夫西地酸及其主要活性代谢物渗透脑脊液评价颅内感染的治疗效果。

IF 2 4区 医学 Q3 ONCOLOGY
Chemotherapy Pub Date : 2023-01-01 DOI:10.1159/000525906
Zhi Rao, Zhong-Fang He, Mao-Hua Zheng, Zi-Long Dang, Gang Yang, Yong-Hong Zhang, Ning Lu, Yu-Hui Wei
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引用次数: 1

摘要

富西地酸因其独特的作用机制而具有良好的抗菌效果。自1962年以来,FA已广泛用于葡萄球菌感染的全身和局部治疗,并表现出对甲氧西林敏感金黄色葡萄球菌、耐甲氧西林金黄色葡萄球菌和耐甲氧西林凝固酶阴性葡萄球菌的良好效力。鉴于FA的活性谱,与其他临床使用的抗生素无交叉耐药,且可能渗透到脑组织,本报告对3例颅内感染患者可能存在的格拉氏阳性菌进行了治疗。在血浆和脑脊液(CSF)中测量FA及其活性代谢物(3-酮FA)以评估FA的治疗,结果表明,每天1,500 mg FA足以达到颅内感染患者血浆和脑脊液的治疗浓度,同时该剂量没有出现意想不到的方案相关毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fusidic Acid and Its Major Active Metabolite Penetration into Cerebrospinal Fluid for Assessing Treatment of Intracranial Infections.

Fusidic acid (FA) had excellent antimicrobial effects due to its unique mechanism of action. Since 1962, FA has been widely used in the systemic and topical treatment of staphylococcal infections and exhibits a well-characterized potency against methicillin-susceptible Staphylococcus aureus, methicillin-resistant Staphylococcus aureus, and methicillin-resistant coagulase-negative Staphylococci. In view of the spectrum of activity, no cross-resistance with other clinically used antibiotics, and potential penetration into brain tissue, FA was used to treat possible gra-positive bacteria in 3 patients with intracranial infections in the present report. FA and its active metabolite (3-keto FA) were measured in plasma and cerebrospinal fluid (CSF) to assess the treatment of FA, and the results indicated that 1,500 mg per day of FA was sufficient to achieve therapeutic concentrations in both plasma and CSF in intracranial infection patients, while the dosage did not experience unexpected regimen-related toxicity.

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来源期刊
Chemotherapy
Chemotherapy 医学-药学
CiteScore
5.80
自引率
0.00%
发文量
34
审稿时长
6-12 weeks
期刊介绍: This journal publishes original research articles and state-of-the-art reviews on all aspects of antimicrobial and antitumor chemotherapy. The results of experimental and clinical investigations into the microbiological and pharmacologic properties of antibacterial, antiviral and antitumor compounds are major topics of publication. Papers selected for the journal offer data concerning the efficacy, toxicology, and interactions of new drugs in single or combined applications. Studies designed to determine the pharmacokinetic and pharmacodynamics properties of similar preparations and comparing their efficacy are also included. Special emphasis is given to the development of drug-resistance, an increasing problem worldwide.
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