Other Supporting Document for Impaired Visual Acuity in Older Adults: Screening
By Roger Chou, MD; Tracy Dana, MLS; Christina Bougatsos, MPH; Sara Grusing, BS; and Ian Blazina, MPH
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 the Journal of the American Medical Association on March 1, 2016.
Importance: Impaired visual acuity is common among older adults and can adversely affect function and quality of life.
Objective: To update a 2009 systematic review on screening for impaired visual acuity among older adults for the US Preventive Services Task Force (USPSTF).
Data Sources: Ovid MEDLINE (2008 to January 2016), Cochrane Central Register of Controlled Trials, and Cochrane Database of Systematic Reviews.
Study Selection: Randomized clinical trials of screening; diagnostic accuracy studies of screening tests in primary care settings; and randomized clinical trials of treatment vs placebo or no treatment for uncorrected refractive errors, cataracts, and dry (atrophic) or wet (exudative) age-related macular degeneration (AMD). Studies of screening and diagnostic accuracy were limited to asymptomatic adults 65 years or older; studies of treatment included asymptomatic adults of any age.
Data Extraction and Synthesis: One investigator abstracted data, a second checked data for accuracy, and 2 investigators independently assessed study quality using predefined criteria. Random-effects meta-analysis was used to estimate the relative and absolute benefits of vascular endothelial growth factor inhibitors (anti-VEGF) for wet AMD.
Main Outcomes and Measures: Visual acuity, vision-related function, functional capacity harms, and diagnostic accuracy.
Results: Three trials (n = 4728) from the 2009 USPSTF review found that screening for impaired visual acuity was not associated with improved visual or clinical outcomes. In 1 good-quality trial (n = 3346), universal screening identified 27% of persons with impaired visual acuity and correctable impairment vs 3.1% with targeted screening, but there was no difference in the likelihood of visual acuity worse than 20/60 after 3 to 5 years (37% vs 35%; relative risk [RR], 1.07; 95% CI, 0.84–1.36). The 2009 review found that effective treatments are available for uncorrected refractive errors and cataracts. Ten-year trial results of dry AMD found an antioxidant/zinc combination was associated with decreased risk of visual acuity loss (46% vs 54%; odds ratio, 0.71; 95% CI, 0.57–0.88). An updated meta-analysis found anti-VEGF for wet AMD was associated with greater likelihood of having vision 20/200 or better vs sham injection (4 trials; RR, 1.47; 95% CI, 1.30–1.66; I2 = 42%; absolute risk difference, 24%; 95% CI, 12%–37% after 1 year). New evidence on the diagnostic accuracy of visual acuity screening tests was limited and consistent with previous findings that screening questions or a visual acuity test was associated with suboptimal accuracy.
Conclusions and Relevance: Screening can identify persons with impaired visual acuity, and effective treatments are available for common causes of impaired visual acuity, such as uncorrected refractive error, cataracts, and dry or wet AMD. However, direct evidence found no significant difference between vision screening in older adults in primary care settings vs no screening for improving visual acuity or other clinical outcomes.
Impaired visual acuity refers to decreased clarity or sharpness of vision. Impaired visual acuity is associated with decreased function and quality of life and increased risk of falls and other accidental injuries.1-5 The prevalence of impaired visual acuity increases with age.6, 7 Impaired visual acuity may be unreported or unrecognized in older persons because vision changes can be relatively subtle, progress slowly over time, or occur in persons with cognitive impairment.
The US Preventive Services Task Force (USPSTF) commissioned this review to update a 2009 review8, 9 and Recommendation Statement10 on screening for impaired visual acuity due to uncorrected refractive errors, cataracts, and dry (atrophic) or wet (exudative) age-related macular degeneration (AMD). The USPSTF previously concluded that the evidence was insufficient to assess the balance of benefits and harms of screening for visual acuity for the improvement of outcomes in older adults (I statement).
Scope of the Review
Using established methods,11 the USPSTF determined the scope and key questions for this review. The final research plan was posted on the USPSTF website prior to conducting the review. The analytic framework and key questions (KQs) used to guide the review are shown in Figure 1.
Detailed methods and data for this review are contained in the full USPSTF review,12 including search strategies, inclusion criteria, and abstraction tables; the full review also includes evidence on effectiveness of older treatments for wet AMD (laser photocoagulation and photodynamic therapy).
Data Sources and Searches
Searches were conducted in Ovid MEDLINE, the Cochrane Central Register of Controlled Trials, and the Cochrane Database of Systematic Reviews from 2008 (searches in the 2009 review were conducted through July 2008) to February 2015 (eAppendix 1 in the Supplement) and reference lists. An updated search conducted on January 6, 2016, using the same databases identified no new studies that would affect the conclusions or understanding of the evidence and therefore the related USPSTF recommendation.
Two reviewers evaluated each study on the basis of predefined criteria. For studies on screening and diagnostic accuracy, we included studies of asymptomatic adults 65 years or older without known impaired visual acuity (based on current corrected vision) who have not sought care for evaluation of vision problems. We included randomized clinical trials (RCTs) of vision screening performed in primary care or community-based settings vs no screening, delayed screening, or usual care (eg, targeted screening) and evaluated visual acuity, vision-related quality of life, functional capacity, mortality, cognition, or harms. We included studies of diagnostic accuracy of vision screening tests, questions, or questionnaires performed in primary care or community settings. For treatment, we included RCTs of asymptomatic adults (not restricted to age ≥65 years) with mild to moderate vision impairment (defined as best visual acuity worse than 20/40 but better than 20/200) that evaluated effects on the outcomes described above for corrective lenses, reading aids, or photorefractive surgery due to uncorrected refractive errors; vitamin and oxidants and vascular endothelial growth factor (VEGF) inhibitors for AMD; or cataract surgery. For screening and treatment, cohort studies were included when evidence from RCTs was insufficient. We excluded studies of screening and diagnostic testing performed in specialty settings and trials of treatment in patients with visual acuity worse than 20/200 or with other causes of vision loss. The selection of literature is summarized in Figure 2.
Data Abstraction and Quality Assessment
Details about the study design, patient population, setting, screening method, interventions, analysis,and results were abstracted. Two investigators independently applied criteria developed by the USPSTF11 to rate the quality of each study as good, fair, or poor (eAppendix 2 in the Supplement). Discrepancies were resolved through consensus.
Data Synthesis and Analysis
The aggregate internal validity (quality) of the body of evidence for each KQ was assessed as good, fair, or poor using methods developed by the USPSTF,11 based on the quality of studies, precision of estimates, consistency of results between studies, and directness of evidence.11 Data synthesis was based on evidence from the 2009 review as well as new evidence. A meta-analysis on effectiveness of VEGF inhibitors vs placebo for wet AMD was performed using a random-effects model with Review Manager 5.2 (Nordic Cochrane Centre) to calculate pooled relative risks (RRs) and absolute risk differences. The meta-analysis was stratified by the VEGF inhibitor used. Results were considered statistically significant if the P value was less than 0.05 based on 2-sided testing, and statistical heterogeneity was measured using the I2.
Screening and Related Harms
Key Question 1. Does vision screening in asymptomatic older adults result in improved vision, morbidity or mortality, quality of life, functional status, or cognition?
Key Question 2. Are there harms of vision screening?
No new trials of vision screening were identified since 2008. Three cluster randomized trials (n = 4728) of vision screening performed as part of a multicomponent screening intervention in older adults (mean age, 76–81 years) were included in the 2009 USPSTF review8 (Table 1 and eTable 1 in the Supplement). The trials found no difference between vision screening vs no vision screening, usual care, or delayed screening on vision and other clinical outcomes after follow-up of 6 months to 5 years.13-15 In the highest-quality and largest trial (n = 3346),15 universal vision screening identified a greater percentage of patients with impaired visual acuity and correctable impairment (27%) than did targeted screening (3.1%), yet there was no difference in likelihood of visual acuity worse than 20/60 after 3- to 5-year follow-up (37% vs 35%; relative risk [RR], 1.07; 95% CI, 0.84–1.36). In this trial, 18 of 40 patients (45%) advised to see an optician after vision screening actually received new lenses and 41 of 75 persons (55%) eligible for referral to an ophthalmologist had clear evidence of a referral, which could have attenuated potential benefits. Other reasons for lack of benefit in the screening trials may include the high loss to follow-up in all trials, similar frequency of vision disorder detection and treatment in the screening and control groups in 1 trial,14 use of a screening question to identify persons for further testing in 1 trial,14 and low uptake of recommended interventions in 1 trial.13 No study addressed harms of vision screening.
One additional screening trial did not meet inclusion criteria because it was conducted in a specialty setting.16 It found vision screening by an optometrist in frail elderly persons increased the risk for falls (2.45 falls/patient vs 1.68 falls/patient; rate ratio, 1.57; 95% CI, 1.20–2.05) along with a non–statistically significant increased risk for fractures (10% vs 5.7%; RR, 1.74; 95% CI, 0.97–3.11) after 1 year compared with usual care.16 Screening led to new eyeglasses or referral for further treatment for 47% of study participants. A subsequent report from this study also found no difference between groups in improvement in vision or vision-related quality of life after 1 year.17
Accuracy of Screening
Key Question 3. What is the accuracy of screening for early impairment in visual acuity due to uncorrected refractive error, cataracts or age-related macular degeneration?
