Development and Validation of the Dystonia-Pain Classification System: A Multicenter Study.


Journal

Movement disorders : official journal of the Movement Disorder Society
ISSN: 1531-8257
Titre abrégé: Mov Disord
Pays: United States
ID NLM: 8610688

Informations de publication

Date de publication:
07 2023
Historique:
revised: 04 04 2023
received: 22 02 2023
accepted: 10 04 2023
medline: 31 7 2023
pubmed: 20 5 2023
entrez: 20 5 2023
Statut: ppublish

Résumé

Dystonia is associated with disabling nonmotor symptoms like chronic pain (CP), which is prevalent in dystonia and significantly impacts the quality of life (QoL). There is no validated tool for assessing CP in dystonia, which substantially hampers pain management. The aim was to develop a CP classification and scoring system for dystonia. A multidisciplinary group was established to develop the Dystonia-Pain Classification System (Dystonia-PCS). The classification of CP as related or unrelated to dystonia was followed by the assessment of pain severity score, encompassing pain intensity, frequency, and impact on daily living. Then, consecutive patients with inherited/idiopathic dystonia of different spatial distribution were recruited in a cross-sectional multicenter validation study. Dystonia-PCS was compared to validated pain, mood, QoL, and dystonia scales (Brief Pain Inventory, Douleur Neuropathique-4 questionnaire, European QoL-5 Dimensions-3 Level Version, and Burke-Fahn-Marsden Dystonia Rating Scale). CP was present in 81 of 123 recruited patients, being directly related to dystonia in 82.7%, aggravated by dystonia in 8.8%, and nonrelated to dystonia in 7.5%. Dystonia-PCS had excellent intra-rater (Intraclass Correlation Coefficient - ICC: 0.941) and inter-rater (ICC: 0.867) reliability. In addition, pain severity score correlated with European QoL-5 Dimensions-3 Level Version's pain subscore (r = 0.635, P < 0.001) and the Brief Pain Inventory's severity and interference scores (r = 0.553, P < 0.001 and r = 0.609, P < 0.001, respectively). Dystonia-PCS is a reliable tool to categorize and quantify CP impact in dystonia and will help improve clinical trial design and management of CP in patients affected by this disorder. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Sections du résumé

BACKGROUND
Dystonia is associated with disabling nonmotor symptoms like chronic pain (CP), which is prevalent in dystonia and significantly impacts the quality of life (QoL). There is no validated tool for assessing CP in dystonia, which substantially hampers pain management.
OBJECTIVE
The aim was to develop a CP classification and scoring system for dystonia.
METHODS
A multidisciplinary group was established to develop the Dystonia-Pain Classification System (Dystonia-PCS). The classification of CP as related or unrelated to dystonia was followed by the assessment of pain severity score, encompassing pain intensity, frequency, and impact on daily living. Then, consecutive patients with inherited/idiopathic dystonia of different spatial distribution were recruited in a cross-sectional multicenter validation study. Dystonia-PCS was compared to validated pain, mood, QoL, and dystonia scales (Brief Pain Inventory, Douleur Neuropathique-4 questionnaire, European QoL-5 Dimensions-3 Level Version, and Burke-Fahn-Marsden Dystonia Rating Scale).
RESULTS
CP was present in 81 of 123 recruited patients, being directly related to dystonia in 82.7%, aggravated by dystonia in 8.8%, and nonrelated to dystonia in 7.5%. Dystonia-PCS had excellent intra-rater (Intraclass Correlation Coefficient - ICC: 0.941) and inter-rater (ICC: 0.867) reliability. In addition, pain severity score correlated with European QoL-5 Dimensions-3 Level Version's pain subscore (r = 0.635, P < 0.001) and the Brief Pain Inventory's severity and interference scores (r = 0.553, P < 0.001 and r = 0.609, P < 0.001, respectively).
CONCLUSIONS
Dystonia-PCS is a reliable tool to categorize and quantify CP impact in dystonia and will help improve clinical trial design and management of CP in patients affected by this disorder. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Identifiants

pubmed: 37208983
doi: 10.1002/mds.29423
doi:

Types de publication

Multicenter Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1163-1174

Informations de copyright

© 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

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Auteurs

Clarice Listik (C)

Department of Neurology, Movement Disorders Center, School of Medicine, University of São Paulo, São Paulo, Brazil.

Eduardo Listik (E)

Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Flávia de Paiva Santos Rolim (F)

Department of Neurology, Hospital Geral de Fortaleza, Fortaleza, Brazil.

Denise Maria Meneses Cury Portela (DM)

Department of Neurology, Instituto de Ensino Superior do Piaui, Teresina, Brazil.

Santiago Perez Lloret (S)

Observatorio de Salud Pública, Pontificia Universidad Católica Argentina, Buenos Aires, Argentina.
Department of Physiology, Faculty of Medicine, University of Buenos Aires, Buenos Aires, Argentina.

Natália Rebeca de Alves Araújo (NR)

Department of Neurology, Instituto de Ensino Superior do Piaui, Teresina, Brazil.

Pedro Rubens Araújo Carvalho (PRA)

Department of Neurology, Hospital Geral de Fortaleza, Fortaleza, Brazil.

Graziele Costa Santos (GC)

Department of Neurology, Universidade Federal de Sao Paulo (UNIFESP), São Paulo, Brazil.

João Carlos Papaterra Limongi (JCP)

Department of Neurology, Movement Disorders Center, School of Medicine, University of São Paulo, São Paulo, Brazil.

Francisco Cardoso (F)

Department of Neurology, Hospital das Clínicas da Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

Veit Mylius (V)

Department of Neurology, Center for Neurorehabilitation, Valens, Switzerland.
Department of Neurology, Philipps University, Marburg, Germany.

Florian Brugger (F)

Department of Neurology, Kantonsspital St. Gallen, St. Gallen, Switzerland.

Ana Mercia Fernandes (AM)

Department of Neurology, Movement Disorders Center, School of Medicine, University of São Paulo, São Paulo, Brazil.

Egberto Reis Barbosa (E)

Department of Neurology, Movement Disorders Center, School of Medicine, University of São Paulo, São Paulo, Brazil.

Manoel Jacobsen Teixeira (M)

Department of Neurology, Movement Disorders Center, School of Medicine, University of São Paulo, São Paulo, Brazil.

Henrique Ballalai Ferraz (HB)

Department of Neurology, Universidade Federal de Sao Paulo (UNIFESP), São Paulo, Brazil.

Sarah Teixeira Camargos (ST)

Department of Neurology, Hospital das Clínicas da Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

Rubens Gisbert Cury (RG)

Department of Neurology, Movement Disorders Center, School of Medicine, University of São Paulo, São Paulo, Brazil.

Daniel Ciampi de Andrade (DC)

Department of Neurology, Movement Disorders Center, School of Medicine, University of São Paulo, São Paulo, Brazil.
Department of Health Science and Technology, Center for Neuroplasticity and Pain (CNAP), Faculty of Medicine, Aalborg University, Aalborg, Denmark.

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