Pivmecillinam for Uncomplicated Acute Cystitis: A Contemporary Review.

IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY Annals of Pharmacotherapy Pub Date : 2024-12-07 DOI:10.1177/10600280241288554
Jessica E Burchette, Kelly Covert, Patrick Tu, Bryan P White, Daniel B Chastain, David B Cluck
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Abstract

Objective: To review the evidence and discuss use of pivmecillinam in uncomplicated acute cystitis.

Data sources: A literature search was conducted utilizing PubMed (from 2000 through August 2024) and ClinicalTrials.gov. Medical Subject Headings (MeSH) terms, such as mecillinam or pivmecillinam and urinary tract infections, were utilized. Additional references were identified by reviewing literature citations.

Study selection and data extraction: Articles were limited to English language publications evaluating the efficacy or safety of pivmecillinam for urinary tract infections (UTIs) in adult populations.

Data synthesis: Data from 6 randomized controlled trials support pivmecillinam for acute uncomplicated cystitis at doses of 200 to 400 mg 3 times daily for 3 to 7 days, with more consistent clinical and bacteriologic cure observed with 400 mg doses and longer therapy durations. Clinical evaluation of 400 mg 2 to 3 times daily is available with use more common in non-US Food and Drug Administration (FDA)-approved populations, such as men, pregnancy, and multidrug resistant infections. There are limited data supporting pivmecillinam for pyelonephritis; routine use is cautioned until further clinical data are available.

Relevance to patient care and clinical practice in comparison with existing drugs: As resistance to first-line antimicrobials rises, the need for safe and effective treatment options remains high. Pivmecillinam represents a new therapeutic option available in the United States for outpatient management of uncomplicated acute cystitis.

Conclusion: Pivmecillinam could be a key agent for uncomplicated acute cystitis. Utilization will likely be cost driven, but the promise of low resistance encourages the place in therapy when other agents are not susceptible to infecting uropathogens.

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匹美西林治疗无并发症急性膀胱炎:当代综述。
目的:回顾证据并探讨哌美西林在无并发症急性膀胱炎中的应用。数据来源:利用PubMed(从2000年到2024年8月)和ClinicalTrials.gov进行文献检索。使用了医学主题标题(MeSH)术语,如美西林或哌美西林和尿路感染。通过回顾文献引文确定其他参考文献。研究选择和数据提取:文章仅限于英文出版物,评估哌美西林治疗成人尿路感染(uti)的有效性或安全性。数据综合:来自6个随机对照试验的数据支持哌美西林治疗急性无并发症膀胱炎,剂量为200 - 400mg,每日3次,持续3 - 7天,400 mg剂量观察到更一致的临床和细菌学治愈,治疗持续时间更长。临床评估400mg每日2 - 3次,在非美国食品和药物管理局(FDA)批准的人群中使用更为常见,如男性、孕妇和多药耐药感染。支持哌美西林治疗肾盂肾炎的数据有限;在获得进一步的临床数据之前,建议常规使用。与现有药物相比,与患者护理和临床实践的相关性:随着对一线抗微生物药物的耐药性上升,对安全有效治疗方案的需求仍然很高。匹美西林代表了一种新的治疗选择,可在美国门诊管理无并发症急性膀胱炎。结论:哌美西林可作为治疗无并发症急性膀胱炎的关键药物。使用可能会受到成本驱动,但低耐药性的前景鼓励在其他药物不易感染尿路病原体的治疗中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.70
自引率
0.00%
发文量
166
审稿时长
3-8 weeks
期刊介绍: Annals of Pharmacotherapy (AOP) is a peer-reviewed journal that advances pharmacotherapy throughout the world by publishing high-quality research and review articles to achieve the most desired health outcomes.The articles provide cutting-edge information about the most efficient, safe and cost-effective pharmacotherapy for the treatment and prevention of various illnesses. This journal is a member of the Committee on Publication Ethics (COPE). Average time from submission to first decision: 14 days
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