Suppr超能文献

头孢他啶/他唑巴坦与美罗培南治疗复杂性尿路感染(包括肾盂肾炎)新生儿和儿童的安全性和疗效:一项 2 期随机临床试验。

Safety and Efficacy of Ceftolozane/Tazobactam Versus Meropenem in Neonates and Children With Complicated Urinary Tract Infection, Including Pyelonephritis: A Phase 2, Randomized Clinical Trial.

机构信息

From the Third Department of Pediatrics, Infectious Diseases Unit, School of Medicine, Aristotle University and Hippokration General Hospital, Thessaloniki, Greece.

Division of Infectious Diseases, CHOC Children's Hospital, Orange, California.

出版信息

Pediatr Infect Dis J. 2023 Apr 1;42(4):292-298. doi: 10.1097/INF.0000000000003832. Epub 2023 Jan 23.

Abstract

BACKGROUND

Ceftolozane/tazobactam, a cephalosporin-β-lactamase inhibitor combination, active against multidrug-resistant Gram-negative pathogens, is approved for treatment of adults with complicated urinary tract infections (cUTI). Safety and efficacy of ceftolozane/tazobactam in pediatric participants with cUTI, including pyelonephritis, were assessed.

METHODS

This phase 2 study (NCT03230838) compared ceftolozane/tazobactam with meropenem for treatment of cUTI in participants from birth to <18 years of age. The primary objective was safety and tolerability. Key secondary end points included clinical cure and per-participant microbiologic response rates at end of treatment (EOT) and test of cure (TOC) visits.

RESULTS

The microbiologic modified intent-to-treat (mMITT) population included 95 participants (ceftolozane/tazobactam, n = 71; meropenem, n = 24). The most common diagnosis and pathogen were pyelonephritis (ceftolozane/tazobactam, 84.5%; meropenem, 79.2%) and Escherichia coli (ceftolozane/tazobactam, 74.6%; meropenem, 87.5%); 5.7% (ceftolozane/tazobactam) and 4.8% (meropenem) of E. coli isolates were extended-spectrum β-lactamase-producers. Rates of adverse events were similar between treatment groups (any: ceftolozane/tazobactam, 59.0% vs. meropenem, 60.6%; drug-related: ceftolozane/tazobactam, 14.0% vs. meropenem, 15.2%; serious: ceftolozane/tazobactam, 3.0% vs. meropenem, 6.1%). Rates of clinical cure for ceftolozane/tazobactam and meropenem at EOT were 94.4% and 100% and at TOC were 88.7% and 95.8%, respectively. Rates of microbiologic eradication for ceftolozane/tazobactam and meropenem at EOT were 93.0% and 95.8%, and at TOC were 84.5% and 87.5%, respectively.

CONCLUSIONS

Ceftolozane/tazobactam had a favorable safety profile in pediatric participants with cUTI; rates of clinical cure and microbiologic eradication were high and similar to meropenem. Ceftolozane/tazobactam is a safe and effective new treatment option for children with cUTI, especially due to antibacterial-resistant Gram-negative pathogens.

摘要

背景

头孢洛扎他唑巴坦是一种头孢菌素-β-内酰胺酶抑制剂复方制剂,对多种耐药革兰氏阴性病原体具有活性,已获批准用于治疗成人复杂性尿路感染(cUTI)。评估了头孢洛扎他唑巴坦在患有 cUTI(包括肾盂肾炎)的儿科参与者中的安全性和疗效。

方法

这是一项 2 期研究(NCT03230838),比较了头孢洛扎他唑巴坦与美罗培南治疗出生至<18 岁的 cUTI 参与者。主要目的是评估安全性和耐受性。主要次要终点包括治疗结束时(EOT)和治疗后测试(TOC)时的临床治愈率和每参与者的微生物学应答率。

结果

微生物学改良意向治疗(mMITT)人群包括 95 名参与者(头孢洛扎他唑巴坦,n=71;美罗培南,n=24)。最常见的诊断和病原体是肾盂肾炎(头孢洛扎他唑巴坦,84.5%;美罗培南,79.2%)和大肠埃希菌(头孢洛扎他唑巴坦,74.6%;美罗培南,87.5%);5.7%(头孢洛扎他唑巴坦)和 4.8%(美罗培南)的大肠埃希菌分离株为扩展谱β-内酰胺酶生产者。治疗组的不良事件发生率相似(任何:头孢洛扎他唑巴坦,59.0% vs. 美罗培南,60.6%;药物相关:头孢洛扎他唑巴坦,14.0% vs. 美罗培南,15.2%;严重:头孢洛扎他唑巴坦,3.0% vs. 美罗培南,6.1%)。头孢洛扎他唑巴坦和美罗培南在 EOT 时的临床治愈率分别为 94.4%和 100%,在 TOC 时分别为 88.7%和 95.8%。头孢洛扎他唑巴坦和美罗培南在 EOT 时的微生物学清除率分别为 93.0%和 95.8%,在 TOC 时分别为 84.5%和 87.5%。

结论

头孢洛扎他唑巴坦在患有 cUTI 的儿科参与者中具有良好的安全性;临床治愈率和微生物学清除率高,与美罗培南相似。头孢洛扎他唑巴坦是一种安全有效的治疗儿童 cUTI 的新选择,特别是针对耐抗菌革兰氏阴性病原体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe72/9990597/28fd80406854/inf-42-292-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验