Diagnosis and management of giant cell arteritis and polymyalgia rheumatica: challenges, controversies and practical tips

被引:6
|
作者
Mackie, Sarah Louise [1 ]
Pease, Colin Thomas [2 ]
机构
[1] Univ Leeds, Chapel Allerton Hosp, NIHR Leeds Musculoskeletal Res Unit, Div Rheumat & Musculoskeletal Dis, Leeds LS7 4SA, W Yorkshire, England
[2] Leeds Teaching Hosp NHS Trust, Dept Rheumatol, Leeds, W Yorkshire, England
基金
美国国家卫生研究院;
关键词
ERYTHROCYTE SEDIMENTATION-RATE; CRANIAL ISCHEMIC COMPLICATIONS; LARGE-VESSEL VASCULITIS; C-REACTIVE PROTEIN; TERM-FOLLOW-UP; TEMPORAL ARTERITIS; RISK-FACTORS; DOUBLE-BLIND; CLASSIFICATION CRITERIA; VISUAL-LOSS;
D O I
10.1136/postgradmedj-2012-131400
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Giant cell arteritis (GCA) and polymyalgia rheumatica (PMR) are inflammatory rheumatic diseases that may present to a variety of disciplines and specialities. The mainstay of treatment is glucocorticoids (steroids); together PMR and GCA now represent one of the most common reasons for medium-to-high dose, long-term glucocorticoid treatment in primary care. However, adverse effects of glucocorticoids are common in these patients. Management of both diseases involves balancing the symptoms and risks of the disease against the adverse effects and risks of glucocorticoids. The crucial first step in management is to make a firm, well-documented diagnosis, since once glucocorticoids are started they can mask the symptoms of a number of other diseases. Diagnosis however can be challenging and there are still substantial gaps in the evidence for treatment.
引用
收藏
页码:284 / 292
页数:9
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