Skip to main content
JAMA Network logoLink to JAMA Network
. 2021 Feb 12;139(5):1–16. doi: 10.1001/jamaophthalmol.2021.0146

A Global Assessment of Eye Health and Quality of Life

A Systematic Review of Systematic Reviews

Lama Assi 1, Fatimah Chamseddine 2, Perla Ibrahim 3, Hadi Sabbagh 3, Lori Rosman 4, Nathan Congdon 5,6, Jennifer Evans 7, Jacqueline Ramke 7,8, Hannah Kuper 9, Matthew J Burton 7,10, Joshua R Ehrlich 11,12, Bonnielin K Swenor 1,13,
PMCID: PMC7881366  PMID: 33576772

Key Points

Question

What is the association between vision impairment, eye diseases, or ophthalmic interventions and quality of life?

Findings

In this cross-sectional study, vision impairment and eye diseases were associated with lower quality of life. More than half of the ophthalmic interventions included had a positive association with quality of life.

Meaning

The associations of quality of life with vision impairment and the improvements in quality of life with ophthalmic interventions support efforts to improve access to ophthalmic treatments globally to reach the millions of people affected by eye disease each year.


This cross-sectional study examines the association between vision impairment or eye disease and quality of life and the outcome of ophthalmic interventions on quality of life globally and across the life span.

Abstract

Importance

More than 1 billion people worldwide have vision impairment or blindness from potentially preventable or correctable causes. Quality of life, an important measure of physical, emotional, and social well-being, appears to be negatively associated with vision impairment, and increasingly, ophthalmic interventions are being assessed for their association with quality of life.

Objective

To examine the association between vision impairment or eye disease and quality of life, and the outcome of ophthalmic interventions on quality of life globally and across the life span, through an umbrella review or systematic review of systematic reviews.

Evidence Review

The electronic databases MEDLINE, Ovid, Embase, Cochrane Database of Systematic Reviews, Proquest Dissertations, and Theses Global were searched from inception through June 29, 2020, using a comprehensive search strategy. Systematic reviews addressing vision impairment, eye disease, or ophthalmic interventions and quantitatively or qualitatively assessing health-related, vision-related, or disease-specific quality of life were included. Article screening, quality appraisal, and data extraction were performed by 4 reviewers working independently and in duplicate. The Joanna Briggs Institute critical appraisal and data extraction forms for umbrella reviews were used.

Findings

Nine systematic reviews evaluated the association between quality of life and vision impairment, age-related macular degeneration, glaucoma, diabetic retinopathy, or mendelian eye conditions (including retinitis pigmentosa). Of these, 5 were reviews of quantitative observational studies, 3 were reviews of qualitative studies, and 1 was a review of qualitative and quantitative studies. All found an association between vision impairment and lower quality of life. Sixty systematic reviews addressed at least 1 ophthalmic intervention in association with quality of life. Overall, 33 unique interventions were investigated, of which 25 were found to improve quality of life compared with baseline measurements or a group receiving no intervention. These interventions included timely cataract surgery, anti–vascular endothelial growth factor therapy for age-related macular degeneration, and macular edema.

Conclusions and Relevance

There is a consistent association between vision impairment, eye diseases, and reduced quality of life. These findings support pursuing ophthalmic interventions, such as timely cataract surgery and anti–vascular endothelial growth factor therapy, for common retinal diseases, where indicated, to improve quality of life for millions of people globally each year.

Introduction

At least 2.2 billion people worldwide have a vision impairment, of whom more than 1 billion have moderate or severe vision impairment or blindness from a preventable or potentially correctable cause, including refractive error, presbyopia, and cataract.1 Existing evidence suggests that vision impairment is associated with lower quality of life,2 defined as physical, emotional, and social well-being. Visual impairment is also linked to lower vision-related quality of life3 or daily visual function and the ability to perform visual tasks.

Over the past decade, quality-of-life measures have gained popularity in ophthalmology research, including clinical trials, as the value of patient-reported outcomes in measuring well-being and visual function is being recognized.4 However, to our knowledge, there has yet to be a global synthesis of the evidence about quality of life and eye health, despite the numerous systematic reviews about vision impairment, eye diseases, or ophthalmic interventions and quality of life.5,6,7

Therefore, the objective of this umbrella review, which is a systematic review of systematic reviews, is to examine the association between vision impairment or specific eye diseases and reduced quality of life, and the effectiveness that ophthalmic interventions can have on improving quality of life.

Methods

This study forms part of the work for the forthcoming Lancet Global Health Commission on Global Eye Health.8 We followed the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) reporting guidelines (eAppendix 1 in the Supplement). A protocol was published9 and registered on the Open Science Framework Registries (https://osf.io/qhv9g). Changes to the protocol are noted in eAppendix 2 in the Supplement.

A comprehensive search was performed using the electronic databases MEDLINE, Ovid, Embase, Cochrane Database of Systematic Reviews, Proquest Dissertations, and Theses Global from inception through June 29, 2020 (a sample search strategy is in the eFigure in the Supplement). OpenGrey, the Agency for Healthcare Research and Quality, and references of included reviews were searched for additional articles. Inclusion and exclusion criteria are listed in Table 1.

Table 1. Inclusion and Exclusion Criteria.

Characteristic Inclusion criteria Exclusion criteria
Study type Systematic reviews, defined as reviews that include all of these items: a research question, search strategy, the sources searched, inclusion/exclusion criteria, screening methods, assessment of included studies’ quality, and information about data synthesis Reviews that did not meet the working definition of a systematic review; systematic reviews that included case series or expert opinion pieces
Population Systematic reviews with participants with vision impairment or eye disease Systematic reviews with participants with stroke-associated vision impairment, since these vision impairments and consequences (eg, visual neglect, visual hallucinations) are different from eye pathologies
Interventions For systematic reviews of interventional studies, systematic reviews that assessed interventions that aim to improve or preserve vision, prevent or stop the progression of vision impairment, or improve vision function For systematic reviews of interventional studies, systematic reviews that assessed psychologic interventions, such as coping strategies
Outcomes Systematic reviews that reported on quality-of-life outcomes, such as health-related, vision-related, or disease-specific quality-of-life questionnaires, or qualitative assessments of physical, emotional, and social well-being and vision function in day-to-day life Systematic reviews that reported on patient satisfaction and patient-reported symptoms
Other None Conference abstracts and articles not in English; systematic reviews that had an updated version available (they were used as an additional reference only if the updated review referred to them)

Study selection, quality appraisal, and data collection were performed by 4 reviewers (L.A., F.C., P.I., and H.S.) independently and in duplicate using Covidence software (Covidence Inc).10 Titles and abstracts were screened to identify potentially relevant articles. Full texts of these articles were assessed for eligibility based on the inclusion and exclusion criteria. Reviews that aimed to identify studies with quality-of-life outcomes but did not find any were excluded, since they had no results to be extracted.

Reviews underwent quality appraisal using the Joanna Briggs Institute Critical Appraisal Checklist for Systematic Reviews and Research Syntheses.11 Reviews for which any of the items “clear review question,” “appropriate inclusion criteria,” “appropriate search strategy,” or “appropriate criteria for critical appraisal” were graded as unclear or no were excluded. Data collection was performed using the Joanna Briggs Institute Data Extraction Form for Systematic Reviews and Research Syntheses.12

Results of the reviews on vision impairment or eye diseases and ophthalmic interventions were presented separately. Within the reviews on ophthalmic interventions, 2 types of comparisons were identified: (1) those that compared the quality of life of a group receiving an intervention with baseline quality of life in the same group or a control group receiving no intervention, a placebo, or sham therapy and (2) those that compared the quality of life of a group receiving 1 intervention with a group receiving another intervention, without comparison with a baseline or a group that received no intervention. Results from each type of comparison were described separately, and only comparisons with baseline or a group receiving no intervention were included in the Tables summarizing findings (Table 2 and Table 3).

Table 2. Findings on the Outcomes of Ophthalmic Interventions and Quality of Life by Systematic Reviewa.

