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Volume 12, Number 43
Monday, October 22, 2012
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OCTOBER IS WORLD BLINDNESS AWARENESS MONTH




In this issue: (click heading to view article)
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######### CNV Complicating GA in AMD

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######### Use of Ranibizumab for the Treatment of Edema of the Macula
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######### Results of Lens Extraction for Visually Significant Cataract in Eyes with Primary Angle Closure
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######### Link Between Parental Smoking and Childhood Refractive Error
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CNV Complicating GA in AMD

The authors of this French retrospective, interventional, consecutive case series sought to investigate the morphological and functional outcomes following intravitreal ranibizumab injections for choroidal neovascularization (CNV) complicating geographic atrophy (GA).

They reviewed the charts of all consecutive patients with GA due to age-related macular degeneration (AMD) who received intravitreal ranibizumab injections for the development of CNV at least 24 months earlier.

Included were 21 treatment-naïve eyes of 21 consecutive patients (four men, 17 women; mean age 86.9 ± 1.6 years). The authors noted that in 95.2% of eyes, a type 2 CNV was present; extrafoveal in 42.8% of cases. They also found that after a mean of 5.0 ± 0.87 (range 1–20) intravitreal ranibizumab injections, best-corrected visual acuity (BCVA) significantly worsened at the 24-month follow-up visit (0.73 ± 0.05 vs. 0.88 ± 0.08 logMAR, respectively; p=0.01). A significant reduction of intraretinal cystic lesions, subretinal fluid and pigment epithelium detachment (p<0.001) and a significant increase of GA area (p=0.003) were present at last visit.

In conclusion, ranibizumab treatment of GA-associated CNVs provides no BCVA improvement at 24 months follow-up despite an anatomic response of CNV. Low effectiveness of ranibizumab in these cases is likely due to GA progression.

SOURCE: Querques G, Massamba N, Coscas F, et al. Choroidal neovascularisation complicating geographic atrophy in age-related macular degeneration. Br J Ophthalmol. 2012;Oct 17. [Epub ahead of print].




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Use of Ranibizumab for the Treatment of Edema of the Macula

To assess the benefit of increased follow-up and treatment with ranibizumab between months 24 and 36 in the Ranibizumab for Edema of the Macula in Diabetes (READ-2) Study, investigators conducted this prospective, interventional, multicenter follow-up.

Patients who agreed to participate between months 24 and 36 (ranibizumab, 28 patients; laser, 22; and ranibizumab + laser, 24) returned monthly and received ranibizumab, 0.5 mg, if foveal thickness (FTH, center subfield thickness) was 250 µm or greater. Improvement in best-corrected visual acuity (BCVA) and reduction in FTH between months 24 and 36 were the main outcome measures.

According to the investigators, mean improvement from the baseline BCVA in the ranibizumab group was 10.3 letters at month 36 vs. 7.2 letters at month 24 (ΔBCVA letters = 3.1, p=.009), and FTH at month 36 was 282 µm vs. 352 µm at month 24 (ΔFTH = 70 µm, p=.006). They reported that changes in BCVA and FTH in the laser group (–1.6 letters and –36 µm, respectively) and the ranibizumab + laser group (+2.0 letters and –24 µm) were not statistically significant. They also noted that the mean number of ranibizumab injections was significantly greater in the ranibizumab group compared with the laser group (5.4 vs. 2.3 injections, p=.008), but not compared with the ranibizumab + laser group (3.3, p=.11).

More aggressive treatment with ranibizumab during year three resulted in a reduction in mean FTH and improvement in BCVA in the ranibizumab group, the investigators concluded. More extensive focal/grid laser therapy in the other two groups may have reduced the need for more frequent ranibizumab injections to control edema. Long-term visual outcomes for treatment of diabetic macular edema with ranibizumab are excellent, but many patients require frequent injections to optimally control edema and maximize vision.

SOURCE: Do DV, Nguyen QD, Khwaja AA, et al.; for the READ-2 Study Group. Ranibizumab for edema of the macula in diabetes study. Arch Ophthalmol. 2012;Oct [Epub ahead of print].



http://www.revophth.com/ChicOS2012






Results of Lens Extraction for Visually Significant Cataract in Eyes with Primary Angle Closure

The following retrospective study examined the clinical outcomes of cataract extraction in eyes with primary angle closure and coexisting cataract.

It included 55 eyes of 39 patients with primary angle closure or occludable angles and visually symptomatic cataract. Approximately 61.8% of eyes had received a peripheral iridotomy and 65% had evidence of glaucomatous optic neuropathy (GON).

At 7.2 months after cataract extraction, a statistically significant reduction in intraocular pressure (IOP) was observed in all eyes with primary angle closure (median 3 mmHg, p=<0.0001). The reduction in IOP was significantly greater in eyes with a higher preoperative IOP (p=<0.0001). On average, one less glaucoma medication was in use postoperatively (p=0.01). Eyes with >180 degrees of peripheral anterior synechiae (PAS) preoperatively achieved a significantly greater reduction in IOP postoperatively compared with those with less PAS (7.5 vs. 4.4 mmHg, p=0.03). They observed reduction in IOP in eyes with PAC and GON was significantly greater compared with those without GON (5.6 vs. 2.5 mmHg, p=0.01). Visual acuity was significantly improved after cataract extraction by a mean of –0.23 LogMAR units (p=0.0001).

Contrary to earlier expectations, the observed reduction in postoperative IOP in eyes with PAC was significantly greater in the presence of a higher preoperative IOP, a larger number of glaucoma medication, narrower iridotrabecular angle width, and greater extent of PAS formation and in eyes with evidence of GON. Lens extraction seems to have a beneficial effect on IOP control in PAC, and is especially efficacious in more advanced cases.

