Evaluation of the Efficacy of Piperacillin/Tazobactam in Extended-Spectrum Beta-Lactamase-Producing Enterobacteriaceae Urinary Tract Infections: A Systematic Review of the Literature.

IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY Annals of Pharmacotherapy Pub Date : 2024-12-07 DOI:10.1177/10600280241291604
Samantha P Sutton, Justin P Reinert
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Abstract

Objective: To evaluate the efficacy of piperacillin/tazobactam (PTZ) for the treatment of extended-spectrum beta-lactamase-producing enterobacteriaceae (ESBL-PE) urinary tract infections (UTIs).

Data sources: A systematic review was conducted in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) standards on PubMed, MEDLINE, Embase, Web of Science Core Collection, and Cochrane Central through July 2024.

Study selection and data extraction: Studies providing efficacy data associated with PTZ in patients ≥18 years old experiencing an ESBL-PE UTI that documented clinical and microbiological cure data were included.

Data synthesis: A total of 577 articles were obtained for screening. After applying the inclusion and exclusion criteria, 7 studies comparing PTZ with carbapenems comprised of 1156 patient cases were analyzed. Piperacillin/tazobactam was found to be noninferior to carbapenems in the treatment of both uncomplicated and complicated UTI's caused by ESBL-PE. The observed noninferiority encompassed clinical response, clinical cure, and microbiological cure outcome metrics. Although not specifically evaluated in this systematic review, adverse effects associated with PTZ were found to be minimal and lesser in incidence than with the carbapenem comparators in aggregate.

Relevance to patient care and clinical practice: While a definitive dosing strategy remains elusive, a PTZ total daily dose of 13.5 g infused over 3 to 4 hours may be appropriate for this indication.

Conclusion: Piperacillin/tazobactam may be an effective carbapenem-sparing agent for the treatment of ESBL-PE UTIs that show in-vitro susceptibility to PTZ. However, additional robust randomized clinical trials are still needed to validate the findings of this review and determine the best dosage regimen of PTZ for ESBL-PE UTIs.

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哌拉西林/他唑巴坦治疗广谱产β -内酰胺酶肠杆菌科尿路感染的疗效评价:文献系统综述。
目的:评价哌拉西林/他唑巴坦(PTZ)治疗广谱β -内酰胺酶产肠杆菌科(ESBL-PE)尿路感染(uti)的疗效。数据来源:根据系统评价和荟萃分析首选报告项目(PRISMA)标准对PubMed、MEDLINE、Embase、Web of Science Core Collection和Cochrane Central进行了系统评价,截止到2024年7月。研究选择和数据提取:研究纳入了对18岁以上ESBL-PE尿路感染患者提供与PTZ相关的疗效数据,并记录了临床和微生物治愈数据。数据综合:共获得577篇文献进行筛选。应用纳入和排除标准,分析7项比较PTZ与碳青霉烯类药物的研究,共1156例患者。哌拉西林/他唑巴坦在治疗ESBL-PE引起的非复杂性和复杂性UTI方面均优于碳青霉烯类药物。观察到的非劣效性包括临床反应、临床治愈和微生物治愈结果指标。虽然在本系统综述中没有特别评估,但总的来说,与碳青霉烯类比较物相比,PTZ相关的不良反应最小,发生率更低。与患者护理和临床实践的相关性:虽然明确的给药策略仍然难以捉摸,但PTZ每日总剂量13.5 g,输注3至4小时可能适用于该适应症。结论:哌拉西林/他唑巴坦可能是一种有效的碳青霉烯保留剂,用于治疗体外对PTZ敏感的ESBL-PE uti。然而,仍然需要更多的随机临床试验来验证本综述的发现,并确定PTZ治疗ESBL-PE uti的最佳给药方案。
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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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