Diagnosis, Treatment, and Follow-Up of Giant-Cell Arteritis: A Retrospective Multicenter Study
Mi-Kyoung Kang1, Yooha Hong1, Yoo Hwan Kim2
1Department of Neurology, Dongtan Sacred Heart Hospital, Hallym University College of Medicine, Hwaseong, Korea.
Insights
Giant-cell arteritis (GCA) management in Korean patients shows high dropout rates and frequent prednisolone side effects. Optimizing treatment requires regular monitoring and extended follow-up for better outcomes.
Area of Science:
- Rheumatology
- Internal Medicine
- Ophthalmology
Background:
- Giant-cell arteritis (GCA) is a prevalent vasculitis in the elderly.
- GCA poses significant risks for visual loss and disease recurrence.
- Management strategies in Asian populations, particularly Koreans, are less understood due to rarity.
Purpose of the Study:
- To characterize the current management status of GCA patients in Korea.
- To analyze treatment patterns, follow-up durations, and outcomes in Korean GCA patients.
- To evaluate the impact of arteritic anterior ischemic optic neuropathy (AAION) on GCA management.
Main Methods:
- Retrospective analysis of medical records from six Korean university hospitals (Feb 2009–Nov 2022).
- Inclusion based on 2022 ACR/EULAR criteria, with original diagnosis by 1990 ACR criteria.
- Evaluation of treatments, follow-up periods, relapse, remission, and adverse drug reactions.
Main Results:
- 18 GCA patients analyzed (median age 75.5 years, 66.7% female).
- Seven patients (38.8%) had AAION; all received initial prednisolone.
- High dropout rate (72.3%), common adverse events (22.2%), and relapses (11.1%) observed during short follow-ups.
Conclusions:
- Korean GCA patients exhibit high dropout rates and short follow-up periods.
- Prednisolone-related adverse effects are common, and relapses occur in approximately 10% of patients.
- Optimizing GCA treatment necessitates consistent monitoring and long-term patient follow-up.
Background And Purpose:
Giant-cell arteritis (GCA) is the most common type of vasculitis in the elderly and is associated with high risks of visual loss and recurrence. Owing to its rarity in Asian populations, the current clinical interventions for these patients are not well known. Here we aimed to characterize the current management status of patients with GCA using Korean multicenter data.
Methods:
This retrospective study analyzed medical records of patients with GCA at six Korean university hospitals from February 2009 to November 2022. GCA had originally been diagnosed based on the 1990 American College of Rheumatology (ACR) criteria, and cases were selected for inclusion in this study based on the 2022 ACR/European Alliance of Associations for Rheumatology criteria. We evaluated treatments, follow-up periods, and outcomes (relapse, remission, and adverse drug reactions) in patients with GCA with or without arteritic anterior ischemic optic neuropathy (AAION).
Results:
This study analyzed 18 patients with a median age of 75.5 years that included 12 females (66.7%). Seven patients (38.8%) had AAION. All patients initially received prednisolone treatment, while four (22.2%) underwent adjuvant treatment with methotrexate and azathioprine during prednisolone tapering. During the median follow-up of 3.5 months (interquartile range: 2.0-23.2 months), 4 patients (22.2%) had prednisolone-related adverse reactions, 2 (11.1%) relapsed, and 13 (72.3%) dropped out. Nine patients (50.0%) experienced remission, with this being sustained in four (36.4%).
Conclusions:
This study observed high dropout rates and short follow-ups. Adverse effects of prednisolone were common, and relapses occurred in approximately one-tenth of Korean patients with GCA. Thus, optimizing GCA treatment necessitates regular monitoring and long-term follow-up.
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