Publication:
Reliability of high-resolution ultrasonography in the assessment of Achilles tendon enthesopathy in seronegative spondyloarthropathies

dc.contributor.authorDİRESKENELİ, RAFİ HANER
dc.contributor.authorsFilippucci, E.; Aydin, S. Zehra; Karadag, O.; Salaffi, F.; Gutierrez, M.; Direskeneli, H.; Grassi, W.
dc.date.accessioned2022-03-12T17:46:52Z
dc.date.accessioned2026-01-11T07:03:07Z
dc.date.available2022-03-12T17:46:52Z
dc.date.issued2009
dc.description.abstractObjective: The present study was mainly aimed at investigating the interobserver and intraobserver reproducibility of ultrasound (US) results in the assessment of Achilles tendon enthesopathy in patients with seronegative spondyloarthropathies (SpA). Methods: A total of 28 patients with a diagnosis of SpA according to the European Spondyloarthropathy Study Group criteria were included. The patient female/male ratio was 1.8 (18/10), mean age was 42 (range 25-75) years and mean disease duration was 9 (range 1-35) years. Mean (SD) Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Bath Ankylosing Spondylitis Functional Index (BASFI) scores were 32.4 (14.5) and 26.3 (9.2), respectively. Bilateral Achilles tendon US examinations were carried out independently by three investigators using a MyLab70 XVG (Esaote Biomedica, Genoa, Italy), equipped with a broadband 6-18 MHz linear probe. Each Achilles tendon was scanned for assessing the presence/absence of US findings indicative of enthesopathy according to the Outcome Measures in Rheumatoid Arthritis Clinical Trials (OMERACT) preliminary definition. The same findings were also scored on a 3-grade semiquantitative scoring system on which investigators reached a consensus prior to the study. Total additive scores per Achilles tendon were calculated. Results: Moderate to excellent interobserver and intraobserver agreements were found for most of the US findings indicative of enthesopathy. Similar results were obtained using semiquantitative assessments, with weighted kappa values estimating the interobserver and intraobserver agreements for soft tissue inflammation of 0.696 and 0.816, respectively and for tissue damage 0.711 and 0.901, respectively. Conclusion: US assessment of Achilles tendon enthesopathy in patients with SpA, using the OMERACT preliminary definition, was found to be reliable. Bone irregularity and entheseal hypoechogenicity were the most difficult abnormalities to reach agreement on.
dc.identifier.doi10.1136/ard.2008.096511
dc.identifier.issn0003-4967
dc.identifier.pubmed19357114
dc.identifier.urihttps://hdl.handle.net/11424/229586
dc.identifier.wosWOS:000271730700010
dc.language.isoeng
dc.publisherB M J PUBLISHING GROUP
dc.relation.ispartofANNALS OF THE RHEUMATIC DISEASES
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectPOWER DOPPLER US
dc.subjectMUSCULOSKELETAL ULTRASOUND
dc.subjectANKYLOSING-SPONDYLITIS
dc.subjectINTEROBSERVER RELIABILITY
dc.subjectPERIPHERAL ENTHESITIS
dc.subjectLOWER-LIMB
dc.subjectRHEUMATOLOGY
dc.subjectCLASSIFICATION
dc.subjectSYNOVITIS
dc.subjectAGREEMENT
dc.titleReliability of high-resolution ultrasonography in the assessment of Achilles tendon enthesopathy in seronegative spondyloarthropathies
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage1855
oaire.citation.issue12
oaire.citation.startPage1850
oaire.citation.titleANNALS OF THE RHEUMATIC DISEASES
oaire.citation.volume68

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