Rate of D‐alloimmunization in trauma does not depend on the number of RhD‐positive units transfused: The BEST collaborative study

Background Evidence indicates the life‐saving benefits of early blood product transfusion in severe trauma resuscitation. Many of these products will be RhD‐positive, so understanding the D‐alloimmunization rate is important. Methods This was a multicenter, retrospective study whereby injured RhD‐ne...

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Veröffentlicht in:Transfusion (Philadelphia, Pa.) Pa.), 2022-08, Vol.62 (S1), p.S185-S192
Hauptverfasser: Seheult, Jansen N., Callum, Jeannie, Delaney, Meghan, Drake, Rosanna, Dunbar, Nancy M., Harm, Sarah K., Hess, John R., Jackson, Bryon P., Javanbakht, Ayda, Moore, Sarah A., Murphy, Michael F., Raval, Jay S., Staves, Julie, Tuott, Erin E., Wendel, Silvano, Ziman, Alyssa, Yazer, Mark H.
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container_end_page S192
container_issue S1
container_start_page S185
container_title Transfusion (Philadelphia, Pa.)
container_volume 62
creator Seheult, Jansen N.
Callum, Jeannie
Delaney, Meghan
Drake, Rosanna
Dunbar, Nancy M.
Harm, Sarah K.
Hess, John R.
Jackson, Bryon P.
Javanbakht, Ayda
Moore, Sarah A.
Murphy, Michael F.
Raval, Jay S.
Staves, Julie
Tuott, Erin E.
Wendel, Silvano
Ziman, Alyssa
Yazer, Mark H.
description Background Evidence indicates the life‐saving benefits of early blood product transfusion in severe trauma resuscitation. Many of these products will be RhD‐positive, so understanding the D‐alloimmunization rate is important. Methods This was a multicenter, retrospective study whereby injured RhD‐negative patients between 18–50 years of age who received at least one unit of RhD‐positive red blood cells (RBC) or low titer group O whole blood (LTOWB) during their resuscitation between 1 January, 2010 through 31 December, 2019 were identified. If an antibody detection test was performed ≥14 days after the index RhD‐positive transfusion then basic demographic information was collected, including whether the patient became D‐alloimmunized. The overall D‐alloimmunization rate, and the rate stratified by the number of units transfused, were calculated. Results Data were collected from nine institutions. Five institutions reported fewer than 10 eligible patients each and were excluded. From the remaining four institutions, all from the USA, there were 235 eligible patients; 77 (random effects estimate: 32.7%; 95% CI: 19.1–50.1%) became D‐alloimmunized. Three of the institutions reported D‐alloimmunization rates ≥38.6%, while the remaining institution's rate was 12.2%. In both random and fixed‐effects models, the rate of D‐alloimmunization was not significantly different between those who received one RhD‐positive unit and those who received multiple RhD‐positive units. Conclusion In this large, multicenter study of injured patients, the overall rate of D‐alloimmunization fell within the range previously reported. The rate of D‐alloimmunization did not increase as the number of transfused RhD‐positive units increased. These data can help to inform RhD type selection decisions.
doi_str_mv 10.1111/trf.16952
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Many of these products will be RhD‐positive, so understanding the D‐alloimmunization rate is important. Methods This was a multicenter, retrospective study whereby injured RhD‐negative patients between 18–50 years of age who received at least one unit of RhD‐positive red blood cells (RBC) or low titer group O whole blood (LTOWB) during their resuscitation between 1 January, 2010 through 31 December, 2019 were identified. If an antibody detection test was performed ≥14 days after the index RhD‐positive transfusion then basic demographic information was collected, including whether the patient became D‐alloimmunized. The overall D‐alloimmunization rate, and the rate stratified by the number of units transfused, were calculated. Results Data were collected from nine institutions. Five institutions reported fewer than 10 eligible patients each and were excluded. From the remaining four institutions, all from the USA, there were 235 eligible patients; 77 (random effects estimate: 32.7%; 95% CI: 19.1–50.1%) became D‐alloimmunized. Three of the institutions reported D‐alloimmunization rates ≥38.6%, while the remaining institution's rate was 12.2%. In both random and fixed‐effects models, the rate of D‐alloimmunization was not significantly different between those who received one RhD‐positive unit and those who received multiple RhD‐positive units. Conclusion In this large, multicenter study of injured patients, the overall rate of D‐alloimmunization fell within the range previously reported. The rate of D‐alloimmunization did not increase as the number of transfused RhD‐positive units increased. These data can help to inform RhD type selection decisions.