Volume 7, Number 31
Monday, August 6, 2007



In this issue: (click heading to view article)
An Interval-Censored Model for Predicting Myopic Regression after LASIK
Risk Factors for Incident Open-Angle Glaucoma in Patients of African Descent
Refractive Surgery for Myopia And Myopic Anisometropic Adults
Antibiotic Prophylaxis and the Incidence of Postop Endophthalmitis After Cataract Surgery
HSV Epithelial Recurrence and Graft Survival After PK in Atopic and Nonatopic Patients
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An Interval-Censored Model for Predicting Myopic Regression after LASIK

This Taiwanese study proposed a time-varying statistical model for predicting the risk of regression toward myopia after laser in situ keratomileusis (LASIK).

Researchers analyzed 615 eyes of 311 patients derived from a retrospective cohort who underwent LASIK in 2003. They recorded refraction outcomes at one day, one week and one, three, six, nine and 12 months or longer after LASIK. They used a cross-validated design to split data into trained (308) and validated (307) data sets. These data sets were then used in an interval-censored model to predict the probability of regression toward myopia and to assess the predictors including demographic features and preoperative and postoperative variables.

Myopia regression was observed in 164 (26.7 percent) of 615 eyes during the follow-up period of 12 months or longer after LASIK. Significant predictors for myopia regression after LASIK included preoperative manifest spherical equivalent, mean preoperative central corneal curvature, size of optic zone, undercorrection and age. The risk of regression toward myopia after LASIK increased rapidly within one month, slowed down between one and six months and became steady after six months, regardless of risk group. The risk of myopia regression up to six months after LASIK was 21 percent in average-risk eyes (based on all eyes).

The authors of this study believe that this interval-censored model may be useful not only for predicting the probability of myopia regression after LASIK, but also for identifying the evolution of patients within low, moderate and high-risk groups.


SOURCE: Chen YI, Chien KL, Wang IJ, et al. An interval-censored model for predicting myopic regression after laser in situ keratomileusis. Invest Ophthalmol Vis Sci 2007;48(8):3516-23.
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Risk Factors for Incident Open-Angle Glaucoma in Patients of African Descent

This investigation by researchers at Stony Brook University School of Medicine, NY, and Johns Hopkins University evaluated risk factors for definite open-angle glaucoma (OAG), based on African-descent participants of the Barbados Eye Studies.

Eighty-one to 85 percent of patients participated over nine years of follow-up; investigators evaluated 3,222 persons at risk (age 40 to 84 years old) who did not have definite OAG at baseline. All had standardized study visits at baseline and after four and nine years, with structured interviews and blood pressure (BP) and other measurements. The ophthalmic protocol included automated perimetry, applanation tonometry, fundus photography and comprehensive ophthalmologic examinations for those referred. Central corneal thickness (CCT) was measured in a subset at the nine-year examination. Incidence was estimated by the product-limit approach; relative risk ratios (RRs) with 95 percent confidence intervals (CIs) were based on Cox regression models with discrete time.

Over nine years, 125 participants developed definite OAG (incidence, 4.4 percent; 95 percent CI, 3.7 to 5.2). Baseline factors influencing risk were age; family history of glaucoma; higher intraocular pressure; lower systolic BP and lower ocular systolic, diastolic and mean perfusion pressures. Thinner CCT was also associated with OAG incidence.

The authors maintain that this is the first report of risk factors for long-term OAG incidence, and they point out that it is also based on a sizable number of new cases. The findings suggest a multifactorial etiology of OAG and suggest that similar risk factors apply across populations. Results are relevant for understanding OAG causation and identifying groups at high risk.


SOURCE: Leske MC, Wu SY, Hennis A, et al. (BESs Study Group). Risk factors for incident open-angle glaucoma: The Barbados Eye Studies. Ophthalmol 2007; Jul 13 [Epub ahead of print].
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Refractive Surgery for Myopia And Myopic Anisometropic Adults

Anisometropia in adults reduces visual acuity in the more myopic eye and can be at least partially reversed by refractive correction, according to results of a study by researchers at Finland"s University of Helsinki.

