16
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Ultrasound detects synovitis in replaced and other surgically operated joints in rheumatoid arthritis patients

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          Joint replacements continue to occur during a rheumatoid arthritis (RA) patient’s lifetime despite significant advances in available treatment options. The purpose of this study was to examine and quantify synovitis in surgically operated joints by ultrasound (US) in RA patients starting a new therapeutic agent.

          Methods

          RA subjects were enrolled in either tocilizumab or tofacitinib open-label, investigator-initiated trials and were assessed by ultrasound. In a subset of RA patients with joint replacements and/or operations of joint areas (OJA; e.g. joint arthroscopies, fusions, and synovectomies), joint-level scores of synovitis were compared between replaced joints, OJAs, and native joints. Joint-level synovitis was measured by grayscale (GSUS (0–3)) and power Doppler (PDUS (0–3)) at baseline and follow-up (3–6 months). McNemar’s test or Wilcoxon signed rank test utilized the mixed effects ordinal logistic regression models.

          Results

          Twenty RA patients had a total of 25 replaced joints and 24 OJA. All replaced joints had GSUS> 1 and 92% had PDUS> 1 at baseline, while OJA and native joints had lower evidence of GSUS> 1 (37.5, 38% respectively) and PDUS> 1 (45.8, 62% respectively). GSUS and PDUS semiquantitative scores improved significantly with treatment in replaced joints ( p = 0.01, p = 0.007), and native joints ( p < 0.001 both), but not OJA.

          Conclusions

          In RA, joint replacement does not eliminate or prevent ultrasound measured synovitis, where all replaced joints have some evidence of US synovitis. US can also act as a potential marker of response to therapy in replaced joints. Scoring US synovitis in replaced joints should be considered in ultrasound RA clinical trials.

          Trial registration

          ClinicalTrials.gov NCT01717859 (registered 10/31/2012); ClinicalTrials.gov NCT02321930 (registered 12/22/2014).

          Related collections

          Most cited references13

          • Record: found
          • Abstract: found
          • Article: not found

          Musculoskeletal ultrasound including definitions for ultrasonographic pathology.

          Ultrasound (US) has great potential as an outcome in rheumatoid arthritis trials for detecting bone erosions, synovitis, tendon disease, and enthesopathy. It has a number of distinct advantages over magnetic resonance imaging, including good patient tolerability and ability to scan multiple joints in a short period of time. However, there are scarce data regarding its validity, reproducibility, and responsiveness to change, making interpretation and comparison of studies difficult. In particular, there are limited data describing standardized scanning methodology and standardized definitions of US pathologies. This article presents the first report from the OMERACT ultrasound special interest group, which has compared US against the criteria of the OMERACT filter. Also proposed for the first time are consensus US definitions for common pathological lesions seen in patients with inflammatory arthritis.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Prevalence of ultrasound-detected residual synovitis and risk of relapse and structural progression in rheumatoid arthritis patients in clinical remission: a systematic review and meta-analysis.

            The aims of this study were to assess the prevalence of US-detected residual synovitis in patients with RA in clinical remission (CR) and evaluate its predictive value for relapse and structural progression.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Adverse reactions to metal debris: histopathological features of periprosthetic soft tissue reactions seen in association with failed metal on metal hip arthroplasties.

              To describe the histopathology of localised adverse reactions to metal debris (ARMD) seen in association with failed metal on metal (MoM) hip arthroplasties. The nature of aseptic lymphocytic vasculitis associated lesion (ALVAL) is investigated. Periprosthetic soft tissues biopsied at time of revision from failed MoM hip arthroplasties from January 2007 to March 2011 were analysed. The inflammatory cell response was categorised into perivascular lymphocytic cuffing (ALVAL), lymphoid aggregate formation with or without germinal centres, metallosis characterised by sheets of macrophages with intracytoplasmic metallic debris and well-defined granulomas. 123 patient samples were analysed, 36 males (29.2%) and 87 females (70.8%). Three cases showing complete tissue necrosis were excluded. Patients were reviewed between 3.27 to 69.6 months postarthroplasty, with an average of 30.92 months. 103 cases (85.8%) showed ALVAL, 18 cases also showed well-defined granulomas. Of the 103 cases with ALVAL, 60 cases also showed a diffuse chronic lymphocytic synovitis, and 40 cases showed lymphoid aggregates with germinal centres. 17 cases (14.2%) showed pure metallosis. Small vessels showing ALVAL expressed peripheral node addressin. ARMD is a spectrum of changes comprising of pure metallosis, ALVAL and granulomatous inflammation. ALVAL, a distinctive inflammatory response seen in ARMD, is a precursor of lymphoid neogenesis. Lymphoid neogenesis documented in a variety of chronic inflammatory conditions most probably contributes to tissue necrosis and prosthetic failure seen in MoM hip arthroplasties. The role of vascular changes in contributing to necrosis is unclear at this stage.
                Bookmark

                Author and article information

                Contributors
                EChoate@mednet.ucla.edu
                Gurjit.Kaeley@jax.ufl.edu
                JBrook@mednet.ucla.edu
                journals@royaltman.com
                JFitzgerald@mednet.ucla.edu
                AFloegelShetty@mednet.ucla.edu
                DElashoff@mednet.ucla.edu
                VRanganath@mednet.ucla.edu
                Journal
                BMC Rheumatol
                BMC Rheumatol
                BMC Rheumatology
                BioMed Central (London )
                2520-1026
                3 February 2020
                3 February 2020
                2020
                : 4
                : 8
                Affiliations
                [1 ]ISNI 0000 0000 9632 6718, GRID grid.19006.3e, Department of Medicine, Division of Rheumatology, , University of California, ; Los Angeles, CA USA
                [2 ]ISNI 0000 0004 1936 8091, GRID grid.15276.37, College of Medicine, , University of Florida, ; Jacksonville, Florida USA
                [3 ]ISNI 0000 0000 9632 6718, GRID grid.19006.3e, Department of Medicine/Biostatistics, Division of General Internal Medicine and Health Services Research, , University of California, ; Los Angeles, CA USA
                Author information
                http://orcid.org/0000-0003-3417-9478
                Article
                107
                10.1186/s41927-019-0107-2
                6996180
                32025629
                4e88c49a-ae66-43f1-820c-ef43de2de18e
                © The Author(s) 2020

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 5 August 2019
                : 20 November 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100004328, Genentech;
                Award ID: ML28542
                Funded by: FundRef http://dx.doi.org/10.13039/100004319, Pfizer;
                Award ID: WI193025
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2020

                arthritis, rheumatoid,synovitis,ultrasonography,surgical procedures operative,joints,response

                Comments

                Comment on this article