Volume 8, Number 14
Monday, April 7, 2008



In this issue: (click heading to view article)
Anterior Chamber Depth and Angle Width: Associations with Ocular and General Parameters
Drivers of Patient Adherence to Topical Ocular Hypotensive Therapy
Link Between Macrovascular Disease and Proliferative Diabetic Retinopathy
Impact of Diabetic Retinopathy on Quantitative RNFL Measurement and Glaucoma Screening
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Anterior Chamber Depth and Angle Width: Associations with Ocular and General Parameters

The Beijing Eye Study 2006, conducted by the Beijing Institute of Ophthalmology, included 3,251 subjects (73.3 percent), aged 45 years and older, out of 4,439 subjects who participated in a 2001 survey and who returned for reexamination. The researchers investigated the normative data of anterior chamber depth (ACD) and angle width and their associations in Chinese adults.

Each of the study participants underwent an ophthalmologic examination including measurement of the anterior chamber dimensions by slit-lamp-based optical coherence tomography (OCT). Out of the 3,251 subjects, OCT measurements were available for 2,985 subjects (91.8 percent). Mean ACD measured 2.42 +/- 0.34 mm and the mean anterior chamber angle (ACA) was 38.3 +/- 16.3 degrees. In multivariate analysis, a shallow chamber depth was significantly associated with age, hyperopic refractive error, female gender, short body stature, nuclear cataract, central corneal thickness (CCT), large optic disc and presence of chronic angle-closure glaucoma. Correspondingly, a narrow ACA was associated with age, female gender, hyperopia, nuclear cataract, short body stature, large optic disc and angle-closure glaucoma. Chamber depth and angle width were not associated with presence of age-related maculopathy and diabetic retinopathy.

The authors believe the results of this study may be helpful in explaining anatomic relationships of the anterior segment of the eye and in elucidating risk factors of angle-closure glaucoma.


SOURCE: Xu L, Cao WF, Wang YX, et al. Anterior chamber depth and chamber angle and their associations with ocular and general parameters: The Beijing Eye Study. Am J Ophthalmol 2008; Mar 11 [Epub ahead of print].
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Drivers of Patient Adherence to Topical Ocular Hypotensive Therapy

Doctor-patient communications and health-related beliefs of patients contribute to patient adherence to medical therapies for open-angle glaucoma, according to a study by Baltimore"s Wilmer Eye Institute and the Johns Hopkins Bloomberg School of Public Health.

The investigators used multiple data sources to determine the drivers of patient adherence to topical ocular hypotensive therapy, including retrospective database and chart reviews in combination with prospective patient surveys. The study covered diverse medical environments where insured patients in the research database sought care. The study included records of 300 patients with a new claim diagnosis for open-angle glaucoma who initially were prescribed one of three prostaglandins, and 103 physicians participating in the same medical plans. Surveyed patients participated in a structured interview addressing self-reported adherence, experiences with medication, communication with the physician and health-related beliefs associated with adherence behavior; phone interviews were conducted with participating ophthalmologists.

Eight variables were associated independently with a lower medication possession ratio: 1) hearing all of what you know about glaucoma from your doctor (compared with some or nothing of what you know); 2) not believing that reduced vision is a risk of not taking medication as recommended; 3) having a problem paying for medications; 4) difficulty adhering to medication regimen while traveling or away from home; 5) not acknowledging stinging and burning; 6) being non-white; 7) receiving medication samples; and 8) not receiving a phone call reminder to visit your doctor. The multivariate model explained 21 percent of the variance.

Based on the results of the study, the authors concluded that patient learning styles associated with less concern about the future effects of glaucoma and the risks of not taking medications are associated with lower adherence. Specifically, knowledge about potential vision loss from glaucoma is a critical element of patient education that tends to be missed by more passive, doctor-dependent patients who tend to be poorly adherent. The findings suggest that educational efforts in the office may improve patient adherence to medical therapies for glaucoma.

SOURCE: Friedman DS, Hahn SR, Gelb L, et al. Doctor-patient communication, health-related beliefs, and adherence in glaucoma results from the Glaucoma Adherence and Persistency Study. Ophthalmol 2008; Mar 3 [Epub ahead of print].
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Link Between Macrovascular Disease and Proliferative Diabetic Retinopathy

Increasing evidence suggests that macrovascular disease and retinopathy may be more closely linked than previously believed. In this study, researchers aimed to determine the relationship between retinopathy and coronary atherosclerosis as measured by computed tomography (CT)-detectable coronary artery calcium (CAC).

The cross-sectional association between CAC and retinopathy was assessed on a Veterans Affairs Diabetes Trial (VADT) sub-sample of 204 subjects with a mean duration of Type II diabetes of 12.3 +/- 8.3 years. Retinopathy was correlated with CAC.

Median CAC increased across retinopathy categories: 197 in those with no retinopathy, 229 with microaneurysms only, 364 with mild nonproliferative diabetic retinopathy (NPDR), 300 with moderate-to-severe NPDR and 981 in those with proliferative diabetic retinopathy (PDR). Stepwise multivariable linear regression analysis found a parsimonious subset of relevant risk factors to include along with PDR in predicting CAC. After investigators adjusted for either this subset of standard factors or a more extensive panel of risk factors, PDR was significantly associated with CAC. Moreover, after logistic regression was used, results showed that individuals with PDR were approximately six times more likely to have CAC greater than 400 compared with those who had no PDR, even after adjustment for other CVD risk factors.

The data indicate an important relationship between retinopathy and extent of coronary atherosclerosis (CAC), and they suggest the potential to identify and treat shared risk factors for these common micro- and macrovascular complications.

