Prevalence and causes of vision loss in South-east Asia and Oceania in 2015: magnitude, temporal trends and projections.


Journal

The British journal of ophthalmology
ISSN: 1468-2079
Titre abrégé: Br J Ophthalmol
Pays: England
ID NLM: 0421041

Informations de publication

Date de publication:
07 2019
Historique:
received: 17 01 2018
revised: 11 06 2018
accepted: 17 06 2018
pubmed: 14 9 2018
medline: 18 2 2020
entrez: 14 9 2018
Statut: ppublish

Résumé

To assess prevalence and causes of vision impairment in South-east Asia and Oceania regions from 1990 to 2015 and to forecast the figures for 2020. Based on a systematic review of medical literature, prevalence of blindness (presenting visual acuity (PVA) <3/60 in the better eye), moderate and severe vision impairment (MSVI; PVA <6/18 but ≥3/60), mild vision impairment (PVA <6/12 but ≥6/18) and near vision impairment (>N5 or N8 in the presence of normal vision) were estimated for 1990, 2010, 2015 and 2020. The age-standardised prevalence of blindness for all ages and both genders was higher in the Oceania region but lower for MSVI when comparing the subregions. The prevalence of near vision impairment in people≥50 years was 41% (uncertainty interval (UI) 18.8 to 65.9). Comparison of the data for 2015 with 2020 predicts a small increase in the numbers of people affected by blindness, MSVI and mild VI in both subregions. The numbers predicted for near VI in South-east Asia are from 90.68 million in 2015 to 102.88 million in 2020. The main causes of blindness and MSVI in both subregions in 2015 were cataract, uncorrected refractive error, glaucoma, corneal disease and age-related macular degeneration. There was no trachoma in Oceania from 1990 and decreasing prevalence in South-east Asia with elimination predicted by 2020. In both regions, the main challenges for eye care come from cataract which remains the main cause of blindness with uncorrected refractive error the main cause of MSVI. The trend between 1990 and 2015 is for a lower prevalence of blindness and MSVI in both regions.

Sections du résumé

BACKGROUND
To assess prevalence and causes of vision impairment in South-east Asia and Oceania regions from 1990 to 2015 and to forecast the figures for 2020.
METHODS
Based on a systematic review of medical literature, prevalence of blindness (presenting visual acuity (PVA) <3/60 in the better eye), moderate and severe vision impairment (MSVI; PVA <6/18 but ≥3/60), mild vision impairment (PVA <6/12 but ≥6/18) and near vision impairment (>N5 or N8 in the presence of normal vision) were estimated for 1990, 2010, 2015 and 2020.
RESULTS
The age-standardised prevalence of blindness for all ages and both genders was higher in the Oceania region but lower for MSVI when comparing the subregions. The prevalence of near vision impairment in people≥50 years was 41% (uncertainty interval (UI) 18.8 to 65.9). Comparison of the data for 2015 with 2020 predicts a small increase in the numbers of people affected by blindness, MSVI and mild VI in both subregions. The numbers predicted for near VI in South-east Asia are from 90.68 million in 2015 to 102.88 million in 2020. The main causes of blindness and MSVI in both subregions in 2015 were cataract, uncorrected refractive error, glaucoma, corneal disease and age-related macular degeneration. There was no trachoma in Oceania from 1990 and decreasing prevalence in South-east Asia with elimination predicted by 2020.
CONCLUSIONS
In both regions, the main challenges for eye care come from cataract which remains the main cause of blindness with uncorrected refractive error the main cause of MSVI. The trend between 1990 and 2015 is for a lower prevalence of blindness and MSVI in both regions.

Identifiants

pubmed: 30209084
pii: bjophthalmol-2018-311946
doi: 10.1136/bjophthalmol-2018-311946
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

878-884

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Informations de copyright

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: JBJ: Consultant for Mundipharma Co. (Cambridge, UK); Patent holder with Biocompatibles UK Ltd. (Farnham, Surrey, UK) (Title: Treatment of eye diseases using encapsulated cells encoding and secreting neuroprotective factor and/or ant-angiogenic factor; Patent number: 20120263794), and Patent application with University of Heidelberg (Heidelberg, Germany) (Title: Agents for use in the therapeutic or prophylactic treatment of myopia or hyperopia; Europäische Patentanmeldung 15 000 771.4.

Auteurs

Jill Elizabeth Keeffe (JE)

L V Prasad Eye Institute, Hyderabad, India jillkeeffe@lvpei.org.

Robert J Casson (RJ)

University of Adelaide, Adelaide, South Australia, Australia.

Hugh R Taylor (HR)

Melbourne School of Population Health, University of Melbourne, Melbourne, Victoria, Australia.

Maria Vittoria Cicinelli (MV)

San Raffaele Scientific Institute, Milan, Italy.

Aditi Das (A)

Health Education Yorkshire, London, UK.

Seth R Flaxman (SR)

Department of Mathematics and Data Science Institute, Imperial College London, London, UK.

Jost B Jonas (JB)

Department of Ophthalmology, Universitätsmedizin, Mannheim, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

John H Kempen (JH)

Immunology and Uveitis Service, Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Boston, Massachusetts, USA.
Discovery Eye Center, Leawood, Kansas, USA.
MyungSung Christian Medical Center, Addis Ababa, Ethiopia.

Janet Leasher (J)

Nova Southeastern University, Fort Lauderdale, Florida, USA.

Hans Limburg (H)

Health Information Services, Grootebroek, The Netherlands.

Kovin Naidoo (K)

African Vision Research Institute, University of Kwazulu-Natal, South Africa & Brien Holden Vision Institute, Sydney, New South Wales, Australia.

Alexander J Silvester (AJ)

St Pauls Eye Unit, Royal Liverpool University Hospital, Prescot Street, Liverpool, UK.

Gretchen A Stevens (GA)

Department of Information, Evidence and Research, World Health Organization, Geneva, Switzerland.

Nina Tahhan (N)

Brien Holden Vision Institute, Sydney, New South Wales, Australia.
School of Optometry and Vision Science, University of New South Wales, Sydney, New South Wales, Australia.

Tien Yin Wong (TY)

Singapore Eye Research Institute, Duke-NUS Graduate Medical School, National University of Singapore, Singapore, Singapore.

Serge Resnikoff (S)

Brien Holden Vision Institute, Sydney, New South Wales, Australia.
School of Optometry and Vision Science, University of New South Wales, Sydney, New South Wales, Australia.

Rupert R A Bourne (RRA)

Vision & Eye Research Unit, Anglia Ruskin University, Cambridge, UK.

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Classifications MeSH