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Updates in the diagnosis and management of Takayasu's arteritis.
Somashekar A, Leung YT. Somashekar A, et al. Postgrad Med. 2023 Jan;135(sup1):14-21. doi: 10.1080/00325481.2022.2159723. Epub 2023 Jan 2. Postgrad Med. 2023. PMID: 36588528 Review.
Takayasu's arteritis is a rare, chronic, large vessel vasculitis which affects the aorta and its large branches. ...We also review the 2021 ACR guidelines for Takayasu's arteritis and correlate them to the updated evidence discussed throughout t …
Takayasu's arteritis is a rare, chronic, large vessel vasculitis which affects the aorta and its large branches. ...We …
2022 American College of Rheumatology/EULAR classification criteria for Takayasu arteritis.
Grayson PC, Ponte C, Suppiah R, Robson JC, Gribbons KB, Judge A, Craven A, Khalid S, Hutchings A, Danda D, Luqmani RA, Watts RA, Merkel PA; DCVAS Study Group. Grayson PC, et al. Ann Rheum Dis. 2022 Dec;81(12):1654-1660. doi: 10.1136/ard-2022-223482. Epub 2022 Nov 9. Ann Rheum Dis. 2022. PMID: 36351705
OBJECTIVE: To develop and validate new classification criteria for Takayasu arteritis (TAK). METHODS: Patients with vasculitis or comparator diseases were recruited into an international cohort. ...The final criteria items and weights were as follows: female sex (+1 …
OBJECTIVE: To develop and validate new classification criteria for Takayasu arteritis (TAK). METHODS: Patients with vasculitis …
EULAR/PRINTO/PRES criteria for Henoch-Schonlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final classification criteria.
Ozen S, Pistorio A, Iusan SM, Bakkaloglu A, Herlin T, Brik R, Buoncompagni A, Lazar C, Bilge I, Uziel Y, Rigante D, Cantarini L, Hilario MO, Silva CA, Alegria M, Norambuena X, Belot A, Berkun Y, Estrella AI, Olivieri AN, Alpigiani MG, Rumba I, Sztajnbok F, Tambic-Bukovac L, Breda L, Al-Mayouf S, Mihaylova D, Chasnyk V, Sengler C, Klein-Gitelman M, Djeddi D, Nuno L, Pruunsild C, Brunner J, Kondi A, Pagava K, Pederzoli S, Martini A, Ruperto N; Paediatric Rheumatology International Trials Organisation (PRINTO). Ozen S, et al. Ann Rheum Dis. 2010 May;69(5):798-806. doi: 10.1136/ard.2009.116657. Ann Rheum Dis. 2010. PMID: 20413568
OBJECTIVES: To validate the previously proposed classification criteria for Henoch-Schonlein purpura (HSP), childhood polyarteritis nodosa (c-PAN), c-Wegener granulomatosis (c-WG) and c-Takayasu arteritis (c-TA). METHODS: Step 1: retrospective/prospective web-data c …
OBJECTIVES: To validate the previously proposed classification criteria for Henoch-Schonlein purpura (HSP), childhood polyarteritis nodosa ( …
Etiology, Diagnosis and Management of Aortitis.
Sharma S, Pandey NN, Sinha M, Chandrashekhara SH. Sharma S, et al. Cardiovasc Intervent Radiol. 2020 Dec;43(12):1821-1836. doi: 10.1007/s00270-020-02486-6. Epub 2020 May 10. Cardiovasc Intervent Radiol. 2020. PMID: 32390100 Review.
Age at onset, geographic predilections, distribution and pattern of involvement in aorta, its branches and pulmonary arteries, and systemic associations provide a clue to etiology. ...Markers of activity include clinical, laboratory and imaging. Medical management remains …
Age at onset, geographic predilections, distribution and pattern of involvement in aorta, its branches and pulmonary arteries, and sy …
Current Diagnosis and Management of Takayasu Arteritis.
As C, Danda D. As C, et al. Int Heart J. 2023;64(4):519-534. doi: 10.1536/ihj.23-195. Int Heart J. 2023. PMID: 37518335 Free article.