The 2009 USPSTF review8 included 8 cross-sectional studies on the diagnostic accuracy of screening for impaired visual acuity in older adults (Table 2 and eTable 2 in the Supplement).18-25 Four studies found screening questions or questionnaires had low accuracy for identifying persons with impaired visual acuity compared with the Snellen eye chart19, 20, 23 or an ophthalmologic examination.24 Positive likelihood ratios ranged from 1.19 to 3.23 and negative likelihood ratios ranged from 0.23 to 0.78. Four studies18, 21, 24, 25 found no visual acuity test had both high sensitivity and specificity compared with a detailed ophthalmologic examination, resulting in positive likelihood ratios that ranged from 1.00 to 8.07 and negative likelihood ratios that ranged from 0.32 to 1.00. Two studies reported areas under the receiver operating characteristic curves of 0.66 and 0.83.18, 21 One study found the Amsler grid had poor accuracy for identifying visual conditions (positive likelihood ratio 1.65 and negative likelihood ratio 0.91).18 A study published in 1988 (n = 50) reported that 100% of patients with cataract and 75% of patients with AMD were correctly identified by a geriatrician compared with an ophthalmologist, with no false positives.22
Three fair-quality cross-sectional studies (reported in 2 publications) published subsequent to the 2009 review evaluated the diagnostic accuracy of screening tests in primary care settings (Table 2 and eTable 2 in the Supplement).26, 27 Two studies (n = 180 and 200) found that a computerized vision screening tool or a flip chart version of the test were not accurate compared with a detailed eye examination.26 Optimal sensitivity (0.80) and specificity (0.68) were observed with the combination of abnormal high contrast visual acuity (threshold >0.19 logarithm of the minimal angle of resolution) or abnormal near visual acuity, resulting in a positive likelihood ratio of 2.5 and a negative likelihood ratio of 0.29. The flip chart instrument performed similarly, based on the low-contrast visual acuity test alone (sensitivity 0.75 and specificity 0.77, for a positive likelihood ratio of 3.26 and negative likelihood ratio of 0.32). A third study (n = 371) compared the scores on the Minimum Data Set (MDS) 2.0 Vision Patterns section against a standard visual acuity test (Early Treatment Diabetic Retinopathy Study chart) for detecting impaired visual acuity.27 Diagnostic accuracy was poor. Using a cutoff score of 1 or greater (0 indicating adequate vision and scores of 1–3 various degrees of impairment), sensitivity of the MDS Visual Patterns section for detecting visual acuity worse than 20/40 was 0.52 and specificity 0.75, for a positive likelihood ratio of 2.11 and a negative likelihood ratio of 0.64.
Key Question 4. Does treatment of early impairment in visual acuity due to uncorrected refractive error, cataracts, or AMD lead to improved visual acuity, morbidity, mortality, vision-related quality of life, functional status, or cognition?
Uncorrected Refractive Error
We identified no new study of treatment vs no treatment for mild uncorrected refractive errors on vision, vision-related quality life, or functional outcomes. The 2009 USPSTF review8 found that refractive lenses and refractive surgery28 were highly effective at restoring normal or near-normal visual acuity, based on a large body of observational data and accumulated clinical experience. It also included 2 randomized trials that reported beneficial effects of corrective lenses on vision-related quality of life, but not in functional status.29, 30 A later report from 1 of these studies,30 published subsequent to the 2009 USPSTF review, also found no effects on function or cognitive status;31 however, 3 observational studies found refractive surgery was associated with improved quality of life.32-34
The 2009 USPSTF review8 found that more than 90% of patients undergoing cataract surgery achieved visual acuity of 20/40 or better based on observational studies.35 It also included 1 trial that found immediate cataract surgery (within 4 weeks) decreased the risk of falls compared with routine surgery (12 months' wait): 1.00/1000 patient days vs 1.52/1000 patient days (rate ratio, 0.66; 95% CI, 0.40–0.96).36 Two cohort studies that were not in the 2009 USPSTF review found no association of cataract surgery vs no surgery with cognitive function or quality of life after 4 months31 and 1 year,37 although visual acuity improved after surgery in both studies.
The 2009 USPSTF review8 included 1 large, good-quality (n = 2556) randomized trial, the Age-Related Eye Disease Study (AREDS) study.38 AREDS reported results stratified according to the severity of AMD at baseline. Among the subgroup of patients in whom treatment is currently recommended (AREDS categories 3 and 4), AREDS found an antioxidant and zinc combination effective for lower likelihood of AMD progression after 6 years of follow-up (adjusted odds ratio [OR], 0.66; 95% CI, 0.47–0.93), although the difference in the likelihood of losing 15 or more letters of visual acuity was not statistically significant (adjusted OR, 0.75; 95% CI, 0.55–1.02). Ten-year follow-up results from AREDS are now available and are consistent with prior results; antioxidant supplements alone (OR, 0.70; 95% CI, 0.56–0.88) or with added zinc (OR, 0.66; 95% CI, 0.53–0.83) were associated with decreased risk of AMD progression vs placebo among persons with AREDS categories 3 and 4 AMD, and the combination was associated with decreased risk of visual acuity loss (46% vs 54%; OR, 0.71; 95% CI, 0.57–0.88).39 The rates of AMD progression were 34% with the combination and 44% with placebo. Mortality outcomes were reported for AREDS severity categories 2, 3, and 4 (n = 3476). Zinc was also associated with a significantly decreased risk of all-cause mortality (22% vs 25%; adjusted HR, 0.83; 95% CI, 0.73–0.95) and cardiovascular mortality (adjusted RR, 0.80; 95% CI, 0.64–0.99), but there was no significant decrease in cancer mortality risk (adjusted RR, 0.84; 95% CI, 0.65–1.08).
A smaller, good-quality trial (n = 300) published since the 2009 USPSTF review found no difference between daily supplementation with fish oil capsules vs placebo in risk of visual acuity loss of 15 or more letters after 3 years (17.8% vs 16.3%; RR, 1.25; 95% CI, 0.69–2.26), although fish oil was associated with decreased risk of developing cataracts, worsening cataract, or need for cataract surgery (50.0% vs 62.5%; RR, 0.80; 95% CI, 0.64–0.99).40 (RRs and CIs calculated based on proportions reported in the original article.40) Evidence on other vitamins and minerals for dry AMD remains limited, with no clear effects on AMD progression or visual acuity (Table 3, Table 4, and eTable 3 in the Supplement).41-44
The 2009 USPSTF review8 included 4 good-quality trials (reported in 3 publications, n = 184 to 716) of intravitreal injection with VEGF inhibitors vs sham therapy.45-47 In the 2009 USPSTF review, pooled results were reported separately for pegaptanib (2 trials) and ranibizumab (2 trials); both VEGF inhibitors were associated with better visual acuity outcomes vs sham injections. A meta-analysis based on all 4 of these trials found VEGF inhibitors associated with greater likelihood for a gain of 15 or more letters in visual acuity (RR, 2.92; 95% CI, 1.20–7.12; I2 = 76%), but the absolute risk difference was not statistically significant (10%; 95% CI, −7% to 27%). VEGF inhibitors were associated with greater likelihood of having vision 20/200 or better vs sham injection (RR, 1.47; 95% CI, 1.30–1.66; I2 = 42%; absolute risk difference, 24%; 95% CI, 12%–37%) after 1 year (Figure 3 and Figure 4). Beneficial effects were also observed in the MARINA trial after 2 years.45 One trial each found intravitreal injection with VEGF inhibitors was associated with small improvements in likelihood of driving among those driving at baseline48 and in vision-related function.49
The MARINA trial found no difference between ranibizumab vs placebo in all-cause mortality (2% vs 3%; RR, 0.91; 95% CI, 0.34–2.44) or vascular mortality (1% vs 2%; RR,0.74; 95% CI, 0.21–2.60) after 2 years.45 In the other trials, there were no deaths47 or mortality was not reported.46
Harms of Treatment
Key Question 5. Are there harms of treating early impairment in visual acuity?
We identified no new study on harms of treatment for uncorrected refractive error compared with no treatment. The 2009 USPSTF review8 included 1 small study (n = 156) that reported a higher risk of falls in older adults using multifocal lenses compared with unifocal lenses (48% vs 37%; adjusted OR, 2.29; 95% CI, 1.06–4.92).50 Three studies reported that incidence of keratitis ranged from 0.3 to 3.6 cases per 10,000 contact lens wearers.51-53 A meta-analysis reported rates of corneal ectasia of 0% to 0.87% based on 5 studies of laser-assisted in situ keratomileusis (LASIK) and rates of keratitis of 0% to 3.4% based on 6 studies of LASIK and 4 studies of laser-assisted subepithelial keratomileusis (LASEK).28
We identified no new study of harms of cataract surgery vs no surgery. The 2009 USPSTF review included 3 systematic reviews35, 54, 55 of observational studies on harms of cataract surgery, which reported pooled rates of posterior lens opacification of 28% after 5 years and 0.13% for endophthalmitis.
We identified no new studies on harms of treatment for AMD vs no treatment. The 2009 USPSTF review8 found use of antioxidant vitamins and mineral supplements not associated with increased risk of most adverse events.41 One trial published subsequent to the 2009 USPSTF review found no difference between supplement use vs placebo in risk of any adverse events (93% vs 89%; RR, 1.05; 95% CI, 0.97–1.13), serious adverse events (31% vs 30%; RR, 1.04; 95% CI, 0.72–1.49), or serious ocular adverse events (8.2% vs 7.0%; RR, 1.18; 95% CI, 0.50–2.75);40 one other trial published subsequent to the 2009 USPSTF review found no difference in risk of withdrawals due to adverse events (7.1% vs 2.3%; RR, 3.00; 95% CI, 0.33–28).43 One of 2 trials found VEGF inhibitors associated with greater likelihood of withdrawal vs sham therapy;45, 46 there were no differences in serious or other adverse events, but estimates for those outcomes were imprecise.
