{"title":"头孢哌酮-舒巴坦联合治疗重症监护病房耐碳青霉烯鲍曼不动杆菌血流感染的疗效:一项多中心回顾性倾向评分匹配研究","authors":"Sheng-Huei Wang, Yu-Chao Lin, Ming-Cheng Chan, Kuang-Yao Yang, Chau-Chyun Sheu, Biing-Ru Wu, Wei-Hsuan Huang, Jia-Yih Feng, Chia-Min Chen, Zi-Xeng Weng, Chung-Kan Peng, Shih-En Tang","doi":"10.1186/s12879-025-11205-w","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>In this study, we aimed to evaluate the efficacy of cefoperazone-sulbactam-containing (CSC) combination therapy for carbapenem-resistant Acinetobacter baumannii (CRAB) bloodstream infections (BSI) patients in intensive care unit (ICU).</p><p><strong>Methods: </strong>This multicenter, retrospective cohort study initially included 407 patients with CRAB BSI in the ICU between 2015 and 2019. Patients were divided into the CSC- and non-cefoperazone-sulbactam-containing (NCSC) groups. Outcomes including mortality, clinical failure, and microbiological eradication were compared after time-window bias adjustment and propensity score matching.</p><p><strong>Results: </strong>There was no statistical difference in baseline characteristics and disease severity between the CSC (n = 50) and NCSC groups (n = 150) after propensity score matching. The CSC group had significantly lower rates of all-cause mortality (30.0% vs. 50.0%, p = 0.014) and clinical failure (32.0% vs. 52.0%, p = 0.015) on day 28 than the NCSC group. The CSC regimen was an independent protective factor against 28-day clinical failure (adjusted odds ratio (aOR) = 0.281, 95% confidence interval [CI] = 0.091-0.864, p = 0.027). Kaplan-Meier analysis showed that the CSC group had a significantly longer survival time than the NCSC group (log-rank test, p = 0.028). The subgroup analysis of clinical factors associated with 28-day mortality showed that female patients and those with body mass index > 25, non-smoker status, and C-reactive protein < 30 especially favored the CSC regimen instead of the NCSC regimen.</p><p><strong>Conclusions: </strong>As an alternative to ampicillin-sulbactam, cefoperazone-sulbactam could be considered as components of combination therapy for critically ill patients with CRAB BSI.</p>","PeriodicalId":8981,"journal":{"name":"BMC Infectious Diseases","volume":"25 1","pages":"872"},"PeriodicalIF":3.0000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12220087/pdf/","citationCount":"0","resultStr":"{\"title\":\"Efficacy of cefoperazone-sulbactam as a component of combination therapy for carbapenem-resistant Acinetobacter baumannii bloodstream infection in intensive care units: a multicenter retrospective propensity score-matched study.\",\"authors\":\"Sheng-Huei Wang, Yu-Chao Lin, Ming-Cheng Chan, Kuang-Yao Yang, Chau-Chyun Sheu, Biing-Ru Wu, Wei-Hsuan Huang, Jia-Yih Feng, Chia-Min Chen, Zi-Xeng Weng, Chung-Kan Peng, Shih-En Tang\",\"doi\":\"10.1186/s12879-025-11205-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>In this study, we aimed to evaluate the efficacy of cefoperazone-sulbactam-containing (CSC) combination therapy for carbapenem-resistant Acinetobacter baumannii (CRAB) bloodstream infections (BSI) patients in intensive care unit (ICU).</p><p><strong>Methods: </strong>This multicenter, retrospective cohort study initially included 407 patients with CRAB BSI in the ICU between 2015 and 2019. Patients were divided into the CSC- and non-cefoperazone-sulbactam-containing (NCSC) groups. Outcomes including mortality, clinical failure, and microbiological eradication were compared after time-window bias adjustment and propensity score matching.</p><p><strong>Results: </strong>There was no statistical difference in baseline characteristics and disease severity between the CSC (n = 50) and NCSC groups (n = 150) after propensity score matching. The CSC group had significantly lower rates of all-cause mortality (30.0% vs. 50.0%, p = 0.014) and clinical failure (32.0% vs. 52.0%, p = 0.015) on day 28 than the NCSC group. The CSC regimen was an independent protective factor against 28-day clinical failure (adjusted odds ratio (aOR) = 0.281, 95% confidence interval [CI] = 0.091-0.864, p = 0.027). Kaplan-Meier analysis showed that the CSC group had a significantly longer survival time than the NCSC group (log-rank test, p = 0.028). The subgroup analysis of clinical factors associated with 28-day mortality showed that female patients and those with body mass index > 25, non-smoker status, and C-reactive protein < 30 especially favored the CSC regimen instead of the NCSC regimen.</p><p><strong>Conclusions: </strong>As an alternative to ampicillin-sulbactam, cefoperazone-sulbactam could be considered as components of combination therapy for critically ill patients with CRAB BSI.</p>\",\"PeriodicalId\":8981,\"journal\":{\"name\":\"BMC Infectious Diseases\",\"volume\":\"25 1\",\"pages\":\"872\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12220087/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"BMC Infectious Diseases\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1186/s12879-025-11205-w\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"INFECTIOUS DISEASES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s12879-025-11205-w","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
Efficacy of cefoperazone-sulbactam as a component of combination therapy for carbapenem-resistant Acinetobacter baumannii bloodstream infection in intensive care units: a multicenter retrospective propensity score-matched study.
Background: In this study, we aimed to evaluate the efficacy of cefoperazone-sulbactam-containing (CSC) combination therapy for carbapenem-resistant Acinetobacter baumannii (CRAB) bloodstream infections (BSI) patients in intensive care unit (ICU).
Methods: This multicenter, retrospective cohort study initially included 407 patients with CRAB BSI in the ICU between 2015 and 2019. Patients were divided into the CSC- and non-cefoperazone-sulbactam-containing (NCSC) groups. Outcomes including mortality, clinical failure, and microbiological eradication were compared after time-window bias adjustment and propensity score matching.
Results: There was no statistical difference in baseline characteristics and disease severity between the CSC (n = 50) and NCSC groups (n = 150) after propensity score matching. The CSC group had significantly lower rates of all-cause mortality (30.0% vs. 50.0%, p = 0.014) and clinical failure (32.0% vs. 52.0%, p = 0.015) on day 28 than the NCSC group. The CSC regimen was an independent protective factor against 28-day clinical failure (adjusted odds ratio (aOR) = 0.281, 95% confidence interval [CI] = 0.091-0.864, p = 0.027). Kaplan-Meier analysis showed that the CSC group had a significantly longer survival time than the NCSC group (log-rank test, p = 0.028). The subgroup analysis of clinical factors associated with 28-day mortality showed that female patients and those with body mass index > 25, non-smoker status, and C-reactive protein < 30 especially favored the CSC regimen instead of the NCSC regimen.
Conclusions: As an alternative to ampicillin-sulbactam, cefoperazone-sulbactam could be considered as components of combination therapy for critically ill patients with CRAB BSI.
期刊介绍:
BMC Infectious Diseases is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of infectious and sexually transmitted diseases in humans, as well as related molecular genetics, pathophysiology, and epidemiology.