European League Against Rheumatism recommendations for calcium pyrophosphate deposition. Part I: terminology and diagnosis
Adult
Male
Delphi Technique
Evidence-Based Medicine/methods
Chondrocalcinosis
Comorbidity
Chondrocalcinosis/diagnosis/epidemiology/etiology
03 medical and health sciences
Age Distribution
0302 clinical medicine
Risk Factors
info:eu-repo/classification/ddc/616
Terminology as Topic
Prevalence
Humans
Sex Distribution
Aged
ddc:616
Aged, 80 and over
Evidence-Based Medicine
Middle Aged
NCEBP 2: Evaluation of complex medical interventions N4i 4: Auto-immunity, transplantation and immunotherapy
3. Good health
Female
DOI:
10.1136/ard.2010.139105
Publication Date:
2011-01-08T02:00:02Z
AUTHORS (15)
ABSTRACT
To agree terminology and to develop recommendations for the diagnosis of calcium pyrophosphate deposition (CPPD).The European League Against Rheumatism (EULAR) CPPD Task Force, comprising 15 experts from 10 countries, agreed the terms and recommendations for diagnosis of CPPD using a Delphi consensus approach. Evidence was systematically reviewed and presented in terms of sensitivity, specificity and positive likelihood ratio (LR) to support diagnosis; ORs were used for association. Strength of recommendation (SOR) was assessed by the EULAR visual analogue scale.It was agreed that 'CPPD' should be the umbrella term that includes acute calcium pyrophosphate (CPP) crystal arthritis, osteoarthritis (OA) with CPPD and chronic CPP crystal inflammatory arthritis. Chondrocalcinosis (CC) defines cartilage calcification, most commonly due to CPPD and detected by imaging or histological examination. A total of 11 key recommendations were generated on the topics of clinical features, synovial fluid (SF) examination, imaging, comorbidities and risk factors. Definitive diagnosis of CPPD relies on identification of SF CPP crystals. Rapid onset inflammatory symptoms and signs are suggestive but not definitive for acute CPP crystal arthritis. Radiographic CC is not highly sensitive or specific, whereas ultrasonography appears more useful (LR=24.2, 95% CI 3.51 to 168.01) for peripheral joints. Recognised risk factors for CPPD include ageing, OA and metabolic conditions such as primary hyperparathyroidism, haemochromatosis and hypomagnesaemia; familial forms are rare. SORs varied from 53 to 99 (maximum 100).New terms for CPPD were agreed and 11 key recommendations for diagnosis of CPPD were developed using research evidence and expert consensus.
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