Diagnosis of calcium pyrophosphate crystal deposition disease by ultrasonography: how many and which sites should be scanned?

Author:

Cipolletta Edoardo12ORCID,Moscioni Erica1,Sirotti Silvia3ORCID,Di Battista Jacopo1,Abhishek Abhishek2ORCID,Rozza Davide4ORCID,Zanetti Anna4ORCID,Carrara Greta4ORCID,Scirè Carlo Alberto4ORCID,Grassi Walter1,Filippou Georgios3ORCID,Filippucci Emilio1ORCID

Affiliation:

1. Rheumatology Unit, Department of Clinical and Molecular Sciences, Polytechnic University of Marche , Ancona, Italy

2. Academic Rheumatology, Injury, Recovery and Inflammation Sciences Department, School of Medicine, University of Nottingham , Nottingham, UK

3. Department of Rheumatology, IRCCS Galeazzi—Sant’Ambrogio Hospital , Milan, Italy

4. Epidemiology Unit, Italian Society of Rheumatology , Milan, Italy

Abstract

Abstract Objective To develop the optimal US scanning protocol for the diagnosis of calcium pyrophosphate crystal deposition (CPPD) disease. Methods In this cross-sectional study, consecutive patients with a crystal-proven diagnosis of CPPD disease, and age-, sex-matched disease controls with a negative synovial fluid analysis were prospectively enrolled in two Italian Institutions. Four rheumatologists, blinded to patients’ clinical details, performed US examinations using a standardized scanning protocol including 20 joints (shoulders, elbows, wrists, metacarpophalangeal joints from second to fifth fingers, hips, knees, ankles). CPPD was identified as presence/absence, according to the OMERACT definitions. Reduced US scanning protocols were developed by selecting the most informative joints to be imaged by US using the LASSO technique. Patients were randomly divided into training and validation sets. Their diagnostic accuracy was tested comparing the area under the receiver operating characteristic curves. Results The number of participants enrolled was 204: 102 with CPPD disease and 102 disease controls [age, mean (s.d.): 71.3 (12.0) vs 71.1 (13.5) years; female: 62.8% vs 57.8%]. The median number of joints with US evidence of CPPD was 5 [interquartile range (IQR): 4–7] and 0 (IQR: 0–1) in patients with CPPD disease and controls, respectively (P < 0.01). The detection of CPPD in ≥2 joints using a reduced scanning protocol (bilateral assessment of knees, wrists and hips) showed a sensitivity of 96.7% (95% CI: 82.8, 99.9) and a specificity of 100 (95% CI: 88.8, 100.0) for the diagnosis of CPPD disease and had good feasibility [mean (s.d.): 12.5 (5.3) min]. Conclusion Bilateral US assessment of knees, wrists and hips had excellent accuracy and good feasibility for the diagnosis of CPPD disease.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

Reference30 articles.

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4. Hospital burden of gout, pseudogout and other crystal arthropathies in France;Maravic;Joint Bone Spine,2015

5. Acute calcium pyrophosphate crystal arthritis flare rate and risk factors for recurrence;Yates;J Rheumatol,2020

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