Evidence map›Paper›PMID 41920210›Full record

ArticleClinical and experimental medicine2026

Development and validation of a risk prediction model and management strategy for red blood cell irregular antibodies a retrospective cohort study of 521 patients.

Liang Wang, Jinjin Yang, Zhaopei Guo, Dongbiao Qiu, Ya Fu, Yongjie Xu

Abstract read
In one paragraph

Article in Clinical and experimental medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Liang Wang *Department of Hepatopancreatobiliary Surgery, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China.
Jinjin Yang *Department of Ultrasound Medicine, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China.
Zhaopei GuoDepartment of Laboratory Medicine, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China.
Dongbiao QiuDepartment of Blood Transfusion, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China. qdbsxk@sina.com.
Ya FuDepartment of Laboratory Medicine, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China. hzxfy@fjmu.edu.cn.
Yongjie XuDepartment of Blood Transfusion, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, China. xuyongjie@fjmu.edu.cn.

Funding

the Innovation of Science and Technology, Fujian Province 2025Y9156the National Natural Science Foundation 82572634
6 · The paper itself

Abstract

This study aimed to systematically identify independent risk factors for difficult cross-matching and to construct a predictive model for early clinical risk warning and stratified management. A derivation cohort of 521 patients with positive red blood cell irregular antibody screening results was retrospectively enrolled. Based on the screening results, patients were categorized into a 1-2 positive wells group (n = 428) and a 3 positive wells group (n = 93). Univariate and multivariate logistic regression analyses were performed to identify independent predictors of difficult cross-matching. A simplified clinical risk scoring system was developed based on the regression coefficients, and the predictive performance of the model was evaluated. Multivariate analysis identified six independent influencing factors: 3 positive wells (OR = 2.34, 95% CI: 1.18-4.65), diagnosis of multiple myeloma (OR = 5.05, 95% CI: 2.54-10.05), hospitalization in the hematology department (OR = 2.25, 95% CI: 1.27-3.98), age ≥ 60 years (OR = 1.97, 95% CI: 1.12-3.48), pregnancy-related diseases (protective factor; OR = 0.24, 95% CI: 0.08-0.73), and difficult blood typing (OR = 4.57, 95% CI: 2.30-9.08). The risk scoring model incorporating these factors demonstrated good predictive performance, with an area under the curve (AUC) of 0.819 (95% CI: 0.766-0.872), a sensitivity of 74.4%, and a specificity of 76.5%. Patients were stratified into three risk tiers (low, medium, and high) based on their scores, with corresponding differentiated clinical management pathways and resource allocation plans established. This study successfully identified and quantified key clinical and laboratory predictors for difficult cross-matching. The established risk scoring model demonstrates good predictive accuracy, providing a reliable tool for precise pre-transfusion risk assessment. The stratified management system based on this model facilitates a shift from reactive to proactive intervention in transfusion workflows, offering significant clinical translational value for optimizing blood bank resource allocation and ensuring transfusion safety for high-risk patients.

Indexed as

Blood Grouping and CrossmatchingErythrocytesIsoantibodiesAdultAgedFemaleHumansMaleMiddle AgedPrediction AlgorithmsRetrospective StudiesRisk AssessmentRisk FactorsIsoantibodiesDifficult cross-matchingIrregular red blood cell antibodiesPrediction modelRisk scoreStratified management

Identifiers

PMID41920210
PMCPMC13079509

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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.