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BY: DR.HASEEB TARIQ
 Blood transfusion is a life
saving procedure and is of
immense importance.
 Sometimes due to different
factors a reaction can
occur which can have
adverse effect on the
patient.
 The objective of this
presentation is to know
different types of
transfusion reactions and
learn their management.
 IMMUNE MEDIATED
 NON-IMMUNE MEDIATED
IMMUNE MEDIATED REACTIONS:
 Febrile non-hemolytic
 Acute hemolytic
 Delayed hemolytic
 Anaphylactic
 GVHD
 Transfusion associated lung injury (TRALI)
 Urticarial transfusion reaction
NON-IMMUNNE MEDIATED:
 Heat/Cold associated injury
 Infections
 Acute hypotensive reaction
 Osmotic injury
 Chemical injury
 Stop the transfusion immediately
 Check & Monitor vitals
 Maintain IV access
 Notify Lab for error
 Check right pack has been transfused
 Obtain CBC report & CXR post-reaction
 Most common
 Occurs during or in 24hrs of transfusion
 Caused by Ab. against donor HLA antigens &
leucocytes
 DIAGNOSIS OF EXCLUSION: Fever may be the
only symptom and may show a delayed
reaction!!
SYMPTOMS:
 FEVER
 DYSPNOEA
Consider and exclude other causes, as fever
alone may be the first manifestation of a life
threatening reaction.
INVESTIGATIONS:
 Clinically assess for Rigors & Chills
 Repeat ABO compatibility
 Exclude hemolytic reaction
 Investigate for sepsis
 Treat the fever with an antipyretic.
 Avoid aspirin in thrombocytopenic and
paediatric patients.
 Follow general management for the reaction.
 Medical Emergency!!
 Transfused red cells are destroyed, due to
incompatibility of antigen on transfused cells
with antibody in the recipient circulation.
 Occurs in 24 hrs of transfusion or during
transfusion.
 Mostly caused due to human error.
Signs & Symptoms:
 Haemolysis
 Haemoglobinuria
 Back pain
 Fever
 ARF
 DIC
INVESTIGATIONS:
 Clinically assess patient
 Check clerical records for error
 DAT, IAT
 RFTs, Serum.Haptoglobulin
 Repeat ABO and screening
MANAGEMENT:
 Stop transfusion immediately and follow
other steps for managing suspected
transfusion reactions.
 Seek urgent medical assistance.
 Maintain blood pressure and renal output.
 Induce diuresis with intravenous fluids and
diuretics.
 This may become a medical emergency so
support blood pressure and maintain an open
airway.
 Do not administer additional blood packs
until cleared by haematologist or Transfusion
Service Provider.
 Generally occurs 2-10 days after transfusion.
 One way this can occur is if a person without
a Kidd blood antigen receives a Kidd antigen
in a transfusion.
 DEFINITION:It is defined as fever and other
symptoms/ signs of hemolysis more than 24
hours after transfusion.
CRITERIA:
 Fall in Hb or failure to rise post-transfusion.
 Rise in billrubin (jaundice)
 In-compatible crossmatch not pre detectable.
 Can occur upto 4 weeks after transfusion.
CLINICAL PICTURE:
 Falling Hb
 Hyprbillirubinemia
 Spherocytes on peripheral smear
 Low grade fever
 Extremely Rare.
 Occurs in Immunocompromised
individuals with identical HLA haplotypes.
 Donor lymphocytes are engrafted by the
recipient which attack the recipient’s
tissues considering them foreign.
 TA-GvHD can develop four to thirty days
after the transfusion.
 Bone marrow Aplasia is common cause of
death.
CLINICAL PRESENTATION:
Skin: Erythroderma, Swollen, Bullae
formation(most common)
GIT: Diarrhoea, Abdominal cramps
LIVER: Elevated LFTs, Hyperbillirubinemia
HEME: Bone marrow aplasia, Thrombocytopenia
persistent
Only supportive treatment is given in GVHD. It
can be prevented by giving Gamma-irradiated
blood to those at risk.
 Occurs during or 6hrs after transfusion.
 Can cause ARDS
 Can cause Non-Cardiogenic Pulmonary
edema
 It is explained by 2-Hit hypothesis
 All bllood products can cause it
2-HIT HYPOTHESIS:
 1st hit is pulmonary pathology causing
localisation of neutrophils
 2nd hit is transfusion of blood products with
sensitized neutrophils
CLINICAL PRESENTATION:
 Hypoxemia (acute respiratory distress)
 Fever
 Tachycardia
 Tachypnoea
 CXR shows bilateral pulmonary infiltrates with
normal cardiac size.
CRITERIA OF DIAGNOSIS:
 No acute injury prior to transfusion
 No relation to risk factor for lung injury
 Bilateral pulmonary infiltrates on CXR
 No circulatory overload, PA
pressure<18mmhg
 Oxygen saturation<90%
MANAGEMENT:
 Follow General Guidelines
 Supportive therapy
 Diurectics has no role and can worsen the
condition
 Majority of patients may require mechanical
ventilation
 Notify Blood Bank for the error
Blood transfusion reactions

