单次肌内剂量头孢曲松的安全性和合理使用:对非复杂淋球菌感染管理的临床见解。

IF 2.2 Q2 HEALTH CARE SCIENCES & SERVICES Drug, Healthcare and Patient Safety Pub Date : 2023-11-03 eCollection Date: 2023-01-01 DOI:10.2147/DHPS.S350763
George P Allen, Haley L Morrill
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引用次数: 0

摘要

淋病是一种由淋病奈瑟菌引起的性传播感染,是一个严重的公共卫生问题。淋病是世界上第二大报告的性传播感染。无并发症淋球菌感染的治疗方法随着抗微生物耐药性的出现而发生了巨大的变化。存在多种耐药机制(例如,β-内酰胺酶的产生、抗菌药物外排和靶位点修饰),其中一些可能导致多药耐药性。1985年,头孢曲松首次被推荐为治疗无并发症淋球菌感染的一种选择,现在它已成为所有临床实践指南中的主要治疗方法。头孢曲松在临床试验中始终显示出较高的微生物治愈率,并且具有良好的安全性。尽管它在对青霉素过敏的患者中的使用可能受到限制,但在这类患者中使用头孢曲松的风险被高估了。淋病奈瑟菌对头孢曲松的易感性降低,再加上缺乏多样化的治疗替代品和新的抗菌药物渠道有限,对淋病的治疗构成了重大威胁。
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Safety Aspects and Rational Use of Single Intramuscular Dose Ceftriaxone: Clinical Insights on the Management of Uncomplicated Gonococcal Infections.

Gonorrhea, a sexually transmitted infection caused by Neisseria gonorrhoeae, is a grave public health concern. Gonorrhea is the second most reported sexually transmitted infection worldwide. The treatment of uncomplicated gonococcal infections has evolved dramatically in response to the emergence of antimicrobial resistance. Multiple resistance mechanisms (for example, beta-lactamase production, antimicrobial efflux, and target site modification) exist, some of which may cause multidrug-resistance. Ceftriaxone was first recommended as an option for uncomplicated gonococcal infections in 1985, and it is now a mainstay of therapy in all clinical practice guidelines. Ceftriaxone has consistently shown high microbiologic cure rates in clinical trials, and it has demonstrated an excellent safety profile. Although its use may be limited in patients with hypersensitivity to penicillins, the risk of using ceftriaxone in such patients is overestimated. The emergence of reduced ceftriaxone susceptibility in N. gonorrhoeae, coupled with a lack of diverse treatment alternatives and the limited pipeline of new antimicrobials, is a significant threat to the treatment of gonorrhea.

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来源期刊
Drug, Healthcare and Patient Safety
Drug, Healthcare and Patient Safety HEALTH CARE SCIENCES & SERVICES-
CiteScore
4.10
自引率
0.00%
发文量
24
审稿时长
16 weeks
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