This retrospective cohort study used the MIMIC-IV database to analyze 11,289 non-diabetic patients with sepsis. The intervention was insulin administration, with a comparator of untreated (no insulin). The primary outcome was 28-day mortality, and secondary outcomes were ICU and hospital length of stay, with a 28-day follow-up.
The main results showed a reduced mortality rate in the insulin group, with a hazard ratio of 0.63-0.67 (p < 0.001). However, the insulin group had a longer median ICU length of stay (5 days vs. 4 days, p < 0.001) and a longer hospital length of stay (12 days vs. 10 days, p < 0.001). Absolute numbers for these outcomes were not reported.
Safety and tolerability data, including adverse events, serious adverse events, and discontinuations, were not reported. Key limitations include the observational design, which cannot prove causality, and the need for further research to elucidate the underlying mechanism and validate these findings.
The practice relevance suggests insulin therapy may improve survival but does not shorten hospitalization. The study evaluates an association; causality is not explicitly claimed. Given the observational nature, clinicians should interpret these findings cautiously.
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ObjectiveTo evaluate the association between insulin administration and 28-day mortality in non-diabetic patients with sepsis.MethodsA retrospective analysis of 11,289 critically ill patients with sepsis in the MIMIC-IV database was conducted. Propensity score matching (PSM) was employed to balance baseline characteristics between the insulin-treated and untreated cohorts. The primary outcome was 28-day mortality; secondary outcome measures included intensive care unit (ICU) and hospital length of stay (LOS). The association between insulin use and mortality was evaluated via Cox regression analysis, and survival was estimated using Kaplan-Meier curves and log-rank tests.ResultsOf the 11,289 non-diabetic patients meeting the inclusion criteria, 1,172 (10.4%) received insulin. After PSM, the final analysis included 2,960 patients (782 in the insulin group and 2,178 in the control group). Baseline characteristics were well-balanced, with standardized mean differences (SMDs) close to zero. Insulin use was significantly associated with a reduced 28-day mortality rate (hazard ratio [HR] 0.63-0.67, p < 0.001), a finding that remained consistent across all subgroups. However, patients receiving insulin therapy had a longer median ICU LOS (5 days vs. 4 days, p < 0.001) and a more extended hospital LOS (12 days vs. 10 days, p < 0.001).ConclusionInsulin therapy may improve the survival rate among non-diabetic patients with sepsis but does not shorten the duration of hospitalization. Further research is warranted to elucidate the underlying mechanism and validate these findings.