Figure 1. Algorithm (flowchart) for randomized infants. *Data were incomplete because of failure to cooperate with monocular testing or failure to have had amblyopia therapy prescribed.
Figure 2. Distribution of grating acuity outcomes for randomized eyes by treatment assignment. Normal indicates 13 or more cycles/degree; below normal, less than 13 to 6.4 or more cycles/degree; poor, measurable acuity of less than 6.4 cycles/degree; blind/low vision, ability to detect only the 2.2-cm-wide stripes on the low-vision Teller acuity card at any distance and at any location in the visual field, light perception only, or no light perception. Visual acuities in the poor and blind/low vision categories were classified as unfavorable outcomes. CM indicates conventional management; ET, early treatment (treated at high-risk prethreshold).
Figure 3. Distribution of grating acuity outcomes for randomized eyes with type 1 (A) and type 2 (B) retinopathy of prematurity by treatment assignment (early treatment [ET] or conventional management [CM]). Grating acuity categories are described in the legend to Figure 2. Visual acuities in the poor and blind/low vision categories were classified as unfavorable outcomes.
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The Early Treatment for Retinopathy of Prematurity Cooperative Group*. Grating Visual Acuity Results in the Early Treatment for Retinopathy of Prematurity Study. Arch Ophthalmol. 2011;129(7):840–846. doi:10.1001/archophthalmol.2011.143
*Authors/Group Information: Velma Dobson, PhD (chair); Graham E. Quinn, MD, MSCE; C. Gail Summers, MD; Robert J. Hardy, PhD; Betty Tung, MS; William V. Good, MD.
Objective To compare grating (resolution) visual acuity at 6 years of age in eyes that received early treatment (ET) for high-risk prethreshold retinopathy of prematurity (ROP) with that in eyes that underwent conventional management (CM).
Methods In a randomized clinical trial, infants with bilateral, high-risk prethreshold ROP (n = 317) had one eye undergo ET and the other eye undergo CM, with treatment only if ROP progressed to threshold severity. For asymmetric cases (n = 84), the high-risk prethreshold eye was randomized to ET or CM.
Main Outcome Measure Grating visual acuity measured at 6 years of age by masked testers using Teller acuity cards.
Results Monocular grating acuity results were obtained from 317 of 370 surviving children (85.6%). Analysis of grating acuity results for all study participants with high-risk prethreshold ROP showed no statistically significant overall benefit of ET (18.1% vs 22.8% unfavorable outcomes; P = .08). When the 6-year grating acuity results were analyzed according to a clinical algorithm (high-risk types 1 and 2 prethreshold ROP), a benefit was seen in type 1 eyes (16.4% vs 25.2%; P = .004) undergoing ET, but not in type 2 eyes (21.3% vs 15.9%; P = .29).
Conclusion Early treatment of eyes with type 1 ROP improves grating acuity outcomes, but ET for eyes with type 2 ROP does not.
Application to Clinical Medicine Type 1 eyes should be treated early; however, based on acuity results at 6 years of age, type 2 eyes should be cautiously monitored for progression to type 1 ROP.
Trial Registration clinicaltrials.gov Identifier: NCT00027222
The Early Treatment for Retinopathy of Prematurity (ETROP) Study1 determined that eyes with high-risk prethreshold ROP would benefit from early peripheral retinal ablation compared with eyes undergoing conventional management (CM). Results of the study, based on assessment of recognition (letter) acuity with Early Treatment Diabetic Retinopathy Study (ETDRS) charts2 when children reached 6 years of age, indicated a benefit of early treatment (ET) in the subset of eyes that had high-risk type 1 ROP at the time of randomization, but not in eyes with high-risk type 2 ROP (Table 1).3
Although the primary ETROP outcome analysis was based on ETDRS recognition acuity at 6 years of age, which is the criterion standard for visual acuity assessment, not all ETROP Study participants had neurodevelopmental skills sufficient to perform a letter acuity task. The 6-year study examination also included assessment of grating (resolution) acuity using the Teller acuity card procedure.4,5 The purpose of the present report is to describe the results of assessment of grating acuity at 6 years of age in ETROP Study participants. Results of ET vs CM are compared for all study eyes (ie, all eyes with high-risk prethreshold ROP) and for eyes with type 1 and type 2 ROP.
