Faulkner Stuart D, Sayuri Ii Suzanne, Pakarinen Chi, Somers Fabian, Jose Vicente Edo Maria, Prieto Remon Lucia, Diaz Ponce Ana, Gove Dianne, Ferrer Elisa, Nafria Begonya, Bertelsen Neil, Boudes Mathieu, Brooke Nicholas, Moutet Alexandra, Fahy Nick
Radcliffe Primary Care Building, Radcliffe Observatory Quarter, Oxford, UK.
The Synergist, Brussels, Belgium.
Health Expect. 2021 Apr;24(2):601-616. doi: 10.1111/hex.13207. Epub 2021 Feb 17.
The holistic evolution of patient engagement in medicines development requires a more detailed understanding of the needs of all involved stakeholders, and one that better accounts for the specific needs of some potentially vulnerable patient populations and key stages in medicines development.
The purpose of this convergent mixed-methods study was to better understand the needs of different stakeholders concerning patient engagement at three key stages in medicines development: research priority setting, clinical trial design and early dialogues with Health Technology Assessment bodies and regulators.
This study brought together findings from three sources: i) an online questionnaire, ii) face-to-face consultations with two potentially vulnerable patient populations, a workshop with Health Technology Assessment bodies, and iii) three-step modified Delphi methodology.
Overall stakeholders still need additional varied support mechanisms to undertake, sustain or measure value of patient engagement. Health Technology Assessment bodies need better rationale for patient engagement in early dialogue and tools to support its implementation. Improved awareness and understanding of the need and value that involving patients, who are often considered as potentially vulnerable, can bring is needed, as is better accommodation of their specific needs. Similarly, weighted Delphi categories were as follows: aims and objectives, and sustainability. Several additional themes were common across the three key stages in medicines development.
This broad-reaching study provides the blocks needed to build a framework for patient engagement in medicines development.
Patients were involved in review and interpretation of data.
患者参与药物研发的全面发展需要更详细地了解所有相关利益相关者的需求,并且要更好地考虑一些潜在弱势患者群体的特殊需求以及药物研发的关键阶段。
这项融合性混合方法研究的目的是更好地了解不同利益相关者在药物研发三个关键阶段(研究优先级设定、临床试验设计以及与卫生技术评估机构和监管机构的早期对话)中关于患者参与的需求。
本研究汇集了来自三个来源的结果:i)在线调查问卷;ii)与两个潜在弱势患者群体进行面对面咨询、与卫生技术评估机构举办一次研讨会;iii)三步改良德尔菲法。
总体而言,利益相关者仍需要更多样化的支持机制来开展、维持或衡量患者参与的价值。卫生技术评估机构在早期对话中需要更好的患者参与理由以及支持其实施的工具。需要提高对让通常被视为潜在弱势的患者参与其中所带来的需求和价值的认识与理解,并且要更好地满足他们的特殊需求。同样,德尔菲法加权类别如下:目标和可持续性。药物研发的三个关键阶段还有几个共同的额外主题。
这项广泛的研究为构建患者参与药物研发的框架提供了所需的要素。
患者参与了数据的审查和解读。