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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
Illness Burden and Unmet Patient Needs in Giant Cell Arteritis: Current State and Future Prospects
Sebastian E Sattui1, Mitra Corral2, Dannielle C O'Donnell2
1Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA, USA.
Insights
Giant cell arteritis (GCA) causes significant patient burdens and healthcare costs. Early diagnosis and optimized treatment, including steroid-sparing options, are crucial for improving outcomes and reducing adverse events in this relapsing vasculitis.
Area of Science:
- Rheumatology
- Internal Medicine
- Vasculitis Research
Background:
- Giant cell arteritis (GCA) is the most prevalent primary systemic vasculitis, affecting large and medium-sized arteries.
- Diagnostic delays and unclear optimal treatment durations pose challenges in GCA management.
- Patients face substantial burdens from GCA, including vision loss and stroke risks, leading to permanent disability.
Purpose of the Study:
- To review the multifaceted burdens of Giant cell arteritis (GCA).
- To identify unmet needs in GCA diagnosis, treatment, and healthcare resource utilization.
- To highlight the impact of GCA on patients' clinical, psychosocial, and economic well-being.
Main Methods:
- This study is a narrative review.
- Literature search on clinical, psychosocial, and economic aspects of GCA.
- Analysis of current diagnostic and treatment strategies and their associated burdens.
Main Results:
- GCA presents significant clinical challenges, including vision impairment and stroke.
- Psychosocial impacts on patients are considerable, affecting quality of life.
- Economic burdens include high direct healthcare spending and resource utilization.
Conclusions:
- Optimizing diagnosis and treatment decisions is key to improving patient care in GCA.
- Reducing diagnostic delays and minimizing adverse effects of treatments like glucocorticoids are critical.
- Emerging glucocorticoid-sparing agents offer promising alternatives for managing this relapsing vasculitis.
Abstract:
Giant cell arteritis (GCA) is the most common form of primary systemic vasculitis and primarily affects large- and medium-sized vessels. Diagnostic delay can occur from underrecognition of symptoms, and optimal treatment duration remains unclear. Patients with GCA can experience significant burdens related to adverse outcomes of GCA, including risk of vision impairment/loss and stroke, which can result in permanent disability. Glucocorticoids, which remain the first line of treatment, are often associated with adverse effects, and emerging glucocorticoid-sparing agents represent an important option for the treatment of this relapsing disease. Moreover, GCA is a costly illness in terms of both direct healthcare spending and healthcare resource utilization. This narrative review summarizes the clinical, psychosocial, and economic burdens of illness as well as the unmet needs of patients with GCA in terms of diagnosis, treatment, and healthcare resource utilization and spending. Reducing delays in diagnosis and making informed treatment decisions that optimize patient response, while minimizing exposure to potential adverse events, can lead to significant improvement in patient care and outcomes.
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