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Volume 12, Number 51
Monday, December 17, 2012
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In this issue: (click heading to view article)
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######### Progression Rates of the Superior, Inferior and Both Hemifield Defects in NTG Patients

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######### Retinal Surface En Face OCT in ERM Surgery
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######### Choroidal Thickness After Extrafoveal PDT with Verteporfin in CSC
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######### Prevalence and Predictors of Sjögren's Syndrome in Patients with Aqueous-Deficient Dry Eye
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Progression Rates of the Superior, Inferior and Both Hemifield Defects in NTG Patients

The authors of the following Korean retrospective, observational cohort study investigated the progression rates of superior and inferior hemifield defects and each hemifield in bihemifield defects in normal-tension glaucoma (NTG) patients and compared the progression rates of each hemifield between groups in eyes with similar baseline hemifield defects.

They analyzed the medical records of 142 NTG patients who performed more than five reliable standard visual field tests with superior (group 2; n=51), inferior (group 1; n=44) or both hemifield (group 3; n=47) defects. They also inspected the changes in the mean thresholds of the 10 zones of the glaucoma hemifield test and the entire hemifield. Additionally, they used a linear mixed-effect model with age, gender, initial IOP, mean deviation and pattern standard deviation controlled.

The authors reported that there were no significant differences in age and systemic and ocular factors between groups except for female gender, which showed a significant difference among the three groups (p=.032). They also noted that the progression rate in group 2 was significantly faster than in group 1 (–0.713 dB/year versus –0.516 dB/year; p=.019), especially in central and nasal zones or than in the superior hemifield of group 3 (–0.717 dB/year versus –0.470 dB/year; p=.001). They found no significant difference in the progression rates between group 1 and the inferior hemifield in group 3 (–0.508 dB/year versus –0.441 dB/year; p=.312) or between the superior and inferior hemifields in group 3 (–0.468 dB/year versus –0.442 dB/year; p=.662).

To conclude, more careful examination and caution is required in the treatment of NTG patients with superior hemifield defect.

SOURCE: Cho HK, Kee C. Comparison of the progression rates of the superior, inferior, and both hemifield defects in normal-tension glaucoma patients. Am J Ophthalmol. 2012;154(6):958–968.




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Retinal Surface En Face OCT in ERM Surgery

Researchers sought to describe the clinical effectiveness of a new imaging approach: en face spectral domain optical coherence tomography (SD-OCT) of the retinal surface before and after epiretinal membrane (ERM) and internal limiting membrane (ILM) peeling.

They performed a retrospective analysis of preoperative and postoperative en face SD-OCT images of the inner face of the macula obtained from 20 eyes of 20 patients undergoing vitrectomy with ILM peeling for ERM.

According to the researchers, preoperatively, en face SD-OCT imaging of the retinal surface clearly showed plaques surrounded by radiating folds because of ERM. It could also disclose areas possibly devoid of ILM secondary to ERM contraction. A rough retinal surface was visible to reserachers in the peeled area during the first postoperative month. At three months, they progressively observed various amounts of dimples in 13 of 15 eyes (87%). In all of these cases, they lasted or increased in size and number at the last follow-up examination. Some residual epiretinal tissue was also detected by this technique.

En face SD-OCT of the retinal surface is an interesting complement to standard retinal OCT section that provides an easy-to-understand global overview of the retinal surface. It can detect and classify tiny progressive morphologic changes in the texture of the retinal surface occurring after ILM peeling.

SOURCE: Rispoli M, Le Rouic F, Lesnoni G, et al. Retinal surface en face optical coherence tomography: a new imaging approach in epiretinal membrane surgery. Retina. 2012;32(10):2070–2076.

http://www.revophth.com/ParkCity2013







Choroidal Thickness After Extrafoveal PDT with Verteporfin in CSC

Danish investigators sought to evaluate the effect of verteporfin photodynamic treatment (PDT) on choroidal thickness in patients with central serous chorioretinopathy (CSC).

They measured choroidal thickness with enhanced depth imaging–optical coherence tomography (EDI–OCT) before and after verteporfin PDT (full-dose verteporfin, half-light dose) in 16 eyes in 16 patients with serous detachment of the fovea secondary to extrafoveal angiographic fluorescein leakage. They confined treatment to the area of leakage, and assessed choroidal thickness before and after treatment over a larger area of the fundus using OCT.

The study investigators reported complete resolution of the serous detachment in all 16 eyes within one month of extrafoveal PDT, while choroidal thickness in the area where PDT was applied decreased from 407 µm [mean; 95% confidence interval (CI95) 356–458 µm] to 349 µm (mean; CI95 300–399 µm; p<0.0001), and subfoveal choroidal thickness was reduced from 421 µm (mean; CI95 352–489 µm) to 346 pm (mean; CI95 278–414 µm; p=0.0001). Initially, subfoveal choroidal thickness was significantly increased in the treated eye compared with the healthy fellow eye (mean 324 µm; CI95 273–376 µm; p=0.0003), but after treatment, the difference was not significant.