Table 5 summarizes the evidence reviewed for this update. We identified no new trials of vision screening vs no screening, delayed screening, or usual care. Three fair- to good-quality cluster randomized trials included in the 2009 USPSTF review8 that enrolled more than 4700 patients found vision screening in older adults as part of a multicomponent screening intervention in primary care settings to be no more effective than no vision screening, delayed screening, or usual care.13-15 A fourth trial found optometrist screening associated with an increased risk of falls in frail elderly individuals.16
Conclusions regarding the suboptimal diagnostic accuracy of vision screening tests in primary care settings are also unchanged from the 2009 USPSTF review. Two new studies found that the accuracy of a computer-based screening tool was limited, and 1 study found that a questionnaire performed poorly as a screening test.26, 27 The 2009 USPSTF review found that no screening question is comparable in accuracy with tests of visual acuity for identifying impaired visual acuity19, 20, 23, 24, 56 and that the Snellen test is inaccurate compared with a detailed eye examination for identifying visual conditions identified on a comprehensive ophthalmological examination. However, the clinical importance of asymptomatic conditions identified on an ophthalmologic examination is unclear and may vary depending on the condition. For example, treatments for cataracts may still be successful after the development of impaired visual acuity, whereas impaired visual acuity due to AMD could be irreversible. Although the Snellen test remains the most widely used tool to measure visual acuity in primary care settings, no clinically relevant reference standard exists to determine its diagnostic accuracy, in part because the Snellen test is often considered the standard for assessing visual acuity in clinical practice. There remains insufficient evidence to assess the accuracy or utility of pinhole testing, the Amsler grid, visual acuity tests other than the Snellen test, physical examination, or funduscopic examination performed in primary care settings.
Conclusions from the 2009 USPSTF review regarding the effectiveness of treatments vs no treatment for common causes of impaired visual acuity also remain unchanged. Based primarily on observational studies, a very high proportion of patients experience favorable vision-related outcomes after treatment for impaired visual acuity due to refractive error and cataracts.8 Correction of refractive error and cataract removal are also associated with improvement in vision-related quality of life, although randomized trials and cohort studies have not shown clear effects on measures of general function, cognition, or depression.29-31, 37, 57
For dry AMD, evidence showing the effectiveness of antioxidant vitamins and minerals for slowing progression of disease or improving visual acuity remains largely restricted to the large AREDS trial.38, 41 Extended (10-year) follow-up from AREDS is now available, showing continued benefits.39 Antioxidants included in the AREDS formulation have been found to be associated with congestive heart failure (vitamin E58) and lung cancer in smokers (beta-carotene59, 60) when prescribed for prevention of cancer or cardiovascular disease, although such harms were not observed in AREDS.
For wet AMD, evidence reviewed in the 2009 USPSTF review found intravitreal injection with VEGF inhibitors to be effective treatment options with a relatively low incidence of serious harms, although they may be associated with an increased risk of acute decline in visual acuity.61 As detailed in the full review, photodynamic therapy and laser photocoagulation also appear to be associated with decreased risk of vision loss in patients with wet AMD but have been replaced as first-line therapy with VEGF inhibitors in most patients because of the risk of acute visual loss, need for retreatment (photodynamictherapy), and risk of permanent retinal damage (laser photocoagulation).12
Our evidence review has limitations. We excluded non–English language studies, which could introduce language bias. However, we identified no relevant non–English language studies, and some research found that exclusion of non–English language studies has little effect on conclusions of reviews of noncomplementary and alternative therapies.62 In addition, trials of therapy for dry AMD evaluated heterogeneous vitamins, antioxidants, and other supplements and could not be pooled. There were also too few randomized trials to perform reliable assessments for publication bias.63
We identified important research gaps. Evidence indicates that screening can identify older patients with decreased visual acuity and there are effective treatments for common causes of impaired visual acuity, yet screening was not associated with improved clinical outcomes. Well-designed studies in primary care settings are needed to identify optimal methods for vision screening and to develop effective strategies for linking older adults with impaired visual acuity to appropriate care, which would help maximize the potential benefits of screening. Studies are needed on the diagnostic accuracy and utility of funduscopic examination, pinhole testing, the Amsler grid, and non-Snellen visual acuity tests in primary care settings for supplementing or replacing the Snellen visual eye chart. Evidence on effectiveness of antioxidants and vitamins for dry AMD remains largely dependent on a single large trial38 and would be strengthened by other, well-designed trials that are also designed to adequately evaluate potential harms associated with components of the supplements, such as congestive heart failure and lung cancer risk. More studies are needed to understand the potential association between correction of refractive errors and risk of falls16 and, if an association is present, to identify methods for mitigating these risks. Research is also needed to understand the effectiveness of new therapies that are being investigated for their effectiveness in AMD, such as statins64 and complement inhibitors (eg, protease inhibitors).65
Screening can identify persons with impaired visual acuity, and effective treatments are available for common causes of impaired visual acuity, such as uncorrected refractive error, cataracts, and dry or wet AMD. However, direct evidence found no significant difference between vision screening in older adults in primary care settings vs no screening for improving visual acuity or other clinical outcomes.
Copyright and Source Information
Source: This article was first published in the Journal of the American Medical Association on March 1, 2016 (JAMA. 2016;315(9):915-933).
Conflict of Interest Disclosures: All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest and none were reported.
Role of the 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 metmethodological 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; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
Additional Information: A draft version of this evidence report underwent external peer review from 5 content experts (Neil M. Bressler, MD, Wilmer Eye Institute, Johns Hopkins University School of Medicine; Zahra Jessa, PhD, BSc, MCOptom, Moorfields Eye Hospital, Royal National Institute of Blind People, London; Gianni Virgili, MD, Careggi Hospital Eye Clinic, University of Florence, Italy; Liam Smeeth, MBChB, FRCGP, FFPH, FRCP, MSc, PhD, London School of Hygiene and Tropical Medicine; Nancy Weintraub,MD, David Geffen School of Medicine, University of California at Los Angeles) and 3 federal partners: Food and Drug Administration/Center for Drug Evaluation and Research; National Institute on Aging/National Institutes of Health; and the Veterans Health Administration. Comments were presented to the USPSTF during its deliberation of the evidence and were considered in preparing the final evidence review.
1. Sims RV, Owsley C, Allman RM, Ball K, Smoot TM. A preliminary assessment of the medical and functional factors associated with vehicle crashes by older adults. J Am Geriatr Soc. 1998;46(5):556-561.
2. Owsley C, Stalvey B,Wells J, Sloane ME. Older drivers and cataract: driving habits and crash risk. J Gerontol A Biol Sci Med Sci. 1999;54(4): M203-M211.
3. McGwin G Jr, Chapman V, Owsley C. Visual risk factors for driving difficulty among older drivers. Accid Anal Prev. 2000;32(6):735-744.
4. Lord SR, Dayhew J. Visual risk factors for falls in older people. J Am Geriatr Soc. 2001;49(5):508-515.
5. Ivers RQ, Cumming RG, Mitchell P, Attebo K. Visual impairment and falls in older adults: the Blue Mountains Eye Study. J Am Geriatr Soc. 1998;46 (1):58-64.
6. Summary health statistics for US adults: National Health Interview Survey. Centers for Disease Control and Prevention National Center for Health Statistics. http://www.cdc.gov/nchs/data/series/sr _10/sr10_256.pdf. Accessed July 16, 2015.
7. Congdon N, O'Colmain B, Klaver CC, et al; Eye Diseases Prevalence Research Group. Causes and prevalence of visual impairment among adults in the United States. Arch Ophthalmol. 2004;122 (4):477-485.
8. Chou R, Dana T, Bougatsos C. Screening for Visual Impairment in Older Adults: Systematic Review to Update the 1996 US Preventive Services Task Force Recommendation: Evidence Synthesis No. 71 [AHRQ Publication No. 09-05135-EF-1]. Rockville, MD: Agency for Healthcare Research and Quality; 2009.
9. Chou R, Dana T, Bougatsos C. Screening older adults for impaired visual acuity: a review of the evidence for the US Preventive Services Task Force. Ann Intern Med. 2009;151(1):44-58,W11-20.
10. US Preventive Services Task Force. Screening for impaired visual acuity in older adults: US Preventive Services Task Force recommendation statement. Ann Intern Med. 2009;151(1):37-43,W10.
11. US Preventive Services Task Force: Methods and Processes: Procedure Manual. http://www.uspreventiveservicestaskforce.org/Page/Name/methods-and-processes. Accessed July 16, 2015.
12. Chou R, Dana T, Bougatsos C, Grusing S, Blazina I. Screening for Impaired Visual Acuity in Older Adults: A Systematic Review to Update the 2009 US Preventive Services Task Force Recommendation: Evidence Synthesis No. 127 [AHRQ Publication No. 14-05209-EF-1]. Rockville, MD: Agency for Healthcare Research and Quality; 2016.
13. Eekhof J, De Bock G, Schaapveld K, Springer M. Effects of screening for disorders among the elderly: an intervention study in general practice. Fam Pract. 2000;17(4):329-333.
14. Moore AA, Siu Al, Partridge JM, Hays RD, Adams J. A randomized trial of office-based screening for common problems in older persons. Am J Med. 1997;102(4):371-378.
15. Smeeth L, Fletcher AE, Hanciles S, Evans J, Wormald R. Screening older people for impaired vision in primary care: cluster randomised trial. BMJ. 2003;327(7422):1027-1031.
16. Cumming RG, Ivers R, Clemson L, et al. Improving vision to prevent falls in frail older people: a randomized trial. J Am Geriatr Soc. 2007; 55(2):175-181.
17. Swamy B, Cumming RG, Ivers R, et al. Vision screening for frail older people: a randomised trial. Br J Ophthalmol. 2009;93(6):736-741.
18. Ariyasu RG, Lee PP, Linton KP, LaBree LD, Azen SP, Siu AL. Sensitivity, specificity, and predictive values of screening tests for eye conditions in a clinic-based population. Ophthalmology. 1996;103 (11):1751-1760.
