Vision in Children Ages 6 Months to 5 Years: Screening
September 05, 2017
Recommendations made by the USPSTF are independent of the U.S. government. They should not be construed as an official position of the Agency for Healthcare Research and Quality or the U.S. Department of Health and Human Services.
By Daniel E. Jonas, MD, MPH; Halle R. Amick, MSPH; Ina F. Wallace, PhD; Cynthia Feltner, MD, MPH; Emily B. Vander Schaaf, MD, MPH; Callie L. Brown, MD, MPH; and Claire Baker
The information in this article is intended to help clinicians, employers, policymakers, and others make informed decisions about the provision of health care services. This article is intended as a reference and not as a substitute for clinical judgment.
This article may be used, in whole or in part, as the basis for the development of clinical practice guidelines and other quality enhancement tools, or as a basis for reimbursement and coverage policies. AHRQ or U.S. Department of Health and Human Services endorsement of such derivative products may not be stated or implied.
This article was first published in JAMA on September 5, 2017.
Importance: Preschool vision screening could allow detection and treatment of vision abnormalities during a critical developmental stage, preserving function and quality of life.
Objective: To review the evidence on screening for and treatment of amblyopia, its risk factors, and refractive error in children aged 6 months to 5 years to inform the US Preventive Services Task Force.
Data Sources: MEDLINE, Cochrane Library, CINAHL, and trial registries through June 2016; references; and experts, with surveillance of the literature through June 7, 2017.
Study Selection: English-language randomized clinical trials (RCTs) or prospective cohort studies that evaluated screening, studies evaluating test accuracy, RCTs of treatment vs inactive controls, and cohort studies or case-control studies assessing harms.
Data Extraction and Synthesis: Dual review of abstracts, full-text articles, and study quality; qualitative synthesis of findings. Studies were not quantitatively pooled because of clinical and methodological heterogeneity.
Main Outcomes and Measures: Visual acuity, amblyopia, school performance, functioning, quality of life, test accuracy, testability, and harms.
Results: Forty studies were included (N = 34,709); 34 evaluated test accuracy. No RCTs compared screening with no screening, and no studies evaluated school performance, function, or quality of life. Studies directly assessing earlier or more intensive screening were limited by high attrition. Positive likelihood ratios were between 5 and 10 for amblyopia risk factors or nonamblyogenic refractive error in most studies of test accuracy and were greater than 10 in most studies evaluating combinations of clinical tests. Inability to cooperate may limit use of some tests in children younger than 3 years. Studies with low prevalence (<10%) of vision abnormalities showed high false-positive rates (usually >75%). Among children with amblyopia risk factors (eg, strabismus or anisometropia), patching improved visual acuity of the amblyopic eye by a mean of less than 1 line on a standard chart after 5 to 12 weeks for children pretreated with glasses (2 RCTs, 240 participants); more children treated with patching than with no patching experienced improvement of at least 2 lines (45% vs 21%; P = 0.003; 1 RCT, 180 participants). Patching plus glasses improved visual acuity by about 1 line after 1 year (0.11 logMAR [95% CI, 0.05-0.17]) for children not pretreated with glasses (1 RCT, 177 participants). Glasses alone improved visual acuity by less than 1 line after 1 year (0.08 logMAR [95% CI, 0.02-0.15], 1 RCT, 177 participants).
Conclusions and Relevance: Studies directly evaluating the effectiveness of screening were limited and do not establish whether vision screening in preschool children is better than no screening. Indirect evidence supports the utility of multiple screening tests for identifying preschool children at higher risk for vision problems and the effectiveness of some treatments for improving visual acuity outcomes.
The most common causes of vision problems in children are amblyopia (a neurodevelopmental disorder that arises from abnormal processing of visual images that leads to a functional reduction of visual acuity) and its associated risk factors (Table 1), nonamblyopic strabismus and nonamblyopic refractive error.9-12 Recent prevalence estimates of amblyopia, strabismus, and anisometropia (a difference in refractive power between the eyes, in which one foveal image is more blurred than the other) among US children younger than 6 years range from 1% to 6%.12-16
A variety of vision screening tools are available to evaluate children (Table 2). Left untreated, vision abnormalities in young children could lead to problems at school, bullying, reduced function and quality of life, depression and anxiety, and injuries. Vision abnormalities are often treatable, but efficacy can decrease as children age, and visual loss can become irreversible.20-24 Untreated amblyopia rarely resolves spontaneously.25,26
In 2011, the US Preventive Services Task Force (USPSTF) recommended screening children to detect amblyopia or its risk factors at least once between the ages of 3 to 5 years (B recommendation) and concluded that the evidence was insufficient to assess the balance of benefits and harms of vision screening for children younger than 3 years (I statement). To inform an updated recommendation, a review was undertaken of the evidence on benefits and harms of vision screening in children; screening test accuracy; and benefits and harms of treatment of amblyopia, its risk factors, and refractive error.
Scope of Review
Detailed methods and additional details of results and analyses are reported in the full evidence report. Figure 1 shows the analytic framework and key questions (KQs) that guided the review.
Data Sources and Searches
PubMed/MEDLINE, the Cochrane Library, and the Cumulative Index to Nursing and Allied Health Literature (CINAHL) were searched for English-language articles published from January 2009 through June 2016. Search strategies are listed in the eMethods in the Supplement. To identify relevant studies published before 2009, all articles included in the 2011 systematic review for the USPSTF were assessed.28-30 ClinicalTrials.gov and the World Health Organization International Clinical Trials Registry platform were searched for unpublished literature. To supplement electronic searches, the reference lists of pertinent articles, all studies suggested by reviewers, and comments received during public commenting periods were reviewed. Since June 2016, ongoing surveillance was conducted through article alerts and targeted searches of high-impact journals to identify major studies published in the interim that may affect the conclusions or understanding of the evidence and therefore the related USPSTF recommendation. The last surveillance was conducted on June 7, 2017.
Two investigators independently reviewed titles, abstracts, and full-text articles to determine eligibility using prespecified criteria for each KQ (eTable 1 in the Supplement). Disagreements were resolved by discussion. The review included English-language studies of children aged 6 months to 5 years conducted in countries categorized as “very high” on the United Nations Human Development Index. Only studies rated as good or fair quality were included.
Data Extraction and Quality Assessment
For each included study, 1 investigator extracted pertinent information about the populations, tests or treatments, comparators, outcomes, settings, and designs, and a second investigator reviewed for completeness and accuracy. To provide a consistent metric for visual acuity outcome measures, results were converted to logarithm of the minimal angle of resolution (logMAR) measurements using established conversion charts.31 Measures of visual acuity are generally reported as Snellen (eg, 20/20, 20/25, 20/30, 20/40, 20/50) or logMAR scales (eg, 0.00, 0.09, 0.18, 0.30, 0.40). Two independent investigators assessed the quality of studies as good, fair, or poor, using predefined criteria developed by the USPSTF and adapted for this topic (eTables 2-5 in the Supplement).32 Disagreements were resolved by discussion. Individual study quality ratings are reported in the Supplement (eTables 2-5).
Data Synthesis and Analysis
Findings for each question were summarized in tabular and narrative format. Results of test accuracy studies were not quantitatively pooled because of considerable clinical and methodological heterogeneity (eg, different tests, target condition definitions, populations, and results), and there were too few treatment trials making similar comparisons to attempt quantitative synthesis.
For KQ2, sensitivities, specificities, likelihood ratios (LRs), and predictive values were calculated when articles reported sufficient data. When qualitatively evaluating LRs, positive LRs indicated a minimal (>1-2), small (>2-5), moderate (>5-10), or large (>10) increase in the risk of the condition of interest (eg, amblyopia or its risk factors). Negative LRs indicated a minimal (0.5 to <1), small (0.2 to <0.5), moderate (0.1 to <0.2), or large (<0.1) decrease in the risk of the condition of interest. Likelihood ratios less than 0.1 or greater than 10 provide strong evidence for ruling out (negative LR <0.1) or ruling in (positive LR >10) diagnoses.33,34
Definitions for what constitutes a minimal clinically important change in visual acuity in young children vary across studies. Recent studies consider a change of 0.2 logMAR (about 2 lines on the Snellen chart) the minimal clinically important change.35-39 Others consider smaller changes clinically meaningful, generally between 0.10 logMAR (about 1 line on the Snellen chart) and 0.15 logMAR (between 1 and 2 lines).40-42 Large treatment studies have calculated sample size requirements based on the ability to detect a change of at least 0.1 logMAR between treatment groups.43-46 When assessing whether improvement in visual acuity represents a clinically meaningful change, practitioners may also consider that visual impairment associated with amblyopia can become permanent and may limit function for the child’s lifetime.23,47
The overall strength of the body of evidence was assessed for each KQ as high, moderate, low, or insufficient using methods developed for the USPSTF (and the Evidence-based Practice Center program29,30), based on the overall quality of studies, consistency of results between studies, precision of findings, and risk of reporting bias.
