Literature DB >> 15606476

Longterm follow-up of patients with multifocal choroiditis and panuveitis.

Raul N G Vianna1, Pinar C Ozdal, João Pessoa Souza Filho, Marcelo Palis Ventura, Vinicius S Saraiva, Jean Deschênes.   

Abstract

PURPOSE: To report the visual prognosis and longterm complications in patients with multifocal choroiditis and panuveitis (MCP).
METHODS: A retrospective study was performed with patients who met inclusion criteria for MCP at the Uveitis Clinic, Royal Victoria Hospital, McGill University, Montreal, Canada. Information collected included duration of follow-up, visual acuity (VA) measured at each clinical visit, ocular and systemic treatment and ocular complications observed during follow-up.
RESULTS: Nineteen patients (37 eyes) with MCP with a mean follow-up of 76.9 months were studied. Kaplan-Meier survival analysis showed a decrease in the proportion of patients with a final VA > or = 20/40 over time. Cystoid macular oedema was seen in 29.7% of the eyes and was the most frequent macular abnormality observed in our group. On the other hand, choroidal neovascularization was detected in only six (16.2%) of the eyes, but was related to VA < 20/200 in four of these eyes. Glaucoma was detected in 10.8% of the eyes. Cataract (posterior subcapsular and/or nuclear) was the most common longterm complication, occurring in 40% of affected eyes. Cataract surgery improved the VA in 83.3% of these eyes.
CONCLUSION: The visual acuity of patients with MCP decreases with time. Visual loss can occur from complications following the inflammation itself and/or iatrogenic induced by the chronic use of corticosteroids.

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Mesh:

Year:  2004        PMID: 15606476     DOI: 10.1111/j.1600-0420.2004.00343.x

Source DB:  PubMed          Journal:  Acta Ophthalmol Scand        ISSN: 1395-3907


  4 in total

Review 1.  [White dot syndrome].

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3.  Observation and Clinical Pattern in Patients with White Dot Syndromes: The Role of Color Photography in Monitoring Ocular Changes in Long-Term Observation.

Authors:  Joanna Brydak-Godowska; Joanna Gołębiewska; Monika Turczyńska; Joanna Moneta-Wielgoś; Agnieszka Samsel; Piotr K Borkowski; Michał Ciszek; Agnieszka Płonecka-Rodzoch; Aleksandra Kużnik-Borkowska; Joanna Ciszewska; Elżbieta Makomaska-Szaroszyk; Lidia B Brydak; Dariusz Kęcik
Journal:  Med Sci Monit       Date:  2017-03-02

Review 4.  Vogt-Koyanagi-Harada disease: review of a rare autoimmune disease targeting antigens of melanocytes.

Authors:  Marcelo Mendes Lavezzo; Viviane Mayumi Sakata; Celso Morita; Ever Ernesto Caso Rodriguez; Smairah Frutuoso Abdallah; Felipe T G da Silva; Carlos Eduardo Hirata; Joyce Hisae Yamamoto
Journal:  Orphanet J Rare Dis       Date:  2016-03-24       Impact factor: 4.123

  4 in total

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