Blood Products and Transfusion Flashcards

1
Q

What are the implications of having Anti-D Antibodies?

A

RhD negative patient must ONLY receive RhD neg blood 🡪 else risks developing Anti-RhD Ab

Otherwise, causes delayed haemolytic transfusion reaction (~5-10 days post-transfusion) where anti-D antibodies latch on to the D positive blood cells transfused which are then recognised & removed in the spleen

Anaemia; high bilirubin from breakdown; jaundice; free haemoglobin released can damage kidneys – renal failure etc.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

How does haemolytic disease of the newborn present?

A

If Severe: Fetus anaemic 🡪 heart beats faster to compensate 🡪 overwhelmed 🡪 fluid backlogs 🡪 Hydrops Fetalis and Death

If Less Severe

  • After birth: Bilirubin rises (no more placenta to remove, only immature liver which cannot cope) 🡪 neonatal jaundice 🡪 brain damage (kernicterus), hyperextended arms +legs + neck, v often fatal
  • Kernicterus = BR Encephalopathy (BR is neurotoxic if concentration is too high)
  • Neonates are most susceptible to Kernicterus
  • Neonates are v susceptible to HyperBR due to time required for hepatic enzymes to upregulate and cope with BR after birth
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is the prophylaxis against maternal sensitisation of Rh-D?

A

Give anti-D Ig at delivery if baby is RhD positive, or for ‘events’ during pregnancy where fetal-maternal haemorrhage is likely to occur (where there is risk of fetal blood entering into maternal circulation)

Works by coating fetal red cells and removing them in mother’s spleen before sensitization can occur.

Must give IM anti-RhD within 72 hours of ‘event’ where fetal-maternal haemorrhage occurs.

Routine Antenatal Anti-D prophylaxis can be given in the third trimester for RhD negative mothers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are the antibodies against infections tested for in pre- transfusion testing?

A

Mandatory in SG:

  • Hepatitis B: HbsAg
  • Hepatitis C: anti-HCV, PCR
  • HIV: anti-HIV 1 & 2, PCR
  • Syphilis: TPPA
  • Malaria
  • Zika

Discretionary: examples include

  • HTLV: anti-HTLV (not tested in BSG Singapore)
  • CMV (can be dangerous in immunosuppressed patients) however no point testing, as most people will be CMV +ve by adulthood
  • Prion disease – vCJD
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the indications for plasma transfusion?

A

If bleeding + abnormal coagulation test results (PT prothrombin time, APTT activated partial thromboplastin time) e.g. liver disease with bleeding/going for invasive procedure

Reversal of warfarin (anticoagulant) e.g. for urgent surgery

  • Prothrombin Complex Concentrate (PCC; contains factors 2, 7, 9, 10 which warfarin acts against) preferred: smaller volume, patients tolerate it better, acts more quickly
  • As well as give VITAMIN K 10mg Infusion on top of PCC

Other conditions occasionally: massive bleeding, disseminated intravascular coagulation

FFP not just to replace volume/ fluid loss – simple non-human products can be used (eg: recombinant F7)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are the indications for cryoprecipitate?

A

If massive bleeding & fibrinogen very low (there is fibrinogen in FFP, but more concentrated in cryoprecipitate)

  • Eg: DIC patients
  • Low fibrinogen is MAIN indicator for using cryoprecipitate

Rarely hypofibrinogenaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is platelet refractoriness?

A

Occurs in pt with severe chronic thrombocytopenia who need many repeated transfusions. Eventually, we will see that the rise in platelet count after each

This is because platelets are given together with WBCs (as part of the buffy coat)

All nucleated cells (platelets and WCC) present HLA Ag. (RBC are anucleate and does not possess HLA).

However, WCC has much MORE HLA than platelets as platelets are merely cell fragments 🡪 will stimulate Anti-HLA Ab production more strongly, which will eventually wipe out Leucocytes and Platelets.

Hence in pt with severe thrombocytopenia that necessitates many transfusions will get leuco-reduced platelets (and leuco-depleted RBC if necessary)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are the 3 indications for leukoreduction?

A

1) To reduce risk of FNHTR
- the most common cause of transfusion related fever
- eg: if patient on fever presents with fever + no other symptoms 🡪 and we have determined it is a FNHTR 🡪 we will proceed by giving leuco-depleted blood/platelets instead

2) To reduce risk of CMV infection (esp if recipient is immunosuppressed and is CMV-ve)
3) To reduce platelet refractoriness

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are the indications for albumin transfusion?

A

4.5%: useful in burns (loss of fluid and plasma proteins due to loss of skin coverage), plasma exchanges. Not indicated in malnutrition

20%: For certain severe liver + kidney conditions (e.g. nephrotic syndrome)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are the indications for clotting factors concentrates?

A

Factor 8 and 9: for Haemophilia A and B respectively

Factor 8 for Von Willebrand’s disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the immediate Adverse Reactions to Transfusions (<24 hours)?

A

Immune

  • Acute Haemolytic Transfusn Rxn: possible DIC!
  • Febrile non-haemolytic reaction (isolated fever) due to WBC in platelet transfusions
  • Allergy (most commonly Urticaria)
  • Anaphylaxis
  • TRALI (transfusion related acute lung injury)

Non immune

  • Bacterial Contamination
  • Transfusion associated cardiac overload
  • Air embolism
  • Massive transfusion: hypothermia, hyperkalemia, hypocalcemia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What are the delayed Adverse Reactions to Transfusions (<24 hours)?

A

Immune
- Delayed haemolytic transfusion reaction (jaundice, renal failure, anaemia)

Non immune

  • Viral infections (hep B, C, etc.)
  • Iron overload (in chronic, multiple transfusions)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

[ACUTE HAEMOLYTIC TRANSFUSION REACTION (WRONG BLOOD)]

What are the early signs?

