Low incidence of anti-D alloimmunization following D+ platelet transfusion: The Anti-D Alloimmunization after D-incompatible Platelet Transfusions (ADAPT) study
Identifieur interne : 002363 ( Main/Exploration ); précédent : 002362; suivant : 002364Low incidence of anti-D alloimmunization following D+ platelet transfusion: The Anti-D Alloimmunization after D-incompatible Platelet Transfusions (ADAPT) study
Auteurs : Joan Cid [Espagne, États-Unis] ; Miguel Lozano [Espagne] ; Alyssa Ziman [États-Unis] ; Kamille A. West [États-Unis] ; Kerry L. O'Brien [États-Unis] ; Michael F. Murphy [Royaume-Uni] ; Silvano Wendel [Brésil] ; Alejandro Vázquez [Espagne] ; Xavier Ortín [Espagne] ; Tor A. Hervig [Norvège] ; Meghan Delaney [États-Unis] ; Willy A. Flegel [États-Unis] ; Mark H. YazerSource :
- British journal of haematology [ 0007-1048 ] ; 2014.
Abstract
The reported frequency of D alloimmunization in D- recipients after transfusion of D+ platelets varies. This study was designed to determine the frequency of D alloimmunization, previously reported to be an average of 5%±2%. A primary anti-D immune response was defined as the detection of anti-D ≥28 days following the first D+ platelet transfusion. Data were collected on 485 D- recipients of D+ platelets in 11 centres between 2010-2012. Their median age was 60 (range 2-100) years. Diagnoses included: haematological (203/485, 42%), oncological (64/485, 13%) and other diseases (218/485, 45%). Only 7/485 (1.44%; 95%CI 0.58-2.97%) recipients had a primary anti-D response after a median serological follow-up of 77 days (range: 28-2111). There were no statistically significant differences between the primary anti-D formers and the other patients, in terms of gender, age, receipt of immunosuppressive therapy, proportion of patients with haematological/oncological diseases, transfusion of whole blood-derived or apheresis platelets or both, and total number of transfused platelet products. This is the largest study with the longest follow-up of D alloimmunization following D+ platelet transfusion. The low frequency of D alloimmunization should be considered when deciding whether to administer Rh Immune Globulin to D- males and D- females without childbearing potential after transfusion of D+ platelets.
Url:
DOI: 10.1111/bjh.13158
PubMed: 25283094
PubMed Central: 4314459
Affiliations:
- Brésil, Espagne, Norvège, Royaume-Uni, États-Unis
- Angleterre, Californie, Catalogne, Maryland, Massachusetts, Oxfordshire, Washington (État), État de São Paulo
- Barcelone, Oxford, São Paulo
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Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Low incidence of anti-D alloimmunization following D+ platelet transfusion: The Anti-D Alloimmunization after D-incompatible Platelet Transfusions (ADAPT) study</title>
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<author><name sortKey="Yazer, Mark H" sort="Yazer, Mark H" uniqKey="Yazer M" first="Mark H." last="Yazer">Mark H. Yazer</name>
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<front><div type="abstract" xml:lang="en"><title>Summary</title>
<p id="P1">The reported frequency of D alloimmunization in D- recipients after transfusion of D+ platelets varies. This study was designed to determine the frequency of D alloimmunization, previously reported to be an average of 5%±2%. A primary anti-D immune response was defined as the detection of anti-D ≥28 days following the first D+ platelet transfusion. Data were collected on 485 D- recipients of D+ platelets in 11 centres between 2010-2012. Their median age was 60 (range 2-100) years. Diagnoses included: haematological (203/485, 42%), oncological (64/485, 13%) and other diseases (218/485, 45%). Only 7/485 (1.44%; 95%CI 0.58-2.97%) recipients had a primary anti-D response after a median serological follow-up of 77 days (range: 28-2111). There were no statistically significant differences between the primary anti-D formers and the other patients, in terms of gender, age, receipt of immunosuppressive therapy, proportion of patients with haematological/oncological diseases, transfusion of whole blood-derived or apheresis platelets or both, and total number of transfused platelet products. This is the largest study with the longest follow-up of D alloimmunization following D+ platelet transfusion. The low frequency of D alloimmunization should be considered when deciding whether to administer Rh Immune Globulin to D- males and D- females without childbearing potential after transfusion of D+ platelets.</p>
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<country name="États-Unis"><region name="Maryland"><name sortKey="Cid, Joan" sort="Cid, Joan" uniqKey="Cid J" first="Joan" last="Cid">Joan Cid</name>
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<country name="Norvège"><noRegion><name sortKey="Hervig, Tor A" sort="Hervig, Tor A" uniqKey="Hervig T" first="Tor A." last="Hervig">Tor A. Hervig</name>
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