19. Eekhof JA, De Bock GH, Schaapveld K, Springer MP. Screening for hearing and visual loss among elderly with questionnaires and tests: which method is the most convincing for action? Scand J Prim Health Care. 2000;18(4): 203-207.
20. Hiller R, Krueger DE. Validity of a survey question as a measure of visual acuity impairment. Am J Public Health. 1983;73(1):93-96.
21. Ivers RQ, Optom B, Macaskill P, Cumming RG, Mitchell P. Sensitivity and specificity of tests to detect eye disease in an older population. Ophthalmology. 2001;108(5):968-975.
22. McMurdo ME, Baines PS. The detection of visual disability in the elderly. Health Bull (Edinb). 1988;46(6):327-329.
23. Chu-Ai Teh R, Lim WS, Basri R, Ismail NH. Utility of a patient-response screening question for visual impairment. J Am Geriatr Soc. 2006;54(2): 370-372.
24. Wang F, Tielsch JM, Ford DE, Quigley HA, Whelton PK. Evaluation of screening schemes for eye disease in a primary care setting. Ophthalmic Epidemiol. 1998;5(2):69-82.
25. Woods RL, Tregear SJ, Mitchell RA. Screening for ophthalmic disease in older subjects using visual acuity and contrast sensitivity. Ophthalmology. 1998;105(12):2318-2326.
26. Jessa Z, Evans BJW, Thomson DW. The development and evaluation of two vision screening tools for correctable visual loss in older people. Ophthalmic Physiol Opt. 2012;32(4):332-348.
27. Swanson MW, McGwin G Jr, Elliott AF, Owsley C. The nursing home minimum data set for vision and its association with visual acuity and contrast sensitivity. J Am Geriatr Soc. 2009;57(3): 486-491.
28. Murray A, Jones L, Milne A, Fraser CM, Lourenco T, Burr J. A systematic review of the safety and efficacy of elective photorefractive surgery for the correction of refractive error. London, UK: National Institute for Health and Clinical Excellence; 2005:149.
29. Coleman AL, Yu F, Keeler E, Mangione CM. Treatment of uncorrected refractive error improves vision-specific quality of life. J Am Geriatr Soc. 2006;54(6):883-890.
30. Owsley C, McGwin G Jr, Scilley K, Meek GC, Seker D, Dyer A. Effect of refractive error correction on health-related quality of life and depression in older nursing home residents. Arch Ophthalmol. 2007;125(11):1471-1477.
31. Elliott AF, McGwin G Jr, Owsley C. Vision-enhancing interventions in nursing home residents and their short-term effect on physical and cognitive function. J Am Geriatr Soc. 2009;57 (2):202-208.
32. McDonnell PJ, Mangione C, Lee P, et al. Responsiveness of the National Eye Institute Refractive Error Quality of Life instrument to surgical correction of refractive error. Ophthalmology. 2003;110(12):2302-2309.
33. Schein OD, Vitale S, Cassard SD, Steinberg EP. Patient outcomes of refractive surgery: the refractive status and vision profile. J Cataract Refract Surg. 2001;27(5):665-673.
34. Tahzib NG, Bootsma SJ, Eggink FA, Nabar VA, Nuijts RM. Functional outcomes and patient satisfaction after laser in situ keratomileusis for correction ofmyopia. J Cataract Refract Surg. 2005; 31(10):1943-1951.
35. Powe NR, Schein OD, Gieser SC, et al; Cataract Patient Outcome Research Team. Synthesis of the literature on visual acuity and complications following cataract extraction with intraocular lens implantation. Arch Ophthalmol. 1994;112(2):239-252.
36. Harwood RH, Foss AJE, Osborn F, Gregson RM, Zaman A, Masud T. Falls and health status in elderly women following first eye cataract surgery: a randomised controlled trial. Br J Ophthalmol. 2005;89(1):53-59.
37. Hall TA, McGwin G Jr, Owsley C. Effect of cataract surgery on cognitive function in older adults. J Am Geriatr Soc. 2005;53(12):2140-2144.
38. Age-Related Eye Disease Study Research Group. A randomized, placebo-controlled, clinical trial of high-dose supplementation with vitamins C and E, beta carotene, and zinc for age-related macular degeneration and vision loss: AREDS report No. 8. Arch Ophthalmol. 2001;119(10):1417-1436.
39. Chew EY, Clemons TE, Agrón E, et al; Age-Related Eye Disease Study Research Group. Long-term effects of vitamins C and E, β-carotene, and zinc on age-related macular degeneration: AREDS report No. 35. Ophthalmology. 2013;120(8): 1604-11.e4.
40. Souied EH, Delcourt C, Querques G, et al; Nutritional AMD Treatment 2 Study Group. Oral docosahexaenoic acid in the prevention of exudative age-related macular degeneration: the Nutritional AMD Treatment 2 study. Ophthalmology. 2013;120(8):1619-1631.
41. Evans JR, Henshaw K. Antioxidant vitamin and mineral supplements for preventing age-related macular degeneration. Cochrane Database Syst Rev. 2008;(1):CD000253.
42. Evans JR, Lawrenson JG. Antioxidant vitamin and mineral supplements for slowing the progression of age-related macular degeneration. Cochrane Database Syst Rev. 2012;11(11):CD000254.
43. Murray IJ, Makridaki M, van der Veen RLP, Carden D, Parry NRA, Berendschot TTJM. Lutein supplementation over a one-year period in early AMD might have a mild beneficial effect on visual acuity: the CLEAR study. Invest Ophthalmol Vis Sci. 2013;54(3):1781-1788.
44. Ma L, Yan SF, Huang YM, et al. Effect of lutein and zeaxanthin on macular pigment and visual function in patients with early age-related macular degeneration. Ophthalmology. 2012;119(11):2290-2297.
45. Rosenfeld PJ, Brown DM, Heier JS, et al; MARINA Study Group. Ranibizumab for neovascular age-related macular degeneration. N Engl J Med. 2006;355(14):1419-1431.
46. Gragoudas ES, Adamis AP, Cunningham ET Jr, Feinsod M, Guyer DR; VEGF Inhibition Study in Ocular Neovascularization Clinical Trial Group. Pegaptanib for neovascular age-related macular degeneration. N Engl J Med. 2004;351(27):2805-2816.
47. Regillo CD, Brown DM, Abraham P, et al. Randomized, double-masked, sham-controlled trial of ranibizumab for neovascular age-related macular degeneration: PIER Study year 1. Am J Ophthalmol. 2008;145(2):239-248.
48. Bressler NM, Chang TS, Varma R, et al. Driving ability reported by neovascular age-related macular degeneration patients after treatment with ranibizumab. Ophthalmology. 2013; 120(1):160-168.
49. Chang TS, Bressler NM, Fine JT, Dolan CM, Ward J, Klesert TR; MARINA Study Group. Improved vision-related function after ranibizumab treatment of neovascular age-related macular degeneration: results of a randomized clinical trial. Arch Ophthalmol. 2007;125(11):1460-1469.
50. Lord SR, Dayhew J, Howland A. Multifocal glasses impair edge-contrast sensitivity and depth perception and increase the risk of falls in older people. J Am Geriatr Soc. 2002;50(11): 1760-1766.
51. Cheng KH, Leung SL, Hoekman HW, et al. Incidence of contact-lens-associated microbial keratitis and its related morbidity. Lancet. 1999;354 (9174):181-185.
52. Nilsson SE, Montan PG. The annualized incidence of contact lens induced keratitis in Sweden and its relation to lens type and wear schedule: results of a 3-month prospective study. CLAO J. 1994;20(4):225-230.
53. Schein OD, McNally JJ, Katz J, et al. The incidence of microbial keratitis among wearers of a 30-day silicone hydrogel extended-wear contact lens. Ophthalmology. 2005;112(12):2172-2179.
54. Schaumberg DA, Dana MR, Christen WG, Glynn RJ. A systematic overview of the incidence of posterior capsule opacification. Ophthalmology. 1998;105(7):1213-1221.
55. Taban M, Behrens A, Newcomb RL, et al. Acute endophthalmitis following cataract surgery: a systematic review of the literature. Arch Ophthalmol. 2005;123(5):613-620.
56. Stone DH, Shannon DJ. Screening for impaired visual acuity in middle age in general practice. BMJ. 1978;2(6141):859-861.
57. Owsley C, McGwin G Jr, Scilley K, Meek GC, Seker D, Dyer A. Impact of cataract surgery on health-related quality of life in nursing home residents. Br J Ophthalmol. 2007;91(10):1359-1363.
58. Lonn E, Bosch J, Yusuf S, et al; HOPE and HOPE-TOO Trial Investigators. Effects of long-term vitamin E supplementation on cardiovascular events and cancer: a randomized controlled trial. JAMA. 2005;293(11): 1338-1347.
59. Omenn GS, Goodman GE, Thornquist MD, et al. Effects of a combination of beta carotene and vitamin A on lung cancer and cardiovascular disease. N Engl J Med. 1996;334(18):1150-1155.
60. The Alpha-Tocopherol Beta Carotene Cancer Prevention Study Group. The effect of vitamin E and beta carotene on the incidence of lung cancer and other cancers in male smokers. N Engl J Med. 1994;330(15):1029-1035.
61. Vedula SS, Krzystolik MG. Antiangiogenic therapy with anti-vascular endothelial growth factor modalities for neovascular age-related macular degeneration. Cochrane Database Syst Rev. 2008;2(2):CD005139.
62. Morrison A, Polisena J, Husereau D, et al. The effect of English-language restriction on systematic review-based meta-analyses: a systematic review of empirical studies. Int J Technol Assess Health Care. 2012;28(2):138-144.
