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七天和十四天抗生素治疗方案对单纯金黄色葡萄球菌菌血症(SAB7)的疗效:一项随机对照试验的研究方案。

Efficacy of seven and fourteen days of antibiotic treatment in uncomplicated Staphylococcus aureus bacteremia (SAB7): study protocol for a randomized controlled trial.

机构信息

Department of Infectious Diseases, Hvidovre Hospital, Copenhagen University Hospital, Kettegaard Alle 30, 2650, Hvidovre, Denmark.

Department of Clinical Microbiology, Hvidovre Hospital, Copenhagen University Hospital, Hvidovre, Denmark.

出版信息

Trials. 2019 May 2;20(1):250. doi: 10.1186/s13063-019-3357-9.

Abstract

BACKGROUND

Staphylococcus aureus bacteremia (SAB) is frequently encountered in the hospital setting, and current guidelines recommend at least 14 days of antibiotic treatment for SAB in order to minimize risks of secondary deep infections and relapse. However, evidence to support these treatment recommendations remains scarce. Patients with uncomplicated SAB are known to have a low of risk of recurrence and death. Reducing treatment length in uncomplicated SAB would reduce the total consumption of antibiotics, duration of hospital admission, and potentially the risk of adverse events. With SAB7 we seek to determine if 7 days of antibiotic treatment in patients with uncomplicated SAB is non-inferior to 14 days of treatment.

METHODS/DESIGN: The study is designed as a randomized, non-blinded, non-inferiority, multicenter interventional study. Primary measure of outcome will be 90-day survival without clinical or microbiological failure to treatment or relapse. Secondary outcomes include the prevalence of severe adverse effects, in particular secondary infection with Clostridium difficile, all-cause mortality, as well as public health related costs. Patients identified with uncomplicated SAB who have received 7 days of protocol-approved antibiotics will be eligible for inclusion and randomized 1:1 in two parallel arms to either (i) discontinue antibiotic treatment at day 7 or (ii) to continue antibiotic treatment for a total of 14 days. Main exclusion criteria include signs of complicated SAB, such as the presence of secondary deep infections, persistent bacteremia, and implantable devices. Patients are followed for 6 months with clinical examinations, consecutive blood tests, and registration of adverse events. A total of 284 patients are to be included at ten centers across Denmark. The primary endpoint will be tested with a statistical non-inferiority margin of 10 percentage points.

DISCUSSION

SAB 7 will determine if 7 days of antibiotic treatment in patients with uncomplicated SAB is sufficient and safe. Results of the study will provide important knowledge on optimized SAB management and could potentially modify the current treatment recommendations.

TRIAL REGISTRATION

ClinicalTrails.gov, H-17027414 . Registered on May 2, 2018. The Danish Medicines Agency (EudraCT), 2017-003529-13. Registered on October 30, 2017.

摘要

背景

金黄色葡萄球菌菌血症(SAB)在医院环境中经常发生,目前的指南建议对 SAB 进行至少 14 天的抗生素治疗,以最大限度地降低继发深部感染和复发的风险。然而,支持这些治疗建议的证据仍然很少。患有单纯性 SAB 的患者复发和死亡的风险较低。在单纯性 SAB 中缩短治疗时间将减少抗生素的总消耗量、住院时间,并可能降低不良事件的风险。我们通过 SAB7 研究来确定在患有单纯性 SAB 的患者中,7 天的抗生素治疗是否不劣于 14 天的治疗。

方法/设计:该研究设计为一项随机、非盲、非劣效、多中心干预研究。主要结局指标为 90 天无临床或微生物学治疗失败、复发或死亡的生存率。次要结局包括严重不良事件的发生率,特别是艰难梭菌继发感染、全因死亡率以及与公共卫生相关的成本。确定患有单纯性 SAB 且已接受 7 天方案批准抗生素治疗的患者符合纳入条件,并随机分为两组,每组 1:1,分别为(i)在第 7 天停止抗生素治疗或(ii)总共接受 14 天的抗生素治疗。主要排除标准包括有复杂 SAB 的迹象,如继发深部感染、持续性菌血症和植入物。患者在 6 个月内接受临床检查、连续血液检查和不良事件登记。将在丹麦的 10 个中心共纳入 284 名患者。主要终点将通过 10 个百分点的统计学非劣效性边际进行检验。

讨论

SAB7 将确定对患有单纯性 SAB 的患者进行 7 天的抗生素治疗是否足够安全。该研究的结果将提供有关优化 SAB 管理的重要知识,并可能改变当前的治疗建议。

试验注册

ClinicalTrails.gov,H-17027414。于 2018 年 5 月 2 日注册。丹麦药品管理局(EudraCT),2017-003529-13。于 2017 年 10 月 30 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62a0/6498575/642b4241164c/13063_2019_3357_Fig1_HTML.jpg

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