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An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
The treatment of giant cell arteritis
J Alexander Fraser1, Cornelia M Weyand, Nancy J Newman
1Department of Clinical Neurological Sciences, University of Western Ontario School of Medicine, London, Ontario, Canada.
Insights
Giant cell arteritis (GCA) treatment requires individualized care, especially for neuro-ophthalmic and neurological complications. High-dose steroids and close monitoring are recommended for acute cases, while long-term steroid-sparing options need further study.
Area of Science:
- Rheumatology
- Neurology
- Ophthalmology
Background:
- Giant cell arteritis (GCA) is a vasculitis responsive to corticosteroids, but long-term management challenges persist.
- GCA presents diverse clinical subtypes, necessitating tailored treatment strategies.
- Existing literature shows varied recommendations for GCA management.
Purpose of the Study:
- To systematically review treatment options for neuro-ophthalmic and neurological complications of GCA.
- To evaluate evidence for adjuvant therapies in GCA management.
- To provide recommendations for managing acute GCA complications.
Main Methods:
- Systematic literature review of treatment options for GCA with ocular and neurological involvement.
- Analysis of evidence for adjuvant therapies.
- Formulation of clinical recommendations based on available data.
Main Results:
- No randomized controlled trials specifically address GCA with ocular/neurological complications.
- Hospital admission for high-dose intravenous methylprednisolone is recommended for acute visual loss or brain ischemia.
- Aspirin may offer benefits; evidence for steroid-sparing agents like methotrexate is debated.
Conclusions:
- Individualized treatment is crucial for GCA, particularly for severe complications.
- Prompt, high-dose corticosteroid therapy and monitoring are vital for acute neuro-ophthalmic/neurological GCA.
- Further research is needed to clarify the role of steroid-sparing agents in long-term GCA management.
Abstract:
Although giant cell arteritis (GCA) is a well-known vasculitis sensitive to corticosteroid-mediated immunosuppression, numerous issues of long-term therapeutic management remain unresolved. Because GCA encompasses a broad spectrum of clinical subtypes, ranging from devastating visual loss and neurological deficits to isolated systemic symptoms, the treatment of GCA must be adjusted to each case, and recommendations vary widely in the literature. This article systematically reviews the treatment options for patients with neuro-ophthalmic and neurological complications of GCA, as well as the evidence for possible adjuvant therapies for patients with GCA. Although there is no randomized controlled clinical trial specifically evaluating GCA patients with ocular and neurological complications, we recommend that GCA patients with acute visual loss or brain ischemia be admitted to the hospital for high-dose intravenous methyl-prednisolone, close monitoring, and prevention of steroid-induced complications. Aspirin may also be helpful in these cases. The evidence supporting the use of steroid-sparing immunomodulatory agents such as methotrexate for long-term management remains debated.
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