Giant cell arteritis
Permanent, severe loss of vision is a feared complication; however, it is not the sole possible devastating outcome of giant cell arteritis. Myocardial infarction, ischemic stroke and limb gangrene may also occur. Thor - acic aortic aneurysms are seen over 17 times more often in patients with giant...
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Published in: | Canadian Medical Association journal (CMAJ) Vol. 183; no. 5; p. 581 |
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Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
Canada
CMA Joule Inc
22-03-2011
CMA Impact, Inc Canadian Medical Association |
Subjects: | |
Online Access: | Get full text |
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Summary: | Permanent, severe loss of vision is a feared complication; however, it is not the sole possible devastating outcome of giant cell arteritis. Myocardial infarction, ischemic stroke and limb gangrene may also occur. Thor - acic aortic aneurysms are seen over 17 times more often in patients with giant cell arteritis than in age-matched controls.1 A thorough history is the most important component of diagnosis. High clinical suspicion can trump a negative biopsy. Neck pain and claudication of the jaw are most suggestive of giant cell arteritis.2 Headache and myalgia are common symptoms but are less helpful in establishing a diagnosis. (Appendix 1, available at www.cmaj .ca /cgi /content /full /cmaj .100920/DC1, highlights the likelihood of diagnosing giant cell arteritis based on several key features.) Progressive loss of vision may occur despite immediate initiation of high doses of oral prednisone (60-100 mg or about 1 mg/kg).5 In these instances, switching to intravenous corticosteroid treatment (e.g., 250 mg of methylprednisolone four times daily) for three days is a common practice. Retrospective studies suggest that adding acetylsalicylic acid may reduce the ischemic complications of giant cell arteritis.6 |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 See related practice article by Zwicker and colleagues, available at www.cmaj.ca |
ISSN: | 0820-3946 1488-2329 |
DOI: | 10.1503/cmaj.100920 |