Benefits of Screening
Key Question 1. Does screening for amblyopia, its risk factors, and refractive error in children aged 6 months to 5 years reduce long-term amblyopia or improve visual acuity, school performance, functioning, and/or quality of life?
Key Question 1a. Does the effectiveness of screening in children aged 6 months to 5 years vary among different age groups?
One randomized clinical trial (RCT)86,89 and 1 cohort study90 enrolling children from the Avon Longitudinal Study of Parents and Children (ALSPAC) project were included (Table 3). The ALSPAC project is a geographically-defined birth cohort study enrolling 14,000 children born in southwest England between April 1991 and December 1992.86 Both studies reported prevalence of amblyopia at age 7.5 years; neither evaluated school performance, function, or quality of life outcomes. The major methodological shortcoming in both studies was high attrition; around half of children did not have results and were excluded from analyses. In addition, the method of randomization in the (self-described) RCT was inadequate (based on last digit of the mother’s day of birth).86,89
The RCT (n = 3490) compared intensive orthoptist screening (clinical examination, age-specific visual acuity testing, and cover-uncover testing) before age 3 years (at 8, 12, 18, 25, 31, and 37 months) with 1-time orthoptist screening at age 37 months.86,89 Baseline data for amblyopia or amblyopia risk factors were not reported. Children in both groups were offered “usual care” in terms of surveillance for visual problems: (1) examination at ages 8 and 18 months by a health visitor (community pediatric nurse), with referrals if a visual problem was suspected86; and (2) visual screening at school entry (ages 4-5 years) by a school nurse.89 The prevalence of amblyopia at 7.5 years was approximately 1% lower in the intensive screening group than in the control group, but the difference was statistically significant for only 1 of their 2 definitions of amblyopia (Table 3).89 Among those who received patching treatment (n = 40 in each group), presence of residual amblyopia at 7.5 years was more likely in the 1-time screening group than in the intensive-screening group, but the difference was statistically significant for only 1 of the 2 amblyopia definitions, and estimates were imprecise; visual acuity at 7.5 years in the worse eye was better in the intensive-screening group than in the 1-time screening group (Table 3).89
The prospective cohort study (n = 6081 completers) compared orthoptist screening at age 3 years in 1 health district with no preschool screening in 2 other health districts.90 Screening examinations by the orthoptist consisted of a monocular vision test, a cover test, and an assessment of binocularity; failure of any part of the examination resulted in referral for further evaluation. All children in the study area were offered vision screening at school entry (ages 4-5 years).90 Among participants who attended the examination at age 7.5 years and were not part of the ALSPAC RCT, no statistically significant differences in amblyopia were apparent between groups based on any of the studies’ 3 definitions of amblyopia (Table 3).90
Accuracy of Screening Tests
Key Question 2. What is the accuracy and reliability of screening tests for amblyopia, its risk factors, and refractive error in children aged 6 months to 5 years?
Thirty-four fair-quality studies (described in 38 articles) were included (eTables 6-17 in the Supplement).48,49,51-62,64-85,88,91 The studies evaluated a variety of test types, including visual acuity tests, stereoacuity tests, ocular alignment tests, autorefractors, photoscreeners, and retinal birefringence scanning. Screening was administered by a variety of personnel across studies (eg, pediatricians, ophthalmologists, nurses, research staff). Sample sizes ranged from 6375 to 4040.70,91
About one-third of the studies included participants younger than 3 years.48,56,65,66,71,72,75,77,80,81,85,88,91 The included studies reported accuracy of tests for a variety of target conditions, ranging from very specific (eg, astigmatism) to broad (eg, amblyopia risk factors). The prevalence of target conditions was generally much higher in samples from ophthalmology clinics53,56,57,62,66,68,69,72,75,77,80,81,85,88 than in those from primary care, community, Head Start, or school settings.
Findings from the Vision In Preschoolers (VIP) study, the largest study for this KQ, were reported in multiple manuscripts (up to 4040 participants).55,60,64,70,78,82,84,91 Phase 1 of the VIP study enrolled 3- to 5-year-olds and compared the accuracy of 11 screening tests.78 Phase 2 compared the performance of nurse screeners with that of lay screeners for 4 tests.84 Unlike many of the included studies, the VIP study evaluated accuracy for a broad range of conditions, including significant nonamblyogenic refractive error. The applicability of the VIP study may be limited because it did not enroll a representative spectrum of patients (as demonstrated by the high prevalence of target conditions, ranging from 21%-36%), study participants may have experienced fatigue from the number of tests, and testing was conducted by skilled personnel in a controlled environment (in phase 1).
Detailed results of studies evaluating test accuracy are provided in the eResults and eTables 6 through 17 in the Supplement. Six publications evaluated visual acuity tests,53,73,74,78,82,84 including 3 from the VIP Study Group.78,82,84 When screening test cutoffs were set to achieve specificities of 90%, phase 1 of the VIP study found that an abnormal result moderately increased the likelihood of amblyopia, amblyopia risk factors (strabismus, astigmatism, hyperopia, myopia, anisometropia), or significant nonamblyogenic refractive error (positive LR, 6.1 [95% CI, 4.8-7.6]).78 A normal result indicated a small decrease in the likelihood (negative LR, 0.43 [95% CI, 0.38-0.50]).
Four fair-quality studies (total, 1854 participants) evaluated a combination of clinical tests, including visual acuity tests, stereoacuity tests, and ocular alignment tests (eTables 6-7 in the Supplement).52,54,67,80 Three of the 4 found that abnormal results indicated a large increase in the likelihood of amblyopia or its risk factors (positive LRs ranged from 12-17).52,67,80 The 4 studies found more variability for negative LRs (range, 0.10-0.91).
Sixteen fair-quality studies (16,712 observations) evaluated autorefractors (eTables 6-17 in the Supplement).49,51,55,57,58,65,66,70,72,74,77,78,84,88,91 Overall, most studies found moderate positive LRs and small negative LRs, although some found large positive and negative LRs.
Eleven fair-quality studies (12 publications, 6187 observations) evaluated photoscreeners (eTables 6-15 in the Supplement).56,59,67-69,73,75,78,81,85 Overall, most studies found moderate positive LRs and small negative LRs, although some found larger or smaller LRs.
Key Question 2a. Does the accuracy or reliability of screening tests for amblyopia, its risk factors, and refractive error vary among different age groups?
Five studies evaluated whether accuracy varies by age (eTable 13 in the Supplement).54,66,69,81,82 All 5 evaluated different screening tests and assessed different age stratifications/comparisons. Overall, data were limited and estimates were somewhat imprecise, but studies did not find any clear differences in test accuracy when results were stratified by age.
Many included studies reported testability information, although few reported data stratified by age or for children younger than 3 years. eTable 14 in the Supplement details the proportion unexaminable reported by studies. Overall, testability exceeded 90% in the majority of studies. Few studies reported testability rates less than 80%, but all that did included children younger than 3 years.48,66,71,77 Some studies demonstrated that testability rates improved somewhat as children age.53,66,71,77,78,80 One study (n = 1170) found that testability rates were 10% for a visual acuity test at ages 24 months to younger than 30 months and steadily improved to 80% by ages 36 months to younger than 42 months and to 95% by ages 48 months to younger than 54 months.71
For autorefractors and photoscreeners, the VIP study found testability rates close to 100% (all participants were 3 years or older).78 Two studies from ophthalmology clinics and 1 from a primary care practice reported better testability for older preschool children than for younger ones (eResults in the Supplement).65,66,77
Harms of Screening
Key Question 3. What are the harms of screening for amblyopia, its risk factors, and refractive error in children aged 6 months to 5 years?
One controlled study that evaluated potential psychosocial effects was included,87 and 16 studies of test accuracy described in KQ2 were used to calculate false-positive rates.48,51,52,55,62,65,67,69,75,78,80,82,85 The controlled study used the ALSPAC population-based cohort (n = 4473) to assess bullying by age 8 years.87 It prospectively compared children who had been offered state-provided preschool screening for amblyopia (at 37 months) with those who had not. Children were asked whether they had repeatedly (≥4 times a month) been bullied. Among the subgroup of patched children, the study showed a lower likelihood of being bullied for children offered screening than for those not offered early screening (25.7% vs 47.1%, P = 0.033; adjusted odds ratio, 0.39 [95% CI, 0.16-0.92], adjusted for sex, paternal socioeconomic class, highest level of maternal education, type of housing).
