{"title":"不同给药方案对耐碳青霉烯肺炎克雷伯菌209例疗效的回顾性分析","authors":"Yao Chen, Qingjiang Guo, Youbao Liang, Erhu Heng","doi":"10.62347/TZFB9853","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Carbapenem-resistant <i>Klebsiella pneumoniae</i> (CRKP) infections pose significant clinical challenges worldwide due to limited therapeutic options and high mortality. Sulperazon (cefoperazone/sulbactam) has demonstrated activity against multidrug-resistant (MDR) organisms; however, the optimal dosing regimen for CRKP remains unclear. This study aimed to evaluate the clinical efficacy, microbiological outcomes, and safety of different sulperazon dosing in CRKP infections.</p><p><strong>Methods: </strong>A retrospective analysis was conducted on 209 adult patients with CRKP infections treated with sulperazon for at least 48 hours at Bengbu First People's Hospital between January 2020 and December 2022. Patients were grouped into a standard-dose group (≤3 g/day, n=112) and a high-dose group (>3 g/day, n=97). Clinical cure, microbiological eradication, treatment failure, 28-day mortality, and incidence of adverse events were compared between groups.</p><p><strong>Results: </strong>The cohort was predominantly elderly (mean age 67.3 ± 15.2 years) and male (65.1%). The most frequent carbapenemase genes were <i>bla</i>_KPC-2 (65.6%) and <i>bla</i>_NDM-1 (23.0%). Virulence factors, including adhesins (72.2%), iron-acquisition systems (63.2%), capsule synthesis genes (58.9%), and the hypermucoviscosity regulator <i>rmpA</i> (42.6%) were frequently detected. Compared with the standard-dose group, the high-dose group showed significantly increased clinical cure rates (64.9% vs. 43.8%; P=0.002) and microbiological eradication rates (69.1% vs. 46.4%; P=0.001), along with lower rates of treatment failure (10.3% vs. 24.1%; P=0.011) and 28-day mortality (8.2% vs. 20.5%; P=0.015), without an increase in adverse events.</p><p><strong>Conclusion: </strong>High-dose sulperazon demonstrated superior clinical efficacy and equivalent safety to standard dosing in the treatment of CRKP infections, supporting dose optimization to improve patient outcomes.</p>","PeriodicalId":7731,"journal":{"name":"American journal of translational research","volume":"17 6","pages":"4764-4773"},"PeriodicalIF":1.6000,"publicationDate":"2025-06-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12261187/pdf/","citationCount":"0","resultStr":"{\"title\":\"Therapeutic efficacy of different sulperazon dosing regimens in carbapenem-resistant Klebsiella pneumoniae: a retrospective analysis of 209 cases.\",\"authors\":\"Yao Chen, Qingjiang Guo, Youbao Liang, Erhu Heng\",\"doi\":\"10.62347/TZFB9853\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>Carbapenem-resistant <i>Klebsiella pneumoniae</i> (CRKP) infections pose significant clinical challenges worldwide due to limited therapeutic options and high mortality. Sulperazon (cefoperazone/sulbactam) has demonstrated activity against multidrug-resistant (MDR) organisms; however, the optimal dosing regimen for CRKP remains unclear. This study aimed to evaluate the clinical efficacy, microbiological outcomes, and safety of different sulperazon dosing in CRKP infections.</p><p><strong>Methods: </strong>A retrospective analysis was conducted on 209 adult patients with CRKP infections treated with sulperazon for at least 48 hours at Bengbu First People's Hospital between January 2020 and December 2022. Patients were grouped into a standard-dose group (≤3 g/day, n=112) and a high-dose group (>3 g/day, n=97). Clinical cure, microbiological eradication, treatment failure, 28-day mortality, and incidence of adverse events were compared between groups.