From October 1, 2000, through September 30, 2002, 401 infants developed high-risk prethreshold ROP and entered the randomized trial. Entry into the study was based on the presence of prethreshold ROP and a risk of blindness of greater than or equal to 15% (high risk) as determined by a risk model (RM-ROP2) that was developed from an analysis of data from the Cryotherapy for Retinopathy of Prematurity Study.1 High-risk prethreshold ROP was noted in both eyes of 317 infants; these infants had one eye randomized to ET (at high-risk prethreshold ROP) and the other eye to CM, with treatment if ROP reached threshold severity. If high-risk prethreshold ROP developed in only 1 eye and the fellow eye had less than severe or no ROP, the high-risk eye was randomized to ET or to CM. This occurred in 84 infants. Details of the design of the ETROP Study6 and details of the model used to calculate whether an infant had high-risk ROP1 have been published elsewhere.
Study protocols were approved by the review boards of all participating institutions, and parents provided written informed consent for participation in the extended follow-up study to allow vision measurements through 6 years of age.
A tester who was masked to the treatment history and ocular status of each eye assessed each child's monocular grating acuity with the Teller acuity card procedure4,5,7-9 (Teller Acuity Cards II; Stereo Optical Company, Inc, Chicago, Illinois). The luminance of the cards was at least 10 candelas per square meter. Test distance was 84 cm but could be reduced to 55, 38, 19, or 9.5 cm for a child with low visual acuity. Testing was usually conducted with a Teller acuity card stage (Vistech Consultants, Inc, Dayton, Ohio), which provided a uniform field in which to display the cards. However, the stage was not used with children who had poor vision, for whom a close test distance was needed, or with children who had nystagmus, for whom the tester used vertical presentation of the cards to allow easier detection of the grating lines.8 The right eye was tested first, followed by the left eye. All eyes were tested with corrective lenses prescribed to meet study protocol criteria.3 Assessment of grating acuity was performed before cycloplegia.
The tester, who was masked to the location of the grating on each card, showed the acuity cards sequentially, starting with a card containing a coarse (2.4 cycles/cm) grating. The tester used the child's eye and head movements and/or the child's pointing behavior in response to repeated presentations of each card to decide whether the child could discriminate the location of the grating on the card. If the child did not give evidence of seeing the initial grating, the tester continued testing with a card containing a coarser grating. The tester proceeded to cards containing finer and finer gratings until the child no longer gave evidence of being able to resolve the grating.4,5 Based on the child's responses, the tester determined the highest spatial frequency (finest grating) that the child could resolve, which was recorded as the grating acuity score for that eye.
Children who could not resolve the coarsest standard acuity card grating (0.32 cycles/cm) were tested with the low vision card, which has 2.2-cm-wide black-and-white stripes filling 1 side of the card. The tester was permitted to display the low vision card at any distance, orientation, or location in the child's visual field to determine whether the child had pattern vision in that eye.
Children were exempted from the visual acuity examination but not from data analysis if an ETROP Study–certified examiner and a parent agreed that both eyes had only light perception or worse vision and the child had bilateral retinal detachments, phthisis bulbi, or bilateral enucleations.
Data were included only if treatment for any amblyopia (judged by the examining ophthalmologist) had been prescribed for at least 4 weeks before the acuity test and if refractive error (measured by cycloplegic retinoscopy) had been measured and corrected within 3 months of the acuity test. Correction was required for myopia of at least 1.00 diopter (D), hyperopia of at least 4.00 D, or astigmatism of at least 1.50 D and for anisometropia of at least 1.50 D spherical equivalent or cylinder.
