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Transfusion medicine

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Transfusion medicine
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Blood Safety: The Right Blood Product to the Right Patient at the Right Time

By Dr Rita Govender, Haematologist

Decision to Transfuse

The clinician must evaluate the risk-benefit ratio for each patient and obtain documented informed consent.
Despite rigorous testing, bedside practices remain a major contributor to adverse events.
- Incorrect patient identification is a leading cause of morbidity in transfusion medicine.

Three Pillars of Blood Safety

1️. Donor Selection

Voluntary, non-remunerated donors complete a detailed questionnaire to screen for:

  • Medical conditions
  • Behavioral risks (e.g. HIV, other infections)
    Donors can self-exclude if needed.

2️.Testing of Donor & Blood Unit

Routine tests include:

  • Serology: Hepatitis B surface antigen, Hepatitis C antibody, HIV 1 & 2 antibodies, Syphilis
  • PCR: HIV, HBV, HCV
    Blood is quarantined until all tests are negative.
    Window period donations still pose a risk.

If a test is positive:

  • Donor is notified, counselled, and deferred.
  • SANBS initiates a look-back programme to trace previous recipients.
    -Since October 2005, no documented HIV transmission due to nucleic acid testing.
3️. Clinician Responsibilities

Before transfusion (if patient is stable):
-Perform clinical & lab evaluations
-Consult a haematologist
-Consider alternatives: haematinics, prohaemostatic agents (e.g. Cyclokapron, DDAVP)
-Explore blood-conserving methods:

  • Acute normovolaemic haemodilution
  • Cell salvage
  • Pre-op autologous donation

If transfusion is necessary:

-Choose correct product
-Obtain informed consent
-Correctly identify patient and label sample at bedside

Bedside Transfusion Protocol

‍‍At least two medical professionals must:

  • Identify the patient
  • Verify unit details (patient info, blood group, expiry)
  • Recheck doctor’s order and previous blood group
  • Inspect unit for leaks, aggregates, discoloration
Transfusion Setup & Monitoring
  • Use strict aseptic technique
  • Regularly inspect cannulation site
  • Monitor vitals: pulse, BP, respiratory rate, temperature
  • Every 15 minutes during transfusion
  • Start slow: 2 ml/min for first 30 mins
  • Red cells: complete within 6 hours
  • Platelets: 15–20 minutes
Adverse Reactions

If symptoms arise (e.g. BP changes, fever, pain, rash):
-Stop transfusion immediately
-Change drip set, maintain vein with saline
-Record vitals, manage symptoms
-Repeat bedside checks
-Contact transfusion service
-Complete legal documentation
-Submit samples: crossmatch, LFTs, cultures, urine, blood unit & set

Key Reminders
  • Use standard recipient set for red cells
  • Use platelet-giving set for platelets
  • Avoid bedside leucodepletion filters on pre-leucodepleted units
  • Microaggregate filters not needed
  • For paediatric cases, request Limited Donor Exposure Programme (LDEP)
  • Use approved blood warmers only when indicated
  • Never add meds/fluids to blood products
  • Only compatible fluids: saline, 4% albumin, plasma protein fractions, ABO-compatible plasma
  • Do not refrigerate platelet products before transfusion
  • Retain empty bags for 48 hours in fridge
References
  • South African standards for blood transfusion
  • Clinical guidelines for blood products in South Africa (4th ed.)
  • Leucocyte depletion guidelines – Blood Transfusion Services of SA
  • SAMJ, May 2006, 96:5
  • The Specialist Forum, April 2002
  • Transfusion, 2004, 44:1S–3S
Useful Websites

🔗 SANBS Official Site
🔗 BCSH Guidelines