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Published on: February 8, 2019
Poor prognosis of visual outcome after visual loss from giant cell arteritis
Helen Danesh-Meyer1, Peter J Savino, Greg G Gamble
1Department of Ophthalmology, University of Auckland, Auckland, New Zealand.
Insights
Visual recovery is rare for patients experiencing vision loss from giant cell arteritis (GCA), even with high-dose corticosteroids. Vision deterioration can occur early, with little improvement in visual fields or color vision.
Area of Science:
- Ophthalmology
- Rheumatology
- Neuro-ophthalmology
Background:
- Giant cell arteritis (GCA) is a systemic vasculitis that can lead to irreversible vision loss.
- Early diagnosis and treatment are crucial to prevent severe complications, including blindness.
Purpose of the Study:
- To determine the incidence and extent of visual recovery in patients with GCA who experienced vision loss.
- To assess the impact of high-dose systemic corticosteroid treatment on visual outcomes in GCA patients.
Main Methods:
- A multicenter prospective case series involving 34 patients with biopsy-proven GCA and visual loss.
- Comprehensive neuro-ophthalmic evaluations, including visual acuity, visual fields, and color vision testing.
- Treatment with high-dose intravenous methylprednisolone followed by oral prednisone, with regular monitoring and dose adjustments.
Main Results:
- Patients presented with a mean visual acuity of 20/400.
- Visual deterioration occurred in 27% of affected eyes within the first week, despite high-dose IV corticosteroids.
- Only 15% of eyes showed improved visual acuity within the first month, with a mere 5% demonstrating concurrent visual field improvement.
Conclusions:
- Visual recovery is uncommon in GCA patients with established vision loss.
- Improvements in visual acuity do not consistently correlate with improvements in visual field or color vision.
- A significant risk of visual deterioration exists within the first week of treatment, even with aggressive corticosteroid therapy.
Objective:
To evaluate the incidence and extent of visual recovery in patients with giant cell arteritis (GCA) treated with high doses of systemic corticosteroids.
Design:
Multicenter prospective case series.
Participants:
Thirty-four consecutive patients with biopsy-proven GCA and visual loss seen at either Wills Eye Hospital in Philadelphia or Auckland Hospital in New Zealand from 2001 to 2004 were evaluated prospectively.
Methods:
All patients underwent a complete neuro-ophthalmic evaluation that included Snellen visual acuity, pseudoisochromatic Ishihara color plates, visual fields, intraocular pressure, slit-lamp examination, and binocular ophthalmoscopy. Formal visual field testing was performed on all patients who were capable of completing the test. All patients were treated with a standard protocol of 1 g of IV methylprednisolone daily for 3 days followed by oral prednisone 60 or 80 mg (depending on patient weight). Patients were evaluated initially at 2-week intervals (14-19 days) and then monthly (4-5 weeks), with subsequent dosages of prednisone modified based on erythrocyte sedimentation rate, C-reactive protein, and patient symptoms. At each visit, patients underwent a repeat complete neuro-ophthalmic evaluation.
Main Outcome Measures:
Alterations in visual acuity, visual field, and color vision.
Results:
Patients with visual loss from GCA had a mean visual acuity of 20/400. Visual deterioration occurred in 27% of eyes within the first week despite high-dose IV corticosteroids. Fifteen percent of eyes showed an improvement of visual acuity within the first month, but only 5% have corresponding improvement in visual field.
Conclusions:
Visual recovery is uncommon in patients who lose vision from GCA. Recovery in visual acuity is not associated with visual field or color vision improvement in this series. Visual deterioration occurs in approximately 27% of eyes despite high-dose IV methylprednisolone. The greatest risk of visual deterioration is in the first 6 days.
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