Reeves Suzanne, Mahdi Josef, Appleby Matthew, Zubko Olga, Lee Teresa, Barber Julie A, Liu Kathy Y, Taylor John-Paul, Henderson Emily J, Schrag Anette, Howard Robert, Weil Rimona S
Division of Psychiatry, University College London, London, UK.
National Hospital for Neurology & Neurosurgery, London, UK.
Psychol Med. 2025 Mar 24;55:e93. doi: 10.1017/S0033291725000534.
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.
幻觉是帕金森病(PD)常见且令人痛苦的症状。临床试验中的治疗反应通过经过验证的问卷进行测量,包括阳性症状评估量表 - 幻觉量表(SAPS - H)和迈阿密大学帕金森病幻觉问卷(UM - PDHQ)。这两种量表的最小临床重要差异(MCID)尚未确定。本研究旨在使用基于共识和统计的方法来估计SAPS - H和UM - PDHQ的MCID范围。
采用德尔菲调查征求研究人员、临床医生和有实际经验者的意见。我们将共识定义为≥75%的一致意见。统计方法使用了昂丹司琼作为帕金森病幻觉治疗试验(TOP HAT,NCT04167813)中前100名PD参与者的盲态数据。基于分布的方法将MCID定义为12周时相对于基线得分变化标准差的0.5。基于锚定的方法将MCID定义为与临床总体印象严重程度量表(CGI - S)1分改善相对应的得分平均变化。
51名研究人员和临床医生参与了三轮德尔菲调查,并达成共识,即两种量表的MCID均为2分。16名有实际经验的专家也达成了相同的共识。基于分布定义的SAPS - H的MCID为2.6分,UM - PDHQ为1.3分,而基于锚定的MCID分别为2.1分和1.3分。
我们使用多种方法进行三角测量,得出两种评定量表的MCID估计范围,SAPS - H为2至2.7分,UM - PDHQ为1.3至2分。