Evidence map›Paper›PMID 22396391›Full record

Trial reportBrain : a journal of neurology2012

A spatiotemporal analysis of gait freezing and the impact of pedunculopontine nucleus stimulation.

Wesley Thevathasan, Michael H Cole, Cara L Graepel, Jonathan A Hyam, Ned Jenkinson, John-Stuart Brittain, Terry J Coyne, Peter A Silburn, Tipu Z Aziz, Graham Kerr and 1 more

2 registry-linked trialsOpen access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Brain : a journal of neurology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 76 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 2 pooled it
10.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03526991 nacompletednot on this mapstarted 2021, after this paper: background citation

Exploring the Effects of Spinal Cord Stimulation in Parkinson's Disease.

TypeinterventionalSponsorNora VanegasRan2021 to 2026Enrolled10ConditionsParkinson DiseaseArmsSpinal Cord Stimulator (SCS)
NCT06272955 unknown statusnot on this mapstarted 2024, after this paper: background citation

Long term effects of spinal cord stimulation in patients with parkinson's disease open label extension to h-49023

Typeobservational_patient_registrySponsorNora VanegasRan2024 to 2025Enrolled10ConditionsParkinson DiseaseArmsSpinal Cord Stimulator (SCS)
3 · Its place in the literature

Who cites it

76 citing papers in PubMed, 2 syntheses or guidelines pooled it, 154 citations in OpenAlex.

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  19. Tractography patterns of pedunculopontine nucleus deep brain stimulation.Journal of neural transmission (Vienna, Austria : 1996) · 2021
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16 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 2 countries.

Wesley ThevathasanNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK. wesley.thevathasan@nds.ox.ac.uk
Michael H Cole
Cara L Graepel
Jonathan A Hyam
Ned Jenkinson
John-Stuart Brittain
Terry J Coyne
Peter A Silburn
Tipu Z Aziz
Graham Kerr
Peter Brown
University of Oxford · GBQueensland University of Technology · AUAustralian Catholic University · AUThe Royal Melbourne Hospital · AUUniversity of Queensland · AUWesley Hospital · AU

Funding

Medical Research Council G0901503
6 · The paper itself

Abstract

Gait freezing is an episodic arrest of locomotion due to an inability to take normal steps. Pedunculopontine nucleus stimulation is an emerging therapy proposed to improve gait freezing, even where refractory to medication. However, the efficacy and precise effects of pedunculopontine nucleus stimulation on Parkinsonian gait disturbance are not established. The clinical application of this new therapy is controversial and it is unknown if bilateral stimulation is more effective than unilateral. Here, in a double-blinded study using objective spatiotemporal gait analysis, we assessed the impact of unilateral and bilateral pedunculopontine nucleus stimulation on triggered episodes of gait freezing and on background deficits of unconstrained gait in Parkinson's disease. Under experimental conditions, while OFF medication, Parkinsonian patients with severe gait freezing implanted with pedunculopontine nucleus stimulators below the pontomesencephalic junction were assessed during three conditions; off stimulation, unilateral stimulation and bilateral stimulation. Results were compared to Parkinsonian patients without gait freezing matched for disease severity and healthy controls. Pedunculopontine nucleus stimulation improved objective measures of gait freezing, with bilateral stimulation more effective than unilateral. During unconstrained walking, Parkinsonian patients who experience gait freezing had reduced step length and increased step length variability compared to patients without gait freezing; however, these deficits were unchanged by pedunculopontine nucleus stimulation. Chronic pedunculopontine nucleus stimulation improved Freezing of Gait Questionnaire scores, reflecting a reduction of the freezing encountered in patients' usual environments and medication states. This study provides objective, double-blinded evidence that in a specific subgroup of Parkinsonian patients, stimulation of a caudal pedunculopontine nucleus region selectively improves gait freezing but not background deficits in step length. Bilateral stimulation was more effective than unilateral.

Indexed as

AgedAnalysis of VarianceCase-Control StudiesDeep Brain StimulationElectrodesFemaleFunctional LateralityGait Disorders, NeurologicHumansMaleMental Status ScheduleMiddle AgedParkinson DiseasePedunculopontine Tegmental NucleusSeverity of Illness IndexStatistics, Nonparametric

Identifiers

PMID22396391
PMCPMC3338924
OpenAlexW1988305799

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.