Continuous subcutaneous apomorphine infusion before subthalamic deep brain stimulation: a prospective, comparative study in 20 patients
| dc.contributor.affiliation | Universidade de Santiago de Compostela. Departamento de Psiquiatría, Radioloxía, Saúde Pública, Enfermaría e Medicina | gl |
| dc.contributor.author | Fernández Pajarín, Gustavo | |
| dc.contributor.author | Sesar Ignacio, Ángel | |
| dc.contributor.author | Ares Pensado, Begoña | |
| dc.contributor.author | Jiménez Martín, Isabel | |
| dc.contributor.author | Gelabert González, Miguel | |
| dc.contributor.author | Arán Echabe, Eduardo | |
| dc.contributor.author | Relova Quinteiro, José Luis | |
| dc.contributor.author | Castro García, Alfonso | |
| dc.date.accessioned | 2022-08-19T06:58:54Z | |
| dc.date.available | 2022-08-19T06:58:54Z | |
| dc.date.issued | 2021 | |
| dc.description.abstract | Background: Background Studies comparing the clinical efficacy of apomorphine infusion (APO) with subsequent subthalamic deep brain stimulation (STN-DBS) in advanced Parkinson’s disease (aPD) are currently lacking. Retrospective data have shown that patients treated with APO are usually older, have a more prolonged disease, and a more severe phenotype. Objective: Objective To compare the benefit of APO with that of STN-DBS on motor, non-motor, cognitive, and quality of life in the same patient when given sequentially. Methods: Methods We prospectively analyzed 20 aPD patients over 3 different treatment phases: baseline (optimized medical treatment), during APO treatment, and during subsequent STN-DBS treatment. The APO and STN-DBS phases were stable for 6 months, and evaluation of the different treatments was separated by 6 months. Results: Results Compared to baseline, APO, and STN-DBS reduced mean daily off time by 70.5% and 89.3% (P = 0.012), respectively, and scores for Unified Parkinson’s Disease Rating Scale (UPDRS) IV by 27.5% and 80.5% (P ≤ 0.001), Non-motor symptoms scale (NMSS) by 24.6% and 49.3% (P ≤ 0.001), Montgomery Asberg depression scale (MADRS) by 7.4% and 39.0% (P = 0.27), Starkstein apathy scale (SAS) by 51.1% and 39.9% (P = 0.734), Parkinson’s disease sleep scale 2 (PDSS-2) by 25.7% and 56.7% (P ≤ 0.001), and Parkinson’s disease questionnaire 39 item (PDQ-39) by 39.6% and 64.9% (P ≤ 0.001). Global cognition did not change with either therapy, but phonetic fluency worsened after STN-DBS compared to APO (P = 0.022). Conclusions: Conclusions Both APO and STN-DBS improved motor and non-motor symptoms and quality of life compared to optimized medical treatment in aPD. Overall, STN-DBS was the most effective treatment, but APO showed a pronounced benefit on motor symptoms. Effective treatment for aPD should not be delayed, even when waiting for surgery. | gl |
| dc.description.peerreviewed | SI | gl |
| dc.identifier.citation | Movement Disorders Clinical Practice 2021; 8(8): 1216–1224. https://doi.org/10.1002/mdc3.13338 | gl |
| dc.identifier.doi | 10.1002/mdc3.13338 | |
| dc.identifier.essn | 2330-1619 | |
| dc.identifier.uri | http://hdl.handle.net/10347/29088 | |
| dc.language.iso | eng | gl |
| dc.publisher | Wiley | gl |
| dc.relation.publisherversion | https://doi.org/10.1002/mdc3.13338 | gl |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International | |
| dc.rights.accessRights | open access | gl |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
| dc.subject | Parkinson’s disease | gl |
| dc.subject | Subthalamic deep brain stimulation | gl |
| dc.subject | Apomorphine | gl |
| dc.subject | Device-aided therapies | gl |
| dc.title | Continuous subcutaneous apomorphine infusion before subthalamic deep brain stimulation: a prospective, comparative study in 20 patients | gl |
| dc.type | journal article | gl |
| dc.type.hasVersion | VoR | gl |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | 0d83ff8a-4d80-49a5-a58d-0bfd5212efc9 | |
| relation.isAuthorOfPublication | c390156b-6464-4686-bd9b-71963e9bc6a5 | |
| relation.isAuthorOfPublication | d61a22a4-9654-42fe-901d-64c975eba878 | |
| relation.isAuthorOfPublication.latestForDiscovery | c390156b-6464-4686-bd9b-71963e9bc6a5 |
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