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OP0200 (2014)
THROMBOEMBOLISM IN RHEUMATOLOGY: INVESTIGATION OF THE RISKS OF DEEP VEIN THROMBOSIS AND PULMONARY EMBOLISM IN INFLAMMATORY ARTHRITIS, CONNECTIVE TISSUE DISEASES, VASCULITIS AND MYOSITIS
J.J. Lee, J.E. Pope
Rheumatology, University of Western Ontario, London, Canada

Background: We performed a meta-analysis investigating the risk of developing deep vein thrombosis (DVT) and/or pulmonary embolisms (PE) in patients with inflammatory arthritis, vasculitis, and connective tissue diseases (CTD) [SLE, Sjogren's syndrome, inflammatory myositis and systemic sclerosis].

Objectives: The objectives were to determine the rate and relative increase in venous thromboembolic events in various inflammatory rheumatologic conditions compared to age and sex matched controls.

Methods: PubMed, Embase, Cochrane Databases, and Medline were searched to identify full text English publications in adults related to rheumatologic inflammatory diseases and VTE. Data regarding rates of DVTs and PEs were extracted. Using random effects models, pooled estimates for VTE in individual and pooled diseases compared with age, sex and co-morbidity matched populations where possible. Studies were excluded if VTEs were in the setting of pregnancy, post-operative outcomes or antiphospholipid antibody syndrome solely but entire SLE cohorts were included.

Results: Most of the 3,929 studies were excluded due to lack of rate or incidence of VTE. Twenty studies remained for analysis. Eight studies of RA identified 5,273,942 patients and 891,530,181 controls with a cumulative incidence of 2% (95% CI:2–3%) and OR 2.23 (95% CI:2.02–2.47) compared to age, sex, and comorbidity matched population. Six studies included 36,582 SLE patients with a cumulative incidence of 9% (95% CI:6–11%). Three Sjogren's syndrome studies with 16,180 subjects demonstrated a VTE cumulative incidence of 3% (95% CI:2–3%). Four studies of inflammatory myositis (N=8,245) yielded a VTE cumulative incidence of 4% (95% CI:2-6%). There were more VTE in SSc (3 studies), ANCA vasculitis (3), PAN (2) and AS (2). Table shows characteristics of some studies included with descriptive statistics on rates of VTEs.

First AuthorYearLocation of StudyCountryTotal DiseaseDisease with VTETotal ControlsControls with DVT
SLE
 Sarabi ZS2005TorontoCanada54430(N/A)(N/A)
 Kaiser R2009UCSFUSA1,930426(N/A)(N/A)
 Chang ER2006McGillCanada42640(N/A)(N/A)
 Calvo-Alen J2005LUMINAUSA57051(N/A)(N/A)
 Romero-Diaz J2009Instituto NacionalMexico24125(N/A)(N/A)
 Gladman DD1980TorontoCanada18017(N/A)(N/A)
 Zoller B2012MigMed2Sweden9,147276(N/A)(N/A)
 Ramagopalan S2011OxfordUK23,544636(N/A)(N/A)
 Avina-Zubieta J2012UBCCanada5,03126550,310533
Sjogren's
 Haga HJ2008HaukelandDenmark904(N/A)(N/A)
 Zoller B2012MigMed2Sweden3,410100(N/A)(N/A)
 Ramagopalan S2011OxfordUK12,680305(N/A)(N/A)
Myositis
 Romero-Diaz J2009Instituto NacionalMexico242(N/A)(N/A)
 Selva-O'Callaghan2011Vall HospitalSpain979(N/A)(N/A)
 Zoller B2012MigMed2Sweden2,12292(N/A)(N/A)
 Ramagopalan S2011OxfordUK6,002167(N/A)(N/A)

Conclusions: Overall, these inflammatory rheumatologic diseases studied were associated with high rates of VTEs, but not all diseases were represented

Disclosure of Interest: None declared

DOI: 10.1136/annrheumdis-2014-eular.2537


Citation: Annals of the Rheumatic Diseases, volume 73, supplement 2, year 2014, page 138
Session: Abstract session: Epidemiology, outcomes and health services research (Oral Presentations )