Evaluating the influence MRSA Co-infection on 28-day mortality among sepsis patients: insights from the MIMIC-IV database

BackgroundSepsis remains a leading cause of mortality in intensive care units (ICUs), with methicillin-resistant Staphylococcus aureus (MRSA) infections presenting significant treatment challenges. The impact of MRSA co-infection on sepsis outcomes necessitates further exploration.MethodsWe conducte...

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Main Authors: Yi-Chang Zhao, Jia-Kai Li, Yu-kun Zhang, Zhi-Hua Sun, Rao Fu, Bi-Kui Zhang, Miao Yan
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-03-01
Series:Frontiers in Pharmacology
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Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2025.1534107/full
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author Yi-Chang Zhao
Yi-Chang Zhao
Jia-Kai Li
Jia-Kai Li
Yu-kun Zhang
Yu-kun Zhang
Zhi-Hua Sun
Zhi-Hua Sun
Rao Fu
Rao Fu
Bi-Kui Zhang
Bi-Kui Zhang
Miao Yan
Miao Yan
author_facet Yi-Chang Zhao
Yi-Chang Zhao
Jia-Kai Li
Jia-Kai Li
Yu-kun Zhang
Yu-kun Zhang
Zhi-Hua Sun
Zhi-Hua Sun
Rao Fu
Rao Fu
Bi-Kui Zhang
Bi-Kui Zhang
Miao Yan
Miao Yan
author_sort Yi-Chang Zhao
collection DOAJ
description BackgroundSepsis remains a leading cause of mortality in intensive care units (ICUs), with methicillin-resistant Staphylococcus aureus (MRSA) infections presenting significant treatment challenges. The impact of MRSA co-infection on sepsis outcomes necessitates further exploration.MethodsWe conducted a retrospective observational cohort study using the Medical Information Mart for Critical Care IV (MIMIC-IV-2.2) database. This cohort study included sepsis patients, scrutinizing baseline characteristics, MRSA co-infection, antimicrobial susceptibility, and their relations to mortality through Cox regression and Kaplan-Meier analyses.ResultsAmong 453 sepsis patients analyzed, significant baseline characteristic differences were observed between survivors (N = 324) and non-survivors (N = 129). Notably, non-survivors were older (70.52 ± 14.95 vs. 64.42 ± 16.05, P < 0.001), had higher lactate levels (2.82 ± 1.76 vs. 2.04 ± 1.56 mmol/L, P < 0.001), and higher SOFA scores (8.36 ± 4.18 vs. 6.26 ± 3.65, P < 0.001). Cox regression highlighted SOFA score (HR = 1.122, P = 0.003), body temperature (HR = 0.825, P = 0.048), and age (HR = 1.030, P = 0.004) as significant predictors of 28-day mortality. MRSA co-infection was found in 98.7% of cases without a significant effect on 28-day mortality (P = 0.9). However, sensitivity to cephalosporins, meropenem, and piperacillin/tazobactam was associated with reduced mortality. The area under the ROC curve for the combined model of age, SOFA, and body temperature was 0.73, indicating a moderate predictive value for 28-day mortality.ConclusionWhile MRSA co-infection’s direct impact on 28-day sepsis mortality is minimal, antimicrobial sensitivity, especially to cephalosporins, meropenem, and piperacillin/tazobactam, plays a critical role in improving outcomes, underscoring the importance of antimicrobial stewardship and personalized treatment strategies in sepsis care.