The most frequently assessed potential harms of screening were false-positive findings (which would lead to unnecessary referrals). In general, studies with a lower prevalence (<10%) of vision abnormalities showed much higher false-positive rates (usually >75%), while those with a high prevalence had lower false-positive rates (usually <35%) (eFigure in the Supplement).
Benefits of Treatment
Key Question 4a. Does treatment of amblyopia, its risk factors, and refractive error in children ages 6 months to 5 years improve visual acuity?
Key Question 4b. Does treatment of amblyopia, its risk factors, and refractive error in children ages 6 months to 5 years reduce long-term amblyopia or improve school performance, functioning, and/or quality of life?
Three trials were included (Table 4)40,44,50; all evaluated patching for amblyopia or amblyopic risk factors. Two compared patching with no patching (children were pretreated with eyeglasses if indicated in both groups),44,50 and 1 compared patching plus eyeglasses vs eyeglasses alone vs no treatment.40 One of the patching vs no patching trials included a run-in phase, during which all participants wore updated eyeglass prescriptions until visual acuity in the amblyopic eye stopped improving44; another trial treated children with refractive error with 6 weeks of corrective lenses before allocation.50 All 3 studies included children based on visual acuity criteria. One of the 3 trials reported enrolling screen-detected children.40 Two of the trials reported best corrected visual acuity,40,44 and 1 measured improvement in visual acuity as a secondary outcome (the trial focused primarily on assessing adherence).50
Overall, the trials indicated that treatments for amblyopia or its risk factors resulted in small mean improvements in visual acuity (Table 4). In the study with the run-in phase,44 patching improved visual acuity by a mean of 0.7 of a line on a standard visual acuity chart, and more children treated with patching than with no patching had at least 2 lines of improvement in acuity (45% vs 21%).
Two included trials40,44 examined treatment outcomes for subgroups defined by baseline visual acuity. First, 1 trial (n = 180) assessed subgroups with either moderate (20/40 to 20/100) or severe (20/125 to 20/400) amblyopia at baseline.44 Findings for these subgroups were similar to the overall trial results for the primary outcome, visual acuity in the amblyopic eye. Second, the trial that compared patching plus eyeglasses, eyeglasses alone, and no treatment among preschoolers (n = 177) assessed subgroups defined by baseline visual acuity abnormalities.40 The authors assessed children with mild (0.18-0.30 logMAR) and moderate or worse (≥0.48 logMAR) refractive error at baseline and examined differences between treatment groups. For children with moderate refractive error at baseline, patching plus eyeglasses resulted in much greater improvement than no treatment at 1 year (0.27 logMAR [95% CI, 0.14-0.39], compared with improvement for all participants of 0.11 logMAR [95% CI, 0.05-0.17]); the difference between eyeglasses alone and no treatment did not reach statistical significance. For children with mild refractive error at baseline, neither treatment was significantly different than no treatment at the end of the trial.
Harms of Treatment
Key Question 5. What are the harms of treatment of amblyopia, its risk factors, and refractive error in children aged 6 months to 5 years?
One trial comparing patching with no patching (n = 180) found that worsening visual acuity in the nonamblyopic eye was not significantly different between groups at 5 weeks (2.4% vs 6.8%, respectively; P = 0.28).44 Among children with no ocular deviation at baseline (n = 118), 5 patients in the patching group and 3 patients in the no-patching group were noted to have a new small-angle strabismus, and 1 patient in the no-patching group was noted to have a new large-angle strabismus.
The trial comparing patching plus eyeglasses, eyeglasses alone, and no treatment found no statistically significant difference between treatment groups at 1-year follow-up in the proportion of children whose uncorrected visual acuity in the amblyopic eye worsened (change >0.1 logMAR) for those with baseline mild acuity loss (9.7% vs 6.5% vs 13.3%, respectively, P = 0.28) or for those with baseline moderate acuity loss (15.0% vs 11.1% vs 23.8%, P = 0.13).40
A substudy63 of the trial40 that compared patching plus eyeglasses, eyeglasses alone, and no treatment examined the emotional status of children undergoing treatment; in the substudy, 144 of 177 parents of participants completed questionnaires at baseline (all participants), 3 months after beginning treatment (participants in active treatment only), and 2 years after recruitment (all participants). They found no significant differences between treatment groups with regard to being happy, cooperative, or good tempered; teasing; problems at preschool; or in emotional and behavioral problems, but found that children were more upset by patching plus eyeglasses than by eyeglasses alone (85% vs 29% at age 4 years, P = 0.03; 62% vs 26% at age 5 years, P = 0.005). Although the study reported some negative effects of glasses or patching for the child (difficulty wearing patch or glasses, upset, coping with treatment) and parent (worry about treatment, upset by treatments, arguments about treatment), it did not report a comparison with the no-treatment group for these outcomes.
One trial (n = 60) comparing no treatment, patching for 3 hours daily, or patching for 6 hours daily reported that no patients experienced an adverse event, such as inverse amblyopia or patch allergy.50
The summary of findings is presented in Table 5. No eligible RCTs directly compared screening with no screening. For the overarching question (KQ1), the strength of evidence was graded as low because of unknown consistency (with a single study making each comparison), imprecision, and methodological limitations. One cohort study showed a reduction in harm (ie, less school-aged bullying) among patched children screened in preschool compared with patched children not screened in preschool.87 In theory, although both glasses and patching have been reported to increase the risk of being bullied,92 preschool screening may allow for treatment before school starts, thus avoiding potential bullying and psychosocial distress.
Harms of preschool vision screening might include unnecessary referrals from false-positive screens, overdiagnosis, and unnecessary treatment. Studies of test accuracy show that screening tests are associated with high false-positive rates among populations with a low prevalence of vision abnormalities. A large (n = 102,508) retrospective study from a statewide photoscreening program found that 19.5% (174/890) of those with false-positive test results were prescribed glasses (ie, unnecessary treatments).93 The study was not eligible for this systematic review because it did not attempt to perform the reference standard in all participants or a random sample of participants.
Regarding test accuracy, estimates for all tests suggest utility for identifying children at higher risk for amblyopia risk factors or other visual conditions. Positive LRs were in the moderate range (>5-10) for most studies, and most studies that evaluated combinations of clinical tests found high (>10) positive LRs. The VIP study, the largest to directly compare multiple tests, generally found similar accuracy across tests. The strength of evidence was graded as low, because of imprecision and methodological limitations of the individual studies. Findings are applicable to a variety of settings and screening personnel.
Accuracy did not clearly differ for preschool children in different age groups. However, unlike studies of photoscreeners, most studies of clinical test accuracy did not enroll children younger than 3 years. Data were relatively limited and estimates were somewhat imprecise, but studies did not find any clear differences in accuracy of tests when results were stratified according to age. Testability may limit the utility of some screening tests, especially clinical tests, in children younger than 3 years. Although relatively few studies assessed changes in testability by age, those that did generally found better testability in children 3 years or older, and some reported low testability rates for visual acuity and stereoacuity tests for those younger than 3 years. In contrast, some data suggest that photoscreeners have high testability rates for children as young as 1 year.94
The review found evidence of moderate strength supporting the effectiveness of some treatments for improving visual acuity outcomes, although mean improvements were small. No studies evaluated potential effectiveness of treatments for reducing long-term amblyopia or for improving school performance, functioning, or quality of life, and no eligible studies evaluated atropine or vision therapy. The included trials all enrolled children 3 years or older, and applicability to those younger than 3 years is unclear. The trials varied somewhat in the populations (with amblyopic risk factors and pretreated with glasses or with amblyopic risk factors but not pretreated with glasses) and interventions compared (2 evaluated patching vs no patching; 1 compared patching plus glasses vs glasses alone vs no treatment). The trial that compared patching plus eyeglasses, eyeglasses alone, and no treatment enrolled screen-detected children, demonstrating the applicability of findings to the main population of interest for this review.40
Taken together, the treatment trials provide evidence of moderate strength that (1) patching improves visual acuity of the amblyopic eye by a mean of less than 1 line on an eye chart after 5 to 12 weeks compared with no patching for children with amblyopic risk factors pretreated with glasses, (2) patching plus glasses improves visual acuity by about 1 line after 1 year compared with no treatment for children with amblyopic risk factors not pretreated with glasses, and (3) glasses alone improve visual acuity by less than 1 line after 1 year compared with no treatment for children with amblyopic risk factors. The magnitude of improvement for patching plus glasses or glasses alone was greater for those with worse baseline visual acuity. Few of the trials reported binary outcomes that may help determine how many participants achieved a clinically meaningful change, although 1 trial reported that more children treated with patching than with no patching experienced improvement of at least 2 lines.44
The review has several limitations. First, for studies of test accuracy conducted in ophthalmology settings, details about the study participants were sometimes limited, making it difficult to determine whether participants had known impaired visual acuity or obvious symptoms of impaired visual acuity. Thus, the review may have included some studies that would not meet eligibility criteria if additional description of the study populations was available. Second, the review did not include comparative effectiveness (ie, head-to-head) studies, such as those comparing atropine with patching. The previous review for the USPSTF described head-to-head trials that compared different patching regimens (eg, 2-hour vs 6-hour patching), different atropine regimens (daily atropine vs weekend atropine), and patching with atropine.43,45,46,95-97 It concluded that the trials found no differences in visual acuity improvement in the amblyopic eye between the treatments. Third, studies published in languages other than English and those conducted in countries not categorized as "very high" on the Human Development Index were excluded.
