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RhD-Positive Whole Blood for Patients With Reproductive Potential After Two Randomized Trials of Prehospital Trauma Resuscitation

Journal
Obstetrics and gynecology (Q1)
Published
15 September 2026
Study design
Randomized controlled trial
Evidence level
Level 1, High (CEBM 1b)
Authors
Jeremy W Jacobs, Jeannie Callum, Brian D Adkins, Elizabeth A Abels, Sheharyar Raza, Deva Sharma, et al.
PMID
42743435
DOI
10.1097/AOG.0000000000006431

Why clinicians should know about it

  • Picked for Emergency Medicine (top studies of the week, 20 September 2026): RhD‑positive whole blood lacks survival benefit

Abstract

Low-titer group O whole blood is increasingly used in civilian trauma resuscitation and is usually RhD-positive because RhD-negative whole blood is scarce. For RhD-negative patients and patients of unknown RhD type who retain reproductive potential, transfusion of RhD-positive red cells can cause anti-D alloimmunization and place a future pregnancy at risk for hemolytic disease of the fetus and newborn, a harm that may emerge years after the trauma encounter. The ethical and clinical justification for accepting this risk has depended on the idea that whole blood provides a survival advantage large enough to outweigh the possibility of future reproductive harm. However, two recently published randomized trials of prehospital traumatic hemorrhage found no survival advantage for whole blood over component therapy. Reflecting this evidence, RhD-positive whole blood is ethically unjustified for RhD-negative patients with reproductive potential when compatible products are available. The reproductive harm is distinctive in being preventable through product selection, concentrated in patients who cannot consent during resuscitation, and often compounded by limited access to obstetric care. Institutions should default patients with reproductive potential to RhD-negative products when available until the RhD type is confirmed, guarantee standardized and cost-free follow-up when RhD-incompatible transfusion occurs, and ensure ethical standards within trial protocols.

Abstract as published, via PubMed.

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For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.