Long-term effect of apomorphine infusion in advanced Parkinson's disease: a real-life study
- PMID: 34117268
- PMCID: PMC8196159
- DOI: 10.1038/s41531-021-00194-7
Long-term effect of apomorphine infusion in advanced Parkinson's disease: a real-life study
Abstract
Long-term effects of continuous subcutaneous apomorphine infusion (CSAI) on health-related quality of life (HRQoL) and predictors of CSAI discontinuation are poorly known. Data from consecutive advanced Parkinson's disease patients treated in routine care were retrospectively collected over 24 months after CSAI initiation, with a focus on the 39-item Parkinson's disease questionnaire (PDQ-39). We determined predictors of CSAI discontinuation and HRQoL improvement using multiple regression analysis. Of the 110 subjects evaluated over a 2-year period, 35% discontinued CSAI. Of those who continued treatment, HRQoL remained stable with a sustained reduction in motor fluctuations. The observed effect on dyskinesias was mild and transient. Of note, patients with preexisting impulse control disorders showed an overall good tolerability. PDQ-39 was the only baseline predictor of HRQoL improvement after 2 years of treatment. The presence of dyskinesias, poorer psychological status, shorter disease duration, male sex, and worse OFF state were predictors of discontinuation. Best candidates for CSAI are patients with: (i) poor baseline HRQoL and (ii) marked motor fluctuations.
Conflict of interest statement
B.D. served on scientific advisory boards for Aguettant, received research support from Orkyn and Elivie, and received travel grant from Orkyn and Elivie; E.B. received travel grant from Vitalaire and PEPS; C.V.-F. received a grant from Association Nationale de la Recherche et de la Technologie and full-time employment by Air Liquide Healthcare; P.D. received a travel grant from UCB pharma; A.M. received travel funding from AbbVie and Merz; L.-L.M. received speech honoraria from Lundbeck and Teva and received travel funding from the Medtronic, Teva, and AbbVie; C.D. received travel grant from Medtronic and Boston Scientific; D.B. received travel grant from Boston Scientific; L.M. received a travel grant from Orkyn (Air Liquide), Abbvie, Elivie, and Medtronic; H.L. received a travel grant from Orkyn (Air Liquide), Abbvie, and Elivie; E.M. received travel grant from Elivie; D.G. served on scientific advisory boards for AbbVie and Zambon, received speech honoraria from Medtronic and Abbvie, received research support from Air Liquide, and received travel grant from Abbvie; E.H. served on scientific advisory boards for Medtronic and Boston Scientific, received honoraria for speeches from Boston Scientific, and received travel grant from Merz; E.R. served on scientific advisory boards for Orkyn and Aguettant, received honoraria for speeches from Orkyn, Aguettant, and EVER Pharma, received research support from Orkyn, Aguettant, Elivie, and EVER Pharma, and received travel grant from Vitalaire, PEPS development, Aguettant, Orkyn, Elivie, and Adelia Medical. B.M, E.C., M.D., F.C.D., N.V, C.T., C.L., Y.W., and M.V. declare absence of commercial or financial relationships that could be construed as potential conflicts of interest.
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