Studies directly evaluating the effectiveness of screening were limited and do not establish whether vision screening in preschool children is better than no screening. Indirect evidence supports the utility of multiple screening tests for identifying preschool children at higher risk for vision problems and the effectiveness of some treatments for improving visual acuity outcomes.
Conflict of Interest Disclosures: All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest and none were reported.
Funding/Support: This research was funded under contract HHSA-290-2012-00015-I, Task Order 6, from the Agency for Healthcare Research and Quality (AHRQ), US Department of Health and Human Services, under a contract to support the USPSTF.
Role of the Funder/Sponsor: Investigators worked with USPSTF members and AHRQ staff to develop the scope, analytic framework, and key questions for this review. AHRQ had no role in study selection, quality assessment, or synthesis. AHRQ staff provided project oversight, reviewed the report to ensure that the analysis met methodological standards, and distributed the draft for peer review. Otherwise, AHRQ had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; and preparation, review, or approval of the manuscript findings. The opinions expressed in this document are those of the authors and do not reflect the official position of AHRQ or the US Department of Health and Human Services.
- Donahue SP, Arthur B, Neely DE, Arnold RW, Silbert D, Ruben JB; POS Vision Screening Committee. Guidelines for automated preschool vision screening: a 10-year, evidence-based update. J AAPOS. 2013;17(1):4-8.
- Doshi NR, Rodriguez ML. Amblyopia. Am Fam Physician. 2007;75(3):361-367.
- Pascual M, Huang J, Maguire MG, et al; Vision In Preschoolers (VIP) Study Group. Risk factors for amblyopia in the vision in preschoolers study. Ophthalmology. 2014;121(3):622-629.
- Ying GS, Huang J, Maguire MG, et al; Vision in Preschoolers Study Group. Associations of anisometropia with unilateral amblyopia, interocular acuity difference, and stereoacuity in preschoolers. Ophthalmology. 2013;120(3):495-503.
- Arnold RW. Amblyopia risk factor prevalence. J Pediatr Ophthalmol Strabismus. 2013;50(4):213-217.
- Pai AS, Rose KA, Leone JF, et al. Amblyopia prevalence and risk factors in Australian preschool children. Ophthalmology. 2012;119(1):138-144.
- Pai AS, Wang JJ, Samarawickrama C, et al. Prevalence and risk factors for visual impairment in preschool children: the Sydney Paediatric Eye Disease Study. Ophthalmology. 2011;118(8):1495-1500.
- Ciner EB, Schmidt PP, Orel-Bixler D, et al. Vision screening of preschool children: evaluating the past, looking toward the future. Optom Vis Sci. 1998;75(8):571-584.
- Mehravaran S, Duarte PB, Brown SI, Mondino BJ, Hendler K, Coleman AL. The UCLA preschool vision program, 2012-2013. J AAPOS. 2016;20(1):63-67.
- Griffith JF, Wilson R, Cimino HC, Patthoff M, Martin DF, Traboulsi EI. The use of a mobile van for school vision screening: results of 63 841 evaluations. Am J Ophthalmol. 2016;163:108-14.
- Tarczy-Hornoch K, Cotter SA, Borchert M, et al; Multi-Ethnic Pediatric Eye Disease Study Group. Prevalence and causes of visual impairment in Asian and non-Hispanic white preschool children: Multi-ethnic Pediatric Eye Disease Study. Ophthalmology. 2013;120(6):1220-1226.
- McKean-Cowdin R, Cotter SA, Tarczy-Hornoch K, et al; Multi-Ethnic Pediatric Eye Disease Study Group. Prevalence of amblyopia or strabismus in Asian and non-Hispanic white preschool children: Multi-Ethnic Pediatric Eye Disease Study. Ophthalmology. 2013;120(10):2117-2124.
- Friedman DS, Repka MX, Katz J, et al. Prevalence of amblyopia and strabismus in white and African American children aged 6 through 71 months the Baltimore Pediatric Eye Disease Study. Ophthalmology. 2009;116(11):2128-2134.
- Multi-Ethnic Pediatric Eye Disease Study (MEPEDS) Group. Prevalence and causes of visual impairment in African-American and Hispanic preschool children: the Multi-Ethnic Pediatric Eye Disease Study. Ophthalmology. 2009;116(10):1990-2000.
- Ying GS, Maguire MG, Cyert LA, et al; Vision In Preschoolers (VIP) Study Group. Prevalence of vision disorders by racial and ethnic group among children participating in head start. Ophthalmology. 2014;121(3):630-636.
- Donahue SP, Baker JD, Scott WE, et al. Lions Clubs International Foundation Core Four Photoscreening: results from 17 programs and 400,000 preschool children. J AAPOS. 2006;10(1):44-48.
- Leat SJ, Pierre JS, Hassan-Abadi S, Faubert J. The moving dynamic random dot stereosize test: development, age norms, and comparison with the Frisby, randot, and stereo smile tests. J Pediatr Ophthalmol Strabismus. 2001;38(5):284-294.
- Miller JM, Lessin HR; American Academy of Pediatrics Section on Ophthalmology; Committee on Practice and Ambulatory Medicine; American Academy of Ophthalmology; American Association for Pediatric Ophthalmology and Strabismus; American Association of Certified Orthoptists. Instrument-based pediatric vision screening policy statement. Pediatrics. 2012;130(5):983-986.
- Choong YF, Chen AH, Goh PP. A comparison of autorefraction and subjective refraction with and without cycloplegia in primary school children. Am J Ophthalmol. 2006;142(1):68-74.
- Epelbaum M, Milleret C, Buisseret P, Dufier JL. The sensitive period for strabismic amblyopia in humans. Ophthalmology. 1993;100(3):323-327.
- Flynn JT, Schiffman J, Feuer W, Corona A. The therapy of amblyopia: an analysis of the results of amblyopia therapy utilizing the pooled data of published studies. Trans Am Ophthalmol Soc. 1998;96:431-450.
- American Academy of Ophthalmology (AAO) Pediatric Ophthalmology/Strabismus Panel. Preferred practice pattern guidelines: amblyopia. https://www.aao.org. 2012. Accessed May 27, 2015.
- Rahi J, Logan S, Timms C, Russell-Eggitt I, Taylor D. Risk, causes, and outcomes of visual impairment after loss of vision in the non-amblyopic eye: a population-based study. Lancet. 2002;360(9333):597-602.
- van Leeuwen R, Eijkemans MJ, Vingerling JR, Hofman A, de Jong PT, Simonsz HJ. Risk of bilateral visual impairment in individuals with amblyopia: the Rotterdam study. Br J Ophthalmol. 2007;91(11):1450-1451.
- Webber AL, Wood J. Amblyopia: prevalence, natural history, functional effects and treatment. Clin Exp Optom. 2005;88(6):365-375.
- Carlton J, Karnon J, Czoski-Murray C, Smith KJ, Marr J. The clinical effectiveness and cost-effectiveness of screening programmes for amblyopia and strabismus in children up to the age of 4-5 years: a systematic review and economic evaluation. Health Technol Assess. 2008;12(25):iii, xi-194.
- US Preventive Services Task Force. US Preventive Services Task Force Procedure Manual, Appendix VI. https://www.uspreventiveservicestaskforce.org/Home/GetFile/6/7/procedure-manual_2016/pdf. 2015. Accessed March 13, 2017.
- Chou R, Dana T, Bougatsos C. Screening for Visual Impairment in Children Ages 1-5 Years: Systematic Review to Update the 2004 US Preventive Services Task Force Recommendation. Evidence Synthesis No. 81. AHRQ Publication No. 11-05151-EF-1. Rockville, MD: Agency for Healthcare Research and Quality; 2011.
- Owens DK, Lohr KN, Atkins D, et al. AHRQ series paper 5: grading the strength of a body of evidence when comparing medical interventions—Agency for Healthcare Research and Quality and the Effective Health-Care Program. J Clin Epidemiol. 2010;63(5):513-523.
