Clinical features, imaging use, and management in giant cell arteritis: a retrospective single-center study.

IF 2.9 3区 医学 Q2 RHEUMATOLOGY
Clinical Rheumatology Pub Date : 2024-11-01 Epub Date: 2024-09-05 DOI:10.1007/s10067-024-07078-0
Aradhna Agarwal, Reid Weisberg, Jiby Mathew, Andreas Reimold, Kyawt Shwin
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引用次数: 0

Abstract

This study examines the characteristics of patients with giant cell arteritis (GCA), the utilization of imaging in GCA diagnosis, and variations in GCA management among specialties. Subjects were identified from the Dallas VAMC database spanning 2010 to 2021 using ICD-9/10 codes for GCA and polymyalgia rheumatica, and a list of temporal artery biopsies (TAB). Patients lacking sufficient data to meet the ACR 1990 classification criteria for GCA were excluded. Categorical variables were compared using Fisher's exact test. Continuous variables were analyzed with the Kruskal-Wallis test. Among 209 identified patients, 41 were excluded due to insufficient data for ACR classification. The cohort comprised 91.9% males with a median age of 69. Of the remaining 168 patients, 42 received a final diagnosis of GCA, and 15 of these were confirmed with a positive TAB. The most reported initial symptoms were visual disturbances (75.5%) and headaches (67.7%). Ophthalmology was the initial physician for 46% of patients. GCA correlated with co-existing autoimmune diseases, glucocorticoid-sparing treatments, and consultation with a rheumatologist (p < 0.05). There were no significant differences in clinical features or management of the positive and negative TAB GCA groups. GCA presents with heterogeneous symptoms making diagnosis challenging. Scalp tenderness and headaches were significantly higher in GCA patients, but sub-group analysis revealed no significant differences among GCA patients. Vascular assessments and adjunct imaging modalities are underutilized. The establishment of multidisciplinary or fast-track clinics may enhance the optimization of GCA management. Key Points • The most common presenting symptoms were blurry vision/visual loss (75.5%), headache (67.7%), and scalp tenderness (35.9%) in descending order. • In sub-group analysis, no significant differences were found between GCA sub-groups, but when compared to the non-GCA group, were found to have significantly higher rates of headache and scalp tenderness. • Compared to other specialties, rheumatologists were more likely to use advanced imaging, and to prescribe glucocorticoid-sparing treatments. • Systematic and comprehensive assessment and multidisciplinary approach could improve diagnosis and management.

巨细胞动脉炎的临床特征、影像学应用和治疗:一项回顾性单中心研究。
本研究探讨了巨细胞动脉炎(GCA)患者的特征、影像学在 GCA 诊断中的应用以及各专科在 GCA 管理方面的差异。研究人员使用 GCA 和多发性风湿痛的 ICD-9/10 编码以及颞动脉活检 (TAB) 列表,从达拉斯 VAMC 数据库中确定了 2010 年至 2021 年的研究对象。缺乏足够数据以满足 ACR 1990 年 GCA 分类标准的患者被排除在外。分类变量的比较采用费雪精确检验。连续变量采用 Kruskal-Wallis 检验进行分析。在已确认的 209 名患者中,有 41 人因 ACR 分类数据不足而被排除。患者中 91.9% 为男性,中位年龄为 69 岁。在剩余的 168 名患者中,42 人最终确诊为 GCA,其中 15 人经 TAB 阳性确诊。报告最多的最初症状是视力障碍(75.5%)和头痛(67.7%)。46%的患者最初的就诊医生是眼科医生。GCA 与并存的自身免疫性疾病、糖皮质激素保留治疗以及风湿免疫科医生的会诊相关(P<0.05)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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