The Progressive Supranuclear Palsy Clinical Deficits Scale

被引:28
|
作者
Piot, Ines [1 ,2 ,3 ]
Schweyer, Kerstin [1 ,2 ]
Respondek, Gesine [1 ,2 ,9 ]
Stamelou, Maria [4 ,5 ,6 ]
Gasser, Thomas
Hermann, Andreas
Hoeglinger, Gunter
Hoellerhage, Matthias
Kimmich, Okka
Klockgether, Thomas
Levin, Johannes
Machetanz, Gerrit
Osterrath, Antje
Palleis, Carla
Prudlo, Johannes
Spottke, Annika
Berg, Daniela
Buerk, Katrin
Classen, Joseph
Eggers, Carsten
Greuel, Andrea
Grimm, Max-Joseph
Hermann, Lennard
Iankova, Vassilena
Jahn, Klaus
Jost, Wolfgang
Klietz, Martin
Kuehn, Andrea
Marxreiter, Franz
Paschen, Steffen
Poetter-Nerger, Monika
Preisl, Marie-Therese
Prilop, Lisa
Toenges, Lars
Trenkwalder, Claudia
Warnecke, Tobias
Wegner, Florian
Winkler, Juergen
Antonini, Angelo
Bhatia, Kailash P.
Boxer, Adam L.
Colosimo, Carlo
Compta, Yaroslau
Corvol, Jean-Christophe
Golbe, Lawrence I.
Hoglinger, Guenter U. [1 ,2 ,9 ]
Lang, Anthony E.
Litvan, Irene
Morris, Huw R.
Nilsson, Christer
机构
[1] German Ctr Neurodegenerat Dis DZNE, Munich, Germany
[2] Tech Univ Munich, Dept Neurol, Munich, Germany
[3] Univ Basel, Dept Neurol, Basel, Switzerland
[4] Natl & Kapodistrian Univ Athens, HYGEIA Hosp, Parkinsons Dis & Movement Disorders Dept, Athens, Greece
[5] Natl & Kapodistrian Univ Athens, Aiginite Hosp, Dept Neurol 1, Athens, Greece
[6] Philipps Univ, Neurol Clin, Marburg, Germany
[7] Ludwig Maximilians Univ Munchen, Dept Psychol, Munich, Germany
[8] Rush Univ, Dept Neurol Sci, Med Ctr, Chicago, IL 60612 USA
[9] Hannover Med Sch, Dept Neurol, Carl Neuberg Str 1, D-30625 Hannover, Germany
关键词
progressive supranuclear palsy; clinical rating scales; outcome measures; power calculation; MONTREAL COGNITIVE ASSESSMENT; MENTAL-STATE-EXAMINATION; DISEASE-RATING-SCALE; QUALITY-OF-LIFE; CORTICOBASAL DEGENERATION; PARKINSONS-DISEASE; NONFLUENT APHASIA; CRITERIA; MANIFESTATION; MULTICENTER;
D O I
10.1002/mds.27964
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background There is currently no undisputed, validated, clinically meaningful measure for deficits in the broad spectrum of PSP phenotypes. Objective To develop a scale to monitor clinical deficits in patients with PSP across its broad phenotypes. Methods The Progressive Supranuclear Palsy Clinical Deficits Scale was conceptualized to cover seven clinical domains (Akinesia-rigidity, Bradyphrenia, Communication, Dysphagia, Eye movements, Finger dexterity, and Gait & balance), each scored from 0 to 3 (no, mild, moderate, or severe deficits). User guidelines were developed to standardize its application. Progressive Supranuclear Palsy Clinical Deficits Scale scores were collected in patients fulfilling the MDS-PSP diagnostic criteria in two independent, multicenter, observational studies, both cross-sectionally (exploratory DescribePSP cohort; confirmatory ProPSP cohort) and longitudinally (12-months' follow-up, both cohorts). Results Cognitive pretesting demonstrated easy scale utility. In total, 164 patients were scored (70.4 +/- 7.6 years; 62% males, 35% variant phenotypes). Mean Progressive Supranuclear Palsy Clinical Deficits Scale completion time was 4 minutes. The Progressive Supranuclear Palsy Clinical Deficits Scale total score correlated with existing scales (e.g., Progressive Supranuclear Palsy Rating Scale: R = 0.88; P < 0.001). Individual Progressive Supranuclear Palsy Clinical Deficits Scale items correlated well with similar constructs in existing scales. Internal consistency (Cronbach's alpha: 0.75), inter-rater reliability (0.96), and test-retest stability (0.99) were acceptable. The PSP-CDS showed significant 12-month change (baseline, 8.6 +/- 3.6; follow-up: 10.8 +/- 3.6; annualized difference: 3.4 +/- 3.4; n = 49; P < 0.0001). Sample sizes required per arm for a two-arm, 1-year follow-up therapeutic trial to detect 50% change in Progressive Supranuclear Palsy Clinical Deficits Scale progression was estimated to be 65 (two-sided, two-sample t test). Conclusion The Progressive Supranuclear Palsy Clinical Deficits Scale is a rapidly completed, clinimetrically sound scale for clinical care and research involving PSP. (c) 2020 International Parkinson and Movement Disorder Society
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页码:650 / 661
页数:12
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