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

FM Weaver, KA Follett, M Stern, P Luo, CL Harris… - Neurology, 2012 - AAN Enterprises
FM Weaver, KA Follett, M Stern, P Luo, CL Harris, K Hur, WJ Marks Jr, J Rothlind, O Sagher…
Neurology, 2012AAN Enterprises
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 …
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® 2012;79:55–65
American Academy of Neurology