- Berkman ND, Lohr KN, Ansari MT, et al. Grading the strength of a body of evidence when assessing health care interventions: an EPC update. J Clin Epidemiol. 2015;68(11):1312-1324.
- Holladay JT. Visual acuity measurements. J Cataract Refract Surg. 2004;30(2):287-290.
- Harris RP, Helfand M, Woolf SH, et al; Methods Work Group, Third US Preventive Services Task Force. Current methods of the US Preventive Services Task Force: a review of the process. Am J Prev Med. 2001;20(3 suppl):21-35.
- Deeks JJ, Altman DG. Diagnostic tests 4: likelihood ratios. BMJ. 2004;329(7458):168-169.
- Guyatt G, Rennie D, Jaeschke R, Guyatt G, Lijmer J. Diagnostic tests. In: Guyatt G, Rennie D, eds. Users’ Guides to the Medical Literature. Chicago, IL: AMA Press; 2002:121-140.
- Sunness JS, El Annan J. Improvement of visual acuity by refraction in a low-vision population. Ophthalmology. 2010;117(7):1442-1446.
- Stewart CE, Moseley MJ, Fielder AR. Defining and measuring treatment outcome in unilateral amblyopia. Br J Ophthalmol. 2003;87(10):1229-1231.
- Holmes JM, Beck RW, Repka MX, et al; Pediatric Eye Disease Investigator Group. The amblyopia treatment study visual acuity testing protocol. Arch Ophthalmol. 2001;119(9):1345-1353.
- Rosser DA, Cousens SN, Murdoch IE, Fitzke FW, Laidlaw DA. How sensitive to clinical change are ETDRS logMAR visual acuity measurements? Invest Ophthalmol Vis Sci. 2003;44(8):3278-3281.
- Rosser DA, Murdoch IE, Fitzke FW, Laidlaw DA. Improving on ETDRS acuities: design and results for a computerised thresholding device. Eye (Lond). 2003;17(6):701-706.
- Clarke MP, Wright CM, Hrisos S, Anderson JD, Henderson J, Richardson SR. Randomised controlled trial of treatment of unilateral visual impairment detected at preschool vision screening. BMJ. 2003;327(7426):1251.
- McGraw PV, Winn B, Gray LS, Elliott DB. Improving the reliability of visual acuity measures in young children. Ophthalmic Physiol Opt. 2000;20(3):173-184.
- Manny RE, Hussein M, Gwiazda J, Marsh-Tootle W; COMET Study Group. Repeatability of ETDRS visual acuity in children. Invest Ophthalmol Vis Sci. 2003;44(8):3294-3300.
- Pediatric Eye Disease Investigator Group. A randomized trial of atropine vs. patching for treatment of moderate amblyopia in children. Arch Ophthalmol. 2002;120(3):268-278.
- Wallace DK, Edwards AR, Cotter SA, et al; Pediatric Eye Disease Investigator Group. A randomized trial to evaluate 2 hours of daily patching for strabismic and anisometropic amblyopia in children. Ophthalmology. 2006;113(6):904-912.
- Repka MX, Beck RW, Holmes JM, et al; Pediatric Eye Disease Investigator Group. A randomized trial of patching regimens for treatment of moderate amblyopia in children. Arch Ophthalmol. 2003;121(5):603-611.
- Repka MX, Cotter SA, Beck RW, et al; Pediatric Eye Disease Investigator Group. A randomized trial of atropine regimens for treatment of moderate amblyopia in children. Ophthalmology. 2004;111(11):2076-2085.
- Tommila V, Tarkkanen A. Incidence of loss of vision in the healthy eye in amblyopia. Br J Ophthalmol. 1981;65(8):575-577.
- Afsari S, Rose KA, Pai AS, et al. Diagnostic reliability and normative values of stereoacuity tests in preschool-aged children. Br J Ophthalmol. 2013;97(3):308-313.
- Arthur BW, Riyaz R, Rodriguez S, Wong J. Field testing of the PlusoptiX S04 photoscreener. J AAPOS. 2009;13(1):51-57.
- Awan M, Proudlock FA, Gottlob I. A randomized controlled trial of unilateral strabismic and mixed amblyopia using occlusion dose monitors to record compliance. Invest Ophthalmol Vis Sci. 2005;46(4):1435-1439.
- Barry JC, König HH. Non-cycloplegic screening for amblyopia via refractive findings with the Nikon Retinomax hand held autorefractor in 3 year old kindergarten children. Br J Ophthalmol. 2001;85(10):1179-1182.
- Barry JC, König HH. Test characteristics of orthoptic screening examination in 3 year old kindergarten children. Br J Ophthalmol. 2003;87(7):909-916.
- Bertuzzi F, Orsoni JG, Porta MR, Paliaga GP, Miglior S. Sensitivity and specificity of a visual acuity screening protocol performed with the Lea Symbols 15-line folding distance chart in preschool children. Acta Ophthalmol Scand. 2006;84(6):807-811.
- Chui L, Fraser T, Hoar K, LaRoche GR. Negative predictive value of a vision screening program aimed at children aged 3 to 4 years old. J AAPOS. 2004;8(6):566-570.
- Ciner E, Carter A, Ying GS, Maguire M, Kulp MT; Vision in Preschoolers (VIP) Study Group. Comparison of the Retinomax and Palm-AR auto-refractors: a pilot study. Optom Vis Sci. 2011;88(7):830-836.
- Cogen MS, Ottemiller DE. Photorefractor for detection of treatable eye disorders in preverbal children. Ala Med. 1992;62(3):16-20.
- Dahlmann-Noor AH, Comyn O, Kostakis V, et al. Plusoptix Vision Screener: the accuracy and repeatability of refractive measurements using a new autorefractor. Br J Ophthalmol. 2009;93(3):346-349.
- Dahlmann-Noor AH, Vrotsou K, Kostakis V, et al. Vision screening in children by Plusoptix Vision Screener compared with gold-standard orthoptic assessment. Br J Ophthalmol. 2009;93(3):342-345.
- Donahue SP, Johnson TM, Ottar W, Scott WE. Sensitivity of photoscreening to detect high-magnitude amblyogenic factors. J AAPOS. 2002;6(2):86-91.
- Freedman H. Vision screening. Ophthalmology. 2006;113(7):1248-1249.
- Harvey EM, Dobson V, Miller JM, et al. Accuracy of the Welch Allyn SureSight for measurement of magnitude of astigmatism in 3- to 7-year-old children. J AAPOS. 2009;13(5):466-471.
- Hope C, Maslin K. Random dot stereogram E in vision screening of children. Aust N Z J Ophthalmol. 1990;18(3):319-324.
- Hrisos S, Clarke MP, Wright CM. The emotional impact of amblyopia treatment in preschool children: randomized controlled trial. Ophthalmology. 2004;111(8):1550-1556.
- Huang J, Maguire MG, Ciner E, et al; Vision In Preschoolers (VIP) Study Group. Intertester agreement in refractive error measurements. Optom Vis Sci. 2013;90(10):1128-1137.
- Jost RM, Stager D Jr, Dao L, Katz S, McDonald R, Birch EE. High specificity of the Pediatric Vision Scanner in a private pediatric primary care setting. J AAPOS. 2015;19(6):521-525.
- Kemper AR, Keating LM, Jackson JL, Levin EM. Comparison of monocular autorefraction to comprehensive eye examinations in preschool-aged and younger children. Arch Pediatr Adolesc Med. 2005;159(5):435-439.
- Kennedy R, Sheps SB, Bagaric D. Field trial of the Otago photoscreener. Can J Ophthalmol. 1995;30(4):193-197.
- Kennedy RA, Sheps SB. A comparison of photoscreening techniques for amblyogenic factors in children. Can J Ophthalmol. 1989;24(6):259-264.
- Kennedy RA, Thomas DE. Evaluation of the iScreen digital screening system for amblyogenic factors. Can J Ophthalmol. 2000;35(5):258-262.
- Kulp MT, Ying GS, Huang J, et al. Accuracy of noncycloplegic retinoscopy, Retinomax autorefractor, and SureSight vision screener for detecting significant refractive errors. Invest Ophthalmol Vis Sci. 2014;55(3):1378-1385.
- Leone JF, Gole GA, Mitchell P, Kifley A, Pai AS, Rose KA. Visual acuity testability and comparability in Australian preschool children: the Sydney Paediatric Eye Disease Study. Eye (Lond). 2012;26(7):925-932.
- Matta NS, Singman EL, Silbert DI. Performance of the Plusoptix vision screener for the detection of amblyopia risk factors in children. J AAPOS. 2008;12(5):490-492.
