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Vision screening in newborns and early childhood

Abstract

We looked at existing recommendations and supporting evidence on the effectiveness of screening for visual disorders in newborns and small infants, and in children between six months and five years of age.

We conducted a literature search up to the 5th of August 2019 by using key terms and manual search in selected sources. We summarized the recommendations and the strength of the recommendations when and as reported by the authors. We summarized the main findings of systematic reviews with the certainty of the evidence as reported on the accuracy of screening tests for detecting visual alterations; the efficacy of treatment for improving visual acuity, school performance, and quality of life; and potential harms derived from vision screening and treating visual alterations.

Although there is little evidence supporting its validity and effectiveness, examining all newborns for congenital cataract and retinoblastoma through the red reflex examination is widely accepted due to the severity of both diseases and the good outcomes reached by early detection and treatment.

Overall, there is a moderate certainty of evidence that visual screening in children between three and five years provides a moderate net benefit, as assessed by the US Preventive Services Task Force: vision screening tests are accurate for detecting amblyopia and its risk factors, and their treatment is associated with visual improvement. There is uncertain evidence on whether vision screening in children under three years of age provides net benefits. Among populations with a low prevalence of vision abnormalities, screening the youngest is associated with an increased rate of false positives, leading to unnecessary additional assessment.

Background

Introduction

The World Health Organization (WHO) European Region is developing a new pocket book for primary health care for children and adolescents in Europe. This article is part of a series of reviews, which aim to summarize the existing recommendations and the most recent evidence on preventive interventions applied to children under five years of age to inform the WHO editorial group to make recommendations for health promotion in primary health care. In this article, we looked at existing recommendations and supporting evidence on the effectiveness of screening for visual disorders in newborns and small infants, and in children between six months and five years of age.

Why is vision screening important in newborns and early childhood?

The aim of vision screening in newborns and early childhood is to detect abnormalities that could lead to severe visual impairment or permanent vision loss if left untreated.

Context

In newborns and small infants, congenital cataract and retinoblastoma are relatively infrequent but can potentially lead to vision loss and even death in the case of retinoblastoma. The median prevalence of congenital cataracts was estimated at 1.7 per 10,000 children globally and the incidence of retinoblastoma was estimated at 6.0 and 7.1 per 100,000 live births in Northern Europe [1,2,3]. Early identification of these disorders could lead to early treatment with improved outcomes.

In infancy and preschool age children, one of the leading causes of vision impairment is amblyopia, known as ‘lazy eye’, with an estimated prevalence between 1 and 5% [4, 5]. Amblyopia refers to a decrease in visual acuity from one or both eyes, that arises during the period of visual development and which is not attributed to a structural alteration of the eye or visual pathways. The main risk factors associated with amblyopia include strabismus (ocular misalignment), significant bilateral refractive errors that cause blurred vision (myopia, hyperopia, astigmatism), and anisometropia (asymmetric retractive error). Less common risk factors are vision deprivation caused by media opacity (such as cataracts) or ptosis. Amblyopia is more common in prematurity, low birth weight, and when there is a positive family history, as those are risk factors for developing amblyogenic factors [4, 5]. Amblyopia and its risk factors are unlikely to resolve spontaneously and, if untreated, they can result in not only vision loss, but also in other consequences such as accidents, poor reading ability and suffering from bullying, depression, anxiety, or poor self-esteem [6]. Screening preschool age children for vision impairment could help identify those who may benefit from early interventions to correct or improve vision.

Key questions

Newborns and small infants

  1. 1.

    Is screening for visual disorders in newborns and small infants associated with improved outcomes?

Children between six months and five years of age

  1. 2.

    How accurate are the screening tests for detecting strabismus, refractive errors, anisometropia, and amblyopia in primary care among children between six months and five years of age?

  2. 3.

    What are the potential harms derived from screening children between six months and five years of age for strabismus, refractive errors, anisometropia, and amblyopia?

  3. 4.

    Is treatment of strabismus, refractive errors, media opacity, and amblyopia in children between six months and five years of age effective for improving visual acuity, school performance, and quality of life?

  4. 5.

    What are the potential harms derived from treating strabismus, refractive errors, anisometropia, and amblyopia in children between six months and five years of age?

  5. 6.

    Is population-based screening in children between six months and five years of age effective for improving long-term visual acuity, school performance and quality of life?

