Evidence map›Paper›PMID 40253764›Full record

SynthesisTransfusion medicine reviews2025

The Utility of a Critical Antibody Titer in Anti-K Alloimmunized Pregnancies: A Systematic Review and Meta-Analysis of Diagnostic Test Accuracy.

Jeremy W Jacobs, Ronan P Sugrue, Jerome Jeffrey Federspiel, Melissa C Funaro, Brian D Adkins, Garrett S Booth, Masja de Haas, Jia Jennifer Ding, Danijela Drndarevic, Sejal Kabre and 5 more

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Transfusion medicine reviews, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Jeremy W JacobsDepartment of Pathology, Microbiology, & Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
Ronan P SugrueDepartment of Obstetrics and Gynecology, Division of Maternal Fetal Medicine, Duke University School of Medicine, Durham, NC, USA.
Jerome Jeffrey FederspielDepartment of Obstetrics and Gynecology, Division of Maternal Fetal Medicine, Duke University School of Medicine, Durham, NC, USA; Department of Population Health Sciences, Duke University School of Medicine, Durham, NC, USA; Department of Medicine, Duke University School of Medicine, Durham, NC, USA.
Melissa C FunaroHarvey Cushing/John Hay Whitney Medical Library, Yale University, New Haven, CT, USA.
Brian D AdkinsDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Garrett S BoothDepartment of Pathology, Microbiology, & Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
Masja de HaasDepartment of Haematology, Leiden University Medical Center, Leiden, The Netherlands; Department of Immunohematology Diagnostics, Sanquin Diagnostic Services, Sanquin, Amsterdam, The Netherlands.
Jia Jennifer DingDepartment of Obstetrics, Gynecology, and Reproductive Sciences, Division of Maternal-Fetal Medicine, Yale School of Medicine, New Haven, CT, USA.
Danijela DrndarevicDepartment of Transfusion, Health Center Užice, Užice, Serbia.
Sejal KabreDepartment of Obstetrics and Gynecology, Bridgeport Hospital/Yale University, Bridgeport, CT, USA.
Shengxin LiuDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Yolentha M SlootwegDepartment of Obstetrics, Leiden University Medical Center, Leiden, The Netherlands; Department of Clinical Transfusion Research, Sanquin Research, Leiden, The Netherlands.
Eleonor TibladDepartment of Medicine Solna, Clinical Epidemiology Division, Karolinska Institutet, Stockholm, Sweden.
Kenneth J MoiseDepartment of Women's Health, Dell Medical School-University of Texas at Austin, Austin, TX, USA; Comprehensive Fetal Care Center, Dell Children's Medical Center, Austin, TX, USA.
Elizabeth A AbelsDepartment of Obstetrics and Gynecology, Bridgeport Hospital/Yale University, Bridgeport, CT, USA; Department of Laboratory Medicine, Yale School of Medicine, New Haven, CT, USA. Electronic address: Elizabeth.AbelsA@gmail.com.

Funding

Duke Women's Reproductive Health Research ScholarsK12HD103083 · NICHD · DUKE UNIVERSITY · PI Cindy Amundsen · 2020 to 2026
$2.2M
NICHD NIH HHS K12 HD103083
6 · The paper itself

Abstract

Anti-Kell (anti-K) alloimmunization is a known cause of severe hemolytic disease of the fetus and newborn (HDFN), yet the utility of a critical maternal antibody titer in guiding clinical management remains debated. We conducted a systematic review and meta-analysis to evaluate the diagnostic accuracy of a maternal anti-K titer threshold of ≥8 for predicting the need for intrauterine intervention due to severe anti-K-mediated HDFN. In parallel, we characterized all reported cases of severe HDFN occurring in the setting of low maternal anti-K titers (<8). Studies were excluded if they lacked reported titers, did not include K-positive or K-unknown fetuses, failed to report fetal outcomes, or included interventions that could lower maternal alloantibody levels. Studies that assessed all alloimmunized patients meeting inclusion criteria were incorporated into a diagnostic test accuracy (DTA) meta-analysis; all eligible studies were included in a qualitative synthesis. Fifty-four studies, comprising 582 fetuses, met inclusion criteria. Of these, 6 studies (350 fetuses) were included in the DTA analysis, which demonstrated a pooled sensitivity of 97.0% (95% CI, 88.7%-99.2%) and specificity of 33.1% (95% CI, 27.9%-38.8%) for an anti-K titer ≥8. Among fetuses affected by severe HDFN, 98.6% (204/207) were associated with maternal anti-K titers ≥8. These findings suggest that severe disease is uncommon in the setting of low anti-K titers and support the use of a critical titer threshold to inform antenatal surveillance. Reevaluation of current clinical guidelines may be warranted in light of these data.

Indexed as

Erythroblastosis, FetalIsoantibodiesKell Blood-Group SystemFemaleHumansInfant, NewbornPregnancyIsoantibodiesKell Blood-Group SystemAlloimmunizationAnti-KHDFNHemolytic diseaseKEL1

Identifiers

PMID40253764
PMCPMC13180262

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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.