{"title":"耐头孢他啶-阿维菌素革兰阴性菌患者临床治疗失败和死亡的风险因素:单中心回顾性分析","authors":"Tingting Liu , Gang Li , Huijie Yue , Xuejiao Liu","doi":"10.1016/j.ipha.2023.11.003","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>In recent years, the number of Gram-negative bacteria (GNB) resistant to ceftazidime-avibactam (CZA) isolated from clinic has been increasing. We aimed to evaluate the clinical efficacy in patients with CZA-resistant GNB infections, and analyze the risk factors for clinical treatment failure and death.</p></div><div><h3>Methods</h3><p>Clinical data of patients with CZA-resistant GNB infections were collected retrospectively, and the influencing factors were analyzed by binary logistic regression.</p></div><div><h3>Results</h3><p>A total of 75 patients with CZA-resistant GNB infections were enrolled in the study, and the clinical effective rate was 56% (42/75). Multivariate analysis showed that continuous renal replacement therapy (CRRT) during anti-infection treatment was an independent risk factor for clinical treatment failure (OR 0.177, 95% CI 0.05–0.63, <em>p</em> = 0.008). The 28-day mortality rate in 75 patients was 18.7% (14/75). Multivariate analysis showed that the regimen of colistin E 750,000 U q12h (OR 0.020, 95% CI 0.00–0.56, <em>p</em> = 0.021), co-administration of tigecycline (OR 8.851, 95% CI 2.38–1316.87, <em>p</em> = 0.012) and CRRT during anti-infection treatment (OR 79.610, 95% CI 4.87–1300.26, <em>p</em> = 0.002) were independent affecting factors for 28-day mortality in patients with CZA-resistant GNB infections.</p></div><div><h3>Conclusions</h3><p>Patients with CZA-resistant GNB infections had a higher possibility of clinical treatment failure and death. The results of the study based on small sample size from a single center showed that clinical treatment failure and death were more likely to happen in patients on CRRT, and the regimen of colistin E 750,000 U q12h or co-administration of tigecycline may reduce or increase mortality, respectively. Further validation in rigorously designed multicenter clinical studies with larger sample sizes is needed.</p></div>","PeriodicalId":100682,"journal":{"name":"Intelligent Pharmacy","volume":"2 2","pages":"Pages 183-189"},"PeriodicalIF":0.0000,"publicationDate":"2023-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949866X2300117X/pdfft?md5=d4fb4e85d261e055c6185e218f28dcf4&pid=1-s2.0-S2949866X2300117X-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Risk factors for clinical treatment failure and death in patients with ceftazidime-avibactam-resistant Gram-negative bacteria: A single-centre retrospective analysis\",\"authors\":\"Tingting Liu , Gang Li , Huijie Yue , Xuejiao Liu\",\"doi\":\"10.1016/j.ipha.2023.11.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><p>In recent years, the number of Gram-negative bacteria (GNB) resistant to ceftazidime-avibactam (CZA) isolated from clinic has been increasing. We aimed to evaluate the clinical efficacy in patients with CZA-resistant GNB infections, and analyze the risk factors for clinical treatment failure and death.</p></div><div><h3>Methods</h3><p>Clinical data of patients with CZA-resistant GNB infections were collected retrospectively, and the influencing factors were analyzed by binary logistic regression.