Papers2814800

Bilateral Deep Brain Stimulation vs Best Medical Therapy for Patients With Advanced Parkinson Disease A Randomized Controlled Trial

JAMA : the journal of the American Medical Association · 7-1-2009 · 2814800 on PMC →
Entities in this paper
Bilateral deep sclerectomy advanced Parkinson disease with motor complications On time without troubling dyskinesia Motor function Quality of Life Neurocognitive function Serious adverse events

Extracted findings (5)

Patients receiving bilateral deep brain stimulation gained a mean of 4.6 hours per day of on time without troubling dyskinesia at 6 months, compared with no change in the best medical therapy group.

Effect: improvement; 4.6 h/d gain (DBS) vs 0 h/d (BMT); between-group difference 4.5 h/d; CI: 95% CI, 3.7-5.4 h/d

Size: 4.6 h/d gain (DBS) vs 0 h/d (BMT); between-group difference CI: 95% CI, 3.7-5.4 h/d

Off-medication UPDRS motor scores improved by 12.3 points in the DBS group versus 1.7 points in the best medical therapy group at 6 months based on blinded assessments, with 71% of DBS patients versus

Effect: improvement; -12.3 points (DBS) vs -1.7 points (BMT) on UPDRS motor score

Size: -12.3 points (DBS) vs -1.7 points (BMT) on UPDRS motor score

Patients receiving deep brain stimulation experienced significant improvements on the PDQ-39 summary measure and 7 of 8 subscales compared with best medical therapy at 6 months.

Effect: improvement; Significant improvement on PDQ-39 summary measure and 7 of 8 subscales

Size: Significant improvement on PDQ-39 summary measure and 7 of 8

Deep brain stimulation was associated with small but statistically significant decrements in working memory, processing speed, phonemic fluency, and visuospatial delayed recall compared with best medi

Effect: adverse; 1.0 to 3.5-point decreases in DBS group vs 1 to 2-point increases in BMT group on composite measures

Size: 1.0 to 3.5-point decreases in DBS group vs 1 to 2-point incr

The overall incidence risk of experiencing a serious adverse event was 3.8 times higher in DBS patients than in BMT patients, with 49 DBS patients (40%) experiencing at least 1 serious adverse event c

Effect: adverse; Incidence risk ratio 3.8 (DBS vs BMT); 40% of DBS patients vs 11% of BMT patients experienced at least 1 serious adverse event; CI: 95% CI, 2

Size: Incidence risk ratio 3.8 (DBS vs BMT); 40% of DBS patients v CI: 95% CI, 2.3-6.3