Study and Year | Country | Study type | Age (years) | Sex | Study sample selection and representativeness | N with dementia | Method of dementia diagnosis | Type of VI/eye disease | Method of VI/eye disease diagnosis |
---|---|---|---|---|---|---|---|---|---|
Abdullah,1965 [12] | UK | Not described | ≥ 65 | Male 26.5% Female 73.5% | 3 patient groups - geriatric patients in London hospital; those of similar age seen on domiciliary visits; those attending a local social club. Moderately representative. | Unclear. 79 or 103 | Not described | General VI Cataract | Ability to read or not Not described |
Amjad, 2019 [13] | USA | Cross-sectional | ≥65; Mean: 82.3 ± 8.1 | Male 41.6% Female 59.4% | Community dwelling adults participating in 2011 NHATS (population- based nationally representative cohort of Medicare beneficiaries aged 65+), who died by 2015. Highly representative | 542 | Based on algorithm: clinician diagnosis of dementia or AD; AD-8 dementia screening interview of proxy respondents | VI | Based on interview questions including: ‘Uses corrective lenses or blind’, ‘Sees well enough to recognize person across street’, ‘Can watch TV across room’, ‘Reads newspaper print’ |
Bayer, 2002 [14] | Germany | Case-control | With glaucoma; Mean: 72.9 ± 10.6 Without glaucoma Mean: 71.4 ± 11.9 | Male 35.7% Female 64.3% | 4 nursing homes in Upper Bavaria, Germany. Low representativeness | 112 | Based on criteria for probable dementia based on NINCDS-ADRDA | Glaucoma | Visual field defects and/or optic disk cup-to-disk ratio of 0.8 or greater with an optic nerve head appearance consistent with glaucoma. Eye exams performed by one of the investigators. |
Bayer, 2002 [15] | Germany | Case- control | With glaucoma; mean: 71.9 ± 11.6 Without glaucoma mean: 73.2 ± 12.3a | Male 38.8% Female 61.2% | 2 nursing homes in Upper Bavaria, Germany. Low representativeness | 49 | Not described | Glaucoma | Visual field defects and/or optic disk cup-to-disk ratio of 0.8 or greater with an optic nerve head appearance consistent with glaucoma. Eye exams performed by two investigators. |
Bennett, 2018 [16] | UK | Cohort study | Not described | Not described | Randomly sampled from primary care list in 3 areas of England. CFAS I, with an 80% response rate, CFAS II, with a 56% response rate. Highly representative. | 83 in CFAS I and 277 in CFAS II. | Diagnosis via an algorithm | VI | Self-reported with no further details. |
Bowen, 2016 [17] | UK | Cross-sectional | 60–89 | Male 37.9% Female 62.1% | Recruited from 20 NHS sites in six English regions. Includes both those in the community and nursing homes. Participation rate not reported but 100 withdrew (12.4%). Highly representative. | 708 (VA measured in only 588) | Known diagnosis of dementia. Unclear how this data was obtained. | VI | Visual acuity (logMAR) worse than 6/12 or worse than 6/18 measured before and after refraction as assessed by an optometrist. Or Blindness – VA of < 3/60 in the better eye with presenting correction (ICD-10,12 categories 3–5) or visual field of no greater than 10 degrees in radius around central fixation. |
AMD | AMD was classified into dry and wet (neovascular) AMD and then graded as mild, moderate or severe. Based on medical records and optometrist exam. | ||||||||
Cataract | Cataract sufficient to be graded on the TOC cataract grading scale. Based on medical records and optometrist exam. | ||||||||
Diabetic Retinopathy | Based on medical records and optometrist exam | ||||||||
Glaucoma | Based on medical records and optometrist exam | ||||||||
Bowen, 2016 [17] | UK | Qualitative | 60–89 | Male 50%; Female 50% | Purposive sampling from community setting and based on those who participated in the prevalence study above. Low representativeness. | 36 | Unclear how this data was obtained. | VI | Visual acuity (logMAR) worse than 6/12 or worse than 6/18 measured before and after refraction as assessed by an optometrist. Or Blindness – VA of < 3/60 in the better eye with presenting correction (ICD-10,12 categories 3–5) or visual field of no greater than 10 degrees in radius around central fixation. |
AMD | AMD was classified into dry and wet (neovascular) AMD and then graded as mild, moderate or severe. Based on medical records and optometrist exam. | ||||||||