</p><p><strong>Results: </strong>The cohort was predominantly elderly (mean age 67.3 ± 15.2 years) and male (65.1%). The most frequent carbapenemase genes were <i>bla</i>_KPC-2 (65.6%) and <i>bla</i>_NDM-1 (23.0%). Virulence factors, including adhesins (72.2%), iron-acquisition systems (63.2%), capsule synthesis genes (58.9%), and the hypermucoviscosity regulator <i>rmpA</i> (42.6%) were frequently detected. Compared with the standard-dose group, the high-dose group showed significantly increased clinical cure rates (64.9% vs. 43.8%; P=0.002) and microbiological eradication rates (69.1% vs. 46.4%; P=0.001), along with lower rates of treatment failure (10.3% vs. 24.1%; P=0.011) and 28-day mortality (8.2% vs. 20.5%; P=0.015), without an increase in adverse events.</p><p><strong>Conclusion: </strong>High-dose sulperazon demonstrated superior clinical efficacy and equivalent safety to standard dosing in the treatment of CRKP infections, supporting dose optimization to improve patient outcomes.</p>\",\"PeriodicalId\":7731,\"journal\":{\"name\":\"American journal of translational research\",\"volume\":\"17 6\",\"pages\":\"4764-4773\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2025-06-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12261187/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American journal of translational research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.62347/TZFB9853\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of translational research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.62347/TZFB9853","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0
摘要
目的:碳青霉烯耐药肺炎克雷伯菌(CRKP)感染由于治疗选择有限和死亡率高,在全球范围内构成了重大的临床挑战。舒拉宗(头孢哌酮/舒巴坦)已被证明具有抗多药耐药(MDR)微生物的活性;然而,CRKP的最佳给药方案仍不清楚。本研究旨在评估不同剂量舒拉松治疗CRKP感染的临床疗效、微生物学结果和安全性。方法:回顾性分析2020年1月至2022年12月蚌埠市第一人民医院接受舒拉松治疗至少48小时的成年CRKP感染患者209例。将患者分为标准剂量组(≤3g /d, n=112)和高剂量组(≤3g /d, n=97)。比较两组患者的临床治愈率、微生物根除率、治疗失败率、28天死亡率和不良事件发生率。结果:该队列以老年人(平均年龄67.3±15.2岁)和男性(65.1%)为主。碳青霉烯酶基因最多的是bla_KPC-2(65.6%)和bla_NDM-1(23.0%)。毒力因子,包括粘附素(72.2%)、铁获取系统(63.2%)、胶囊合成基因(58.9%)和高黏液粘度调节剂rmpA(42.6%)经常被检测到。与标准剂量组比较,高剂量组临床治愈率显著提高(64.9% vs 43.8%;P=0.002)和微生物根除率(69.1% vs. 46.4%;P=0.001),治疗失败率也较低(10.3% vs. 24.1%;P=0.011)和28天死亡率(8.2% vs. 20.5%;P=0.015),不良事件未增加。结论:大剂量舒拉松治疗CRKP感染的临床疗效优于标准剂量,安全性与标准剂量相当,支持剂量优化以改善患者预后。
Therapeutic efficacy of different sulperazon dosing regimens in carbapenem-resistant Klebsiella pneumoniae: a retrospective analysis of 209 cases.
Objectives: Carbapenem-resistant Klebsiella pneumoniae (CRKP) infections pose significant clinical challenges worldwide due to limited therapeutic options and high mortality. Sulperazon (cefoperazone/sulbactam) has demonstrated activity against multidrug-resistant (MDR) organisms; however, the optimal dosing regimen for CRKP remains unclear. This study aimed to evaluate the clinical efficacy, microbiological outcomes, and safety of different sulperazon dosing in CRKP infections.
Methods: A retrospective analysis was conducted on 209 adult patients with CRKP infections treated with sulperazon for at least 48 hours at Bengbu First People's Hospital between January 2020 and December 2022. Patients were grouped into a standard-dose group (≤3 g/day, n=112) and a high-dose group (>3 g/day, n=97). Clinical cure, microbiological eradication, treatment failure, 28-day mortality, and incidence of adverse events were compared between groups.
Results: The cohort was predominantly elderly (mean age 67.3 ± 15.2 years) and male (65.1%). The most frequent carbapenemase genes were bla_KPC-2 (65.6%) and bla_NDM-1 (23.0%). Virulence factors, including adhesins (72.2%), iron-acquisition systems (63.2%), capsule synthesis genes (58.9%), and the hypermucoviscosity regulator rmpA (42.6%) were frequently detected. Compared with the standard-dose group, the high-dose group showed significantly increased clinical cure rates (64.9% vs. 43.8%; P=0.002) and microbiological eradication rates (69.1% vs. 46.4%; P=0.001), along with lower rates of treatment failure (10.3% vs. 24.1%; P=0.011) and 28-day mortality (8.2% vs. 20.5%; P=0.015), without an increase in adverse events.
Conclusion: High-dose sulperazon demonstrated superior clinical efficacy and equivalent safety to standard dosing in the treatment of CRKP infections, supporting dose optimization to improve patient outcomes.