# Differential analysis of mean blood glucose levels from venous and fingertip in predicting 30-day mortality among ICU patients with severe trauma: A retrospective study utilizing the MIMIC-IV database

**Authors:** Fei Yin, Zhenguo Qiao, Xiaofei Wu, Yuzhou Xu, Yun Liu, Aleksandra Klisic, Aleksandra Klisic, Aleksandra Klisic, Aleksandra Klisic, Aleksandra Klisic

PMC · DOI: 10.1371/journal.pone.0343401 · PLOS One · 2026-02-23

## TL;DR

This study shows that both venous and fingertip blood glucose levels in ICU trauma patients are linked to 30-day mortality, with venous measurements being more accurate.

## Contribution

The study introduces a comparative analysis of venous and fingertip blood glucose as predictors of mortality in ICU trauma patients using the MIMIC-IV database.

## Key findings

- Venous blood glucose (VMBG) showed better predictive accuracy for 30-day mortality than fingertip blood glucose (FMBG).
- Both VMBG and FMBG had a nonlinear 'J-shaped' relationship with mortality, with specific glucose thresholds identified.
- Early-stage glucose monitoring was significantly associated with 30-day mortality, highlighting the importance of timely tracking.

## Abstract

To investigate the correlation between mean blood glucose of venous (VMBG) and mean blood glucose of fingertip (FMBG) within 30 days and 30-day mortality in trauma patients in intensive care unit (ICU), and to systematically evaluate the prognostic value of early-stage and long-term monitoring intervals.

Utilizing data from the MIMIC-IV database, we employed receiver operating characteristic (ROC) curves, restricted cubic splines (RCS), and Cox proportional hazards models to assess glucose-outcome relationships. Sensitivity analyses using complete datasets, propensity score matching (PSM), and subgroup analyses were conducted to verify result robustness. Furthermore, to minimize the bias of immortal time, the Landmark analysis was employed to investigate the correlation between the early-stage VMBG, FMBG and 30-day mortality rate. Secondary outcomes included 90-, 180-, and 360-day all-cause mortality.

A total of 2,699 patients were enrolled in the study. The AUC values (95% CI) for VMBG and FMBG were 0.705 (0.675-0.735) and 0.640 (0.608-0.672), respectively. VMBG demonstrated superior predictive ability for 30-day mortality compared to FMBG (Z=5.833, P<0.001). Multivariate-adjusted Cox regression revealed independent associations between VMBG, FMBG, and 30-day mortality, with HRs of 1.019 (1.016-1.023) and 1.009 (1.006-1.013), respectively. RCS analysis further indicated a nonlinear “J-shaped” relationship between VMBG, FMBG, and outcomes (P for nonlinearity<0.001), with two thresholds at 88.1 mg/dL and 125.4 mg/dL for VMBG, and 95.4 mg/dL and 134.0 mg/dL for FMBG. The threshold values for FMBG were observed to be higher than those of VMBG. According to the thresholds of VMBG and FMBG, patients were stratified into hypoglycemic, normoglycemic, and hyperglycemic groups, respectively. Whether in the pre-PSM or post-PSM cohort, with the normoglycemic group as the reference, both the hypoglycemic and hyperglycemic groups of VMBG and FMBG were associated with an increased 30-day mortality rate. Subgroup analyses revealed that the impact of elevated VMBG and FMBG on prognosis was more pronounced in patients aged <65 years, non-White individuals, and those without diabetes(P for interaction<0.05). VMBG and FMBG during different time intervals were all non - linearly correlated with the 30 - day mortality rate. The Landmark analysis indicated that during the early-stages, there was also a significant statistical correlation among VMBG, FMBG and prognosis. For secondary outcomes, VMBG and FMBG also showed significant associations with 90-day, 180-day, and 360-day all-cause mortality.

In ICU trauma patients, both VMBG and FMBG across various time intervals exhibited nonlinear associations with 30-day mortality. Although venous blood glucose monitoring typically demonstrated higher prognostic predictive accuracy compared to fingertip measurements, the early - warning value of fingertip blood glucose should not be overlooked. In clinical monitoring, the characteristics of both measurement methods should be comprehensively recognized.

## Linked entities

- **Diseases:** trauma (MONDO:0021178)

## Full-text entities

- **Genes:** GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, SH2B2 (SH2B adaptor protein 2) [NCBI Gene 10603] {aka APS}, SKAP2 (src kinase associated phosphoprotein 2) [NCBI Gene 8935] {aka PRAP, RA70, SAPS, SCAP2, SKAP-HOM, SKAP55R}, GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}
- **Diseases:** liver disease (MESH:D008107), inflammatory (MESH:D007249), shock (MESH:D012769), Injury (MESH:D014947), hyperglycemia (MESH:D006943), critically ill (MESH:D016638), metabolic disturbances (MESH:D024821), traumatic brain injury (MESH:D000070642), ORCID iD (MESH:C535742), GV (MESH:C537362), cancer (MESH:D009369), diabetes (MESH:D003920), endothelial damage (MESH:D014652), cerebral hyperemia (MESH:D006940), AKI (MESH:D058186), cerebral edema (MESH:D001929), Distant Organ Dysfunction (MESH:D009102), microcirculation disorder (MESH:D009358), metabolic disorder (MESH:D008659), Kidney Dis (MESH:D007680), hypoglycemic (MESH:C000721848), APS III (MESH:D000208), death (MESH:D003643), hyperglycemic (MESH:D006944), hypothermia (MESH:D007035), cerebrovascular disease (MESH:D002561), insulin resistance (MESH:D007333), infections (MESH:D007239), hypoglycemia (MESH:D007003), coagulopathy (MESH:D001778), peripheral hypoperfusion (MESH:D010523), neuronal damage (MESH:D009410), renal disease (MESH:D007674), congestive heart failure (MESH:D006333), Coma (MESH:D003128), chronic pulmonary disease (MESH:D002908), necrosis (MESH:D009336), microcirculation disorder[1 (MESH:C538557), septic (MESH:D001170)
- **Chemicals:** oxygen (MESH:D010100), epinephrine (MESH:D004837), cortisol (MESH:D006854), blood glucose (MESH:D001786), norepinephrine (MESH:D009638), FGV (-), bicarbonate (MESH:D001639), catecholamine (MESH:D002395), Glucose (MESH:D005947), creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12928430/full.md

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Source: https://tomesphere.com/paper/PMC12928430