Blood Products and Transfusion Flashcards

1
Q

Indications for Blood Transfusion - Example Question

A

A 68-year-old patient is referred to the on-call medical team by their General Practitioner (GP) when they are found to have low Haemoglobin (Hb) on a routine set of blood tests taken for fatigue. The results, repeated in hospital, are as follows:

Hb 72 g/l
MCV 69 fl
Platelets 351 * 109/l
Film comment Microcytic hypochromic red cells with pencil cells and target cells

You assess the patient and they give no history suggestive of bleeding. On examination, they are haemodynamically stable with no melaena. Which of the following would be the strongest indication for transfusion in this patient?

	> A history of exertional angina
	A history of myocardial infarction treated with angioplasty
	A history of exertional dyspnoea
	A history of worsening fatigue
	A history of myelodysplastic syndrome

Symptomatic anaemia should be treated unless there is a contraindication.

Fatigue and exertional dyspnoea are ‘soft’ symptoms that should not cause the clinician to rush into transfusion.

The data regarding blood transfusion in ischaemic heart disease are mixed. The current Cochrane consensus is that there is no good evidence to support a liberal (<10g/L) versus restrictive (<7-8g/L) transfusion strategy in any patient cohort, including those with pre-existing ischaemic heart disease. Therefore a history of MI with no current symptoms would not be an indication for transfusion in this patient.

Patients with myelodysplastic syndrome may tolerate low haemoglobin levels well, and moreover are at risk of iron overload from repeated transfusions, and therefore generally would not be transfused at this level in the absence of symptoms.

Exertional chest pain implies cardiac ischaemia, i.e. inadequate oxygen delivery to cardiac tissue, and therefore the patient would benefit from transfusion in this case.

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2
Q

Blood Products: Packed Red Cells

A

Used for transfusion in chronic anaemia and cases where infusion of large volumes of fluid may result in cardiovascular compromise. Product obtained by centrifugation of whole blood.

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3
Q

Blood Products: Platelet Rich Plasma

A

Usually administered to patients who are thrombocytopaenic and are bleeding or require surgery. It is obtained by low speed centrifugation.

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4
Q

Blood Products: Platelet Concentrate

A

Prepared by high speed centrifugation and administered to patients with thrombocytopaenia.

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5
Q

Blood Products: Fresh Frozen Plasma

A

Fresh frozen plasma
Prepared from single units of blood.
Contains clotting factors, albumin and immunoglobulin.
Unit is usually 200 to 250ml.
Usually used in correcting clotting deficiencies in patients with hepatic synthetic failure who are due to undergo surgery.
Usual dose is 12-15ml/Kg-1.
It should not be used as first line therapy for hypovolaemia.

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6
Q

Blood Products: Cryoprecipitate

A

Formed from supernatant of FFP.
Rich source of Factor VIII and fibrinogen.
Allows large concentration of factor VIII to be administered in small volume.

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7
Q

Blood Products: SAG-Mannitol Blood

A

Removal of all plasma from a blood unit and substitution with:
Sodium chloride
Adenine
Anhydrous glucose
Mannitol
Up to 4 units of SAG M Blood may be administered. Thereafter whole blood is preferred. After 8 units, clotting factors and platelets should be considered.

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8
Q

Cell Saver Devices

A

Cell saver devices
These collect patients own blood lost during surgery and then re-infuse it. There are two main types:
Those which wash the blood cells prior to re-infusion. These are more expensive to purchase and more complicated to operate. However, they reduce the risk of re-infusing contaminated blood back into the patient.
Those which do not wash the blood prior to re-infusion.
Their main advantage is that they avoid the use of infusion of blood from donors into patients and this may reduce risk of blood borne infection. It may be acceptable to Jehovah’s witnesses. It is contraindicated in malignant disease for risk of facilitating disease dissemination.

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9
Q

Blood products used in Warfarin Reversal

A

Blood products used in warfarin reversal
In some surgical patients the use of warfarin can pose specific problems and may require the use of specialised blood products

Immediate or urgent surgery in patients taking warfarin(1) (2):

  1. Stop warfarin
  2. Vitamin K (reversal within 4-24 hours)
    - IV takes 4-6h to work (at least 5mg)
    - Oral can take 24 hours to be clinically effective
  3. Fresh frozen plasma
    Used less commonly now as 1st line warfarin reversal
    -30ml/kg-1
    -Need to give at least 1L fluid in 70kg person (therefore not appropriate in fluid overload)
    -Need blood group
    -Only use if human prothrombin complex is not available
  4. Human Prothrombin Complex (reversal within 1 hour)
    - Bereplex 50 u/kg
    - Rapid action but factor 6 short half life, therefore give with vitamin K
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10
Q

‘Reversal’ of NOAC: Example Question

A

A 64-year-old man referred by the emergency department has fluctuating confusion and a severe headache of 4-hour duration. His only past history is a deep vein thrombosis 3 months ago for which he takes rivaroxaban 20mg OD.

