Pathophysiology of TRALI: current concepts
Transfusion-related acute lung injury (TRALI) is a life-threatening adverse event in blood transfusion and is considered the most common cause of transfusion-related fatalities in the United States and the United Kingdom. TRALI and acute respiratory distress syndrome (ARDS) share a common clinical d...
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Veröffentlicht in: | Intensive care medicine 2007-06, Vol.33 Suppl 1 (S1), p.S3-S11 |
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description | Transfusion-related acute lung injury (TRALI) is a life-threatening adverse event in blood transfusion and is considered the most common cause of transfusion-related fatalities in the United States and the United Kingdom. TRALI and acute respiratory distress syndrome (ARDS) share a common clinical definition except that TRALI is temporally and mechanistically related to blood transfusion. Two different mechanisms have been proposed. The first is leuko-agglutination due to infusion of leukocyte Antibodies with the blood product transfused. The second proposes a two-event model where the first event is the clinical condition of the patient, and the second the infusion of lipids that accumulate in blood products during storage. An emerging common pathway of granulocyte activation is discussed, as is the relevance of immune and non-immune TRALI from a practical point of view. Some unresolved questions in TRALI pathophysiology, including the relevance of Antibodies to HLA class-II antigens and the participation of the endothelium, are examined, as are the suggested preventive measures for both immune and non-immune TRALI. It is concluded that further clinical and experimental data are necessary before any recommendations can be made regarding non-immune TRALI. In contrast, in immune TRALI, preventive measures to avoid transfusion of blood products that contain leukocyte Antibodies should be taken now. |
doi_str_mv | 10.1007/s00134-007-2873-3 |
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TRALI and acute respiratory distress syndrome (ARDS) share a common clinical definition except that TRALI is temporally and mechanistically related to blood transfusion. Two different mechanisms have been proposed. The first is leuko-agglutination due to infusion of leukocyte Antibodies with the blood product transfused. The second proposes a two-event model where the first event is the clinical condition of the patient, and the second the infusion of lipids that accumulate in blood products during storage. An emerging common pathway of granulocyte activation is discussed, as is the relevance of immune and non-immune TRALI from a practical point of view. Some unresolved questions in TRALI pathophysiology, including the relevance of Antibodies to HLA class-II antigens and the participation of the endothelium, are examined, as are the suggested preventive measures for both immune and non-immune TRALI. It is concluded that further clinical and experimental data are necessary before any recommendations can be made regarding non-immune TRALI. In contrast, in immune TRALI, preventive measures to avoid transfusion of blood products that contain leukocyte Antibodies should be taken now.</description><identifier>ISSN: 0342-4642</identifier><identifier>EISSN: 1432-1238</identifier><identifier>DOI: 10.1007/s00134-007-2873-3</identifier><identifier>PMID: 17676436</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Agglutination ; Antibodies ; Blood products ; Blood transfusions ; Blood vessels ; Edema ; Endothelium ; Fatalities ; Granulocytes ; Humans ; Hypotheses ; Intensive care ; Leukocytes ; Leukocytes - immunology ; Lipids ; Lungs ; Neutrophil Activation ; Neutrophils ; Pathophysiology ; Physiology ; Respiratory distress syndrome ; Respiratory Distress Syndrome, Adult - immunology ; Respiratory Distress Syndrome, Adult - physiopathology ; Respiratory Distress Syndrome, Adult - prevention & control ; Transfusion Reaction</subject><ispartof>Intensive care medicine, 2007-06, Vol.33 Suppl 1 (S1), p.S3-S11</ispartof><rights>Springer-Verlag Berlin Heidelberg 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c241t-1337397e41c6ab3a15e940d0ad7ddc50f60e031a7e4e7567e2b6f90557279ff33</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17676436$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sachs, U J H</creatorcontrib><title>Pathophysiology of TRALI: current concepts</title><title>Intensive care medicine</title><addtitle>Intensive Care Med</addtitle><description>Transfusion-related acute lung injury (TRALI) is a life-threatening adverse event in blood transfusion and is considered the most common cause of transfusion-related fatalities in the United States and the United Kingdom. TRALI and acute respiratory distress syndrome (ARDS) share a common clinical definition except that TRALI is temporally and mechanistically related to blood transfusion. Two different mechanisms have been proposed. The first is leuko-agglutination due to infusion of