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        <title>Editor's picks</title>
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        <description>The editor's pick of recent articles published by BMC Ophthalmology</description>
        <dc:date>2013-04-24T00:00:00Z</dc:date>
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                                <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2415/13/18" />
                                <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2415/13/6" />
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        <title>Systemic therapies for inflammatory eye disease: Past, Present and Future</title>
        <description>In this review we consider the current evidence base for treatments in inflammatory eye disease, and in particular uveitis, from a historical perspective. We consider the challenges that have traditionally hindered progress in inflammatory eye disease including small target populations, heterogeneous disease groups, poorly defined phenotypes, diagnostic inconsistency, subjective outcome measures, specific issues around visual acuity as an outcome measure and low commercial interest. Strategies to address these issues are considered de novo and with reference to recent advances outside of ophthalmology and highlight the promise for ocular inflammation. Progress in these specialties has included the development of thriving clinical-trial cultures, public-private partnerships, pathogenetic- and structure-led drug design, efficient drug development pipelines, and biomarker-defined treatment protocols enabling personalization of medicine. Although there are challenges, these are exciting opportunities as we seek to develop safe and effective treatments for patients with inflammatory eye disease.</description>
        <link>http://www.biomedcentral.com/1471-2415/13/18</link>
                <dc:creator>Alastair K Denniston</dc:creator>
                <dc:creator>Andrew D Dick</dc:creator>
                <dc:source>BMC Ophthalmology 2013, 13:18</dc:source>
        <dc:date>2013-04-24T00:00:00Z</dc:date>
        <dc:identifier>10.1186/1471-2415-13-18</dc:identifier>
                            <dc:title>Inflamatory eye disease in translation</dc:title>
                            <dc:description>&lt;p&gt;Associate Editor Alastair Denniston and Section Editor Andrew Dick review past remedies, current treatments what the future might hold for inflammatory eye disease research in translation.&lt;/p&gt;</dc:description>
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                <prism:publicationName>BMC Ophthalmology</prism:publicationName>
        <prism:issn>1471-2415</prism:issn>
        <prism:volume>13</prism:volume>
        <prism:startingPage>18</prism:startingPage>
        <prism:publicationDate>2013-04-24T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.biomedcentral.com/1471-2415/13/6">
        <title>Over-expression of human cystatin C in pterygium &lt;it&gt;versus&lt;/it&gt; healthy conjunctiva</title>
        <description>Background:
A prospective, non-randomised, transversal and comparative study, carried out in INOVA Vision Institute and Autonomous University of Aguascalientes. Pterygium is an important illness that affects 22% people from tropic and equatorial zones. Is an inflammatory process caused by UV rays, and it has a behavior similar to a neoplasm. For this study was taken into consideration 191 samples from the INOVA Vision Institute, Aguascalientes, Mexico. Include 73 pterygia samples, which were obtained during resection under sterile conditions. 44 normal conjunctiva samples were obtained from the same patients when harvesting the conjunctival autograft, or from other patients undergoing extracapsular cataract extraction from the superior bulbar region. Tears from patients with pterygium (n&#8201;=&#8201;50) and normal volunteers (n&#8201;=&#8201;24) were obtained using a calibrated glass micro capillary tube. The surgical conjunctiva and pterygia samples were subjected to reverse-transcription polymerase chain reaction (RT-PCR), western blot, and immunohistochemistry. Tears were analyzed by enzyme-linked immunosorbent assays.
Methods:
This was a prospective, non-randomised study involving 191 biological samples taken from patients with pterygium and normal volunteers, whom were operated under local anaesthesia by either complete resection of the lesion with primary closure, or resection with conjunctival autograft. Tissue samples were fixed in 10% formaldehyde. Sections were routinely stained with hematoxylin and eosin. HCC expression was evaluated by reverse-transcription polymerase chain reaction (RT-PCR), immunohistochemistry, and by western blotting. All tears samples were analyzed by enzyme-linked immunosorbent assays (ELISA).