Source Year Country of lead author Quality of life outcome or measure Assessment tools Assessment Participants, No.b Studies, No. Study Type Countries of primary studiesc Findings Quality of evidence
Age-related cataract
Chou, et al13 2016 UK VRQOL after cataract surgery NR Treatment of early impairment in visual acuity due to cataract error 1627 5 Cohort studies NR Three studies found moderate improvement in VRQOL and function after cataract surgery. Two studies found similar VRQOL in the groups with vs without cataract surgery (measures of association not provided). Fair
Hodge, et al14 2007 Canada Patient QOL and satisfaction NR Expedited (<6 wk waiting time) first-eye or second-eye cataract surgery vs control group awaiting surgery NR 2 RCTs The UK Better QOL in the group that received cataract surgery in <6 wk vs a group awaiting surgery (routine waiting time, >6 mo) at 6 mo after randomization (measures of association not provided). NR
Conner-Spady, et al15 2007 Canada VRQOL VF-14 Expedited (<6 wk waiting time) first-eye or second-eye cataract surgery vs control group awaiting surgery 514 2 RCTs The UK Significant VRQOL benefits in the groups that received cataract surgery vs control groups still awaiting cataract surgery 6 mo after randomization. Deterioration in VRQOL in the control group while waiting (measures of association not provided). NR
Casparis, et al16 2017 Switzerland VRQOL Impact of Vision Impairment questionnaire Immediate vs no or delayed cataract surgery (>6 mo) among patients with AMD 56 1 RCT Australia Better VRQOL in the immediate-cataract surgery group vs the control group awaiting surgery (waiting time >6 mo) after 6 mo of follow-up (MD, 1.60 [95% CI, 0.61-2.59]; I2 = NA). Low
Ishikawa, et al17 2013 Canada Self-reported visual functioning VF-14, Tailored questionnaire, or ADVS Second-eye cataract surgery vs cataract surgery in 1 eye only 1554 7 3 RCTs, 4 cohort studies NR Better VRQOL after second-eye cataract surgery vs cataract surgery in 1 eye only was reported in all studies. Four studies found that the magnitude of improvement was smaller after second-eye surgery than after first-eye surgery (measures of association not provided). Moderate
Frampton, et al18 2014 UK VRQOL VF-14 Second-eye cataract surgery vs cataract surgery in 1 eye only 535 2 RCT The UK and Spain Better VRQOL existed in those post–expedited second-eye surgery vs those awaiting second-eye cataract surgery, but the difference was not clinically meaningful (VF-14: study 1: MD, 7.5 [95% CI, 5.1-9.9]; P < .001; study 2: MD, 8.24 [95% CI, 4.35-12.36]; P < .001). NR
Ishikawa, et al17 2013 Canada HRQOL SIP, HRQOL, SF-12, SF-36, EQ-5D, or SRS Second-eye cataract surgery vs cataract surgery in 1 eye only 1261 6 3 RCTs, 3 cohort studies NR Inconsistent and mixed results. One study found improvement in HRQOL after second-eye cataract surgery, 3 found no improvement in HRQOL, and 2 found mixed results (measures of association not provided). NR
Frampton, et al18 2014 UK HRQOL SF-12, SF-36, or EQ-5D Second-eye cataract surgery vs cataract surgery in 1 eye only 743 3 RCT The UK and Spain Mixed results; 2 studies found no significant improvement in HRQOL after second-eye cataract surgery. One study found clinically relevant improvement in the mental health component of HRQOL after expedited vs no second-eye surgery (point difference, 1.90 [95% CI, 0.03-3.79]; P < .05). NR
Riaz, et al19 2009 UK VRQOL NR Extracapsular cataract extraction with posterior chamber IOL vs intracapsular cataract extraction with aphakic glasses 3400 1 RCT India Improved VRQOL in both groups, with the advantage of extracapsular cataract extraction with posterior chamber IOL vs aphakic glasses across all categories (measures of association not provided). NR
Refractive error
Chou, et al13 2016 UK VRQOL NEI-VFQ Treatment of early impairment in visual acuity due to uncorrected refractive error 282 2 RCT NR Beneficial effects of corrective lenses on VRQOL or vision-related function in the group with immediate correction of refractive error with eyeglasses compared with delayed treatment (scores on the NEI-VFQ were improved by a mean of approximately 10 of 100 points in the immediate-treatment groups). Fair
Age-related macular degeneration
Chou, et al13 2016 UK VRQOL NR Anti-VEGF injections vs control for neovascular AMD NR 3 Trials?? NR Mild to moderate improvements in VRQOL in the groups who took anti-VEGF vs sham injections, but the differences were not always significant (measures of association not provided). Fair
Solomon, et al20 2019 UK VRQOL NEI-VFQ Anti-VEGF injections vs control for neovascular AMD 1134 2 RCT The US, France, Germany, Hungary, Czech Republic, and Australia Greater improvement in VRQOL in the ranibizumab than control groups (no anti-VEGF) after 1 y of follow-up (MD, 6.7 [95% CI, 3.4-10.0]; I2 = 68.3%). Moderate
Sarwar, et al21 2016 US VRQOL NEI-VFQ-25 Aflibercept or ranibizumab therapy vs baseline for AMD 2412 2 RCT The US, Canada, Argentina, Australia, Austria, Brazil, Belgium, Colombia, Czech Republic, France, Germany, Hungary, India, Israel, Italy, Japan, Latvia, Mexico, the Netherlands, Poland, Portugal, South Korea, Singapore, Slovakia, Spain, Sweden, Switzerland, and the UK Improvement in VRQOL from baseline to 1 y in both aflibercept and ranibizumab groups to a similar extent (MD, −0.39 [95% CI, −1.71 to 0.93]; I2 = 54.71%). High
Giansanti, et al22 2009 Italy VRQOL NEI-VFQ-25 Macular/submacular surgery vs observation for subfoveal neovascular AMD 689 2 RCT The US Better VRQOL in the surgery vs observation group at 1 y (RR, 1.35 [95% CI, 1.09-1.68]; I2 = 0.0%). Low
Evans, et al23 2010 UK VRQOL Daily Living Tasks Dependent on Vision questionnaire Radiotherapy vs observation for neovascular AMD 203 1 RCT The UK No differences in VRQOL between treatment and observation groups 12 or 24 mo after treatment (measures of association not provided). NR
Evans, et al23 2017 UK VRQOL NEI-VFQ-25 Multivitamin supplements vs placebo or no treatment for AMD 110 1 RCT Italy Better VRQOL in the multivitamin supplements group vs placebo at 24 mo (MD, 12.3 [95% CI, 4.24-20.36]). Low
Evans, et al23 2017 UK QOL NEI VFQ-25 Lutein and/or zeaxanthin vs placebo for AMD 108 1 RCT China Similar VRQOL changes in the intervention and placebo groups at 12 mo (MD, 1.48 [95% CI, −5.53 to 8.49]). Low
Liu, et al24 2014 China VRQOL VFQ Lutein and/or zeaxanthin vs placebo for AMD 253 2 RCT NR No significant difference in VRQOL improvement between groups (weighted MD, 6.51 [95% CI, −6.16 to 19.17]). NR
Retina (other)
Virgili, et al25 2018 Italy VRQOL NEI-VFQ-25 Anti-VEGF therapy vs laser photocoagulation for diabetic macular edema 412 3 RCT Canada, Europe, Australia, Canada, and Turkey Improvement in VRQOL from baseline to 6 or 12 mo in both groups; greater improvement in the ranibizumab group vs laser photocoagulation group (mean change in composite score, 5.14 [95% CI, 2.96-7.32]). Moderate
Braithwaite, et al26 2014 UK VRQOL NEI-VFQ-25 Anti-VEGF injection vs sham injection for macular edema secondary to central retinal vein occlusion 743 3 RCT Argentina, Asia/Pacific, Canada, Colombia, Europe, India, Israel, and the US Significant improvement in VRQOL in the anti-VEGF vs sham groups at 6 mo (MD not provided; range, 6.2 to 7.5, based on 1 study). Moderate
Zhou, et al27 2014 China VRQOL NEI-VFQ-25 Anti-VEGF injection vs sham injection for macular edema secondary to central retinal vein occlusion 743 3 RCT Argentina, Asia/Pacific, Canada, Colombia, Europe, India, Israel, and the US Significant improvement in VRQOL in the anti-VEGF vs sham groups at 6 mo (MD, 4.58 [95% CI, 2.93-6.23]; P < .001; I2 = 0%). High
Ford, et al28 2014 UK VRQOL NEI-VFQ-25 Anti-VEGF injection vs sham injection for macular edema secondary to central retinal vein occlusion 782 3 RCT NR Significantly better changes in VRQOL in both the aflibercept and ranibizumab groups vs sham groups at 6 mo (MDs, 6.4, 4.0, nad 3.4, respectively; confidence intervals not provided). NR
