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Half of Takayasu's Arteritis Relapse

A French retrospective study of 318 Takayasu's arteritis (TA) patients shows that 50% of patients will relapse and experience a vascular complication ≤10 years from diagnosis. 

A multicenter study examined 318 TA patients meeting both ACR and and Ishikawa criteria to assess event-free survival, relapse-free survival, vascular complications and risk factors for vascular complications.  At diagnosis, TA primarily affects younger (mean age 36 [25–47] years) women (86.8%).

With 6.1 years of follow-up, relapses were observed in 43%, vascular complications in 38%, and death in 5%.

Progressive disease course (P=0.018) and carotidynia (P=0.036) were independently associated with event-free survival.

Outomes observed:

 5 Year10 YearAssociations
Event-Free Survival48.2%36.4%Progressive disease course (P=0.018) and carotidynia (P=0.036)
Relapse-Free Survival58.6%47.7%Male sex (P=0.048), elevated C-reactive protein (P=0.013), and carotidynia (P=0.003)
Complication-Free Survival69.9%53.7%Progressive disease course (P=0.017), thoracic aorta involvement (P=0.009), and retinopathy (P=0.002)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Conclusions: This nationwide study shows that 50% of patients with TA will relapse and experience a vascular complication ≤10 years from diagnosis. 

Disclosures: 
The author has no conflicts of interest to disclose related to this subject

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