- Miller JM, Dobson V, Harvey EM, Sherrill DL. Comparison of preschool vision screening methods in a population with a high prevalence of astigmatism. Invest Ophthalmol Vis Sci. 2001;42(5):917-924.
- Miller JM, Harvey EM, Dobson V. Visual acuity screening versus noncycloplegic autorefraction screening for astigmatism in Native American preschool children. J AAPOS. 1999;3(3):160-165.
- Morgan KS, Johnson WD. Clinical evaluation of a commercial photorefractor. Arch Ophthalmol. 1987;105(11):1528-1531.
- Ottar WL, Scott WE, Holgado SI. Photoscreening for amblyogenic factors. J Pediatr Ophthalmol Strabismus. 1995;32(5):289-295.
- Rogers DL, Neely DE, Chapman JB, et al. Comparison of the MTI Photoscreener and the Welch-Allyn SureSight autorefractor in a tertiary care center. J AAPOS. 2008;12(1):77-82.
- Schmidt P, Maguire M, Dobson V, et al; Vision In Preschoolers Study Group. Comparison of preschool vision screening tests as administered by licensed eye care professionals in the Vision In Preschoolers study. Ophthalmology. 2004;111(4):637-650.
- Schmidt P, Maguire M, Kulp MT, Dobson V, Quinn G; Vision in Preschoolers Study Group. Random Dot E stereotest: testability and reliability in 3- to 5-year-old children. J AAPOS. 2006;10(6):507-514.
- Shallo-Hoffmann J, Coulter R, Oliver P, Hardigan P, Blavo C. A study of pre-school vision screening tests’ testability, validity and duration: do group differences matter? Strabismus. 2004;12(2):65-73.
- Tong PY, Bassin RE, Enke-Miyazaki E, et al. Screening for amblyopia in preverbal children with photoscreening photographs, II: sensitivity and specificity of the MTI photoscreener. Ophthalmology. 2000;107(9):1623-1629.
- Vision in Preschoolers (VIP) Study Group. Effect of age using Lea Symbols or HOTV for preschool vision screening. Optom Vis Sci. 2010;87(2):87-95.
- Vision in Preschoolers Study Group. Preschool visual acuity screening with HOTV and Lea symbols: testability and between-test agreement. Optom Vis Sci. 2004;81(9):678-683.
- Vision in Preschoolers Study Group. Preschool vision screening tests administered by nurse screeners compared with lay screeners in the vision in preschoolers study. Invest Ophthalmol Vis Sci. 2005;46(8):2639-2648.
- Weinand F, Gräf M, Demming K. Sensitivity of the MTI photoscreener for amblyogenic factors in infancy and early childhood. Graefes Arch Clin Exp Ophthalmol. 1998;236(11):801-805.
- Williams C, Harrad RA, Harvey I, Sparrow JM; ALSPAC Study Team. Screening for amblyopia in preschool children: results of a population-based, randomised controlled trial. Ophthalmic Epidemiol. 2001;8(5):279-295.
- Williams C, Horwood J, Northstone K, Herrick D, Waylen A, Wolke D; ALSPAC Study Group. The timing of patching treatment and a child’s wellbeing. Br J Ophthalmol. 2006;90(6):670-671.
- Williams C, Lumb R, Harvey I, Sparrow JM. Screening for refractive errors with the Topcon PR2000 pediatric refractometer. Invest Ophthalmol Vis Sci. 2000;41(5):1031-1037.
- Williams C, Northstone K, Harrad RA, Sparrow JM, Harvey I; ALSPAC Study Team. Amblyopia treatment outcomes after screening before or at age 3 years: follow up from randomised trial. BMJ. 2002;324(7353):1549.
- Williams C, Northstone K, Harrad RA, Sparrow JM, Harvey I; ALSPAC Study Team. Amblyopia treatment outcomes after preschool screening v school entry screening: observational data from a prospective cohort study. Br J Ophthalmol. 2003;87(8):988-993.
- Ying GS, Maguire M, Quinn G, Kulp MT, Cyert L; Vision In Preschoolers (VIP) Study Group. ROC analysis of the accuracy of noncycloplegic retinoscopy, Retinomax Autorefractor, and SureSight Vision Screener for preschool vision screening. Invest Ophthalmol Vis Sci. 2011;52(13):9658-9664.
- Horwood J, Waylen A, Herrick D, Williams C, Wolke D. Common visual defects and peer victimization in children. Invest Ophthalmol Vis Sci. 2005;46(4):1177-1181.
- Donahue SP. How often are spectacles prescribed to “normal” preschool children? J AAPOS. 2004;8(3):224-229.
- Donahue SP, Johnson TM, Leonard-Martin TC. Screening for amblyogenic factors using a volunteer lay network and the MTI photoscreener: initial results from 15,000 preschool children in a statewide effort. Ophthalmology. 2000;107(9):1637-1644.
- Pediatric Eye Disease Investigator Group. Pharmacological plus optical penalization treatment for amblyopia: results of a randomized trial. Arch Ophthalmol. 2009;127(1):22-30.
- Repka MX, Wallace DK, Beck RW, et al; Pediatric Eye Disease Investigator Group. Two-year follow-up of a 6-month randomized trial of atropine vs patching for treatment of moderate amblyopia in children. Arch Ophthalmol. 2005;123(2):149-157.
- Stewart CE, Stephens DA, Fielder AR, Moseley MJ; ROTAS Cooperative. Objectively monitored patching regimens for treatment of amblyopia: randomised trial. BMJ. 2007;335(7622):707.
- Does screening for amblyopia, its risk factors, and refractive error in children aged 6 months to 5 years reduce long-term amblyopia or improve visual acuity, school performance, functioning, and/or quality of life?
- Does the effectiveness of screening in children aged 6 months to 5 years vary among different age groups?
- What are the accuracy and reliability of screening tests for amblyopia, its risk factors, and refractive error in children aged 6 months to 5 years?
- Do the accuracy and reliability of screening tests for amblyopia, its risk factors, and refractive error vary among different age groups?
- What are the harms of screening for amblyopia, its risk factors, and refractive error in children aged 6 months to 5 years?
- a. Does treatment of amblyopia, its risk factors, and refractive error in children aged 6 months to 5 years improve visual acuity?
- Does treatment of amblyopia, its risk factors, and refractive error in children aged 6 months to 5 years reduce long-term amblyopia or improve school performance, functioning, and/or quality of life?
- What are the harms of treating amblyopia, its risk factors, and refractive error in children aged 6 months to 5 years?
Evidence reviews for the US Preventive Services Task Force (USPSTF) use an analytic framework to visually display the key questions that the review will address to allow the USPSTF to evaluate the effectiveness and safety of a preventive service. The questions are depicted by linkages that relate interventions and outcomes. Further details are available in the USPSTF procedure manual.27
a Amblyopia risk factors include anisometropia, strabismus, hyperopia, any media opacity, astigmatism, and abnormal visual acuity (which includes substantial isoametropic refractive error).
b Determination of refractive error is based on age-appropriate standards.
This figure is the analytic framework depicting the five key questions and the research approach that guided the evidence review. In general, the figure illustrates the overarching question (key question 1): whether screening children ages 6 months to 5 years for visual impairment leads to improved health outcomes. The framework starts on the left with the patient population of interest: children ages 6 months to 5 years. Moving from left to right, the figure depicts the availability of tools to screen children for visual impairment and the accuracy and reliability of such tools (key question 2). There are potential harms of screening (key question 3). For children with visual impairment, treatment may improve health outcomes, such as visual acuity, reduced long-term amblyopia, school performance, functioning, and quality of life (key question 4). Treatment may also result in harms (key question 5).
CINAHL indicates Cumulative Index to Nursing and Allied Health Literature; KQ, key question; WHO ICTRP, World Health Organization International Clinical Trials Registry.
a Sum of the numbers of studies or articles per KQ exceeds the total number of included studies or articles because some were included in multiple KQs.