Mitry, et al29 2013 UK VRQOL NEI-VFQ-25 Anti-VEGF injection vs sham injection for macular edema secondary to branch retinal vein occlusion 397 1 RCT The US Greater VRQOL improvement in the ranibizumab groups vs sham group at 6 mo of treatment (change in NEI-VFQ-25 composite score, 9.3 [95% CI, 7.2-11.4] in the 0.3-mg ranibizumab group; 10.4 [95% CI, 8.3-12.4] in the 0.5-mg ranibizumab group; and 5.4 [95% CI, 3.6-7.3] in the sham group; P < .005 for each group vs the sham group). NR
Zhu, et al30 2016 China VRQOL NEI-VFQ-25 Anti-VEGF injection vs sham injection for choroidal neovascularization secondary to pathological myopia 121 1 RCT Hong Kong, Japan, Korea, Singapore, and Taiwan Better VRQOL outcomes in the anti-VEGF vs sham groups (mean change in NEI-VFQ-25 score, 5.72 [95% CI, 1.60-9.84]. Moderate
Lescrauwaet, et al31 2019 Belgium VRQOL NEI-VFQ-25 Ocriplasmin injection vs sham or placebo injection for symptomatic vitreomacular traction 870 2 RCT NR A higher proportion of people in the ocriplasmin group had a clinically meaningful improvement in VRQOL vs those in the control group (difference in proportions, 11.8% [95% CI, 3.8%-19.7%]; P = .004). NR
Neffendorf, et al32 2017 UK VRQOL VFQ Ocriplasmin injection vs sham or placebo injection for symptomatic vitreomacular adhesion 656 2 RCT The US, Belgium, Czech Republic, Germany, Poland, Spain, and the UK Greater improvement in VRQOL in the ocriplasmin group vs sham/placebo group at 6 mo (MD in improvement, 2.7 [95% CI, 0.8-4.6] points). Moderate
Brito-García, et al33 2017 Spain VRQOL VAQ and VF-14 Nutritional supplementation treatments for hereditary retinal dystrophies (retinitis pigmentosa, Best disease) 52 2 RCT The US and Canada No significant differences in VRQOL were noted between the groups of participants with retinitis pigmentosa and Best disease who received nutritional supplementation vs those who did not. NR
Glaucoma
Rolim de Moura, et al34 2007 Brazil VRQOL NEI VFQ-25 Laser trabeculoplasty and topical β-blocker vs placebo for early open-angle glaucoma 255 1 RCT NR No significant difference in VRQOL between the treatment and placebo groups at 3 y. NR
Chi, et al35 2020 Taiwan QOL GQL-15 Selective laser trabeculoplasty and medication or medication only for open-angle glaucoma 41 1 RCT Unspecified countries in Asia No significant change in QOL from baseline to follow-up at 6 mo in the selective laser trabeculoplasty and medication and medication-only groups. NR
Low vision
van Nispen, et al36 2020 the Netherlands VRQOL NEI-VFQ- 25, VA-LV-VFQ48, Activity Inventory, IVI Vision rehabilitation using methods of enhancing vision (eg, low-vision outpatient service, customized prism glasses) vs passive control for adults with vision impairment 262 5 RCT The US, Germany, and Canada Small benefit in VRQOL favoring low vision rehabilitation, but the effects were moderately heterogenous and imprecisely estimated, including no benefit (standardized MD, −0.19 [95% CI, −0.54 to 0.15]; I2 = 34%). Very low
van Nispen, et al36 2020 The Netherlands HRQOL EQ-5D, SF-36 Multidisciplinary vision rehabilitation (eg, low-vision rehabilitation plus home visit) vs passive control for adults with vision impairment 183 2 RCT The UK and the US Rehabilitation resulted in more favorable HRQOL, but estimates were very imprecise and included no effect (standardized MD, −0.08 [95% CI, −0.37 to 0.21]; I2 = 0%). Very low
van Nispen, et al36 2020 The Netherlands VRQOL NEI- VFQ-25, VFQ-48 questionnaire Multidisciplinary vision rehabilitation (eg, low-vision rehabilitation plus home visit) vs passive control for adults with vision impairment 193 2 RCT The UK and the US Both studies found better VRQOL with rehabilitation, but the effect was large in a large trial delivering intensive rehabilitation (standardized MD, 1.64 [95% CI, −2.05 to −1.24]) and small in the other study (standardized MD, −0.42 [95% CI, −0.90 to 0.07]). Very low
Vision screening
Evans, et al37 2018 UK VRQOL NEI- RQL-42 School vision screening and ready-made spectacles vs vision screening and custom-made spectacles 188 1 RCT China Improvement in VRQOL to a similar extent in both groups after wearing spectacles for 2 mo (change in NEI-RQL-42 score in the ready-made spectacles group, 4.65 [95% CI, 2.45-6.86]; similar change in the custom-made spectacles group). Moderate
Rhinoconjunctivitis
Erekosima, et al38 2014 UK QOL RQOL questionnaire Subcutaneous immunotherapy vs placebo for rhinoconjunctivitis 539 4 RCT NR Greater improvement in disease-specific QOL among adults in the subcutaneous immunotherapy group vs placebo group (measures of association not provided). High
Kim, et al39 2013 US QOL RQOL questionnaire Subcutaneous immunotherapy vs placebo for rhinoconjunctivitis 350 2 RCT NR Significant improvement in disease-specific QOL in the subcutaneous immunotherapy arm vs the control group (measures of association not provided). Low
Kim, et al39 2013 US QOL Pediatric and Adolescent RQOL questionnaires Sublingual immunotherapy vs placebo for rhinoconjunctivitis among children only 461 2 RCT NR No improvement in disease-specific QOL in the sublingual immunotherapy group vs placebo among children. NR
Lin, et al40 2013 US Disease-specific quality of life for rhinoconjunctivitis and asthma RQOL questionnaire Sublingual immunotherapy vs placebo for rhinoconjunctivitis among children and adults 819 8 RCT NR Improvement in disease-specific QOL in the sublingual immunotherapy group in 7 of 8 studies. Results were statistically significant in 4 of the studies, and a strong magnitude of association (>40% difference in effect) was reported in 2 studies. Moderate
Rodrigo, et al41 2010 Uruguay QOL RQOL Questionnaire Intranasal fluticasone furoate vs placebo for seasonal allergic rhinitis 2219 5 RCT NR Significant improvement in disease-specific QOL in the intranasal fluticasone furoate group vs placebo (weighted MD, −0.68 [95% CI, −0.80 to −0.56]; I2 = 0%). NR
Rodrigo, et al41 2010 Uruguay QOL RQOL Questionnaire Intranasal fluticasone furoate vs placebo for perennial allergic rhinitis 919 3 RCT NR Significant improvement in disease-specific QOL in the intranasal fluticasone furoate group vs placebo (weighted MD, −0.51 [95% CI, −0.76 to −0.22]; I2 = 44%). NR
Uveitis
Urruti-coechea-Arana, et al42 2019 Spain VRQOL NEI-VFQ-25 Adalimumab or dexamethasone vs placebo in the treatment of uveitis 443 2 RCT NR Significantly greater improvement in VRQOL in the adalimumab group vs placebo among participants with active uveitis (measures of association not provided). However, no differences were found in the treatment group vs placebo among those with inactive uveitis. NR
Squires, et al43 2017 UK VRQOL NEI-VFQ-25 Adalimumab or dexamethasone vs placebo in the treatment of uveitis 681 3 RCT Europe, North America, and Australia Significantly greater improvement in VRQOL in the adalimumab vs placebo group in patients with active uveitis (MD, 4.20 [95% CI, 1.02-7.38]; P = .01), but not in those with inactive uveitis (MD, 2.12 [95% CI, −0.84 to 5.08]; P = .16). Similarly, significant VRQOL benefits noted using dexamethasone implant vs sham procedure. NR
Squires, et al43 2017 UK HRQOL EQ-5D Adalimumab or dexamethasone vs placebo in the treatment of uveitis 452 2 RCT Europe, North America, and Australia Significantly greater improvement in HRQOL in the adalimumab vs placebo groups among participants with active uveitis (MD, 0.04 [95% CI, 0.00-0.07]). However, no differences were found in the treatment group vs placebo among those with inactive uveitis (MD, 0.00 [95% CI, –0.03 to 0.04]). NR
Trichiasis
Burton, et al44 2015 UK VRQOL ?? Perioperative azithromycin vs no azithromycin 1903 2 RCT Gambia and Ethiopia VRQOL (vision function, eye comfort, and physical functioning) improved following surgery; however, studies did not analyze by groups allocated to azithromycin vs control (measures of association not provided). NR
Thyroid eye disease or Graves ophthalmopathy
Viani, et al45 2012 Brazil QOL NR Radiotherapy vs sham radiotherapy for thyroid eye disease 88 1 RCT NR No differences in QOL in the radiotherapy vs sham radiotherapy groups. NR
Rajendram, et al46 2012 UK QOL Graves Ophthalmopathy QOL, Euro-QoL, Sickness Impact Profile, and Medical Outcomes Study Short-General Health Survey questionnaires Radiotherapy vs sham radiotherapy for thyroid eye disease 88 1 RCT NR No significant differences in QOL between the radiotherapy vs sham radiotherapy groups. NR

