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      Definitions and reliability assessment of elementary ultrasound lesions in giant cell arteritis: a study from the OMERACT Large Vessel Vasculitis Ultrasound Working Group

      research-article
      1 , 2 , 3 , 4 , 5 , 6 , 7 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 19 , 20 , 17 , 21 , 22 , 23 , 24 , 25 , 18 , 25 , 26 , 27 , 28 , 29
      RMD Open
      BMJ Publishing Group
      giant cell arteritis, ultrasonography, systemic vasculitis

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          Abstract

          Objectives

          To define the elementary ultrasound (US) lesions in giant cell arteritis (GCA) and to evaluate the reliability of the assessment of US lesions according to these definitions in a web-based reliability exercise.

          Methods

          Potential definitions of normal and abnormal US findings of temporal and extracranial large arteries were retrieved by a systematic literature review. As a subsequent step, a structured Delphi exercise was conducted involving an expert panel of the Outcome Measures in Rheumatology (OMERACT) US Large Vessel Vasculitis Group to agree definitions of normal US appearance and key elementary US lesions of vasculitis of temporal and extracranial large arteries. The reliability of these definitions on normal and abnormal blood vessels was tested on 150 still images and videos in a web-based reliability exercise.

          Results

          Twenty-four experts participated in both Delphi rounds. From originally 25 statements, nine definitions were obtained for normal appearance, vasculitis and arteriosclerosis of cranial and extracranial vessels. The ‘halo’ and ‘compression’ signs were the key US lesions in GCA. The reliability of the definitions for normal temporal and axillary arteries, the ‘halo’ sign and the ‘compression’ sign was excellent with inter-rater agreements of 91–99% and mean kappa values of 0.83–0.98 for both inter-rater and intra-rater reliabilities of all 25 experts.

          Conclusions

          The ‘halo’ and the ‘compression’ signs are regarded as the most important US abnormalities for GCA. The inter-rater and intra-rater agreement of the new OMERACT definitions for US lesions in GCA was excellent.

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          Most cited references46

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          Disease pattern in cranial and large-vessel giant cell arteritis.

          To identify variables that distinguish large-vessel giant cell arteritis (GCA) with subclavian/axillary/brachial artery involvement from cranial GCA. Seventy-four case patients with subclavian/axillary GCA diagnosed by angiography and 74 control patients with temporal artery biopsy-proven GCA without large vessel involvement matched for the date of first diagnosis were identified. Pertinent initial symptoms, time delay until diagnosis, and clinical symptoms, as well as clinical and laboratory findings at the time of diagnosis, were recorded by retrospective chart review. Expression of cytokine messenger RNA in temporal artery tissue from patients with large-vessel and cranial GCA was determined by semiquantitative polymerase chain reaction analysis. Distribution of disease-associated HLA-DRB1 alleles in patients with aortic arch syndrome and cranial GCA was assessed. The clinical presentation distinguished patients with large-vessel GCA from those with classic cranial GCA. Upper extremity vascular insufficiency dominated the clinical presentation of patients with large-vessel GCA, whereas symptoms related to impaired cranial blood flow were infrequent. Temporal artery biopsy findings were negative in 42% of patients with large-vessel GCA. Polymyalgia rheumatica occurred with similar frequency in both patient groups. Large-vessel GCA was associated with higher concentrations of interleukin-2 gene transcripts in arterial tissue and overrepresentation of the HLA-DRB1*0404 allele, indicating differences in pathogenetic mechanisms. GCA is not a single entity but includes several variants of disease. Large-vessel GCA produces a distinct spectrum of clinical manifestations and often occurs without involvement of the cranial arteries. Large-vessel GCA requires a different approach to the diagnosis and probably also to treatment.
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            Ultrasound of proximal upper extremity arteries to increase the diagnostic yield in large-vessel giant cell arteritis.

            To describe characteristic ultrasound findings and clinical features of patients with newly diagnosed cranial and large-vessel (LV) GCA in a specialized ultrasound clinic. This case-control study includes all consecutive patients between 1997 and 2006 with newly diagnosed GCA. Duplex ultrasound of the temporal, subclavian, axillary and proximal brachial arteries was performed in all patients with suspected temporal arteritis, PMR, arm claudication, unclear inflammation or pyrexia of unknown origin (PUO). In 53 of 176 patients, ultrasound depicted characteristic vasculitic homogeneous wall swelling of the axillary, subclavian and/or proximal brachial arteries. These were affected in 98, 61 and 21%, respectively, in the 53 patients. The findings were bilateral in 79%. Axillary arteries were stenotic or occluded in 51 and 2% and temporal artery ultrasound and histology were positive in 62 and 67% of LV-GCA cases, respectively. A significantly greater number of LV-GCA patients were female (83 vs 65%) and younger (mean 66 vs 72 yrs) as compared with those without proximal arm involvement. Headaches (38 vs 75%), jaw claudication (24 vs 48%) and anterior ischaemic optic neuropathy (4 vs 19%) occurred significantly less frequently. The median time until diagnosis was significantly longer (31 vs 8 weeks). ESR and presence of PMR were similar in both groups. Performing axillary artery ultrasound in all patients with suspected temporal arteritis, PMR, arm claudication, unclear inflammation or PUO increases the diagnostic yield for LV-GCA. Patients with LV-GCA differ from those without arm involvement.
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              • Abstract: found
              • Article: not found

              Reliability of a consensus-based ultrasound score for tenosynovitis in rheumatoid arthritis.

