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Intermediate uveitis: pattern of etiology, complications, treatment and outcome in a tertiary academic center

Overview of attention for article published in Orphanet Journal of Rare Diseases, April 2017
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Title
Intermediate uveitis: pattern of etiology, complications, treatment and outcome in a tertiary academic center
Published in
Orphanet Journal of Rare Diseases, April 2017
DOI 10.1186/s13023-017-0638-9
Pubmed ID
Authors

Thomas Ness, Daniel Boehringer, Sonja Heinzelmann

Abstract

Patients with intermediate uveitis (IU) represent a heterogenous group characterized by a wide spectrum of etiologies and regional differences. Aim of the study was to analyze the characteristics of patients with IU examined in an academic center in Germany. We conducted a retrospective analysis of the clinical records of all patients with intermediate uveitis referred to the Eye Center, University of Freiburg from 2007 to 2014. Diagnosis followed the Standardization in Uveitis Nomenclature (SUN) criteria. Data analysis included: etiology of IU, demographics, complications, treatment and visual acuity. We identified 159 patients with intermediate uveitis during that period. Mean age at diagnosis was 35 years. Most are female (64%), and the mean duration of IU was 6.1 years (range 1 month - 35 years). Etiology of IU was idiopathic in 59%. Multiple sclerosis (MS) (20%) and sarcoidosis (10%) were frequent systemic causes of IU. Other etiologies including infectious diseases (tuberculosis, borreliosis) or immune-mediated conditions (eg, after vaccination) were present in 11%. The pattern of complications included macular edema (CME) (36%), cataract (24%), secondary glaucoma (7%), and epiretinal membrane formation (19%). Periphlebitis and optic neuritis were more frequent in conjunction with MS. Treatment comprised local and systemic steroids, immunosuppressive agents, biologics, and surgery. Best corrected visual acuity was better than 20/25 in 60% of the eyes after more than 10 years of follow-up. In our German academic center, most IU cases were idiopathic or associated with MS or sarcoidosis. In contrast to other countries, infectious cases were rare. Patients' overall visual prognosis is favorable even when the duration of IU has been long and and despite numerous complications.

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Geographical breakdown

Country Count As %
Unknown 75 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 10 13%
Student > Bachelor 9 12%
Other 7 9%
Researcher 7 9%
Student > Ph. D. Student 6 8%
Other 11 15%
Unknown 25 33%
Readers by discipline Count As %
Medicine and Dentistry 30 40%
Nursing and Health Professions 7 9%
Immunology and Microbiology 2 3%
Agricultural and Biological Sciences 1 1%
Computer Science 1 1%
Other 5 7%
Unknown 29 39%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 30 April 2017.
All research outputs
#20,418,183
of 22,968,808 outputs
Outputs from Orphanet Journal of Rare Diseases
#2,480
of 2,636 outputs
Outputs of similar age
#269,443
of 309,813 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#50
of 53 outputs
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