Evidence map›Paper›PMID 39940054›Full record

ArticleEuropean journal of medical research2025

Constructing a logistic regression-based prediction model for subsequent early pregnancy loss in women with pregnancy loss.

Nan Ding, Peili Wang, Xiaoping Wang, Fang Wang

Abstract read
In one paragraph

Article in European journal of medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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

4 authors.

Nan DingReproductive Medicine Center, The Second Hospital of Lanzhou University, No.82, Cuiying Road, Chengguan District, Lanzhou, Gansu, China.
Peili WangReproductive Medicine Center, The Second Hospital of Lanzhou University, No.82, Cuiying Road, Chengguan District, Lanzhou, Gansu, China.
Xiaoping WangReproductive Medicine Center, The Second Hospital of Lanzhou University, No.82, Cuiying Road, Chengguan District, Lanzhou, Gansu, China.
Fang WangReproductive Medicine Center, The Second Hospital of Lanzhou University, No.82, Cuiying Road, Chengguan District, Lanzhou, Gansu, China. ery_fwang@lzu.edu.cn.

Funding

the Medical Innovation and Development Project of Lanzhou University No. lzuyxcx-2022-137the Science Foundation of Lanzhou University No. 071100132 and 071100186the Science Foundation of Lanzhou University Second Hospital Grant No. YJS-BD-19
6 · The paper itself

Abstract

objectivesThe aim of this study is to construct a nomogram for predicting subsequent early pregnancy loss in women with a history of pregnancy loss, which may increase well-being and the capacity for managing reproductive options. MATERIALS AND

methodsWe conducted a retrospective analysis of medical records from women with a history of pregnancy loss at the Reproductive Medicine Center of Lanzhou University Second Hospital between January 2019 and December 2022. A cohort of 718 patients was selected for the study. We structured our data into a training set of 575 cases (80% of the cohort) and a test set of 143 cases (20%). To identify significant predictors, we applied a stepwise forward algorithm guided by the Akaike Information Criterion (AIC) to the training set. Model validation was conducted using the test set. For the validation process, we employed various methods to assess the predictive power and accuracy of the model. Receiver Operating Characteristic (ROC) curves provided insights into the model's ability to distinguish between outcomes effectively. Calibration curves assessed the accuracy of the probability predictions against actual outcomes. The clinical utility of the model was further evaluated through Decision Curve Analysis, which quantified the net benefits at various threshold probabilities. In addition, a nomogram was developed to visually represent the risk factors.

resultsAmong the 36 candidate variables initially considered, 10 key predictors were identified through logistic regression analysis and incorporated into the nomogram. These selected variables include age, education, thrombin time (TT), antithrombin III (AT-III), D-dimer levels, 25-hydroxy Vitamin D, immunoglobulin G(IgG), complement components C4, anti-cardiolipin antibody (ACA) and lupus anticoagulant (LA). In addition, based on clinical experience, the number of previous pregnancy losses was also included as a predictive variable. The prediction model revealed an area under the curve (AUC) of approximately 0.717 for the training set and 0.725 for the validation set. Calibration analysis indicated satisfactory goodness-of-fit, with a Hosmer-Lemeshow test yielding a χ2 value of 7.78 (p = 0.55). Decision curve analysis confirmed the clinical utility of the nomogram. Internal validation confirmed the robust performance of the predictive model.

conclusionsThe constructed nomogram provides a valuable tool for predicting subsequent early pregnancy loss in women with a history of pregnancy loss. This nomogram can assist clinicians and patients in making informed decisions regarding the management of pregnancy and improving clinical outcomes.

trial registrationThis study was registered in the Chinese Clinical Trial Registry under the registration number ChiCTR2000039414 on October 27, 2020. The registration was done retrospectively.

Indexed as

Abortion, SpontaneousNomogramsAdultFemaleHumansLogistic ModelsPregnancyRetrospective StudiesRisk FactorsROC CurveEarly pregnancy lossLogistic regressionPrediction model

Identifiers

PMID39940054
PMCPMC11823067

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.