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The  diagnostic   scope  of The  diagnostic   scope  of

The diagnostic scope of - PowerPoint Presentation

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The diagnostic scope of - PPT Presentation

SensorBased Gait Analysis in Atypical Parkinsonism supported study by Dr Heiko Gaßner and Dr Cecilia Raccagni Early diagnosis of MSA a medical challenge Postural instability and gait difficulty PIGD are disabling symptoms of Parkinsons disease PD and atypic ID: 933375

based gait msa analysis gait based analysis msa parameters apd patients sensor compared psp pigd cohorts disease supporting variability

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Slide1

The diagnostic scope of Sensor-Based Gait Analysis in Atypical Parkinsonism

supported

studyby Dr. Heiko Gaßner and Dr. Cecilia Raccagni

Slide2

Early diagnosis of MSA – a medical challenge!

Postural instability and gait difficulty (PIGD) are disabling symptoms of Parkinson´s disease (PD) and atypical parkinsonian syndromes (APD), including MSA and Progressive

Supranuclear Palsy (PSP).Sensor-based gait analysis revealed more quantitative gait deficits in MSA compared to PD.However, the diagnostic value of instrumented bedside tests (e.g. sensor-based gait analysis) compared to clinical evaluation in differential diagnosis has not been assessed so far.

Slide3

Study designWe compared gait parameters (gait velocity, stride length, gait variability etc.) of patients with MSA and PSP to those of sporadic PD patients. Cohorts were matched by disease duration, gender and age. Gait parameters were evaluated in standardized gait tests using an instrumented gait-analysis system.

Figure designed by Jochen Klucken

and P

-HCT

Slide4

Key findings

The PIGD score

identified APD patients correctly in most of the cases analyzed

(>90% accuracy). The objective gait variability parameters reflecting instability of gait (e.g. stance time CV) discriminated APD from PD with similar accuracy.

Gaßner, Raccagni et al. 2019

Frontiers in Neurology

Slide5

ConclusionsSensor-based gait parameters support the neurologist in differentiating APD from PD. Importantly, they provide metric, objective added value, and serve as complementary outcomes supporting diagnostics and clinical trials.

Our data need to be replicated and validated in larger patient cohorts.

Slide6

AcknowledgmentsWe are

grateful to for:

A grant in 2017 supporting this and other projects.

We further thank

Gregor Wenning (Innsbruck, Austria) and Jochen Klucken (Erlangen, Germany)

for supportingour

research

activities

.