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Neurostimulation for Advanced Parkinson Disease and Quality of Life at 5 Years: A Nonrandomized Controlled Trial.
Jost, Stefanie T; Aloui, Salima; Evans, Julian; Ashkan, Keyoumars; Sauerbier, Anna; Rizos, Alexandra; Petry-Schmelzer, Jan Niklas; Gronostay, Alexandra; Fink, Gereon R; Visser-Vandewalle, Veerle; Antonini, Angelo; Silverdale, Monty; Timmermann, Lars; Martinez-Martin, Pablo; Chaudhuri, K Ray; Dafsari, Haidar S.
Afiliação
  • Jost ST; University of Cologne, Faculty of Medicine and University Hospital Cologne, Department of Neurology, Cologne, Germany.
  • Aloui S; University of Cologne, Faculty of Medicine and University Hospital Cologne, Department of Neurology, Cologne, Germany.
  • Evans J; Department of Neurology and Neurosurgery, Salford Royal NHS Foundation Trust, Manchester, UK.
  • Ashkan K; Parkinson Foundation International Centre of Excellence, King's College Hospital, London, UK.
  • Sauerbier A; Academic Health Science Centre, University of Manchester, Greater Manchester, UK.
  • Rizos A; University of Cologne, Faculty of Medicine and University Hospital Cologne, Department of Neurology, Cologne, Germany.
  • Petry-Schmelzer JN; Parkinson Foundation International Centre of Excellence, King's College Hospital, London, UK.
  • Gronostay A; Academic Health Science Centre, University of Manchester, Greater Manchester, UK.
  • Fink GR; University of Cologne, Faculty of Medicine and University Hospital Cologne, Department of Neurology, Cologne, Germany.
  • Visser-Vandewalle V; University of Cologne, Faculty of Medicine and University Hospital Cologne, Department of Neurology, Cologne, Germany.
  • Antonini A; University of Cologne, Faculty of Medicine and University Hospital Cologne, Department of Neurology, Cologne, Germany.
  • Silverdale M; Cognitive Neuroscience, Institute of Neuroscience and Medicine (INM-3), Research Centre Jülich, Jülich, Germany.
  • Timmermann L; University of Cologne, Faculty of Medicine and University Hospital Cologne, Department of Stereotactic and Functional Neurosurgery, Cologne, Germany.
  • Martinez-Martin P; Department of Neurosciences (DNS), Padova University, Padova, Italy.
  • Chaudhuri KR; Department of Neurology and Neurosurgery, Salford Royal NHS Foundation Trust, Manchester, UK.
  • Dafsari HS; Department of Neurology, University Hospital Giessen and Marburg, Campus Marburg, Marburg, Germany.
JAMA Netw Open ; 7(1): e2352177, 2024 01 02.
Article em En | MEDLINE | ID: mdl-38236600
ABSTRACT
Importance Deep brain stimulation of the subthalamic nucleus (STN-DBS) improves quality of life (QOL) in patients with advanced Parkinson disease (PD). However, controlled studies with more than 3 years of follow-up are lacking.

Objective:

To investigate the long-term effects of STN-DBS on QOL compared with standard-of-care medication (MED). Design, Setting, and

Participants:

In this prospective, observational, quasi-experimental, longitudinal nonrandomized controlled trial, 183 patients were screened for eligibility and 167 were enrolled from March 1, 2011, to May 31, 2017, at 3 European university centers. Propensity score matching for demographic and clinical characteristics was applied to 108 patients with PD (62 in the STN-DBS group and 46 in the MED group), resulting in a well-balanced, matched subcohort of 25 patients per group. Data analysis was performed from September 2022 to January 2023. Exposure Treatment for PD of STN-DBS or MED. Main Outcomes and

Measures:

Assessments included Parkinson's Disease Questionnaire 8 (PDQ-8), Unified PD Rating Scale-motor examination, Scales for Outcomes in PD-activities of daily living (ADL) and motor complications, and levodopa-equivalent daily dose. Within-group longitudinal outcome changes, between-group differences, and correlations of change scores were analyzed.

Results:

The study population in the analysis included 108 patients (mean [SD] age, 63.7 [8.3] years; 66 [61.1%] male). At 5-year follow-up, PDQ-8 and ADL worsened only in the MED group (PDQ-8 change, -10.9; 95% CI, -19.0 to -2.7; P = .01; ADL change -2.0; 95% CI, -3.1 to -0.8; P = .002), whereas both outcomes remained stable in the STN-DBS group (PDQ-8 change, -4.3; 95% CI, -13.2 to 4.7; P = .34; ADL change, -0.8; 95% CI, -2.5 to 1.0; P = .38). Changes in PDQ-8 and ADL correlated moderately (rs = .40, P = .008). Furthermore, STN-DBS outcomes were favorable for motor complications (median difference in change scores between STN-DBS and MED, -2.0; 95% CI, -4.0 to -1.0; P = .003), mobility (-1.0; 95% CI, -2.0 to 0; P = .03), and levodopa-equivalent daily dose reduction (-821.4; 95% CI, -1111.9 to -530.8; P < .001). Conclusions and Relevance This study provides evidence of differences in QOL outcomes at 5-year follow-up between STN-DBS (stable) and MED (worsened), mainly driven by the favorable effect of STN-DBS on mobility (class IIb evidence). The association between changes in QOL and ADL, but not motor impairment or complications, highlights the relative importance of ADL outcomes for long-term DBS assessments. Trial Registration German ClinicalTrials Registry DRKS00006735.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Qualidade de Vida Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Qualidade de Vida Idioma: En Ano de publicação: 2024 Tipo de documento: Article