63. Sterne JA, Sutton AJ, Ioannidis JPA, et al. Recommendations for examining and interpreting funnel plot asymmetry inmeta-analyses of randomised controlled trials. BMJ. 2011;343:d4002.
64. Guymer RH, Baird PN, Varsamidis M, et al. Proof of concept, randomized, placebo-controlled study of the effect of simvastatin on the course of age-related macular degeneration. PLoS One. 2013; 8(12):e83759.
65. Williams MA, McKay GJ, Chakravarthy U. Complement inhibitors for age-related macular degeneration. Cochrane Database Syst Rev. 2014;1 (1):CD009300.
Figure 1. Analytic Framework and Key Questions
“Asymptomatic” individuals are those without known impaired visual acuity (based on current corrected vision) who have not sought care for evaluation of vision problems.
This figure depicts the analytic framework, which outlines the evidence areas covered in the review, including the population, interventions and related harms, and outcomes. The population includes asymptomatic adults without known vision impairment (based on current corrected vision) and who have not sought care for evaluation of vision problems. An arrow from the population leads to screening, followed by normal or abnormal diagnosis. A subsequent arrow from the screening intervention assesses resulting harms. An arrow leading from abnormal screening results incorporates treatment and leads to the outcomes examined in the review, which are improved visual acuity, morbidity, mortality, vision-related quality of life, functional status, and cognition. A subsequent arrow from treatment assesses resulting harms. An additional overarching arrow in the framework examines the effect of screening on outcomes.
Figure 2. Literature Flow Diagram
Cochrane databases include the Cochrane Central Register of Controlled Trials and the Cochrane Database of Systematic Reviews. Other sources include prior reviews, references lists, and referrals from experts.
AMD indicates age-related macular degeneration; VEGF, vascular endothelial growth factor.
a Studies and reviews may be included for more than 1 key question (KQ).
This figure is a literature flow diagram depicting the search and selection of articles for the present review. The diagram shows that 4,506 abstracts of potentially relevant articles were identified through MEDLINE, Cochrane, and other sources. 273 articles were reviewed at the full-text level after excluding 4,233 nonrelevant abstracts and background articles. From these, 225 were excluded due to: wrong population (55), wrong intervention (30), wrong outcome (23), wrong study design for key question (39), not a study (13), in systematic review and not directly used (26), wrong comparison (23), using original studies instead (14), and screening conducted by an optometrist (1 study in 2 publications). After excluding these studies, 48 publications, including 10 studies and 1 systematic review in the update and 29 studies (in 30 publications) and 7 systematic reviews from the prior report, were included.
Table 1. Trials of Screening for Impaired Visual Acuity in Older Adults (Key Question 1)
No./Total No. %)
|Mean age, y||Baseline Visual Acuity||Intervention||Results||Qualityb|
|Eekhof et al,13 2000||The Netherlands||General practice||717/1121
|81||NR||G1, screening: Snellen eye chart and/or functional visual assessment
G2, delayed screening
|G1 vs G2:
Vision problem detected: 49% vs NR
Visual disorder in second year: 51% (95% CI, 45%–58%) vs 47% (95% CI, 42%–52%); P = 0.68)
|Moore et al,14 1997||United States||Community-based office practice||161/261 (62)||76||NR||G1, screening: question to assess difficulty performing everyday activities, followed by Snellen eye chart if positive
G2, usual care
|G1 vs G2:
Vision problem detected: 20% vs 19%
Improvement in vision at 6 mo: 20% (20/99) vs 24% (31/131); RR, 0.85 (95% CI, 0.52–1.40)
|Smeeth et al,15 2003||United Kingdom||General practice||2065/3346 (62)||89||Difficulty seeing newsprint:
|G1, universal screening: health assessment by a trained nurse, including Glasgow eye chart and pinhole testing if visual acuity <6/18 in either eye
G2, targeted screening: brief health assessment
|G1 vs G2:
Found to have visual acuity <6/18 in either eye: 27% (451/1662) vs 3.1% (53/1684)
Visual acuity <6/18 (20/60) at 3 y: RR, 1.07 (95% CI, 0.84 to 1.36)
Mean NEI-VFQ composite score: 86.0 vs 85.6 (range, 1 to 100); mean difference, 0.4 (95% CI, −1.7 to 2.5)
Abbreviations: G1, G2, group 1, group 2; NEI-VFQ, National Eye Institute Vision Function Questionnaire; NR, not reported; RCT, randomized clinical trial; RR, relative risk.
a Race was not reported in any of the 3 trials.
b See eTable 1 in the Supplement for detailed quality assessment.
Table 2. Studies of Diagnostic Accuracy for Impaired Visual Acuity in Older Adults
(Key Question 3)a
|Reference Standard||Target Vision Condition||Screening Test||Sensitivity
|Positive Likelihood Ratio
|Negative Likelihood Ratio
|Studies From Update|
|Jessa et al,26 2012 (study 1)||180||"Gold standard eye examination"c||Any ocular disease||High-contrast visual acuity >0.19 logMAR or abnormal near visual acuity||0.80 (0.72-0.86)||0.68 (0.57-0.77)||2.48 (1.76-3.49)||0.29 (0.20-0.45)||8.55|
|Jessa et al,26 2012 (study 2)||200||"Gold standard eye examination"c||Any ocular disease||A: High-contrast visual acuity >0.9 logMAR or abnormal near visual acuity
B: Low-contrast visual acuity >0.49 logMAR
|Swanson et al,27 2009||371||ETDRS chart||Any ocular disease||MDS vision patterns ection score >0 (adequate)||0.52 (0.45-0.59)||0.75 (0.68-0.82)||2.11 (1.56-2.86)||0.64 (0.54-0.75)||3.30|
|Studies From 2009 Review|
|Ariyasu et al,18 1996||317||Ophthalmologic examination||Any ocular disease, excluding refractive error||Amsler grid abnormal||0.20 (0.14-0.27)||0.88 (0.80-0.94)||1.65 (0.90-3.06)||0.91 (0.82-1.01)||1.82 (0.90-3.69)|
|McMurdo and Baines,22 1988||50||Ophthalmologist examination||A: Cataract
|Positive finding on physical examination||A: 1.0 (9/9)
B: 0.75 (3/4)
|A: 1.0 (41/41)
B: 1.0 (46/46)
|Eekhof et al,19 2000||1121||Snellen chart||Visual acuity ≤0.3 (about 20/60 on Snellen)||Trouble recognizing face by questionnaire||0.60 (0.51-0.69)||0.82 (0.79-0.84)||3.23 (2.66-3.93)||0.49 (0.40-0.61)||6.56 (4.42-9.72)|
|Difficulty with low vision chart at reading distance||Trouble recognizing face by questionnaire||0.83 (0.76-0.88)||0.67 (0.64-0.70)||2.47 (2.20-2.78)||0.26 (0.18-0.37)||9.45 (6.08-14.7)|
|Hiller and Krueger,20 1983||3997||Snellen chart||A: Visual acuity ≤20/50
B: Visual acuity ≤20/100
|Trouble seeing, by questionnaire||A: 0.34 (0.28-0.41)
B: 0.48 (0.32-0.63)
|A: 0.84 (0.82-0.86)
B: 0.82 (0.80-0.84)
|A: 2.15 (1.72-2.69)
B: 2.69 (1.94-3.74)
|A: 0.78 (0.71-0.86)
B: 0.64 (0.48-0.84)
|A: 2.75 (2.00-3.78)
B: 4.24 (2.33-7.72)
|Chu-Ai Teh et al,23 2006||124||Snellen chart||Visual acuity ≤20/40||Problem with vision by questionnaire||0.68 (0.58-0.78)||0.43 (0.22-0.66)||1.19 (0.80-1.77)||0.74 (0.42-1.33)||1.60 (0.62-4.16)|
|Wang et al,24 1998||405||Ophthalmologic examination||Any ocular disease||A: Problem with vision by questionnaire
B: Problem with vision by questionnaire followed by visual acuity ≤20/40
|A: 0.90 (0.85-0.94)
B: 0.57 (0.50-0.64)
|A: 0.44 (0.37-0.51)
B: 0.79 (0.73-0.84)
|A: 1.60 (1.41-1.83)
B: 2.72 (2.03-3.65)
|A: 0.23 (0.15-0.36)
B: 0.54 (0.46-0.65)
|A: 6.88 (4.06-11.7)
B: 5.00 (3.23-7.74)
|Visual acuity testing|
|Ariyasu et al,18 1996||317||Ophthalmologic examination||Any ocular disease, excluding refractive error||Near visual acuity ≤20/30||0.83 (0.75-0.89)||0.32 (0.23-0.44)||1.23 (1.04-1.46)||0.52 (0.32-0.86)||2.34 (1.23-4.47)|
|Near visual acuity ≤20/40||0.76 (0.68-0.83)||0.49 (0.38-0.61)||1.50 (1.19-1.90)||0.49 (0.33-0.71)||3.09 (1.71-5.55)|
