Evidence map›Paper›PMID 42564011›Full record

ArticleFrontiers in neurology

Neutrophil-to-albumin ratio as a predictor of sepsis-associated encephalopathy in patients with rheumatoid arthritis: an exploratory machine learning study.

Tong Xin, Che Wang, Fan Gong, Yanxia Zhao, Jingjing He, Xiaoping Wang, Daqing Nie, Guorong Jin, Aijing Liu

Abstract read
In one paragraph

Article in Frontiers in neurology. 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

9 authors.

Tong Xin *Department of Rheumatology and Immunology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Che Wang *Department of Medical and Pharmaceutical Informatics, Hebei Medical University, Shijiazhuang, Hebei, China.
Fan GongDepartment of Rheumatology and Immunology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Yanxia ZhaoDepartment of Rheumatology and Immunology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Jingjing HeDepartment of Rheumatology and Immunology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Xiaoping WangDepartment of Rheumatology and Immunology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Daqing NieDepartment of Rheumatology, The Affiliated Hospital to Changchun University of Chinese Medicine, Changchun, Jilin, China.
Guorong JinDepartment of Spine and Traumatic Orthopedics, Beibei Hospital of Chongqing Medical University, Chongqing, China.
Aijing LiuDepartment of Rheumatology and Immunology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and purpose: Patients with rheumatoid arthritis (RA) face an elevated risk of sepsis and its associated neurological complications, most notably sepsis-associated encephalopathy (SAE). Nonetheless, early identification of SAE in this population remains a substantial clinical challenge. To address this gap, we aimed to develop and validate a predictive model that incorporates the neutrophil-to-albumin ratio (NAR) to estimate SAE risk in RA patients with sepsis. Methods: This retrospective multicenter cohort study included a derivation cohort of 89 patients with RA and sepsis from two centers and an independent external validation cohort of 37 patients from a third center. Patients in the derivation cohort were classified into SAE and non-SAE groups. Three machine learning algorithms (LASSO, random forest, and XGBoost) were applied for feature selection, and the optimal model was selected based on area under the receiver operating characteristic curve (AUC). Model performance was evaluated using bootstrap resampling, calibration curves, and decision curve analysis. The final XGBoost model was subsequently evaluated in the external validation cohort. A web-based dynamic prediction tool was developed for clinical application. Kaplan-Meier analysis and Cox regression were performed to evaluate 28-day survival. Results: SAE occurred in 23.6% of patients and was associated with significantly higher 28-day mortality (61.9% vs. 33.8%, Conclusion: The NAR-integrated XGBoost model provides a robust and interpretable tool for early SAE prediction in RA patients with sepsis, showing potential clinical utility for bedside risk stratification.

Indexed as

machine learningneutrophil-to-albumin ratiorheumatoid arthritissepsis-associated encephalopathyXGBoost

Identifiers

PMID42564011
PMCPMC13441812

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.