ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 1878

The Utility of the Omeract Ultrasound Tenosynovitis Scoring System in Multicenter Clinical Trials

Mads Ammitzbøll-Danielsen1, Mikkel Østergaard1, Esperanza Naredo2, Annamaria Iagnocco3, Ingrid Moller4, Maria Antonietta D'Agostino5, Frédérique Gandjbakhch6 and Lene Terslev7, 1Center for Rheumatology and Spine Diseases, Rigshospitalet, Copenhagen Center for Arthritis Research, Copenhagen, Denmark, 2Rheumatology, Joint and Bone Research Unit, IIS-FJD, Hospital Universitario Fundación Jiménez Díaz., Madrid, Spain, 3Academic Rheumatology Unit, Università degli Studi di Torino, Torino, Italy, 4Rheumatology, Instituto Poal, Barcelona, Spain, 5Department of Rheumatology, Assistance publique-Hôpitaux de Paris Ambroise Paré Hospital, Boulogne-Billancourt , Université Versailles Saint Quentin en Yvelines, Paris, France, 6Department of Rheumatology, APHP, Pitié Salpétrière Hospital, Universite Paris 6, Paris, France, 7Copenhagen Center for Arthritis Research, Center for Rheumatology and Spine Diseases, Rigshospitalet, Denmark, Copenhagen, Denmark

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Imaging, Outcome measures, rheumatoid arthritis (RA) and tendonitis/bursitis

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Monday, November 6, 2017

Title: Imaging of Rheumatic Diseases I: Novel Imaging and Scoring Systems

Session Type: ACR Concurrent Abstract Session

Session Time: 4:30PM-6:00PM

Background/Purpose :Tenosynovitis is very common in patients with RA and is associated with lower physical function.  Several studies have confirmed the limitations of clinical examination for detection of tenosynovitis in comparison with ultrasound (US) and a highly validated and reliable US scoring system is therefore needed if implementing US-tenosynovitis as an outcome measure in clinical trials. The OMERACT US group’s tenosynovitis scoring system has a good single and multicenter intra- and inter-observer agreement, whereas the sensitivity to change in a multicenter design has never been tested.

Furthermore, it is unknown whether low grade synovial hypertrophy without Doppler Signal represents true inflammation, i.e. can be eliminated by anti-inflammatory therapy and is sensitive to change.

The aim of this study was to test the sensitivity to change of the OMERACT US scoring system for tenosynovitis, including minimal signs of tenosynovitis, in a multicenter design in order to validate it as an outcome measure in RA multicenter clinical trials. Furthermore, to assess the association between US and HAQ and DAS28.

Methods: Forty-nine patients with established RA (duration ≥1 year) and 18 early RA patients (<1 year) with US-verified tenosynovitis were recruited from six rheumatology outpatient clinics in four different countries, if they were scheduled for treatment intensification with synthetic and/or biological DMARD. Tenosynovitis was assessed at baseline, and at three and six months’ follow-up, by GS and Doppler, using the semi-quantitative OMERACT scoring system. Furthermore, HAQ and DAS28 were assessed.  

Results: At baseline tenosynovitis was most frequently found at the extensor carpi ulnaris and tibialis posterior tendons (70.7% and 44.4%, respectively). The overall GS score showed a statistically significant decrease from baseline median 5 (25th;75th percentile: 2;7) to 6 months 0 (0;3) and the overall Doppler score decreased statistically significant from baseline 3 (2;6) to 6 months 0 (0;1), both with a p<0.01. Both GS and Doppler showed high responsiveness (SRM>0.9), as did HAQ and DAS28 (table 1).  Among tendons with grey scale (GS)=1/Doppler=0, 36 of 39 (92.3%) showed therapy-induced improvements. Changes in US-scores were statistically significantly associated with DAS28 (p=0.02), but not with HAQ.

Conclusion:   In conclusion, this RA multicenter study documented a high sensitivity to change of both GS and Doppler US tenosynovitis scores, indicating utility of the OMERACT US scoring system for diagnosing and monitoring tenosynovitis in multicenter trials. Secondly, synovial hypertrophy without Doppler signal, do respond to therapy, suggesting it reflects true inflammation. Finally, changes in US tenosynovitis scores are associated with changes in DAS28.


All Sites – Imaging modality

Baseline

Δ 0-3 month

P

SRM

Δ 3-6 month

P

SRM

Δ 0-6 month

P

SRM

(n=67)

Grey scale

Median [25p;75p]

4

[2;7]

-2

[-3;-0]

<0.01

0.8

-1.0

[-2;0]

<0.01

0.4

-2

[-5;-5]

<0.01

0.9

Mean ±SD

5.0

±3.4

-2.4

±2.9

-0.9

±2.4

-3.3

±3.8

Doppler

Median [25p;75p]

3

[2;6]

-2

[-4;-1]

<0.01

0.8

0

[-2;0]

<0.01

0.3

-3

[-5;2]

<0.01

0.9

Mean ± SD

1.2

 ±0.66

-0.8

±0.6

0

±0.2

-0.7

±0.6

DAS28

Median [25p;75p]

4.6

[3.7;5.3]

-1.4

[-48;-2]

<0.01

0.9

-0.4

[-1.3;0.1]

<0.01

0.3

-1.6

[-3.2;-0.7]

<.0.01

1.1

Mean ±SD

4.4

±1.3

-1.4

±1.5

-0.5

±1.5

-1.8

±1.7

HAQ

Median [25p;75p]

1.0

[0.5;1.5]

-0.25

[-0.75;0]

<0.01

0.8

0

[-0.25;0]

0.02

0.3

-0.375

[-0.875;0]

<.0.01

0.9

Mean ± SD

1.0

±0.6

-0.4

±0.4

-0.1

± 0.3

-0.5

± 0.5

P, p-value for Wilcoxon’s test for change of paired data between 2 time points; N, number of patients; SRM, standardized response mean.



Disclosure: M. Ammitzbøll-Danielsen, None; M. Østergaard, AbbVie, BMS, Celgene, Crescendo Bioscience, Janssen, Merck, 2,Abbvie, BMS, Boehringer-Ingelheim, Celgene, Eli-Lilly, Centocor, GSK, Hospira, Janssen, Merck, Novartis, Orion, Pfizer, Regeneron, Roche, Takeda, and UCB, 5; E. Naredo, Abbvie, Roche, BMS, Pfizer, UCB, Novartis, Lilly, Janssen, 5; A. Iagnocco, None; I. Moller, None; M. A. D'Agostino, None; F. Gandjbakhch, None; L. Terslev, None.

To cite this abstract in AMA style:

Ammitzbøll-Danielsen M, Østergaard M, Naredo E, Iagnocco A, Moller I, D'Agostino MA, Gandjbakhch F, Terslev L. The Utility of the Omeract Ultrasound Tenosynovitis Scoring System in Multicenter Clinical Trials [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/the-utility-of-the-omeract-ultrasound-tenosynovitis-scoring-system-in-multicenter-clinical-trials/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2017 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/the-utility-of-the-omeract-ultrasound-tenosynovitis-scoring-system-in-multicenter-clinical-trials/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology