (PBB). Transfusing only the required component (eg fresh whole blood, packed red blood cells, fresh frozen plasma, cryoprecipitate; Pet Blood Bank, 2020) reduces the volume of the product to be administered and reduces both the anaphylactic risk and the development of any inadvertent recipient sensitisation to the unnecessary blood components that may affect the safety of future transfusions.

Compatibility testing

Prior to transfusion of any blood product, but particularly a red cell product, blood typing to determine the dog erythro­cyte antigen (DEA) 1 status of the recipient should be estab­lished. This can be done quickly and easily even in an out of hours or emergency setting using an in-house kit. Establish­ing the recipient as DEA 1 negative or positive allows a com­patible red cell product to be administered which reduces the risk of an adverse transfusion reaction during subsequent transfusions as a result of DEA 1 sensitisation. In addition, as only 30 percent of PBB blood donors are DEA 1 negative and 70 percent are DEA 1 positive, using type-matched red cells supports PBB in managing their stock levels.

A major cross-match detects existing recipient anti-bodies to any donated red cell antigen, including and beyond DEA 1, as even when DEA 1-typed blood is given correctly to patients there is still the potential to introduce other antigens that may be seen as foreign and that the patient may create antibodies against (Young et al., 1949). It is therefore recommended in dogs to perform a cross-match prior to transfusion if:

  • The transfusion history of the dog is unknown
  • Previous transfusions have caused a reaction
  • A transfusion has been administered more than four days previously

A cross-match should be carried out prior to transfusion for the lifetime of the dog.

A compatible cross-match result means that an acute haemolytic transfusion reaction (AHTR) would be unlikely. As with blood typing, a cross-match can be carried out in-house using a commercial test kit in under 30 minutes.

STEP-BY-STEP BLOOD PRODUCT PREPARATION

Select the blood product and check the unit for any unusual discoloration, cloudiness or particles and check the bag for signs of external damage. If any of these are observed, do not administer the unit and inform PBB. Check that the unit is in date and has been stored correctly and the appropri­ate temperature range was maintained during storage. It is sensible to have a double-check process to confirm that the blood product selected and the DEA 1 status are correct prior to unit preparation.

FIGURE (1A) Prior to the administration of plasma it will need to be defrosted. This can be done for non-urgent transfusions by laying the unit on a flat surface at room temperature and will take approximately three hours. Alternatively, the unit can be placed in a plastic ziplock bag to prevent contamination of the administration ports and the bag placed in a warm water bath. The water bath should contain water not exceeding 37°C; this will defrost a large unit in approximately 11 to 15 minutes if the temperature is maintained by topping up with warm water as the bath temperature reduces. Before removing the unit, make sure that all the plasma is defrosted and no frozen crystals remain by gently palpating the unit. Red cell products that have been refrigerated do not need to be warmed before administration; however, warming can be carried out if preferred using a 37°C water bath in the same way and is definitely recommended where the recipient is very young or is hypothermic. Blood products should never be placed in a microwave as this will damage the cells and proteins
FIGURE (1B) Prior to the administration of plasma it will need to be defrosted. This can be done for non-urgent transfusions by laying the unit on a flat surface at room temperature and will take approximately three hours. Alternatively, the unit can be placed in a plastic ziplock bag to prevent contamination of the administration ports and the bag placed in a warm water bath. The water bath should contain water not exceeding 37°C; this will defrost a large unit in approximately 11 to 15 minutes if the temperature is maintained by topping up with warm water as the bath temperature reduces. Before removing the unit, make sure that all the plasma is defrosted and no frozen crystals remain by gently palpating the unit. Red cell products that have been refrigerated do not need to be warmed before administration; however, warming can be carried out if preferred using a 37°C water bath in the same way and is definitely recommended where the recipient is very young or is hypothermic. Blood products should never be placed in a microwave as this will damage the cells and proteins
FIGURE (2) Once warmed, the red cell/ plasma unit should be removed from the plastic ziplock bag and hung on a drip stand. Don non-sterile gloves and apply hand sanitiser then access one of the administration ports on the unit by tearing the protective cover using aseptic technique
FIGURE (3) Remove a blood administration set from its outer packaging and prepare for use by closing off the drip wheel and closing any in-line clamps. All blood products must be passed through a filter before reaching the patient to remove micro clots and cellular debris
FIGURE (4A) Unsheathe the administration set insertion spike and in an aseptic manner push fully into the revealed administration port using a rotating motion ensuring it reaches the blood product. The unit is now breached and must be discarded after four hours at room temperature
FIGURE (4B) Unsheathe the administration set insertion spike and in an aseptic manner push fully into the revealed administration port using a rotating motion ensuring it reaches the blood product. The unit is now breached and must be discarded after four hours at room temperature
FIGURE (5) Fill the drip chamber to approximately a half to two thirds by gently squeezing the drip chamber taking care not to damage the chamber filter. Ensure the fill level is above the filter but not so full that the drip rate cannot be observed
FIGURE (6) Open any clamps on the administration line then slowly release the drip wheel
FIGURE (7) Prime the entire length of the administration line to the very end, leaving the cover in place
FIGURE (8) Only remove the cover immediately before attaching to the patient’s intravenous catheter

Preparation of the patient

Blood products can be given by the intraosseous and central venous routes but are generally administered via a peripheral intravenous catheter. Due to blood being an ideal growth medium for bacteria, gloves should always be worn when handling the blood product and line or the intrave­nous catheter (IvC) being used. Confirm the IvC is in situ by disinfecting the port and flushing with sterile saline before disinfecting the port again and attaching the blood adminis­tration/extension set.

