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DBS Multicenter Four-Year Follow-up


Bilateral deep brain stimulation in Parkinson's disease: A multicentre study
with 4 years follow-up
 MC Rodriguez-Oros, JA Obeso, AE Lang, JL Houeto, P Pollak, S Rehncrona, J
Kulisevsky, A Albanese, J Volkmann, MI Hariz, NP Quinn, JD Speelman, J
Furidi, I Zamarbide, A Gironell, J Molet, B Pascual-Sedano, B Pidoux, AM
Bonnet, Y Agid, J Xie, A-L Benabid, AM Lozano, J Saint-Cyr, L Romito, MF
Contarino, M Scerrati, V Fraix, N Van Blercom
 Brain 2005;128:2240-2249


 Deep brain stimulation of either the subthalamic nucleus or the globus
pallidus continues to provide significant benefit after 4 years of treatment,
according to the study.


 Long-term follow-up was conducted at 8 centers in Europe and Canada, of
patients originally enrolled in a multicenter trial of deep brain
stimulation. Patients were enrolled if they had been treated for a minimum of
3 years and less than 5 years. Forty-nine of 68 DBS-STN patients were
available for follow-up, and 20 of 37 DBS-GPi patients. Compared to GPi
patients, STN patients at baseline were slightly older, had slightly higher
UPDRS off-medication scores, and slightly higher daily levodopa equivalent
doses.


Results showed:
 --for STN, at baseline the percent of waking time spent off, on with
dyskinesias, and on without dyskinesias was 53%, 23%, and 24%, respectively.
At 3-4 years, it was 23%, 13%, and 64%.


 --For GPi, these same percentages were 37%, 37%, and 26% at baseline, and
21%, 10%, and 69% at 3-4 years.


 --for STN, UPDRS off-medication motor scores were 56.7 at baseline and 28.6
at 3-4 years (with stimulation on). For GPi, the scores were 51.7 and 31.7.


 --for STN, levodopa equivalent dose intake fell from 1309 mg/day to 859
mg/day (p<0.001). For GPi, it rose from 1074 to 1418 (difference not
significant).


 Persistent adverse events were reported in 53% of STN patients, and 35% of
GPi patients. The severity of adverse events did not warrant suspension of
DBS in any case. Major adverse events present at 3-4 years included:


 --memory decline and/or psychiatric disturbance in 12 STN patients (4 mild, 7
moderate, 1 severe) and 1 GPi patient (mild).


 --moderate depression in 3 STN patients


 --speech difficulties in 9 STN patients (2 mild, 3 moderate, 4 severe) and 1
GPi patient (severe)


 --falls and/or balance disturbances in 8 STN patients (2 mild, 5 moderate, 1
severe)


 --gait disorders in 9 STN patients (2 mild, 3 moderate, 4 severe)


 The authors note that while the adverse events encountered are also seen in
patients on medication alone, the higher rate in STN patients versus GPi
patients "implies some specificity to the findings." The study was not
designed to evaluate the relative contributions to risk of the procedure or
initial severity of PD or other factors, however.


A Commentary by Hans Joachim Freund accompanies the report.


 Sponsored by Medtronic.

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