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Volume 13, Number 10
Monday, March 11, 2013
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MARCH IS NATIONAL NUTRITION MONTH




In this issue: (click heading to view article)
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######### Influence of Systemic Beta-Blockers on the Need for Repeated Intravitreal Injections in Wet AMD Treated by Bevacizumab

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######### Five-year Results of PDT for PCV
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######### Use of Reduced-fluence PDT for CSC
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######### Contributing Factors for Progression of VF Loss in NTG Patients with Medical Treatment
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Influence of Systemic Beta-Blockers on the Need for Repeated Intravitreal Injections in Wet AMD Treated by Bevacizumab

To evaluate the effect of concomitant systemic therapy in patients with choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD) treated by intravitreal bevacizumab and to propose a mechanism for different interindividual response, investigators performed this retrospective, nonrandomized, single-center, consecutive interventional case series study.

They treated 46 eyes from 46 patients with CNV secondary to AMD by monthly intravitreal 1.25 mg bevacizumab injections on a pro re nata regimen. They also recorded changes in Early Treatment Diabetic Retinopathy Study best-corrected visual acuity (BCVA), central foveal thickness as determined by spectral domain optical coherence tomography, number of injections performed, occurrence of severe adverse effects and systemic concomitant medication. Additionally, they evaluated the effect of systemic medication on final BCVA, central foveal thickness and number of injections performed.

The investigators reported that the most frequent systemic medications recorded were angiotensin-converting-enzyme inhibitors in 19 patients, beta-adrenergic blocking agents (n=18), nonsteroidal anti-inflammatory drugs (n=17), diuretics (n=16), calcium channel blockers (n=14), benzodiazepines (n=11), proton-pump inhibitors (n=9) and statins (n=8). They noted that 32 patients had arterial hypertension. Average follow-up was 25.1 months (standard deviation [SD]=8.9) and average gain in BCVA was 0.9 (SD=13.6) and –2.1 letters (SD=15.9) at 12 months and 24 months, respectively. The investigators also noted that the average reduction in central foveal thickness was 111 µm (SD=54) and 105 µm (SD=71) at 12 months and 24 months, respectively. The average number of intravitreal injections required was 6.7 (SD=3.2). Furthermore, patients on treatment with systemic beta-adrenergic blocking agents required less intravitreal injections (5.2, SD=2.4 vs. 7.9, SD=3.4) and this difference was statistically significant (p=0.0068, multiple linear regression).

The study investigators concluded that concomitant systemic beta-adrenergic blocking agents treatment may reduce the need for repeated intravitreal injections of bevacizumab in patients with choroidal neovascularization associated with AMD.

SOURCE: Montero JA, Ruiz-Moreno JM, Sanchis-Merino E, Perez-Martin S. Systemic beta-blockers may reduce the need for repeated intravitreal injections in patients with wet age-related macular degeneration treated by bevacizumab. Retina. 2013;33(3):508–512.


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Five-year Results of PDT for PCV

The following retrospective Korean study evaluated the five-year efficacy of photodynamic therapy (PDT) in patients with polypoidal choroidal vasculopathy (PCV).

A total of 42 eyes of 36 patients with PCV followed up for at least 60 months after PDT were reviewed. All eyes were primarily treated with PDT. Main outcome measure was best-corrected visual acuity (BCVA; logarithm of minimal angle of resolution [logMAR]) at baseline and at each follow-up visit. The eyes were also classified into three groups: improved (improvement ≥0.3 logMAR), decreased (deterioration ≥0.3 logMAR) and stable.

It was determined that during the mean follow-up duration, 73.64 ± 13.47 months, the mean number of PDT was 2.21 ± 1.62 treatments. Recurrence was noted in 33 eyes (78.6%) during follow-up. Moreover, the mean baseline BCVA was 0.78 ± 0.48 logMAR (20/120 Snellen equivalent), and the final BCVA at 60 months was 0.67 ± 0.52 logMAR (20/93 Snellen equivalent) (p=.050, paired t test). On the final evaluation at 60 months, the mean BCVA was improved in 14 eyes (33.3%), stable in 23 eyes (54.8%) and decreased in five eyes (11.9%).

At 60 months after initial PDT, 88.1% of PCV patients showed stable or improved BCVA after PDT. Despite a high recurrence rate, PDT remained effective for five years, and represents a good therapeutic approach to PCV.

SOURCE: Kang HM, Kim YM, Koh HJ. Five-year follow-up results of photodynamic therapy for polypoidal choroidal vasculopathy. Am J Ophthalmol. 2013;155(3):438–447.