Grating acuity results were categorized as normal (≥13 cycles/degree), below normal (<13 cycles/degree and ≥6.4 cycles/degree), poor (measurable acuity <6.4 cycles/degree), or blind/low vision (only the ability to detect the 2.2-cm-wide stripes on the low vision acuity card at any distance and at any location in the visual field, light perception only, or no light perception). Furthermore, acuity results in the normal and below-normal categories were classified as favorable outcomes, and acuity results in the poor and blind/low vision categories were classified as unfavorable outcomes.
For statistical analysis, an adaptation of the Mantel-Haenszel χ2 procedure for matched pairs was used.10 This method allows data from children with bilateral disease to be combined with data from children with asymmetric disease. When analyzing only symmetric disease, the paired eyes were analyzed using the McNemar test for matched pairs.
Of the 401 randomized infants, 370 survived until 6 years of age (Figure 1), and 329 (88.9%) had grating acuity assessed (n = 317) or were exempted from acuity assessment owing to bilateral blindness (n = 12). A total of 329 children were included in the data analysis. Of these, 260 children had symmetric (bilateral) disease, and 69 had asymmetric disease. Grating acuity data were incomplete for 8 children with symmetric disease and 4 children with asymmetric disease.
The proportion of randomized eyes with unfavorable grating acuity at 6 years of age is shown in Table 2. Overall, 18.1% of ET high-risk prethreshold eyes and 22.8% of CM eyes had unfavorable outcomes, a difference that did not reach statistical significance (P = .08). Within-subject comparisons in the children with bilateral disease showed that there were 30 children with favorable outcomes in their ET eyes and unfavorable outcomes in their CM eyes (discordant pairs), and 17 children with unfavorable outcomes in ET eyes and favorable outcomes in CM eyes. This difference approached but did not reach statistical significance (P = .06). Figure 2 provides the distribution of 6-year grating acuity outcomes by treatment assignment for randomized eyes.
We analyzed the grating acuity data using type 1 and type 2 categories, as proposed in the initial publication of ETROP Study results,11 and our results are shown in Table 3 for eyes that were high risk based on the RM-ROP2 algorithm.1 Type 1 high-risk prethreshold eyes receiving ET had a significantly lower rate of unfavorable outcomes (16.4%) than did type 1 eyes receiving CM (25.2%) (P = .004). In contrast, type 2 eyes that were high risk showed a higher, but not statistically different, percentage of unfavorable outcomes with ET (21.3%) than CM eyes (15.9%) (P = .29).
Figure 3 shows the distribution of grating acuity scores for eyes that had high-risk prethreshold ROP. Results are shown for ET and CM type 1 (Figure 3A) and type 2 (Figure 3B) eyes. The data clearly indicate that there is a benefit of early treatment in type 1 eyes but not in type 2 eyes.
Table 4 presents the discordant pairs for grating acuity outcome at 6 years of age for subgroups of children with bilateral high-risk prethreshold ROP by International Classification of ROP12 category, RM-ROP2 risk, and types 1 and 2 disease. The greatest benefit of ET was seen in eyes with zone I, stage 3, with or without plus disease. The benefit of ET was observed for all risk categories but was most pronounced in children with 30% to less than 45% risk for unfavorable outcome. This analysis also shows a significant benefit of ET for eyes with type 1 disease, but not for eyes with type 2 disease.
The results of grating acuity assessment of ET vs CM eyes with high-risk prethreshold ROP at 6 years of age in the ETROP Study are consistent with the results of ETDRS recognition acuity assessment at 6 years,3 indicating a clear benefit of ET in eyes with type 1 high-risk prethreshold ROP, but not in eyes with type 2 high-risk prethreshold ROP. In eyes with type 1 ROP, the rate of unfavorable grating acuity outcomes (ie, grating acuity <6.4 cycles/degree) was 16.4% in ET eyes compared with 25.2% in CM eyes (P = .004). In contrast, the rate of unfavorable outcomes in eyes with type 2 high-risk prethreshold ROP was greater in ET compared with CM eyes (21.3% vs 15.9%).
