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Patients’ perception of Parkinson’s disease-associated pain following initiation of rotigotine: a multicenter non-interventional study
- Source :
- Postgraduate Medicine. 129:46-54
- Publication Year :
- 2016
- Publisher :
- Informa UK Limited, 2016.
-
Abstract
- To evaluate Parkinson's disease (PD)-associated pain as perceived by the patients (subjective characterization), and how this may change following initiation of rotigotine transdermal patch.SP1058 was a non-interventional study conducted in routine clinical practice in Germany and Austria in patients experiencing PD-associated pain (per the physician's assessment). Data were collected at baseline (ie, before rotigotine initiation) and at a routine visit after ≥25 days (-3 days allowed) of treatment on a maintenance dose of rotigotine (end of study [EoS]). Pain perception was assessed using the 12-item Pain Description List of the validated German Pain Questionnaire (each item ranked 0 = 'not true' to 3 = 'very true'). Primary effectiveness variable: change from baseline to EoS in the sum score of the 4 'affective dimension' items of the Pain Description List. Secondary effectiveness variables: change from baseline to EoS in Unified Parkinson's Disease Rating Scale (UPDRS) II, III, and II+III scores, and Parkinson's Disease Questionnaire (PDQ-8) total score (PD-related quality-of-life). Other variables included scores of the eight 'sensory dimension' items of the Pain Description List.Of 93 enrolled patients (mean [SD] age: 71.1 [9.0] years; male: 48 [52%]), 77 (83%) completed the study, and 70 comprised the full analysis set. The mean (SD) change from baseline in the sum score of the four 'affective dimension' items was -1.3 (2.8) indicating a numerical improvement (baseline: 3.9 [3.4]). In the 'sensory dimension', pain was mostly perceived as 'pulling' at baseline (49/70 [70%]); 'largely true'/'very true'). Numerical improvements were observed in all UPDRS scores (mean [SD] change in UPDRS II+III: -5.3 [10.5]; baseline: 36.0 [15.9]), and in PDQ-8 total score (-2.0 [4.8]; baseline: 10.7 [5.9]). Adverse drug reactions were consistent with dopaminergic stimulation and transdermal administration.The perception of the 'affective dimension' of PD-associated pain numerically improved in patients treated with rotigotine. ClinicalTrials.gov identifier: NCT01606670; https://clinicaltrials.gov/ct2/show/NCT01606670?term=NCT01606670rank=1.
- Subjects :
- Male
Levodopa
medicine.medical_specialty
Parkinson's disease
Tetrahydronaphthalenes
Pain
Thiophenes
Administration, Cutaneous
Placebo
law.invention
03 medical and health sciences
0302 clinical medicine
Randomized controlled trial
law
Rating scale
Germany
Surveys and Questionnaires
Activities of Daily Living
Humans
Medicine
030212 general & internal medicine
Aged
Aged, 80 and over
business.industry
Maintenance dose
Parkinson Disease
Rotigotine
General Medicine
Middle Aged
medicine.disease
Austria
Dopamine Agonists
Physical therapy
Female
Observational study
business
030217 neurology & neurosurgery
Follow-Up Studies
medicine.drug
Subjects
Details
- ISSN :
- 19419260, 00325481, and 01606670
- Volume :
- 129
- Database :
- OpenAIRE
- Journal :
- Postgraduate Medicine
- Accession number :
- edsair.doi.dedup.....dcbe332440fbb1cb70bf2494494c4d4e
- Full Text :
- https://doi.org/10.1080/00325481.2017.1258953