Petra Schwingenschuh

Dr. Petra Schwingenschuh

orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
28 February 2020 in Journal of Neurology, Neurosurgery & Psychiatry
Verified
Journal Article
Open access
PDF file
SPSusannah Pick
Susannah Pick
DADavid G Anderson
David G Anderson
AAAli Asadi-Pooya
Ali Asadi-Pooya
SASelma Aybek
Selma Aybek
GBGaston Baslet
Gaston Baslet
TNTimothy R Nicholson
Timothy R Nicholson
Objectives We aimed to identify existing outcome measures for functional neurological disorder (FND), to inform the development of recommendations and to guide future research on FND outcomes. Methods A systematic review was conducted to identify existing FND-specific outcome measures and the most common measurement domains and measures in previous treatment studies. Searches of Embase, MEDLINE and PsycINFO were conducted between January 1965 and June 2019. The findings were discussed during two international meetings of the FND-Core Outcome Measures group. Results Five FND-specific measures were identified—three clinician-rated and two patient-rated—but their measurement properties have not been rigorously evaluated. No single measure was identified for use across the range of FND symptoms in adults. Across randomised controlled trials (k=40) and observational treatment studies (k=40), outcome measures most often assessed core FND symptom change. Other domains measured commonly were additional physical and psychological symptoms, life impact (ie, quality of life, disability and general functioning) and health economics/cost–utility (eg, healthcare resource use and quality-adjusted life years). Conclusions There are few well-validated FND-specific outcome measures. Thus, at present, we recommend that existing outcome measures, known to be reliable, valid and responsive in FND or closely related populations, are used to capture key outcome domains. Increased consistency in outcome measurement will facilitate comparison of treatment effects across FND symptom types and treatment modalities. Future work needs to more rigorously validate outcome measures used in this population.

1 February 2015 in Neurobiology of Aging
Verified
Journal Article
Closed access
CGChristine Ghadery
Christine Ghadery
LPLukas Pirpamer
Lukas Pirpamer
EHEdith Hofer
Edith Hofer
CLChristian Langkammer
Christian Langkammer
KPKatja Petrovic
Katja Petrovic
RSReinhold Schmidt
Reinhold Schmidt

16 February 2016 in Movement Disorders
Verified
Journal Article
Closed access
PDF file
Petra SchwingenschuhPetra Schwingenschuh
Petra Schwingenschuh
TSTabish A. Saifee
Tabish A. Saifee
PKPetra Katschnig‐Winter
Petra Katschnig‐Winter
AMAntonella Macerollo
Antonella Macerollo
MKMariella Koegl‐Wallner
Mariella Koegl‐Wallner
MEMark Edwards
Mark Edwards

11 August 2024 in npj Parkinson's Disease
Verified
Journal Article
Open access
PDF file
COConor Owens-Walton
Conor Owens-Walton
TNTalia M. Nir
Talia M. Nir
SASarah Al-Bachari
Sarah Al-Bachari
SASonia Ambrogi
Sonia Ambrogi
TATim Anderson
Tim Anderson
YWYsbrand Van Der Werf
Ysbrand Van Der Werf
The progression of Parkinson’s disease (PD) is associated with microstructural alterations in neural pathways, contributing to both motor and cognitive decline. However, conflicting findings have emerged due to the use of heterogeneous methods in small studies. Here we performed a large diffusion MRI study in PD, integrating data from 17 cohorts worldwide, to identify stage-specific profiles of white matter differences. Diffusion-weighted MRI data from 1654 participants diagnosed with PD (age: 20–89 years; 33% female) and 885 controls (age: 19–84 years; 47% female) were analyzed using the ENIGMA-DTI protocol to evaluate white matter microstructure. Skeletonized maps of fractional anisotropy (FA) and mean diffusivity (MD) were compared across Hoehn and Yahr (HY) disease groups and controls to reveal the profile of white matter alterations at different stages. We found an enhanced, more widespread pattern of microstructural alterations with each stage of PD, with eventually lower FA and higher MD in almost all regions of interest: Cohen’s d effect sizes reached d = −1.01 for FA differences in the fornix at PD HY Stage 4/5. The early PD signature in HY stage 1 included higher FA and lower MD across the entire white matter skeleton, in a direction opposite to that typical of other neurodegenerative diseases. FA and MD were associated with motor and non-motor clinical dysfunction. While overridden by degenerative changes in the later stages of PD, early PD is associated with paradoxically higher FA and lower MD in PD, consistent with early compensatory changes associated with the disorder.

4 March 2022 in Journal of the Neurological Sciences
Verified
Journal Article
Open access
Petra SchwingenschuhPetra Schwingenschuh
Petra Schwingenschuh
AEAlberto J. Espay
Alberto J. Espay
Functional tremor is the most common functional movement disorder. It can be diagnosed with clinically definite certainty at the bedside by ascertaining its inconsistent (distractibility, frequency variability) and incongruent features (entrainment, ballistic suppression), requiring no additional neurological investigations except, in selected cases, those serving to elevate the diagnostic category to laboratory supported using accelerometry and surface electromyography. In the background of excessive attention to the affected body part and abnormal beliefs and expectations, functional correlates include the impairment of emotion processing, sense of agency, and abnormal connectivity between limbic and motor regions. While the treatment options remain under-studied, promising interventions in physiotherapy, cognitive behavioral therapy, and other psychotherapies are under evaluation to assessing their efficacy in attenuating this important source of neurological disability. This article is part of the Special Issue "Tremor" edited by Daniel D. Truong, Mark Hallett, and Aasef Shaikh.

1 March 2014 in Parkinsonism & Related Disorders
Verified
Journal Article
Closed access
MKMariella Koegl-Wallner
Mariella Koegl-Wallner
PKPetra Katschnig-Winter
Petra Katschnig-Winter
TPTamara Pendl
Tamara Pendl
BMBarbara Melisch
Barbara Melisch
MTMartin Trummer
Martin Trummer
Petra SchwingenschuhPetra Schwingenschuh
Petra Schwingenschuh