Patients are generally not given food during a transfu­sion, but water can be provided. It is best to avoid using the catheter to administer drugs and other fluids, especially flu­ids containing calcium such as Hartmann’s solution, during the transfusion. Where a drug is time critical, for example an analgesic, and cannot be given earlier or later, the drug can be administered if a second IvC is available.

Once started, the blood administration set should not be disconnected, or the transfusion stopped, except when a potential adverse reaction is occurring. Make sure patients have been walked out and have no owner visits scheduled during the transfusion window.

Monitoring for adverse transfusion reactions

The recipient should be placed in a kennel that permits constant visualisation and a transfusion nurse assigned. It is preferable to have the same nurse monitoring the entire transfusion for consistency and so subtle changes are more likely to be identified, and a specific transfusion monitoring form completed. Staff availability may need to be considered when planning a non-urgent transfusion on a busy shift.

FIGURE (9) Patient undergoing a packed red blood cell transfusion attached to a multiparameter monitor

Prior to starting the transfusion, obtain the baseline values. Pulse rate and quality, respiratory rate and effort, temperature, mentation, mucous membrane colour and capillary refill time are the minimum parameters to be monitored, as well as recording the passage of urine and faeces and their appearance, any episodes of vomiting and noting any changes in behaviour. In addition, SpO2 and arterial blood pressure can be recorded. The author prefers to attach transfusion patients to a multiparameter monitor with the ECG and blood pressure cuff attached (Figure 9) and where tolerated the rectal and pulse oximetry probes placed. This allows continuous monitoring without repeat­edly disturbing the patient.

There are various forms of acute adverse transfusion reactions, including immunological reactions such as acute haemolytic transfusion reaction, febrile transfusion reaction and transfusion-related lung injury, as well as non-immunological reactions such as allergic reaction/ anaphylactic shock, erythrocyte haemolysis circulatory overload and sepsis. Signs of an acute adverse transfusion reaction include increased body temperature, increase or decrease in heart rate, weak or bounding pulses, increased respiratory rate or effort, dyspnoea, cyanosis, weakness or collapse, urticaria/erythema/oedema, hyperaemic mucous membranes, reduced mentation or responsiveness, shak­ing/trembling/seizures, vomiting or diarrhoea, or demon­stration of unusual behaviours.

There is no one transfusion monitoring schedule; the fol­lowing is based on the author’s experience:

  • First 20 to 30 minutes: The nurse will remain with the patient continuously during this time, recording observations every 10 minutes
  • 30 minutes to 1 hour: If there are no signs of an adverse transfusion reaction, monitoring can continue every 10 to 15 minutes
  • 1 to 2 hours: If progressing uneventfully, monitor at 30-minute intervals
  • 2 to 4 hours: Monitoring can be reduced to hourly

Administration of the blood product

When small volumes of blood product need to be delivered, or if the desired volume cannot be completed within four hours, the unit may be separated into smaller volumes and stored labelled in a sterile empty blood bag or syringes. If kept in the fridge at +2 to +6˚C, each syringe must be discarded after four hours at room temperature and the syringes can be kept refrigerated for 24 hours. The blood product must be passed through a filter and the product is then delivered using a syringe driver (Figure 10).

FIGURE (10) The blood product must be passed through a filter and the product is then delivered using a syringe driver

The transfusion rate is started slowly at 0.5 to 1ml/kg/hr, as the severity of an adverse reaction is, in part, related to the volume of blood that has been administered. If no signs of an adverse transfusion reaction have been observed in the first 15 to 30 minutes, the rate can be increased to 5 to 10ml/ kg/hr. Any breached unit must be discarded after four hours. Lower rates of 1 to 2ml/kg/hr should be used for patients with circulatory compromise.

The ability to control the delivery of the blood product is important for recipient safety and use of an infusion pump or syringe driver for smaller volumes allows this. The current recommendation is to check with the manufacturer if the infusion pump is compatible for delivering blood products as some studies have reported a reduced red cell survival time with this type of delivery versus gravity flow (McDevitt et al., 2011).

The blood administration set should be changed after four hours or when a new unit is to be administered. Simi­larly, Hemo-nate filters should be changed after every 50ml blood product, after four hours of use or whenever a new unit is attached.

Unit traceability

Once the transfusion is complete, it is vital that a transfu­sion log is maintained recording each unit and its recipient so the recipient of a given unit can always be traced.

References

Heikes, B. and Ruaux, C.

2013

Effect of syringe and aggregate filter administration on survival of transfused autologous fresh feline red blood cells. Journal of Veterinary Emergency and Critical Care, 24, 162-167

McDevitt, R., Ruaux, C. and Baltzer, W.

2011

Influence of transfusion technique on survival of autologous red blood cells in the dog. Journal of Veterinary Emergency and Critical Care, 21, 209-216

Pet Blood Bank

2020

Canine blood component table

Young, L., Ervin. D. and Yuile, C.

1949

Hemolytic reactions produced in dogs by transfusion of incompatible dog blood and plasma. Blood, 4, 1218-1231

Helen Rooney

Helen Rooney, BSc (Hons), CVN, Cert Ed, Dip AVN (Medical), Cert VNECC, RVN, qualified as a veterinary nurse in 1996 and has worked in referral practice and as a veterinary nursing lecturer. She has an interest in emergency and critical care and transfusion medicine, enjoying the fast pace and intense nursing input of these cases. She is the Pet Blood Bank UK Training and Induction Manager.


More from this author

Looking for a range of resources, insights and CPD all in one place?

Join the ALL-NEW Veterinary Practice community; the online platform with nugget-sized, CPD-accredited veterinary training and resources!

Everything you need for your professional development, delivered by experts.

One place. One login. It’s online. All the time.

Annual subscription: £299 for Vets and £199 for Vet Nurses

Subscribe Now