Gao Weiwen, Yang Jian, Zhang Xiangwang, Tian Lei, Xu Dong, Xu Shuyun, Liu Dong, He Yan
Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.
Department of Pharmacy, Central People's Hospital of Zhanjiang, Zhanjiang, 524045, People's Republic of China.
Infect Dis Ther. 2024 Dec;13(12):2509-2526. doi: 10.1007/s40121-024-01065-3. Epub 2024 Oct 22.
The efficacy and safety of omadacycline have been primarily documented through Phase III clinical trials; however, there are limited data from real-world clinical settings. This study aims to explore the real-world use of omadacycline in China and identify the factors associated with its efficacy.
We conducted a retrospective review of medical records for patients treated with omadacycline at a single center from March 2022 to March 2024. We analyzed demographic characteristics, laboratory results, antibiotic regimens, and clinical outcomes. Logistic regression was employed to identify risk factors associated with clinical treatment failure or failure of microbial clearance.
A total of 183 patients were included in the final analysis. Clinical success was achieved in 71.0% (130/183) of patients, with a bacterial clearance rate of 61.9% (26/42). Renal impairment was observed in 20.8% (38/183) of patients, with 39.5% (15/38) of these patients receiving nephrotoxic antibiotic treatments. Noteworthy adverse drug reactions were rare during the course of the treatment. Multivariate logistic regression analysis identified several independent factors associated with treatment failure: moderate to severe liver damage (OR: 3.073, 95% CI 1.345-7.021, p = 0.008), admission to the respiratory department (OR: 2.573, 95% CI 1.135-5.834, p = 0.024), and a duration of omadacycline therapy of less than 7 days (OR: 3.762, 95% CI 1.626-8.706, p = 0.002).
Our study demonstrates that omadacycline treatment can achieve favorable clinical success and bacterial clearance, with positive safety and tolerability outcomes. However, high-quality randomized controlled trials are needed to validate these initial findings.
奥马环素的疗效和安全性主要通过III期临床试验得到证实;然而,来自真实临床环境的数据有限。本研究旨在探讨奥马环素在中国的实际应用情况,并确定与其疗效相关的因素。
我们对2022年3月至2024年3月在单一中心接受奥马环素治疗的患者的病历进行了回顾性分析。我们分析了人口统计学特征、实验室检查结果、抗生素治疗方案和临床结局。采用逻辑回归分析确定与临床治疗失败或微生物清除失败相关的危险因素。
最终纳入分析的患者共有183例。71.0%(130/183)的患者临床治疗成功,细菌清除率为61.9%(26/42)。20.8%(38/183)的患者出现肾功能损害,其中39.5%(15/38)的患者接受了肾毒性抗生素治疗。治疗过程中值得注意的药物不良反应罕见。多因素逻辑回归分析确定了几个与治疗失败相关的独立因素:中度至重度肝损伤(OR:3.073,95%CI 1.345-7.021,p = 0.008)、入住呼吸内科(OR:2.573,95%CI 1.135-5.834,p = 0.024)以及奥马环素治疗疗程少于7天(OR:3.762,95%CI 1.626-8.706,p = 0.002)。
我们的研究表明,奥马环素治疗可取得良好的临床治疗成功和细菌清除效果,安全性和耐受性良好。然而,需要高质量的随机对照试验来验证这些初步发现。