Why the study?
The prognostic significance of ST-segment deviation on ECG in non-cardiac ICU populations remains unclear.
Does the presence of ST-segment deviation on admission 12-lead ECG predict 30-day all-cause mortality and improve risk stratification beyond the SOFA score in non-cardiac critically ill ICU patients?
Does the presence of ST-segment deviation on admission 12-lead ECG predict 30-day all-cause mortality and improve risk stratification beyond the SOFA score in non-cardiac critically ill ICU patients?
ST-segment deviation on an admission 12-lead ECG is present in 41% of non-cardiac ICU patients and serves as an independent predictor of 30-day all-cause mortality beyond the SOFA score.
STD on admission may refine mortality risk in non-cardiac ICU patients; leaves open incremental value beyond SOFA for prospective validation.
Background/Objectives: ST-segment deviation (STD) on electrocardiography (ECG) may reflect myocardial injury in critically ill patients. However, its prognostic significance in non-cardiac intensive care unit (ICU) populations remains unclear. We aimed to assess the association between STD on ICU admission and 30-day mortality and to evaluate its incremental prognostic value beyond the SOFA score. Methods: In this retrospective single-center study, we included 307 consecutive ICU patients (median age: 64.0 years; 65.5% men). Patients with acute cardiac conditions were excluded. STD was defined as ≥1 mm ST elevation or depression in any lead on standard 12-lead ECG performed on admission. The primary outcome was 30-day all-cause mortality. Prognostic associations were assessed using multivariable Cox regression adjusted for SOFA score. Discriminative performance was evaluated by comparing ROC curves for models with and without STD, with bootstrap-based testing (1000 iterations) to assess significance. Results: STD was present in 126 patients (41.0%) and occurred more frequently in non-survivors (47.6% vs. 36.5%, p = 0.033. In Cox regression, STD was independently associated with 30-day mortality (HR = 1.534; 95% CI: 1.081–2.177; p = 0.017), even after adjustment for SOFA score. This association remained statistically robust in bootstrap validation. The addition of STD amplitude to the SOFA score modestly improved model discrimination with a borderline significant difference between the areas under the curve (ΔAUC = 0.005, p = 0.0581). Conclusions: ST-segment deviation on the admission ECG is an independent predictor of 30-day mortality in non-cardiac critically ill patients and may enhance risk stratification beyond the SOFA score.
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Świstek et al. (2025) studied this question.
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