The majority of patients respond rapidly to initial treatment with glucocorticoids, and vision loss in treated patients is rare. Lack of response to glucocorticoid therapy should alert the physician to question the diagnosis; however, up to 50% of adequately treated patients experience unpredictable disease relapses and recurrence of symptoms.[2]Dinkin M, Johnson E. One giant step for giant cell arteritis: updates in diagnosis and treatment. Curr Treat Options Neurol. 2021;23(2):6.
https://www.doi.org/10.1007/s11940-020-00660-2
http://www.ncbi.nlm.nih.gov/pubmed/33488050?tool=bestpractice.com
[97]Moreel L, Betrains A, Molenberghs G, et al. Epidemiology and predictors of relapse in giant cell arteritis: a systematic review and meta-analysis. Joint Bone Spine. 2023 Jan;90(1):105494.
http://www.ncbi.nlm.nih.gov/pubmed/36410684?tool=bestpractice.com
Glucocorticoid-related adverse effects are common, occurring in over 60% of patients.[21]Salvarani C, Cantini F, Boiardi L, et al. Polymyalgia rheumatica and giant-cell arteritis. N Engl J Med. 2002 Jul 25;347(4):261-71.
http://www.ncbi.nlm.nih.gov/pubmed/12140303?tool=bestpractice.com
Major consequences of glucocorticoid therapy include diabetes mellitus and osteoporotic fractures. Use of tocilizumab may allow for more accelerated glucocorticoid tapering, but the optimal duration of tocilizumab therapy remains unclear.
The overall survival for patients with GCA is similar to that of the general population;[12]Salvarani C, Crowson CS, O'Fallon WM, et al. Reappraisal of the epidemiology of giant cell arteritis in Olmsted County, Minnesota, over a fifty-year period. Arthritis Rheum. 2004 Apr 15;51(2):264-8.
http://www.ncbi.nlm.nih.gov/pubmed/15077270?tool=bestpractice.com
however, the risk of developing aortic aneurysms is markedly increased in patients with GCA. In a population-based study, GCA patients were 17 times more likely to develop thoracic aortic aneurysms and 2.4 times more likely to develop isolated abdominal aortic aneurysms, compared with people of the same age and sex.[98]Evans JM, O'Fallon WM, Hunder GG. Increased incidence of aortic aneurysm and dissection in giant cell (temporal) arteritis. A population-based study. Ann Intern Med. 1995 Apr 1;122(7):502-7.
http://www.ncbi.nlm.nih.gov/pubmed/7872584?tool=bestpractice.com
Thoracic aortic aneurysms may result in dissection and markedly increased mortality.[99]Nuenninghoff DM, Hunder GG, Christianson TJ, et al. Mortality of large-artery complication (aortic aneurysm, aortic dissection, and/or large-artery stenosis) in patients with giant cell arteritis: a population-based study over 50 years. Arthritis Rheum. 2003 Dec;48(12):3532-7.
http://www.ncbi.nlm.nih.gov/pubmed/14674005?tool=bestpractice.com
Risk factors for the development of aortic aneurysm in GCA are incompletely understood. However, the presence of aortic inflammation at baseline appears to predispose some patients to progressive aortic dilatation.[7]Bongartz T, Matteson EL. Large-vessel involvement in giant cell arteritis. Curr Opin Rheumatol. 2006 Jan;18(1):10-7.
http://www.ncbi.nlm.nih.gov/pubmed/16344614?tool=bestpractice.com
[38]Dejaco C, Ramiro S, Bond M, et al. EULAR recommendations for the use of imaging in large vessel vasculitis in clinical practice: 2023 update. Ann Rheum Dis. 2024 May 15;83(6):741-51.
https://www.doi.org/10.1136/ard-2023-224543
http://www.ncbi.nlm.nih.gov/pubmed/37550004?tool=bestpractice.com
Epidemiological evidence suggests that patients with GCA may have an increased risk of cardiovascular disease. Therefore, monitoring for, and management of, cardiovascular risk factors is particularly warranted in this patient population.[100]Tomasson G, Peloquin C, Mohammad A, et al. Risk for cardiovascular disease early and late after a diagnosis of giant-cell arteritis: a cohort study. Ann Intern Med. 2014 Jan 21;160(2):73-80.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381428
http://www.ncbi.nlm.nih.gov/pubmed/24592492?tool=bestpractice.com
[101]Amiri N, De Vera M, Choi HK, et al. Increased risk of cardiovascular disease in giant cell arteritis: a general population-based study. Rheumatology (Oxford). 2016 Jan;55(1):33-40.
http://www.ncbi.nlm.nih.gov/pubmed/26248811?tool=bestpractice.com