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Use of Reduced-fluence PDT for CSC

The authors of the following study sought to evaluate the efficacy of reduced-fluence photodynamic therapy (RFPDT) for central serous chorioretinopathy (CSC). They determined that RFPDT appears to be an effective treatment method for CSC and that outer nuclear layer (ONL) thickness is an important visual predictive factor of RFPDT for CSC.

This retrospective medical record review of consecutive CSC patients treated with RFPDT (full-dose verteporfin and laser fluence of 25 J/cm²) examined 22 eyes of 21 patients (20 males and one female). The authors followed all patients for one year and evaluated best-corrected visual acuity (BCVA), complete resolution of subretinal fluid (CR of SRF), central retinal thickness (CRT), the outer nuclear layer (ONL) thickness and the photoreceptor inner and outer segments (IS/OS) line determined by optical coherence tomography imaging at baseline, one, three, six, nine and 12 months after initial RFPDT.

The study authors performed a single RFPDT session in all cases during a 12-month period. They identified CR of SRF in all patients. They also observed that BCVA significantly improved between three and 12 months (p<0.05). According to the authors, the CRT significantly decreased between one and 12 months. They observed a significantly thicker ONL at one month, and 17 eyes (77.2%) showed recovery of the continuous foveal IS/OS line. The authors of this study determined that ONL thickness was correlated with BCVA at 12 months (p<0.01). Stepwise analysis indicated that pre-treatment BCVA (p<0.01) and ONL thickness (p<0.01) were significant predictive factors for BCVA at 12 months. Neither ocular nor systemic adverse effects were observed during the follow-up period.

SOURCE: Ohkuma Y, Hayashi T, Sakai T, et al. One-year results of reduced fluence photodynamic therapy for central serous chorioretinopathy: the outer nuclear layer thickness is associated with visual prognosis. Graefes Arch Clin Exp Ophthalmol. March 2013.






Contributing Factors for Progression of VF Loss in NTG Patients with Medical Treatment

Researchers retrospectively analyzed 92 eyes in 92 normal-tension glaucoma (NTG) patients treated with only topical anti-glaucoma medications for five or more years to investigate the prognostic factors responsible for the progression of visual field defects (VFDs).

To identify subfield-based prognostic factors, they divided the central 30-degree visual field (Humphrey Field Analyzer) into six subfields: upper and lower arcuate, paracentral and cecocentral subfields. The evaluated factors related to subfield-based progression (age, refraction, mean intraocular pressure (IOP), IOP variability, central corneal thickness and disc hemorrhage) using a linear mixed model.

According to the researchers, the mean observation period was 7.7 ± 2.7 (5.0 to 15.5) years, and the estimated rate of change in the mean deviation value was –0.16 ± 0.31 dB/y (p<0.001). A subfield-based linear mixed model analysis of the time course of changes in the mean of total deviation identified a greater extent of myopia as a significant positive prognostic factor for VFD progression in the upper paracentral area (p=0.016). The mean IOP, central corneal thickness, disc hemorrhage, age and IOP variation showed no significant contribution in any of the subfields.

In conclusion, the extent of myopia was found to be a significant positive prognostic factor for VFD progression in the upper paracentral subfield for non-high-myopic NTG eyes with an average IOP of 14.2 mmHg under topical anti-glaucoma medication.

SOURCE: Sakata R, Aihara M, Murata H, et al. Contributing factors for progression of visual field loss in normal-tension glaucoma patients with medical treatment. J Glaucoma. 2013;22(3):250–254.




