PERI - Blood Transfusion Flashcards

1
Q

5 features of haemolytic disease of the newborn (HDN)

Rhesus Blood Groups
Sensitization Phase
Effector Phase
Treatment
Clinical Features x2

A

1.) Rhesus Blood Groups - D antigen is most important
- Rh+ = D antigens present, Rh- = D antigens absent
- D antibodies are produced when Rh- mothers are exposed to D antigens during pregnancy

2.) Sensitization Phase - pregnancy w/ 1st Rh+ fetus
- occurs if Rh antigens from the fetus enters the mother’s circulation during delivery/miscarriage etc.
- mother produces anti-Rh+ antibodies (IgG)

3.) Effector Phase - pregnancy w/ 2nd Rh+ fetus
- anti-Rh+ antibodies cross the placenta in T3, damaging the fetal RBCs causing haemolytic anaemia in newborn

4.) Treatment - RhoGAM (antibodies for Rh antigens)
- binds to Rh antigens in the newborn, so the mother doesn’t become sensitized (not exposed to Rh antigens)
- it is given to unsensitized Rh- women within 3 days after miscarriage or delivery of an Rh+ fetus

5.) Clinical Features
- ↑bilirubin leads to jaundice
- bilirubin can enter the the brain to cause kernicterus which can cause permanent neurological damage

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2
Q

4 features of the ABO system and haemolytic transfusion reactions

ABO Blood Groups
Type of Antibody
Donors and Receipients
Haemolytic Transfusion Reaction

A

1.) ABO Blood Groups - antigens on RBCs
- A has B antibodies whilst B has A antibodies
- AB has no antibodies, O has A and B antibodies

2.) Type of Antibody - usually all IgM
- IgM cannot cross the placenta so mixture of antigens does not cause haemolytic disease in the newborn
- IgG can be produced during a blood transfusion

3.) Donors and Recipients
- A receives A, B receives B, preventing RBC damage
- Rh- women only receive Rh- blood to prevent sensitisation
- AB+ is a universal acceptor as it can receive A, B or rhesus -ve since it has no antibodies in its circulation
- O- is a universal donor since it has no A, B or rhesus antigens so no immune reaction would occur

4.) Haemolytic Transfusion Reaction - life-threatening
- cardiovascular shock/collapse, kidney failure

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3
Q

Blood Tests

Group and Save
Crossmatch

A

1.) Group and Save
- determines the patient’s blood group (ABO and RhD)
- screens the blood for any atypical antibodies
- takes roughly 40mins and no blood is issued
- recommended if blood loss is not anticipated

2.) Crossmatch - mixes patient’s blood with donor blood to check compatibility for transfusion
- also takes 40mins in addition to G/S
- done if blood loss is anticipated and emergency situation where blood is needed straight away

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4
Q

Blood Products

Requesting Blood Products
Administering Blood Products
Irradiated Blood Products
Cytomegalovirus (CMV)

A

1.) Requesting Blood Products - procedures in place to prevent patient being given incorrect blood
- 3 points of identification e.g. name, DOB, patient no.
- label bottle and complete request form at bedside
- consent patient appropriately

2.) Administering Blood Products
- Hb <70g/L w/out bleeding or ACS need transfusion
- each unit must be prescribed individually, must reassess the patient after each unit
- rate of infusion should be 3-4 hours (from the blood leaves storage)
- observations taken before and after transfusion (15-20mins, 1hr, completion)
- only given in green or grey cannulas

3.) Irradiated Blood Products - required to reduce graft-versus-host disease in at risk populations (Immunocompromised):
- receiving blood from 1st/2nd degree family members
- intra-uterine transfusions, Hodgkin’s lymphoma
- haematopoetic stem cell (HSC) transplants, after
anti-thymocyte globulin or alemtuzumab therapy
- those receiving purine analogues as chemotherapy

4.) Cytomegalovirus (CMV) - common congenital infection causing deafness and cerebral palsy
- CMV negative blood should be given to pregnant women, intra-uterine transfusions, and neonates (up to 28days)

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5
Q

Types of Blood Products

Packed Red Cells
Platelets
Fresh Frozen Plasma (FFP)
Cryoprecipitate

A

1.) Packed Red Cells - contains RBCs
- indications: acute blood loss, chronic anaemia (<70 or <80 ACS) or symptomatic anaemia
- 1 unit increases Hb by 10g/L
- given over 2-4hrs, must be completed within 4 hrs
- new G/S is needed before future transfusions

