Abstract
OBJECTIVE:
To describe the clinical spectrum and outcome of patients with presumed tubercular uveitis and choroidal involvement.
METHODS:
A retrospective case series nested in a cohort study was enrolled at a tertiary referral eye care center in the UK. Failure was defined as recurrence of lesion within 6 months of completion of antitubercular therapy (ATT) or corticosteroid therapy.
RESULTS:
Seventy-seven patients with presumed ocular tuberculosis and choroidal involvement were included in the study. Mean age was 45.5 ± 15.7 years, 44 (57.1%) patients were male, and 51 (66.2%) presented with bilateral disease. Choroidal granuloma was the most frequent clinical presentation (n = 27, 35.07%), followed by multifocal choroiditis (n = 24, 31.17%) and serpiginous-like choroiditis (n = 18, 23.38%). Quantiferon Gold in Tube Test (QFT) was positive in 64 (83.11%) patients. Fifty (64.94%) patients received ATT.
CONCLUSIONS:
Choroidal involvement in presumed ocular tuberculosis can present with a variable spectrum. Treatment failure rates were equivalent between ATT and non-ATT treated groups.
| Original language | English |
|---|---|
| Pages (from-to) | 97-104 |
| Journal | Ocular Immunology and Inflammation |
| Volume | 25 |
| Issue number | 1 |
| Early online date | 25 Jan 2016 |
| DOIs | |
| Publication status | Published - 31 Jan 2017 |
| Externally published | Yes |
Keywords
- Epidemiology and public health
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