PDT of active CSC was followed by choroidal thickness reduction, not only locally, but also at considerable distance from the treated area. Thus, the process that causes choroidal thickening in CSC appears to spread laterally within the choroid.

SOURCE: Pryds A, Larsen M. Choroidal thickness following extrafoveal photodynamic treatment with verteporfin in patients with central serous chorioretinopathy. Acta Ophthalmol. 2012;90(8):738–743.



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Prevalence and Predictors of Sjögren's Syndrome in Patients with Aqueous-Deficient Dry Eye

To assess the prevalence and determine predictors of Sjögren's syndrome (SS) in patients with clinically significant aqueous-deficient dry eye, patients enrolled in an industry-sponsored, multicenter clinical trial (NCT00784719) were evaluated prospectively for the presence of SS.

Ocular testing included Schirmer test, corneal fluorescein staining, conjunctival lissamine green staining and tear-film breakup time. Review of systems questionnaire, medical history, dry eye questionnaire and laboratory workup (Sjögren-specific antibody A (SSA), Sjögren-specific antibody B (SSB), rheumatoid factor (RF) and antinuclear antibody (ANA)) were obtained.

Of 327 patients, 38 (11.6%) had SS: 21 (6.4%) with primary SS (pSS) and 17 (5.2%) with secondary SS. Nine patients (3%) were newly diagnosed using the applied diagnostic criteria based on American–European consensus criteria. Patients with SS had significantly worse conjunctival and corneal staining, Schirmer test (with and without anaesthesia) and symptoms compared with patients without SS. Furthermore, pSS was significantly more likely to occur in patients with positive ANA (OR: 13.9) and RF (OR: 4.8).

Ophthalmologists caring for patients with clinically significant dry eye should have a high index of suspicion for underlying SS and low threshold for serological workup. RF and ANA are recommended as useful tests in SSA/SSB-negative patients for further diagnostic referral.

SOURCE: Liew M, Zhang M, Kim E, Akpek EK. Prevalence and predictors of Sjögren's syndrome in a prospective cohort of patients with aqueous-deficient dry eye. Br J Ophthalmol. 2012;96(12):1498–1503.





  • ORAYA AND OPTEGRA EYE HOSPITAL GROUP LAUNCH NEW WET AMD THERAPY. In a press release, Oraya Therapeutics Inc. announced that an agreement has been reached with UK specialist eye hospital group Optegra to establish Optegra as the world's first clinical centers to offer Oraya Therapy Stereotactic Radiotherapy for the treatment of wet age-related macular degeneration (AMD). Oraya Therapy is a noninvasive, low-energy X-ray treatment intended as a one-time procedure to reduce or eliminate the need for chronic injections while preserving or enhancing a patient's vision outcomes. It is delivered by the IRay Radiotherapy System in a simple outpatient procedure lasting approximately 20 minutes, with no limitations on patient activities following treatment. The IRay is a CE-marked medical device. In the United States, it is an investigational device and is not available for sale. The new therapy will initially be offered at Optegra Surrey Eye Hospital in Guildford.
  • FDA APPROVES AN SNDA FOR RESCULA. Sucampo Pharmaceuticals Inc. has received approval of an sNDA for RESCULA (unoprostone isopropyl ophthalmic solution) 0.15% for the lowering of IOP in patients with open-angle glaucoma or ocular hypertension from the FDA. The company intends to commercialize RESCULA in the first quarter of 2013. Read more here.
  • PHASE 1B CLINICAL STUDY OF NOVEL IL-1 INHIBITOR PROTEIN FOR THE TREATMENT OF DRY EYE DISEASE INITIATED. Eleven Biotherapeutics has initiated a Phase Ib clinical trial to evaluate EBI-005, its lead ophthalmic protein, in patients with dry eye disease. The company is rapidly advancing EBI-005, a rationally designed topical protein that inhibits the Interleukin-1 (IL-1) receptor to treat ocular surface inflammatory disorders. According to Eleven Biotherapeutics, the Phase Ib clinical trial has a robust study design as a double-blind, multicenter, randomized, placebo-controlled study to evaluate two doses of EBI-005 over a six-week period in subjects with dry eye disease. The trial is expected to enroll up to 80 subjects and will be conducted in about nine centers throughout the United States. The primary objective of the study is to determine the safety of EBI-005. Additionally, an assessment of biological activity of EBI-005 will be measured by the Ocular Surface Disease Index and corneal fluorescein staining. Eleven Biotherapeutics expects the clinical study to be completed in the first half of 2013. Additional information is available at www.elevenbio.com.
  • LPATH TO OFFER AND SELL SHARES OF COMMON STOCK. Lpath Inc. recently announced that intends to offer and sell shares of its common stock in an underwritten public offering subject to market conditions. According to the company, there can be no assurance as to whether or when the offering may be complete, or as to the actual size or terms of the offering. Copies of the preliminary prospectus supplement and the accompanying prospectus relating to this offering may be obtained from Summer Street Research Partners, Attention: Prospectus Department, 101 Arch Street, Boston, MA 02110, or by telephone at (617) 532-6433. Check with the company's website for updates.




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