A
  • Fever, Chills, N&V, Flushing
  • Chest / Loin / Back Pain
  • Pain along infusion vein (occurs rapidly, hence pain upon infusion)
  • Haematuria – red urine (due to Hb release 🡪 ATN)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

[ACUTE HAEMOLYTIC TRANSFUSION REACTION (WRONG BLOOD)]

What are the late signs?

A

Hypotension – can even lead to DIC ☹

Hemoglobinuria

Jaundice MAY occur – however since occurs at the start 🡪 may not have sufficiently high BR to cause jaundice

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

[ACUTE HAEMOLYTIC TRANSFUSION REACTION (WRONG BLOOD)]

What are the relevant investigations?

A

Haemolysis panel: Br, Haptoglobin, Hemopexin, LDH

Assess organ involvement: Renal Panel, K, Ca, Pi, Mg

Confirm AHTR: Direct Coomb’s Test, Check pt identifiers, perform GXM once again

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

[ACUTE HAEMOLYTIC TRANSFUSION REACTION (WRONG BLOOD)]

What is the management?

A

While waiting for above result to arrive, provide supportive therapy + saline resuscitation

17
Q

[Allergy during transfusion? ] what is the management?

A

If only urticaria with no other symptoms and signs (aka no anaphylaxis)

  • Stop the transfusion
  • Antihistamines
  • Restart the unit slowly

If urticaria is associated with extensive rash, swelling etc
- Stop the transfusion

DO NOT restart transfusion in any other transfusion reactions EXCEPT isolated urticaria

18
Q

What are the signs and symptoms of anaphylaxis?

A

CV – hypotension, shock

Respi – cough, dyspnoea, wheeze

Mucocutaneous – Generalised urticaria, angioedema

GIT – N&V, Diarrhoea, Abdominal Pain

19
Q

What is the management of anaphylaxis?

A
  • IV Hydrocortisone + H1 & H2 Antihistamines (Diphenhydramine & Ranitidine etc)
  • If shock 🡪 IM Adrenaline 0.5ml of 1:1000 dilution 🡪 making up to 0.5mg
  • Stop blood, start plain IV fluids (resuscitate circulatory collapse)
  • Avoid further transfusion
20
Q

What are the relevant investigations for anaphylaxis?

A
  • Test IgA Levels

- IgA deficient blood products may need to be selected next time (e.g. used washed blood) if patient is IgA Deficient

21
Q

[FEBRILE NON-HAEMOLYTIC TRANFUSION REACTION]

In what groups of patient is febrile non haemolytic transfusion reacton more common in?

A

More common with Platelet Transfusion (since platelets are transfused together with WBC)

More prevalent in female patients who have been previously pregnant and patients who have previously received transfusion

22
Q

[FEBRILE NON-HAEMOLYTIC TRANFUSION REACTION]

What is the management?

A

Just transfuse more slowly + give anti-pyretic

Can opt to use leuco-reduced blood products to reduce risk of FNHTR

23
Q

What are the clinical features of TRALI?

A
  • fever
  • hypotension
  • acute dyspnea
  • JVP unchanged
  • auscultation: rales
  • X ray: diffuse bilateral infiltrates
  • Ejection fraction: normal
  • Pulmonary oedema: fluid exudate
  • Response to diuretic: minimal
24
Q

What are the clinical features of TACO?

A
  • no fever
  • hypertension
  • acute dyspnea
  • JVP can be changed
  • auscultation: rales + S3
  • X ray: diffuse bilateral infiltrates
  • Ejection fraction decreased
  • pulmonary edema fluid: transudate
  • response to diuretic: significant improvement?
25
Q

What is the management of TRALI?

A

If suspected TRALI 🡪 may need ventilation (can be fatal)

May need to contact blood bank to remove the original donor from donor pool!

26
Q

How do you prevent TRALI?

A

Reduce plasma from female donors

  • Most FFP is male donor
  • If platelets pooled from 4 donors, plasma they are re-suspended in is from a male donor

Virally inactivated FFP (pooled, solvent detergent treated) does not cause TRALI

Stop unnecessary use. Use Vitamin K or PCC for reversing warfarin

27
Q

What is the management for bacterial infection?

A

Discontinue transfusion with supportive treatment plus IV broad spectrum antibiotics

Send blood pack(s) to transfusion lab - for culture

Take blood cultures from patient

28
Q

How is bacterial contamination of blood prevented?

A

Donor questioning (exclude if ill) + arm cleaning (alcohol/iodine)

Store always in controlled 4 ̊C fridge - if out for >1⁄2 hour, cannot put back in: wasted

Complete transfusion of blood within 5h of leaving fridge i.e. give over 4hrs max

Look for abnormalities of blood or components e.g.: clumps of discolored debris; brown plasma etc.

29
Q

How does delayed haemolytic transfusion reaction occur?

A

Occurs in Non-ABO Ag -ve patient who has previously been SENSITIZED to the Ag (via prev blood transfusion / pregnancy) 🡪 has developed Anti-Ag Ab

  • Eg: Kell, Duffy, Kidd, RhD
  • The sensitisation dose does NOT lead to DHTR

However occasionally, Ab levels are very low 🡪 hence negative pre-transfusion test 🡪 erroneously given Ag +ve blood

Reaction happens after days – weeks

30
Q

What are the signs and symptoms of delayed haemolytic transfusion?

A

Usually mild: causing Fever, Jaundice, Anemia (and ↓Haptoglobin, ↑BR, ↑LDH), Increased reticulocytes

If severe: Haemaglobinuria, Haematuria (due to ATN from Hb released), Renal Failure