统一全球试验网络的质量改进指标,推进儿科临床试验的实施。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2024-09-01 Epub Date: 2024-06-20 DOI:10.1007/s43441-024-00663-0
Sabah Attar, Angie Price, Collin Hovinga, Breanne Stewart, Thierry Lacaze-Masmonteil, Fedele Bonifazi, Mark A Turner, Ricardo M Fernandes
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引用次数: 0

摘要

背景:尽管全球都在努力改善儿科临床试验,但儿科药物审批仍然严重滞后。要解决这些延误问题,需要研究网络之间开展合作。本文通过比较临床试验行为指标的驱动因素和内容,为促进不同辖区儿科网络之间的互操作性迈出了第一步:三个儿科网络--儿童高级临床试验研究所、母婴儿童和青少年研究网络以及 conect4children--分别制定了指标,以解决延误问题并提高效率。我们确定了每个网络确定衡量标准的方法,描述了每个网络的衡量标准,并绘制了一致性图,以便就网络可共享的核心衡量标准达成共识:结果:在一个网络(11 项指标)中,指标选择的驱动因素是网站质量的提高;在一个网络中,指标选择的驱动因素是网络绩效(13 项指标);在一个网络中,指标选择的驱动因素是两者(5 项指标)。衡量标准的领域包括研究能力/胜任力、研究机构的确定/可行性、试验启动和招募/注册。由研究机构质量改进驱动的网络没有能力/适配性或鉴定/可行性指标。确定了 15 个试验启动和开展的指标。所有三个网络中都有与研究机构批准相关的指标。衡量标准的主题可为制定 "共享 "衡量标准提供参考:我们发现在驱动因素、方法和指标方面存在差异。消除这种差异将有助于采用统一的方法来解决儿科药物审批的延误问题。概述了在全球范围内定义可互操作指标的合作工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Harmonizing Quality Improvement Metrics Across Global Trial Networks to Advance Paediatric Clinical Trials Delivery.

Harmonizing Quality Improvement Metrics Across Global Trial Networks to Advance Paediatric Clinical Trials Delivery.

Background: Despite global efforts to improve paediatric clinical trials, significant delays continue in paediatric drug approvals. Collaboration between research networks is needed to address these delays. This paper is a first step to promote interoperability between paediatric networks from different jurisdictions by comparing drivers for, and content of, metrics about clinical trial conduct.

Methods: Three paediatric networks, Institute for Advanced Clinical Trials for Children, the Maternal Infant Child and Youth Research Network and conect4children, have each developed metrics to address delays and create efficiencies. We identified the methodology by which each network identified metrics, described the metrics of each network, and mapped consistency to come to consensus about core metrics that networks could share.

Results: Metric selection was driven by site quality improvement in one network (11 metrics), by network performance in one network (13 metrics), and by both in one network (five metrics). The domains of metrics were research capacity/capability, site identification/feasibility, trial start-up, and recruitment/enrolment. The network driven by site quality improvement did not have indicators for capacity/capability or identification/feasibility. Fifteen metrics for trial start up and conduct were identified. Metrics related to site approvals were found in all three networks. The themes for metrics can inform the development of 'shared' metrics.

Conclusion: We found disparity in drivers, methodology and metrics. Tackling this disparity will result in a unified approach to addressing delays in paediatric drug approvals. Collaborative work to define inter-operable metrics globally is outlined.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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