The investigators tested the hypothesis that anisometropic adults without significant amblyopia suffer from mild visual impairment probably due to aniseikonia, which might be improved by corneal refractive surgery. Fifty-seven patients presenting with myopic anisometropia of 3.25 diopters (D) or greater and 174 myopic controls appropriate for refractive surgery were included in the study. Surgeons performed photorefractive keratectomy (PRK) or LASIK on 57 anisometropic eyes. Because 43 of the 174 myopic control patients had bilateral surgery, PRK or LASIK was performed on 217 myopic control eyes. Investigators measures best spectacle-corrected visual acuity (BSCVA), refraction and refractive correction preoperatively and at one, three, five to seven, eight to 13 and 25 months following surgery.

Preoperative mean spherical equivalent was -7.20 +/- 2.40 D for anisometropic patients and -6.40 +/- 1.90 D for myopic patients. At eight to 13 months postoperatively, when 23 (40 percent) anisometropic eyes and 94 (43 percent) myopic eyes were examined, the mean spherical equivalent refractions were -0.80 +/- 1.60 D and -0.30 +/- 0.60 D, respectively. Preoperatively, the mean BSCVA on a logMAR scale was -0.0143 +/- 0.0572 (Snellen 0.98 +/- 0.12) in the anisometropic group and 0.0136 +/- 0.0361 (Snellen 1.04 +/- 0.09) in the control group. Eight to 13 months postoperatively, these values were 0.0076 +/- 0.0659 (Snellen 1.03 +/- 0.15) and 0.0495 +/- 0.0692 (Snellen 1.13 +/- 0.18); this difference remained statistically significant. For the myopic patients, the improvement in BSCVA reached almost maximum at three months, and this improvement was found to be highly significant three months after surgery. The improvement in BSCVA was significantly slower for anisometropic patients and became statistically significant only after eight to 13 months postoperatively. The slower improvement in BSCVA for anisometropic patients suggests plastic changes in the visual cortex following refractive surgery.

SOURCE: Vuori E, Tervo TM, Holopainen MV, Holopainen JM. Improvement of visual acuity following refractive surgery for myopia and myopic anisometropia. J Refract Surg 2007;23(5):447-55.
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Antibiotic Prophylaxis and the Incidence of Postop Endophthalmitis After Cataract Surgery

The European Society of Cataract & Refractive Surgeons (ESCRS) Endophthalmitis Study Group conducted this study aimed at identifying risk factors and describing the effects of antibiotic prophylaxis on the incidence of postoperative endophthalmitis after cataract surgery. The study was based on analysis of the findings of the ESCRS multicenter study, which included 24 ophthalmology units in Austria, Belgium, Germany, Italy, Poland, Portugal, Spain, Turkey and the United Kingdom; the prospective, randomized, partially masked multicenter cataract surgery study recruited 16,603 patients and was based on a 2 x 2 factorial design, with intracameral cefuroxime and topical perioperative levofloxacin factors resulting in four treatment groups.

In the current study, investigators performed a comparison of case and non-case data using multivariable logistic regression analyses; they estimated odds ratios (ORs) associated with treatment effects and other risk factors. Twenty-nine patients presented with endophthalmitis, of whom 20 were classified as having proven infective endophthalmitis. The absence of an intracameral cefuroxime prophylactic regimen at 1 mg in 0.1 mL normal saline was associated with a 4.92-fold increase (95 percent confidence interval [CI], 1.87 to 12.9) in the risk for total postoperative endophthalmitis. In addition, the use of clear corneal incisions (CCIs) compared to scleral tunnels was associated with a 5.88-fold increase (95 percent CI, 1.34 to 25.9) in risk and the use of silicone intraocular lens (IOL) optic material compared to acrylic with a 3.13-fold increase (95 percent CI, 1.47 to 6.67). The presence of surgical complications increased the risk for total endophthalmitis 4.95-fold (95 percent CI, 1.68 to 14.6), and more experienced surgeons were more likely to be associated with endophthalmitis cases. When considering only proven infective endophthalmitis cases, the absence of cefuroxime and the use of silicone IOL optic material were significantly associated with an increased risk. Additionally, evidence showed that men were more predisposed to infection (OR, 2.70; 95 percent CI, 1.07 to 6.8).

SOURCE: ESCRS Endophthalmitis Study Group. Prophylaxis of postoperative endophthalmitis following cataract surgery: Results of the ESCRS multicenter study and identification of risk factors. J Cataract Refract Surg 2007;33(6):978-88.
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HSV Epithelial Recurrence and Graft Survival After PK in Atopic and Nonatopic Patients

Investigators compared the incidence of herpes simplex virus (HSV) epithelial recurrence and graft survival after penetrating keratoplasty (PK) in patients with and without self-reported atopy in this retrospective cohort comparative study.

