Initial Clinical Outcome With Bilateral, Dual-Target Deep Brain Stimulation Trial in Parkinson Disease Using Summit RC + S.

dc.contributor.author

Mitchell, Kyle T

dc.contributor.author

Schmidt, Stephen L

dc.contributor.author

Cooney, Jeffrey W

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Grill, Warren M

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Peters, Jennifer

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Rahimpour, Shervin

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Lee, Hui-Jie

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Jung, Sin-Ho

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Mantri, Sneha

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Scott, Burton

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Lad, Shivanand P

dc.contributor.author

Turner, Dennis A

dc.date.accessioned

2022-05-12T16:37:59Z

dc.date.available

2022-05-12T16:37:59Z

dc.date.issued

2022-04-07

dc.date.updated

2022-05-12T16:37:56Z

dc.description.abstract

Background

Deep brain stimulation (DBS) is an effective therapy in advanced Parkinson disease (PD). Although both subthalamic nucleus (STN) and globus pallidus (GP) DBS show equivalent efficacy in PD, combined stimulation may demonstrate synergism.

Objective

To evaluate the clinical benefit of stimulating a combination of STN and GP DBS leads and to demonstrate biomarker discovery for adaptive DBS therapy in an observational study.

Methods

We performed a pilot trial (n = 3) of implanting bilateral STN and GP DBS leads, connected to a bidirectional implantable pulse generator (Medtronic Summit RC + S; NCT03815656, IDE No. G180280). Initial 1-year outcome in 3 patients included Unified PD Rating Scale on and off medications, medication dosage, Hauser diary, and recorded beta frequency spectral power.

Results

Combined DBS improved PD symptom control, allowing >80% levodopa medication reduction. There was a greater decrease in off-medication motor Unified PD Rating Scale with multiple electrodes activated (mean difference from off stimulation off medications -18.2, range -25.5 to -12.5) than either STN (-12.8, range -20.5 to 0) or GP alone (-9, range -11.5 to -4.5). Combined DBS resulted in a greater reduction of beta oscillations in STN in 5/6 hemispheres than either site alone. Adverse events occurred in 2 patients, including a small cortical hemorrhage and seizure at 24 hours postoperatively, which resolved spontaneously, and extension wire scarring requiring revision at 2 months postoperatively.

Conclusion

Patients with PD preferred combined DBS stimulation in this preliminary cohort. Future studies will address efficacy of adaptive DBS as we further define biomarkers and control policy.
dc.identifier

00006123-990000000-00199

dc.identifier.issn

0148-396X

dc.identifier.issn

1524-4040

dc.identifier.uri

https://hdl.handle.net/10161/25039

dc.language

eng

dc.publisher

Ovid Technologies (Wolters Kluwer Health)

dc.relation.ispartof

Neurosurgery

dc.relation.isversionof

10.1227/neu.0000000000001957

dc.title

Initial Clinical Outcome With Bilateral, Dual-Target Deep Brain Stimulation Trial in Parkinson Disease Using Summit RC + S.

dc.type

Journal article

duke.contributor.orcid

Mitchell, Kyle T|0000-0003-4788-1581

duke.contributor.orcid

Cooney, Jeffrey W|0000-0002-9903-5400

duke.contributor.orcid

Jung, Sin-Ho|0000-0002-1473-7236

duke.contributor.orcid

Mantri, Sneha|0000-0003-4556-0522

duke.contributor.orcid

Scott, Burton|0000-0003-4608-4062

duke.contributor.orcid

Lad, Shivanand P|0000-0003-4991-5319

duke.contributor.orcid

Turner, Dennis A|0000-0001-7118-0764

pubs.organisational-group

Duke

pubs.organisational-group

School of Medicine

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Clinical Science Departments

pubs.organisational-group

Neurology

pubs.organisational-group

Neurology, Movement Disorders

pubs.publication-status

Published

pubs.volume

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