# From microbial dynamics to risk prediction: a nomogram-based model for hospital-acquired infections in rehabilitation settings

**Authors:** Bangying Yu, Yunping Guo, Chenchao Wu, Meidan Fang, Weiwei Ma, Ali Li, Minhua Zheng, Jing Wang

PMC · DOI: 10.3389/fcimb.2026.1723835 · Frontiers in Cellular and Infection Microbiology · 2026-02-17

## TL;DR

This study develops a predictive model for hospital-acquired infections in rehabilitation patients using clinical data and microbial trends.

## Contribution

A novel nomogram-based model and web tool for predicting HAIs in rehabilitation settings using clinical and microbiological data.

## Key findings

- Key pathogens like Klebsiella pneumoniae and Pseudomonas aeruginosa showed distinct temporal trends in infections.
- The nomogram model achieved good performance with an AUC of 0.741 internally and 0.799 for the simplified score in external validation.
- Age, prothrombin time, D-dimer, and C-reactive protein were identified as significant risk factors for HAIs.

## Abstract

To analyze microbial infection patterns and develop a predictive model for hospital−acquired infection (HAI) in rehabilitation inpatients.

A retrospective cohort study included 635 patients admitted between August 2018 and February 2025; 4,523 clinical specimens were analyzed. After exclusions, 361 patients were classified into HAI (n=213) and non−HAI (n=148) groups. Significant variables from univariate analysis were incorporated into LASSO and logistic regression to build a prediction model, which was visualized as a nomogram. A simplified scoring tool and a web application were developed. External validation was performed using 332 patients from three hospitals.

Among 4,523 specimens from 635 rehabilitation inpatients, the overall positivity rate was 61.2%. Sputum cultures were most frequent, while urine cultures increased over time. Key pathogens like Klebsiella pneumoniae and Pseudomonas aeruginosa showed distinct temporal trends. High antimicrobial resistance was prevalent, especially among multidrug-resistant organisms, with carbapenem-resistant Enterobacteriaceae being the most common MDRO type. Regression analyses identified age, prothrombin time, D−dimer, and C−reactive protein as key risk factors of HAI, while albumin and high−density lipoprotein cholesterol were protective.The nomogram demonstrated good discriminatory ability and calibration internally (AUC = 0.741) and maintained robust, generalizable performance in external validation, with the simplified risk score achieving an AUC of 0.799, while also showing stable performance before and during the COVID-19 pandemic. The tool is publicly accessible at: https://wjing-enzemed.shinyapps.io/hospital-infection-risk-en/.

Our findings elucidate key microbiological patterns and predictive factors for HAI in rehabilitation inpatients. The developed model, utilizing readily available clinical parameters, shows robust and generalizable performance in stratifying infection risk, which can aid early intervention and optimize resource allocation in rehabilitation care.

## Linked entities

- **Species:** Klebsiella pneumoniae (taxon 573), Pseudomonas aeruginosa (taxon 287), Enterobacteriaceae (taxon 543)

## Full-text entities

- **Genes:** SAA [NCBI Gene 6287], UROD (uroporphyrinogen decarboxylase) [NCBI Gene 7389] {aka PCT, UPD}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** fever (MESH:D005334), neurological dysfunction (MESH:D009461), microbial (MESH:D015163), pneumonia (MESH:D011014), hypoalbuminemia (MESH:D034141), cryptococcal infection (MESH:D016919), dysbiosis (MESH:D064806), impaired antimicrobial defense (MESH:D060825), critically ill (MESH:D016638), inflammation (MESH:D007249), trauma (MESH:D014947), skin/soft tissue infections (MESH:D018461), Respiratory infections (MESH:D012141), cerebrospinal fluid (MESH:D002559), fungal (MESH:D009181), PT (MESH:D007020), infectious diseases (MESH:D003141), Bloodstream infections (MESH:D018805), MRSA (MESH:D013203), neurological impairments (MESH:D009422), colonization (MESH:D003108), CoNS (MESH:D064726), tuberculosis (MESH:D014376), COVID-19 (MESH:D000086382), bacteremia (MESH:D016470), immune dysfunction (MESH:D007154), coagulation (MESH:D001778), infection (MESH:D007239), urinary tract and bloodstream infections (MESH:D014552), cough (MESH:D003371), endothelial injury (MESH:D057772), pressure ulcers (MESH:D003668), hypoproteinemia (MESH:D007019), Hospital-acquired Infections (MESH:D003428), malnutrition (MESH:D044342), CRBSI (MESH:D055499)
- **Chemicals:** chlorhexidine (MESH:D002710), moxifloxacin (MESH:D000077266), cholesterol (MESH:D002784), erythromycin (MESH:D004917), methicillin (MESH:D008712), clindamycin (MESH:D002981), levofloxacin (MESH:D064704), carbapenem (MESH:D015780), penicillin G (MESH:D010400), uric acid (MESH:D014527), ciprofloxacin (MESH:D002939), cefoxitin (MESH:D002440), phosphorus (MESH:D010758), alcohol (MESH:D000438), calcium (MESH:D002118), magnesium (MESH:D008274), glucose (MESH:D005947), Oxacillin (MESH:D010068), ticarcillin/clavulanic acid (MESH:C043215), imipenem (MESH:D015378), Ampicillin (MESH:D000667), iodine (MESH:D007455), trimethoprim-sulfamethoxazole (MESH:D015662), lipid (MESH:D008055), macrolides (MESH:D018942), quinolones (MESH:D015363), abumin (-), nitrofurantoin (MESH:D009582), Penicillin (MESH:D010406)
- **Species:** Fungi (kingdom) [taxon 4751], Pseudomonas aeruginosa (species) [taxon 287], Mus musculus (house mouse, species) [taxon 10090], Staphylococcus hominis (species) [taxon 1290], Klebsiella pneumoniae (species) [taxon 573], Escherichia coli (E. coli, species) [taxon 562], Klebsiella aerogenes (species) [taxon 548], Enterococcus faecium (species) [taxon 1352], Enterobacteriaceae (enterobacteria, family) [taxon 543], Acinetobacter baumannii (species) [taxon 470], Serratia marcescens (species) [taxon 615], Staphylococcus aureus (species) [taxon 1280], Homo sapiens (human, species) [taxon 9606], Staphylococcus epidermidis (species) [taxon 1282], Haemophilus influenzae (species) [taxon 727], Stenotrophomonas maltophilia (species) [taxon 40324]

## Full text

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## Figures

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## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12953564/full.md

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Source: https://tomesphere.com/paper/PMC12953564