Search methods and selected manuscripts

We described the search methods, data collection and data synthesis in the second paper of this supplement (Sophie Jullien, Gottfried Huss & Ralf Weige. Supporting recommendations for childhood preventive interventions for primary health care: elaboration of evidence synthesis and lessons learnt. BMC Pediatrics. 2021. https://0-doi-org.brum.beds.ac.uk/10.1186/s12887-021-02638-8).

The search was conducted on the 5th of August 2019, by manual search and by using the search term “vision screening”, “vision test”, “vision disorder”, or “amblyopia”. We included any document that addressed at least one of the key questions. The WHO has developed several strategies and promotional activities to address blindness and vision impairment worldwide [7]. This WHO World report will contain recommendations including comprehensive and integrated eye care with the objective of helping to decrease the burden of eye diseases and vision impairment globally. However, we did not find any specific recommendations on screening measures for children other than eye examination in newborns. We found recommendations and their supporting evidence from the US Preventive Services Task Force (USPSTF) (2017) and the PrevInfad workgroup (Spanish Association of Primary Care Pediatrics) (2016). We looked at the National Institute for Health and Care Excellence (NICE) and Centers for Disease Control and Prevention (CDC) guidelines, as well as the recommendations from the American Academy of Pediatrics (AAP) in collaboration with the American Academy of Ophthalmology (AAO), the Royal College of Paediatrics and Child Health (RCPCH), and the UK National Screening Committee, and we included the brief recommendations that each of them provided.

The supporting evidence document for the USPSTF included a systematic review on screening for amblyopia and its risk factors in children. We searched in the Cochrane library for the identification of other systematic reviews on any topic related to our key questions. By using the search terms cited above, the search returned 99 reviews and two protocols. By screening the titles and abstracts, we included seven systematic reviews that addressed any of the key questions, two on screening and five on treatment of vision impairment. Among the two reviews on screening, one was published in 2017 and looked at tests for detecting strabismus in children between 1 and 6 years of age in the community. The other review assessed vision screening for amblyopia in childhood. Although it was published in 2009, we decided to include it due to the relevance of the topic and the lack of updated Cochrane review addressing this question.

All the included manuscripts for revision in this article are displayed in Table 1.

Table 1 Included manuscripts for revision

Existing recommendations

We summarized the existing recommendations and the strength of recommendations as per their authors in Table 2.

Table 2 Summary of existing recommendations

Existing evidence

The USPSTF 2017 recommendations result from a systematic review that the USPSTF commissioned in order to update their 2011 recommendations on screening for amblyopia and its risk factors in children [6]. Overall, 40 studies reported in 46 manuscripts were included, addressing one or several of the authors’ key questions on screening test accuracy, and benefits and harms of vision screening in children, and of treatment of amblyopia, its risk factors, and refractive error. For each key question, authors assessed the quality of each included study (good, fair or poor, although poor studies were excluded) and the overall strength of the body of evidence (high, moderate, low or insufficient) mentioned in the text as ‘strength of the evidence’ as per the review authors.

The supportive document developed from PrevInfad consists on a comprehensive summary of systematic reviews addressing these topics [5]. PrevInfad addressed visual screening for newborns and infants, and for children aged between 12 months and 5 years, while the systematic review conducted by Jonas et al. included children between 6 months and 5 years of age. In the present document, we decided to first address screening in newborns and small infants to address congenital cataracts and retinoblastoma, and then screening in children between 6 months and 5 years of age in order to be inclusive. It should be noted that the 6 or 12 months threshold is very unlikely to make any difference on the inclusion of the studies as there is very little evidence on this age group.

Visual disorders screening in newborns and small infants

Congenital cataract and retinoblastoma cause opacities of the transparent media, which can be detected by a simple and safe ocular examination assessing the red reflex with an ophthalmoscope. Although there is little evidence supporting the validity of this examination or the effectiveness of screening both diseases, it is widely accepted to routinely search in the neonatal period for opacities of the transparent media or leukocoria, as both disorders can be treated [5, 12].

From several national studies, screening newborns within the first six weeks of life detected between 47% (in the UK) and 75% (in Sweden) of newborns with congenital cataract that needed surgery. It seems that the sensitivity of the red reflex to detect retinoblastoma is low, however the use of this low sensitivity screening tool is accepted in this case as it is a potentially lethal disorder and there is no alternative screening test as of today [5]. In addition, early diagnosis for early treatment is essential in both disorders. In the case of congenital cataract, surgery should be conducted within the first three months of age with the aim to achieve optimum outcome. Delay in the treatment can lead to irreversible amblyopia and consequent vision loss of the affected eye. In the case of retinoblastoma, it remains curable if treated within the first three to six months after the detection of leukocoria. Therefore, a child with leukocoria should be referred immediately. With early diagnosis and adequate treatment, the cure rate is up to 98% mostly with preservation of the vision, while survival will decrease with delay in the treatment [5].