              To produce consensus-based scoring systems for ultrasound (US) tenosynovitis and to assess the intraobserver and interobserver reliability of these scoring systems in rheumatoid arthritis (RA).
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                Author and article information

                Journal
                RMD Open
                RMD Open
                rmdopen
                rmdopen
                RMD Open
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                2056-5933
                2018
                17 May 2018
                : 4
                : 1
                : e000598
                Affiliations
                [1 ] departmentDepartment of Rheumatology , Hospital of Southwest Jutland , Esbjerg, Denmark
                [2 ] departmentDepartment of Internal Medicine, Clinical Division of Internal Medicine II , Medical University of Innsbruck , Innsbruck, Austria
                [3 ] departmentDepartment of Rheumatology , Medical University of Graz , Graz, Austria
                [4 ] departmentDepartment of Rhematology , Hospital of Bruneck , Bruneck, Italy
                [5 ] departmentIII. Medical Clinic, Department of Oncology, Hematology and Rheumatology , University Hospital Bonn , Berlin, Germany
                [6 ] Leiden University Medical Center , Leiden, The Netherlands
                [7 ] departmentEpidemiology Unit , Italian Society for Rheumatology (SIR) , Milan, Italy
                [8 ] departmentDepartment of Rheumatology , University of Ferrara , Ferrara, Italy
                [9 ] departmentDepartment of Rheumatology , University Medical Centre Ljubljana , Ljubljana, Slovenia
                [10 ] Martina Hansens Hospital , Bærum, Oslo, Norway
                [11 ] departmentDipartimento Scienze Cliniche e Biologiche - Reumatologia , Università degli Studi di Torino , Torino, Italy
                [12 ] departmentDepartment of Rheumatology , Norfolk and Norwich University Hospital , Norwich, UK
                [13 ] departmentHospital de Santa Maria - CHLN , Lisbon Academic Medical Centre , Lisbon, Portugal
                [14 ] Hospital Universitario Fundación Jiménez Díaz , Madrid, Spain
                [15 ] University Hospital La Paz , Madrid, Spain
                [16 ] MC Groep Hospitals , Lelystad, The Netherlands
                [17 ] departmentRheumatology , Mayo Clinic , Rochester, Minnesota, USA
                [18 ] Copenhagen Center for Arthritis Research (COPECARE) , Copenhagen, Denmark
                [19 ] departmentDepartment of Rheumatology and Internal Medicine , Pomeranian Medical University , Szczecin, Poland
                [20 ] Hôpital Ambroise Paré , Boulogne-Billancourt, France
                [21 ] St. Elizabeth’s Medical Center , Boston, Massachusetts, USA
                [22 ] departmentDepartment of Rheumatology, First Faculty of Medicine , Charles University of Prague , Prague, Czech Republic
                [23 ] Arcispedale Santa Maria Nuova , Reggio Emilia, Italy
                [24 ] departmentDepartment of Rheumatology , University of California , Los Angeles, California, USA
                [25 ] Diagnostic Centre Region Hospital Silkeborg , Silkeborg, Denmark
                [26 ] departmentDepartment of Rheumatology , Odense University Hospital , Odense, Denmark
                [27 ] Asklepios Medical Center , Bad Abbach, Germany
                [28 ] Southend University Hospital NHS Foundation Trust & Anglia Ruskin University , Southend-on-Sea, UK
                [29 ] departmentMedical Centre for Rheumatology , Immanuel Krankenhaus Berlin , Berlin, Germany
                Author notes
                [Correspondence to ] Dr Christina Duftner; christina.duftner@ 123456gmx.at
                Author information
                http://orcid.org/0000-0001-7451-0271
                http://orcid.org/0000-0002-0943-8768
                http://orcid.org/0000-0002-5347-0060
                Article
                rmdopen-2017-000598
                10.1136/rmdopen-2017-000598
                5976098
                29862043
                82c16d9d-996a-4a32-b34b-08328d1e847f
                © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

                This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

                History
                : 11 October 2017
                : 04 March 2018
                : 06 March 2018
                Categories
                Vasculitis
                1506
                Original article
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                giant cell arteritis,ultrasonography,systemic vasculitis

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