Patient involvement in RSV research: towards patients setting the research agenda

Journal article

Respiratory syncytial virus (RSV) causes a substantial disease burden among children, elderly and immunocompromised adults. Recognition of patient involvement in research is gradually increasing. Most research is being carried out without active patient involvement other than patients participating as study subjects, and most knowledge gained through research only partially reaches the general public. Since 2016, the RSV Patient Advisory Board has officially been involved as an advisory group in the Respiratory Syncytial Virus Consortium in Europe (RESCEU). What started as a small single-center initiative, is now growing towards an international organization providing patient perspectives as inputs to scientists, and improving awareness of RSV. This article summarizes the history, current role, and future aims of the RSV Patient Advisory Board as an advocate to improve patient involvement in research. RSV patients and their representatives are important stakeholders in setting the global research agenda, and educating patients, professionals, and the general public.

Authors: Derksen-Lazet, ND; Parmentier, CEJ; Wildenbeest, JG; Bont, LJ; Pollard, AJ

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: Oxford University Press
• Journal: The Journal of Infectious Diseases
• Volume: 226
• Issue: Suppl 1
• Pages: S130-S134
• Place of publication: United States
• Publication date: 2022-04-29
• DOI: 10.1093/infdis/jiac110
• EISSN: 1537-6613
• ISSN: 0022-1899
• Pmid: 35485175
• Language: English
• Keywords: patient involvement; awareness; FFR; patient participation; RESCEU Investigators; patient network; patient perspective