Abbreviations: anti-VEGF, anti–vascular endothelial growth factor; EQ-5D, EuroQol-5 Dimension; GQL-15, Glaucoma Quality of Life-15; HRQOL, health-related quality of life; IVI, impact of vision impairment; MD, mean difference; NEI-RQL-42, National Eye Institute Refractive Error Quality of Life Instrument–42; NEI-VFQ-25, National Eye Institute 25-Item Visual Function Questionnaire; NR, not reported; QOL, quality of life; RCT, randomized clinical trial; RR, risk ratio; RQOL, rhinoconjunctivitis quality of life; SF-12, 12-Item Short Form Survey; SF-36, 36-Item Short Form Health Survey; SIP, Sickness Impact Profile; VRQOL, vision-related quality of life.

a

List of included studies in eTable 4 in the Supplement.

b

Informing the specific outcome (a given systematic review may have included more studies for other outcomes).

c

Indicates overlap of studies. In this column, we report the name of the study or first author and year of publication (as reported by the systematic review). Only applicable for outcomes assessed by more than 1 systematic review.

Table 3. Findings on the Association Between Vision Impairment or Eye Disease and Quality of Life by Systematic Reviewa.

Systematic reviewa Year Country of lead author Quality of life outcome or measure Assessment instruments Participants, No.b Participant type Studies, No. Study type Countries of primary studiesb Results/findings
Systematic reviews of quantitative studies
Nyman, et al47 2010 UK Mental health subscale in QOL questionnaires NEI-VFQ-25 and SF-36 33 648 Working-age adults (18-59 y) 11 NR The US, Korea, and India Vision impairment was associated with modestly lower mental health scores on the NEI-VFQ-25 than control participants (average mean difference, 14.5% [range, 0.6%-35%]). The SF-36 was less sensitive than the NEI-VFQ-25 in detecting lower mental health among those with vision impairment vs controls (mean difference, 3%; 1 study only).
Nyman, et al47 2010 UK QOL NR 2622 Working-age adults (18-59 y) 3 NR The US, Sweden, and Australia Vision impairment was associated with lower QOL across a range of measures, such as higher odds of reporting “not feeling full of life” vs control participants (OR, 4.63 [95% CI, 2.1-9.8])
Tseng, et al49 2018 Taiwan QOL WHOQOL-BREF, CDCHRQOL, SF-36, IVI, NHVQOL, EQ-5D, NEI-VFQ-25, and WHO/PBD VF20 NR Older adults 15 14 cross-sectional and 1 longitudinal study Australia, Canada, Europe, Germany, Korea, Nepal, New Zealand, Nigeria, Philippines, Taiwan, and the US Vision impairment was associated with lower QOL in 14 of 15 studies (eg, OR, 2.20 [95% CI, 1.10-4.90] in 1 study examining vision impairment and generic health-related QOL; in another study examining vision impairment among older adults, the difference in SF-36 scores was 6.7 (95% CI, 3.37-10.1; P < .001). An increase in vision impairment severity was associated with lower QOL (eg, β, 0.31 [95% CI, 0.11-0.52]; P = .003).
Schakel, et al48 2019 The Netherlands Fatigue severity SF-36 vitality subscale or Fatigue Assessment Scale 10 870 Adults 14 7 case-control and 7 cross-sectional studies Australia, Brazil, China, Greece, Japan, Nepal, the Netherlands, Taiwan, and the US Vision impairment was associated with higher levels of fatigue in affected participants vs control participants with normal sight (standardized mean difference [SMD], −0.36 [95% CI, −0.50 to −0.22]; I2 = 84%).
Schakel, et al48 2019 The Netherlands Fatigue odds SF-36 vitality subscale or Fatigue Assessment Scale 8053 Adults 4 2 cross-sectional and 2 case-control studies Canada, Czech Republic, Germany, and the Netherlands Vision impairment was associated with higher odds of fatigue in affected participants vs control participants with normally sight (pooled adjusted OR, 2.61 [95% CI, 1.69-4.04]; I2 = 90%).
Wang, et al50 2017 China Disease-specific QOL GQL-15 questionnaire 253 Individuals with glaucoma 2 NR Australia and Nigeria Glaucoma was associated with significantly higher (ie, poorer) QOL summary scores (SMD , 0.94 [95% CI, 0.73-1.16]; P < .001; I2 = 0%), and subscale scores for all 4 factors (central and near vision: SMD, 0.82 (95% CI, 0.61-1.04]; P < .001; peripheral vision: SMD, 0.74 [95% CI, 0.53-0.96]; P < .001; dark adaption and glare: SMD, 1.02 [95% CI, 0.80-1.24]; P < .001; outdoor mobility: SMD, 0.60 [95% CI, 0.39-0.81]; P < .001) vs control group without glaucoma.
Khoo, et al6 2019 Singapore Psychosocial functioning Depression or anxiety questionnaires and mental health QOL subscale scores NR Individuals with diabetic retinopathy 28 Cross-sectional NR Diabetic retinopathy was significantly associated with poor psychosocial functioning in 20 of 28 observational studies (measures of association not provided).
D’Amanda, et al53 2020 US QOL NEI-VFQ-25, VF-14, SF-12, HRQOL-14, WHOQOL-BREF, CHQ, SF-36, and PedsQL 905 Individuals with mendelian eye conditions 11 Cross-sectional Brazil, Canada, France, Greece, Israel, Korea, the Netherlands, and the UK Retinitis pigmentosa, Usher syndrome, mixed retinal dystrophies, and retinoblastoma (in children) were associated with lower overall QOL in 5 studies. CHARGE syndrome, albinism, retinoblastoma, and mixed retinal dystrophies were associated with lower QOL on certain subscales (not specified) in 6 studies (measures of association not provided).
Systematic reviews of qualitative studies
Nyman, et al7 2012 UK Emotional well-being NA NR Older adults NR Qualitative NR Diagnosis of vision impairment was identified as a traumatic event in 8 studies. An array of emotions was reported around the time of diagnosis, including feelings of shock, fear, panic, distress, helplessness, and frustration.
Nyman, et al7 2012 UK General functioning NA NR Older adults NR Qualitative NR Vision impairment had a dramatic outcome on individuals’ daily lives and functioning. People reported having to relinquish independence (11 studies) and leisure pursuits (8 studies).
Bennion, et al51 2012 UK Emotional well-being NA 121 Individuals with age-related macular degeneration 5 Qualitative NR The diagnosis of age-related macular degeneration was described as a shocking even by participants. Some accepted the diagnosis, while others felt powerless and in despair. Negative thoughts and depression symptoms were not confined to those with the most severe cases.
D’Amanda, et al53c 2020 US General and visual functioning NA 430 Individuals with mendelian eye conditions 9c Qualitative Australia, the Netherlands, Ireland, Sweden, Tanzania, the UK, the US, and Zimbabwe Vision impairment had a considerable association with visual and global daily functioning and specific aspects of life, such as education, employment, and relationships among people with mendelian eye conditions (albinism, mixed retinal dystrophies, Leber hereditary optic neuropathy, retinitis pigmentosa, Alstrom syndrome, and retinoblastoma).
Garip, et al52 2019 UK Emotional well-being NA 223 Individuals with retinitis pigmentosa 10c Qualitative Australia, the US, Republic of Korea, Ireland, the Netherlands, and the UK The diagnosis of retinitis pigmentosa was commonly accompanied by shock, negative emotional states, and a loss of confidence. Participants reported fatigue, fear, isolation, and vulnerability as they coped with the disease and dealt with their own judgements and perceived stigma.
Garip, et al52 2019 UK Visual functioning NA 223 Individuals with retinitis pigmentosa 10c Qualitative Australia, the US, Republic of Korea, Ireland, the Netherlands, and the UK The diagnosis of retinitis pigmentosa was accompanied by loss of visual acuity, hobbies, pastimes, and social support. Participants reported difficulty performing day-to-day tasks, such as reading, seeing in changing light conditions, shopping, driving, playing sports, taking part in leisure activities, and doing household chores.

Abbreviations: CDCHRQOL, Centers for Disease Control and Prevention Health-Related Quality of Life; CHARGE syndrome, coloboma, heart defects, atresia choanae, growth retardation, genital abnormalities, and ear abnormalities; CHQ, Children’s Health Questionnaire; EQ-5D, EuroQoL–5 Dimension; GQL-15 questionnaire, Glaucoma Quality of Life–15 questionnaire; HRQOL-14, Health-Related Quality of Life–14; IVI, impact of vision impairment; NA, not applicable; NEI-VFQ-25, National Eye Institute 25-Item Visual Function Questionnaire; NHVQoL, Nursing Home Vision-Targeted Health-Related Quality of Life; NR, not reported; OR, odds ratio; PedsQL, Pediatric Quality of Life Inventory; QOL, quality of life; SF-12, 12-Item Short Form Survey; SF-36, 36-Item Short Form Health Survey; VF-14, Visual Function Index; WHOQOL-BREF, World Health Organization Quality of Life BREF; WHO/PBD VF20, World Health Organization Prevention of Blindness and Deafness Visual Function–20.

a

Quality of evidence ratings were not reported for any study.

b

Informing the specific outcome (a given systematic review may have included more studies for other outcomes).

c

Two identical primary studies were included in both reviews.

When the same intervention or outcome was assessed by more than 1 review, the primary studies used by the reviews to inform the results were compared to assess the extent to which individual studies were included in more than 1 review. Results about associations were based on the reviews’ interpretation of the estimates and accompanied by the measure of association and quality of the evidence assessment when available in the published review. Overall findings were presented in Table 2 and Table 3.

Results

As described in the PRISMA flowchart (eTable 1 in the Supplement), 8070 unique titles and abstracts were screened; of these, 685 relevant full-text articles were assessed for eligibility. Ten eligible systematic reviews addressed quality of life and vision impairment or eye diseases, and 205 assessed ophthalmic interventions. Of the reviews concerning ophthalmic interventions, 143 were excluded because they did not identify any eligible studies with quality-of-life data in the literature.

Results of the quality assessment are presented in eTable 2 in the Supplement. Three reviews were excluded, 2 for not having appropriate critical appraisal criteria, and 1 for not having appropriate inclusion criteria. This left 9 reviews on vision impairment or eye diseases and 60 reviews on ophthalmic interventions included in the current analysis. Review characteristics are summarized in eTable 2 in the Supplement.

Vision Impairment and Eye Diseases

In total, 9 systematic reviews6,7,47,48,49,50,51,52,53 published between 2010 and 2020 evaluated the association between vision impairment or eye disease and quality of life. Four of them had corresponding authors in the UK7,47,51,52; the rest were in the US,53 Netherlands,48 Taiwan,49 China,50 and Singapore.6 Five6,47,48,49,50 were systematic reviews of observational quantitative studies, 37,51,52 were reviews of qualitative studies, and 153 was a review of both quantitative and qualitative studies (Table 3). None of the reviews graded the quality of the evidence.

The systematic reviews of observational quantitative studies focused on people with vision impairment, including adults48 and specifically working-age47 and older adults,49 people with glaucoma,50 diabetic retinopathy,6 and children and adults with mendelian eye conditions, including retinitis pigmentosa, Usher syndrome, and mixed retinal dystrophies.53 Among all the populations examined, vision impairment or eye diseases were associated with lower quality of life, including vision-related and health-related49 and glaucoma-specific50 quality of life. Moreover, people with vision impairment had poorer scores on quality-of-life subscales, such as mental health,47 psychosocial functioning,6 and fatigue (odds ratio, 2.61 [95% CI, 1.69-4.04]).48

The systematic reviews of qualitative studies assessed emotional well-being and daily functioning among older adults with vision impairment7 and age-related macular degeneration (AMD)51 and children and adults with mendelian eye conditions,53 including retinitis pigmentosa specifically in a second review.52 The 2 reviews52,53 that addressed retinitis pigmentosa included 2 overlapping primary studies. Emotional well-being among people with vision impairment, AMD, and retinitis pigmentosa was especially affected at the initial diagnosis, which was described as a shocking or traumatic event in the 3 reviews.7,51,52 Moreover, coping with AMD and retinitis pigmentosa was associated with negative thoughts, including depressive symptoms, fatigue, and isolation.51,52 Vision impairment and mendelian eye conditions specifically also affected general daily functioning; people reported having to relinquish their independence and giving up on leisure activities.7,52,53 Difficulties performing visual tasks, such as reading and seeing in changing light conditions, were also reported by people with retinitis pigmentosa.52

Overall, 5 exposures (vision impairment; AMD; diabetic retinopathy; mendelian eye conditions, including retinitis pigmentosa; and glaucoma) were evaluated for their association with quality of life. A summary of findings is presented in the Box.

Box. Summary of Findings From Systematic Reviews of Vision Impairment or Eye Disease Associated With Lower Quality of Life.

Vision Impairment
  • Vitality subscale (fatigue) of health-related quality of life among adults with vision impairment48

  • Mental health subscale of health-related and vision-related quality of life among working-age adults with vision impairment47

  • Vision-related and health-related quality of life among older adults with vision impairment49

  • Emotional well-being and general functioning among older adults with vision impairment7

Age-Related Macular Degeneration
  • Emotional well-being among people with age-related macular degeneration51

Diabetic Retinopathy
  • Psychosocial functioning among people with diabetic retinopathy6

Mendelian Eye Conditions
  • Emotional well-being among people with retinitis pigmentosa52

  • General and visual functioning among people with mendelian eye conditions, including retinitis pigmentosa53

Glaucoma
  • Glaucoma-specific quality of life among people with glaucoma50

Ophthalmic Interventions

In total, 60 systematic reviews published between 2005 and 2020 evaluated ophthalmic interventions using quality-of-life outcomes. Seventeen had corresponding authors in the UK,18,19,23,26,28,29,32,37,42,43,44,46,54,55,56,57,58,59 13 in the US,13,20,21,38,39,40,60,61,62,63,64,65,66 6 in China,24,27,30,67,68,69 6 in Italy,22,25,70,71,72,73 3 in Brazil,34,45,74 3 in Canada,14,15,17 2 in Denmark,75,76 2 in Spain,33,42 and 1 each in Uruguay,41 Switzerland,16 Bahrain,73 Germany,77 Belgium,31 the Netherlands,36 Taiwan,35 and Australia.78 Thirty-nine reviews reported vision-related quality-of-life measures13,15,16,19,21,22,23,24,25,26,27,28,29,30,31,32,33,34,37,42,44,54,55,58,59,60,61,62,66,67,68,69,70,71,73,74,75,76,77; 7, disease-specific measures35,38,39,40,41,57,65; 4, generic measures14,45,56,72; and 10, more than 1 measure type.17,18,20,36,43,46,63,64,78,79 Reviews that assessed and reported the quality of the evidence either used the Grading of Recommendations, Assessment, Development, and Evaluations (GRADE) tool with 4 possible levels of evidence (very low, low, moderate, or high)80 or the US Preventive Services Task Force scale for overall quality of the evidence (poor, fair, or good).81

