Sudden Onset, Fixed Dystonia and Acute Peripheral Trauma as Diagnostic Clues for Functional Dystonia.

acute peripheral trauma fixed dystonia functional dystonia idiopathic dystonia sudden onset

Journal

Movement disorders clinical practice
ISSN: 2330-1619
Titre abrégé: Mov Disord Clin Pract
Pays: United States
ID NLM: 101630279

Informations de publication

Date de publication:
Oct 2021
Historique:
received: 24 04 2021
revised: 16 07 2021
accepted: 26 07 2021
entrez: 11 10 2021
pubmed: 12 10 2021
medline: 12 10 2021
Statut: epublish

Résumé

The differentiation of functional dystonia from idiopathic dystonia may be clinically challenging. To identify clinical features suggestive of functional dystonia to guide physicians to distinguish functional dystonia from idiopathic dystonia. Patient data were extracted from the Italian Registry of Functional Motor Disorders and the Italian Registry of Adult Dystonia. Patients with functional and idiopathic dystonia were followed up at the same clinical sites, and they were similar in age and sex. We identified 113 patients with functional dystonia and 125 with idiopathic dystonia. Sudden onset of dystonia, evidence of fixed dystonia, and acute peripheral trauma before dystonia onset were more frequent in the functional dystonia group. No study variable alone achieved satisfactory sensitivity and specificity, whereas a combination of variables yielded 85% sensitivity and 98% specificity. A diagnostic algorithm was developed to reduce the risk of misclassifying functional dystonia. Our findings extend the current diagnostic approach to functional dystonia by showing that clinical information about symptom onset, fixed dystonia, and history of peripheral trauma may provide key clues in the diagnosis of functional dystonia.

Sections du résumé

BACKGROUND BACKGROUND
The differentiation of functional dystonia from idiopathic dystonia may be clinically challenging.
OBJECTIVE OBJECTIVE
To identify clinical features suggestive of functional dystonia to guide physicians to distinguish functional dystonia from idiopathic dystonia.
METHODS METHODS
Patient data were extracted from the Italian Registry of Functional Motor Disorders and the Italian Registry of Adult Dystonia. Patients with functional and idiopathic dystonia were followed up at the same clinical sites, and they were similar in age and sex.
RESULTS RESULTS
We identified 113 patients with functional dystonia and 125 with idiopathic dystonia. Sudden onset of dystonia, evidence of fixed dystonia, and acute peripheral trauma before dystonia onset were more frequent in the functional dystonia group. No study variable alone achieved satisfactory sensitivity and specificity, whereas a combination of variables yielded 85% sensitivity and 98% specificity. A diagnostic algorithm was developed to reduce the risk of misclassifying functional dystonia.
CONCLUSION CONCLUSIONS
Our findings extend the current diagnostic approach to functional dystonia by showing that clinical information about symptom onset, fixed dystonia, and history of peripheral trauma may provide key clues in the diagnosis of functional dystonia.

Identifiants

pubmed: 34631946
doi: 10.1002/mdc3.13322
pii: MDC313322
pmc: PMC8485608
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1107-1111

Informations de copyright

© 2021 The Authors. Movement Disorders Clinical Practice published by Wiley Periodicals LLC. on behalf of International Parkinson and Movement Disorder Society.

Déclaration de conflit d'intérêts

No specific funding was received for this work and the authors declare that there are no conflicts of interest relevant to this work.

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Auteurs

Tommaso Ercoli (T)

Department of Medical Sciences and Public Health University of Cagliari Cagliari Italy.

Giovanni Defazio (G)

Department of Medical Sciences and Public Health University of Cagliari Cagliari Italy.

Christian Geroin (C)

Neurology Unit, Movement Disorders Division, Department of Neurosciences, Biomedicine and Movement Sciences University of Verona Verona Italy.

Enrico Marcuzzo (E)

Neurology Unit, Movement Disorders Division, Department of Neurosciences, Biomedicine and Movement Sciences University of Verona Verona Italy.

Giovanni Fabbrini (G)

Department of Human Neurosciences Sapienza University of Rome Rome Italy.
IRCCS Neuromed Pozzilli Italy.

Francesco Bono (F)

Botulinum Toxin Center, Neurology Unit A.O.U. Mater Domini Catanzaro Italy.

Alessandro Mechelli (A)

Botulinum Toxin Center, Neurology Unit A.O.U. Mater Domini Catanzaro Italy.

Roberto Ceravolo (R)

Neurology Unit, Department of Clinical and Experimental Medicine University of Pisa Pisa Italy.

Luigi Michele Romito (LM)

Parkinson and Movement Disorders Unit Fondazione IRCCS Istituto Neurologico Carlo Besta Milan Italy.

Alberto Albanese (A)

Department of Neurology IRCCS Humanitas Research Hospital Rozzano Italy.

Antonio Pisani (A)

Department of Brain and Behavioral Sciences University of Pavia Pavia Italy.
IRCCS Mondino Foundation Pavia Italy.

Maurizio Zibetti (M)

Department of Neuroscience-Rita Levi Montalcini University of Turin Turin Italy.

Maria Concetta Altavista (MC)

UOC di Neurologia Ospedale San Filippo Neri Rome Italy.

Luca Maderna (L)

Department of Neurology-Stroke Unit and Laboratory of Neurosciences Istituto Auxologico Italiano, IRCCS Milan Italy.

Martina Petracca (M)

Fondazione Policlinico Universitario 'Agostino Gemelli'-IRCCS Rome Italy.

Paolo Girlanda (P)

Department of Clinical and Experimental Medicine University of Messina Messina Italy.

Marcello Mario Mascia (MM)

Department of Medical Sciences and Public Health University of Cagliari Cagliari Italy.

Alfredo Berardelli (A)

Department of Human Neurosciences Sapienza University of Rome Rome Italy.
IRCCS Neuromed Pozzilli Italy.

Michele Tinazzi (M)

Neurology Unit, Movement Disorders Division, Department of Neurosciences, Biomedicine and Movement Sciences University of Verona Verona Italy.

Classifications MeSH