One study was found that assessed cost-effectiveness of cataract screening in newborns. This study, conducted in Sweden, found that this screening performed in maternity wards after birth and during the routine health visits of the infant was cost-effective when compared to the screening performed only after birth [5].

Accuracy of screening tests for detecting strabismus, refractive errors, anisometropia, and amblyopia in children under five years of age

We summarized the main tests used for detecting strabismus, refractive errors, anisometropia and amblyopia in Table 3. Three systematic reviews addressed accuracy of these screening tests, which are summarized in Tables 4 and 5.

Table 3 Available screening tests for visual impairment [4, 5]
Table 4 Systematic reviews on accuracy of vision screening tests
Table 5 Main findings on accuracy of vision screening tests

Influence of age in accuracy and testability of screening tests

The screening of low age children could lead to an increased rate of false positives. In addition, the youngest might present less ability to complete the screening test, known as testability [5]. Jonas et al. included five studies that looked at the variation of the accuracy of visual acuity tests, a combination of clinical tests, an autorefractor and two photo-screeners due to age [4, 6]. They found that children under the age of three were not included in most of the studies. They reached the conclusion that ‘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.’

Although testability is reported in many studies included in the Jonas et al. review, few of them reported their findings stratified by age, or for children under three years of age [4, 6]. Testability was over 90% in most of the studies, and under 80% in few studies (all the studies with testability under 80% included children under three years of age). Higher testability rates were found in older children, and testability rates for visual acuity and stereoacuity tests were lower among children under the age of three. From the VIP study, testability of Lea and HOTV optotypes was over 95% among children between 3 and 5 years, and testability of the Random Dot E was 86 and 93% among 3 and 5-year-old children respectively. For autorefractors and photo-screeners, testability rate were close to 100% among children aged 3 years or above [4,5,6].

Potential harms of screening children between six months and five years of age for strabismus, refractive errors, anisometropia and amblyopia

False-positive findings in visual screening would lead to unnecessary referrals, and the associated anxiety and costs for the families and the health system. Jonas et al. reported the false-positive rates calculated from 16 studies [6]. They found false-positive rates above 75% in studies with a low prevalence of vision abnormalities (under 10%), and between 5 and 39% in populations with a high prevalence of vision abnormalities (above 20%) [4,5,6].

One controlled study identified by Jonas et al. evaluated the potential psychosocial effects of visual screening [23]. This prospective study compared bullying victimization (≥4 times a month) by the age of 8 among children who were patched between two groups of schools: one group that received preschool screening for amblyopia and one group that did not. Among the included 4473 children, 122 were patched. The reduction in bullying victimization among children who were offered preschool screening compared to the control group was almost 50% (25.7% versus 47.1%, with an AOR 0.39 [95%CI 0.16 to 0.92], adjusted for sex, paternal socioeconomic class, highest level of maternal education, and type of housing). Early screening leading to early intervention was associated with a decreased risk of bullying among patched children, probably because children are younger by the time they can remove the patch.

Based on the 16 observational studies and the cohort study included in the Jonas et al. review (14,196 observations), the strength of the evidence was rated as low for bullying, moderate for false-positive rates, and insufficient for other harms.

No studies were found that assessed possible harms derived from wearing glasses when unnecessary (long term outcomes and impacts in the vision), nor that evaluated rate of children who received unnecessary treatment for amblyopia or any of its risk factors [4, 5].

Effectiveness of treatment of strabismus, refractive errors, anisometropia, and amblyopia in children between six months and five years of age

The success of the visual screening will partly depend on the effectiveness of the treatment to improve or correct amblyopia and its risk factors, in order to improve visual acuity, avoid permanent vision loss, and subsequently to improve school performance and functionality for a better quality of life. There are however no studies evaluating school performance or other functional outcomes, or quality of life [4]. There are several treatment strategies for treating amblyopia, including the correction of refractive errors by using glasses, with the addition or not of occlusive patches, opaque lens or eye drops to blur the better seeing eye. Several factors could influence the effectiveness of the treatment: age of the child when starting the treatment, the intensity of amblyopia, and therapeutic compliance [5].