</p></div><div><h3>Results</h3><p>A total of 75 patients with CZA-resistant GNB infections were enrolled in the study, and the clinical effective rate was 56% (42/75). Multivariate analysis showed that continuous renal replacement therapy (CRRT) during anti-infection treatment was an independent risk factor for clinical treatment failure (OR 0.177, 95% CI 0.05–0.63, <em>p</em> = 0.008). The 28-day mortality rate in 75 patients was 18.7% (14/75). Multivariate analysis showed that the regimen of colistin E 750,000 U q12h (OR 0.020, 95% CI 0.00–0.56, <em>p</em> = 0.021), co-administration of tigecycline (OR 8.851, 95% CI 2.38–1316.87, <em>p</em> = 0.012) and CRRT during anti-infection treatment (OR 79.610, 95% CI 4.87–1300.26, <em>p</em> = 0.002) were independent affecting factors for 28-day mortality in patients with CZA-resistant GNB infections.</p></div><div><h3>Conclusions</h3><p>Patients with CZA-resistant GNB infections had a higher possibility of clinical treatment failure and death. The results of the study based on small sample size from a single center showed that clinical treatment failure and death were more likely to happen in patients on CRRT, and the regimen of colistin E 750,000 U q12h or co-administration of tigecycline may reduce or increase mortality, respectively. 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引用次数: 0
摘要
目的近年来,从临床中分离到的对头孢他啶-阿维巴坦(CZA)耐药的革兰阴性菌(GNB)数量不断增加。方法回顾性收集对头孢他啶-阿维菌素耐药的革兰阴性菌(GNB)感染患者的临床数据,并通过二元逻辑回归分析影响因素。结果共纳入75例对头孢他啶-阿维菌素耐药的革兰阴性菌(GNB)感染患者,临床有效率为56%(42/75)。多变量分析显示,抗感染治疗期间的持续肾脏替代治疗(CRRT)是临床治疗失败的独立风险因素(OR 0.177,95% CI 0.05-0.63,P = 0.008)。75名患者的28天死亡率为18.7%(14/75)。多变量分析显示,在抗感染治疗期间使用可乐定 E 750,000 U q12h 的方案(OR 0.020,95% CI 0.00-0.56,P = 0.021)、联合使用替加环素(OR 8.851,95% CI 2.38-1316.87,P = 0.012)和 CRRT(OR 79.610,95% CI 4.87-1300.26,P = 0.002)是CZA耐药GNB感染患者28天死亡率的独立影响因素。结论CZA耐药GNB感染患者临床治疗失败和死亡的可能性较高。基于单个中心小样本量的研究结果表明,临床治疗失败和死亡更有可能发生在接受 CRRT 的患者身上,而使用可乐定 E 750,000 U q12h 或联合使用替加环素的方案可能会分别降低或增加死亡率。还需要在设计严格、样本量更大的多中心临床研究中进一步验证。
Risk factors for clinical treatment failure and death in patients with ceftazidime-avibactam-resistant Gram-negative bacteria: A single-centre retrospective analysis
Objective
In recent years, the number of Gram-negative bacteria (GNB) resistant to ceftazidime-avibactam (CZA) isolated from clinic has been increasing. We aimed to evaluate the clinical efficacy in patients with CZA-resistant GNB infections, and analyze the risk factors for clinical treatment failure and death.
Methods
Clinical data of patients with CZA-resistant GNB infections were collected retrospectively, and the influencing factors were analyzed by binary logistic regression.
Results
A total of 75 patients with CZA-resistant GNB infections were enrolled in the study, and the clinical effective rate was 56% (42/75). Multivariate analysis showed that continuous renal replacement therapy (CRRT) during anti-infection treatment was an independent risk factor for clinical treatment failure (OR 0.177, 95% CI 0.05–0.63, p = 0.008). The 28-day mortality rate in 75 patients was 18.7% (14/75). Multivariate analysis showed that the regimen of colistin E 750,000 U q12h (OR 0.020, 95% CI 0.00–0.56, p = 0.021), co-administration of tigecycline (OR 8.851, 95% CI 2.38–1316.87, p = 0.012) and CRRT during anti-infection treatment (OR 79.610, 95% CI 4.87–1300.26, p = 0.002) were independent affecting factors for 28-day mortality in patients with CZA-resistant GNB infections.
Conclusions
Patients with CZA-resistant GNB infections had a higher possibility of clinical treatment failure and death. The results of the study based on small sample size from a single center showed that clinical treatment failure and death were more likely to happen in patients on CRRT, and the regimen of colistin E 750,000 U q12h or co-administration of tigecycline may reduce or increase mortality, respectively. Further validation in rigorously designed multicenter clinical studies with larger sample sizes is needed.