Findings about quality of life after ophthalmic interventions compared with quality of life at baseline or in a group receiving no intervention are presented in Table 2. Seven systematic reviews13,14,15,16,17,18,19 addressed interventions for age-associated cataract. One review13 found improvement in vision-related quality of life after treatment of early vision impairment attributable to cataract in 3 of the 5 studies included (with fair-quality evidence). Two reviews14,15 using results from the same primary studies showed improved vision-related quality of life in the group receiving expedited cataract surgery compared with the control group with a routine waiting time for surgery, and a third16 found benefits to immediate cataract surgery among people with AMD specifically, compared with those having no or delayed surgery (low-quality evidence). Two reviews17,18 with some overlap of primary studies found a nonclinically meaningful improvement in vision-related quality of life after a second eye cataract surgery compared with surgery in 1 eye only (with moderate-quality evidence in 1 review17). Both extracapsular cataract extraction with posterior chamber intraocular lens (IOL) implantation and intracapsular cataract extraction with aphakic glasses were associated with improvement in vision-related quality-of-life outcomes, but extracapsular cataract extraction resulted in greater improvement.19 Only 1 systematic review assessed interventions associated with refractive error. Using corrective lenses for vision impairment because of uncorrected refractive error improved vision-related quality of life (fair-quality evidence).13

Seven systematic reviews13,20,21,22,23,24,54 assessed interventions for AMD. Anti–vascular endothelial growth factor (anti-VEGF) therapy was associated with improved vision-related quality of life compared with no anti-VEGF therapy in 2 reviews,13,14,15,16,17,18,19,20 with some overlap in primary studies (described as mild to moderate improvements, with fair-quality evidence13 and moderate-quality evidence20). Treatment using aflibercept and ranibizumab resulted in improved vision-related quality of life from baseline to a similar extent (high-quality evidence that quality of life is similar in both groups).21 Macular surgery compared with observation (relative risk, 1.35 [95% CI, 1.09-1.68]; low-quality evidence),22 and antioxidant vitamin supplementation compared with placebo (low-quality evidence)23 were associated with improved vision-related quality of life, while radiotherapy compared with observation54 was not. Two reviews23,24 with some overlap of primary studies found that supplementation with lutein and/or zeaxanthin compared with placebo was not associated with better vision-related quality of life (with low-quality evidence in 1 review23).

Nine systematic reviews25,26,27,28,29,30,31,32,33 examined interventions for other retinal diseases. One systematic review reported that both anti-VEGF therapy and laser photocoagulation improved vision-related quality of life for diabetic retinopathy, but anti-VEGF therapy resulted in a greater improvement (moderate-quality evidence).25 Likewise, 3 reviews26,27,28 using identical primary studies found that anti-VEGF therapy, compared with a sham treatment, was associated with improvement in vision-related quality of life in people with macular edema secondary to central retinal vein occlusion (high-quality evidence in 1 review27 and moderate-quality evidence in another review26). Anti-VEGF therapy was also found to improve vision-related quality of life in those with branch retinal vein occlusion29 and choroidal neovascularization secondary to pathological myopia (moderate-quality evidence).30 Ocriplasmin injection compared with a sham treatment was associated with clinically meaningful improvement in vision-related quality of life among those with symptomatic vitreomacular traction31 and adhesion (moderate-quality evidence).32 In people with hereditary retinal dystrophies, vision-related quality of life was similar among those who received nutritional supplementation and placebo.33

Two systematic reviews34,35 addressed glaucoma interventions. Treatment of early open-angle glaucoma with laser trabeculoplasty and topical β-blockers compared with placebo was not associated with differences in vision-related quality of life.34 Selective laser trabeculoplasty and/or medication use did not result in changes in disease-specific quality of life in open-angle glaucoma.35

One systematic review36 addressed vision rehabilitation interventions. Compared with a passive control arm (delayed or no care), methods for enhancing vision (eg, low-vision service, customized prism glasses) resulted in an imprecisely estimated benefit in vision-related quality of life (very low-quality evidence), and multidisciplinary rehabilitation resulted in beneficial vision-related quality-of-life effects (with very low-quality evidence).36

One systematic review37 addressed vision screening. After-school vision screenings and the use of ready-made or custom-made spectacles both resulted in improvement in vision-related quality of life to a similar extent (with moderate-quality evidence that quality of life was similar in both groups).37

Subcutaneous immunotherapy for rhinoconjunctivitis was shown to result in greater improvement in rhinoconjuctivitis-specific quality of life compared with placebo among children in 1 systematic review39 (low-quality evidence) and among adults in another review38 (high-quality evidence). Sublingual immunotherapy was associated with better quality of life in 1 review40 (moderate-quality evidence), but not in another 1 that focused on children only.39 Intranasal fluticasone furoate was associated with better rhinoconjunctivitis-specific quality of life compared with placebo in people with allergic rhinoconjunctivitis.41

Two systematic reviews with some overlap of primary studies reported that adults with active uveitis who received adalimumab, relative to those receiving placebo, had a greater improvement in quality of life, but those with inactive uveitis did not have improvements in quality of life with therapy.42,43 Surgery for people with trichiasis improved vision-related quality of life regardless of perioperative azithromycin administration in 1 review.44 There were no differences in quality of life among people with thyroid eye disease who received radiotherapy or sham, according to 2 reviews45,46 based on results from the same primary study.

Thirty-three interventions among specific populations (eg, people with AMD, people with inactive disease, children only) were identified, after accounting for duplicate interventions assessed by multiple reviews and combining quality-of-life outcomes (health-related, vision-related, or disease-specific quality of life). A summary of findings is presented in Table 4. Overall, only 11 interventions23,24,33,34,35,39,42,43,45,46,54 were not associated with improved quality of life compared with baseline or compared with a group receiving no intervention: radiotherapy54 and supplementation with lutein and zeaxanthin23,24 for AMD, supplementation with nutrients for hereditary retinal dystrophies,33 early open-angle glaucoma treatment with laser trabeculoplasty and topical β-blockers,34 open-angle glaucoma treatment with selective laser trabeculoplasty and/or medications,35 adalimumab for the treatment of inactive uveitis (treatment improved quality of life among those with active disease),42,43 radiotherapy for the treatment of thyroid eye disease,45,46 and sublingual immunotherapy for rhinoconjunctivitis among children39 (however, this treatment improved quality of life in a review covering both children and adults40).

Table 4. Summary of Findings From Systematic Reviews of Ophthalmic Interventions.

Area Findings on quality of life
Improvementa No difference
Age-related cataract Cataract surgery for the treatment of early impairment in visual acuity (1); expedited cataract surgery vs awaiting cataract surgery (routine wait time) (2); expedited surgery vs routine wait time among people with age-related macular degeneration (1); second-eye surgery vs surgery in 1 eye only (2); cataract surgery by extracapsular cataract extraction with posterior chamber intraocular lens or intracapsular cataract extraction with aphakic glasses (1) None
Cornea and refractive error Corrective lenses for refractive error (1) None
Age-related macular degeneration Anti-VEGF vs no anti-VEGF (2); aflibercept or ranibizumab (1); macular surgery vs observation (1); multivitamin supplements vs placebo (1) Radiotherapy vs observation (1); Lutein and/or zeaxanthin vs placebo (2)
Retina (other) Anti-VEGF or laser photocoagulation for diabetic retinopathy (1); anti-VEGF vs sham for macular edema secondary to central retinal vein occlusion (3); anti-VEGF vs sham for macular edema secondary to branch retinal vein occlusion (1); anti-VEGF vs sham for choroidal neovascularization secondary to pathological myopia (1); ocriplasmin injection vs sham for symptomatic vitreomacular traction (1); ocriplasmin injection vs sham for symptomatic vitreomacular adhesion (1) Nutritional supplementation vs placebo for hereditary retinal dystrophies (1)
Glaucoma None Laser trabeculoplasty and topic β-blockers vs placebo for early open glaucoma (1); Selective laser trabeculoplasty and medication or medication only for open-angle glaucoma (1)
Low vision Multidisciplinary rehabilitation vs waiting list or no care (1); methods of enhancing vision (eg, low-vision service, customized prism glasses) vs waiting list or no care (1) None
Vision screening Ready-made spectacles or custom-made spectacles after school vision screening (1) None
Rhinoconjunctivitis Subcutaneous immunotherapy vs placebo (2); Sublingual immunotherapy vs placebo (all ages) (1); intranasal fluticasone furoate vs placebo for seasonal allergic rhinitis (1); intranasal fluticasone furoate vs placebo for perennial allergic rhinitis (1) Sublingual immunotherapy vs placebo among children only (1)
Uveitis Adalimumab vs placebo for active uveitis (2) Adalimumab vs placebo for inactive uveitis (2)
Trichiasis Surgery with or without preoperative azithromycin (1) None
Thyroid eye disease None Radiotherapy vs sham (2)

Abbreviations: anti-VEGF, anti–vascular endothelial growth factor; QOL, quality of life.

a

Number of systematic reviews informing the intervention and outcome are shown in parentheses.

Comparisons of quality of life between 2 different ophthalmic interventions are presented in eTable 3 in the Supplement. Similar quality of life was reported across the interventions for most interventions compared. Interventions that were associated with small or moderate improvements in quality of life when compared with other interventions were immediate sequential cataract surgery compared with different date bilateral cataract surgery (moderate-quality evidence),75 multifocal IOLs compared with monofocal IOLs (very low-quality evidence in 1 review),55,60,61 toric IOLs compared with nontoric IOLs,61 macular translocation compared with photodynamic therapy (described as “insufficient evidence”70(p2)), the use of handheld electronic devices with optical devices compared with optical devices alone (moderate-quality evidence),71 vision rehabilitation using methods for enhancing vision (eg, low-vision service, customized prism glasses) compared with other interventions (moderate-quality evidence),36 and posterior lamellar tarsal rotation surgery for minor trichiasis compared with epilation.44

Discussion

In this umbrella review, we performed a global, broad assessment of eye disease, vision impairment, and ophthalmic interventions on quality of life. There was a consistent association between vision impairment and eye disease with reduced quality of life across eye conditions, especially among adults. Seventy-five percent of ophthalmic interventions evaluated had evidence of a positive outcome on quality of life. Most notably, cataract surgery and the use of anti-VEGF therapy for AMD, diabetic macular edema, and macular edema secondary to other causes resulted in improved quality of life.

