Frequency settings of subthalamic nucleus DBS for Parkinson's disease: A systematic review and network meta-analysis.


Journal

Parkinsonism & related disorders
ISSN: 1873-5126
Titre abrégé: Parkinsonism Relat Disord
Pays: England
ID NLM: 9513583

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 13 08 2023
accepted: 13 08 2023
medline: 13 11 2023
pubmed: 22 8 2023
entrez: 21 8 2023
Statut: ppublish

Résumé

Deep Brain Stimulation (DBS) is an effective treatment for the motor symptoms of Parkinson's Disease. The targeted physiological structure for lead location is commonly the subthalamic nucleus (STN). The efficacy of DBS for improving motor symptoms is assessed via the Unified Parkinson's Disease Rating III Scale (UPDRS-III). In this study, we sought to compare the efficacy of frequency settings utilized for STN-DBS. Following PRISMA Guidelines, a search on PUBMED and MEDLINE was performed to include full-length randomized controlled trials evaluating STN-DBS. The frequency stimulation parameters and Unified Parkinson's Disease Rating Scale (UPDRS-III) outcomes were extracted in the search. High-frequency stimulation (HFS) was defined as ≥100 Hz and low-frequency stimulation (LFS) was defined as <100 Hz. A frequentist network meta-analysis was performed with odds ratios (OR) and pooling performed using the Mantel-Haenszel method. Statistics are presented as OR [95% CI]. 15 studies consisting of 298 patients were included for analysis. Bilateral HFS -0.68 [-0.89; -0.46] was associated with better UPDRS-III scores compared to bilateral LFS. On the other hand, bilateral LFS with medications (MEDS) was favored over HFS with MEDS (-0.28 [-0.63; 0.07]). Bilateral LFS and MEDS, HFS and MEDS, stimulation (STIM) OFF MEDS ON, HFS, LFS, STIM OFF MEDS OFF UPDRS outcomes were ranked from best to worst outcomes. The outcomes of this study suggest that bilateral HFS has better utility for those with no response to medication, while LFS has additive benefits to medication by improving unique symptoms via different neurophysiological mechanisms.

Identifiants

pubmed: 37604755
pii: S1353-8020(23)00888-X
doi: 10.1016/j.parkreldis.2023.105809
pii:
doi:

Types de publication

Meta-Analysis Systematic Review Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

105809

Informations de copyright

Copyright © 2023. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of competing interest RD: Nothing to disclose. LSD: Nothing to disclose. AN: Nothing to disclose MB: Nothing to disclose MA: Nothing to disclose SI: Nothing to disclose MCP: Nothing to disclose.

Auteurs

Rajiv Dharnipragada (R)

University of Minnesota Medical School, University of Minnesota Twin-Cities, Minneapolis, MN, 55455, USA. Electronic address: dharn001@umn.edu.

Lalitha S Denduluri (LS)

College of Liberal Arts, University of Minnesota Twin-Cities, Minneapolis, MN, 55455, USA.

Anant Naik (A)

Carle Illinois College of Medicine, University of Illinois Urbana Champaign, Champaign, IL, 61801, USA.

Mario Bertogliat (M)

University of Minnesota Medical School, University of Minnesota Twin-Cities, Minneapolis, MN, 55455, USA.

Matthew Awad (M)

University of Minnesota Medical School, University of Minnesota Twin-Cities, Minneapolis, MN, 55455, USA.

Salman Ikramuddin (S)

Department of Neurology, University of Minnesota Twin-Cities, Minneapolis, MN, 55455, USA.

Michael C Park (MC)

Department of Neurology, University of Minnesota Twin-Cities, Minneapolis, MN, 55455, USA; Department of Neurosurgery, University of Minnesota Twin-Cities, Minneapolis, MN, 55455, USA.

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Classifications MeSH