leukocyte Antibodies with the blood product transfused. The second proposes a two-event model where the first event is the clinical condition of the patient, and the second the infusion of lipids that accumulate in blood products during storage. An emerging common pathway of granulocyte activation is discussed, as is the relevance of immune and non-immune TRALI from a practical point of view. Some unresolved questions in TRALI pathophysiology, including the relevance of Antibodies to HLA class-II antigens and the participation of the endothelium, are examined, as are the suggested preventive measures for both immune and non-immune TRALI. It is concluded that further clinical and experimental data are necessary before any recommendations can be made regarding non-immune TRALI. In contrast, in immune TRALI, preventive measures to avoid transfusion of blood products that contain leukocyte Antibodies should be taken now.</description><subject>Agglutination</subject><subject>Antibodies</subject><subject>Blood products</subject><subject>Blood transfusions</subject><subject>Blood vessels</subject><subject>Edema</subject><subject>Endothelium</subject><subject>Fatalities</subject><subject>Granulocytes</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Intensive care</subject><subject>Leukocytes</subject><subject>Leukocytes - immunology</subject><subject>Lipids</subject><subject>Lungs</subject><subject>Neutrophil Activation</subject><subject>Neutrophils</subject><subject>Pathophysiology</subject><subject>Physiology</subject><subject>Respiratory distress syndrome</subject><subject>Respiratory Distress Syndrome, Adult - immunology</subject><subject>Respiratory Distress Syndrome, Adult - physiopathology</subject><subject>Respiratory Distress Syndrome, Adult - 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immunology</topic><topic>Lipids</topic><topic>Lungs</topic><topic>Neutrophil Activation</topic><topic>Neutrophils</topic><topic>Pathophysiology</topic><topic>Physiology</topic><topic>Respiratory distress syndrome</topic><topic>Respiratory Distress Syndrome, Adult - immunology</topic><topic>Respiratory Distress Syndrome, Adult - physiopathology</topic><topic>Respiratory Distress Syndrome, Adult - prevention & control</topic><topic>Transfusion Reaction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sachs, U J H</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Intensive care medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sachs, U J H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pathophysiology of TRALI: current concepts</atitle><jtitle>Intensive care medicine</jtitle><addtitle>Intensive Care Med</addtitle><date>2007-06</date><risdate>2007</risdate><volume>33 Suppl 1</volume><issue>S1</issue><spage>S3</spage><epage>S11</epage><pages>S3-S11</pages><issn>0342-4642</issn><eissn>1432-1238</eissn><abstract>Transfusion-related acute lung injury (TRALI) is a life-threatening adverse event in blood transfusion and is considered the most common cause of transfusion-related fatalities in the United States and the United Kingdom. TRALI and acute respiratory distress syndrome (ARDS) share a common clinical definition except that TRALI is temporally and mechanistically related to blood transfusion. Two different mechanisms have been proposed. The first is leuko-agglutination due to infusion of leukocyte Antibodies with the blood product transfused. The second proposes a two-event model where the first event is the clinical condition of the patient, and the second the infusion of lipids that accumulate in blood products during storage. An emerging common pathway of granulocyte activation is discussed, as is the relevance of immune and non-immune TRALI from a practical point of view. Some unresolved questions in TRALI pathophysiology, including the relevance of Antibodies to HLA class-II antigens and the participation of the endothelium, are examined, as are the suggested preventive measures for both immune and non-immune TRALI. It is concluded that further clinical and experimental data are necessary before any recommendations can be made regarding non-immune TRALI. In contrast, in immune TRALI, preventive measures to avoid transfusion of blood products that contain leukocyte Antibodies should be taken now.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>17676436</pmid><doi>10.1007/s00134-007-2873-3</doi></addata></record> |
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subjects | Agglutination Antibodies Blood products Blood transfusions Blood vessels Edema Endothelium Fatalities Granulocytes Humans Hypotheses Intensive care Leukocytes Leukocytes - immunology Lipids Lungs Neutrophil Activation Neutrophils Pathophysiology Physiology Respiratory distress syndrome Respiratory Distress Syndrome, Adult - immunology Respiratory Distress Syndrome, Adult - physiopathology Respiratory Distress Syndrome, Adult - prevention & control Transfusion Reaction |
title | Pathophysiology of TRALI: current concepts |
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