The original design of the ETROP Study involved randomization of high-risk prethreshold eyes to ET or CM. The study showed a clear benefit for ET among high-risk prethreshold eyes.3 We also identified in 2003 that eyes could be segregated into 2 types according to the International Classification of ROP characteristics. Eyes with type 1 characteristics should receive ET and eyes with type 2 characteristics could be observed and treated if progression to type 1 occurred (Table 1). Most type 2 eyes have ROP that regresses and does not require treatment. The results for grating acuity at 6 years of age support these earlier recommendations. The results for grating acuity also are consistent with those reported for ETDRS acuity (optotype acuity) at 6 years of age. However, these grating acuity results differ from the grating acuity results at 9 months of age when a statistically significant difference was noted between ET and CM eyes.11 This is most likely due to dramatic visual development that occurs in the young child and the ability to detect more subtle differences at the older age.
The present report has strengths and limitations. The first strength is that grating acuity data could be obtained from nearly all study eyes. Only 10 of 298 ET eyes (3.4%) and 10 of 291 CM eyes (3.4%) had no grating acuity score available. A second strength of the present study is the masking of the visual acuity testers to the treatment status and the current retinal status of each eye. A final strength is the high follow-up rate (342 patients [92.4%]), 6 years after their enrollment in the study, for the 370 surviving study participants. A disadvantage of assessment of grating acuity is that, in certain conditions that reduce optotype acuity (eg, amblyopia,13 age-related maculopathy,14 and retinal residua of ROP15), grating acuity results may underestimate the loss in optotype acuity.
In conclusion, the grating acuity results at 6 years of age in children enrolled in the ETROP Study show an enduring benefit for early treatment for most eyes with ROP. However, this benefit exists only for eyes with type 1 disease. Looking at all eyes in the study, early treatment did not reach statistical significance when grating acuity was assessed but, when eyes were distinguished by type 1 or 2 characteristics, type 1 eyes showed a significant benefit for grating acuity outcome and type 2 eyes did not. This finding supports the ETDRS acuity outcome results,3 making careful observation and identification of the International Classification of ROP characteristics even more important as one contemplates whether laser ablation should be performed.
Correspondence: Graham E. Quinn, MD, MSCE, Pediatric Ophthalmology, Wood Center, First Floor, The Children's Hospital of Philadelphia, Philadelphia, PA 19104.
Submitted for Publication: September 9, 2010; final revision received January 6, 2011; accepted January 10, 2011.
Reprint Requests: William V. Good, MD, Smith-Kettlewell Eye Research Institute, 2318 Fillmore St, San Francisco, CA 94115.
Financial Disclosure: Velma Dobson, PhD, has received royalties from the sale of Teller acuity cards.
Funding/Support: This study was supported by cooperative agreements 5U10 EY12471 and 5U10 EY12472 with the National Eye Institute of the National Institutes of Health, US Department of Health and Human Services.
Velma Dobson, PhD (chair); Graham E. Quinn, MD, MSCE; C. Gail Summers, MD; Robert J. Hardy, PhD; Betty Tung, MS; William V. Good, MD.
Stanford Center, Palo Alto, California
Lucille Packard Children's Hospital, Stanford University: Ashima Madan, MD (principal investigator); M. Bethany Ball, BS, and Judith Y. Hall, RNC (study center coordinators); and William V. Good, MD (coinvestigator).
San Francisco Center, San Francisco, California
California Pacific Medical Center, Oakland Children's Hospital, University of California, San Francisco Medical Center: William V. Good, MD (principal investigator); Judith Gancasz (study center coordinator); and David Durand, MD, Terri Slagle, MD, and Gordon Smith, MD (coinvestigators).
Chicago Center, Chicago, Illinois
University of Illinois at Chicago Hospital and Medical Center: Michael Shapiro, MD (principal investigator); Nydia Santiago (study center coordinator); and Rama Bhat, MD, Lawrence Kaufman, MD, Marilyn Miller, MD, and David Mittelman, MD (coinvestigators).
