ArticleThe Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale2026
The Systemic Inflammation Response Index (SIRI) for Stratifying Mortality Risk in Multidrug-Resistant Lower Respiratory Tract Infections Acquired in Hospital Settings.
Article in The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale, 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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Abstract
Background: Timely risk assessment is important in the management of patients with multidrug-resistant (MDR) hospital-acquired lower respiratory tract infections (LRTI). The Systemic Inflammation Response Index (SIRI), an inflammatory biomarker derived from peripheral neutrophil, monocyte, and lymphocyte counts, has shown prognostic potential across several clinical settings. However, its prognostic value and clinically interpretable threshold in patients with MDR hospital-acquired LRTI remain uncertain. This study aimed to evaluate the association between SIRI and in-hospital mortality in this population. Methods: This single-center retrospective cohort study included 214 patients diagnosed with MDR hospital-acquired LRTI, with all-cause in-hospital mortality as the primary outcome. Cox proportional hazards models were used to assess the prognostic value of SIRI. Restricted cubic splines were applied to examine potential nonlinear associations. A data-driven cutoff was evaluated using Kaplan-Meier survival analysis and stratified receiver operating characteristic (ROC) analysis. Results: When analyzed as a dichotomized variable using the data-driven cutoff, high SIRI was associated with increased in-hospital mortality (hazard ratio [HR] = 2.93, 95% confidence interval [CI]: 1.66-5.14, Conclusion: SIRI may help identify a subgroup of patients with MDR hospital-acquired LRTI who have a higher mortality risk, particularly when interpreted using a threshold of approximately 3.0. Given the modest ROC performance and retrospective single-center design, this cutoff should be regarded as an exploratory risk-stratification signal rather than a stand-alone clinical decision tool. External prospective validation is required before clinical implementation.
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