  • PHASE IIb RESULTS OF LATANOPROSTENE BUNOD FOR REDUCTION OF IOP PRESENTED. Robert N. Weinreb, MD, presented the Phase IIb results for latanoprostene bunod (previously known as BOL-303259-X) at the American Glaucoma Society 23rd Annual Meeting on March 2. Dr. Weinreb is chairman and distinguished professor of Ophthalmology, University of California San Diego and director, Shiley Eye Center and Hamilton Glaucoma Center. Latanoprostene bunod, a nitric oxide-donating prostaglandin F2 alpha analog, licensed by Nicox to Bausch + Lomb, is being developed for the reduction of IOP in patients with glaucoma or ocular hypertension. This dose-ranging study showed that latanoprostene bunod is effective at lowing IOP at multiple concentrations in a dose-dependent manner and that latanoprostene bunod 0.024% q.d. statistically significantly reduced IOP greater than latanoprost with a similar side effect profile. The randomized, investigator-masked study enrolled 413 patients across 23 sites in the United States and Europe. In light of the positive results of this study, Bausch + Lomb initiated a Phase III clinical program of latanoprostene bunod in January 2013 that includes two separate, randomized, multicenter, double-masked, parallel-group clinical studies, APOLLO and LUNAR, designed to compare the efficacy and safety of lantoprostene bunod administered q.d. with timolol maleate 0.5% administered b.i.d. in lowering IOP in patients with open-angle glaucoma or ocular hypertension. Read more here.
  • CENTERVUE INTRODUCES HANDHELD BINOCULAR REFRACTOMETER. CenterVue recently introduced the 2WIN For Vision, a handheld binocular refractometer. In five seconds, at one-meter distance, the 2WIN accurately measures refraction in the most natural vision conditions. It is also a vision analyzer, as it provides an objective assessment of the visual function, including pupil distance, pupil size, gaze and check of lens correction in use. The 2WIN is handheld, lightweight and easy-to-use. The company is also launching a new proprietary telemedicine platform, the Eye Knowledge Network (EKN). The EKN is a fully tested cloud system that transmits retinal images over the Internet and makes them available for online consultation by authorized users. It ensures fully encrypted, HIPPA-compliant data transmission and works seamlessly with CenterVue's automated fundus camera, the DRS. Visit the company's website for additional information.
  • PROGRESSIVE CHOICE FREEFORM LENS SERIES LAUNCHED BY ZEISS. Carl Zeiss Vision has launched a new customized progressive lens series designed for the competitive market environment that eye-care professionals face today. The Choice series consists of three new progressive lenses: ZEISS Progressive Choice, ZEISS Progressive Choice Plus and ZEISS Progressive Choice Plus V. ZEISS Progressive Choice lenses are optically optimized for up to 30% larger fields of clear vision. Four corridor options, sized for 13 mm, 15 mm, 17 mm and 19 mm fitting heights, are available. No compensated powers are required for verification of the lenses. With ZEISS Progressive Individual 2, the Choice series creates a complete ZEISS customized lens portfolio with multiple levels of customization and price points, to meet more patients' vision and affordability needs. ZEISS Progressive Choice Plus offers the five corridor options for fitting heights of 13 mm, 15 mm, 17 mm, 19 mm and 21 mm. ZEISS Progressive Choice Plus V employs a corridor sized automatically in 0.1-mm increments to the fitting height of the patient's frame. Visit the company's website for more information.
  • WILLS EYE INSTITUTE'S JERRY SHIELDS, MD, TO RECEIVE NATIONWIDE HONOR. Wills Eye Institute recently announced that Dr. Jerry A. Shields, director of the Wills Eye Ocular Oncology Service, is to receive The National Physician of the Year Award in Clinical Excellence. The Awards recognize and honor five exemplary physicians, as well as the many thousands of other excellent physicians practicing in communities throughout the United States. For 40 years, Dr. Shields has diagnosed and treated countless patients with ocular tumors and has led clinical research to improve methods for the diagnosis and treatment of eye cancers, including tumors of the eyelids, conjunctiva, intraocular structures and orbit. He will receive the honor at a ceremony on Monday, March 18, 2013 at The Pierre Hotel in New York City.
  • OWL TO HOST AWARDS RECEPTION AT ASCRS. Ophthalmic Women Leaders (OWL) will be hosting its annual awards reception honoring influential women in ophthalmology during the 2013 American Society of Cataract & Refractive Surgeons meeting in San Francisco. Three awards will be presented: Visionary Woman Award, sponsored by the Lindstrom Family Foundation; the Rising Star Award, sponsored by Link Consulting; and the Catalyst Award. Through March 15, OWL members will be able to nominate candidates for each of the three awards being presented. Nominations can be completed here. The reception will be held at the W Hotel San Francisco (Industry Room, 2nd floor) on April 22 from 5:30 p.m. to 7:00 p.m. Admission is free for OWL members and $25 for non-members. Registration at www.owlsite.org.
  • CHRISTOPHER THATCHER NAMED DIVISION VICE PRESIDENT AND BUSINESS UNIT MANAGER AT REICHERT TECHNOLOGIES. Reichert Technologies, a unit of AMETEK Ultra Precision Technologies, recently named Christopher A. Thatcher as Division Vice President and Business Unit Manager. He will be based at the company's Buffalo, NY, headquarters and have responsibility for Reichert's global businesses.


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