Extravascular hemolytic transfusion reaction: Difference between revisions

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(Expand: DHTR mechanism, Kidd/Rh/Duffy antibodies, evaluation, blood bank notification)
 
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==Background==
==Background==
*Occurs days to weeks after transfusion
*Delayed immune-mediated destruction of transfused RBCs by recipient antibodies (IgG)
*Occurs '''2-10 days''' after transfusion (delayed hemolytic transfusion reaction, DHTR)
*Caused by anamnestic antibody response: recipient was previously sensitized (prior transfusion, pregnancy) but antibody titer fell below detection at time of crossmatch
*Hemolysis occurs extravascularly in the spleen, liver, and bone marrow (reticuloendothelial system)
*Most common clinically significant antibodies: Kidd (Jk), Rh, Duffy (Fy), Kell


==Clinical Features==
==Clinical Features==
*[[hemolytic anemia|Hemolysis]] occurs in spleen, liver, and bone marrow
*Often subclinical or mild
*Unexplained drop in hemoglobin or failure of expected post-transfusion hemoglobin rise
*Low-grade [[fever]]
*Mild [[jaundice]] (indirect [[hyperbilirubinemia]])
*Dark urine (less common than in [[intravascular hemolytic transfusion reaction|intravascular hemolysis]])
*Rarely progresses to clinically significant hemolysis


==Differential Diagnosis==
==Differential Diagnosis==
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==Evaluation==
==Evaluation==
*[[Hyperbilirubinemia]]
*Positive direct antiglobulin test (DAT/Coombs)
*Poor response to transfusion
*Elevated indirect bilirubin, LDH
*Decreased haptoglobin
*Positive antibody screen with new alloantibody identified
*Inadequate hemoglobin rise after transfusion
*Reticulocytosis


==Management==
==Management==
*None necessary; rarely fatal
*'''Rarely requires specific treatment''' — usually self-limited
*Notify blood bank immediately for antibody identification
*Future transfusions must be antigen-negative for the identified antibody
*Supportive care; transfuse if clinically indicated (with antigen-negative units)
*Monitor for rare progression to severe hemolysis


==Disposition==
==Disposition==
 
*May not require admission if hemodynamically stable and hemolysis is mild
*Ensure blood bank notification and updated antibody record


==See Also==
==See Also==
{{Transfusion reactions see also}}
{{Transfusion reactions see also}}
==External Links==


==References==
==References==

Latest revision as of 01:43, 21 March 2026

Background

  • Delayed immune-mediated destruction of transfused RBCs by recipient antibodies (IgG)
  • Occurs 2-10 days after transfusion (delayed hemolytic transfusion reaction, DHTR)
  • Caused by anamnestic antibody response: recipient was previously sensitized (prior transfusion, pregnancy) but antibody titer fell below detection at time of crossmatch
  • Hemolysis occurs extravascularly in the spleen, liver, and bone marrow (reticuloendothelial system)
  • Most common clinically significant antibodies: Kidd (Jk), Rh, Duffy (Fy), Kell

Clinical Features

  • Often subclinical or mild
  • Unexplained drop in hemoglobin or failure of expected post-transfusion hemoglobin rise
  • Low-grade fever
  • Mild jaundice (indirect hyperbilirubinemia)
  • Dark urine (less common than in intravascular hemolysis)
  • Rarely progresses to clinically significant hemolysis

Differential Diagnosis

Transfusion Reaction Types

Evaluation

  • Positive direct antiglobulin test (DAT/Coombs)
  • Elevated indirect bilirubin, LDH
  • Decreased haptoglobin
  • Positive antibody screen with new alloantibody identified
  • Inadequate hemoglobin rise after transfusion
  • Reticulocytosis

Management

  • Rarely requires specific treatment — usually self-limited
  • Notify blood bank immediately for antibody identification
  • Future transfusions must be antigen-negative for the identified antibody
  • Supportive care; transfuse if clinically indicated (with antigen-negative units)
  • Monitor for rare progression to severe hemolysis

Disposition

  • May not require admission if hemodynamically stable and hemolysis is mild
  • Ensure blood bank notification and updated antibody record

See Also

References