This figure is a flow chart that summarizes the search and selection of articles. There were 2069 references identified by searching PubMed (N=1,851), CINAHL (N=2), the Cochrane Library (N=41), and the ClinicalTrials.gov and WHO ICTRP databases (N=175). In addition, there were 113 references identified from hand searching and reference list review (N=33), from peer reviewer suggestions (N=20), and from the 2011 USPSTF review of this literature (N=60). The titles and abstracts of 2182 references were screened for potential inclusion. Of these, 366 were deemed appropriate for full-text review to determine eligibility. After full-text review, 320 were excluded: 29 for ineligible language/non-English; 20 for ineligible publication type/not original research; 106 for ineligible population; 14 for ineligible screening or intervention; 70 for ineligible comparator; 37 for ineligible outcome; 29 for ineligible study design; 9 for ineligible country; and 6 for poor quality. Forty-six articles representing 40 studies were included in this report’s qualitative synthesis. Two studies were included for key question 1; 34 studies were included for key question 2; 17 studies were included for key question 3; 3 studies were included for key question 4; and 3 studies were included for key question 5.
|Risk Factorc||Age, mo|
|Manifest strabismus in primary position, prism diopters||>8||>8||>8|
|Media opacity, mm||>1||>1||>1|
a Adapted from Donahue et al.1
b Amblyopia is a neurodevelopmental disorder that arises from abnormal processing of visual images that leads to a functional reduction of visual acuity.2 It results from conditions that interfere with normal binocular vision. Specific conditions associated with amblyopia are anisometropia (a difference in refractive power between the eyes, in which one foveal image is more blurred than the other), strabismus (ocular misalignment, in which each eye does not have the same image on the fovea), and deprivation (caused by the blockage of the visual pathway, often attributable to cataracts, ptosis, or refractive error due tomyopia, hyperopia, and/or astigmatism).3-7 Strabismic and anisometropic amblyopia can coexist. Strabismus can also inhibit development of normal binocular vision in the absence of amblyopia.8
c Ptosis has been removed from the list because nearly all amblyopia-related ptosis occurs in the setting of superimposed anisometropia.1
|Category||Screening Test||Description of Test|
|Visual acuity test||Picture identification tests
(eg, LEA Symbols)
|Figure identification from various distances (eg, the LEA Symbols test uses a circle, apple, square, and house; symbols gradually decrease in size)|
|Visual acuity test||HOTV eye test||Identification of letters HOTV; letters gradually decrease in size|
|Visual acuity test||Snellen||Letter or number identification; letters or numbers gradually decrease in size|
|Visual acuity test||Tumbling E||Identification of the direction of arms of the letter E; letters gradually decrease in size|
|Stereoacuity test||Contour stereotests
(eg, Frisby, Random Dot E, Randot Stereo Smile, Titmus Fly)
|Use of polarized glasses and stereo cards to determine whether a child can correctly identify a 3-dimensional image|
|Stereoacuity test||Moving dynamic random dot stereosize test17||Computer-generated moving stereotest dots|
|Ocular alignment test||Corneal light reflex test
|Symmetric light reflex in both pupils from light held 2 feet away; can also detect cataracts and tumors|
|Ocular alignment test||Cover-uncover test
(cross cover test)
|Alignment changes when covering or uncovering a single focusing eye|
|Ocular alignment test||Simultaneous red reflex test
|Equal red reflexes when viewed through ophthalmoscope; can also detect cataracts and tumors|
|Photoscreeninga||A trained observer evaluates images of corneal light reflexes from a calibrated camera; binocular; can assess ocular alignment, media opacity, and visual acuity|
(automated visual acuity test)
|Autorefractive screeningb||Estimates refractive error using an automated device; monocular; does not assess ocular alignment|
a Photoscreening devices use optical images (photographs) of the eye’s red reflex to identify risk factors in both eyes simultaneously. Most photoscreeners can estimate refractive error, media opacity, and ocular alignment.18 Interpretation of the image is subjective and based on pre-established pass/fail criteria; older devices require a trained interpreter, but newer machines often include computerized interpretation or relay information to a central reading system. Image acquisition takes a few seconds and captures images from both eyes at once, making photoscreeners especially useful for preverbal or developmentally delayed children and children unable to tolerate longer examinations.18
b Autorefractors are computerized instruments that provide objective refractive status by measuring how light changes as it enters and reflects off the back of the eye. For patients with reduced visual acuity, it determines the lens power required to accurately focus light on the retina. Advantages of autorefractors include ease and time of use, ready availability, and patient tolerance. Handheld autorefractors require only a few seconds of a child’s attention, potentially increasing testability rates vs traditional tabletop models, especially among young children.19 A disadvantage of autorefraction is that it typically measures 1 eye at a time, limiting its ability to detect strabismus without refractive error.18
|Source||Study Design||Screening Intervention vs Control||Sample Size||Age||Female, No. (%)b||Non-White, No (%)||Main Results (at Age 7.5 y)|
|Williams et al,86 2001
Williams et al,89 2002
|RCT||Screening at 8, 12, 18, 25, 31, and 37 moc vs screening at 37 mod||3490 randomized
(2029 intensive screening, 1490 1-time screening)
|Initially tested at 8-37 mo and followed up to age 7.5 y||924 (48)||96 (5)||Amblyopia A: 1.5% (16/1088) vs 2.7% (22/826); RR, 0.55 (95% CI, 0.29-1.04)e
Amblyopia B: 0.6% (69/1088) vs 1.8% (15/876); RR, 0.35 (95% CI, 0.15-0.86)f
Residual amblyopia A among children treated with occlusion: 25% (10/40) vs 8% (3/40); OR, 1.56 (95% CI, 0.62-3.92)
Residual amblyopia B among children treated with occlusion: OR, 4.11 (95% CI,1.04-16.29)
Mean visual acuity in worse eye after patching treatment (adjusted for confounding variables): 0.15 (95% CI, 0.08-0.22) vs 0.26 (95% CI, 0.17-0.35); P < 0.0001
|Williams et al,90 2003||Cohort||Screening at 37 mo vs no preschool screeningg||6081 analyzed
(1516 screened; 4565 not screened)
|Screening offered at 37 mo; tested at 7.5 y||2852 (47)||NR||Amblyopia A: 1.1% (11/1019) vs 2.0% (100/5062); adjusted OR, 0.63 (95% CI, 0.32-1.23)e,h
Amblyopia B: 0.7% (7/1019) vs 1.3% (65/5062); adjusted OR, 0.72 (95% CI, 0.32-1.60)f,h
Amblyopia C: 1.9% (19/1019) vs 3.4% (171/5062); adjusted OR, 0.65 (95% CI, 0.38-1.10)h,i
Mean visual acuity in worse eye after patching treatment (adjusted for confounding variables): 0.14 (95% CI, 0.11-0.18) (n = 25) vs 0.22 (95% CI, 0.20-0.23) (n = 166); P < 0.001
a All studies in this table were conducted in community orthoptic clinics and were of fair quality.
b No. and percent among those analyzed.
c Cover-uncover test; Cardiff cards at ages 8 and 12 months; Cardiff and Kay picture test at ages 18, 25, and 31 months; Kays picture test and HOTV crowded symbols distance visual acuity test at age 37 months; noncycloplegic autorefraction (performed at all visits but only used for referral at age 37 months).
d Cover-uncover test; Kays picture test and HOTV test; noncycloplegic autorefraction.
e Amblyopia A indicates interocular difference in acuity of 0.2 logMAR (2 lines on standard chart) or greater.
f Amblyopia B indicates interocular difference in acuity of 0.3 logMAR or greater.
g Kay pictures or Sheridan Gardiner singles visual acuity test, cover-uncover test, and 20-diopter prism or stereopsis test (or both).
h Adjusted for sex, highest level of maternal education, birth weight, family history of strabismus or amblyopia, and duration of breastfeeding.
i Amblyopia C indicates visual acuity in amblyopic eye of 0.18 logMAR or worse (20/30 or worse on Snellen chart).
|Source||Duration||Age, Mean (Range), y||Diagnoses||Baseline Mean Acuity||Country
|Intervention vs Control||Main Results for Amblyopic Eye|
|Wallace et al,44 2006 (PEDIG)
n = 180
|5 wk of treatment (up to 52 wk follow-up)||5.2 (3-7)||Strabismus, 23%; anisometropia, 47%; strabismus and anisometropia, 30%||0.56 logMAR
(≈Snellen equivalent 20/75)
(46 clinical sites)
|Patching for 2 h/d (with ≥1 h of near activities) vs no patching.