Vision impairment and eye diseases, namely glaucoma, diabetic retinopathy, AMD, and retinitis pigmentosa were associated with lower quality of life, using a range of outcome measures. Quantitative studies showed significant associations and sometimes a graded response, with worse vision impairment being associated with worse quality of life. Qualitative studies provided insight into the mechanisms of the associations, specifically on well-being and functioning. While the significant associations were expected, previous literature suggests that even more eye diseases are associated with worse quality of life. Notably, dry eye has been studied extensively, and a systematic review82 (excluded because of a lack of appropriate criteria for critical appraisal) has suggested that dry eye syndrome has a substantial association with reduced quality of life across countries in Europe, North America, and Asia.

Ophthalmic interventions differed in their association with quality of life. In general, treating cataract immediately after diagnosis, even in those with competing eye conditions such as AMD and who had already received a first cataract surgery, improved quality of life. Moreover, anti-VEGF therapy for a number of conditions, including AMD and diabetic macular edema, and the use of corrective lenses for refractive error were associated with improved quality of life. Projections from 2015 suggested that in 2020, 127.7 million people will have moderate or severe vision impairment because of uncorrected refractive error, 57.1 million because of cataract, 8.8 million because of AMD, and 3.2 million because of diabetic retinopathy.83 Three interventions (cataract surgery, corrective lenses, and anti-VEGF therapy) provide opportunities to improve the quality of life of more than 150 million individuals globally. Other interventions, such as treating rhinoconjunctivitis in children and adults, trichiasis in endemic areas, and uveitis in those with active and inactive disease, and low-vision rehabilitation, also have the potential to improve quality of life.

The 8 interventions that were not found to improve quality of life included 2 that focused on specific populations. This included the use of adalimumab, which did not improve quality of life among people with inactive uveitis but improved it in those with active disease, and sublingual immunotherapy for rhinoconjunctivitis, which did not improve quality of life among children but improved it when people of all ages were included in another review. Two of the interventions involved nutritional supplements; one was lutein or zeaxanthin for AMD, and the other was nutritional supplements for hereditary retinal dystrophies.

There were gaps in the evidence available on the outcomes of leading causes of visual impairment (eg, cataract, refractive error), among particular groups (eg, children, people from racial/ethnic minorities), and in low- and middle-income countries compared with high-income countries. Interventions for dry eye, refractive error, glaucoma, and diabetic retinopathy were underrepresented in this review in comparison with their prevalence globally. While systematic reviews about some topics may be lacking, there may be a lack of primary studies as well: 70% of the interventional systematic reviews that aimed to assess quality of life outcomes were subsequently excluded because they did not identify any primary studies reporting quality-of-life outcomes. Moreover, almost half of the interventions and outcomes identified in this review were comparing one intervention with another without presenting information about the change in quality of life from baseline in any of the groups, making it impossible to know whether any of the interventions had an association with quality of life to begin with. While this may be standard practice, as more and more eye diseases have well-established treatments, delaying treatment or using placebo control arms will not be possible. Thinking of ways to answer questions about potential advantages of interventions without depriving a group of beneficial therapy will be important. Researchers could be encouraged to analyze and present data such as overall changes from baseline values by treatment arm, or regardless of treatment arm, even if they are not the primary outcomes.

The review process highlighted the need for a unified definition for quality of life to study and understand the association with vision impairment and ophthalmic interventions on well-being and vision function from the patient perspective. Many systematic reviews were excluded because they considered patient satisfaction or patient-reported symptoms and discomfort as quality-of-life measures. While these measures fall under the umbrella of patient-reported outcomes and capture valuable information, they do not describe general well-being or vision function in day-to-day life. Moreover, in the included reviews, a wide range of quality of life measures were used between and within the systematic reviews, which limits the ability to compare findings between studies or combine them into meta-analyses.

Limitations

Umbrella reviews findings are limited to results that have been synthesized in published reviews, which may be affected by publication bias themselves. Although this may have limited the availability of studies about specific topics, it is this approach that allowed for a global assessment of a broad topic in a systematic manner. Moreover, umbrella reviews are limited by the quality of the reviews and the data reported by the reviews; not all reviews reported specific estimates, tools used to measure outcomes, or enough context to interpret the results. However, we applied strict criteria for systematic reviews, including the working definition and critical appraisal criteria used, and excluded reviews with case series. This approach may have further limited the number of systematic reviews included, but it ensured the inclusion of reviews of higher quality. Finally, there were overlaps in primary studies used by the reviews, and many reviews reported findings based on results from 1 or 2 primary studies only; these were presented in both the text and Tables to allow readers to take them into account when interpreting the findings.

There is evidence that vision impairment and eye diseases in general are associated with lower quality of life, and most ophthalmic interventions are associated with improved quality of life. Reviews and primary studies addressing underrepresented diseases and reviews focusing on specific populations, such as people from low- and middle-income countries, are needed to expand generalizable knowledge on the association between eye health and quality of life.

Conclusions

Vision impairment and eye conditions are associated with lower quality of life, and ophthalmic interventions can lead to significant improvement in quality of life. Scaling up interventions, such as cataract surgery, refractive error correction, and anti-VEGF therapy at a global level, has the potential to improve the quality of life of millions of people worldwide.

Supplement.

eAppendix 1. Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) reporting guidelines

eAppendix 2. Changes to the Protocol

eAppendix 3. MEDLINE Ovid Search Strategy

eFigure. PRISMA Flow Chart

eTable 1. Quality Appraisal Using the Joanna Briggs Institute Critical Appraisal Checklist for Systematic Reviews and Research Syntheses

eTable 2. Systematic Review Characteristics (Selected from the Joanna Briggs Institute Data Extraction Form for Systematic Reviews and Research Syntheses)

eTable 3. Comparisons of Quality of Life Impact of Different Ophthalmic Interventions by Systematic Review

eTable 4. Studies Included

eReferences.

