Optimizing short-term antibiotic treatment in patients with acute cholangitis: study protocol for an open-label randomized controlled trial (the BOLT-P3 trial).

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2025-09-01 DOI:10.1186/s13063-025-09077-1
Sakue Masuda, Yoshinori Imamura, Karen Kimura, Makomo Makazu, Jun Kubota, Hiroshi Takihara, Ryuhei Jinushi, Tomoaki Fujikawa, Kyohei Maejima, Aya Kawanishi, Ryuichi Yamamoto, Shogo Noda, Taiji Koyama, Ayumu Sugitani, Shomei Ryozawa, Kazuya Koizumi
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引用次数: 0

Abstract

Background: Acute cholangitis (AC) frequently presents as a community-acquired infection and is associated with a high prevalence of antibiotic use among infectious diseases. The Tokyo Guidelines 2018 (TG18) recommend 4-7 days of antibiotic administration after biliary drainage. However, this recommendation lacks strong evidence of its effectiveness and is primarily based on heterogeneous clinical findings and expert opinions. Recent retrospective studies have advocated a shorter 1- to 3-day antibiotic course as effective for AC treatment, prompting the need to reassess the treatment duration to achieve therapeutic efficacy while minimizing resistance and adverse effects.

Methods: We designed a multicenter, non-blinded, randomized trial to evaluate the efficacy of short-course therapy compared to standard-course therapy for AC management. The short-course therapy group will receive 1-3 days of intravenous (IV) antibiotic treatment after successful biliary drainage compared to 4-7 days of IV antibiotics after successful biliary drainage for the standard-course therapy group. The primary outcome is the clinical cure rate within 14 days from the endoscopic retrograde cholangiopancreatography (ERCP) procedure. Participants will be allocated to either treatment course using a minimization method in a non-blinded, randomized manner, with stratification factors including condition severity and facility. We determined that 210 participants would be required to achieve a statistical power of 90% with a one-sided significance threshold of 2.5% and a non-inferiority limit of 10%.

Discussion: This phase 3 trial aims to determine the non-inferiority of short-course therapy over standard-course therapy. Shortening the duration of antibiotic administration may mitigate the emergence of resistant bacteria, adverse events, and reduce hospital stay length and healthcare costs. https://jrct.niph.go.jp/re/reports/detail/73862 TRIAL REGISTRATION: This study was registered at the Japan Registry of Clinical Trials under registry number jRCT1031230709. Registered on 14 March 2024, https://jrct.niph.go.jp/re/reports/detail/73862.

Abstract Image

Abstract Image

优化急性胆管炎患者的短期抗生素治疗:一项开放标签随机对照试验(BOLT-P3试验)的研究方案
背景:急性胆管炎(AC)经常表现为社区获得性感染,并与传染病中抗生素使用的高流行率相关。东京指南2018 (TG18)建议胆道引流后4-7天使用抗生素。然而,这一建议缺乏强有力的证据证明其有效性,主要是基于不同的临床发现和专家意见。最近的回顾性研究主张较短的1- 3天抗生素疗程对AC治疗有效,这提示需要重新评估治疗时间,以达到治疗效果,同时最大限度地减少耐药性和不良反应。方法:我们设计了一项多中心、非盲、随机试验来评估短期治疗与标准疗程治疗在AC治疗中的疗效。短期治疗组在胆道引流成功后给予1-3天静脉抗生素治疗,而标准疗程组在胆道引流成功后给予4-7天静脉抗生素治疗。主要结果是内镜逆行胆管造影(ERCP)术后14天内的临床治愈率。参与者将以非盲、随机的方式使用最小化方法分配到任何一个疗程,分层因素包括病情严重程度和设施。我们确定需要210名参与者才能达到90%的统计能力,单侧显著性阈值为2.5%,非劣效性极限为10%。讨论:这项3期试验旨在确定短期治疗相对于标准疗程治疗的非劣效性。缩短抗生素使用时间可以减轻耐药细菌的出现,减少不良事件,减少住院时间和医疗费用。https://jrct.niph.go.jp/re/reports/detail/73862试验注册:本研究在日本临床试验注册中心注册,注册号为jRCT1031230709。于2024年3月14日注册,网址:https://jrct.niph.go.jp/re/reports/detail/73862。
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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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