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spelling doaj-art-b849bbcccd5c4c5b8789c5fca6512e6e2025-08-20T02:47:45ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122025-03-011610.3389/fphar.2025.15341071534107Evaluating the influence MRSA Co-infection on 28-day mortality among sepsis patients: insights from the MIMIC-IV databaseYi-Chang Zhao0Yi-Chang Zhao1Jia-Kai Li2Jia-Kai Li3Yu-kun Zhang4Yu-kun Zhang5Zhi-Hua Sun6Zhi-Hua Sun7Rao Fu8Rao Fu9Bi-Kui Zhang10Bi-Kui Zhang11Miao Yan12Miao Yan13Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, Hunan, ChinaInternational Research Center for Precision Medicine, Transformative Technology and SoftwareServices, Changsha, Hunan, ChinaDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, Hunan, ChinaInternational Research Center for Precision Medicine, Transformative Technology and SoftwareServices, Changsha, Hunan, ChinaDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, Hunan, ChinaXiangya School of Medicine, Central South University, School of Pharmacy, Changsha, Hunan, ChinaInternational Research Center for Precision Medicine, Transformative Technology and SoftwareServices, Changsha, Hunan, ChinaSchool of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu, ChinaDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, Hunan, ChinaInternational Research Center for Precision Medicine, Transformative Technology and SoftwareServices, Changsha, Hunan, ChinaDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, Hunan, ChinaInternational Research Center for Precision Medicine, Transformative Technology and SoftwareServices, Changsha, Hunan, ChinaDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, Hunan, ChinaInternational Research Center for Precision Medicine, Transformative Technology and SoftwareServices, Changsha, Hunan, ChinaBackgroundSepsis remains a leading cause of mortality in intensive care units (ICUs), with methicillin-resistant Staphylococcus aureus (MRSA) infections presenting significant treatment challenges. The impact of MRSA co-infection on sepsis outcomes necessitates further exploration.MethodsWe conducted a retrospective observational cohort study using the Medical Information Mart for Critical Care IV (MIMIC-IV-2.2) database. This cohort study included sepsis patients, scrutinizing baseline characteristics, MRSA co-infection, antimicrobial susceptibility, and their relations to mortality through Cox regression and Kaplan-Meier analyses.ResultsAmong 453 sepsis patients analyzed, significant baseline characteristic differences were observed between survivors (N = 324) and non-survivors (N = 129). Notably, non-survivors were older (70.52 ± 14.95 vs. 64.42 ± 16.05, P < 0.001), had higher lactate levels (2.82 ± 1.76 vs. 2.04 ± 1.56 mmol/L, P < 0.001), and higher SOFA scores (8.36 ± 4.18 vs. 6.26 ± 3.65, P < 0.001). Cox regression highlighted SOFA score (HR = 1.122, P = 0.003), body temperature (HR = 0.825, P = 0.048), and age (HR = 1.030, P = 0.004) as significant predictors of 28-day mortality. MRSA co-infection was found in 98.7% of cases without a significant effect on 28-day mortality (P = 0.9). However, sensitivity to cephalosporins, meropenem, and piperacillin/tazobactam was associated with reduced mortality. The area under the ROC curve for the combined model of age, SOFA, and body temperature was 0.73, indicating a moderate predictive value for 28-day mortality.ConclusionWhile MRSA co-infection’s direct impact on 28-day sepsis mortality is minimal, antimicrobial sensitivity, especially to cephalosporins, meropenem, and piperacillin/tazobactam, plays a critical role in improving outcomes, underscoring the importance of antimicrobial stewardship and personalized treatment strategies in sepsis care.https://www.frontiersin.org/articles/10.3389/fphar.2025.1534107/fullMRSAantimicrobial susceptibilitysepsis28-day mortalityMIMIC database
spellingShingle Yi-Chang Zhao
Yi-Chang Zhao
Jia-Kai Li
Jia-Kai Li
Yu-kun Zhang
Yu-kun Zhang
Zhi-Hua Sun
Zhi-Hua Sun
Rao Fu
Rao Fu
Bi-Kui Zhang
Bi-Kui Zhang
Miao Yan
Miao Yan
Evaluating the influence MRSA Co-infection on 28-day mortality among sepsis patients: insights from the MIMIC-IV database
Frontiers in Pharmacology
MRSA
antimicrobial susceptibility
sepsis
28-day mortality
MIMIC database
title Evaluating the influence MRSA Co-infection on 28-day mortality among sepsis patients: insights from the MIMIC-IV database
title_full Evaluating the influence MRSA Co-infection on 28-day mortality among sepsis patients: insights from the MIMIC-IV database
title_fullStr Evaluating the influence MRSA Co-infection on 28-day mortality among sepsis patients: insights from the MIMIC-IV database
title_full_unstemmed Evaluating the influence MRSA Co-infection on 28-day mortality among sepsis patients: insights from the MIMIC-IV database
title_short Evaluating the influence MRSA Co-infection on 28-day mortality among sepsis patients: insights from the MIMIC-IV database
title_sort evaluating the influence mrsa co infection on 28 day mortality among sepsis patients insights from the mimic iv database
topic MRSA
antimicrobial susceptibility
sepsis
28-day mortality
MIMIC database
url https://www.frontiersin.org/articles/10.3389/fphar.2025.1534107/full
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