4.7 Article

Randomized trial of deep brain stimulation for Parkinson disease Thirty-six-month outcomes

期刊

NEUROLOGY
卷 79, 期 1, 页码 55-65

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0b013e31825dcdc1

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资金

  1. Medtronic Neurological, Inc.
  2. Cooperative Studies Program, Department of Veterans Affairs Office of Research and Development
  3. NINDS
  4. Teva
  5. Ipsen
  6. Medtronic
  7. Adamas Pharma
  8. Schering-Plough
  9. GSK
  10. GE Healthcare
  11. EMD Serono
  12. Boehringer Ingelheim
  13. St Jude Medical
  14. Impax Pharma
  15. Novartis
  16. Biogen
  17. Xenoport
  18. Solvay
  19. Eisai
  20. NIH/NINDS
  21. NPF
  22. Allon
  23. Acadia
  24. Valeant
  25. Kyowa
  26. Johnson Johnson
  27. Schering
  28. Santhera

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Objectives: Our objective was to compare long-term outcomes of deep brain stimulation (DBS) of the globus pallidus interna (GPi) and subthalamic nucleus (STN) for patients with Parkinson disease (PD) in a multicenter randomized controlled trial. Methods: Patients randomly assigned to GPi (n = 89) or STN DBS (n = 70) were followed for 36 months. The primary outcome was motor function on stimulation/off medication using the Unified Parkinson's Disease Rating Scale motor subscale. Secondary outcomes included quality of life and neurocognitive function. Results: Motor function improved between baseline and 36 months for GPi (41.1 to 27.1; 95% confidence interval [CI] -16.4 to -10.8; p < 0.001) and STN (42.5 to 29.7; 95% CI -15.8 to -9.4; p < 0.001); improvements were similar between targets and stable over time (p = 0.59). Health-related quality of life improved at 6 months on all subscales (all p values significant), but improvement diminished over time. Mattis Dementia Rating Scale scores declined faster for STN than GPi patients (p = 0.01); other neurocognitive measures showed gradual decline overall. Conclusions: The beneficial effect of DBS on motor function was stable and comparable by target over 36 months. Slight declines in quality of life following initial gains and gradual decline in neurocognitive function likely reflect underlying disease progression and highlight the importance of nonmotor symptoms in determining quality of life. Classification of Evidence: This study provides Class III evidence that improvement of motor symptoms of PD by DBS remains stable over 3 years and does not differ by surgical target. Neurology (R) 2012; 79:55-65

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