|Near visutal acuity ≤20/60||0.60 (0.52-0.69)||0.64 (0.53-0.74)||1.67 (1.22-2.30)||0.62 (0.47-0.81)||2.70 (1.53-4.77)|
|Ariyasu et al,18 1996||317||Ophthalmologic examination||Any ocular disease, excluding refractive error||Presenting distance visual acuity ≤20/30||0.75 (0.69-0.81)||0.51 (0.42-0.61)||1.54 (1.26-1.90)||0.48 (0.36-0.65)||3.18 (1.96-5.18)|
|Presenting distance visual acuity ≤20/40||0.68 (0.61-0.74)||0.67 (0.58-0.76)||2.08 (1.57-2.76)||0.47 (0.37-0.60)||4.40 (2.69-7.18)|
|Presenting distance visual acuity ≤20/60||0.53 (0.46-0.60)||0.86 (0.78-0.92)||3.76 (2.34-6.03)||0.54 (0.46-0.64)||6.90 (3.82-12.5)|
|Ivers et al,21 2001||3654||Ophthalmologic examination||A: Nuclear cataract
B: Early AMD
C: Any eye disease
|Pinhole distance acuity ≤20/30||A: 0.31 (0.28-0.34)
B: 0.45 (0.37-0.53)
C: 0.34 (0.31-0.37)
|A: 0.89 (0.87-0.91)
B: 0.79 (0.78-0.80)
C: 0.86 (0.84-0.87)
|A: 2.83 (2.35-3.40)
B: 2.16 (1.80-2.59)
C: 2.43 (2.14-2.76)
|A: 0.78 (0.74-0.81)
B: 0.69 (0.60-0.80)
C: 0.77 (0.74-0.80)
|A: 3.65 (2.93-4.55)
B: 3.11 (2.26-4.30)
C: 3.17 (2.69-3.73)
|Pinhole distance acuity ≤20/40||A: 0.13 (0.11-0.15)
B: 0.21 (0.15-0.28)
C: 0.15 (0.13-0.17)
|A: 0.98 (0.97-0.99)
B: 0.92 (0.91-0.93)
C: 0.96 (0.95-0.97)
|A: 6.57 (4.29-10.1)
B: 2.59 (1.87-3.58)
C: 3.74 (2.95-4.73)
|A: 0.89 (0.87-0.91)
B: 0.86 (0.80-0.93)
C: 0.89 (0.86-0.91)
|A: 7.40 (4.78-11.5)
B: 3.01 (2.01-4.49)
C: 4.22 (3.27-5.45)
|Pinhole distance acuity ≤20/60||A: 0.08 (0.06-0.10)
B: 0.10 (0.06-0.16)
C: 0.09 (0.07-0.11)
|A: 0.99 (0.98-1.00)
B: 0.95 (0.94-0.96)
C: 0.97 (0.96-0.98)
|A: 8.07 (4.44-14.7)
B: 2.01 (1.24-3.28)
C: 2.98 (2.23-3.97)
|A: 0.93 (0.91-0.95)
B: 0.95 (0.90-1.00)
C: 0.94 (0.92-0.96)
|A: 8.69 (4.76-15.8)
B: 2.13 (1.25-3.63)
C: 3.17 (2.34-4.30)
|Ivers et al,21 2001||3654||Ophthalmologic examination||A: Nuclear cataract
B: Early AMD
C: Any eye disease
|Presenting distance visual acuity ≤20/30||A: 0.44 (0.41-0.47)
B: 0.56 (0.48-0.64)
C: 0.47 (0.44-0.50)
|A: 0.77 (0.74-0.79)
B: 0.66 (0.64-0.68)
C: 0.74 (0.72-0.76)
|A: 1.91 (1.69-2.16)
B: 1.65 (1.42-1.90)
C: 1.81 (1.65-1.98)
|A: 0.73 (0.68-0.77)
B: 0.67 (0.56-0.80)
C: 0.72 (0.68-0.76)
|A: 2.63 (2.20-3.15)
B: 2.47 (1.79-3.40)
C: 2.53 (2.19-2.92)
|Presenting distance visual acuity ≤20/40||A: 0.25 (0.22-0.28)
B: 0.34 (0.27-0.42)
C: 0.27 (0.24-0.29)
|A: 0.90 (0.88-0.92)
B: 0.82 (0.81-0.83)
C: 0.87 (0.86-0.88)
|A: 2.50 (2.05-3.05)
B: 1.89 (1.50-2.37)
C: 2.07 (1.81-2.38)
|A: 0.83 (0.80-0.87)
B: 0.80 (0.72-0.90)
C: 0.84 (0.81-0.87)
|A: 3.00 (2.38-3.79)
B: 2.34 (1.67-3.28)
C: 2.47 (2.08-2.94)
|Presenting distance visual acuity ≤20/60||A: 0.13 (0.11-0.15)
B: 0.13 (0.08-0.20)
C: 0.14 (0.12-0.16)
|A: 0.96 (0.95-0.97)
B: 0.92 (0.91-0.93)
C: 0.94 (0.93-0.95)
|A: 3.22 (2.35-4.41)
B: 1.65 (1.09-2.49)
C: 2.33 (1.89-2.88)
|A: 0.91 (0.88-0.93)
B: 0.94 (0.89-1.00)
C: 0.92 (0.89-0.94)
|A: 3.55 (2.54-4.96)
B: 1.75 (1.09-2.80)
C: 2.55 (2.02-3.21)
|Ivers et al,21 2001||3654||Ophthalmologic examination||A: Nuclear
B: Early AMD
C: Any eye
|Reading acuity ≤20/30
||A: 0.97 (0.96-0.98)
B: 0.99 (0.96-1.00)
C: 0.98 (0.97-0.99)
|A: 0.03 (0.02-0.04)
B: 0.03 (0.02-0.04)
C: 0.03 (0.02-0.04)
|A: 1.00 (0.99-1.01)
B: 1.02 (1.00-1.04)
C: 1.01 (1.00-1.02)
|A: 1.00 (0.63-1.60)
B: 0.42 (0.10-1.69)
C: 0.66 (0.42-1.03)
|A: 1.00 (0.62-1.61)
B: 2.42 (0.65-8.98)
C: 1.53 (0.97-2.42)
|Reading acuity ≤20/40||A: 0.88 (0.86-0.90)
B: 0.95 (0.90-0.98)
C: 0.89 (0.87-0.91)
|A: 0.20 (0.18-0.22)
B: 0.16 (0.15-0.17)
C: 0.19 (0.18-0.21)
|A: 1.10 (1.06-1.14)
B: 1.13 (1.09-1.18)
C: 1.10 (1.07-1.13)
|A: 0.60 (0.49-0.73)
B: 0.32 (0.16-0.62)
C: 0.58 (0.49-0.68)
|A: 1.84 (1.46-2.32)
B: 3.59 (1.78-7.26)
C: 1.90 (1.55-2.32)
|Reading acuity ≤20/60||A: 0.57 (0.54-0.60)
B: 0.70 (0.62-0.77)
C: 0.59 (0.56-0.62)
|A: 0.59 (0.56-0.62)
B: 0.53 (0.51-0.55)
C: 0.59 (0.57-0.61)
|A: 1.39 (1.28-1.52)
B: 1.48 (1.33-1.65)
C: 1.44 (1.35-1.54)
|A: 0.73 (0.67-0.79)
B: 0.57 (0.45-0.72)
C: 0.70 (0.64-0.75)
|A: 1.91 (1.62-2.26)
B: 2.61 (1.85-3.68)
C: 2.07 (1.80-2.38)
|Wang et al,24 1998||405||Ophthalmologic examination||Any ocular disease||Presenting distance visual acuity ≤20/40||0.61 (0.54-0.68)||0.72 (0.65-0.78)||2.18 (1.70-2.79)||0.54 (0.45-0.66)||4.02 (2.65-6.09)|
|Woods et al,25 1998||3283||Ophthalmologic examination||Any ocular disease, excluding refractive error||Near visual acuity ≤20/30||0.77 (0.74-0.80)||0.68 (0.63-0.73)||2.41 (2.08-2.80)||0.34 (0.30-0.38)||7.15 (5.52-9.26)|
|Woods et al,25 1998||3283||Ophthalmologic examination||Any ocular disease, excluding refractive error||Presenting distance visual acuity ≤20/30||0.74 (0.71-0.77)||0.87 (0.83-0.90)||5.66 (4.36-7.34)||0.30 (0.27-0.33)||18.9 (13.6-26.3)|
Abbreviations: AMD, age-related macular degeneration; ETDRS, Early Treatment Diabetic Retinopathy Study; logMAR, logarithm of the minimal angle of resolution; MDS, Minimum Data Set; NC, not calculated; OR, odds ratio.
a All studies had a cross-sectional design. See eTable 2 in the Supplement for detailed quality assessment.
b Diagnostic OR is the ratio of the positive likelihood ratio to the negative likelihood ratio.
c Included computerized high-contrast visual acuity and low-contrast visual acuity tests.
Table 3. Treatment Studies of Antioxidant Vitamins, Minerals, and Other Supplements for Dry AMD Published Since the 2009 Review: Systematic Review (n = 6150 Participants) (Key Question 4)
Searched, Date of
|No. and Design of
|Interventions||Methods for Rating
Quality of Primary Studies
of Primary Studies
|Evans et al,42 2012||Antioxidant vitamin or mineral supplementation vs placebo/no intervention||MEDLINE, EMBASE, Cochrane Central Register of Controlled Trials, Allied and Complementary Medicine Database, OpenGrey, metaRegister of Controlled Trials, ClinicalTrials.gov through August 2012||13 RCTs: zinc (5 trials), lutein (2 trials), vitamin E (1 trial), antioxidant combination (4 trials); multiple interventions (1 trial)||A: Antioxidant vitamin or mineral supplementation
A1: Multivitamin or mineral supplement
B: Placebo/no intervention
|Risk of bias assessment using criteria from Cochrane Handbook for Systematic Review Interventions (2011)||For dichotomous outcomes, calculated RRs and standard error and converted reported ORs to RRs when possible. Random-effects model used assessing SMD for continuous outcomes. If ≤3 trials, fixed-effects model was used.||A vs B (SMD):
Visual acuity, loss of ≥3 lines (3 trials): OR, 0.81; 95% CI, 0.67 to 0.98
Mean visual acuity (4 trials): no meta- analysis; SMD range, −0.80 to 0.14; CI significant for 1 study (SMD, −0.80; 95% CI, −1.27 to −0.32)
Mean change in visual acuity (3 trials): no meta-analysis; SMD range, −0.34 to 0.42; CI not significant for any trial AMD progression, dichotomous: no meta-analysis; OR ranged from 0.50 to 2.31; CI not significant for any trial
|No meta-analysis; narrative review suggested higher rates of withdrawals due to adverse events in participants taking zinc vs placebo. Other harms not well reported.||Good|
|A1 vs B:
Mean visual acuity (2 trials): SMD, 0.00; 95% CI, −0.45 to 0.45
Mean change in visual acuity (2 trials): SMD, 0.34; 95% CI, −0.10 to 0.79
AMD progression, continuous (2 trials): no meta-analysis conducted; results from individual trials found no significant difference
AMD progression, dichotomous (1 trial): adjusted OR (for age, sex, smoking, and AMD category), 0.68; 95% CI, 0.53 to 0.87
|A2 vs B:
Visual acuity, loss of ≥3 lines (2 trials): OR, 0.81; 95% CI, 0.66 to 0.99
Mean visual acuity (1 trial): SMD, 0.15; 95% CI, −0.29 to 0.60
Mean change in visual acuity (1 trial): SMD, −0.34; 95% CI, −0.79 to 0.11
AMD progression, dichotomous (3 trials): OR, 0.73; 95% CI, 0.58 to 0.93
Abbreviations: AMD, age-related macular degeneration; OR, odds ratio; RCT, randomized clinical trial; RR, risk ratio; SMD, standardized mean difference.
