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一项旨在减少中国农村基层医疗机构急性呼吸道感染不合理抗生素处方的抗生素管理计划:一项整群随机对照试验的研究方案。

An antibiotic stewardship programme to reduce inappropriate antibiotic prescribing for acute respiratory infections in rural Chinese primary care facilities: study protocol for a clustered randomised controlled trial.

机构信息

National Center for Respiratory Diseases, State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, Laboratory of Guangdong-Hong Kong -Macao Great Bay, Guangzhou Medical University, 151 Yanjiang Xi Rd, Guangzhou City, 510120, Guangdong, China.

Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada.

出版信息

Trials. 2020 May 12;21(1):394. doi: 10.1186/s13063-020-04303-4.

Abstract

BACKGROUND

Inappropriate prescribing of antibiotics for acute respiratory infections at the primary care level represents the major source of antibiotic misuse in healthcare, and is a major driver for antimicrobial resistance worldwide. In this study we will develop, pilot and evaluate the effectiveness of a comprehensive antibiotic stewardship programme in China's primary care hospitals to reduce inappropriate prescribing of antibiotics for acute respiratory infections among all ages.

METHODS

We will use a parallel-group, cluster-randomised, controlled, superiority trial with blinded outcome evaluation but unblinded treatment (providers and patients). We will randomise 34 primary care hospitals from two counties within Guangdong province into the intervention and control arm (1:1 overall ratio) stratified by county (8:9 within-county ratio). In the control arm, antibiotic prescribing and management will continue through usual care. In the intervention arm, we will implement an antibiotic stewardship programme targeting family physicians and patients/caregivers. The family physician components include: (1) training using new operational guidelines, (2) improved management and peer-review of antibiotic prescribing, (3) improved electronic medical records and smart phone app facilitation. The patient/caregiver component involves patient education via family physicians, leaflets and videos. The primary outcome is the proportion of prescriptions for acute respiratory infections (excluding pneumonia) that contain any antibiotic(s). Secondary outcomes will address how frequently specific classes of antibiotics are prescribed, how frequently key non-antibiotic alternatives are prescribed and the costs of consultations. We will conduct a qualitative process evaluation to explore operational questions regarding acceptability, cultural appropriateness and burden of technology use, as well as a cost-effectiveness analysis and a long-term benefit evaluation. The duration of the intervention will be 12 months, with another 24 months' post-trial long-term follow-up.

DISCUSSION

Our study is one of the first trials to evaluate the effect of an antibiotic stewardship programme in primary care settings in a low- or middle-income country (LMIC). All interventional activities will be designed to be embedded into routine primary care with strong local ownership. Through the trial we intend to impact on clinical practice and national policy in antibiotic prescription for primary care facilities in rural China and other LMICs.

TRIAL REGISTRATION

ISRCTN, ID: ISRCTN96892547. Registered on 18 August 2019.

摘要

背景

基层医疗机构对急性呼吸道感染的抗生素处方不当是造成抗生素滥用的主要原因,也是全球抗生素耐药性的主要驱动因素。本研究旨在开发、试点和评估中国基层医疗机构全面抗生素管理计划的有效性,以减少各年龄段急性呼吸道感染的抗生素处方不当。

方法

我们将采用平行组、集群随机、对照、优效性试验,对结果进行盲法评估,但对治疗(提供者和患者)进行开放。我们将从广东省的两个县中随机抽取 34 家基层医疗机构,按照县(8:9 县内比例)分为干预组和对照组(1:1 总比例)。在对照组中,抗生素的开具和管理将继续通过常规护理进行。在干预组中,我们将针对家庭医生和患者/照护者实施抗生素管理计划。家庭医生部分包括:(1)使用新操作指南进行培训,(2)改善抗生素开具的管理和同行审查,(3)改善电子病历和智能手机应用程序的便利性。患者/照护者部分包括通过家庭医生进行患者教育、发放传单和播放视频。主要结局是急性呼吸道感染(不包括肺炎)处方中包含任何抗生素的比例。次要结局将包括特定类别的抗生素的开具频率、关键非抗生素替代品的开具频率以及咨询费用。我们将进行定性的过程评估,以探索关于可接受性、文化适宜性和技术使用负担的操作性问题,以及成本效益分析和长期效益评估。干预的持续时间为 12 个月,随后进行 24 个月的试验后长期随访。

讨论

我们的研究是评估中低收入国家(LMIC)基层医疗环境中抗生素管理计划效果的首批试验之一。所有干预活动都将设计为嵌入常规基层医疗服务中,并具有强烈的地方所有权。通过该试验,我们旨在影响中国农村和其他 LMIC 地区基层医疗机构的临床实践和国家抗生素处方政策。

试验注册

ISRCTN,编号:ISRCTN85044553。于 2019 年 8 月 18 日注册。

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