SOURCE: Reaven PD, Emanuele N, Moritz T, et al.; for the VADT. Proliferative diabetic retinopathy in Type 2 diabetes is related to coronary artery calcium in the Veterans Affairs Diabetes Trial (VADT). Diabetes Care 2008; Mar 3 [Epub ahead of print].
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Impact of Diabetic Retinopathy on Quantitative RNFL Measurement and Glaucoma Screening

Researchers at Japan"s Senshokai Eye Institute investigated the impact of diabetic retinopathy on quantitative retinal nerve fiber layer (RNFL) assessment and diagnostic power for glaucoma by scanning laser polarimetry and optical coherence tomography (OCT).

The individual RNFL parameters of GDx and OCT were obtained for 170 eyes (one eye from each of 170 subjects: 45 healthy, 47 with glaucoma, 40 with diabetes and 38 with glaucoma with diabetes). The parameters were compared among the four groups. Diabetic eyes had mild-to-moderate nonproliferative diabetic retinopathy (NPDR) without maculopathy. In glaucomatous eyes with or without diabetes, the ability to discriminate glaucoma was assessed by the areas under the receiver operating characteristic curves (AUROCs) and the sensitivities at more than 80 percent and 90 percent of specificities for each technique.

Using GDx-VCC, significant differences in RNFL measurement parameters were found for all comparisons except those between glaucomatous eyes with diabetes and without diabetes. OCT parameters did not detect significant differences between age-matched healthy and diabetic eyes. Among the parameters included, the nerve fiber indicator (NFI) of GDx-VCC and the inferior quadrant thickness (IQT) of OCT had the largest AUROCs and sensitivities at specificities greater than 80 percent: 86 percent for NFI and 85 percent for IQT in glaucomatous eyes with diabetes; 92 percent for NFI and 91 percent for IQT in simple glaucomatous eyes.

The results suggest that mild-to-moderate NPDR causes a quantitative discrepancy in RNFL measurements between GDx-VCC and OCT in simple diabetic eyes. However, mild-to-moderate glaucomatous optic neuropathy can be highly discriminated by the two imaging devices in eyes with diabetic retinopathy.

SOURCE: Takahashi H, Chihara E. Impact of diabetic retinopathy on quantitative retinal nerve fiber layer measurement and glaucoma screening. Invest Ophthalmol Vis Sci 2008;49(2):687-92.
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BRIEFLY
  • CMS DESIGNATES STAAR COLLAMER IOL AS A NEW TECHNOLOGY IOL. The Centers for Medicare and Medicaid Services (CMS) has designated STAAR Surgical"s Afinity Collamer Aspheric foldable intraocular lens (IOL) CQ2015A as a New Technology Intraocular Lens (NTIOL). To receive this designation, an IOL must be FDA approved, with labeling and advertising consistent with the specific claim or characteristic for which CMS approval is being sought. In addition, the product"s manufacturer must show evidence that use of the IOL results in measurable, clinically meaningful improved patient outcomes in comparison with use of currently available IOLs. The Afinity Collamer Aspheric IOL has been proven to reduce spheric aberrations, leading to improved visual acuity and increased contrast sensitivity. The CMS approval for NTIOL reimbursement status means that Medicare will provide an additional reimbursement of $50 per Afinity lens when provided to a Medicare patient in an ambulatory surgical center (this type of center performs more than half of all cataract surgeries in the United States and most of STAAR"s current IOL business is in this segment). The NTIOL subset, Reduced Spherical Aberrations, for which the Afinity Collamer Aspheric IOL has been approved, began allowing the enhanced reimbursement beginning March 17, 2008 and will do so until February 26, 2011.

  • PARADIGM INTRODUCES EARLY GLAUCOMA DETECTION DEVICE. Paradigm Medical Industries introduced its Glaid-PERG electrophysiology instrument for the early detection of glaucoma at this weekend"s American Society for Cataract Refractive Surgeons (ASCRS) Conference in Chicago, IL. The Glaid-PERG is the earliest means of detecting cellular losses attributed to glaucoma and other ocular ailments, according to a company spokesperson. Earlier this year, Paradigm signed an exclusive agreement with LACE Elettronica srl (Rome, Italy) to distribute the Glaid-PERG instrument. In U.S. and European clinical studies, the device has been proven to provide high test repeatability and a high level of accuracy. Ongoing research is indicating testing application for ocular ailments other than glaucoma. Paradigm will also introduce the prototype version of its redesigned LD400 Autoperimetry system at the ASCRS show. The LD400 is used to measure patient visual fields to determine the severity of glaucoma and to aid in managing the disease.
  • CLINICAL TRIAL RESULTS ANNOUNCED FOR NEW XIBROM ONCE-DAILY FORMULATION. ISTA Pharmaceuticals, Inc. recently reported the results of a clinical trial of Xibrom (bromfenac sodium ophthalmic solution) QD (once-daily) 0.18%, a new formulation of the company"s ocular nonsteroidal anti-inflammatory agent. The findings demonstrated this formulation"s equivalence with ISTA"s 0.09% formulation, given once daily in achieving the primary efficacy endpoint of absence of ocular inflammation 15 days following surgery. No statistically significant difference was recorded between the two formulations in achieving the secondary efficacy endpoints (elimination of ocular pain and mean reduction of markers of inflammation). The results also indicated that both formulations of bromfenac produced a low overall incidence of ocular adverse events. A spokesperson for ISTA says that the nearly identical performance of the two concentrations was unexpected; it suggests that the 0.09% formulation is near the top of the dose-response curve. The company plans to complete the data analysis and confer with the FDA to determine the next step; it will also consider other options for new Xibrom products, including the possibility of a label change for the currently marketed 0.09% formulation of Xibrom so that it can be administered once daily. For more information, go to www.istavision.com.


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