Transfusion associated microchimerism: a heretofore little-recognized complication following transfusion

J Thromb Thrombolysis. 2009 Jan;27(1):57-67. doi: 10.1007/s11239-008-0268-0. Epub 2008 Sep 3.

Abstract

Potent antiplatelet and antithrombotic agents have significantly reduced mortality in the setting of acute coronary syndromes and percutaneous coronary intervention. However these agents are associated with increased bleeding which is in turn associated with adverse clinical outcomes. In many centers, transfusion is often used to correct for blood loss. Blood transfusion in the setting of acute coronary syndrome has been associated with adverse clinical outcomes including increased mortality. Transfusion associated microchimerism (TA-MC) is a newly recognized complication of blood transfusion. There is engraftment of the donor's hematopoietic stem cells in patients who then develop microchimerism. This article discusses the association of bleeding/blood transfusion with adverse outcomes and the potential role of TA-MC in clinical outcomes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Acute Coronary Syndrome / blood
  • Acute Coronary Syndrome / drug therapy
  • Acute Coronary Syndrome / mortality
  • Acute Coronary Syndrome / therapy
  • Anemia / epidemiology
  • Anemia / etiology
  • Anemia / physiopathology
  • Anemia / therapy
  • Angioplasty, Balloon, Coronary / adverse effects
  • Blood Preservation
  • Blood Transfusion / statistics & numerical data
  • Cell Survival
  • Chimerism*
  • Clinical Trials as Topic / statistics & numerical data
  • Cytokines / metabolism
  • Female
  • Fetomaternal Transfusion
  • Fibrinolytic Agents / adverse effects
  • Fibrinolytic Agents / therapeutic use
  • Hemorrhage / chemically induced
  • Hemorrhage / epidemiology
  • Hemorrhage / etiology
  • Hemorrhage / physiopathology
  • Humans
  • Incidence
  • Leukocytes / cytology
  • Leukocytes / immunology
  • Platelet Aggregation Inhibitors / adverse effects
  • Platelet Aggregation Inhibitors / therapeutic use
  • Pregnancy
  • Transfusion Reaction*
  • Treatment Outcome

Substances

  • Cytokines
  • Fibrinolytic Agents
  • Platelet Aggregation Inhibitors