Exploring remission concept in axial spondyloarthritis through the perception of rheumatologists using vignettes and priority ratings.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
30 05 2022
Historique:
received: 01 07 2021
revised: 01 09 2021
pubmed: 17 9 2021
medline: 3 6 2022
entrez: 16 9 2021
Statut: ppublish

Résumé

The optimal treatment target in axial spondyloarthritis (axSpA) is remission; however, a consensual definition of remission is lacking. Our objective was to explore rheumatologists' perception of remission using vignette cases and a priority exercise. A cross-sectional survey of rheumatologists' perceptions of remission in axSpA was performed in 2020 using (i) 36 vignette cases, with a single clinical picture and three varying parameters [axial pain (ranging from 2 to 5 on a 0-10 scale)], fatigue (2-8), and morning stiffness (<15 min, 30 min or 1 h), assessed as remission yes/no; and (ii) prioritization of elements to consider for remission from a list of 12 items: BASDAI, ASDAS, elements of BASDAI and ASDAS including CRP, NSAID use, extra-articular manifestations (EAMs), and other explanations of symptoms, e.g. fibromyalgia. Analyses were descriptive. Overall, 200 French rheumatologists participated in 2400 vignette evaluations. Of these, 463 (19%) were classified as remission. The six vignette cases representing 56% of all remission cases had <15 min duration of morning stiffness and axial pain ≤3/10, regardless of fatigue levels. Prioritized items for remission were: morning stiffness (75%), EAMs (75%), NSAID use (71%), axial pain (68%) and CRP (66%). When conceptualizing remission in axSpA, rheumatologists took into account morning stiffness and axial pain as expected; the link between remission and fatigue was much weaker. Furthermore, rheumatologists also included EAMs and NSAID use in the concept of remission. Consensus is needed for definition of remission in axSpA.

Identifiants

pubmed: 34528070
pii: 6370975
doi: 10.1093/rheumatology/keab711
doi:

Substances chimiques

Anti-Inflammatory Agents, Non-Steroidal 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2603-2608

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Krystel Aouad (K)

Institut Pierre Louis d'Epidémiologie et de Santé Publique, Sorbonne Université, INSERM, Paris.

Daniel Wendling (D)

Rheumatology Department, Besançon University Hospital, Besançon.

Maxime Breban (M)

Service de Rhumatologie, Hôpital Ambroise Paré, AP-HP, Boulogne.
Infection & Inflammation, UMR 1173, Inserm, UVSQ/Université Paris Saclay.
Laboratoire d'Excellence Inflamex, Université de Paris.

Sabrina Dadoun (S)

Rheumatology, Private Practice.
Rheumatology, CeSOA, MGEN Action Sociale.

Christophe Hudry (C)

Rheumatology, CeSOA, MGEN Action Sociale.

Anna Moltó (A)

Rheumatology Department, Cochin Hospital, APHP.
Rheumatology, INSERM U-1153 (ECAMO), CRESS, Université de Paris, Paris.

Edouard Pertuiset (E)

Rheumatology Department, Rene Dubos Hospital, Pontoise.

Laure Gossec (L)

Institut Pierre Louis d'Epidémiologie et de Santé Publique, Sorbonne Université, INSERM, Paris.
Rheumatology Department, Pitié-Salpêtrière Hospital, AP-HP, Sorbonne Université, Paris, France.

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