Rw. Read et al., Revised diagnostic criteria for Vogt-Koyanagi-Harada disease: Report of aninternational committee on nomenclature, AM J OPHTH, 131(5), 2001, pp. 647-652
PURPOSE: To present revised criteria for the diagnosis of Vogt-Koyanagi-Har
ada disease, a chronic, bilateral, granulomatous ocular and multisystem inf
lammatory condition of unknown cause,
METHODS: Diagnostic criteria and nomenclature were subjects of discussion a
t the First International Workshop on Vogt-Koyanagi-Harada Disease on Octob
er 19-21, 1999, at the University of California, Los Angeles, Conference Ce
nter, Lake Arrowhead, California. A committee appointed by the workshop par
ticipants was charged with drafting revised criteria for Vogt-Koyanagi-Hara
da disease, based on discussions held during the conference. This article i
s the consensus committee report.
RESULTS: New criteria, taking into account the multisystem nature of Vogt-K
oyanagi-Harada disease, with allowance for the different ocular findings pr
esent in the early and late stages of the disease, were formulated and agre
ed upon by the committee. These criteria are based on additional knowledge
and experience of experts in the field and are believed to reflect disease
features more fully than previously published criteria,
CONCLUSIONS: The revised definition of Vogt-Koyanagi-Harada disease, with e
xpanded diagnostic criteria, will facilitate performance of studies involvi
ng homogeneous populations of patients, at various stages of disease, that
address unanswered questions regarding treatment and disease mechanisms, (C
) 2001 by Elsevier Science Inc. All rights reserved.