Continuous subcutaneous apomorphine infusion before subthalamic deep brain stimulation: a prospective, comparative study in 20 patients

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Psiquiatría, Radioloxía, Saúde Pública, Enfermaría e Medicinagl
dc.contributor.authorFernández Pajarín, Gustavo
dc.contributor.authorSesar Ignacio, Ángel
dc.contributor.authorAres Pensado, Begoña
dc.contributor.authorJiménez Martín, Isabel
dc.contributor.authorGelabert González, Miguel
dc.contributor.authorArán Echabe, Eduardo
dc.contributor.authorRelova Quinteiro, José Luis
dc.contributor.authorCastro García, Alfonso
dc.date.accessioned2022-08-19T06:58:54Z
dc.date.available2022-08-19T06:58:54Z
dc.date.issued2021
dc.description.abstractBackground: 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.peerreviewedSIgl
dc.identifier.citationMovement Disorders Clinical Practice 2021; 8(8): 1216–1224. https://doi.org/10.1002/mdc3.13338gl
dc.identifier.doi10.1002/mdc3.13338
dc.identifier.essn2330-1619
dc.identifier.urihttp://hdl.handle.net/10347/29088
dc.language.isoenggl
dc.publisherWileygl
dc.relation.publisherversionhttps://doi.org/10.1002/mdc3.13338gl
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectParkinson’s diseasegl
dc.subjectSubthalamic deep brain stimulationgl
dc.subjectApomorphinegl
dc.subjectDevice-aided therapiesgl
dc.titleContinuous subcutaneous apomorphine infusion before subthalamic deep brain stimulation: a prospective, comparative study in 20 patientsgl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
relation.isAuthorOfPublication0d83ff8a-4d80-49a5-a58d-0bfd5212efc9
relation.isAuthorOfPublicationc390156b-6464-4686-bd9b-71963e9bc6a5
relation.isAuthorOfPublicationd61a22a4-9654-42fe-901d-64c975eba878
relation.isAuthorOfPublication.latestForDiscoveryc390156b-6464-4686-bd9b-71963e9bc6a5

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