</description><identifier>ISSN: 0041-1132</identifier><identifier>EISSN: 1537-2995</identifier><identifier>DOI: 10.1111/trf.16952</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>alloimmunization ; Antibodies ; anti‐D ; Blood transfusion ; Erythrocytes ; Institutions ; Isoimmunization ; rate ; red blood cell ; Resuscitation ; RhD ; Transfusion ; Trauma ; whole blood</subject><ispartof>Transfusion (Philadelphia, Pa.), 2022-08, Vol.62 (S1), p.S185-S192</ispartof><rights>2022 AABB.</rights><rights>2022 AABB</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3652-c26d86a6a44732f843d67669fb19daa5a8a0c1bb1fc349bd8e79936adb5771883</citedby><cites>FETCH-LOGICAL-c3652-c26d86a6a44732f843d67669fb19daa5a8a0c1bb1fc349bd8e79936adb5771883</cites><orcidid>0000-0002-2375-7503 ; 0000-0003-1089-5787 ; 0000-0001-6740-2758 ; 0000-0001-8601-5438</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Ftrf.16952$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ftrf.16952$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids></links><search><creatorcontrib>Seheult, Jansen N.</creatorcontrib><creatorcontrib>Callum, Jeannie</creatorcontrib><creatorcontrib>Delaney, Meghan</creatorcontrib><creatorcontrib>Drake, Rosanna</creatorcontrib><creatorcontrib>Dunbar, Nancy M.</creatorcontrib><creatorcontrib>Harm, Sarah K.</creatorcontrib><creatorcontrib>Hess, John R.</creatorcontrib><creatorcontrib>Jackson, Bryon P.</creatorcontrib><creatorcontrib>Javanbakht, Ayda</creatorcontrib><creatorcontrib>Moore, Sarah A.</creatorcontrib><creatorcontrib>Murphy, Michael F.</creatorcontrib><creatorcontrib>Raval, Jay S.</creatorcontrib><creatorcontrib>Staves, Julie</creatorcontrib><creatorcontrib>Tuott, Erin E.</creatorcontrib><creatorcontrib>Wendel, Silvano</creatorcontrib><creatorcontrib>Ziman, Alyssa</creatorcontrib><creatorcontrib>Yazer, Mark H.</creatorcontrib><creatorcontrib>The Biomedical Excellence for Safer Transfusion collaborative</creatorcontrib><title>Rate of D‐alloimmunization in trauma does not depend on the number of RhD‐positive units transfused: The BEST collaborative study</title><title>Transfusion (Philadelphia, Pa.)</title><description>Background Evidence indicates the life‐saving benefits of early blood product transfusion in severe trauma resuscitation. Many of these products will be RhD‐positive, so understanding the D‐alloimmunization rate is important. Methods This was a multicenter, retrospective study whereby injured RhD‐negative patients between 18–50 years of age who received at least one unit of RhD‐positive red blood cells (RBC) or low titer group O whole blood (LTOWB) during their resuscitation between 1 January, 2010 through 31 December, 2019 were identified. If an antibody detection test was performed ≥14 days after the index RhD‐positive transfusion then basic demographic information was collected, including whether the patient became D‐alloimmunized. The overall D‐alloimmunization rate, and the rate stratified by the number of units transfused, were calculated. Results Data were collected from nine institutions. Five institutions reported fewer than 10 eligible patients each and were excluded. From the remaining four institutions, all from the USA, there were 235 eligible patients; 77 (random effects estimate: 32.7%; 95% CI: 19.1–50.1%) became D‐alloimmunized. Three of the institutions reported D‐alloimmunization rates ≥38.6%, while the remaining institution's rate was 12.2%. In both random and fixed‐effects models, the rate of D‐alloimmunization was not significantly different between those who received one RhD‐positive unit and those who received multiple RhD‐positive units. Conclusion In this large, multicenter study of injured patients, the overall rate of D‐alloimmunization fell within the range previously reported. The rate of D‐alloimmunization did not increase as the number of transfused RhD‐positive units increased. These data can help to inform RhD type selection decisions.