TY - JOUR
T1 - Why do people still make anti-D over 50 years after the introduction of Rho(D) immune globulin? A Biomedical Excellence for Safer Transfusion (BEST) Collaborative study
AU - BEST foRmation of Anti-D After Rhogam (RADAR) Study Investigators and the Biomedical Excellence for Safer Transfusion (BEST) Collaborative
AU - DelBaugh, Regina M.
AU - Murphy, Michael F.
AU - Staves, Julie
AU - Fachini, Roberta Maria
AU - Wendel, Silvano
AU - Hands, Katie
AU - Bonet-Bub, Carolina
AU - Kutner, Jose Mauro
AU - Cohn, Claudia S.
AU - Cox, Cody A.
AU - Jacquot, Cyril
AU - Hasan, Rida A.
AU - Lu, Wen
AU - Juskewitch, Justin E.
AU - Raval, Jay S.
AU - Rollins-Raval, Marian A.
AU - Fung, Mark K.
AU - Ziman, Alyssa
AU - Fermon, Erica J.
AU - Gorlin, Jed B.
AU - Peters, Jessica
AU - Dunbar, Nancy M.
AU - Callum, Jeannie
AU - Scholey, Aiden
AU - Parsons, Meredith G.
AU - Virk, Mrigender Singh
AU - Wali, Junaid Ahmad
AU - Wong, Stephen Hong Chun
AU - Charlewood, Richard
AU - Mishra, Sonam
AU - Tehseen, Sarah
AU - Anthony, Sheila
AU - Alquist, Caroline R.
AU - Thant, Mamie M.
AU - Williams, Lance A.
AU - Lu, Qun
AU - Andrews, Jennifer
AU - Tucci, Jonathan J.
AU - VanderMeulen, Heather
AU - Azzeh, Mahmoud
AU - Thibodeaux, Suzanne R.
AU - Wallace, Lisa R.
AU - Muñiz, Maria De Los Angeles
AU - Mabagos, Geraldine
AU - Lokhandwala, Parvez M.
AU - Williams, Nathan A.
AU - Thomasson, Reggie R.
AU - Narasimhan, Ramya
AU - Greebon, Leslie J.
AU - Prajapati, Vipulkumar
AU - Campbell-Lee, Sally A.
AU - Johnson, Carolyn
AU - Tordon, Bryan
AU - Radwi, Ghazala
N1 - Publisher Copyright:
© 2025 AABB.
PY - 2025/5
Y1 - 2025/5
N2 - Background: Rho(D) immune globulin (RhIg) is used to reduce RhD alloimmunization in pregnancy. This study describes potential causes for RhD alloimmunization after the development and implementation of RhIg. Study Design and Methods: This retrospective descriptive study investigated RhD-negative patients born in 1965–2005 with anti-D newly identified during 2018–2022. Transfusion, pregnancy, intravenous drug abuse, and transplantation were considered potential alloimmunization sources. Results: There were 1200 study patients (852 females; 348 males) at 30 institutions in 5 countries (USA, Canada, UK, New Zealand, Brazil). Most patients had a single potential source of alloimmunization identified (857/1200, 71%), most commonly pregnancy among females (537/852, 63%) and transfusion among males (180/348, 52%). When multiple potential sources were included, males were more likely than females to have a history of transfusion (235/348 [68%] vs. 149/852 [17%], p <.0001) and confirmed or suspected intravenous drug abuse (100/348 [29%] vs. 138/852 [16%], p <.0001). Among females with a history of pregnancy, 119/718 (17%) had healthcare access issues, 120/718 (17%) had pregnancy in a country where they may not have received RhIg, and 21/718 (3%) refused RhIg. Among patients with a history of transfusion, males were more likely than females to have received RhD-positive red blood cells or whole blood (143/235 [61%] vs. 30/149 [20%], p <.0001) and/or platelets (84/235 [36%] vs. 19/149 [13%], p <.0001). Discussion: Pregnancy was the most frequently identified potential source of RhD alloimmunization among females. Transfusion was most frequent in males. Intravenous drug abuse as a common potential source among patients with RhD alloimmunization merits further study.
AB - Background: Rho(D) immune globulin (RhIg) is used to reduce RhD alloimmunization in pregnancy. This study describes potential causes for RhD alloimmunization after the development and implementation of RhIg. Study Design and Methods: This retrospective descriptive study investigated RhD-negative patients born in 1965–2005 with anti-D newly identified during 2018–2022. Transfusion, pregnancy, intravenous drug abuse, and transplantation were considered potential alloimmunization sources. Results: There were 1200 study patients (852 females; 348 males) at 30 institutions in 5 countries (USA, Canada, UK, New Zealand, Brazil). Most patients had a single potential source of alloimmunization identified (857/1200, 71%), most commonly pregnancy among females (537/852, 63%) and transfusion among males (180/348, 52%). When multiple potential sources were included, males were more likely than females to have a history of transfusion (235/348 [68%] vs. 149/852 [17%], p <.0001) and confirmed or suspected intravenous drug abuse (100/348 [29%] vs. 138/852 [16%], p <.0001). Among females with a history of pregnancy, 119/718 (17%) had healthcare access issues, 120/718 (17%) had pregnancy in a country where they may not have received RhIg, and 21/718 (3%) refused RhIg. Among patients with a history of transfusion, males were more likely than females to have received RhD-positive red blood cells or whole blood (143/235 [61%] vs. 30/149 [20%], p <.0001) and/or platelets (84/235 [36%] vs. 19/149 [13%], p <.0001). Discussion: Pregnancy was the most frequently identified potential source of RhD alloimmunization among females. Transfusion was most frequent in males. Intravenous drug abuse as a common potential source among patients with RhD alloimmunization merits further study.
KW - Rho(D) immune globulin (RhIg)
KW - alloimmunization
KW - anti-D
KW - intravenous drug abuse
KW - pregnancy
KW - transfusion
KW - transplant
UR - https://www.scopus.com/pages/publications/105000824065
U2 - 10.1111/trf.18202
DO - 10.1111/trf.18202
M3 - Article
C2 - 40059673
AN - SCOPUS:105000824065
SN - 0041-1132
VL - 65
SP - 957
EP - 967
JO - Transfusion
JF - Transfusion
IS - 5
ER -