We summarized the main findings on the effectiveness of different interventions for vision impairment in children from the USPSTF review, five Cochrane reviews, and an additional review from the UK National Screening Committee (NSC) that was identified in the PrevInfad document, in Table 6. The UK NSC review that was published in 2019 by the same authors to look at recent evidence to make evidence-based decisions on whether the 2012 recommendations from the UK NSC needed to be amended found no new evidence on these topics [13, 14].

Table 6 Systematic reviews on treatment effectiveness

Influence of age in effectiveness of treatment

Evidence on the impact of age in the effectiveness of treatment is controversial, and we report here findings from the PrevInfad summary document [5]. No clinical trial included children under three years of age. Among children between 3 and 6 years of age, most of the studies showed no association between age and effects of treatment. A meta-analysis of four trials conducted in the US including 996 children between 3 and 12 years of age, looked at three age groups: 3 to less than 5 years, 5 to less than 7 years, and 7 to less than 13 years. Treatment in the oldest group was less effective than in the other two groups (p < 0.04 for moderate intensity amblyopia and p < 0.01 for severe intensity amblyopia). There were no significant differences in treatment between the two younger groups for both moderate and severe intensity amblyopia, although there was a trend to a minor effect in older children with severe amblyopia. From another study, delaying patching by one year in children aged between three and five years was associated to poorer results after six months of follow-up. Another study compared less than three hours with three to six hours of daily occlusion in two age groups. There were no significant differences between the two regiments among children under four years (p = 0.54), but treatment was more effective with three to six hours daily occlusion among older children (p = 0.03 in 4 to 6-year-old children and p < 0.001 in children older than 6 years).

Although it was considered that amblyopia was irreversible if left untreated until the age of 6–10 years, some studies have shown that treatment can be effective in older children, although effectiveness is less from the age of 7 [5].

Potential harms of treating strabismus, refractive errors, anisometropia, and amblyopia in children between six months and five years of age

Potential harms derived from treatment of visual impairment were evaluated by the Jonas review and the PrevInfad document [5, 6]. Some studies have associated the treatment of amblyopia with a reversible vision loss in the non-amblyopic eye. In one study, this was higher among children treated with occlusion, compared to atropine (decrease in visual acuity of two or more lines: RR 0.93 [95% CI 0.88 to 0.97]). Another study also showed a decrease in the visual acuity of the non-amblyopic eye, which was higher among the group treated with atropine and flat lens compared to atropine alone (decrease in visual acuity of one or more lines: RR 0.86 [95% CI 0.78 to 0.95]). This loss in visual acuity was recovered in 19 out of the 20 affected children and in 17 out of the 18 affected children in the first and second study respectively. However, other studies showed no association between treatment and increased risk of vision loss in the non-amblyopic eye, such as two trials included in the Jonas review (one trial with patching and the other comparing eyeglasses plus patching versus eyeglasses alone versus no treatment) [5].

Two clinical trials included in the Jonas review assessed the psychosocial adverse effects of treatment for amblyopia. One trial found no differences on being happy, cooperative, or good tempered, on teasing, on problems at preschool, or in emotional and behavioural problems between three groups of 4-year-old children treated with patch and eyeglasses, eyeglasses alone, and no treatment. However, they found that children treated with patch and eyeglasses were more upset than those treated with eyeglasses alone (85% versus 29% at 4 years of age [p = 0.03], and 62% versus 26% at 5 years of age [p = 0.005]). The limitation of this study is the high attrition bias, with data available for only 44% of the recruited children. The other trial showed a decrease in the emotional well-being of children treated with atropine or patch, with a larger effect among patched children. Other observational studies evaluated the association between psychosocial effects and stigma and treatment of amblyopia, with diverging findings [5, 6].

Treatment with patches was associated with cutaneous irritation in 5% of children included in one trial [5]. Another trial including 60 children comparing daily 3 h of patching, 6 h of patching and no treatment showed no inverse amblyopia and no patch allergy [6]. Some local and systemic adverse effects associated with atropine were also reported in some clinical trials [5].

The strength of the evidence rated by Jonas et al. based on the three clinical trials included for this topic (n = 417) was low.

