Evidence map›Paper›PMID 40708459›Full record

ArticleTransfusion2025

The prevalence and timing of seroconversion during pregnancy-A retrospective study to enable safe transfusion.

E Dreyfuss, V Yahalom, Y Barer, I Ambar, A Pardo, A Shmueli, O Houri, E Hadar, S Barbash-Hazan

Abstract read
In one paragraph

Article in Transfusion, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

E DreyfussHelen Schneider Hospital for Women, Rabin Medical Center, Petach Tikva, Israel.ORCID https://orcid.org/0009-0003-3332-1142
V YahalomGray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.ORCID https://orcid.org/0000-0001-5043-8690
Y BarerSchool of Public Health, Tel Aviv University, Tel Aviv, Israel.
I AmbarHelen Schneider Hospital for Women, Rabin Medical Center, Petach Tikva, Israel.
A PardoHelen Schneider Hospital for Women, Rabin Medical Center, Petach Tikva, Israel.
A ShmueliHelen Schneider Hospital for Women, Rabin Medical Center, Petach Tikva, Israel.
O HouriHelen Schneider Hospital for Women, Rabin Medical Center, Petach Tikva, Israel.ORCID https://orcid.org/0000-0002-3393-813X
E HadarHelen Schneider Hospital for Women, Rabin Medical Center, Petach Tikva, Israel.
S Barbash-HazanHelen Schneider Hospital for Women, Rabin Medical Center, Petach Tikva, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDuring pregnancy, exposure to fetal red blood cell antigens can trigger alloimmunization. To enable safe transfusion of compatible blood for pregnant individuals where urgent surgery might be necessary, blood bank standards mandate a valid blood type and antibody screening every 72 h ("3-day rule"). This practice requires frequent blood drawings contributing to patient discomfort and costs. To investigate if this practice is required, we evaluated the proportion of pregnant individuals who develop clinically significant alloantibodies within 72 h of a previous negative antibody screen. STUDY DESIGN AND

methodsRetrospective cohort of RhD-positive pregnant individuals with initial negative antibody screens, undergoing repeated screens at variable intervals. Seroconversion rates were compared with healthy male blood donors. Characteristics of pregnant individuals with and without seroconversion were analyzed.

resultsAmong 8659 RhD-positive pregnant individuals with initial negative antibody screens, 56 (0.6%) converted to a positive antibody screen, while only 15 (0.2%) developed clinically significant alloantibodies. Of these 15, only one converted within 3 days of testing, while others converted within 5-95 days. Two of the 15 women received a blood transfusion, 8-97 days before seroconversion. No male donors seroconverted during 9 months of follow up. Pregnant individuals with seroconversion were more likely to have systemic lupus erythematosus and antiphospholipid antibody syndrome. DISCUSSION: Only one pregnant individual developed clinically significant alloantibodies within 72 h of a negative screening, compared to none of the control group. For pregnant individuals without recent transfusion, extending antibody screening intervals to 1 week appears safe.

Indexed as

Blood TransfusionIsoantibodiesRh-Hr Blood-Group SystemSeroconversionAdultBlood DonorsFemaleHumansMalePregnancyPrevalenceRetrospective StudiesTime FactorsIsoantibodiesRh-Hr Blood-Group System“3‐day rule”alloimmunizationpregnancytransfusion

Identifiers

PMID40708459
PMCPMC12432806

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.