TGO2 May 2025 Flashcards
(41 cards)
Compassion
- Kindness
- Empathy
- Sympathy
- Concern
Help others without judgement or expectation
Excellence
- Dependable
- Accurate
Exceed client’s expectation
Accountable
- Reliable (do what we say we’ll do)
Work efficiently individually to work towards shared goals
Respect
- Polite
- Careful
Accept and embrace our differences
Integrity
- Consistent
- Honest
Own your mistakes and successes
Transfusion Reaction: Fever
- Acute haemolytic (ABO incompatible)
- Bacterial contamination
- Febrile non-haemolytic (cytokine release from donor WBC)
- TRALI
Transfusion Reaction: Short of Breath
- Anaphylaxis
- Bacterial contamination
- TACO
- TRALI
- Acute haemolytic transfusion reaction
Transfusion Reaction: Rash/Itch
- Minor allergic reaction
- Anaphylaxis
Transfusion Reaction: Hypotension
- Bacterial Contamination
- Acute haemolytic transfusion reaction
- Anaphylaxis
Transfusion Reaction: Hypertension
- Circulatory Overload
Transfusion Reaction: Tachycardia
- Bacterial Contamination
Not all antibodies can be excluded on a complex ABID. How would you provide blood for that patient?
- Phenotype the units as negative for the antigens unable to be excluded
- In conjunction with senior scientist/haematologist, explore provision “most suitable” phenotyped blood
A patient has a complex ABID and ARCBS can’t find pheno matched units. How would you provide blood for them?
- See if we have blood suitable for them at other sites, including private pathology providers
- See if there are any units assigned to other patients who may be able to share for the time being
- With senior scientist/haematologist approval, drop phenotype requirements to see if we can find blood that may be incompatible and issue least reactive.
Screen + panel = positive, but they are few, weak reactions. How would you continue?
Consider changing the phase to enhance reactivity (enzyme enhancement, PEG, room temperature)
Could also be an HLA reactor; if all clinically significant antibodies are excluded refer to senior scientist.
Screen + panel = non-specific panagglutination. How would you continue?
- Warm auto
* DAT would be up, Elution would show panagglutination, adsorb to ensure no underlying alloantibodies - Additive
* Change phase; glass for gel card, no potentiator (NISS), change cells or wash and resuspend with a neutral red cell diluent - Drug interference (mAb)
* Test with DTT treated cells, check with nurse for clinical information - Multiple antibodies
* Consider differentiation with different testing phases (RT, Enz) - High incidence antibodies
* Try to find negative red cells for testing, or consider neutralisation or adsorption if the protocol is supported
A patient has a history of [RhK, Fy, Jk, Ss] antibody. Do you need to serologically crossmatch?
Yes, whether reactive or not. Also phenotype the unit as negative.
A patient has a history of [M, N, Lea, Leb, P1]. Do you need to serologically crossmatch?
Only if currently reactive.
Provision of Rx- typed units is best practice, but random units are fine.
A patient has a history of a low incidence antigen [Cob, Kpa, Lua, Wra, Cw]. Do you need to serologically crossmatch?
Yes.
A patient has a history of A1 antibody. Do you need to serologically crossmatch?
Only if currently reactive at 37*C.
A patient has a history of HTLA antibodies. Do you need to serologically crossmatch?
Yes. Phenotype matched if currently reactive.
A patient has a history of anti-HI. Do you need to serologically crossmatch?
Only if its currently reactive. Technically only if A1 or A1B but I would probably err on the side of caution if its not urgent and serocrossmatch for A2 and B.
What blood group do you select for a patient with anti-A1 antibodies reactive at 37*C?
Group O can be given to everyone.
Group A2 can be given to A/AB patients.
Group B can be given to AB patients.
What’s the difference between a Quality Control program and a Quality Assurance program.
QC = TER
T echniques,
E quipment,
R eagents are in working order.
QA = accuracy
T echniques,
E quipment and
K nowledge is sufficient to ensure accurate results.
How do you ensure attention to detail?
- Only work on one specimen at a time.
- If interrupted, start again.
- Ensure QC is read first ahead of patients (e.g. phenotyping)
- Do not trust your memory. Write down every well/test tube is read.