Cataract | Cataract sufficient to be graded on the TOC cataract grading scale. Based on medical records and optometrist exam. | ||||||||
Diabetic Retinopathy | Based on medical records and optometrist exam | ||||||||
Glaucoma | Based on medical records and optometrist exam | ||||||||
Carcenac, 2009 [18] | Canada | Cross-sectional | Not described | Not described | Nursing home setting. Only includes those who have died between April 2000 and April 2004. Not representative as only includes those who have died. | 228 | Not described. Extracted from clinical files of deceased patients. | AMD; Glaucoma | Based on clinical files of deceased patients. |
Chandra, 1986 [19] | USA | Case-control | Mean: 80.1 | Male 40.6% Female 59.4% | Community setting. Only includes those who have died (as dementia status is based on cause of death). Not representative. | 7195 | Listed as cause of death | Cataract Glaucoma Blindness | Listed on death certificate |
Chriqui, 2017 [20] | Canada | Cross-sectional | ≥ 65; Range 68 to 102; Mean: 87.2 ± 7.5 | Male 26.7%; Female 73.3% | Residents of nursing homes. Populations of these facilities are representative of community nursing homes in the US. Response/completion rate of 50.8%. Moderately representative for nursing home setting. | 150 | Diagnosis recorded in medical chart. | VI | Distance VA lower than 6/12 (0.30 logMAR 20/40) in the better seeing eye as assessed by an optometrist. |
Chung, 2015 [21] | Taiwan | Case-control | ≥45; Mean 76.8 ± 9.6 | Male 45.2% Female 54.8% | 1,000,000 individuals randomly sampled from the Registry for Beneficiaries (n = 23.72 million) of the Taiwan National Health Insurance (NHI) program. Highly representative as most people in Taiwan are covered by the NHI. | 7770 | Diagnosis of dementia on claims records with ICD-9 codes. At least one diagnosis made by certified neurologist or psychiatrist. | Glaucoma | Based on ICD-9 codes in claims data. |
Clague, 2017 [22] | UK | Cross-sectional | Mean: 82.6 ± 7.4; | Male 29.4% Female 70.6% | All registered patients who were alive and permanently registered in the Primary Care Clinical Informatics Unit with 314 general practices on 31 March 2007. Representative sample of the Scottish population. Highly representative. | 10,528 | Diagnosis from electronic medical records | Blindness or low vision | Identified open angle glaucoma cases by the principal diagnosis of ICD-9-CM codes 365.1, 365.10, or 365.11 in a medical claim during ambulatory care visits. |
Deardorff, 2019 [23] | USA | Cross-sectional | ≥65 | Not described | Community-dwelling Medicare beneficiaries, enrolled in the MCBS between 1999 and 2006. Highly representative. | 871 | Self-report | VI | Based on question: How much trouble do you have with your vision? (no trouble, little trouble, or a lot of trouble). Subjects who reported “little trouble” or “a lot of trouble” were classified as having VI. |
Frost, 2016 [24] | Australia | Case-control | Mean: 70.2 ± 9.0 | Male 59% Female 41% | Community setting. Recruited from AIBL study in Western Australia (a study of over 2000 people with long-term follow up over 10 years). Moderately representative | 22 | NINCDS-ADRDA criteria for probable AD. | AMD | Retinal photos reviewed by experienced grader from Centre for Eye Research plus categorized as AMD based on software |
Hamedani, 2019 [25] | USA | Cross-sectional | Not described | Not described | Community setting. Medicare database includes 97% of those aged 65+ in US (47,582,342 beneficiaries). Highly representative. | Not described | ICD-9 in claims data | Blindness or low vision | Blindness/low vision was defined by ICD-9 diagnosis codes (369.0–369.4) in claims data. |
Heun, 2013 [26] | UK | Case-control | Mean 85.1 ± 8.2; | Male 34.9% Female 65.1% | Based on hospital register so likely included all patients meeting criteria during a defined period but unclear. Low representativeness. | 634 | ICD-10 codes in hospital discharge data | Glaucoma | ICD-10 codes in hospital discharge data |
John, 1999 [27] | UK | Case-control | Mean 84.7 (Range 73.6–96.4) | Male 33.3% Female 66.7% | Community setting. Sample of 500 older persons from Oxfordshire in the UK. Low representativeness. | 79 | Port-mortem diagnosis established by consortium. | Cataract | Based on medical records from annual physical and neurological assessments |
