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Journal of Neurology, Neurosurgery, and Psychiatry 2006;77:450-453; doi:10.1136/jnnp.2005.078659
Copyright © 2006 by the BMJ Publishing Group Ltd.

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PAPER

Clinical and neuropsychological follow up at 12 months in patients with complicated Parkinson’s disease treated with subcutaneous apomorphine infusion or deep brain stimulation of the subthalamic nucleus

D De Gaspari1,*, C Siri1,*, A Landi2, R Cilia1, A Bonetti1, F Natuzzi1, L Morgante3, C B Mariani1, E Sganzerla2, G Pezzoli1, A Antonini1

1 Centro Parkinson, Istituti Clinici di Perfezionamento, Milan, Italy
2 Clinica Neurochirurgica, Ospedale San Gerardo, Università Milano–Bicocca, Monza, Italy
3 Clinica Neurologica, Università di Messina, Messina, Italy

Correspondence to:
Correspondence to:
Angelo Antonini
Centro Parkinson, Istituti Clinici di Pefezionamento, 20126 Milan, Italy; angelo3000{at}yahoo.com

Background: The clinical condition of advanced Parkinson’s disease (PD) patients is often complicated by motor fluctuations and dyskinesias which are difficult to control with available oral medications.

Objective: To compare clinical and neuropsychological 12 month outcome following subcutaneous apomorphine infusion (APO) and chronic deep brain stimulation of the subthalamic nucleus (STN-DBS) in advanced PD patients.

Methods: Patients with advanced PD and medically untreatable fluctuations underwent either APO (13 patients) or STN-DBS (12 patients). All patients were clinically (UPDRS-III, AIMS, 12 h on-off daily) and neuropsychologically (MMSE, Hamilton-17 depression, NPI) evaluated at baseline and at 12 months. APO was discontinued at night.

Results: At 12 months APO treatment (74.78±24.42 mg/day) resulted in significant reduction in off time (–51%) and no change in AIMS. Levodopa equivalent medication doses were reduced from 665.98±215 mg/day at baseline to 470±229 mg/day. MMSE, NPI, and Hamilton depression scores were unchanged. At 12 months STN-DBS resulted in significant clinical improvement in terms of reduction in daily off time (–76%) and AIMS (–81%) as well as levodopa equivalent medication doses (980±835 to 374±284 mg/day). Four out of 12 patients had stopped oral medications. MMSE was unchanged (from 28.6±0.3 to 28.4±0.6). Hamilton depression was also unchanged, but NPI showed significant worsening (from 6.58±9.8 to 18.16±10.2; p<0.02). Category fluency also declined.

Conclusions: Both APO and STN-DBS resulted in significant clinical improvement in complicated PD. STN-DBS resulted in greater reduction in dopaminergic medications and provided 24 h motor benefit. However, STN-DBS, unlike APO, appears to be associated with significant worsening on NPI resulting from long term behavioral problems in some patients.


Abbreviations: AIMS, Abnormal Involuntary Movement Scale; APO, subcutaneous apomorphine infusion; CF, category fluency; CPM, Raven’s Coloured Progressive Matrices; CVLT, the California Verbal Learning Test; HDRS-17, Hamilton Depression Rating Scale-17; H&Y stage, Hoehn and Yahr stage; MMSE, Mini-Mental State Examination; NPI, Neuro-Psychiatric Inventory; PD, Parkinson’s disease; PF, phonemic fluency; PWL, Paired Word Learning; STN-DBS, deep brain stimulation of the subthalamic nucleus; UPDRS-III, Unified Parkinson’s Disease Rating Scale motor examination

Keywords: apomorphine; deep brain stimulation of the subthalamic nucleus; neuropsychology; Parkinson’s disease; STN-DBS







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