Takayasu arteritis (TA or TAK) is a chronic large vessel vasculitis with predilection to affect the aorta and its branches. The new 2022 ACR/EULAR classification criteria for Takayasu arteritis incorporated imaging characteristics as an absolute …
Takayasu arteritis (TA or TAK) is a chronic large vessel vasculitis with predilection to affect the aorta and its branc …
Diagnosis and differential diagnosis of large-vessel vasculitides.
Keser G, Aksu K. Keser G, et al. Rheumatol Int. 2019 Feb;39(2):169-185. doi: 10.1007/s00296-018-4157-3. Epub 2018 Sep 17. Rheumatol Int. 2019. PMID: 30221327 Review.
There are no universally accepted diagnostic criteria for large-vessel vasculitides (LVV), including giant cell arteritis (GCA) and Takayasu arteritis (TAK). Currently, available classification criteria cannot be used for the diagnosis of GCA and TAK. ...Vari …
There are no universally accepted diagnostic criteria for large-vessel vasculitides (LVV), including giant cell arteritis (GCA) and …
Diagnosis, Management, and Outcome of Aortitis at a Single Center.
Skeik N, Ostertag-Hill CA, Garberich RF, Alden PB, Alexander JQ, Cragg AH, Manunga JM, Stephenson EJ, Titus JM, Sullivan TM. Skeik N, et al. Vasc Endovascular Surg. 2017 Oct;51(7):470-479. doi: 10.1177/1538574417704296. Epub 2017 Aug 31. Vasc Endovascular Surg. 2017. PMID: 28859604 Review.
METHODS: We retrospectively reviewed all patients' charts who were diagnosed with giant cell arteritis, Takayasu arteritis, or noninfectious aortitis presenting at a single center between January 1, 2009, and April 17, 2015. ...RESULTS: Among the included 15 …
METHODS: We retrospectively reviewed all patients' charts who were diagnosed with giant cell arteritis, Takayasu arteritis …
Updates in Pathophysiology, Diagnosis and Management of Takayasu Arteritis.
Serra R, Butrico L, Fugetto F, Chibireva MD, Malva A, De Caridi G, Massara M, Barbetta A, Cannistrà M, de Franciscis S. Serra R, et al. Ann Vasc Surg. 2016 Aug;35:210-25. doi: 10.1016/j.avsg.2016.02.011. Epub 2016 May 27. Ann Vasc Surg. 2016. PMID: 27238990 Review.
BACKGROUND: Takayasu arteritis (TA) is a rare, systemic, inflammatory vasculitis of granulomatous nature, and still of unknown etiology. ...CONCLUSIONS: This review presents the last updates in all fields of Takayasu arteritis. Still today, large areas …
BACKGROUND: Takayasu arteritis (TA) is a rare, systemic, inflammatory vasculitis of granulomatous nature, and still of unknown …
Clinical diagnosis and management of large vessel vasculitis: giant cell arteritis.
Chatterjee S, Flamm SD, Tan CD, Rodriguez ER. Chatterjee S, et al. Curr Cardiol Rep. 2014 Jul;16(7):498. doi: 10.1007/s11886-014-0498-z. Curr Cardiol Rep. 2014. PMID: 24893935 Review.
Large vessel vasculitis (LVV) covers a spectrum of primary vasculitides predominantly affecting the aorta and its major branches. The two main subtypes are giant cell arteritis (GCA) and Takayasu arteritis (TA). ...Acute phase reactants can be normal a …
Large vessel vasculitis (LVV) covers a spectrum of primary vasculitides predominantly affecting the aorta and its major branches. The …
Clinical diagnosis and management of large vessel vasculitis: Takayasu arteritis.
Chatterjee S, Flamm SD, Tan CD, Rodriguez ER. Chatterjee S, et al. Curr Cardiol Rep. 2014 Jul;16(7):499. doi: 10.1007/s11886-014-0499-y. Curr Cardiol Rep. 2014. PMID: 24893936 Review.
Takayasu arteritis (TA) is 1 of the 2 main causes of large vessel vasculitides (LVV), giant cell arteritis being the other. ...Available vascular imaging modalities may be acceptable in defining vascular anatomy, but are notoriously inaccurate in delineating …
Takayasu arteritis (TA) is 1 of the 2 main causes of large vessel vasculitides (LVV), giant cell arteritis being the ot …
50 results