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Published on: February 8, 2019
Fast-Track Clinics and Visual Outcomes in Giant Cell Arteritis: A Systematic Review and Meta-Analysis
Tiago M B D M Beirão1, Catarina Rua1, Catarina Silva1
1Rheumatology Department, Unidade Local de Saúde Gaia e Espinho, Porto, Portugal.
Insights
Fast-track clinics (FTC) significantly reduce permanent sight loss and visual disturbances in giant cell arteritis (GCA) patients compared to conventional practice. This approach shows promise for improving GCA patient outcomes.
Area of Science:
- Rheumatology
- Ophthalmology
- Clinical Medicine
Background:
- Giant cell arteritis (GCA) is a serious inflammatory condition affecting large arteries, primarily in individuals over 50.
- Delayed diagnosis of GCA can lead to severe complications, including irreversible vision loss.
- Conventional diagnostic methods may cause significant delays, impacting patient outcomes.
Purpose of the Study:
- To compare the effectiveness of fast-track clinics (FTC) versus conventional practice (CP) in managing GCA.
- To evaluate the impact of FTC on visual outcomes and diagnostic timelines in GCA patients.
Main Methods:
- A systematic review and meta-analysis adhering to PRISMA guidelines.
- Included studies compared FTC and CP for GCA, reporting outcomes like visual disturbances, sight loss, biopsy rates, and time to diagnosis.
- Statistical analysis involved pooled odds ratios (OR) with 95% confidence intervals (CI) and random-effects modeling.
Main Results:
- FTC was associated with significantly decreased permanent sight loss (OR: 0.31; p<0.001) and visual disturbances (OR: 0.58; p=0.04).
- Temporal artery biopsy rates were lower in the FTC group (OR: 0.19; p=0.49).
- The median time to diagnosis was marginally reduced with FTC but not statistically significant (OR: 0.96; p=0.83).
Conclusions:
- Fast-track clinics show potential for improving visual outcomes in GCA patients.
- FTC represents a promising strategy for GCA management that requires further prospective validation.
Introduction:
Giant cell arteritis (GCA) is a chronic inflammatory disease that primarily affects medium and large arteries, predominantly in individuals over 50 years of age. Delayed diagnosis and treatment can result in severe complications, including irreversible vision loss. Conventional diagnostic pathways, often involving temporal artery biopsy, can lead to significant delays. Fast-track clinics (FTC) have been developed to expedite diagnosis and treatment, potentially improving patient outcomes. This meta-analysis aimed to compare the effectiveness of FTC and conventional practice (CP) in managing GCA.
Materials And Methods:
A systematic review and meta-analysis were conducted following the Preferred Reporting Items for Systematic Reviews and Meta-analysis (PRISMA) guidelines. Relevant studies that compared FTC and CP in GCA management were retrieved from the MEDLINE, Cochrane, and Embase databases. Inclusion criteria required studies to report at least one of the following outcomes: visual disturbances, permanent sight loss, biopsy rates, or median days to diagnosis. The QUADAS-2 tool was used to assess the study quality and bias risk. Statistical analyses included pooled odds ratios (OR) with 95% confidence intervals (CI), heterogeneity assessment using the I2 statistic, and a random-effects model to account for study variability. Funnel plots were used to assess the publication bias.
Results:
Three studies included 348 patients (173 in the FTC group and 175 in the CP group). FTC implementation was linked to decreased permanent sight loss (8.09% vs. 24.57%, OR: 0.31; p <0.001) and visual disturbances (20.23% vs. 32.57%, OR: 0.58; p =0.04), and use of temporal artery biopsy was lower in the FTC group (47.40% vs. 65.14%, OR: 0.19; p =0.49). The median number of days to diagnosis was slightly lower in the FTC group (57.6 vs. 58.3 d), although the difference was not statistically significant (OR: 0.96; p =0.83).
Conclusion:
Fast-track clinics may improve visual outcomes in patients with GCA and represent a promising approach that warrants further validation in prospective studies.
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