Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/94961
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dc.creatorGBD 2019 Ageing Collaboratorsen_US
dc.date.accessioned2022-09-05T09:04:21Z-
dc.date.available2022-09-05T09:04:21Z-
dc.identifier.urihttp://hdl.handle.net/10397/94961-
dc.language.isoenen_US
dc.publisherBMJ Groupen_US
dc.rightsThis is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/.en_US
dc.rightsThe following publication GBD 2019 Ageing Collaborators. (2022). Global, regional, and national burden of diseases and injuries for adults 70 years and older: systematic analysis for the Global Burden of Disease 2019 Study. bmj, 376(8329), e068208 is available at https://doi.org/10.1136/bmj-2021-068208en_US
dc.titleGlobal, regional, and national burden of diseases and injuries for adults 70 years and older : systematic analysis for the Global Burden of Disease 2019 Studyen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume376en_US
dc.identifier.issue8329en_US
dc.identifier.doi10.1136/bmj-2021-068208en_US
dcterms.abstractObjectives To use data from the Global Burden of Diseases, Injuries, and Risk Factors Study 2019 (GBD 2019) to estimate mortality and disability trends for the population aged ≥70 and evaluate patterns in causes of death, disability, and risk factors.en_US
dcterms.abstractDesign Systematic analysis.en_US
dcterms.abstractSetting Participants were aged ≥70 from 204 countries and territories, 1990-2019.en_US
dcterms.abstractMain outcomes measures Years of life lost, years lived with disability, disability adjusted life years, life expectancy at age 70 (LE-70), healthy life expectancy at age 70 (HALE-70), proportion of years in ill health at age 70 (PYIH-70), risk factors, and data coverage index were estimated based on standardised GBD methods.en_US
dcterms.abstractResults Globally the population of older adults has increased since 1990 and all cause death rates have decreased for men and women. However, mortality rates due to falls increased between 1990 and 2019. The probability of death among people aged 70-90 decreased, mainly because of reductions in non-communicable diseases. Globally disability burden was largely driven by functional decline, vision and hearing loss, and symptoms of pain. LE-70 and HALE-70 showed continuous increases since 1990 globally, with certain regional disparities. Globally higher LE-70 resulted in higher HALE-70 and slightly increased PYIH-70. Sociodemographic and healthcare access and quality indices were positively correlated with HALE-70 and LE-70. For high exposure risk factors, data coverage was moderate, while limited data were available for various dietary, environmental or occupational, and metabolic risks.en_US
dcterms.abstractConclusions Life expectancy at age 70 has continued to rise globally, mostly because of decreases in chronic diseases. Adults aged ≥70 living in high income countries and regions with better healthcare access and quality were found to experience the highest life expectancy and healthy life expectancy. Disability burden, however, remained constant, suggesting the need to enhance public health and intervention programmes to improve wellbeing among older adults.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBMJ, 12 Mar. 2022, v. 376, no. 8329, e068208en_US
dcterms.isPartOfBMJen_US
dcterms.issued2022-03-12-
dc.identifier.isiWOS:000769387900013-
dc.identifier.scopus2-s2.0-85127409980-
dc.identifier.pmid35273014-
dc.identifier.eissn1756-1833en_US
dc.identifier.artne068208en_US
dc.description.validate202208 bckwen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera1687-
dc.identifier.SubFormID45801-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextBill and Melinda Gates Foundationen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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