Indianapolis Center, Indianapolis, Indiana
Indiana University School of Medicine, James Whitcomb Riley Hospital for Children, Indiana University Hospital, Wishard Memorial Hospital, Methodist Hospital, Community Hospitals of Indianapolis: Daniel Neely, MD (principal investigator); Elizabeth A. Hynes, RN (study center coordinator); and David Plager, MD (coinvestigator).
Louisville Center, Louisville, Kentucky
Kosair Children's Hospital, University of Louisville Hospital: Charles C. Barr, MD (principal investigator); Michelle Bottorff (study center coordinator); and Greg K. Whittington, PsyS, Peggy H. Fishman, MD, and Paul J. Rychwalski, MD (coinvestigators).
New Orleans Center, New Orleans, Louisiana
Tulane University Medical Center, Medical Center of Louisiana at New Orleans: Robert A. Gordon, MD (principal investigator); Deborah S. Neff, LPN (study center coordinator); and James G. Diamond, MD, and William L. Gill, MD (coinvestigators).
Baltimore G Center, Baltimore, Maryland
University of Maryland Medical Systems, Mercy Medical Center, Franklin Square Hospital: Mark W. Preslan, MD (principal investigator); Kevin Powdrill (study center coordinator); and Kelly A. Hutcheson, MD, Eric Jones, MD, Scott M. Steidl, MD, DMA, and Joanne Marie Waeltermann, MD (coinvestigators).
Baltimore R Center
Johns Hopkins Hospital, Johns Hopkins Bayview Medical Center, Howard County General Hospital, Greater Baltimore Medical Center, St Joseph Medical Center: Michael X. Repka, MD (principal investigator); Jennifer A. Shepard, NNP, and Pamela Donahue, PA-C, ScD (study center coordinators); and Susan W. Aucott, MD, Mary Louise Z. Collins, MD, Maureen M. Gilmore, MD, and James T. Handa, MD (coinvestigators).
Boston Center, Boston, Massachusetts
Beth Israel Deaconess Medical Center, Children's Hospital Boston, New England Medical Center, Brigham and Women's Hospital: Deborah K. VanderVeen, MD (principal investigator); Theresa Mansfield, RN, and Brenda MacKinnon, RNC (study center coordinators); Cynthia H. Cole, MD, MPH, Anthony Fraioli, MD, David Hunter, MD, O’Ine McCabe, MD, Robert Petersen, MD, and Mitchell Brent Strominger, MD (coinvestigators); and Sarah MacKinnon, OC(C), COMT, Rhiannon Johnson, OC(C), and Mariette Tyedmers, CO (orthoptists).
Detroit Center, Detroit, Michigan
William Beaumont Hospital, Children's Hospital of Michigan, St John's Hospital Detroit: John Baker, MD (principal investigator); Kristi Cumming, MSN, and Pat Manatrey, RN (study center coordinators); and Mary P. Bedard, MD, Renato Casabar, MD, Antonio Capone, MD, Edward O’Malley, MD, Rajesh Rao, MD, John Roarty, MD, Michael Trese, MD, and George Williams, MD (coinvestigators).
Minneapolis Center, Minneapolis, Minnesota
Fairview University Medical Center, Children's Health Care, Minneapolis, Hennepin County Medical Center: C. Gail Summers, MD (principal investigator); Sally Cook, BA, Ann Holleschau, BA, and Molly Maxwell, RN (study center coordinators); and Stephen P. Christiansen, MD, and David Brasel, MD (coinvestigators).
St Louis Center, St Louis, Missouri
Cardinal Glennon Children's Medical Center, St Mary's Health Center: Bradley V. Davitt, MD (principal investigator); Linda Breuer, LPN (study center coordinator); and Oscar Cruz, MD, William Keenan, MD, Greg Mantych, MD, and Gregg Lueder, MD (coinvestigators).
