Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China; Department of Pharmacy, Jingzhou Hospital of Traditional Chinese Medicine, Jingzhou, People's Republic of China.
Clinical Pharmacy, No. 920 Hospital, Joint Logistic Center of Chinese People's Liberation Army, Kunming, People's Republic of China.
Int J Antimicrob Agents. 2024 Sep;64(3):107273. doi: 10.1016/j.ijantimicag.2024.107273. Epub 2024 Jul 11.
Colistin sulphate for injection (CSI) became clinically available in China in July 2019. To date, there is no published data regarding its usage in children. Our research group has been following data on the efficacy and safety of CSI in Chinese paediatric patients with carbapenem-resistant organism infections. The purpose of this short communication is to provide a brief overview of the findings to date.
We reviewed the electronic medical records of paediatric patients (aged 9-17 y) who were administered CSI during their hospital stay at Tongji Hospital in Wuhan, China, between June 2021 and November 2023. Drug efficacy was evaluated based on clinical and microbiological outcomes, while drug safety was assessed using surveillance markers that reflect adverse reactions.
A total of 20 patients met the inclusion criteria. The predominant pathogens were Klebsiella pneumoniae (8 strains), followed by Acinetobacter baumannii (5 strains) and Pseudomonas aeruginosa (2 strains). The clinical response rate of CSI was 85%, with a bacterial clearance rate of 79%. None of the patients experienced colistin-related nephrotoxicity or neurotoxicity during the treatment.
In this real-world setting, CSI demonstrated a high level of clinical response and was well tolerated for the treatment of carbapenem-resistant organism infections in Chinese children.
硫酸粘菌素注射液(CSI)于 2019 年 7 月在中国上市。迄今为止,尚无关于其在儿童中应用的数据。我们的研究小组一直在关注 CSI 在我国儿童耐碳青霉烯类肠杆菌科细菌感染患者中的疗效和安全性数据。本短通讯旨在简要介绍迄今为止的研究结果。
我们回顾了 2021 年 6 月至 2023 年 11 月期间在我院住院的年龄为 9-17 岁的儿童患者(n=20)的电子病历,这些患者接受了 CSI 治疗。根据临床和微生物学结果评估药物疗效,使用反映不良反应的监测指标评估药物安全性。
共纳入 20 例符合条件的患者。主要病原体为肺炎克雷伯菌(8 株),其次为鲍曼不动杆菌(5 株)和铜绿假单胞菌(2 株)。CSI 的临床有效率为 85%,细菌清除率为 79%。治疗过程中无患者发生粘菌素相关肾毒性或神经毒性。
在本真实世界研究中,CSI 对治疗中国儿童耐碳青霉烯类肠杆菌科细菌感染显示出较高的临床疗效和良好的耐受性。