Continued use of eyeglasses if needed, regardless of randomization group.
|Mean logMAR acuity: 0.44 (SD, 0.22) vs 0.51 (SD, 0.28)a
Mean difference in logMAR acuity, adjusted for baseline acuity: 0.07 (95% CI, 0.02-0.12)
Mean improvement in lines at 5 wk: 1.1 (SD, 1.6) vs 0.5 (SD, 1.7)
Mean improvement in lines, best measured acuity (from 5-52 wk): 2.2 (SD, 1.8) vs 1.3 (SD, 1.4)
Difference in mean best logMAR acuity, adjusted for baseline acuity (up to week 52): 0.10 (95% CI, 0.05-0.14)
Proportion of children with ≥2 lines of improvement in acuity: 38/85 (45%) vs 18/88 (21%), P = 0.003
|Clarke et al,40 2003
n = 177
|1 y of treatment
(78 wk follow-up)
|4 (3-5)||Anisometropia, 72%||0.36 logMAR
(8 eye clinics)
|Patching + eyeglasses vs eyeglasses only vs no treatment||Mean best corrected logMAR acuity at 1 y: 0.19 (SD, 0.12) vs 0.22 (SD, 0.17) vs 0.30 (SD, 0.20)
Mean difference from no treatment, patching + eyeglasses: 0.11 (95% CI, 0.05-0.17)b
Eyeglasses only: 0.08 (95% CI, 0.02-0.15)b
Among the subgroup with moderate acuity loss at baseline (n = 63), mean difference from no treatment, patching + eyeglasses: 0.27 (95% CI, 0.14-0.39)
Eyeglasses only: 0.11 (95% CI, -0.03 to 0.24)
n = 60
(up to 8)
|Strabismus, 45%; mixed amblyopia, 42%||0.63, 0.69, and 0.59 logMAR
(≈Snellen 20/85, 20/100, and 20/80)
(ophthalmology and orthoptic clinics)
|Patching for 3 h/d vs patching for 6 h/d vs no treatmentc||Mean improvement in logMAR acuity: 0.29 (SD, 0.14) vs 0.34 (SD, 0.19) vs 0.24 (SD, 0.17),
P = 0.11d
Approximate mean Snellen equivalents, lines of improvement: 1.9 (SD, 1.0) vs 2.3 (SD, 1.2) vs 1.6 (SD, 0.12)
a Equivalent to 20/50 vs 20/63 on standard Snellen chart.
b Between-group differences in acuity were not significant at 6 months posttrial, after all groups had received treatment (after the 1-year follow-up visit, children in the no-treatment and glasses-only groups received treatment following the same protocol as those in the combined-treatment group).
c Eyeglasses were prescribed for all who needed them (all groups).
d Although the difference was not statistically significant, the point estimates of the effect were in favor of the patching groups, adherence was suboptimal (participants wore patching for 58% of the prescribed time in the 3-hour group [mean, 103 minutes] and for 41% in the 6-hour group [mean, 153 minutes]), and the study was underpowered to find a small difference between groups.
|No. of Studies
|No. of Participants||Summary of Main Findings
(Including Consistency and Precision)
(Including Reporting Bias)
|Strength of Evidence||Applicability|
|KQ1: Benefits of Screening|
|2 (1 RCT and 1 prospective cohort study)||7995
|School performance, function, QOL: NR
Prevalence of amblyopia at 7.5 y: In the RCT, approximately 1% lower for intensive screening (at 8, 12, 18, 25, 31, and 37 mo) than for screening at 37 mo; difference was statistically significant for 1 of 2 definitions of amblyopia.a
In cohort study, no statistically significant difference between screened (at 37 mo) and nonscreened groups for any definition of amblyopia.b
Consistency of findings is unknown, and findings were imprecise.
|Fair||Studies had high overall attrition (approximately 50%) and compared different screening strategies; RCT did not use a valid randomization method. Reporting bias not detected.||Low||Healthy preschool children who receive vision screening at ages 4 to 5 y by a school nurse as part of usual care. Trained orthoptists conducted screening examinations.|
|KQ2: Test Accuracy|
|34 (studies of test accuracy)||45,588 observationsc||Estimates for all tests suggest utility for identification of children at higher risk for amblyopia risk factors or other visual conditions, with positive LRs most commonly in the moderate range (>5-10). Evidence suggests that combinations of clinical tests have higher positive LRs (>10). The VIP study, the largest to directly compare multiple tests, generally found similar LRs across tests.
Accuracy did not clearly differ for children stratified according to age. Findings were mostly consistent but were imprecise.
|Fair||Many studies recruited from specialty clinics or enrolled populations with high prevalence; heterogeneity of populations, settings, and target conditions evaluated; common shortcomings included high (or NR) rates of uninterpretable results or noncompliance with tests, not reporting whether uninterpretable results or noncompliance were included in analyses, lacking a representative spectrum, and lacking a random or consecutive sample. Reporting bias not detected.||Low||Most studies of clinical tests did not include children <3 y; however most studies of photoscreeners and 5 of 16 studies of autorefractors included them. Applicable to a variety of settings and screening personnel, although only 1 study was conducted completely in a primary care setting and another was described as conducted partly in primary care.|
|KQ3: Harms of Screening|
|17 (1 cohort study and 16 observational studies of test accuracy)||14,196||One cohort reported lower likelihood of being bullied for the subgroup of patched children offered screening at 37 mo than those not screened (25.7% vs 47.1%, P = 0.033; adjusted OR, 0.39 [95% CI, 0.16-0.92]).d
Studies of test accuracy with a lower prevalence (<10%) of vision abnormalities had higher false-positive rates (1−PPV) than studies with higher prevalence (usually >75% vs usually <35%).
Evidence on bullying was imprecise.
For false-positive rates, findings were reasonably consistent (for studies of similar prevalence) and reasonably precise.
|Fair||Medium risk of selection bias and confounding in the cohort study that reported bullying. Studies did not assess psychological effects or other harms of the false-positive findings. Reporting bias not detected.||Low for bullying, moderate for false-positive rates, insufficient for other harms||Children (<6 y) being screened for amblyopia or its risk factors.|
|KQ4: Benefits of Treatment|
|3 (RCTs)||417||Patching vs no patching: on average, <1 line (on Snellen chart) improvement after 5-12 wks for visual acuity of amblyopic eye; more children experienced improvement of ≥2 lines (45% vs 21%, P = 0.003) in the one study reporting it.
Patching + glasses vs glasses alone vs no treatment: on average, improvement of about 1 line on Snellen chart after 1 y for patching + glasses vs no treatment, logMAR, 0.11 (95% CI, 0.05-0.17) and <1 line for glasses alone; magnitude of improvement was greater for those with worse baseline acuity. Findings were consistent and precise.
|Adherence to treatment was low in the fair-quality study; the fair-quality study was focused on adherence and underpowered to find a small difference between groups in visual acuity. Reporting bias not detected.||Moderate for improved visual acuity||For patching vs no patching: children aged ≥3 y with amblyopic risk factors pretreated with glasses. For patching + glasses vs glasses alone vs no treatment: children aged ≥3 y with amblyopic risk factors.|
|KQ5: Harms of Treatment|
|3 (RCTs)||417||Worsening visual acuity in the nonamblyopic eye: risk not increased with patching vs no patching at 5 wk (2.4% vs 6.8%, P = 0.28).
Loss of visual acuity in the amblyopic eye: No significant difference between patching + glasses, glasses alone, and no treatment at 1 y.e
Child happiness or behavior problems: No difference between patching + glasses, glasses alone, and no treatment.
Child or parent upset or worry about treatment: Greater with patching than with glasses alone.
Consistency was unknown (single study reported each outcome), and findings were imprecise.
|Overall sparse evidence on harms of treatment; no included studies examined atropine; assessment did not compare glasses and patching with the no-treatment group for the psychological harms identified (eg, child difficulty coping, upset, parental worry). Reporting bias not detected.||Low||Children receiving treatment for amblyopia or its risk factors with eyeglasses or patching|
Abbreviations: KQ, key question; logMAR, logarithm of the minimum angle of resolution; LR, likelihood ratio; NR, not reported; OR, odds ratio; PPV, positive predictive value; QOL, quality of life; RCT, randomized clinical trial; VIP, Vision In Preschoolers.
a Amblyopia A: 1.5% vs 2.7% (RR, 0.55 [95% CI, 0.29-1.04]); amblyopia B: 0.6% vs 1.8% (RR, 0.35 [95% CI, 0.15-0.86]). Refer to Table 3 notes for definitions of amblyopia A and B.
b Amblyopia A: adjusted OR, 0.63 (95% CI, 0.32-1.23); amblyopia B: adjusted OR, 0.72 (95% CI, 0.32-1.60); amblyopia C: adjusted OR, 0.65 (95% CI, 0.38-1.10). Refer to Table 3 notes for definitions of amblyopia A, B, and C. All ORs adjusted for sex, highest level of maternal education, birth weight, family history of strabismus/amblyopia, and duration of breastfeeding.
c Some study participants contributed multiple observations (eg, if they were evaluated with multiple tests).
d The effects were observed in children who received patches but not those prescribed only glasses.
e Values were 9.7% vs 6.5% vs 13.3% (P = 0.28) for those with mild baseline acuity loss and 15.0% vs 11.1% vs 23.8% (P = 0.13) for those with moderate baseline acuity loss, respectively, for patching plus eyeglasses, eyeglasses alone, and no treatment.