References

  • 1.World Health Organization . World Report of Vision. World Health Organization;2019. [Google Scholar]
  • 2.Chia EM, Wang JJ, Rochtchina E, Smith W, Cumming RR, Mitchell P. Impact of bilateral visual impairment on health-related quality of life: the Blue Mountains Eye Study. Invest Ophthalmol Vis Sci. 2004;45(1):71-76. doi: 10.1167/iovs.03-0661 [DOI] [PubMed] [Google Scholar]
  • 3.Chiang PP, Zheng Y, Wong TY, Lamoureux EL. Vision impairment and major causes of vision loss impacts on vision-specific functioning independent of socioeconomic factors. Ophthalmology. 2013;120(2):415-422. doi: 10.1016/j.ophtha.2012.07.077 [DOI] [PubMed] [Google Scholar]
  • 4.Braithwaite T, Calvert M, Gray A, Pesudovs K, Denniston AK. The use of patient-reported outcome research in modern ophthalmology: impact on clinical trials and routine clinical practice. Patient Relat Outcome Meas. 2019;10:9-24. doi: 10.2147/PROM.S162802 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Boyle J, Vukicevic M, Koklanis K, Itsiopoulos C. Experiences of patients undergoing anti-VEGF treatment for neovascular age-related macular degeneration: a systematic review. Psychol Health Med. 2015;20(3):296-310. doi: 10.1080/13548506.2014.936886 [DOI] [PubMed] [Google Scholar]
  • 6.Khoo K, Man REK, Rees G, Gupta P, Lamoureux EL, Fenwick EK. The relationship between diabetic retinopathy and psychosocial functioning: a systematic review. Qual Life Res. 2019;28(8):2017-2039. doi: 10.1007/s11136-019-02165-1 [DOI] [PubMed] [Google Scholar]
  • 7.Nyman SR, Dibb B, Victor CR, Gosney MA. Emotional well-being and adjustment to vision loss in later life: a meta-synthesis of qualitative studies. Disabil Rehabil. 2012;34(12):971-981. doi: 10.3109/09638288.2011.626487 [DOI] [PubMed] [Google Scholar]
  • 8.Burton MJ, Faal HB, Ramke J, et al. Announcing the Lancet Global Health Commission on Global Eye Health. Lancet Glob Health. 2019;7(12):e1612-e1613. doi: 10.1016/S2214-109X(19)30450-4 [DOI] [PubMed] [Google Scholar]
  • 9.Assi L, Rosman L, Chamseddine F, et al. Eye health and quality of life: an umbrella review protocol. BMJ Open. 2020;10(8):e037648. doi: 10.1136/bmjopen-2020-037648 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Covidence Inc . Covidence systematic review software: better systematic review management. Accessed January 29, 2021. https://www.covidence.org/
  • 11.Aromataris E, Fernandez R, Godfrey CM, Holly C, Khalil H, Tungpunkom P. Summarizing systematic reviews: methodological development, conduct and reporting of an umbrella review approach. Int J Evid Based Healthc. 2015;13(3):132-140. doi: 10.1097/XEB.0000000000000055 [DOI] [PubMed] [Google Scholar]
  • 12.Aromataris E, Fernandez R, Godfrey C, Holly C, Khalil H, Tungpunkom P.. Chapter 10: Umbrella reviews. In: Aromataris E, Munn Z, eds. JBI Manual for Evidence Synthesis. Joanna Briggs Institute;2020. doi: 10.46658/JBIMES-20-11 [DOI] [Google Scholar]
  • 13.Chou R, Dana T, Bougatsos C, Grusing S, Blazina I. Screening for impaired visual acuity in older adults: updated evidence report and systematic review for the US Preventive Services Task Force. JAMA. 2016;315(9):915-933. doi: 10.1001/jama.2016.0783 [DOI] [PubMed] [Google Scholar]
  • 14.Hodge W, Horsley T, Albiani D, et al. The consequences of waiting for cataract surgery: a systematic review. CMAJ. 2007;176(9):1285-1290. doi: 10.1503/cmaj.060962 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Conner-Spady B, Sanmartin C, Sanmugasunderam S, et al. A systematic literature review of the evidence on benchmarks for cataract surgery waiting time. Can J Ophthalmol. 2007;42(4):543-551. doi: 10.3129/i07-094 [DOI] [PubMed] [Google Scholar]
  • 16.Casparis H, Lindsley K, Kuo IC, Sikder S, Bressler NM. Surgery for cataracts in people with age-related macular degeneration. Cochrane Database Syst Rev. 2017;2(2):CD006757. doi: 10.1002/14651858.CD006757.pub4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Ishikawa T, Desapriya E, Puri M, Kerr JM, Hewapathirane DS, Pike I. Evaluating the benefits of second-eye cataract surgery among the elderly. J Cataract Refract Surg. 2013;39(10):1593-1603. doi: 10.1016/j.jcrs.2013.08.033 [DOI] [PubMed] [Google Scholar]
  • 18.Frampton G, Harris P, Cooper K, Lotery A, Shepherd J. The clinical effectiveness and cost-effectiveness of second-eye cataract surgery: a systematic review and economic evaluation. Health Technol Assess. 2014;18(68):1-205, v-vi. doi: 10.3310/hta18680 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Riaz Y, Mehta JS, Wormald R, et al. Surgical interventions for age-related cataract. Cochrane Database Syst Rev. 2006;(4):CD001323. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Solomon SD, Lindsley K, Vedula SS, Krzystolik MG, Hawkins BS. Anti-vascular endothelial growth factor for neovascular age-related macular degeneration. Cochrane Database Syst Rev. 2019;3:CD005139. doi: 10.1002/14651858.CD005139.pub4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Sarwar S, Clearfield E, Soliman MK, et al. Aflibercept for neovascular age-related macular degeneration. Cochrane Database Syst Rev. 2016;2:CD011346. doi: 10.1002/14651858.CD011346.pub2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Giansanti F, Eandi CM, Virgili G. Submacular surgery for choroidal neovascularisation secondary to age-related macular degeneration. Cochrane Database Syst Rev. 2009;(2):CD006931. doi: 10.1002/14651858.CD006931.pub2 [DOI] [PubMed] [Google Scholar]
  • 23.Evans JR, Lawrenson JG. Antioxidant vitamin and mineral supplements for slowing the progression of age-related macular degeneration. Cochrane Database Syst Rev. 2017;7(7):CD000254. doi: 10.1002/14651858.CD000254.pub4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Liu R, Wang T, Zhang B, et al. Lutein and zeaxanthin supplementation and association with visual function in age-related macular degeneration. Invest Ophthalmol Vis Sci. 2014;56(1):252-258. doi: 10.1167/iovs.14-15553 [DOI] [PubMed] [Google Scholar]
  • 25.Virgili G, Parravano M, Evans JR, Gordon I, Lucenteforte E. Anti-vascular endothelial growth factor for diabetic macular oedema: a network meta-analysis. Cochrane Database Syst Rev. 2018;10(10):CD007419. doi: 10.1002/14651858.CD007419.pub6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Braithwaite T, Nanji AA, Lindsley K, Greenberg PB. Anti-vascular endothelial growth factor for macular oedema secondary to central retinal vein occlusion. Cochrane Database Syst Rev. 2014;(5):CD007325. doi: 10.1002/14651858.CD007325.pub3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Zhou S, Gao J, Xu X. Antivascular endothelial growth factors in the treatment of macular oedema secondary to central retinal vein occlusion: a meta-analysis. Clin Exp Ophthalmol. 2014;42(7):637-649. doi: 10.1111/ceo.12286 [DOI] [PubMed] [Google Scholar]
  • 28.Ford JA, Clar C, Lois N, et al. Treatments for macular oedema following central retinal vein occlusion: systematic review. BMJ Open. 2014;4(2):e004120. doi: 10.1136/bmjopen-2013-004120 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Mitry D, Bunce C, Charteris D. Anti-vascular endothelial growth factor for macular oedema secondary to branch retinal vein occlusion. Cochrane Database Syst Rev. 2013;(1):CD009510. doi: 10.1002/14651858.CD009510.pub2 [DOI] [PubMed] [Google Scholar]
  • 30.Zhu Y, Zhang T, Xu G, Peng L. Anti-vascular endothelial growth factor for choroidal neovascularisation in people with pathological myopia. Cochrane Database Syst Rev. 2016;12:CD011160. doi: 10.1002/14651858.CD011160.pub2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Lescrauwaet B, Blot K, Jackson TL. Patient-reported outcomes of ocriplasmin for the treatment of vitreomacular traction: a systematic review and synthesis of the literature. Patient Relat Outcome Meas. 2019;10:101-116. doi: 10.2147/PROM.S153718 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Neffendorf JE, Kirthi V, Pringle E, Jackson TL. Ocriplasmin for symptomatic vitreomacular adhesion. Cochrane Database Syst Rev. 2017;10:CD011874. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Brito-García N, Del Pino-Sedeño T, Trujillo-Martín MM, et al. Effectiveness and safety of nutritional supplements in the treatment of hereditary retinal dystrophies: a systematic review. Eye (Lond). 2017;31(2):273-285. doi: 10.1038/eye.2016.286 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Rolim de Moura C, Paranhos A Jr, Wormald R. Laser trabeculoplasty for open angle glaucoma. Cochrane Database Syst Rev. 2007;(4):CD003919. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Chi SC, Kang YN, Hwang DK, Liu CJ. Selective laser trabeculoplasty versus medication for open-angle glaucoma: systematic review and meta-analysis of randomised clinical trials. Br J Ophthalmol. 2020;104(11):1500-1507. doi: 10.1136/bjophthalmol-2019-315613 [DOI] [PubMed] [Google Scholar]
  • 36.van Nispen RM, Virgili G, Hoeben M, et al. Low vision rehabilitation for better quality of life in visually impaired adults. Cochrane Database Syst Rev. 2020;1:CD006543. doi: 10.1002/14651858.CD006543.pub2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Evans JR, Morjaria P, Powell C. Vision screening for correctable visual acuity deficits in school-age children and adolescents. Cochrane Database Syst Rev. 2018;2(2):CD005023. doi: 10.1002/14651858.CD005023.pub3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Erekosima N, Suarez-Cuervo C, Ramanathan M, et al. Effectiveness of subcutaneous immunotherapy for allergic rhinoconjunctivitis and asthma: a systematic review. Laryngoscope. 2014;124(3):616-627. doi: 10.1002/lary.24295 [DOI] [PubMed] [Google Scholar]
  • 39.Kim JM, Lin SY, Suarez-Cuervo C, et al. Allergen-specific immunotherapy for pediatric asthma and rhinoconjunctivitis: a systematic review. Pediatrics. 2013;131(6):1155-1167. doi: 10.1542/peds.2013-0343 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Lin SY, Erekosima N, Kim JM, et al. Sublingual immunotherapy for the treatment of allergic rhinoconjunctivitis and asthma: a systematic review. JAMA. 2013;309(12):1278-1288. doi: 10.1001/jama.2013.2049 [DOI] [PubMed] [Google Scholar]
  • 41.Rodrigo GJ, Neffen H. Efficacy of fluticasone furoate nasal spray vs. placebo for the treatment of ocular and nasal symptoms of allergic rhinitis: a systematic review. Clin Exp Allergy. 2011;41(2):160-170. doi: 10.1111/j.1365-2222.2010.03654.x [DOI] [PubMed] [Google Scholar]
  • 42.Urruticoechea-Arana A, Cobo-Ibáñez T, Villaverde-García V, et al. Efficacy and safety of biological therapy compared to synthetic immunomodulatory drugs or placebo in the treatment of Behçet’s disease associated uveitis: a systematic review. Rheumatol Int. 2019;39(1):47-58. doi: 10.1007/s00296-018-4193-z [DOI] [PubMed] [Google Scholar]