Results:
Expression levels and distribution patterns of HCC in normal conjunctiva and pterygium. Higher levels of HCC mRNAs and proteins were detected in pterygium compared with a normal conjunctiva. Immunohistochemistry revealed that HCC was localized in the apical cells of the epithelium in the normal conjunctiva. In contrast, HCC was detected in all extension of epithelial tissue, from apical to basal cells in pterygia. The concentration of HCC protein in tears was higher in patients with pterygium versus controls.
Conclusion:
HCC may play an important role in protecting normal conjunctiva, and regulating inflammatory conditions of the anterior ocular surface.</description>
        <link>http://www.biomedcentral.com/1471-2415/13/6</link>
                <dc:creator>Luis Fernando Barba-Gallardo</dc:creator>
                <dc:creator>Javier Ventura-Juárez</dc:creator>
                <dc:creator>David Kershenobich Stalnikowitz</dc:creator>
                <dc:creator>Rafael Gutiérrez-Campos</dc:creator>
                <dc:creator>Eugenia Torres-Bernal</dc:creator>
                <dc:creator>Luis Fernando Torres-Bernal</dc:creator>
                <dc:source>BMC Ophthalmology 2013, 13:6</dc:source>
        <dc:date>2013-02-27T00:00:00Z</dc:date>
        <dc:identifier>10.1186/1471-2415-13-6</dc:identifier>
                            <dc:title>Cystatin role in ocular inflammation?</dc:title>
                            <dc:description>&lt;p&gt;Human cystatin C is more highly expressed and in a wider range of cells in the conjunctiva of people with pterygium (a fibrovascular lesion of the ocular surface), suggesting it may have a role in inflammatory ocular conditions.&lt;/p&gt;</dc:description>
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        <prism:issn>1471-2415</prism:issn>
        <prism:volume>13</prism:volume>
        <prism:startingPage>6</prism:startingPage>
        <prism:publicationDate>2013-02-27T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.biomedcentral.com/1471-2415/13/5">
        <title>Prognostic factors for corneal graft recovery after severe corneal graft rejection following penetrating keratoplasty</title>
        <description>Background:
To investigate the outcome and prognostic factors for corneal graft recovery after severe corneal graft rejection following penetrating keratoplasty (PKP) treated with topical and systemic steroids.
Methods:
Fifty-eight eyes in 58 patients with severe corneal graft rejection following PKP were treated with topical and systemic steroids. Factors affecting the reversibility and maintenance of graft transparency were analyzed.
Results:
Graft transparency was restored in 37 of 58 eyes (63.8%). Clarity of the graft was maintained in 25 of 37 eyes after transparency was restored, while corneal decompensation developed at a mean of 6.0&#8201;&#177;&#8201;4.3 months in the remainder. The interval between rejection and treatment with systemic steroids was shorter in cases that recovered graft transparency (OR, 0.88, 95% CI. 0.80&#8211;0.97, P&#8201;=&#8201;0.0093). Corneal decompensation after the recovery of corneal transparency tend to occur in cases of regraft (OR, 0.09, 95% CI. 0.01&#8211;0.54, P&#8201;=&#8201;0.0091).
Conclusions:
Severe corneal graft rejection after PKP was reversible in approximately two-thirds of the cases, with graft transparency being maintained in two-thirds of them when treated with both topical and systemic steroids. Early treatment confers a benefit in terms of the recovery of graft transparency.</description>
        <link>http://www.biomedcentral.com/1471-2415/13/5</link>
                <dc:creator>Katsuya Yamazoe</dc:creator>
                <dc:creator>Kyoko Yamazoe</dc:creator>
                <dc:creator>Seika Shimazaki-Den</dc:creator>
                <dc:creator>Jun Shimazaki</dc:creator>
                <dc:source>BMC Ophthalmology 2013, 13:5</dc:source>
        <dc:date>2013-02-25T00:00:00Z</dc:date>
        <dc:identifier>10.1186/1471-2415-13-5</dc:identifier>
                            <dc:title>Steroids may save rejected corneal grafts</dc:title>
                            <dc:description>&lt;p&gt;Corneal grafts which are severely rejected following penetrating keratoplasty can have their transparency saved in approximately two thirds of cases by the use of topical and systemic steroids, with earlier treatment being beneficial.&lt;/p&gt;</dc:description>
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                <prism:publicationName>BMC Ophthalmology</prism:publicationName>
        <prism:issn>1471-2415</prism:issn>
        <prism:volume>13</prism:volume>
        <prism:startingPage>5</prism:startingPage>
        <prism:publicationDate>2013-02-25T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.biomedcentral.com/1471-2415/13/4">
        <title>Driving patterns in older adults with glaucoma</title>
        <description>Background:
The ability to drive is important for ensuring quality of life for many older adults. Glaucoma is prevalent in this age group and may affect driving. The purpose of this study is to determine if glaucoma and glaucomatous visual field (VF) loss are associated with driving cessation, limitations, and deference to another driver in older adults.
