QT interval prolongation and mortality in sepsis: a retrospective cohort study from the MIMIC-IV database
- PMID: 41545939
- PMCID: PMC12825248
- DOI: 10.1186/s12872-026-05519-z
QT interval prolongation and mortality in sepsis: a retrospective cohort study from the MIMIC-IV database
Abstract
Background: Sepsis is a leading cause of mortality in patients admitted to the intensive care unit (ICU), and QT prolongation (QTP) is common in critically ill patients. However, the association between QTP and long-term mortality in sepsis remains unexamined.
Methods: This retrospective study included patients meeting the Sepsis-3 criteria upon ICU admission between 2008 and 2019, identified from the Intensive Care Medical Information Mart IV (MIMIC-IV) database. Patients were categorized into two groups based on the presence (QTP group) or absence (non-QTP group) of QTP. Clinical outcomes were compared between patients with and without QTP. We used Kaplan–Meier analysis to compare the 28-day and 1-year all-cause mortality between septic patients with and without QTP. Furthermore, we utilized multivariate regression, propensity score matching (PSM), inverse probability of treatment weighting (IPTW), and a survey-weighted generalized linear model to assess the association of QTP with 28-day and 1-year all-cause mortality in patients with sepsis.
Results: A total of 4,845 patients were enrolled, with 1,424 (29.4%) in the QTP group. Compared with the non-QTP patients, the QTP group had significantly higher 28-day mortality (19.17% vs. 13.15%, p < 0.001) and 1-year mortality (33.99% vs. 24.82%, p < 0.001). Following PSM, the QTP group exhibited significantly higher mortality at both 28-day mortality (18.81% vs. 15.51%, p < 0.05) and 1-year mortality (33.60% vs. 27.64%, p < 0.001) compared to the non-QTP group. Patients in the QTP group exhibited increased risk of both 28-day mortality (adjusted OR = 1.34, 95% CI: 1.11–1.61, p = 0.002) and 1-year mortality (adjusted OR = 1.40, 95% CI: 1.20–1.63, p < 0.001).
Conclusion: The incidence of QTP was significantly elevated in ICU patients with sepsis compared with the general population and QTP was associated with increased risk-adjusted 28-day and 1-year mortality in ICU patients with sepsis.
Supplementary Information: The online version contains supplementary material available at 10.1186/s12872-026-05519-z.
Keywords: Mortality; Multivariable analysis; Propensity score matching; QT prolongation; Sepsis.
Conflict of interest statement
Declarations. Ethics approval and consent to participate: The MIMIC database was approved by the Institutional Review Boards (IRBs) of the Massachusetts Institute of Technology and Beth Israel Deaconess Medical Center. This study adhered to the ethical principles of the Declaration of Helsinki and was approved by both institutions. As patient data was de-identified, individual informed consent was not required. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests.
Figures
References
-
- PenttiM R, Borys S, Leonard S G, James J B, Rory C, Barbara J D, et al. AHA/ACCF/HRS recommendations for the standardization and interpretation of the electrocardiogram: part IV: the ST segment, T and U waves, and the QT interval: a scientific statement from the American Heart Association Electrocardiography and Arrhythmias Committee, Council on Clinical Cardiology; the American College of Cardiology Foundation; and the Heart Rhythm Society. Endorsed by the International Society for Computerized Electrocardiology. J Am Coll Cardiol. 2009;53(11):982–91. 10.1016/j.jacc.2008.12.014. - PubMed
-
- Syed Raza S, Ki P, Richard A. Long QT Syndrome: A Comprehensive Review of the Literature and Current Evidence. Curr Probl Cardiol. 2018;44(3):92–106. 10.1016/j.cpcardiol.2018.04.002. - PubMed
-
- DavidP, Eric H, Julie A S, Garrett C, Marjorie F, Ann W, et al. High prevalence of corrected QT interval prolongation in acutely ill patients is associated with mortality: results of the QT in Practice (QTIP) Study. Crit Care Med. 2011;40(2):394–9. 10.1097/CCM.0b013e318232db4a. - PubMed
LinkOut - more resources
Full Text Sources
Miscellaneous