Kang, 2012 [28] | USA | Cross-sectional | ≥ 60 | Male 35.3%; Female 64.7% | 17 Nursing homes in Iowa. 10 participants from each NH randomly selected from list of residents with dementia. Refusal rate of 10%. Highly representative of nursing home setting. | 153 | Diagnosis of AD or other dementia in medical chart | VI | Assessed by MDS section D1 Vision questionnaire. |
Kiely, 2018 [29] | Australia | Cross-sectional | ≥65; range 73 to 79; Mean: 75.3 ± 1.5 | Male 62.5% Female 37.5% | Sampled from wave four of the oldest cohort of the PATH study, a representative community-based longitudinal cohort commencing in 2001 with follow-up every four years. Highly representative. | 64 | DSM-IV criteria for dementia or 5th Edition criteria for major neurocognitive disorder | VI | Impaired VA defined as > 0.3 logMAR (worse than 20/40 or 6/12) as assessed by a trained interviewer |
Kosse, 2015 [30] | Netherlands | Cross-sectional | Not described | Male 60% Female 40% | Residents living in a 20-bed closed psychogeriatric ward in nursing home between September 2011 and April 2013. Low representativeness. | 20 | Extracted from electronic medical records. | Visual problems | Extracted from electronic medical records. |
Lai, 2017 [31] | Taiwan | Case-control | ≥45; Mean 78.7 ± 6.6 | Male 42.6% Female 57.4% | Database of NHI. People 65+ with ICD-9 diagnosis of AD in 2000–2011 + 4 controls for each AD case. Highly representative as most people in Taiwan are covered by the NHI. | 1351 | ICD-9 codes listed on insurance claims for 2 or more visits | Glaucoma | ICE-9 codes in medical claims data for 2 or more visits. |
Lawrence, 2009 [9] | UK | Qualitative | 65–99 | Male 36.8% Female 63.2% | Participants drawn from 4 socially and ethnically diverse south London boroughs. Highly representative. | 19 | Using a dementia service OR using a vision service + the “MMBlind”, the “Short Form of the Informant Questionnaire of Cognitive Decline in the Elderly” and the CDR scale | VI | Assessed with Snellen acuity and Seeing Severity Scale. |
Löppönen, 2004 [32] | Finland | Cross-sectional | Mean 82.4 ± 7 | Male 32% Female 68% | Community sample. 12% of the population in Lieto was invited. Participation rate of 82%. Highly representative. | 112 | Clinical assessment and DSM-IV + NINDS-AIREN for vascular dementia | Cataract Glaucoma | ICD-10 code in medical records. |
Luo, 2018 [33] | China | Cross-sectional | Not described | Male 38.6% Female 52.5% | Data from Second National Samples Survey on Disability from April to May 31,2006. Covers all provincial administrative areas in Mainland China. Highly representative. | 1208 | Combination of self-report and on-site diagnosis by psychiatrist according to ICD-10. | VI | Used WHO criteria but limited to VI due to uncorrectable causes. Assessed by ophthalmologist. |
Marquie, 2019 [34] | Spain | Cross-sectional | Mean age 81.4 ± 7.2. | Male 31.6% Female 69.4% | Recruited from public memory clinic; program that assesses cognition in community for free without referral; and a cohort study. Response rate 96.3%. Moderately representative. | 833 | Clinical diagnosis based on DSM-IV | Glaucoma AMD Low VA High IOP | Based on examination by an optometrist |
Morse, 2004 [35] | USA | Cross-sectional | Mean: 84 | Not described | Randomly selected from 11 New York city long-term-care facilities. Highly representative. | 391 | Not described | VI | Normal VA = 20/20–20/40; mild VI 20/50–20/70; moderate VI 20/80–20/200; severe VI 20/250–20/1000, very severe VI = counting fingers, hand motion, or no light perception. Assessed by Vistech Consultant. |
Muurinen, 2014 [36] | Finland | Cross-sectional | > 65; Mean: 83 | Male 22% Female 78% | All permanent residents in assisted living facilities in two cities in 2007. 70% participation rate. Moderately representative. | 833 (1398) | Not described | VI | Based on answer to question “Is the resident’s vision good enough for reading regular print” yes/no (with or without glasses). Response of no = VI. Reported from trained nurses who knew the residents well. |
