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    <title>AMA Publishing Group: Retinal Neovascularization Topic Collection</title>
    <link>http://pubs.jamanetwork.com/</link>
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    <language>en-us</language>
    <pubDate>Wed, 19 Dec 2012 00:00:00 GMT</pubDate>
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      <title>Optical Coherence Tomographic Imaging of Sub-Retinal Pigment Epithelium Lipid OCT Imaging of Sub-RPE Lipid </title>
      <link>http://pubs.jamanetwork.com/article.aspx?articleID=1308386</link>
      <pubDate>Sat, 01 Dec 2012 00:00:00 GMT</pubDate>
      <author>Mukkamala S, Costa RA, Fung A, et al. </author>
      <description>&lt;span class="paragraphSection"&gt;&lt;div class="boxTitle"&gt;Objective&lt;/div&gt;To describe an optical coherence tomographic finding of layered hyperreflective bands beneath the retinal pigment epithelium (RPE), the so-called onion sign believed to represent lipid within a vascularized pigment epithelial detachment.&lt;div class="boxTitle"&gt;Methods&lt;/div&gt;This retrospective observational case series involved reviewing clinical histories of patients with the onion sign. Imaging studies analyzed included spectral-domain optical coherence tomography, color and red-free photographs, near infrared reflectance, fundus autofluorescence, and blue-light fundus autofluorescence.&lt;div class="boxTitle"&gt;Results&lt;/div&gt;A total of 22 eyes of 20 patients with sub-RPE hyperreflective bands were identified. There were 15 women and 5 men with a mean patient age of 76 years (range, 60-92 years). Snellen best-corrected visual acuities ranged from 20/25 to counting fingers, with a median of 20/80. Two patients had bilateral involvement, and 3 of 17 eyes had multifocal onion signs in the same eye. All eyes had neovascular age-related macular degeneration, with type 1 (sub-RPE) neovascularization. In all patients, the onion sign correlated with areas of yellow-gray exudates seen clinically that appeared bright on red-free and near infrared reflectance imaging. No specific fundus autofluorescence or blue-light fundus autofluorescence pattern was identified.&lt;div class="boxTitle"&gt;Conclusions&lt;/div&gt;The onion sign refers to layered hyperreflective bands in the sub-RPE space usually associated with chronic exudation from type 1 neovascularization in patients with age-related macular degeneration. With an associated bright near infrared reflectance, these bands may correspond to lipid, collagen, or fibrin. Because the onion sign colocalizes to areas of exudation that are known to consist of lipoprotein, we propose that this finding may represent layers of precipitated lipid in the sub-RPE space. To our knowledge, this is the first report of lipid detected in the sub-RPE space on clinical examination.&lt;/span&gt;</description>
      <prism:volume xmlns:prism="prism">130</prism:volume>
      <prism:number xmlns:prism="prism">12</prism:number>
      <prism:startingPage xmlns:prism="prism">1547</prism:startingPage>
      <prism:endingPage xmlns:prism="prism">1553</prism:endingPage>
      <prism:doi xmlns:prism="prism">10.1001/archophthalmol.2012.2491</prism:doi>
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      <title>Long-term Use of Aspirin and Age-Related Macular Degeneration Aspirin and Age-Related Macular Degeneration </title>
      <link>http://pubs.jamanetwork.com/article.aspx?articleID=1486830</link>
      <pubDate>Wed, 19 Dec 2012 00:00:00 GMT</pubDate>
      <author>Klein BK, Howard KP, Gangnon RE, et al. </author>
      <description>&lt;span class="paragraphSection"&gt;&lt;div class="boxTitle"&gt;Context&lt;/div&gt;Aspirin is widely used for relief of pain and for cardioprotective effects. Its use is of concern to ophthalmologists when ocular surgery is being considered and also in the presence of age-related macular degeneration (AMD).&lt;div class="boxTitle"&gt;Objective&lt;/div&gt;To examine the association of regular aspirin use with incidence of AMD.&lt;div class="boxTitle"&gt;Design, Setting, and Participants&lt;/div&gt;The Beaver Dam Eye Study, a longitudinal population-based study of age-related eye diseases conducted in Wisconsin. Examinations were performed every 5 years over a 20-year period (1988-1990 through 2008-2010). Study participants (N = 4926) were aged 43 to 86 years at the baseline examination. At subsequent examinations, participants were asked if they had regularly used aspirin at least twice a week for more than 3 months.&lt;div class="boxTitle"&gt;Main Outcome Measure&lt;/div&gt;Incidence of early AMD, late AMD, and 2 subtypes of late AMD (neovascular AMD and pure geographic atrophy), assessed in retinal photographs according to the Wisconsin Age-Related Maculopathy Grading System.&lt;div class="boxTitle"&gt;Results&lt;/div&gt;The mean duration of follow-up was 14.8 years. There were 512 incident cases of early AMD (of 6243 person-visits at risk) and 117 incident cases of late AMD (of 8621 person-visits at risk) over the course of the study. Regular aspirin use 10 years prior to retinal examination was associated with late AMD (hazard ratio [HR], 1.63 [95% CI, 1.01-2.63]; P = .05), with estimated incidence of 1.76% (95% CI, 1.17%-2.64%) in regular users and 1.03% (95% CI, 0.70%-1.51%) in nonusers. For subtypes of late AMD, regular aspirin use 10 years prior to retinal examination was significantly associated with neovascular AMD (HR, 2.20 [95% CI, 1.20-4.15]; P = .01) but not pure geographic atrophy (HR, 0.66 [95% CI, 0.25-1.95]; P = .45). Aspirin use 5 years (HR, 0.86 [95% CI, 0.71-1.05]; P = .13) or 10 years (HR, 0.86 [95% CI, 0.65-1.13]; P = .28) prior to retinal examination was not associated with incident early AMD.&lt;div class="boxTitle"&gt;Conclusions&lt;/div&gt;Among an adult cohort, aspirin use 5 years prior to observed incidence was not associated with incident early or late AMD. However, regular aspirin use 10 years prior was associated with a small but statistically significant increase in the risk of incident late and neovascular AMD.&lt;/span&gt;</description>
      <prism:volume xmlns:prism="prism">308</prism:volume>
      <prism:number xmlns:prism="prism">23</prism:number>
      <prism:startingPage xmlns:prism="prism">2469</prism:startingPage>
      <prism:endingPage xmlns:prism="prism">2478</prism:endingPage>
      <prism:doi xmlns:prism="prism">10.1001/jama.2012.65406</prism:doi>
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