Figure 3. Gain of 15 Letters or More of Visual Acuity With Use of VEGF Inhibitors at 1-Year Follow-up (Key Question 4)
The 2-year results for MARINA: risk ratio, 7.86 (95% CI, 4.08 to 15). VEGF indicates vascular endothelial growth factor.
This figure is a forest plot showing gain of 15 letters or more of visual acuity with use of VEGF inhibitors at 1-year followup. Two studies comparing ranibizumab versus sham and 2 studies of pegaptanib versus sham were pooled for a total risk ratio of 2.92 (95% CI, 1.20 to 7.12); I2=76%.
Figure 4. Visual Acuity of 20/200 or Better With Use of VEGF Inhibitors at 1-Year Follow-up (Key Question 4)
The 2-year results for MARINA: risk ratio, 1.63 (95% CI, 1.44 to 1.86). VEGF indicates vascular endothelial growth factor.
This figure is a forest plot showing visual acuity of 20/200 or better with use of VEGF inhibitors at 1-year followup. Two studies comparing ranibizumab versus sham and 2 studies of pegaptanib versus sham were pooled for a total risk ratio of 1.47 (95% CI, 1.30 to 1.66); I2=42%.
Table 4. Treatment Studies of Antioxidant Vitamins, Minerals, and Other Supplements for Dry AMD Published Since the 2009 Review: Trials
|Interventions and Follow-up||Age, y||Female||Race||Clinical Factors||Vision-Related Outcomes||Other Outcomes||Adverse Events|
|Chew et al,39 2013 AREDS (report No. 35)||n = 4753b||A: Antioxidant supplement (vitamin C, 500 mg + vitamin E, 400 IU + beta-carotene, 15 mg/d)
B: Zinc, 80 mg/d
C: Antioxidant supplement + zinc
D: Placebo Follow-up: 10 y
|A: 97% white, 2% black, 1% other
B: 96% white, 3% black, 1% other
C: 97% white, 3% black, <1% other
D: 96% white, 4% black, <1% otherc
A: 28% category 2, 40% category 3, 24% category 4
B: 30% category 2, 41% category 3, 22% category 4
C: 28% category 2, 42% category 3, 22% category 4
D: 30% category 2, 40% category 3, 22% category 4
|A vs D:d
Loss of visual acuity ≥15 letters ETDRS: OR, 0.83; 95% CI, 0.67-1.02
Visual acuity <20/100: OR, 0.82; 95% CI, 0.64-1.07
Progression to advanced AMD: OR, 0.70; 95% CI, 0.56-0.88
B vs D:d
Loss of visual acuity ≥15 letters ETDRS: OR, 0.86; 95% CI, 0.70-1.07
Visual acuity <20/100: OR, 0.88; 95% CI, 0.69-1.14
Progression to advanced AMD: OR, 0.82; 95% CI, 0.66-1.02
C vs D:d
Loss of visual acuity ≥15 letters ETDRS: OR, 0.71; 95% CI, 0.57-0.88
Visual acuity <20/100: OR, 0.72; 95% CI, 0.56-0.94
Progression to advanced AMD:OR, 0.66; 95% CI, 0.53-0.83
|A + C (antioxidant) vs B + D (no antioxidant):e
All-cause mortality: 24.0% (439/1831) vs 23.6% (427/1806); aHR,f 1.06; 95% CI, 0.93-1.21
CV mortality: aRR,f 1.20; 95% CI, 0.97-1.49
Cancer mortality: aRR, 1.07; 95% CI, 0.83-1.38
Non-CV, noncancer mortality: aRR, 0.94; 95% CI, 0.74-1.20
B + C (zinc) vs A + D (no zinc):e
All-cause mortality: 22.4% (401/1790) vs 25.2% (465/1847); aHR, 0.83; 95% CI, 0.73-0.95
CV mortality: aRR, 0.80; 95% CI, 0.64-0.99
Cancer mortality: aRR, 0.84; 95% CI, 0.65-1.08
Non-CV, noncancer mortality: aRR, 0.93; 95% CI, 0.73-1.18
|NR by treatment group; narrative report of no significant increase in incidence of hospitalization after adjustment for age, sex, smoking, and treatment group|
|Ma et al,44 2012||n = 108||A: Lutein, 10 mg/d
B: Lutein, 20 mg/d
C: Lutein, 10 mg/d + zeaxanthin, 10 mg/d
D: Placebo Follow-up: 48 wk
|A vs D:
BCVA, mean change from baseline: −0.04 (95% CI, −0.11 to 0.03) vs −0.00 (95% CI, −0.06 to 0.05);P = NS
B vs D:
BCVA, mean change from baseline: −0.02 (95% CI, −0.11 to 0.06) vs −0.00 (95% CI, −0.06 to 0.05); P = NS
C vs D:
BCVA, mean change from baseline: −0.04 (95% CI, −0.10 to 0.01) vs −0.00 (95% CI, −0.06 to 0.05); P = NS
|NR||NR by treatment group; narrative report of no AEs related to interventions|
|Murray et al,43 2013 (CLEAR)||n = 84||A: Lutein, 10 mg/d
Follow-up: 1 y
|NR||Visual acuity (logMAR)
|A vs B:
Visual acuity, mean change from baseline: 0.01 vs −0.04; P < .05
|NR||A vs B:
Withdrawals due to AEs: 7.1% (3/42) vs 2.3% (1/42); RR, 3.00; 95% CI, 0.33-28
|Souied et al,40 2013 (NAT2)||n = 300||A: Fish oil capsules (DHA, 280 mg + EPA, 90 mg + vitamin E, 2 mg) 3x/d
B: Placebo (olive oil 602 mg)
Follow-up: 3 y
|NR||Mean visual acuity in study eye (logMAR):
|A vs B:g
Visual acuity, mean (SD) change from baseline logMAR: 0.155 (0.297) vs 0.116 (0.258); P = .31
Loss of visual acuity, participants with decrease >15 letters ETDRS: 17.8% (21/118) vs 14.3% (16/112); RR, 1.25; 95% CI, 0.69-2.26
|A vs B:
All-cause mortality: 2.2% (3/134) vs 4.7% (6/129); RR, 0.48; 95% CI, 0.12-1.88
Any AE: 93.3% (125/134) vs 89.1% (115/129); RR 1.05; 95% CI, 0.97-1.13
Any serious AE: 31.3% (42/134) vs 30.2% (39/129); RR, 1.04; 95% CI, 0.72-1.49
Serious ocular AE: 8.2% (11/134) vs 7.0% (9/129); RR, 1.18; 95% CI, 0.50-2.75
Cataract development, worsening, or need for cataract surgery: 50% (67/134) vs 62.5% (81/129); RR, 0.80; 95% CI, 0.64-0.99
|A vs B:
Any AE: 93.3% (125/134) vs 89.1% (115/129); RR, 1.05 (95% CI, 0.97-1.13)
Any serious AE: 31.3% (42/134) vs 30.2% (39/129); RR, 1.04 (95% CI, 0.72-1.49)
Treatment-related AE (investigator-determined): 3.7% (5/134) vs 1.6% (2/129); RR, 2.41 (95% CI, 0.48-12)
Serious ocular AE: 8.2% (11/134) vs 7.0% (9/129); RR, 1.18 (95% CI, 0.50-2.75)
Ocular AE: 65.7% (88/134) vs 57.4% (74/129); RR, 1.14 (95% CI, 0.94-1.39)
Cataract development, worsening or need for cataract surgery: 50% (67/134) vs 62.5% (81/129); RR, 0.80 (95% CI, 0.64-0.99)
Serious nonocular AE: 23.1% (31/134) vs 23.2% (30/129); RR, 0.99 (95% CI, 0.64-1.54)
Abbreviations: AE, adverse event; aHR, adjusted hazard ratio; AMD, age-related macular degeneration; AREDS, Age-Related Eye Disease Study; aRR, adjusted risk ratio; BCVA, best-corrected visual acuity; CV, cardiovascular; DHA, docosahexaenoic acid; ETDRS, Early Treatment Diabetic Retinopathy Study; EPA, eicosapentaenoic acid; logMAR, logarithm of the minimum angle of resolution; NS, not significant; NR, not reported; OR, odds ratio; RR, relative risk.
a All 4 trials were rated good quality according to assessment detailed in eTable 3 in the Supplement.
b Focusing on AREDS categories 3 and 4 for vision-related outcomes, n = 2459; for categories 2, 3, and 4, n = 3476.
