Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/31209
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dc.contributor.authorDuncan, Andrew D Sen_UK
dc.contributor.authorHapca, Simonaen_UK
dc.contributor.authorDe Souza, Nicoshaen_UK
dc.contributor.authorMorales, Danielen_UK
dc.contributor.authorBell, Samiraen_UK
dc.date.accessioned2020-05-30T00:00:21Z-
dc.date.available2020-05-30T00:00:21Z-
dc.date.issued2020-11en_UK
dc.identifier.urihttp://hdl.handle.net/1893/31209-
dc.description.abstractObjectives to establish and quantify any observable association between the exposure to community prescriptions for quinine and acute kidney injury (AKI) events in a population of older adults. Design two observational studies using the same dataset, a retrospective longitudinal cohort study and a self-controlled case series (SCCS). Setting NHS health board in Scotland. Participants older adults (60+ years) who received quinine prescriptions in Tayside, Scotland, between January 2004 and December 2015. The first study included 12,744 individuals. The SCCS cohort included 5,907 people with quinine exposure and more than or equal to one AKI event. Main outcome measured in the first study, multivariable logistic regression was used to calculate odds ratios (ORs) for AKI comparing between episodes with and without recent quinine exposure after adjustment for demographics, comorbidities and concomitant medications. The SCCS study divided follow-up for each individual into periods ‘on’ and ‘off’ quinine, calculating incidence rate ratios (IRRs) for AKI adjusting for age. Results during the study period, 273,596 prescriptions for quinine were dispensed in Tayside. A total of 13,616 AKI events occurred during follow-up (crude incidence 12.5 per 100 person-years). In the first study, exposure to quinine before an episode of care was significantly associated with an increased probability of AKI (adjusted OR = 1.27, 95% confidence interval (CI) 1.21–1.33). In the SCCS study, exposure to quinine was associated with an increased relative incidence of AKI compared to unexposed periods (IRR = 1.20, 95% CI 1.15–1.26), with the greatest risk observed within 30 days following quinine initiation (IRR = 1.48, 95% CI 1.35–1.61). Conclusion community prescriptions for quinine in an older adult population are associated with an increased risk of AKI.en_UK
dc.language.isoenen_UK
dc.publisherOxford University Press (OUP)en_UK
dc.relationDuncan ADS, Hapca S, De Souza N, Morales D & Bell S (2020) Quinine exposure and the risk of acute kidney injury: a population-based observational study of older people. Age and Ageing, 49 (6), pp. 1042-1047. https://doi.org/10.1093/ageing/afaa079en_UK
dc.rights© The Author(s) 2020. Published by Oxford University Press on behalf of the British Geriatrics Society. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.subjectacute kidney injuryen_UK
dc.subjectquinineen_UK
dc.subjectleg crampsen_UK
dc.subjectolder peopleen_UK
dc.subjectepidemiology and pharmacovigilanceen_UK
dc.titleQuinine exposure and the risk of acute kidney injury: a population-based observational study of older peopleen_UK
dc.typeJournal Articleen_UK
dc.rights.embargodate2020-05-29en_UK
dc.identifier.doi10.1093/ageing/afaa079en_UK
dc.identifier.pmid32463438en_UK
dc.citation.jtitleAge and Ageingen_UK
dc.citation.issn1468-2834en_UK
dc.citation.issn0002-0729en_UK
dc.citation.volume49en_UK
dc.citation.issue6en_UK
dc.citation.spage1042en_UK
dc.citation.epage1047en_UK
dc.citation.publicationstatusPublisheden_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.contributor.funderWellcome Trusten_UK
dc.author.emailsimona.hapca@stir.ac.uken_UK
dc.citation.date28/05/2020en_UK
dc.contributor.affiliationNinewells Hospital & Medical Schoolen_UK
dc.contributor.affiliationComputing Scienceen_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.contributor.affiliationUniversity of Dundeeen_UK
dc.identifier.isiWOS:000591582900027en_UK
dc.identifier.scopusid2-s2.0-85094685082en_UK
dc.identifier.wtid1625351en_UK
dc.contributor.orcid0000-0003-3148-9657en_UK
dc.contributor.orcid0000-0001-9100-1575en_UK
dc.date.accepted2020-03-15en_UK
dcterms.dateAccepted2020-03-15en_UK
dc.date.filedepositdate2020-05-29en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.typeJournal Article/Reviewen_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorDuncan, Andrew D S|en_UK
local.rioxx.authorHapca, Simona|0000-0003-3148-9657en_UK
local.rioxx.authorDe Souza, Nicosha|en_UK
local.rioxx.authorMorales, Daniel|en_UK
local.rioxx.authorBell, Samira|0000-0001-9100-1575en_UK
local.rioxx.projectProject ID unknown|Wellcome Trust|en_UK
local.rioxx.freetoreaddate2020-05-29en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2020-05-29|en_UK
local.rioxx.filenameafaa079.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source1468-2834en_UK
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