Replacement of dopaminergic medication with subthalamic nucleus stimulation in Parkinson's disease: Long‐term observation

Stimulation of the subthalamic nucleus (STN) is an effective treatment for advanced Parkinson's disease (PD), but the medication requirements after implant are poorly known. We performed a long‐term prospective evaluation of 20 patients maintained at stable dopaminergic therapy for 5 years after bilateral STN implants, who were evaluated 6 months, 1 year, 3 years, and 5 years after surgery. We measured, during the entire observation period, the effect of deep brain stimulation on motor and functional outcome measures, the levodopa equivalent daily dose and the total electrical energy delivered. At 5 years, the UPDRS motor score had improved by 54.2% and levodopa equivalent dose was reduced by 61.9%, compared with preimplant. Dopaminergic medication remained stable during the observation period, but energy was progressively increased over time. Rest tremor, rigidity, gait, lower and upper limb akinesia, and total axial score were improved in decreasing order. Postural stability and speech improved transiently, whereas on‐period freezing of gait, motor fluctuations and dyskinesias recovered durably. Functional measures did not show improvement in autonomy and daily living activities after STN implant. Chronic STN stimulation allows to replace for dopaminergic medications in the long‐term at the expense of an increase of the total energy delivered. This is associated with marked improvement of motor features without a matching benefit in functional measures. © 2008 Movement Disorder Society

[1]  J. Bloch,et al.  Long-term outcome of 50 consecutive Parkinson's disease patients treated with subthalamic deep brain stimulation. , 2008, Parkinsonism & related disorders.

[2]  N. Tandon Neurosurgery at an earlier stage of Parkinson disease: A randomized, controlled trial , 2008 .

[3]  R. Goodman,et al.  Relationship of clinical efficacy to postmortem-determined anatomic subthalamic stimulation in Parkinson syndrome. , 2007, Clinical neuropathology.

[4]  P. Stanzione,et al.  Bilateral deep brain stimulation of the pedunculopontine and subthalamic nuclei in severe Parkinson's disease. , 2007, Brain : a journal of neurology.

[5]  P. Gubellini,et al.  High-Frequency Stimulation of the Subthalamic Nucleus Potentiates l-DOPA-Induced Neurochemical Changes in the Striatum in a Rat Model of Parkinson's Disease , 2007, The Journal of Neuroscience.

[6]  Alessandro Stefani,et al.  High‐frequency stimulation of the subthalamic nucleus modulates the activity of pedunculopontine neurons through direct activation of excitatory fibres as well as through indirect activation of inhibitory pallidal fibres in the rat , 2007, The European journal of neuroscience.

[7]  P. Kempster,et al.  Longitudinal study of the motor response to levodopa in Parkinson's disease , 2006, Movement disorders : official journal of the Movement Disorder Society.

[8]  G. Baltuch,et al.  Long-Term Outcomes of Bilateral Subthalamic Nucleus Stimulation in Patients with Advanced Parkinson’s Disease , 2006, Stereotactic and Functional Neurosurgery.

[9]  Hideki Oshima,et al.  Direct Effect of Subthalamic Nucleus Stimulation on Levodopa-Induced Peak-Dose Dyskinesia in Patients with Parkinson’s Disease , 2006, Stereotactic and Functional Neurosurgery.

[10]  G. Deuschl,et al.  Subthalamic nucleus deep brain stimulation: Summary and meta‐analysis of outcomes , 2006, Movement disorders : official journal of the Movement Disorder Society.

[11]  J. Volkmann,et al.  Stimulation of subthalamic fibre tracts reduces dyskinesias in STN-DBS. , 2006, Movement disorders : official journal of the Movement Disorder Society.

[12]  Y. Agid,et al.  Stimulation of the subthalamic nucleus in Parkinson’s disease: a 5 year follow up , 2005, Journal of Neurology, Neurosurgery & Psychiatry.

[13]  R. P. Maguire,et al.  Disease progression continues in patients with advanced Parkinson’s disease and effective subthalamic nucleus stimulation , 2005, Journal of Neurology, Neurosurgery & Psychiatry.

[14]  Michele Tagliati,et al.  Calculating total electrical energy delivered by deep brain stimulation systems , 2005, Annals of neurology.

[15]  A. Benabid,et al.  Five-year follow-up of bilateral stimulation of the subthalamic nucleus in advanced Parkinson's disease. , 2003, The New England journal of medicine.

[16]  A. Bentivoglio,et al.  Long-term follow up of subthalamic nucleus stimulation in Parkinson's disease. , 2002, Neurology.

[17]  A L Benabid,et al.  Unilateral lesion of the nigrostriatal pathway induces an increase of neuronal activity of the pedunculopontine nucleus, which is reversed by the lesion of the subthalamic nucleus in the rat , 2001, The European journal of neuroscience.

[18]  M. Hariz,et al.  Hardware failure in parkinsonian patients with chronic subthalamic nucleus stimulation is a medical emergency , 2001, Movement disorders : official journal of the Movement Disorder Society.

[19]  A. Benabid,et al.  Dyskinesias and the subthalamic nucleus. , 2000, Annals of neurology.

[20]  Y. Agid,et al.  Levodopa-induced dyskinesias in Parkinson's disease: is sensitization reversible? , 2000, Annals of neurology.

[21]  E. Moro,et al.  Chronic subthalamic nucleus stimulation reduces medication requirements in Parkinson’s disease , 1999, Neurology.

[22]  P. Remy,et al.  Core assessment program for surgical interventional therapies in Parkinson's disease (CAPSIT‐PD) , 1999, Movement disorders : official journal of the Movement Disorder Society.

[23]  A. Benabid,et al.  Effect on parkinsonian signs and symptoms of bilateral subthalamic nucleus stimulation , 1995, The Lancet.

[24]  J. Hughes,et al.  Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. , 1992, Journal of neurology, neurosurgery, and psychiatry.

[25]  F Lhermitte,et al.  Does long‐term aggravation of Parkinson's disease result from nondopaminergic lesions? , 1987, Neurology.

[26]  R. Barker,et al.  Movement Disorders , 1994, Stereotactic and Functional Neurosurgery.