eMedicine Specialties > Ophthalmology > Unclassified Disorders
Vogt-Koyanagi-Harada Disease: Follow-up
Updated: Jan 5, 2008
Follow-up
Further Outpatient Care
- This chronic disorder requires monitoring for many years.
Complications
- Cataract
- Glaucoma
- Closed-angle glaucoma - Pupillary block, forward rotation of the ciliary body
- Open-angle glaucoma
- Subretinal fibrosis
- Choroidal neovascularization
- Neovascularization of the disc
- Pigmentary changes of the fundus
- Optic atrophy
Prognosis
- Visual loss in patients with VKH disease often is due to cataracts, glaucoma, and choroidal neovascularization. However, choroidal neovascularization is a major cause of late visual loss.
- The prognosis may be improved by the use of early high-dose corticosteroids during the acute phase of the disease and afterward a slow tapering reduction in dosage until therapy is discontinued. In most cases, therapy should not be discontinued during the 3 months after onset of the disease because of the high rate of recurrence during this period. Many patients require at least a 3- to 6-month tapering period (or longer) before the corticosteroids can be discontinued.
Patient Education
- Patients need to be educated so that they will have proper monitoring and care.
Miscellaneous
Medicolegal Pitfalls
- Misdiagnosis of infectious uveitis can lead to inappropriate treatment and potential toxicity, while losing valuable ground without the needed steroid therapy. On the other hand, infectious uveitis misdiagnosed as VKH disease and treated with systemic immunosuppression can lead to disastrous results. In particular, syphilis and tuberculosis may demonstrate significant deterioration when treated with steroids alone prior to aggressive appropriate antibiotic therapy.
More on Vogt-Koyanagi-Harada Disease |
| Overview: Vogt-Koyanagi-Harada Disease |
| Differential Diagnoses & Workup: Vogt-Koyanagi-Harada Disease |
| Treatment & Medication: Vogt-Koyanagi-Harada Disease |
Follow-up: Vogt-Koyanagi-Harada Disease |
| Multimedia: Vogt-Koyanagi-Harada Disease |
| References |
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References
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Further Reading
Keywords
Vogt-Koyanagi-Harada syndrome, VKH syndrome, VKH disease, Harada disease, Vogt-Koyanagi syndrome, uveoencephalitis, uveomeningitis, granulomatous panuveitis
Follow-up: Vogt-Koyanagi-Harada Disease