Establishing Consensus to Support and Enhance Parkinson’s Disease Management
A UK Modified Delphi Consensus Study
This study was initiated and funded by Bial Pharma UK.
Background and Rationale
Motor fluctuations, including wearing off and dyskinesia, affect up to 40% of patients within 4–6 years of L Dopa use2. Although L Dopa remains the cornerstone of Parkinson’s disease (PD) treatment, long term therapy is associated with motor complications4,2. Current guidelines recommend adjunctive therapies but provide limited practical guidance, contributing to variation in clinical practice and sub optimal care3.
This UK‑wide consensus sought to provide real‑world, expert‑led guidance to support earlier and more individualised treatment decisions.
Study Objectives
Agree a set strategy to optimise and implement L-Dopa therapy with adjunctive therapies
Agree on a set framework on the best practices for Parkinson’s disease management within NHS capacity
Gain consensus to support and enhance Parkinson's disease management
Methodology
Delphi consensus is a widely recognised and well-established methodology for capturing expert opinion and driving alignment where evidence is limited or evolving.
By using a structured, anonymised, and iterative process, it reduces bias and builds credible agreement among healthcare professionals. This rigour makes Delphi outputs both highly useful in clinical decision-making and suitable for peer-reviewed publication.
There is a growing need for healthcare consensus
The Delphi method is a credible, approach to support healthcare decision-making
Delphi process summary
Statement development (Steering committee): 59 draft statements across 4 domains.
Survey testing (wider expert panel, n=150): Ratings using a 4-point Likert scale.
Consensus threshold: ≥75% agreement.
Results analysis workshop (Steering committee): Interpretation of results.
Manuscript development (Steering committee): Peer-reviewed article submission.
Expert consensus methodology
Using a modified Delphi approach
Expert Panel
The steering committee consisted of nine highly experienced UK experts across neurology, geriatrics, nursing, and clinical neuroscience. A wider multidisciplinary expert panel (n=150) participated in the Delphi survey, with balanced representation by role and level of experience.
Steering committee members
9 experts in the panel across the UK
3 neurologists
2 geriatricians
1 professor of clinical neuroscience
1 professor of nursing
1 advanced nurse practitioner
1 Parkinson's disease specialist nurse
Consensus Results
Consensus was achieved for all 59 statements (100%).
Consensus results by topic and statement, final statement set (59 statements)
Agreement levels
Overview of consensus domains:
Consensus domains
A: Initiating and monitoring L Dopa (14 statements).
B: Early identification of motor fluctuations (27 statements).
C: Use of adjunctive therapies (12 statements).
D: Best practice and education (6 statements).
Key Recommendations
Recomendations
Full Peer‑Reviewed Article
The full peer‑reviewed manuscript describing the methodology and detailed findings of this Delphi consensus study is available online.
Article link: A modified Delphi consensus study to support and enhance Parkinson's disease management
Conclusion
This modified Delphi consensus was led by 9 multidisciplinary experts across the UK.
All consensus statements achieved high levels of agreement from a multidisciplinary panel of 150 healthcare professionals involved in PD management.
Six evidence-based recommendations were reported in this study, aiming to enhance the management of PD. They emphasise earlier, individualised treatment decisions aligned with patient goals, timely detection of motor fluctuations such as wearing off, and the early* use of adjunctive therapies when appropriate within license.
By promoting earlier intervention and more structured follow-up, this consensus supports a proactive approach that may improve long-term outcomes and quality of life for people living with PD.
Use of medicines outside of their licensed indications cannot be recommended by Bial Pharma UK.
Sign up to our website
Enjoyed this content and want to see more? Sign up to access more. The Bial website contains promotional material.
Aradi SD, Hauser RA. Neurotherapeutics. 2020;17:1339–1365.
NICE BNF. Parkinson’s disease treatment summaries. NICE; 2025.
Antonini A, Stoessl AJ, Kleinman LS, et al. Developing consensus among movement disorder specialists on clinical indicators for identifying advanced Parkinson’s disease: a multi-country Delphi-panel approach. Curr Med Res Opin. 2018;34(12):2063–2073.
Fox S, Antonini A, Ferreira J. EMJ. 2022;7(4):20–27.
National Institute for Health and Care Excellence (NICE). Parkinson’s disease in adults: diagnosis and management (NG71). NICE; 2017.
Fox SH, Katzenschlager R, Lim S‑Y, et al. International Parkinson and Movement Disorder Society evidence-based medicine review: update on treatments for the motor symptoms of Parkinson’s disease. Mov Disord. 2018;33(8):1248–1266.
Armstrong MJ, Okun MS. Diagnosis and treatment of Parkinson disease: a review. JAMA. 2020;323(6):548–560.
Goetz CG, Tilley BC, Shaftman SR, et al. Movement Disorder Society–sponsored revision of the Unified Parkinson’s Disease Rating Scale (MDS‑UPDRS): scale presentation and clinimetric testing results. Mov Disord. 2008;23(15):2129–2170.
Hauser RA, Auinger P; Parkinson Study Group. Determination of minimal clinically important change in early and advanced Parkinson’s disease. Mov Disord. 2011;26(5):813–818.
Pavese N, et al. J Parkinsons Dis. 2026. SAGE Journals. DOI: 10.1177/1877718X261427577.
Grissinger M. Pharmacy and Therapeutics 2018; 43: 10.
Cabrera-Martos I, Ortiz-Rubio A, Torres-Sánchez I, et al. Clin Rehabil 2019; 33: 465–472.
Grosset KA, Grosset DG. Movement Disorders 2005; 20: 616–619.
Ziebell M, Khalid U, Klein AB, et al. Neurobiol Aging 2012; 33: 428.e1-428.e5.
Sampaio TB, Savall AS, Gutierrez MEZ, et al. Neural Regen Res 2017; 12: 549–557.
Hansen L, Witzig V, Schulz JB, et al. Neurological Sciences 2023; 44: 3905.
Stern MB. Parkinsonism Relat Disord 2000; 7: 27–33.
Parkinson’s UK. Patient initiated follow up/review, 2025.
NICE, Guidance, Parkinson’s disease in adults information for the public follow-up checks. NICE, 2025.
Caillava-Santos F, Margis R, de Mello Rieder CR. Neuropsychiatr Dis Treat 2015; 11: 1175.
Ferreira JJ, Lee JY, Ma H Il, et al. J Neurol 2024; 271: 6729–6738.
Stocchi F. et al Parkinsonism Relat Disord (2014) 20:204-11 DOI: 10.1016/j.parkreldis.2013.10.027
Tinelli M, Kanavos P, Grimaccia F. A literature review of the potential clinical and socioeconomic impact of targeting unmet needs in Parkinson’s disease.
Antonini A, Stoessl AJ, Kleinman LS, et al. Curr Med Res Opin 2018; 34: 2063–2073.
Parkinson’s UK People with Parkinson’s can’t wait any longer. Parkinson’s UK, 2025.
WEB-NPD-UNB-GB-26-0005
April 2026