2.) Platelets - contains platelets
- indications: thrombocytopenia (<20), bleeding w/ thrombocytopenia, haemorrhagic shock in trauma, pre-operative platelet level <50
- 1 dose ↑plt levels by 20-40, given over 30mins

3.) Fresh Frozen Plasma (FFP) - contains clotting factors
- indications: DIC, massive haemorrhage, haemorrhage secondary to liver disease
- given over 30mins
- universal donor for FFP is AB (O for RBCs)

4.) Cryoprecipitate - contains fibrinogen, vWF, factor VIII, fibronectin
- indications: DIC w/ low fibrinogen (<1), vWF disease, massive haemorrhage
- given stat (all at once)

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6
Q

General Complications of Blood Transfusions

Clotting Abnormalities
Electrolyte Abnormalities x2
Hypothermia

A

1.) Clotting Abnormalities - due to dilution effect
- packed red cells have no platelets or clotting factors
- FFP and platelets should be given to patients receiving more than 4 units of RBCs

2.) Electrolyte Abnormalities
- hypocalcaemia: chelation of Ca by calcium-binding agent in preservative –> ↓Ca2+
- hyperkalaemia: inevitable partial haemolysis of RBCs causing the release of intracellular potassium

3.) Hypothermia - drop in core body temperature
- blood products thawed from frozen and kept at cool temperatures so still cold by time of transfusion

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7
Q

Acute Transfusion Specific Complications

Acute Haemolytic Reaction
Transfusion Associated Circulatory Overload (TACO)
Transfusion Related Acute Lung Injury (TRALI)
Non-Haemolytic Febrile and Allergic Reactions
Others

A

1.) Acute Haemolytic Reaction - ABO incompatibility causing RBC destruction by IgM antibodies
- sx starts mins after transfusion: fever, urticaria, abdo and chest pain, hypotension, haematuria
- Ix: DAT/Coombs (definitive), repeat crossmatch, FBC (↓Hb), ↓haptoglobin, ↑bilirubin, ↑LDH
- Mx: stop transfusion, IV fluid resus, inform blood bank, and O2, seek specialist advice
- complications: DIC, renal failure

2.) Transfusion Associated Circulatory Overload
- sx: SOB, hypertension, afebrile, ↑JVP, S3 present
- urgent CXR, treat w/ O2 and IV furosemide
- common in those already overloaded e.g. HF, can be prescribed 20mg furosemide prophylactically

3.) Transfusion-Related Acute Lung Injury - a form of ARDS, a non-cardiogenic cause of pulmonary oedema
- antibodies against alveolar macrophages
- sx: SOB, fever, hypotension, normal JVP
- Mx: stop transfusion, urgent CXR (diffuse bilateral infiltrates), high flow O2, specialist input
- need to differentiate from TACO

4.) Non-Haemolytic Febrile and Allergic Reactions
- febrile reaction: fever or chills, slow/stop the transfusion and give paracetamol
- mild allergic reaction: itching/urticaria, temporarily stop the transfusion and treat w/ anti-histamines

5.) Others - anaphylaxis and sepsis
- anaphylaxis: stop transfusion and treat accordingly, more likely in IgA deficiency w/ anti-IgA antibodies
- septic shock: stop transfusion and treat accordingly

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8
Q

Delayed Transfusion Complications

Infection
Graft vs Host Disease (GvHD)
Iron Overload

A

1.) Infection - theoretical risk with any transfusion
- HepB/C, HIV, syphilis, malaria, vCJD
- uncommon due to screening of blood donors

2.) Graft vs Host Disease - rare but often fatal
- T lymphocytes in transfused blood attacks the host due to HLA mismatch between donor and recipient
- common in transfusion of non-irradiated blood products to an immunocompromised recipient
- can occur weeks after a transfusion
- symptoms: culture-negative fever, painful maculopapular rash, persistent N+V, watery/bloody diarrhoea, jaundice

3.) Iron Overload - repeated transfusions, affects
- multiple organs: liver (cirrhosis), pancreas (diabetes), heart (cardiomegaly), joint pain, skin(hyperpigmentation)

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