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患者和公众参与一项平台随机试验的设计和方案制定,该试验旨在评估诊断测试以优化抗菌治疗(PROTECT)。

Patient and public involvement in the design and protocol development for a platform randomised trial to evaluate diagnostic tests to optimise antimicrobial therapy (PROTECT).

作者信息

Svobodova Martina, Keating Liza, Gager Melanie, Waldron Cherry-Ann, Ainsworth Sammy, Carman Julie, Jones Sarah, Ogden Margaret, Prestwich Graham

机构信息

Centre for Trials Research, Cardiff University, Cardiff, Wales, CF14 4YS, UK.

Intensive Care Unit, Royal Berkshire NHS Foundation Trust, Reading, England, RG1 5AN, UK.

出版信息

NIHR Open Res. 2024 Sep 20;4:52. doi: 10.3310/nihropenres.13591.1. eCollection 2024.

Abstract

BACKGROUND

Our patient and public involvement activities were part of a project aiming to develop a master protocol and National Institute for Health and Care research application for the PROTECT trial aiming to assess the effectiveness, implementation, and efficiency of antimicrobial stewardship interventions, to safely reduce unnecessary antibiotic usage by excluding severe bacterial infection in acutely unwell patients.

METHODS

Three public involvement sessions were held with representation from young people and parents, people from diverse backgrounds and people with experience of presenting to the emergency department with undifferentiated illness. The teleconference meetings lasted between 60-90 minutes, were recorded, notes were subsequently taken, and findings summarised. The data was collected on September 13, 2023, October 14, 2023 and February 28, 2024.

RESULTS

Working with public involvement contributors and public involvement groups at the protocol development stage provided an opportunity for the public to shape and influence the trial. We were able to establish the feasibility of the trial in the proposed setting and gain insights into how it would be perceived by potential trial participants. Antibiotic resistance was viewed as an urgent problem and research evaluating new technologies was deemed timely and important. The platform design was considered appropriate, time and cost-effective. Deferred and electronic methods of consent were viewed as acceptable if a clear and inclusive explanation is provided.

CONCLUSIONS

Having access to public contributors with relevant lived experience was an important resource for the trial team. Identification and recruitment of public contributors via working with existing public involvement groups across the UK enabled the trial team to involve public members with varied life experiences and from diverse backgrounds. This project was a good practice example of how public involvement groups and practitioners across the UK can work together to deliver public involvement that is inclusive of relevant groups.

摘要

背景

我们的患者和公众参与活动是一个项目的一部分,该项目旨在制定一项主方案,并为PROTECT试验申请英国国家卫生与保健研究所的研究资金。该试验旨在评估抗菌药物管理干预措施的有效性、实施情况和效率,通过排除急性不适患者的严重细菌感染来安全减少不必要的抗生素使用。

方法

举办了三次公众参与会议,参与者包括年轻人及其父母、来自不同背景的人以及有因未分化疾病到急诊科就诊经历的人。电话会议持续60 - 90分钟,会议进行了录音,随后做了笔记并总结了结果。数据收集于2023年9月13日、2023年10月14日和2024年2月28日。

结果

在方案制定阶段与公众参与贡献者和公众参与团体合作,为公众提供了塑造和影响试验的机会。我们能够确定试验在提议环境中的可行性,并深入了解潜在试验参与者对它的看法。抗生素耐药性被视为一个紧迫问题,评估新技术的研究被认为是及时且重要的。平台设计被认为是合适的,具有时间和成本效益。如果能提供清晰且包容的解释,延期同意和电子同意方法被视为可以接受。

结论

接触有相关生活经验的公众贡献者对试验团队来说是一项重要资源。通过与英国各地现有的公众参与团体合作来识别和招募公众贡献者,使试验团队能够让具有不同生活经历和背景的公众成员参与进来。该项目是英国公众参与团体和从业者如何共同努力实现包容相关群体的公众参与的一个良好实践范例。

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