SOURCE: Shams PN, Foster PJ. Clinical outcomes after lens extraction for visually significant cataract in eyes with primary angle closure. J Glaucoma. 2012;21(8):545–550.



Link Between Parental Smoking and Childhood Refractive Error

Researchers assessed the relationship between parental smoking and childhood refractive errors in Singapore Chinese children aged six to 72 months recruited through the STrabismus, Amblyopia, and Refractive errors in Singaporean children study.

They recruited a total of 4,164 children, with a positive response rate of 72.3% (n=3,009). They also obtained cycloplegic refraction measurements from all children by trained eye professionals. Parents underwent an interviewer-administered questionnaire that obtained information on demographics, lifestyle and parental smoking history.

The study researchers obtained spherical equivalent readings for 87.7% of the children. They noted that in all, 52.1% were male (n=1,375). They also reported that the overall prevalence of myopia (at least –0.5D) was 11.0%. Overall, 37.1% of the fathers interviewed gave a history of smoking and among the mothers interviewed, 9.2% gave a history of smoking, 6.6% had smoked during the child's life and 2.2% had smoked during the pregnancy. Maternal history of ever smoking, smoking during child's life, and smoking during pregnancy were associated with decreased odds ratio (OR) of childhood myopia (OR 0.50 (p=0.01), OR 0.39 (p=0.01), and OR 0.3 (p=0.14), respectively). Furthermore, paternal history of smoking was associated with decreased OR of childhood myopia (OR of 0.72 (p=0.02)).

In light of this finding of an inverse association between parental smoking and childhood myopia, the researchers suggest further studies to better understand the role of nicotinic acetylcholine receptor pharmacology in ocular development. This may pave the way for the development of targeted treatment strategies for prevention of myopia.

SOURCE: Iyer JV, Low WC, Dirani M, Saw SM. Parental smoking and childhood refractive error: the STARS study. Eye. 2012;26(10):1324–1328.





  • FDA APPROVES JETREA FOR TREATMENT OF SYMPTOMATIC VMA. In a recent press release, ThromboGenics NV announced that the FDA has approved its JETREA (oriplasmin) in the United States for the treatment of symptomatic vitreomacular adhesion (VMA). The approval was based on data from ThromboGenics' Phase III program, where JETREA was shown to be superior to placebo for the treatment of symptomatic VMA (26.5% vs. 10.1%; p<0.01). The recommended dose of JETREA is 0.125 mg (0.1 mL) of the diluted solution administered by intravitreal injection to the affected eye once as a single injection. The agent is provided as a single-use glass vial containing 0.5 mg in 0.2 mL solution for intravitreal injection (2.5 mg/mL). View important safety and prescribing information about JETREA at www.jetrea.com.
  • TEARSCAN OCULAR DIAGNOSTIC LAB SYSTEM NOW AVAILABLE. Advanced Tear Diagnostics (ATD) recently unveiled its new TearScan ocular diagnostic testing platform, which is specifically designed to assist eye-care physicians in detecting and quantifying biomarkers associated with the diagnosis and treatment of a variety of ocular surface disorders. The company says the unit incorporates a compact, low-cost computerized multi-channel analytical reflectance photometer designed to quickly and accurately process ATD's proprietary test cassettes. ATD will be demonstrating its new TearScan System at the American Academy of Ophthalmology in Chicago beginning November 10th. For additional information, visit http://teardiagnostics.com.
  • LPATH'S COMMON STOCK TO BE LISTED ON NASDAQ. The NASDAQ Stock Market has approved Lpath Inc.'s application to list the company's common stock on the NASDAQ Capital Market. Lpath's common stock is expected to begin trading at the open of trading on October 22, 2012 under the ticker symbol LPTN. The company initiated dosing of its ocular drug iSONEP last month to determine how it can best be used to benefit wet age-related macular degeneration patients. Visit Lpath's website to learn more.
  • 1-YEAR RESULTS OF PHASE III VIEW 1 AND VIEW 2 STUDIES PUBLISHED. According to Regeneron Pharmaceuticals Inc., detailed one-year results from its VIEW 1 and VIEW 2 Phase III studies of EYLEA (aflibercept) Injection were published online in the journal Ophthalmology. These randomized, multicenter, double-masked, active-controlled studies assessed the safety and efficacy of EYLEA in patients with wet age-related macular degeneration. EYLEA was dosed every eight weeks following three initial monthly injections and was shown to be clinically equivalent to Lucentis (ranibizumab injection) dosed every four weeks, as measured by the primary endpoint of maintenance of best-corrected visual acuity (<15 letters of vision loss on an eye chart as measured on an ETDRS scale) over 52 weeks.
  • FIRST OCT-GUIDED FEMTOLASER-ASSISTED CORNEAL SURGERY DEMONSTRATED. At the recent European Society of Cataract & Refractive Surgeons meeting last month in Milan, first pictures of Ziemer Ophthalmic System AG's proprietary in-house developed OCT technology were shown to a broad audience. The company's new FEMTO LDV Z Models launched in February 2012 and are CE marked and FDA cleared. The OCT module is an add-on option for the FEMTO LDV Z6. The integrated OCT system performs online imaging for refractive and corneal procedures and allows precise placement of the laser focal point relative to the Bowman's and Descemet's membranes. Introduction of the OCT module—pending CE marking and FDA clearance—is planned for the first half of 2013. Click here to read more.




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