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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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 |
format | Article |
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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><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 & 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 & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2375-7503</orcidid><orcidid>https://orcid.org/0000-0003-1089-5787</orcidid><orcidid>https://orcid.org/0000-0001-6740-2758</orcidid><orcidid>https://orcid.org/0000-0001-8601-5438</orcidid></search><sort><creationdate>202208</creationdate><title>Rate of D‐alloimmunization in trauma does not depend on the number of RhD‐positive units transfused: The BEST collaborative study</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3652-c26d86a6a44732f843d67669fb19daa5a8a0c1bb1fc349bd8e79936adb5771883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>alloimmunization</topic><topic>Antibodies</topic><topic>anti‐D</topic><topic>Blood transfusion</topic><topic>Erythrocytes</topic><topic>Institutions</topic><topic>Isoimmunization</topic><topic>rate</topic><topic>red blood cell</topic><topic>Resuscitation</topic><topic>RhD</topic><topic>Transfusion</topic><topic>Trauma</topic><topic>whole blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & 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. These data can help to inform RhD type selection decisions.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><doi>10.1111/trf.16952</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-2375-7503</orcidid><orcidid>https://orcid.org/0000-0003-1089-5787</orcidid><orcidid>https://orcid.org/0000-0001-6740-2758</orcidid><orcidid>https://orcid.org/0000-0001-8601-5438</orcidid><oa>free_for_read</oa></addata></record> |
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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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