The study included patients who presented with previously diagnosed ocular HSV between March 2003 and March 2004 and who underwent primary PK for ocular HSV at the Cornea Service of Wills Eye Hospital, Philadelphia, PA. From the 58 patients invited, 49 patients (50 eyes) were included. Nine patients were ineligible in accordance with the exclusion criteria: no active classic HSV episode before PK, immunosuppression, less than one year of follow-up and previous history of PK before presentation at the Service. Eligible patients filled out a questionnaire regarding their history of atopic disease, considering the presence of allergic rhinitis, asthma or atopic dermatitis. Researchers obtained ocular history through chart review. Main outcome measures were the incidence of epithelial HSV recurrences and corneal graft survival in both groups. Each group (atopic and nonatopic) included 25 eyes.

The atopic patients had a mean incidence of 0.07 episode per eye year (SD +/- 0.9) compared with 0.12 per eye year (standard deviation [SD] +/- 0.21) in the nonatopics. At 10 years of follow-up, the survival rate in the atopics was 92 percent and in the nonatopics was 79 percent. Although nonatopics had significantly more epithelial recurrences after PK compared to atopics, both groups presented low incidences of recurrences and high graft survival rates.

SOURCE: Rezende RA, Bisol T, Hammersmith K, et al. Epithelial herpetic simplex keratitis recurrence and graft survival after corneal transplantation in patients with and without atopy. Am J Ophthalmol 2007;143(4):623-8.
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BRIEFLY
  • TOPCON INTRODUCES NEW COLOR BALANCE TOOL FOR RETINAL IMAGING SOFTWARE. Topcon Medical Systems, Inc. has launched a new Color Balance Tool for its Imagenet Digital Imaging Software. The new tool allows the user to adjust the histogram curves of the individual red, green, and blue channels of the retinal images at capture. After capturing a color fundus image, the user can see the effects of adjusting color balance in a preview image before taking additional photographs of a patient"s eye, thereby reducing trial and error in fine-tuning adjustments of color and exposure. The Color Balance Tool may also be used in monochrome imaging, such as fluorescein angiography, monochromatic photography and fundus autofluorescence imaging, to adjust contrast to maximize diagnostic information. For more information, call 800-223-1130 or go to www.topconmedical.com.

  • IMPROVED GENE THERAPY APPROACH MAY HELP TREAT INHERITED BLINDNESS. Researchers at Washington University School of Medicine in St. Louis have identified DNA elements that control when and where genes linked to blindness are "switched on," a finding that may help treat some of the almost 200 inherited forms of blindness. Using a computational analysis of DNA to search for elements that can turn on genes in the photoreceptor cells of the eye, the investigators have identified hundreds of potential cis-regulatory elements (DNA segments involved in activating and deactivating genes). They confirmed 19 of these elements, more than doubling the number known to scientists. The newly discovered elements can be used as switches to activate blindness therapies; with further studies of the new and previously established sites, the researchers expect to determine the basic rules that appear to govern how the sites work. The results of this study are also being used to design gene therapy vectors for a form of Leber"s congenital amaurosis.
    SOURCE: Hsiau TH-C, Diaconu C, Myers CA, et al. The cis-regulatory logic of the mammalian photoreceptor transcriptional network. Pub Lib Sci ONE 2007; July 25.

  • LENS AND OLFACTORY CELLS MAY HAVE THE SAME ORIGIN. Researchers at Umea University in Sweden have discovered that the same signal molecule determines the formation of both the lens of the eye and the olfactory cells of the nose. The mucous membrane for smelling and the lens of the eye develop early in the fetal stage of human development, but the signals governing their formation have been unknown until now. Umea"s researchers discovered that the same signal molecule regulates the formation of both cell types, but that cells exposed to the signal for short periods become olfactory cells, while cells exposed for longer periods become lens cells. The finding that exposure time, not the concentration of the same signal, determines the formation of two sensory organs is considered of vital importance to the study of cell formation during the fetal period.
    SOURCE: Sjodal M, Edlund T, Gunhaga L. Time of exposure to BMP signals plays a key role in the specification of the olfactory and lens placodes ex vivo. Developmental Cell 2007;13(1):141-9.


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