Takayasu's arteritis natural history, complications and prognosis: Difference between revisions
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===Prognosis=== | ===Prognosis=== | ||
* Takayasu arteritis is a chronic relapsing and remitting disorder.<ref name="pmid16195161">{{cite journal |vauthors=Park MC, Lee SW, Park YB, Chung NS, Lee SK |title=Clinical characteristics and outcomes of Takayasu's arteritis: analysis of 108 patients using standardized criteria for diagnosis, activity assessment, and angiographic classification |journal=Scand. J. Rheumatol. |volume=34 |issue=4 |pages=284–92 |date=2005 |pmid=16195161 |doi=10.1080/03009740510026526 |url=}}</ref> | * Takayasu arteritis is a chronic relapsing and remitting disorder.<ref name="pmid16195161">{{cite journal |vauthors=Park MC, Lee SW, Park YB, Chung NS, Lee SK |title=Clinical characteristics and outcomes of Takayasu's arteritis: analysis of 108 patients using standardized criteria for diagnosis, activity assessment, and angiographic classification |journal=Scand. J. Rheumatol. |volume=34 |issue=4 |pages=284–92 |date=2005 |pmid=16195161 |doi=10.1080/03009740510026526 |url=}}</ref> | ||
* Takayasu arteritis is associated with significant morbidity. | |||
* | * The five year survival rate in Takayasu arteritis is over 90%. | ||
* The 5- and 10-year survival rates are approximately 69% and 36%, respectively, in patients with 2 or more complications. | |||
* The 5- and 10-year survival rates associated with 1 or fewer complications are 100% and 96%, respectively | |||
==References== | ==References== | ||
Revision as of 14:05, 6 April 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Farnaz Khalighinejad, MD [2]
Overview
Natural History
Natural History
Complications
Common complications of Takayasu's arteritis include:[1]
- Hardening and narrowing of blood vessels
- High blood pressure
- Inflammation of the heart
- Heart failure
- Stroke
- Transient ischemic attack (TIA)
- Aneurysm in the aorta
- Heart attack
Prognosis
- Takayasu arteritis is a chronic relapsing and remitting disorder.[2]
- Takayasu arteritis is associated with significant morbidity.
- The five year survival rate in Takayasu arteritis is over 90%.
- The 5- and 10-year survival rates are approximately 69% and 36%, respectively, in patients with 2 or more complications.
- The 5- and 10-year survival rates associated with 1 or fewer complications are 100% and 96%, respectively
References
- ↑ Phillip R, Luqmani R (2008). "Mortality in systemic vasculitis: a systematic review". Clin. Exp. Rheumatol. 26 (5 Suppl 51): S94–104. PMID 19026150.
- ↑ Park MC, Lee SW, Park YB, Chung NS, Lee SK (2005). "Clinical characteristics and outcomes of Takayasu's arteritis: analysis of 108 patients using standardized criteria for diagnosis, activity assessment, and angiographic classification". Scand. J. Rheumatol. 34 (4): 284–92. doi:10.1080/03009740510026526. PMID 16195161.