Evidence map›Paper›PMID 42602147›Full record

ArticleFrontiers in neurology2026

Frailty combined with nutritional risk for predicting stroke-associated pneumonia: a cohort study based on a nomogram model.

Kailibinuer Aimaier, Jiarui Xiong, Chunrui Liu, Shuhong Zhou, Guangwei Liu, Feng Li

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Article in Frontiers in neurology, 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.

Kailibinuer AimaierDepartment of Neurology & Nursing, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Jiarui XiongDepartment of Neurology & Nursing, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Chunrui LiuDepartment of Neurology & Nursing, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Shuhong ZhouCollege of Culture and Tourism, Chongqing Business Vocational College, Chongqing, China.
Guangwei LiuDepartment of Neurology & Nursing, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Feng LiDepartment of Neurology & Nursing, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Stroke-associated pneumonia (SAP) is a common and serious complication in patients with acute severe stroke, and existing risk assessment tools have limited predictive accuracy in critically ill populations. This study innovatively incorporated frailty and nutritional risk, which reflect stress tolerance and overall physiological reserve, into an early SAP prediction model. Methods: A retrospective cohort study was conducted on 293 critically ill stroke patients admitted to the Neurocritical Care Unit of the First Affiliated Hospital of Chongqing Medical University between 2013 and 2024. Collect clinical characteristics and laboratory indicators of patients, assess their frailty status and nutritional risk, and analyze the additive interaction effect between the two on the occurrence of SAP. Independent predictors were identified through multivariate logistic regression and incorporated into a visual nomogram. Model performance was evaluated using the area under the receiver operating characteristic curve (AUC), calibration plots, decision curve analysis, and 10-fold cross-validation. Results: A total of 293 patients with severe stroke were included in this study, among whom 126 (43%) developed SAP. The results of the additive interaction analysis showed a positive additive interaction between frailty and nutritional risk in the development of SAP, with an attributable proportion (AP) of 0.711 (95% CI = 0.358 ~ 1.065) and a synergy index (SI) of 3.694 (95% CI = 1.200 ~ 11.364). A SAP risk prediction model incorporating age, nasogastric tube use, neutrophil-to-lymphocyte ratio (NLR), frailty status, and nutritional risk demonstrated good discriminative performance, with an area under the curve (AUC) of 0.848, which was significantly higher than that of the conventional SAP prediction score (ISAN score: AUC = 0.589). Internal validation showed that the model achieved an accuracy of 73.93%, sensitivity of 77.30%, and specificity of 71.95%, indicating good stability. The calibration curve demonstrated good agreement between predicted and observed outcomes. Decision curve analysis (DCA) indicated that the model provided substantially greater clinical net benefit than the ISAN score. Discussion: This study is the first to integrate frailty and nutritional risk into an SAP prediction model, significantly improving early risk identification and providing an innovative, practical tool for precision prevention and targeted intervention in critically ill stroke patients.

Indexed as

FrailtyNomogramsNutritional StatusPneumoniaStrokeAgedAged, 80 and overCohort StudiesFemaleHumansMaleMiddle AgedRetrospective StudiesRisk AssessmentRisk Factorsfrailtynutritionpulmonary infectionrisk predictionstroke

Identifiers

PMID42602147
PMCPMC13473277

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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.