Effectiveness of population-based screening in children between six months and five years of age

No RCT was found that assessed population-based screening for vision impairments in children versus no screening, looking at long-term outcomes such as amblyopia prevalence, schooling performance or quality of life [5]. The Jonas et al. review identified two studies (one RCT and one cohort study) conducted in England in 1991–92, that evaluated the prevalence of amblyopia at the age of 7.5 years [6]. The RCT recruited 3490 children and compared intensive orthoptist screening six times between 8 and 37 months and one time at 37 months of age. The risk of presenting amblyopia at 7.5 years was lower in the group with multiple times screening compared to single time screening (0.6% versus 1.8%; RR 0.35 [95% CI: 0.15 to 0.86]), however this was only significant for one of the wo amblyopia definitions evaluated (interocular difference in acuity ≥0.3 logMAR). Mean visual acuity in the worse eye after treatment (patching) was better among children screened several times versus a single time (0.15 versus 0.26 logMAR; p < 0.0001) [6]. The cohort study recruited 6081 children and compared single screening at 37 months of age in one health district versus no preschool screening in two other health districts. There were no significant differences in the prevalence of amblyopia at 7.5 years of age, assessed by three definitions. Both studies were at high risk of attrition bias. Indeed, data was available for only 55% of the recruited children at the end of the follow-up period [6]. In addition, the RCT was at high risk of selection bias as the method of randomization was inadequate and the baseline characteristics for amblyopia or its risk factors were not reported. Based on these two studies (n = 7795), the strength of the evidence was rated as low.

Few retrospective population-based studies found an association between vision screening and a reduced prevalence of amblyopia, but the low quality of methodology raises concern about the internal and external validity of these findings [5].

It is worth to mention that there is no evidence to determine the optimal vision screening interval in children under five years of age [4].

Summary of findings

  • Although there is little evidence supporting the validity and effectiveness of examining all newborns for congenital cataract and retinoblastoma through the red reflex examination, examining routinely the eyes of all newborns is widely accepted due to the severity of both diseases, if left untreated, and the good outcomes reached by early detection and treatment.

  • Visual tests used for screening children aged three to five years were assessed to be useful for detecting amblyopia and its risk factors. Estimates showed higher positive likelihood ratio for the detection of children at higher risk, and for the combination of clinical tests.

  • Overall, there is a moderate certainty of evidence that visual screening in children between three and five years provides a moderate net benefit, as assessed by the US Preventive Services Task Force (USPSTF): vision screening tests are accurate for detecting amblyopia and its risk factors, and treatment of these visual abnormalities is associated with visual improvement.

  • Overall, there is uncertain evidence on whether screening amblyopia and its risk factors in children under three years of age provides net benefits. Among populations with a low prevalence of vision abnormalities, screening the youngest is associated with an increased rate of false positives, leading to unnecessary additional assessment.

  • There is limited evidence on harms from treatment, but patching may have some psychological harms.

  • There are several gaps in the evidence to acquire a better understanding of the best combination of screening tests, the optimal age for initiation of screening, the optimal screening intervals, the net benefit of screening and treatment in children under three years of age, and the long-term outcomes of preschool screening such as school performance and quality of life.

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Acknowledgments

I am very grateful to María Jesús Esparza, Laura Reali, and Gottfried Huss for carefully reviewing and providing valuable feedback for each article. I am also grateful to Ralf Weigel and Gottfried Huss for proofreading the final version of this document.

About this supplement

This article has been published as part of BMC Pediatrics Volume 21, Supplement 1 2021: Defined preventive interventions for children under five years of age: evidence summaries for primary health care in the WHO European region. The full contents of the supplement are available at https://0-bmcpediatrics-biomedcentral-com.brum.beds.ac.uk/articles/supplements/volume-21-supplement-1.

Funding

Publication charges for this article have been funded by the Friede Springer endowed professorship for Global Child Health at the Witten Herdecke University, Germany.

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SJ was identified as the researcher in the development of the synthesis of evidence and writing the report. For each selected topic on preventive interventions, SJ defined the key questions, established and run the literature search, screened the returned manuscripts for eligibility, extracted data and summarized the existing recommendations and supporting evidence. The principal advisors of this project were Dr. Gottfried Huss, MPH General Secretary of ECPCP, Project- Coordinator and Prof. Ralf Weigel, Friede Springer endowed professorship of Global Child Health, Witten/Herdecke University (scientific advice). The author(s) read and approved the final manuscript.

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Correspondence to Sophie Jullien.

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SJ had a contract and was paid as an independent consultant by the WHO via Witten/ Herdecke University, ECPCP and EPA/UNEPSA for developing the different articles of this supplement.

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Jullien, S. Vision screening in newborns and early childhood. BMC Pediatr 21 (Suppl 1), 306 (2021). https://0-doi-org.brum.beds.ac.uk/10.1186/s12887-021-02606-2

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