c Baseline characteristics for the original AREDS cohort.
d Results for the subgroup of participants with AREDS category 3 or 4 AMD; results including AREDS category 2 AMD reported in the full review.12
e Results for participants with AREDS category 2, 3, or 4 AMD.
f Adjusted for age; sex; race; education; smoking status; body mass index; and presence of diabetes, angina, cancer, and hypertension.
g Six-month, 1-year, and 2-year outcomes reported in the full review.12
Table 5. Summary of Evidence: Screening for Impaired Visual Acuity in Older Adults
|Key Question Topic||Main Findings
From 2009 USPSTF Review
|No. of Studies
Identified for Update
|Summary of Findings
(Including Reporting Bias)
|Key question 1: Benefits of screening||Three cluster RCTs found no difference between vision screening and usual care, no vision screening, or delayed screening on vision and other clinical outcomes; 1 RCT found vision screening by an optometrist in frail elderly persons to be associated with an increased risk for falls (RR, 1.57 [95% CI, 1.20-2.05]) and a trend toward increased risk for fractures (RR, 1.74 [CI, 0.97-3.11])||None||Unchanged from the 2009 review; no new studies. Evidence was consistent and imprecise.||Good (mainly primary care-applicable settings, as part of multicomponent screening intervention)||All studies had different types of comparators. Reporting bias was not detected.||Fair|
|Key question 2: Harms of
|See Key Question 1 for evidence on falls.||None||Unchanged from the 2009 review; no new studies. Evidence was precise; unable to assess consistency (1 study).||Moderate (screening was done by n optometrist)||1 study only. Reporting bias was possible since most screening studies
did not report harms.
|Key question 3: Accuracy of screening||Four studies found screening questions are not accurate for identifying persons with vision impairment compared with Snellen chart. Four studies found visual acuity testing is not accurate for identifying presence of vision conditions compared with detailed ophthalmologic examination. One study found the Amsler grid is not accurate for identifying presence of vision conditions compared with detailed ophthalmologic examination. One very small (n = 50) study found nonophthalmologists are as accurate as ophthalmologists for identifying presence of cataracts. All studies were cross-sectional.||3 (n = 751)||Two new studies found that a computerized vision screening tool or a flip-chart version were not accurate compared with a detailed eye examination, and a third study found the MDS 2.0 Vision Patterns section associated with poor diagnostic accuracy compared with an eye chart; overall conclusions unchanged from the 2009 review. Evidence was consistent and precise.||Moderate (tests are practical for primary care but were sometimes performed by optometrists)||Sometimes unclear if the reference standards were interpreted independently of the target test, lack of predefined thresholds for positive results. Reporting bias was possible as some studies reported accuracy based on optimal criteria for a positive test.||Fair|
|Key question 4: Benefits of reatment|
|Uncorrected refractive error||In 1 large population-based study, 60% of older adults with vision impairment can achieve visual acuity ≥20/40 with refractive correction. Two RCTs found use of corrective lenses associated with improvements in vision-related function, but effects on overall function inconsistent. Numerous observational studies show that >85% of patients achieve visual acuity 20/40 or better following photorefractive surgery for myopia or hyperopia.||None||Unchanged from the 2009 review; no new studies. Evidence was consistentand precise.||Moderate||Mainly observational data and accumulated clinical experience. Reporting bias was not detected.||Fair|
|Cataract||Numerous observational studies found that >90% of patients achieve visual acuity ≥20/40 after cataract extraction and intraocular lens implantation. Three observational studies found cataract surgery associated with improved vision-related function. One trial found immediate first-eye cataract surgery associated with a decreased rate of second (but not first) fall compared with delayed surgery, resulting in a lower overall rate of falls (rate ratio, 0.66; 95% CI, 0.40-0.96, P = 0.03), but a second trial found no effect of second-eye cataract surgery on falls.||2 prospective cohort studies
(n = 346)
|Two new studies reported improved visual acuity with surgery with no differences between groups on cognitive function or quality of life; overall conclusions unchanged from the 2009 review. Evidence was consistent for visual acuity and inconsistent for falls and precise.||Moderate||Mainly observational data. Reporting bias was not detected.||Fair|
|Dry AMD: vitamin and mineral supplements||A large, good-quality (n = 2556) randomized trial, AREDS reported results stratified according to the severity of AMD at baseline. Among subgroup of patients in whom treatment is currently recommended (AREDS categories 3 and 4), AREDS found an antioxidant and zinc combination effective for lower likelihood of AMD progression after 6 y of follow-up (adjusted OR, 0.66; 95% CI, 0.47-0.93), although the difference in the likelihood of ≥15 letters of visual acuity loss was not statistically significant (adjusted OR, 0.75; 95% CI, 0.55-1.02). A systematic review of 9 trials (including AREDS) found insufficient evidence to determine efficacy of vitamins and minerals other than the AREDS combination.||1 systematic review (updated version of the previously included systematic review, with 4 new RCTs) 3 RCTs + 2 additional reports from the AREDS trial with 10-y follow-up (total n = 10,010)||Ten-year follow-up from AREDS is consistent with prior results, with antioxidant supplements alone (OR, 0.70; 95% CI, 0.56-0.88) or with added zinc (OR, 0.66; 95% CI, 0.53-0.83) associated with decreased risk of AMD progression and the combination associated with decreased risk of visual acuity loss (OR, 0.71; 95% CI, 0.57-0.88). Evidence on the effects of other vitamins and mineral treatments remains limited, with no clear effects on AMD progression or visual acuity; overall conclusions unchanged from the 2009 review. Evidence was consistent and precise.||Good (participants in AREDS and other studies generally had mild visual impairment at baseline)||Substantial heterogeneity in interventions assessed and outcomes reported. Reporting bias was not detected.||Good|
|Wet AMD: VEGF inhibitors||RR, 0.71, 95% CI, 0.61-0.84, 2 RCTs for pegaptanib (1 trial) and RR, 0.21, 95% CI, 0.16-0.27, 2 RCTs for ranibizumab (2 trials).||Additional publication from previously included trial||Unchanged from the 2009 review; no new studies. Evidence was consistent and precise.||Moderate||No new trials published since the prior review; study population in the 4 included trials was older (>75 y) with moderate to severe impaired visual acuity at baseline. Reporting bias was not detected.||Fair|
|Key question 5: Harms of treatment|
|Uncorrected refractive error||One small prospective study found multifocal lenses associated with higher risk of falls in older adults compared with unifocal lenses (OR, 2.09; 95% CI, 1.06-4.92). Three studies found incidence of infectious keratitis ranges from 0.3 to 3.6 cases per 10,000 contact lens wearers; 1 study found incidence to be higher in persons >50 y. Corneal ectasia rates range from 0% to 0.87% in 5 studies of LASIK, keratitis rates range from 0% to 3.4% in 6 studies of LASIK and 4 studies of LASEK.||None||Unchanged from the 2009 review; no new studies. Evidence was consistent for contact lenses and refractive surgery (only 1 study for corrective lenses) and imprecise.||Moderate||Only 1 study on corrective lenses. Reporting bias was not detected.||Corrective lenses: poor
Contact lenses, refractive surgery: fair
|Cataract||Systematic reviews of numerous observational studies of cataract surgery found a pooled rate of posterior capsule opacification of 28% after 5 y and a pooled rate of 0.13% for endophthalmitis.||None||Unchanged from the 2009 review; no new studies. Evidence was consistent and precise.||Moderate||Mainly observational studies. Reporting bias was not detected.||Fair|
|Dry AMD: vitamin and mineral supplements||The large AREDS trial found zinc aassociated with significantly increased risk of hospitalization for genitourinary causes compared with nonuse of zinc (RR, 1.47; 95% CI, 1.19-1.80) and antioxidants associated with increased risk of yellow skin compared with nonuse of antioxidants (RR, 1.38; 95% CI, 1.09-1.75).||2 RCTs
(n = 384)
|Two new trials found no difference between supplement use vs placebo in risk of any AE (RR, 1.05; 95% CI, 0.97-1.13), serious AEs (RR, 1.05; 95% CI, 0.72-1.49), serious ocular AEs (RR, 1.18; 95% CI, 0.50-2.75), or withdrawals due to AEs (RR, 3.00; 95% CI, 0.33-28). No new evidence on AEs associated with zinc or antioxidants; overall conclusions unchanged from the 2009 review. Evidence was consistent and precise for any AEs but imprecise for other AEs.||Good (participants in both studies had relatively mild visual impairment at baseline)||Neither trial was designed to assess harms and sample sizes were relatively small (n = 94 and 300). Reporting bias was possible due to inconsistent reporting of harms.||Good|
|Wet AMD: VEGF inhibitors||More cases of endophthalmitis and uveitis compared with placebo, but small numbers of events. No increase in risk of systemic hypertension or arterial thromboembolic events.||None||Unchanged from the 2009 review; no new studies. Evidence was consistent and imprecise.||Moderate||Evidence limited to 4 older trials; few AEs reported. Reporting bias was possible due to inconsistent reporting of harms.||Fair|
Abbreviations: AE, adverse event; AREDS, Age-Related Eye Disease Study; AMD, age-related macular degeneration; LASEK, laser assisted subepithelial keratomileusis; LASIK, laser assisted in situ keratomileusis; MDS, Minimum Data Set; OR, odds ratio; RCT, randomized clinical trial; RR, relative risk; SR, systematic review; USPSTF, US Preventive Services Task Force; VEGF, vascular endothelial growth factor.
a Overall study quality, summary of findings, applicability, and limitations are based on new evidence plus previously reviewed evidence.
Internet Citation: Evidence Summary: Impaired Visual Acuity in Older Adults: Screening. U.S. Preventive Services Task Force. March 2016.