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革兰氏染色指导的呼吸机相关性肺炎抗生素选择(GRACE-VAP)试验:一项随机对照试验的原理与研究方案

GRam stain-guided Antibiotics ChoicE for Ventilator-Associated Pneumonia (GRACE-VAP) trial: rationale and study protocol for a randomised controlled trial.

作者信息

Yoshimura Jumpei, Yamakawa Kazuma, Kinoshita Takahiro, Ohta Yoshinori, Morimoto Takeshi

机构信息

Division of Trauma and Surgical Critical Care, Osaka General Medical Center, 3-1-56 Bandai-Higashi, Sumiyoshi, Osaka, 558-8558, Japan.

Division of General Medicine, Department of Internal Medicine, Hyogo College of Medicine, 1-1 Mukogawa, Nishinomiya, Hyogo, 663-8501, Japan.

出版信息

Trials. 2018 Nov 8;19(1):614. doi: 10.1186/s13063-018-2971-2.

Abstract

BACKGROUND

Optimising the use of antibiotic agents is a pressing challenge to overcoming the rapid emergence and spread of multidrug-resistant pathogens in intensive care units (ICUs). Although Gram staining may possibly provide immediate information for predicting pathogenic bacteria, Gram stain-guided initial antibiotic treatment is not well established in the ICU setting. We planned the GRam stain-guided Antibiotics ChoicE for Ventilator-Associated Pneumonia (GRACE-VAP) trial to investigate whether Gram staining can safely restrict the use of broad-spectrum antibiotics in patients with ventilator-associated pneumonia (VAP), which is one of the most common hospital-acquired infections in ICUs.

METHODS/DESIGN: The GRACE-VAP trial is a multicentre, randomised, open-label parallel-group trial to assess the non-inferiority of Gram stain-guided initial antibiotic treatment to guidelines-based initial antibiotic treatment for the primary endpoint of clinical response rate in patients with VAP. Secondary endpoints include the coverage rates of initial antibiotic therapies, the selected rates of anti-pseudomonal agents and anti-methicillin-resistant Staphylococcus aureus (anti-MRSA) agents as initial antibiotic therapies, 28-day all-cause mortality, ICU-free days, ventilator-free days and adverse events. Patients are randomly assigned to receive Gram stain-guided treatment or guidelines-based treatment at a ratio of 1:1. In the Gram stain group, results of Gram staining of endotracheal aspirate are used to guide the selection of antibiotics. In the guidelines group, the combination of an anti-pseudomonal agent and an anti-MRSA agent is administered. A total sample size of 200 was estimated to provide a power of 80% with a one-sided alpha level of 2.5% and a non-inferiority margin of 20%, considering 10% non-evaluable patients.

DISCUSSION

The GRACE-VAP trial is expected to reveal whether Gram staining can reduce the use of broad-spectrum antibiotics without impairing patient outcomes and thereby provide evidence for an antibiotic selection strategy in patients with VAP.

TRIAL REGISTRATION

Clinicaltrials.gov, NCT03506113 . Registered on 29 March 2018. University Hospital Medical Information Network, UMIN000031933. Registered on 26 March 2018.

摘要

背景

优化抗生素的使用是克服重症监护病房(ICU)中多重耐药病原体迅速出现和传播这一紧迫挑战的关键。尽管革兰氏染色可能为预测病原菌提供即时信息,但在ICU环境中,革兰氏染色指导下的初始抗生素治疗尚未得到充分确立。我们开展了呼吸机相关性肺炎革兰氏染色指导下的抗生素选择(GRACE-VAP)试验,以研究革兰氏染色是否能安全地限制呼吸机相关性肺炎(VAP)患者使用广谱抗生素,VAP是ICU中最常见的医院获得性感染之一。

方法/设计:GRACE-VAP试验是一项多中心、随机、开放标签平行组试验,旨在评估革兰氏染色指导下的初始抗生素治疗相对于基于指南的初始抗生素治疗在VAP患者临床反应率这一主要终点上的非劣效性。次要终点包括初始抗生素治疗的覆盖率、作为初始抗生素治疗的抗假单胞菌药物和抗耐甲氧西林金黄色葡萄球菌(抗MRSA)药物的选择率、28天全因死亡率、无ICU天数、无呼吸机天数和不良事件。患者按1:1的比例随机分配接受革兰氏染色指导的治疗或基于指南的治疗。在革兰氏染色组中,气管内吸出物的革兰氏染色结果用于指导抗生素的选择。在指南组中,给予抗假单胞菌药物和抗MRSA药物联合治疗。考虑到10%不可评估的患者,估计总样本量为200时,检验效能为80%,单侧α水平为2.5%,非劣效界值为20%。

讨论

GRACE-VAP试验有望揭示革兰氏染色是否能在不影响患者预后的情况下减少广谱抗生素的使用,从而为VAP患者的抗生素选择策略提供证据。

试验注册

Clinicaltrials.gov,NCT03506113。于2018年3月29日注册。大学医院医学信息网络,UMIN000031933。于2018年3月26日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dfd/6225572/b062454b7663/13063_2018_2971_Fig1_HTML.jpg

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