North Carolina Center, Durham, North Carolina
Duke University Medical Center: Sharon Freedman, MD (principal investigator); David Wallace, MD, MPH (coprincipal investigator); Lori Hutchins Parkman, RN, and Sarah K. Jones (study center coordinators); and Laura Enyedi, MD, and Ricki F. Goldstein, MD (coinvestigators).
Buffalo Center, Buffalo, New York
Women's and Children's Hospital of Buffalo, Sisters of Charity Hospital: James D. Reynolds, MD (principal investigator); Kristine Ziemann, RN, BSN (study center coordinator); and George P. Albert, MD, Steven Awner, MD, and Rita Ryan, MD (coinvestigators).
Long Island/Westchester Center, Westchester, New York
Stony Brook University Hospital, Westchester Medical Center: Pamela Ann Weber, MD (principal investigator); Marc Horowitz, MD (coprincipal investigator); Cherylene Behrendt, Adriann Combs, and Natalie Dweck, RN (study center coordinators); and Richard Koty, MD, Edmund LaGamma, MD, and Maury Marmor, MD (coinvestigators).
New York Center, New York, New York
New York Presbyterian Hospital, Columbia and Cornell Campus: John Flynn, MD (principal investigator); Osode Coki, RNC, BSN (study center coordinator); and Michael Chiang, MD, MPH, Steven Kane, MD, Alfred Krauss, MD, Thomas C. Lee, MD, PhD, Robert F. Lopez, MD, and Richard Polin, MD (coinvestigators).
Rochester/Syracuse Center, Rochester, New York
University of Rochester Medical Center, Crouse-Irving Memorial Hospital: Dale L. Phelps, MD (principal investigator); Cassandra Horihan, MS, and Jane Phillips (study center coordinators); and Gary Markowitz, MD, Walter Merriam, MD, Leon-Paul Noel, MD, Donald Tingley, MD, and Matthew Gearinger, MD (coinvestigators).
Columbus Center, Columbus, Ohio
Nationwide Children's Hospital: Gary L. Rogers, MD (principal investigator); Don Bremer, MD (coprincipal investigator); Rae Fellows, MEd, and Sharon Klamfoth, LPN (study center coordinators); and Brian Arthur, MD, Cybil Bean Cassady, MD, Richard Golden, MD, and Mary Lou McGregor, MD (coinvestigators).
Oklahoma City Center, Oklahoma City, Oklahoma
University of Oklahoma Health Sciences Center, Dean A. McGee Eye Institute: R. Michael Siatkowski, MD (principal investigator); Cheryl Harris, COA, and Vanessa Yazdanipanah (study center coordinators); and Reagan H. Bradford, MD, Robert E. Leonard, MD, and Mary Anne McCaffree, MD (coinvestigators).
Portland Center, Portland, Oregon
Doernbecher Children's Hospital at Oregon Health and Science University: David T. Wheeler, MD (principal investigator); Nancy Dolphin, RN (study center coordinator); and Earl A. Palmer, MD, Ann Stout, MD, Brian Nichols, MD, and David Epley, MD (coinvestigators).
Philadelphia Center, Philadelphia, Pennsylvania
The Children's Hospital of Philadelphia, The Hospital of the University of Pennsylvania, Pennsylvania Hospital: Graham E. Quinn, MD, MSCE (principal investigator); Jamie G. Koh, RN, MSN, CCRC, and Marianne Letterio, RN, BSN (study center coordinators); and Soraya Abbasi, MD, Jane C. Edmond, MD, Brian J. Forbes, MD, PhD, Albert M. Maguire, MD, Monte D. Mills, MD, Eric A. Pierce, MD, Terri L. Young, MD, and Stephanie Davidson, MD (coinvestigators).
Pittsburgh Center, Pittsburgh, Pennsylvania
Magee-Women's Hospital: Kenneth Cheng, MD (principal investigator); Janice Kelchner-Cheng, RN, and Judith Jones, RNC, BSN (study center coordinators); and Robert Bergren, MD, Bernard Doft, MD, Louis Lobes, MD, and Karl Olsen, MD (coinvestigators).