Methods:
Cross-sectional study. Eighty-one glaucoma subjects and 58 glaucoma suspect controls between age 60 and 80 reported if they had ceased driving, limited their driving in various ways, or preferred another to drive.
Results:
Twenty-three percent of glaucoma subjects and 6.9% of suspects had ceased driving (p&#8201;=&#8201;0.01). Glaucoma subjects also had more driving limitations than suspects (2.0 vs. 1.1, p&#8201;=&#8201;0.007). In multivariable models, driving cessation was more likely for glaucoma subjects as compared to suspects (OR&#8201;=&#8201;4.0; 95% CI&#8201;=&#8201;1.1-14.7; p&#8201;=&#8201;0.03). The odds of driving cessation doubled with each 5 decibel (dB) decrement in the better-eye VF mean deviation (MD) (OR&#8201;=&#8201;2.0; 95% CI&#8201;=&#8201;1.4-2.9; p&#8201;&lt;&#8201;0.001). Glaucoma subjects were also more likely than suspects to report a greater number of driving limitations (OR&#8201;=&#8201;4.7; 95% CI&#8201;=&#8201;1.3-16.8; p&#8201;=&#8201;0.02). The likelihood of reporting more limitations increased with the VF loss severity (OR&#8201;=&#8201;1.6 per 5 dB decrement in the better-eye VF MD; 95% CI&#8201;=&#8201;1.1-2.4; p&#8201;=&#8201;0.02). Neither glaucoma nor VF MD was associated with other driver preference (p&#8201;&gt;&#8201;0.1 for both).
Conclusions:
Glaucoma and glaucomatous VF loss are associated with greater likelihood of driving cessation and greater limitation of driving in the elderly. Further prospective study is merited to assess when and why people with glaucoma change their driving habits, and to determine if their observed self-regulation of driving is adequate to ensure safety.</description>
        <link>http://www.biomedcentral.com/1471-2415/13/4</link>
                <dc:creator>Suzanne W van Landingham</dc:creator>
                <dc:creator>Chad Hochberg</dc:creator>
                <dc:creator>Robert W Massof</dc:creator>
                <dc:creator>Emilie Chan</dc:creator>
                <dc:creator>David S Friedman</dc:creator>
                <dc:creator>Pradeep Y Ramulu</dc:creator>
                <dc:source>BMC Ophthalmology 2013, 13:4</dc:source>
        <dc:date>2013-02-21T00:00:00Z</dc:date>
        <dc:identifier>10.1186/1471-2415-13-4</dc:identifier>
                            <dc:title>Glaucoma impacts driving habits</dc:title>
                            <dc:description>&lt;p&gt;Older people with glaucoma and visual field loss associated with glaucoma are more likely to stop or limit their driving, although whether this is sufficient to ensure safety without impacting quality of life remains to be established.&lt;/p&gt;</dc:description>
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                <prism:publicationName>BMC Ophthalmology</prism:publicationName>
        <prism:issn>1471-2415</prism:issn>
        <prism:volume>13</prism:volume>
        <prism:startingPage>4</prism:startingPage>
        <prism:publicationDate>2013-02-21T00:00:00Z</prism:publicationDate>
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