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Abstract
Background
Programming deep brain stimulation in dystonia is difficult because of the delayed benefits and absence of evidence-based guidelines. Therefore, we evaluated the efficacy of a programming algorithm applied in a double-blind, sham-controlled multicenter study of pallidal deep brain stimulation in dystonia.
Methods
A standardized monopolar review to identify the contact with the best acute antidystonic effect was applied in 40 patients, who were then programmed 0.5 V below the adverse effect threshold and maintained on these settings for at least 3 months, if tolerated. If no acute effects were observed, contact selection was based on adverse effects or anatomical criteria. Three-year follow-up data was available for 31 patients, and five-year data for 32 patients. The efficacy of the algorithm was based on changes in motor scores, adverse events, and the need for reprogramming.
Results
The mean (±standard deviation) dystonia motor score decreased by 73 ± 24% at 3 years and 63 ± 38% at 5 years for contacts that exhibited acute improvement of dystonia (n = 17) during the monopolar review. Contacts without acute benefit improved by 58 ± 30% at 3 years (n = 63) and 53 ± 31% at 5 years (n = 59). Interestingly, acute worsening or induction of dystonia/dyskinesia (n = 9) correlated significantly with improvement after 3 years, but not 5 years.
Conclusions
Monopolar review helped to detect the best therapeutic contact in approximately 30% of patients exhibiting acute modulation of dystonic symptoms. Acute improvement, as well as worsening of dystonia, predicted a good long-term outcome, while induction of phosphenes did not correlate with outcome.
Trial registration
ClinicalTrials.gov NCT00142259.
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1 Department of Neurology, University Hospital Würzburg, Würzburg, Germany; Department of Neurology and Neurological Critical Care, Rhön-Klinikum, Bad Neustadt, Germany; Department of Neurology, Christian Albrechts University, Kiel, Germany
2 Department of Neurology, University Hospital Würzburg, Würzburg, Germany
3 Department of Neurology, Campus Mitte, Charité - Universitätsmedizin Berlin, Berlin, Germany
4 Neurology Moves, Movement Disorder Center Berlin, Berlin, Germany
5 Department of Neurology, Vivantes Hospital Berlin Spandau, Berlin, Germany; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria
6 Department of Neurosurgery, Medical University of Innsbruck, Innsbruck, Austria
7 Department of Neurology, Christian Albrechts University, Kiel, Germany
8 Department of Neurosurgery, Christian Albrechts University, Kiel, Germany
9 Department of Neurology and Institute of Clinical Neuroscience and Medical Psychology, Heinrich Heine University, Düsseldorf, Germany
10 Department of Neurology, Oslo University Hospital, Oslo, Norway
11 MVZ, Evang. Kliniken, Gelsenkirchen, Germany
12 Department of Neurosurgery, University of Lübeck, Lübeck, Germany
13 Department of Functional Neurosurgery and Stereotaxy, Albert Ludwig University Freiburg, Freiburg, Germany; Department of Functional Neurosurgery and Stereotaxy, Heinrich Heine University Düsseldorf, Düsseldorf, Germany
14 Department of Neurology, University Hospital Würzburg, Würzburg, Germany; Department of Neurology, Klinikum Augsburg, Augsburg, Germany
15 Department of Neurology, University Hospital Würzburg, Würzburg, Germany; Department of Neurology, Christian Albrechts University, Kiel, Germany