  • 43.Squires H, Poku E, Bermejo I, et al. A systematic review and economic evaluation of adalimumab and dexamethasone for treating non-infectious intermediate uveitis, posterior uveitis or panuveitis in adults. Health Technol Assess. 2017;21(68):1-170. doi: 10.3310/hta21680 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Burton M, Habtamu E, Ho D, Gower EW. Interventions for trachoma trichiasis. Cochrane Database Syst Rev. 2015;2015(11):CD004008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Viani GA, Boin AC, De Fendi LI, Fonseca EC, Stefano EJ, Paula JS. Radiation therapy for Graves’ ophthalmopathy: a systematic review and meta-analysis of randomized controlled trials. Arq Bras Oftalmol. 2012;75(5):324-332. doi: 10.1590/S0004-27492012000500006 [DOI] [PubMed] [Google Scholar]
  • 46.Rajendram R, Bunce C, Lee RWJ, Morley AMS. Orbital radiotherapy for adult thyroid eye disease. Cochrane Database Syst Rev. 2012;(7):CD007114. doi: 10.1002/14651858.CD007114.pub2 [DOI] [PubMed] [Google Scholar]
  • 47.Nyman SR, Gosney MA, Victor CR. Psychosocial impact of visual impairment in working-age adults. Br J Ophthalmol. 2010;94(11):1427-1431. doi: 10.1136/bjo.2009.164814 [DOI] [PubMed] [Google Scholar]
  • 48.Schakel W, Bode C, Elsman EBM, et al. The association between visual impairment and fatigue: a systematic review and meta-analysis of observational studies. Ophthalmic Physiol Opt. 2019;39(6):399-413. doi: 10.1111/opo.12647 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Tseng Y-C, Liu SH-Y, Lou M-F, Huang G-S. Quality of life in older adults with sensory impairments: a systematic review. Qual Life Res. 2018;27(8):1957-1971. doi: 10.1007/s11136-018-1799-2 [DOI] [PubMed] [Google Scholar]
  • 50.Wang Y, Alnwisi S, Ke M. The impact of mild, moderate, and severe visual field loss in glaucoma on patients’ quality of life measured via the Glaucoma Quality of Life-15 Questionnaire: a meta-analysis. Medicine (Baltimore). 2017;96(48):e8019. doi: 10.1097/MD.0000000000008019 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Bennion AE, Shaw RL, Gibson JM. What do we know about the experience of age related macular degeneration? a systematic review and meta-synthesis of qualitative research. Soc Sci Med. 2012;75(6):976-985. doi: 10.1016/j.socscimed.2012.04.023 [DOI] [PubMed] [Google Scholar]
  • 52.Garip G, Kamal A. Systematic review and meta-synthesis of coping with retinitis pigmentosa: implications for improving quality of life. BMC Ophthalmol. 2019;19(1):181. doi: 10.1186/s12886-019-1169-z [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.D’Amanda CS, Nolen R, Huryn LA, Turriff A. Psychosocial impacts of mendelian eye conditions: a systematic literature review. Surv Ophthalmol. 2020;65(5):562-580. doi: 10.1016/j.survophthal.2020.02.002 [DOI] [PubMed] [Google Scholar]
  • 54.Evans JR, Sivagnanavel V, Chong V. Radiotherapy for neovascular age-related macular degeneration. Cochrane Database Syst Rev. 2010;(5):CD004004. doi: 10.1002/14651858.CD004004.pub3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.de Silva SR, Evans JR, Kirthi V, Ziaei M, Leyland M. Multifocal versus monofocal intraocular lenses after cataract extraction. Cochrane Database Syst Rev. 2016;12(12):CD003169. doi: 10.1002/14651858.CD003169.pub4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Spiteri CK, Lois N, Scott N, et al. Vitrectomy with internal limiting membrane (ILM) peeling versus vitrectomy with no peeling for idiopathic full‐thickness macular hole (FTMH). 2013(6). doi: 10.1002/14651858.CD009306.pub2 [DOI] [PubMed]
  • 57.Lim BX, Lim CH, Lim DK, Evans JR, Bunce C, Wormald R. Prophylactic non-steroidal anti-inflammatory drugs for the prevention of macular oedema after cataract surgery. Cochrane Database Syst Rev. 2016;11:CD006683. doi: 10.1002/14651858.CD006683.pub3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Burr J, Azuara-Blanco A, Avenell A, Tuulonen A. Medical versus surgical interventions for open angle glaucoma. Cochrane Database Syst Rev. 2012;(9):CD004399. doi: 10.1002/14651858.CD004399.pub3 [DOI] [PubMed] [Google Scholar]
  • 59.Clarke EL, Evans JR, Smeeth L. Community screening for visual impairment in older people. Cochrane Database Syst Rev. 2018;2:CD001054. doi: 10.1002/14651858.CD001054.pub3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Khandelwal SS, Jun JJ, Mak S, Booth MS, Shekelle PG. Effectiveness of multifocal and monofocal intraocular lenses for cataract surgery and lens replacement: a systematic review and meta-analysis. Graefes Arch Clin Exp Ophthalmol. 2019;257(5):863-875. doi: 10.1007/s00417-018-04218-6 [DOI] [PubMed] [Google Scholar]
  • 61.Wang SY, Stem MS, Oren G, Shtein R, Lichter PR. Patient-centered and visual quality outcomes of premium cataract surgery: a systematic review. Eur J Ophthalmol. 2017;27(4):387-401. doi: 10.5301/ejo.5000978 [DOI] [PubMed] [Google Scholar]
  • 62.Herretes S, Wang X, Reyes JMG. Topical corticosteroids as adjunctive therapy for bacterial keratitis. Cochrane Database Syst Rev. 2014;(10):CD005430. doi: 10.1002/14651858.CD005430.pub3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Low A, Faridi A, Bhavsar KV, et al. Comparative effectiveness and harms of intravitreal antivascular endothelial growth factor agents for three retinal conditions: a systematic review and meta-analysis. Br J Ophthalmol. 2019;103(4):442-451. doi: 10.1136/bjophthalmol-2018-312691 [DOI] [PubMed] [Google Scholar]
  • 64.Ollendorf DA, Colby JA, Pearson SD. Comparative effectiveness of anti-VEGF agents for diabetic macular edema. Int J Technol Assess Health Care. 2013;29(4):392-401. doi: 10.1017/S0266462313000500 [DOI] [PubMed] [Google Scholar]
  • 65.Li T, Qureshi R, Taylor K. Conventional occlusion versus pharmacologic penalization for amblyopia. Cochrane Database Syst Rev. 2019;8(8):CD006460. doi: 10.1002/14651858.CD006460.pub3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Brady CJ, Villanti AC, Law HA, et al. Corticosteroid implants for chronic non-infectious uveitis. Cochrane Database Syst Rev. 2016;2(2):CD010469. doi: 10.1002/14651858.CD010469.pub2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Jin S, Friedman DS, Cao K, et al. Comparison of postoperative visual performance between bifocal and trifocal intraocular lens based on randomized controlled trails: a meta-analysis. BMC Ophthalmol. 2019;19(1):78. doi: 10.1186/s12886-019-1078-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Xu Z, Cao D, Chen X, Wu S, Wang X, Wu Q. Comparison of clinical performance between trifocal and bifocal intraocular lenses: a meta-analysis. PLoS One. 2017;12(10):e0186522. doi: 10.1371/journal.pone.0186522 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Yang J-J, Liu Q-P, Li J-M, Qin L. Comparison of visual outcomes with implantation of trifocal versus bifocal intraocular lens after phacoemulsification: a meta-analysis. Int J Ophthalmol. 2018;11(3):484-492. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Eandi CM, Giansanti F, Virgili G. Macular translocation for neovascular age-related macular degeneration. Cochrane Database Syst Rev. 2008;(4):CD006928. doi: 10.1002/14651858.CD006928.pub2 [DOI] [PubMed] [Google Scholar]
  • 71.Virgili G, Acosta R, Bentley SA, Giacomelli G, Allcock C, Evans JR. Reading aids for adults with low vision. Cochrane Database Syst Rev. 2018;4:CD003303. doi: 10.1002/14651858.CD003303.pub4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Virgili G, Bini A. Laser photocoagulation for neovascular age-related macular degeneration. Cochrane Database Syst Rev. 2007;18(3):CD004763. doi: 10.1002/14651858.CD004763.pub2 [DOI] [PubMed] [Google Scholar]
  • 73.Lawrence D, Fedorowicz Z, van Zuuren EJ. Day care versus in-patient surgery for age-related cataract. Cochrane Database Syst Rev. 2015;(11):CD004242. doi: 10.1002/14651858.CD004242.pub5 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Lake JC, Victor G, Clare G, Porfírio GJ, Kernohan A, Evans JR. Toric intraocular lens versus limbal relaxing incisions for corneal astigmatism after phacoemulsification. Cochrane Database Syst Rev. 2019;12:CD012801. doi: 10.1002/14651858.CD012801.pub2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.Kessel L, Andresen J, Erngaard D, Flesner P, Tendal B, Hjortdal J. Immediate sequential bilateral cataract surgery: a systematic review and meta-analysis. J Ophthalmol. 2015;2015:912481. doi: 10.1155/2015/912481 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Kessel L, Andresen J, Erngaard D, Flesner P, Tendal B, Hjortdal J. Indication for cataract surgery. do we have evidence of who will benefit from surgery? a systematic review and meta-analysis. Acta Ophthalmol. 2016;94(1):10-20. doi: 10.1111/aos.12758 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Schuster AK, Tesarz J, Vossmerbaeumer U. The impact on vision of aspheric to spherical monofocal intraocular lenses in cataract surgery: a systematic review with meta-analysis. Ophthalmology. 2013;120(11):2166-2175. doi: 10.1016/j.ophtha.2013.04.011 [DOI] [PubMed] [Google Scholar]
  • 78.Rees G, Ponczek E, Hassell J, Keeffe JE, Lamoureux EL. Psychological outcomes following interventions for people with low vision: a systematic review. Expert Rev Ophthalmol. 2010;5(3):385-403. doi: 10.1586/eop.10.32 [DOI] [Google Scholar]
  • 79.Li E, Donati S, Lindsley KB, Krzystolik MG, Virgili G. Treatment regimens for administration of anti-vascular endothelial growth factor agents for neovascular age-related macular degeneration. Cochrane Database Syst Rev. 2020;5(5):CD012208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80.Siemieniuk R, Guyatt G. What is GRADE? BMJ Best Practice: EBM Toolkit website. Accessed January 26, 2021. https://bestpractice.bmj.com/info/us/toolkit/learn-ebm/what-is-grade/
  • 81.US Preventive Services Task Force . Grade definitions. Published 2018. Accessed January 26, 2021. https://www.uspreventiveservicestaskforce.org/uspstf/grade-definitions
  • 82.McDonald M, Patel DA, Keith MS, Snedecor SJ. Economic and humanistic burden of dry eye disease in Europe, North America, and Asia: a systematic literature review. Ocul Surf. 2016;14(2):144-167. doi: 10.1016/j.jtos.2015.11.002 [DOI] [PubMed] [Google Scholar]
  • 83.Flaxman SR, Bourne RRA, Resnikoff S, et al. ; Vision Loss Expert Group of the Global Burden of Disease Study . Global causes of blindness and distance vision impairment 1990-2020: a systematic review and meta-analysis. Lancet Glob Health. 2017;5(12):e1221-e1234. doi: 10.1016/S2214-109X(17)30393-5 [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplement.

eAppendix 1. Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) reporting guidelines

eAppendix 2. Changes to the Protocol

eAppendix 3. MEDLINE Ovid Search Strategy

eFigure. PRISMA Flow Chart

eTable 1. Quality Appraisal Using the Joanna Briggs Institute Critical Appraisal Checklist for Systematic Reviews and Research Syntheses

eTable 2. Systematic Review Characteristics (Selected from the Joanna Briggs Institute Data Extraction Form for Systematic Reviews and Research Syntheses)

eTable 3. Comparisons of Quality of Life Impact of Different Ophthalmic Interventions by Systematic Review

eTable 4. Studies Included

eReferences.


Articles from JAMA Ophthalmology are provided here courtesy of American Medical Association

RESOURCES