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Blood transfusion reactions

  • 1.
  • 3.  Blood transfusion is a life saving procedure and is of immense importance.  Sometimes due to different factors a reaction can occur which can have adverse effect on the patient.  The objective of this presentation is to know different types of transfusion reactions and learn their management.
  • 4.  IMMUNE MEDIATED  NON-IMMUNE MEDIATED IMMUNE MEDIATED REACTIONS:  Febrile non-hemolytic  Acute hemolytic  Delayed hemolytic  Anaphylactic  GVHD  Transfusion associated lung injury (TRALI)  Urticarial transfusion reaction
  • 5. NON-IMMUNNE MEDIATED:  Heat/Cold associated injury  Infections  Acute hypotensive reaction  Osmotic injury  Chemical injury
  • 6.
  • 7.  Stop the transfusion immediately  Check & Monitor vitals  Maintain IV access  Notify Lab for error  Check right pack has been transfused  Obtain CBC report & CXR post-reaction
  • 8.  Most common  Occurs during or in 24hrs of transfusion  Caused by Ab. against donor HLA antigens & leucocytes  DIAGNOSIS OF EXCLUSION: Fever may be the only symptom and may show a delayed reaction!!
  • 9. SYMPTOMS:  FEVER  DYSPNOEA Consider and exclude other causes, as fever alone may be the first manifestation of a life threatening reaction. INVESTIGATIONS:  Clinically assess for Rigors & Chills  Repeat ABO compatibility  Exclude hemolytic reaction  Investigate for sepsis
  • 10.  Treat the fever with an antipyretic.  Avoid aspirin in thrombocytopenic and paediatric patients.  Follow general management for the reaction.
  • 11.  Medical Emergency!!  Transfused red cells are destroyed, due to incompatibility of antigen on transfused cells with antibody in the recipient circulation.  Occurs in 24 hrs of transfusion or during transfusion.  Mostly caused due to human error.
  • 12. Signs & Symptoms:  Haemolysis  Haemoglobinuria  Back pain  Fever  ARF  DIC INVESTIGATIONS:  Clinically assess patient  Check clerical records for error  DAT, IAT  RFTs, Serum.Haptoglobulin  Repeat ABO and screening
  • 13. MANAGEMENT:  Stop transfusion immediately and follow other steps for managing suspected transfusion reactions.  Seek urgent medical assistance.  Maintain blood pressure and renal output.  Induce diuresis with intravenous fluids and diuretics.  This may become a medical emergency so support blood pressure and maintain an open airway.  Do not administer additional blood packs until cleared by haematologist or Transfusion Service Provider.
  • 14.  Generally occurs 2-10 days after transfusion.  One way this can occur is if a person without a Kidd blood antigen receives a Kidd antigen in a transfusion.  DEFINITION:It is defined as fever and other symptoms/ signs of hemolysis more than 24 hours after transfusion.
  • 15. CRITERIA:  Fall in Hb or failure to rise post-transfusion.  Rise in billrubin (jaundice)  In-compatible crossmatch not pre detectable.  Can occur upto 4 weeks after transfusion. CLINICAL PICTURE:  Falling Hb  Hyprbillirubinemia  Spherocytes on peripheral smear  Low grade fever
  • 16.  Extremely Rare.  Occurs in Immunocompromised individuals with identical HLA haplotypes.  Donor lymphocytes are engrafted by the recipient which attack the recipient’s tissues considering them foreign.  TA-GvHD can develop four to thirty days after the transfusion.  Bone marrow Aplasia is common cause of death.
  • 17. CLINICAL PRESENTATION: Skin: Erythroderma, Swollen, Bullae formation(most common) GIT: Diarrhoea, Abdominal cramps LIVER: Elevated LFTs, Hyperbillirubinemia HEME: Bone marrow aplasia, Thrombocytopenia persistent Only supportive treatment is given in GVHD. It can be prevented by giving Gamma-irradiated blood to those at risk.
  • 18.  Occurs during or 6hrs after transfusion.  Can cause ARDS  Can cause Non-Cardiogenic Pulmonary edema  It is explained by 2-Hit hypothesis  All bllood products can cause it
  • 19.
  • 20. 2-HIT HYPOTHESIS:  1st hit is pulmonary pathology causing localisation of neutrophils  2nd hit is transfusion of blood products with sensitized neutrophils CLINICAL PRESENTATION:  Hypoxemia (acute respiratory distress)  Fever  Tachycardia  Tachypnoea
  • 21.  CXR shows bilateral pulmonary infiltrates with normal cardiac size. CRITERIA OF DIAGNOSIS:  No acute injury prior to transfusion  No relation to risk factor for lung injury  Bilateral pulmonary infiltrates on CXR  No circulatory overload, PA pressure<18mmhg  Oxygen saturation<90%
  • 22.
  • 23. MANAGEMENT:  Follow General Guidelines  Supportive therapy  Diurectics has no role and can worsen the condition  Majority of patients may require mechanical ventilation  Notify Blood Bank for the error

Editor's Notes

  1. No treatment is given in absence of rapid hemolysis. Avoid offending agent in future.
  2. Diagnosis is made on skin biopsy and occasionally on liver & bone marrow biopsy.
  3. Immunocompromised, those receiving blood from family, leucoreduction filters can prevent but are not documented.
  4. Use of male plasma has been shown to reduce the risk of TRALI as females contain more anti-HLA & anti-neutrophil antibodies.