Georgios Filippou1, Antonella Adinolfi2, Marco A Cimmino3, Carlo A Scirè4, Serafino Carta5, Sauro Lorenzini2, Pierpaolo Santoro2, Luca M Sconfienza6, Ilaria Bertoldi2, Valentina Picerno2, Valentina Di Sabatino2, Paolo Ferrata5, Mauro Galeazzi2, Bruno Frediani2. 1. Department of Medicine, Surgery and Neurosciences, Rheumatology Section, University of Siena, Italy. gf.filippou@gmail.com. 2. Department of Medicine, Surgery and Neurosciences, Rheumatology Section, University of Siena, Italy. 3. Academic Unit of Clinical Rheumatology and Research Laboratory, Dipartimento di Medicina Interna, University of Genova, Italy. 4. Epidemiology Unit, Italian Society for Rheumatology, Milano, Italy. 5. Department of Medicine, Surgery and Neurosciences, Orthopaedics Section, University of Siena, Italy. 6. Servizio di Radiologia, IRCCS Policlinico San Donato, San Donato Milanese; and Dipartimento di Scienze Biomediche per la Salute, Università degli Studi di Milano, Italy.
Abstract
OBJECTIVES: To assess the diagnostic performance of ultrasound (US), x-rays, and microscopic analysis of synovial fluid (SF) for calcium pyrophosphate dihydrate crystal deposition disease (CPPD) using histology as a reference standard. METHODS: We enrolled consecutive patients with osteoarthritis waiting to undergo knee replacement surgery. Each patient underwent US of the knee, focusing on menisci and the hyaline cartilage, the day before surgery. During surgery, SF, menisci and condyles were retrieved and examined microscopically. For the meniscus and cartilage microscopic analysis, 8 samples were collected from each specimen and knee radiographs, performed up to 3 months before surgery, were also assessed. A dichotomous score was given for the presence/absence of CPP for each method. Microscopic findings of the specimens were considered the reference standard. All the procedures followed were in accordance with the ethical standards of the local responsible committee. RESULTS: 42 patients (14 males) were enrolled. All patients underwent US, 34 had eligible radiographs and 32 had SF analysis. 25 patients (59.5%) were positive for CPP at US, 15 (44.1%) at X-ray and 14 (43.7%) at SF. Sensitivity and specificity values were 96% and 87% for US, 75% and 93% for radiography and 77% and 100% for SF respectively. There were no statistically significant differences between the diagnostic performance across single tests. CONCLUSIONS: US proved to be at least as accurate as SF analysis for the diagnosis of CPPD. US, which is feasible and harmless, could be considered the first exam of choice for CPPD diagnosis.
OBJECTIVES: To assess the diagnostic performance of ultrasound (US), x-rays, and microscopic analysis of synovial fluid (SF) for calcium pyrophosphate dihydratecrystal deposition disease (CPPD) using histology as a reference standard. METHODS: We enrolled consecutive patients with osteoarthritis waiting to undergo knee replacement surgery. Each patient underwent US of the knee, focusing on menisci and the hyaline cartilage, the day before surgery. During surgery, SF, menisci and condyles were retrieved and examined microscopically. For the meniscus and cartilage microscopic analysis, 8 samples were collected from each specimen and knee radiographs, performed up to 3 months before surgery, were also assessed. A dichotomous score was given for the presence/absence of CPP for each method. Microscopic findings of the specimens were considered the reference standard. All the procedures followed were in accordance with the ethical standards of the local responsible committee. RESULTS: 42 patients (14 males) were enrolled. All patients underwent US, 34 had eligible radiographs and 32 had SF analysis. 25 patients (59.5%) were positive for CPP at US, 15 (44.1%) at X-ray and 14 (43.7%) at SF. Sensitivity and specificity values were 96% and 87% for US, 75% and 93% for radiography and 77% and 100% for SF respectively. There were no statistically significant differences between the diagnostic performance across single tests. CONCLUSIONS: US proved to be at least as accurate as SF analysis for the diagnosis of CPPD. US, which is feasible and harmless, could be considered the first exam of choice for CPPD diagnosis.
Authors: Vito Chianca; Domenico Albano; Carmelo Messina; Federico Midiri; Giovanni Mauri; Alberto Aliprandi; Michele Catapano; Lorenzo Carlo Pescatori; Cristian Giuseppe Monaco; Salvatore Gitto; Anna Pisani Mainini; Angelo Corazza; Santi Rapisarda; Grazia Pozzi; Antonio Barile; Carlo Masciocchi; Luca Maria Sconfienza Journal: Acta Biomed Date: 2018-01-19
Authors: Federico Bruno; Antonio Barile; Francesco Arrigoni; Antonella Laporta; Anna Russo; Marina Carotti; Alessandra Splendiani; Ernesto Di Cesare; Carlo Masciocchi Journal: Acta Biomed Date: 2018-01-19