Objective
To determine the incidence of permanent visual loss from giant cell arteritis (GCA).
Design
Retrospective, population-based cohort
Participants
All residents of Olmsted Country, Minnesota, USA, diagnosed with GCA between January 1, 1950 and December 31, 2009
Methods
All cases of GCA were identified using the Rochester Epidemiology Project, which is a record-linkage system of medical records for all patient-physician encounters among Olmsted County, Minnesota residents. The medical records were reviewed to identify and determine the cause of permanent vision loss among patients with GCA. Systemic symptoms of GCA and visual outcomes were also determined.
Main Outcome Measures
Incidence and outcomes of permanent vision loss from GCA.
Results
Among the 245 new cases of GCA over the 60-year period, 20 (8.2%) patients suffered permanent vision loss due to GCA. The frequency of arteritic ischemic optic neuropathy (A ION) was 6.9% (95%CI: 4.0%–11.1%) accounting for 85% of cases of permanent vision loss. The frequency of central retinal artery occlusion (CRAO) was 1.6% (95%CI: 0.4%–4.2%) and cilioretinal artery occlusion was 0.4% (95%CI: 0.01%–2.3%). The population-based age- and sex-adjusted annual incidence of A-ION from GCA among persons age ≥ 50 years was 1.3 (95%CI: 0.7–2.0) per 100,000 population. 20% of patients with permanent vision loss from GCA had vision loss without constitutional symptoms of GCA. Overall, there was no significant difference between presenting and final visual acuities.
Conclusion
This population-based data provides the most accurate incidence of permanent vision loss from GCA. This study confirms that visual outcomes from GCA-related vision loss are poor and that 20% of patients with permanent visual loss from GCA can present without systemic symptoms of GCA.