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外科脓毒症患者持续性炎症免疫抑制分解代谢综合征的早期预测
Authors Zhong M, Pan T, Sun NN, Tan RM, Xu W, Qiu YZ, Liu JL, Chen EZ, Qu HP
Received 28 July 2021
Accepted for publication 30 August 2021
Published 9 September 2021 Volume 2021:14 Pages 5441—5448
DOI https://doi.org/10.2147/IJGM.S331411
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Scott Fraser
Objective: To find the predictors for persistent inflammation-immunosuppression catabolism syndrome in ICU surgical septic patients.
Design: Single center observation study.
Participants: Inclusion: 1) patients ≥ 18, 2) admitted to the ICU after major surgery or transferred to the ICU within 48 hours after the diagnosis of sepsis following the definition of sepsis-3.0. Exclusion: 1) pregnant or lactating patients, 2) patients with severe immune deficiency, 3) patients that expired within 14 days after the diagnosis of sepsis.
Results: A total of 169 participants were included. After propensity score matching, PICS patients were found to have higher intensive care unit (ICU) mortality (32.4% vs 12.4%, p=0.046), 90-day mortality (32.4% vs 9.1%, p=0.006), and ICU-acquired infection rate (44.1% vs 12.7%, p< 0.001), and longer ICU stays (29 vs 11 days, p< 0.001) comparing to non-PICS patients. In multivariate logistic regression, it demonstrated that the SOFA score, Charlson co-morbidity index (CCI), albumin level on the ICU day 1, and lymphocyte count on the ICU day 3 were statistically significant. Sensitivity analysis was conducted with the receiver operating characteristic curve for a combination of the four parameters and the area under the curve was 0.838 (95% confidence interval 0.774– 0.901).
Conclusion: The chronic disease condition and decreased immunity in the early course of sepsis were crucial for PICS. The combination of CCI, SOFA score, albumin level on ICU Day 1 and lymphocyte count on ICU Day 3 can be early predictor for PICS.
Keywords: sepsis, persistent inflammation-immunosuppression catabolism syndrome