Charleston Center, Charleston, South Carolina
Medical University of South Carolina: Richard A. Saunders, MD (principal investigator); Dilip Purohit, MD (coprincipal investigator); Linda Stevens, RN (study center coordinator); and Kimberly Lenhart (vision tester).
Houston Center, Houston, Texas
Baylor College of Medicine, Texas Children's Hospital, The Woman's Hospital of Texas, Ben Taub General Hospital: David K. Coats, MD (principal investigator); Michele L. Parker, COA, Maria Castanes, MPH, and Alison Brown (study center coordinators); and Jane Edmond, MD, Joseph Garcia-Prats, MD, Eric Holz, MD, W. Scott Jarriel, MD, Karen Johnson, MD, George Mandy, MD, Evelyn A. Paysee, MD, A. Melinda Rainey, MD, Paul G. Steinkuller, MD, and Kimberly G. Yen, MD (coinvestigators).
San Antonio Center, San Antonio, Texas
University of Texas Health Science Center, University Hospital, Christus Santa Rosa Children's Hospital: John P. Stokes, MD (principal investigator); Yolanda Trigo, COT (study center coordinator); and Alice K. Gong, MD, and W. A. J. van Heuven, MD (coinvestigators).
Salt Lake City Center, Salt Lake City, Utah
University of Utah Health Science Center, Primary Children's Medical Center: Robert Hoffman, MD (principal investigator); Susan Bracken, RN, and Deborah Y. Harrison, MS (study center coordinators); and Paul Bernstein, MD, Jerald King, MD, and Michael Teske, MD (coinvestigators).
National Eye Institute, Bethesda, Maryland: Maryann Redford, DDS, MPH (June 2001 to present); Richard L. Mowery, PhD (October 2000 to May 2001); and Donald F. Everett, MA (September 1999 to September 2000).
Smith-Kettlewell Eye Research Institute, San Francisco, California: William V. Good, MD (principal investigator); and Michelle Quintos, BA (project coordinator).
School of Public Health, Coordinating Center for Clinical Trials, University of Texas Health Science Center, Houston: Robert J. Hardy, PhD (principal investigator); Betty Tung, MS (coinvestigator); and Gordon Tsai, MS (coordinating center staff).
Vision Testing Center
University of Arizona College of Medicine, Tucson: Velma Dobson, PhD (principal investigator); Deborah D. Hargadon and Jeffrey Wood (vision testers); and Graham E. Quinn, MD, and Erin M. Harvey, PhD (coinvestigators).
Data and Safety Monitoring Committee
John Connett, PhD (chair); Edward F. Donovan, MD, Argye Hillis, PhD, Jonathan M. Holmes, MD, Joseph M. Miller, MD, and Carol R. Taylor, RN, CSFN, PhD (members); and William V. Good, MD, Robert J. Hardy, PhD, and Maryann Redford, DDS, MPH (ex-officio members).
Permanent members: William V. Good, MD (chair), Robert J. Hardy, PhD, Velma Dobson, PhD, Earl A. Palmer, MD, Dale L. Phelps, MD, and Maryann Redford, DDS, MPH. Elected members: W. A. J. van Heuven, MD (2000-2001 and 2004-2007); Charles Barr, MD (2001-2002); Michael Gaynon, MD (2002-2003); Michael Shapiro, MD (2003-2004); David Wallace, MD (2007-2008); Bradley V. Davitt, MD (2008 to present); Rae Fellows, MEd (2000-2001 and 2006 to present); Judith Jones, RNC, BSN (2001-2002); Kristi Cumming, MSN (2002-2003); Deborah S. Neff, LPN (2003-2004); Jennifer A. Shepard, NNP (2004-2006); and Nancy Dolphin, RN (2006 to present).
William V. Good, MD (chair), Robert J. Hardy, PhD, Velma Dobson, PhD, Earl A. Palmer, MD, Dale L. Phelps, MD, Michelle Quintos, BA, and Betty Tung, MS.
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