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Abstract Number: 1344

Impact of Fibromyalgic RA on Composite Scores; Results from a Longitudinal Study of RA Patients Initiating Bdmard Therapy

Hilde B Hammer1, Sella A. Provan2, Brigitte Michelsen3, Till Uhlig4, Jon Lampa5 and Tore K Kvien6, 1Rheumatology, Dept. of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway, 2Department of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway, 3Rheumatology, Hospital of Southern Norway trust, Kristiansand, Norway, 4Dept. of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway, 5Karolinska Institute, Department of Medicine, Rheumatology Unit, Stockholm, Sweden, Stockholm, Sweden, 6On behalf of the NOR-DMARD registry, Oslo, Norway

Meeting: 2017 ACR/ARHP Annual Meeting

Date of first publication: September 18, 2017

Keywords: Assessment, remission, rheumatoid arthritis (RA) and ultrasonography

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Session Information

Date: Monday, November 6, 2017

Title: Rheumatoid Arthritis – Clinical Aspects Poster II: Pathophysiology, Autoantibodies, and Disease Activity Measures

Session Type: ACR Poster Session B

Session Time: 9:00AM-11:00AM

Background/Purpose:

The composite scores DAS28, CDAI and SDAI all include number of tender and swollen joints (of 28). Rheumatoid arthritis (RA) patients with tender to swollen joint count difference (TSJD) >0 had reduced composite score remission and TSJD of ≥7 was shown to have ≥ 80% sensitivity and specificity to have “fibromyalgic RA” (FM-RA) (Pollard et al. Rheumatology 2010). Ultrasonography (US) is a sensitive imaging technique to detect synovitis including grey scale synovitis (GS) and power Doppler (PD) activity. The present purpose was to explore the impact of FM-RA on the composite scores in comparison to other clinical assessments including US in a longitudinal study of established RA patients initiating bDMARD therapy.

Methods:

A total of 209 patients with RA (mean (SD) age 53 (13) years, disease duration 10 (9) years, 81% women, 79% anti-CCP positive) were included when initiating bDMARDs and assessed at baseline and after 1, 2, 3, 6 and 12 months with joint pain VAS, patient’s global VAS, RAID score, MHAQ, clinical examinations (performed by a study nurse; assessor’s disease activity VAS, tender and swollen joint counts (of 28) and laboratory variables (ESR and CRP). All US examinations (semi-quantitative scoring (0-3)) of GS and PD (PIP 2-3, MCP 1-5, wrist (radiocarpal, intercarpal, radioulnar), elbow, knee, tibiotalar, MTP 1-5 and ext.carpi ulnaris/tib.post.tendons bilaterally) were performed by one rheumatologist (HBH) (Siemens Acuson Antares, excellence version, 5-13 MHz probe). To explore the impact of tender minus swollen joint count, patients were divided into three groups depending on TSJD at baseline; Gr.1=≤0 (n=125), Gr.2=1-6 (n=62), Gr.3=≥7 (n=22, FM-RA). Statistical calculations included frequency of DAS28(ESR), CDAI, SDAI and ACR/EULAR (Boolean) remission, one-way ANOVA and cross-tabs.

Results:

There were significantly higher DAS28(ESR), CDAI, SDAI, joint pain VAS, patient’s global VAS, RAID score and M-HAQ in the FM-RA group at all time points (p≤0.003), while there were no differences between the groups regarding assessor’s global VAS or ESR/CRP. On the other hand, sum scores GS and PD were higher in Gr.1 and 2 (figure 1). The table illustrates that the FM-RA group has a very low percentage of composite score remission both at 6 and 12 months follow-up.

Conclusion:

In spite of having the lowest degree of US pathology, the 10.5% FM-RA patients had significantly higher levels of all the commonly used composite scores at all time points and they seldom reached remission. Thus, the small RA-FM group should be identified and other than composite scores should be used for assessing their disease activity.

Percentages of patients in composite score remission

6 months

12 months

Group 1; TSJD=≤0

Group 2; TSJD=1-6

Group 3; TSJD=≥7, FM-RA

Group 1; TSJD=≤0

Group 2; TSJD=1-6

Group 3; TSJD=≥7, FM-RA

DAS28

27.2

11.4

2.3

26.3

12.5

0.0

SDAI

15.2

7.1

1.1

17.8

9.2

0.7

CDAI

12.5

6.5

1.6

16.4

7.9

0.7

Boolean

13.0

7.1

1.1

14.5

7.9

0.7


Disclosure: H. B. Hammer, AbbVie Norway, 2,Abbvie, 8,Novartis Pharmaceutical Corporation, 5,Pfizer Inc, 8,Roche Pharmaceuticals, 8; S. A. Provan, None; B. Michelsen, None; T. Uhlig, None; J. Lampa, None; T. K. Kvien, AbbVie, 2,Pfizer Inc, 2,Roche Pharmaceuticals, 2,UCB, 2,BMS, 2,MSD, 2,AbbVie, 5,Pfizer Inc, 5,BMS, 8,MSD, 8,Roche Pharmaceuticals, 8,UCB, 8,AbbVie, 8.

To cite this abstract in AMA style:

Hammer HB, Provan SA, Michelsen B, Uhlig T, Lampa J, Kvien TK. Impact of Fibromyalgic RA on Composite Scores; Results from a Longitudinal Study of RA Patients Initiating Bdmard Therapy [abstract]. Arthritis Rheumatol. 2017; 69 (suppl 10). https://acrabstracts.org/abstract/impact-of-fibromyalgic-ra-on-composite-scores-results-from-a-longitudinal-study-of-ra-patients-initiating-bdmard-therapy/. Accessed .
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