On examination, he is orientated to person but cannot recall the time or where he is. There is no evidence of head injury. Temperature is 36.5 degrees, pulse 90 bpm, blood pressure 149/80 mmHg. A brief examination of the peripheral nervous system elicits no abnormal signs and his pupils are size 3 and equal.

An urgent CT head shows blood in the ventricular system.

What is the best immediate management to limit the bleeding?

	Vitamin K 10mg IV
	Pooled platelets
	> Prothrombin complex concentrate (PCC)
	Haemofiltration
	Fresh frozen plasma (FFP) 15mls/kg

The new oral anticoagulants (NOACs) unlike warfarin have as yet no single reversal agent or readily available method of monitoring the clinical effect. Recommendations from the company summary of product characteristics can aid the management of severe bleeding associated with the use of NOACs.

The likely diagnosis here is an intracerebral haemorrhage resulting in depression of GCS, which is a severe or life-threatening bleeding complication of the rivaroxaban.

In addition to haemodynamic support and blood transfusion when necessary, it is recommended to stop the rivaroxaban, consider tranexamic acid, consider prothrombin complex concentrate in conjunction with a consultant haematologist Haemodialysis may be used in the presence of renal failure. Activated charcoal may be useful if a history of recent ingestion is given. Haemodialysis, however, is minimally effective due to the high proportion of rivaroxaban bound to plasma proteins.

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11
Q

Blood Product Transfusion Complications

A

Blood product transfusion complications

Complications
haemolytic: immediate or delayed
febrile reactions
transmission of viruses, bacteria, parasites, vCJD
hyperkalaemia
iron overload
ARDS
clotting abnormalities
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12
Q

Blood Transfusion Cx:

Immediate Haemolytic Reaction

A

Immediate haemolytic reaction
e.g. ABO mismatch
massive intravascular haemolysis

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13
Q

Blood Transfusion Cx:

Febrile Reactions

A

Febrile reactions
due to white blood cell HLA antibodies
often the result of sensitization by previous pregnancies or transfusions

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14
Q

Blood Transfusion Cx:

Immunosuppression

A

Causes a degree of immunosuppression

e.g. patients with colorectal cancer who have blood transfusions have a worse outcome than those who do not

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15
Q

Blood Transfusion Cx:

Transmission of vCJD

A

Transmission of vCJD
although the absolute risk is very small, vCJD may be transmitted via blood transfusion
a number of steps have been taken to minimise this risk, including:
→ from late 1999 onward, all donations have undergone removal of white cells (leucodepletion) in order to reduce any vCJD infectivity present
→from 1999, plasma derivatives have been fractionated from imported plasma rather than being sourced from UK donors. Fresh Frozen Plasma (FFP) used for children and certain groups of adults needing frequent transfusions is also imported
→ from 2004 onward, recipients of blood components have been excluded from donating blood

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16
Q

Blood Transfusion Cx:

Transfusion Associated Lung Injury (TRALI)

A

TRALI presents with acute shortness of breath and hypoxia within six hours of transfusion. Bilateral pulmonary infiltrates are seen on chest X-ray and it is often accompanied by a temperature. Whilst uncommon it is the leading cause of transfusion-related mortality. It is caused by human leucocyte antibodies/human neutrophil antibodies from donor plasma. It occurs more commonly with platelets and FFP than with packed red cells. Blood can be sent for serology and anti-leucocyte antibodies are seen in the donor plasma which react with recipient neutrophil antigens. The mainstay of management is supportive care but intubation and ventilation are often required.

17
Q

Blood Transfusion Cx:

Transfusion-associated Circulatory Overload (TACO)

A

Transfusion-associated circulatory overload (TACO) is an increasingly recognised complication of transfusion which can result in significant morbidity and even death. Patients aged over 70 are at increased risk of TACO. The concept that one unit of packed red cells leads to a 1g/dL increment only applies to a patient weighing 70-80 kg. As a general guide transfusing, a volume of 4ml/kg typically gives an increment of 1g/dL. TACO can occur anytime within six hours of transfusion.
NB The risk of TACO is higher with packed red cells than with FFP or platelets (in contrast to TRALI)
TACO can present with any of the following:
acute respiratory distress
tachycardia
increased blood pressure
acute or worsening pulmonary oedema
Management of TACO is with diuretics and the haematocrit should be measured. In cases where there has been a dramatic elevation in haematocrit, venesection may be required to reduce the risk of a stroke.

18
Q

Blood Transfusion - Cx: Example Question

A

A 75-year-old male presents following a fall whilst intoxicated. He has sustained a fractured right neck of femur and is admitted under the orthopaedic team. He has a past medical history of liver cirrhosis, ischaemic heart disease and congestive cardiac failure. There is a suspicion that he drinks excessively.

On examination, his right leg is externally rotated and shortened. He is thin and has mild pitting oedema to his mid-shins. His pulse is 92 beats per minute and regular, respiratory rate 18 breaths per minute, blood pressure 121/72 mmHg, Sa02 94% on room air. Apart from a slight expiratory wheeze, his chest is clear to auscultation.

Bloods show:

Hb 112 g/l
Platelets 48 * 109/l
WBC 11.2* 109/l
INR 1.9

The orthopaedic team arrange for a transfusion of two units of fresh frozen plasma (FFP) and two units of platelets before taking the patient to theatre.

Four hours after the transfusion the patient has become unwell.
Observations show a respiratory rate of 34 breaths per minute, Sa02 80% on room air. Heart rate is 120 beats per minute and regular. Temperature is 38.5ºC. A chest X-ray is performed at the bedside which shows bilateral shadowing.

What is the most likely cause of the patient’s deterioration?

Community acquired pneumonia
Transfusion associated circulatory overload
Acute myocardial infarction
> Transfusion associated acute lung injury
Atrial fibrillation with a rapid ventricular response

The history is not suggestive of a community-acquired pneumonia so this is unlikely.

Transfusion-associated circulatory overload (TACO) is an increasingly recognised complication of transfusion which can result in significant morbidity and even death. Whilst TACO is an important differential, in this case, the patient’s symptoms start later than would be expected. In addition, the risk of TACO is higher with packed red cells than with FFP or platelets again making this choice less likely.

Again acute myocardial infarction would be a differential to consider but there is no chest pain in the history to suggest this, so this is not the most likely answer here.

Similarly, atrial fibrillation leading to acute left ventricular failure is a differential to consider and an electrocardiogram would be an important investigation but the pulse feels regular in the patient which makes this a less likely diagnosis.

Transfusion-related acute lung injury (TRALI) is the most likely answer in this case.

19
Q

Isolated Pyrexia - Example Question

A

You are called to see a 55-year-old gentleman who is having a blood transfusion for symptomatic anaemia secondary to colon cancer. The nurses have been doing regular observations as documented below.

10am: Baseline observations prior to blood transfusion

Respiratory rate 20 breaths/min
Saturations 96% on air 
Temperature 37.5 ºc
Blood pressure 145/78 mmHg
Heart rate 74 beats/min

10:15 am: repeat observations after 15 mins of transfusion

Respiratory rate 19 breaths/min
Saturations 97% on air
Temperature 38.2 ºc
Blood pressure 150/80 mmHg
Heart rate 72 beats/min

The nurses have already stopped the blood transfusion by the time you arrive to see the patient. On questioning the patient he feels well with no complaints of pain, itch or rashes. On examination his heart sounds are pure and chest is clear. He has no previous documented reactions to blood transfusions although the patient informs you he is allergic to penicillin. What instructions do you give the nurses?

Take blood cultures and commence antibiotics
Dispose of the remaining blood in the bag
> Restart the blood transfusion after giving the patient paracetemol
Take blood cultures, repeat chest x ray and perform urinalysis
Restart the blood transfusion an hour after giving the patient paracetemol

Blood transfusion reaction are common and can be serious. This patient is well and has no clinical evidence of haemodynamic compromise. He has an isolated pyrexia which is likely to be secondary to commencement of the blood transfusion. After confirming this his blood transfusion should be restarted as soon as possible and paracetemol given for symptomatic relief. Disposal of the blood should be considered if a serious adverse reaction occurs. Septic screen and antibiotics should be considered if any underlying infection is suspected. Blood transfusion should be completed within 4 hours and waiting an hour prior to restarting is a waste of valuable time.

20
Q

Blood Products - Example Question

A

A 24 year old man undergoing his second cycle of ABVD (Doxorubicin, Bleomycin, Vinblastine, Dacarbazine) chemotherapy for Hodgkin lymphoma feels tired and short of breath on exertion. His temperature is 36.5°c and he reports no bleeding.

Bloods show:

Hb 69 g/L
WCC 1 x 10^9 /L
Neutrophils 0.7 x 10^9 /L
Platelets 19 x 10^9 /L

What is the most appropriate treatment?

	CMV negative blood
	Phenotyped blood
	> Irradiated blood
	CMV negative and irradiated blood
	Leucodepleted blood

Guidance has recently changed regarding the uses of CMV negative blood. The indications for CMV negative blood are for pregnant patients, intrauterine transfusions and neonates. Indications for irradiated blood include Hodgkin lymphoma, previous purine analogue, stem cell transplant, HLA matched products. Indications for phenotyped blood include sickle cell disease and patients with clinically significant antibodies. All blood products are leucodepleted; this does not have to be requested. Platelets are not required as the patient is afebrile and not bleeding.

21
Q

Indications for CMV negative blood

A

The indications for CMV negative blood are for:

  • pregnant patients
  • intrauterine transfusions
  • neonates.
22
Q

Indications for Irradiated Blood

A

Indications for irradiated blood include:

  • Hodgkin lymphoma
  • previous purine analogue
  • stem cell transplant
  • HLA matched products.
23
Q

Indications for phenotyped blood

A

Indications for phenotyped blood include:

  • sickle cell disease
  • patients with clinically significant antibodies.
24
Q

Leucodepleted Blood

A

All blood products are leucodepleted; this does not have to be requested.

25
Q

Which Immunoglobulin is responsible for Haemolytic Blood transfusions?

A

IgM