Engaging stakeholders in pharmacoepidemiology research: Current state and recommendations

Purpose Given current efforts to enhance patient‐centered care and shared decision‐making, the International Society of Pharmacoepidemiology Workgroup on Patient Engagement assessed patient and other stakeholder engagement in pharmacoepidemiology research and provides recommendations for the field....

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Published in:Pharmacoepidemiology and drug safety 2019-06, Vol.28 (6), p.766-776
Main Authors: Camelo Castillo, Wendy, Heath, Nicholas, Kim, John, Yang, Kimberly, Ritchey, Mary E., dosReis, Susan, Santanello, Nancy, West, Suzanne L.
Format: Article
Language:English
Subjects:
benefit‐risk assessment
Decision making
Decision Making, Shared
Humans
Local government
patient engagement
patient involvement
Patient Participation - methods
Patient-Centered Care - methods
Patient-Centered Care - organization & administration
pharmacoepidemiology
Pharmacoepidemiology - methods
Pharmacoepidemiology - organization & administration
pharmacovigilance
Research Design
stakeholder participation
Stakeholders
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Summary:Purpose Given current efforts to enhance patient‐centered care and shared decision‐making, the International Society of Pharmacoepidemiology Workgroup on Patient Engagement assessed patient and other stakeholder engagement in pharmacoepidemiology research and provides recommendations for the field. Methods A systematic review used MEDLINE and EMBASE to identify published literature from 2005 to 2016 addressing how stakeholders—patients, caregivers, and others—assisted researchers conducting pharmacoepidemiologic research. Three pairs of Workgroup members screened titles and s to select articles for full‐text review and analysis. Two Workgroup members ed the following data: research focus, characterization and role of stakeholders, and type(s) of engagement strategy employed. Data were summarized descriptively. Results We identified 5717 references for screening. Of these, 69 met the criteria for full‐text screening, and 11 were selected for data ion. Of these 11 studies, seven focused on the development of a research agenda and eight had stakeholders react or advise on an aspect of the study. Although patients were the most commonly identified stakeholders, advocacy groups and health care professionals were also frequently identified. Some studies reported the engagement of other stakeholders, including local government or policy experts. Engagement strategies varied, with five studies using more than one strategy. Studies often did not indicate the involvement of stakeholders in developing the study design or with implementation. Conclusions Currently, few pharmacoepidemiology publications mention patient or other stakeholder engagement in the design, analysis, or reporting of research. This suggests that there are opportunities to expand stakeholder engagement and/or increase the transparency of reporting stakeholder engagement.
ISSN:1053-8569
1099-1557
DOI:10.1002/pds.4786