</description><subject>alloimmunization</subject><subject>Antibodies</subject><subject>anti‐D</subject><subject>Blood transfusion</subject><subject>Erythrocytes</subject><subject>Institutions</subject><subject>Isoimmunization</subject><subject>rate</subject><subject>red blood cell</subject><subject>Resuscitation</subject><subject>RhD</subject><subject>Transfusion</subject><subject>Trauma</subject><subject>whole blood</subject><issn>0041-1132</issn><issn>1537-2995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp10b1OwzAUBWALgUQpDLyBJRYY0voncWI2KBSQkJBKmCMndoRRYhfbAZWJhZ1n5ElwKRMSXu7g71xd6QBwiNEExzcNrp1gxjOyBUY4o3lCOM-2wQihFCcYU7IL9rx_QggRjvAIfCxEUNC28OLr_VN0ndV9Pxj9JoK2BmoDgxNDL6C0ykNjA5RqqYyE8TM8KmiGvlZunV88rjcsrddBvygYdwS_DhvfDl7JU1hGfn55X8LGdp2orRM_0IdBrvbBTis6rw5-5xg8zC_L2XVye3d1Mzu7TRrKMpI0hMmCCSbSNKekLVIqWc4Yb2vMpRCZKARqcF3jtqEpr2Whcs4pE7LO8hwXBR2D483epbPPg_Kh6rVvVLzHKDv4irACI0oKlkZ69Ic-2cGZeF1UPEspzwmK6mSjGme9d6qtlk73wq0qjKp1IVUspPopJNrpxr7qTq3-h1W5mG8S3zT_j30</recordid><startdate>202208</startdate><enddate>202208</enddate><creator>Seheult, Jansen N.</creator><creator>Callum, Jeannie</creator><creator>Delaney, Meghan</creator><creator>Drake, Rosanna</creator><creator>Dunbar, Nancy M.</creator><creator>Harm, Sarah K.</creator><creator>Hess, John R.</creator><creator>Jackson, Bryon P.</creator><creator>Javanbakht, Ayda</creator><creator>Moore, Sarah A.</creator><creator>Murphy, Michael F.</creator><creator>Raval, Jay S.</creator><creator>Staves, Julie</creator><creator>Tuott, Erin E.</creator><creator>Wendel, Silvano</creator><creator>Ziman, Alyssa</creator><creator>Yazer, Mark H.</creator><general>John Wiley &amp; 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Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Transfusion (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seheult, Jansen N.</au><au>Callum, Jeannie</au><au>Delaney, Meghan</au><au>Drake, Rosanna</au><au>Dunbar, Nancy M.</au><au>Harm, Sarah K.</au><au>Hess, John R.</au><au>Jackson, Bryon P.</au><au>Javanbakht, Ayda</au><au>Moore, Sarah A.</au><au>Murphy, Michael F.</au><au>Raval, Jay S.</au><au>Staves, Julie</au><au>Tuott, Erin E.</au><au>Wendel, Silvano</au><au>Ziman, Alyssa</au><au>Yazer, Mark H.</au><aucorp>The Biomedical Excellence for Safer Transfusion collaborative</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rate of D‐alloimmunization in trauma does not depend on the number of RhD‐positive units transfused: The BEST collaborative study</atitle><jtitle>Transfusion (Philadelphia, Pa.)</jtitle><date>2022-08</date><risdate>2022</risdate><volume>62</volume><issue>S1</issue><spage>S185</spage><epage>S192</epage><pages>S185-S192</pages><issn>0041-1132</issn><eissn>1537-2995</eissn><abstract>Background Evidence indicates the life‐saving benefits of early blood product transfusion in severe trauma resuscitation. Many of these products will be RhD‐positive, so understanding the D‐alloimmunization rate is important. Methods This was a multicenter, retrospective study whereby injured RhD‐negative patients between 18–50 years of age who received at least one unit of RhD‐positive red blood cells (RBC) or low titer group O whole blood (LTOWB) during their resuscitation between 1 January, 2010 through 31 December, 2019 were identified. If an antibody detection test was performed ≥14 days after the index RhD‐positive transfusion then basic demographic information was collected, including whether the patient became D‐alloimmunized. The overall D‐alloimmunization rate, and the rate stratified by the number of units transfused, were calculated. Results Data were collected from nine institutions. Five institutions reported fewer than 10 eligible patients each and were excluded. From the remaining four institutions, all from the USA, there were 235 eligible patients; 77 (random effects estimate: 32.7%; 95% CI: 19.1–50.1%) became D‐alloimmunized. Three of the institutions reported D‐alloimmunization rates ≥38.6%, while the remaining institution's rate was 12.2%. In both random and fixed‐effects models, the rate of D‐alloimmunization was not significantly different between those who received one RhD‐positive unit and those who received multiple RhD‐positive units. Conclusion In this large, multicenter study of injured patients, the overall rate of D‐alloimmunization fell within the range previously reported. The rate of D‐alloimmunization did not increase as the number of transfused RhD‐positive units increased. 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source Wiley Online Library Journals Frontfile Complete
subjects alloimmunization
Antibodies
anti‐D
Blood transfusion
Erythrocytes
Institutions
Isoimmunization
rate
red blood cell
Resuscitation
RhD
Transfusion
Trauma
whole blood
title Rate of D‐alloimmunization in trauma does not depend on the number of RhD‐positive units transfused: The BEST collaborative study
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