Nyman, 2017 [37] | UK | Qualitative | Mean: 82.1; Range: 58–96 | Male 34.6% Female 65.4% | Not described | 26 | Has received a formal diagnosis of dementia or has been referred for/in the process of receiving dementia assessment. | VI | Certified as having VI, registered blind or partially sighted, or self-reported low vision. |
Patel, 2019 [38] | USA | Cross-sectional | ≥ 65 | Not described | Recruited from 2011 to 2016 from the NHATS, a nationally representative survey of 11,558 Medicare enrollees age ≥ 65. Highly representative. | Not described | Unclear but based on tests of memory, orientation and executive function | VI | Difficulty recognizing someone across the street. Self- reported with no further details. |
Pelletier, 2014 [39] | Canada | Case-control | Mean 83.7 ± 6.3; Range: 66–101 | Male 29.6% Female 71.4% | Recruited people with dementia from 2 academic hospitals, admitted from April 2008 to April 2009. Highly representative. | 220 | Clinical diagnosis with DSM-IV criteria. Had to have received diagnosis either before or during admission. | Glaucoma | Based on medical records or use of medication |
Prince, 2011 [40] | China, India, Cuba, Dominican Republic, Venezuela, Mexico, Peru | Cross-sectional | ≥ 65 | More females than males in all sites | All residents aged 65+ in 11 geographically defined sites in seven LAMIC (India, China, Cuba, Dominican Republic, Venezuela, Mexico and Peru). Highly representative. | Not described | Diagnosis based on meeting either 10/66 or DSM-IV criteria. | VI | Eyesight problems which result in at least some difficulty, and/or an observer-rated item by the interviewer of ‘near total blindness’ |
Smilnak, 2019 [41] | USA | Case-control | ≥ 75 Mean age 88.6 ± 5.9 | Male 33.9% Female 66.1% | Pathologic specimens of eyes and brains of autopsy subjects aged 75 and above who presented to Duke University Medical Center. Low representativeness as only includes those who have died. | 115 | Autopsy and pathological diagnosis | AMD Glaucoma (severe) | Autopsy and histopathological diagnosis. |
Tamura, 2006 [42] | Japan | Case- control | Mean: 80.9 ± 8.4 | Male 17.2% Female 82.8% | Institutionalized residents or those accessing treatment at 4 hospitals. Highly representative. | 172 | Diagnosis of probable AD was based on clinical findings according to NINCDS-ADRDA | Glaucoma | Probable OAG was diagnosed by width of the angle of the anterior chamber >grade 2, a vertical cup-to-disc ratio of the optic nerve head > 0.7 and/or difference between the vertical cup-to-disc ratio in the eyes > 0.2 with characteristic glaucomatous disc change. Ophthalmic examination was performed and diagnosis was made by two glaucoma specialists |
Varadaraj, 2020 [43] | USA | Cross-sectional | > 65; | Not described | Recruited form the NHATS, a nationally representative survey of Medicare beneficiaries aged 65 years and older. Highly representative. | Not described | Diagnosis of probable dementia based on (a) participant- or proxy-reported physician diagnosis of dementia or AD, or (b) an AD8 score ≥ 2; or (c) participant cognitive test scores ≤1.5 SDs below mean in at least two of the three cognitive domains. Possible dementia based on cognitive test scores ≤1.5 SDs below mean in one domain in the absence of meeting the physician diagnosis or AD8 criteria described above. | VI | Vision impairment was defined as self-reported blindness or difficulty with distance/near vision |
Williams, 2014 [44] | UK | Case-control | Mean 80.1 ± 7.7 | Male 36.8% Female 63.2% | Opportunistic rather than consecutive recruitment of cases to a primary care clinic. Low representativeness. | 258 | Clinical examination and NINCDS criteria | AMD | Based on photos and Wisconsin AMD grading system. |
Wittich, 2019 [45] | Canada | Cross-sectional | Not described | Not described | Not described | 21 | Clinical diagnosis by consensus. Specific clinical criteria used are not described. | Reduced visual acuity | Reduced reading acuity (MNRead) (> .5 logMAR [20/63]). Moderate to severe loss of contrast sensitivity (Mars test) (< 1.48 log CS [3.3% contrast]). |
Wong, 2015 [46] | Singapore | Cross-sectional | > 60 | Not described | Recruited from 3 tertiary hospitals. Consecutive recruitment from July 2009 to December 2012. Moderately representative. | 268 (outcome data on only 264) | DSM-IV criteria | AMD Diabetic retinopathy Cataract Glaucoma | Retinal photographs reviewed by ophthalmologist |