Literature DB >> 25058456

Patterns of Uveitis in a University-based Tertiary Referral Center in Riyadh, Saudi Arabia.

Huda Al Dhahri1, Khalid Al Rubaie1, Suhail Hemachandran1, Ahmed Mousa1, Priscilla W Gikandi1, Hani S Al-Mezaine1, Ahmed M Abu El-Asrar1.   

Abstract

PURPOSE: To investigate the referral patterns and diagnosis of uveitis in a university-based tertiary referral center in Riyadh, Saudi Arabia.
METHODS: We retrospectively reviewed the medical records of 642 patients (1220 eyes).
RESULTS: There were 295 (46%) males and 347 (54%) female patients, with a mean age of 36.4 ± 16.1 years at presentation. Panuveitis was most common (47.1%), followed by anterior uveitis (36.8%), posterior uveitis (10.7%), and intermediate uveitis (5.4%). Nongranulomatous (85.2%) and noninfectious (69.3%) were the most frequent types of uveitis. The most identifiable specific diagnoses were Vogt-Koyanagi-Harada (VKH) disease (19.6%), presumed tuberculous uveitis (PTU) (17.8%), Behçet disease (BD) (8.4%), and toxoplasmosis (6.9%). After a mean follow-up period of 31.3 ± 31.5 months, 73.5% of the eyes achieved visual acuity of 20/40 or better.
CONCLUSIONS: The most common anatomic diagnosis was panuveitis. VKH disease, PTU, BD, and toxoplasmosis are the most frequently diagnosed entities.

Entities:  

Keywords:  Behçet disease; Vogt-Koyanagi-Harada disease; epidemiology; tuberculosis; uveitis

Year:  2014        PMID: 25058456     DOI: 10.3109/09273948.2014.939197

Source DB:  PubMed          Journal:  Ocul Immunol Inflamm        ISSN: 0927-3948            Impact factor:   3.070


  9 in total

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Authors:  Daniel M Albert; Meisha L Raven
Journal:  Microbiol Spectr       Date:  2016-11

3.  The Association between QuantiFERON-TB Gold Test and Clinical Manifestations of Uveitis in the United States.

Authors:  Mehmet Yakin; Natasha Kesav; Shuk Kei Cheng; Sonny Caplash; Sapna Gangaputra; H Nida Sen
Journal:  Am J Ophthalmol       Date:  2021-05-02       Impact factor: 5.488

Review 4.  Vogt-Koyanagi-Harada syndrome - current perspectives.

Authors:  Abeir Baltmr; Sue Lightman; Oren Tomkins-Netzer
Journal:  Clin Ophthalmol       Date:  2016-11-24

5.  Soluble cytokine receptor levels in aqueous humour of patients with specific autoimmune uveitic entities: sCD30 is a biomarker of granulomatous uveitis.

Authors:  Ahmed M Abu El-Asrar; Nele Berghmans; Saleh A Al-Obeidan; Priscilla W Gikandi; Ghislain Opdenakker; Jo Van Damme; Sofie Struyf
Journal:  Eye (Lond)       Date:  2019-12-05       Impact factor: 3.775

Review 6.  Sarcoid Uveitis: An Intriguing Challenger.

Authors:  Pia Allegri; Sara Olivari; Federico Rissotto; Roberta Rissotto
Journal:  Medicina (Kaunas)       Date:  2022-07-04       Impact factor: 2.948

7.  Identification of immune hub genes participating in the pathogenesis and progression of Vogt-Koyanagi-Harada disease.

Authors:  Yiqi Wang; Yahan Ju; Jiajing Wang; Na Sun; Zhimin Tang; Huiqin Gao; Ping Gu; Jing Ji
Journal:  Front Immunol       Date:  2022-07-25       Impact factor: 8.786

8.  Patterns of Uveitis at a Tertiary Referral Center in Northeastern Iran.

Authors:  Seyedeh Maryam Hosseini; Nasser Shoeibi; Raheleh Ebrahimi; Mehdi Ghasemi
Journal:  J Ophthalmic Vis Res       Date:  2018 Apr-Jun

9.  PRKCQ rs4750316 is associated with Vogt-Koyanagi-Harada syndrome in a Han Chinese population.

Authors:  Lei Xu; Tingting Zhao; Gangxiang Yuan; Shengping Hou; Wenxin Zeng; Feilan Chen
Journal:  Mol Vis       Date:  2019-12-02       Impact factor: 2.367

  9 in total

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