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.

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Tác giả: Carolina Bonet-Bub, Claudia S Cohn, Cody A Cox, Regina M DelBaugh, Nancy M Dunbar, Roberta Maria Fachini, Erica J Fermon, Mark K Fung, Jed B Gorlin, Katie Hands, Rida A Hasan, Cyril Jacquot, Justin E Juskewitch, Jose Mauro Kutner, Wen Lu, Michael F Murphy, Jessica Peters, Jay S Raval, Marian A Rollins-Raval, Julie Staves, Silvano Wendel, Alyssa Ziman

Ngôn ngữ: eng

Ký hiệu phân loại: 621.18 Generating and transmitting steam

Thông tin xuất bản: United States : Transfusion , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 742152

 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 <
  .0002) and confirmed or suspected intravenous drug abuse (100/348 [29%] vs. 138/852 [16%], p <
  .0002). 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 <
  .0002) and/or platelets (84/235 [36%] vs. 19/149 [13%], p <
  .0002). 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.
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