Minimal clinically important differences for treatment of hallucinations in Parkinson’s disease and dementia with Lewy bodies.

Publication date: Mar 24, 2025

Hallucinations are common and distressing symptoms in Parkinson’s disease (PD). Treatment response in clinical trials is measured using validated questionnaires, including the Scale for Assessment of Positive Symptoms-Hallucinations (SAPS-H) and University of Miami PD Hallucinations Questionnaire (UM-PDHQ). The minimum clinically important difference (MCID) has not been determined for either scale. This study aimed to estimate a range of MCIDs for SAPS-H and UM-PDHQ using both consensus-based and statistical approaches. A Delphi survey was used to seek opinions of researchers, clinicians, and people with lived experience. We defined consensus as agreement ≥75%. Statistical approaches used blinded data from the first 100 PD participants in the Trial for Ondansetron as Parkinson’s Hallucinations Treatment (TOP HAT, NCT04167813). The distribution-based approach defined the MCID as 0. 5 of the standard deviation of change in scores from baseline at 12 weeks. The anchor-based approach defined the MCID as the average change in scores corresponding to a 1-point improvement in clinical global impression-severity scale (CGI-S). Fifty-one researchers and clinicians contributed to three rounds of the Delphi survey and reached consensus that the MCID was 2 points on both scales. Sixteen experts with lived experience reached the same consensus. Distribution-defined MCIDs were 2. 6 points for SAPS-H and 1. 3 points for UM-PDHQ, whereas anchor-based MCIDs were 2. 1 and 1. 3 points, respectively. We used triangulation from multiple methodologies to derive the range of MCID estimates for the two rating scales, which was between 2 and 2. 7 points for SAPS-H and 1. 3 and 2 points for UM-PDHQ.

Concepts Keywords
Hallucinations Aged
Miami Consensus
Nct04167813 Delphi consensus
Parkinson Delphi Technique
Researchers Female
Hallucinations
hallucinations
Humans
Lewy Body Disease
Male
Middle Aged
Ondansetron
Ondansetron
Parkinson Disease
Parkinson’s disease
SAPS-H
Surveys and Questionnaires
UM-PDHQ

Semantics

Type Source Name
disease MESH hallucinations
disease MESH Parkinson’s disease
disease MESH dementia
drug DRUGBANK Ondansetron
disease MESH Lewy Body Disease
disease MESH Minimal Clinically Important Difference
pathway KEGG Parkinson disease

Original Article

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