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Abstract Number: 809

Risk Factors for Severe Ischemic Complications in Takayasu Arteritis: A French Multicenter Retrospective Cohort of 182 Patients

Cloé Comarmond1, Tristan Mirault2, Jean-Emmanuel Kahn3, Philippe Cluzel4, Fabien Koskas5, Laurent Chiche6, Julien Gaudric7, Emmanuel Messas8, Patrice Cacoub9 and David Saadoun10, 1Internal Medicine and Clinical Imunology, Referal Center for Autoimmune diseases, Internal Medicine and Clinical Imunology, Hôpital Pitié Salpétrière, Paris, France, 2HEGP vascular department, paris, France, 3Internal Medicine, Foch Hospital, Suresnes, France, 4Vascular and Interventional Imaging Department, Paris, France, 5Vascular Surgery, Assistance Publique-Hôpitaux de Paris, Hopital Pitié-Salpétrière, Paris, France, 6Vascular Surgery, Paris, France, 7Department of Vascular surgery GHPS, Paris, France, 8Vascular Department, Paris, France, 9Groupe Hospitalier Pitié Salpétrière, Service de Médecine Interne, DHU i2B, Paris, France, 10DHU 2iB Internal Medicine Referal Center for Autoimmune diseases Pitie Hospital, Paris, France

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: Complications and takayasu arteritis

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Session Information

Title: Vasculitis

Session Type: Abstract Submissions (ACR)

Background/Purpose .Takayasu arteritis (TA) is a chronic inflammatory disease that primarily affects large vessels, such as the aorta and its main branches. To report clinical features, morphologic findings, treatment and long-term outcome of a large cohort of patients with TA, and to determine risk factors for the occurrence of severe ischemic complications (SIC) during follow-up.

Methods .We performed a retrospective multicenter study of characteristics and outcomes of 182 patients with TA fulfilling the American College of Rheumatology criteria. Characteristics at presentation, SIC, relapses and deaths were recorded.

Results . The median age [interquartile range] at onset of symptoms was 31 [24 ; 45] years and with a predominance of females (85%). The median delay of diagnosis was 10 [0 ; 47] months. The most common clinical findings were vascular bruits (52%), unequal or absent pulses (47%), and upper extremity blood pressure discrepancy >10 mm Hg (44%). Major complications at diagnosis were hypertension (36%), aneuvrysm (24%), and aortic regurgitation (18%). Forty six percent of patients had extensive disease at diagnosis according to Numano type V. Twenty percent of patients had another inflammatory or auto-immune disease associated to TA, mostly ankylosing spondylitis, crohn disease and sarcoidosis. Stenotic lesions were 3.1-fold more common than were aneuvrysms (78% versus 25%, respectively). Revascularization procedure was required for 49% of patients. The median delay between diagnosis and first surgery or endovascular intervention was 5 [0 ; 17.5] months. Glucocorticoids were prescribed in 151 (83%) patients. The median delay in initiation of corticosteroids was 1 [0 ; 5] months. Fifty eight percent of patients required additional immunosuppressive agent. The median delay in initiation of the first immunosuppressor was 11 [2 ; 29.5] months. Twenty six percent of patients required three or more antihypertensive drugs. SIC occurred in 38 (21%) patients after TA diagnosis. SIC-free survival at 10 years was 82% in patients without refractory hypertension versus 34% in patients with refractory hypertension (i.e. requiring ≥ 3 antihypertensive drugs) (P = 0.003). SIC-free survival at 5 years was 89% in patients with immunosuppressive agent versus 78% without immunosuppressive agent (P = 0.175). In multivariable analysis, predictive variables for the occurrence of SIC after TA diagnosis were refractory hypertension (OR 12.03 [95%CI 2.78-52.07], P = 0.001), relapse (OR 7.11 [95%CI 1.82-27.78], P = 0.005) and SIC at time of TA diagnosis (OR 4.65 [95%CI 1.10-19.67], P = 0.036). Forty four percent relapsed after a median follow-up of 69 [31 ; 145] months. The median relapse-free survival was 16 [7 ; 62] months. The mortality rate was 12%. Five of 7 (71%) deaths were related to cardiovascular complication.

Conclusion . In this cohort of TA patients, risk factors for late-developing SIC were refractory hypertension, relapse and SIC at time of TA diagnosis. Immunosuppressive agents may reduce late-developing SIC. Despite prolonged and intensive therapy, TA remains a major cause of cardiovascular morbi-mortality.


Disclosure:

C. Comarmond,
None;

T. Mirault,
None;

J. E. Kahn,
None;

P. Cluzel,
None;

F. Koskas,
None;

L. Chiche,
None;

J. Gaudric,
None;

E. Messas,
None;

P. Cacoub,

Astra Zeneca, Bayer, Boehringer Ingelheim, Gilead, Glaxo Smith Kline, Janssen, Merck Sharp Dohme, Roche, Servier, Vifor.,

5;

D. Saadoun,
None.

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