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海盗项目:基于信息学的即时护理随机对照试验,用于减少革兰氏阴性菌血症中抗生素治疗的过度使用。

PIRATE project: point-of-care, informatics-based randomised controlled trial for decreasing overuse of antibiotic therapy in Gram-negative bacteraemia.

作者信息

Huttner Angela, Albrich Werner C, Bochud Pierre-Yves, Gayet-Ageron Angèle, Rossel Anne, Dach Elodie von, Harbarth Stephan, Kaiser Laurent

机构信息

Division of Infectious Diseases, Geneva University Hospitals, Geneva, Switzerland.

Infection Control Program, Geneva University Hospitals, Geneva, Switzerland.

出版信息

BMJ Open. 2017 Jul 13;7(7):e017996. doi: 10.1136/bmjopen-2017-017996.

Abstract

INTRODUCTION

Antibiotic overuse drives antibiotic resistance. The optimal duration of antibiotic therapy for Gram-negative bacteraemia (GNB), a common community and hospital-associated infection, remains unknown and unstudied via randomised controlled trials (RCTs).

METHODS AND ANALYSIS

This investigator-initiated, multicentre, non-inferiority, informatics-based point-of-care RCT will randomly assign adult hospitalised patients receiving microbiologically efficacious antibiotic(s) for GNB to (1) 14 days of antibiotic therapy, (2) 7 days of therapy or (3) an individualised duration determined by clinical response and 75% reduction in peak C reactive protein (CRP) values. The randomisation will occur in equal proportions (1:1:1) on day 5 (±1) of efficacious antibiotic therapy as determined by antibiogram; patients, their physicians and study investigators will be blind to treatment duration allocation until the day of antibiotic discontinuation. Immunosuppressed patients and those with GNB due to complicated infections (endocarditis, osteomyelitis, etc) and/or non-fermenting bacilli ( spp, spp, spp) spp, spp or polymicrobial growth with Gram-positive organisms will be ineligible. The primary outcome is incidence of clinical failure at day 30; secondary outcomes include clinical failure, all-cause mortality and incidence of infection in the 90-day study period. An interim safety analysis will be performed after the first 150 patients have been followed for ≤30 days. Given a chosen margin of 10%, the required sample size to determine non-inferiority is roughly 500 patients. Analyses will be performed on both intention-to-treat and per-protocol populations.

ETHICS AND DISSEMINATION

Ethics approval was obtained from the cantonal ethics committees of all three participating sites. Results of the main trial and each of the secondary endpoints will be submitted for publication in a peer-reviewed journal.

TRIAL REGISTRATION NUMBER

This trial is registered at www.clinicaltrials.gov (NCT03101072; pre-results).

摘要

引言

抗生素的过度使用导致了抗生素耐药性。革兰氏阴性菌血症(GNB)是一种常见的社区和医院相关感染,抗生素治疗的最佳疗程仍不明确,且尚未通过随机对照试验(RCT)进行研究。

方法与分析

这项由研究者发起的、多中心、非劣效性、基于信息学的即时护理RCT将把因GNB接受微生物学有效抗生素治疗的成年住院患者随机分为三组:(1)接受14天抗生素治疗;(2)接受7天治疗;(3)根据临床反应和C反应蛋白(CRP)峰值降低75%确定个体化疗程。随机分组将在根据抗菌谱确定的有效抗生素治疗第5天(±1天)以相等比例(1:1:1)进行;患者、其医生和研究调查人员在抗生素停用前对治疗疗程分配情况不知情。免疫抑制患者以及因复杂感染(心内膜炎、骨髓炎等)和/或非发酵菌(如嗜麦芽窄食单胞菌、洋葱伯克霍尔德菌、铜绿假单胞菌等)导致GNB的患者,以及伴有革兰氏阳性菌的多微生物生长患者不符合入选条件。主要结局是第30天临床失败的发生率;次要结局包括临床失败、全因死亡率以及90天研究期内再次感染的发生率。在对首批150例患者随访≤30天后将进行中期安全性分析。鉴于选定的非劣效性界值为10%,确定非劣效性所需的样本量约为500例患者。将对意向性治疗人群和符合方案人群进行分析。

伦理与传播

已获得所有三个参与地点的州伦理委员会的伦理批准。主要试验结果和每个次要终点结果将提交至同行评审期刊发表。

试验注册号

本试验已在www.clinicaltrials.gov注册(NCT03101072;预结果)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d60/5541592/46c71801997c/bmjopen-2017-017996f01.jpg

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