Evidence map›Paper›PMID 42707493›Full record

ArticleBMJ neurology open2026

Moving beyond monitoring: wearable technology (PKG) for the diagnosis of Parkinson's disease.

Michael William Hayes, Niroshan Jeyakumar, James Burrell

Abstract read
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Article in BMJ neurology open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Michael William HayesNeurology, Concord Repatriation General Hospital, Concord, New South Wales, Australia.ORCID https://orcid.org/0000-0001-8124-854X
Niroshan JeyakumarSydney Medical School, The University of Sydney, Sydney, New South Wales, Australia.
James BurrellMedicine, Macquarie University Health Services, Macquarie Park, New South Wales, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The use of wearable technology results in objective and reliable monitoring of motor activity in Parkinson's disease (PD) but its utility as a diagnostic aid has not been assessed. Objectives: To assess whether a Personal KinetiGraph (PKG) performed at baseline and again following a long-form levodopa (LD) challenge (increasing to 300 mg daily over a minimum of 6 weeks) is a useful discriminator in those with parkinsonism but diagnostic uncertainty. Methods: Over a 10-year period, 26 patients with parkinsonism in whom there was diagnostic uncertainty due to clinical complexity or conflicting evidence were tested with a PKG, recording bradykinesia and tremor before and after formalised treatment with LD. Patients were followed for a median of 46.5 months (mean 49.8) to establish a 'final' clinical diagnosis. Results: Of the 15/26 diagnostically uncertain patients with a 'final' diagnosis of PD, the PKG demonstrated bradykinesia (mean bradykinesia score ≥25) at baseline in 14/15; in 12/15, bradykinesia improved with LD and, when present, tremor was similarly reduced. In the 11/26 patients who had a final diagnosis other than PD, the PKG recorded bradykinesia in 3/11 with improved bradykinesia and reduced tremor in only 1/11. PKG-defined bradykinesia coupled with LD responsiveness was 88% sensitive (95% CI 57% to 98%) and 89% specific (95% CI 52% to 99%) for a 'final' PD diagnosis in this select group. Additionally, PKG-defined tremor and LD responsiveness had a sensitivity of 85% (95% CI 55% to 98%) and specificity of 89% (95% CI 52% to 99%). Conclusion: PKG-defined bradykinesia and tremor coupled with LD responsiveness appear to be predictive of an eventual PD diagnosis in diagnostically challenging cases. Larger studies are required to verify these conclusions.

Indexed as

MOVEMENT DISORDERSPARKINSON'S DISEASETELEMETRY

Identifiers

PMID42707493
PMCPMC13548271

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