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dc.contributor.authorBech, Anne Berit
dc.contributor.authorClausen, Thomas
dc.contributor.authorWaal, Helge
dc.contributor.authorSaltyte Benth, Jurate
dc.contributor.authorSkeie, Ivar
dc.date.accessioned2020-04-16T13:01:44Z
dc.date.available2020-04-16T13:01:44Z
dc.date.created2019-08-20T16:25:36Z
dc.date.issued2019
dc.identifier.citationBMC Health Services Research. 2019, 19 .en_US
dc.identifier.issn1472-6963
dc.identifier.urihttps://hdl.handle.net/11250/2651340
dc.description.abstractBACKGROUND: Mortality rates and causes of death among individuals in opioid agonist treatment (OAT) vary according to several factors such as geographical region, age, gender, subpopulations, drug culture and OAT status. Patients in OAT are ageing due to effective OAT as well as demographic changes, which has implications for morbidity and mortality. Norway has one of the oldest OAT populations in Europe. Because of the varying mortality rates and causes of death in different subgroups and countries, research gaps still exist. The aims of this study were to describe the causes of death among OAT patients in Norway, to estimate all-cause and cause-specific crude mortality rates (CMRs) during OAT and to explore characteristics associated with drug-induced cause of death compared with other causes of death during OAT. METHODS: This was a national, observational register study. Data from the Norwegian Cause of Death Registry and the Norwegian Patient Registry were combined with data from medical records. We included all patients in the Norwegian OAT programme who died not more than 5 days after the last intake of OAT medication, between 1 January 2014 and 31 December 2015. RESULTS: In the 2-year observation period, 200 (1.4%) of the OAT patients died. A forensic or medical autopsy was performed in 63% of the cases. The mean age at the time of death was 48.9 years (standard deviation 8.4), and 74% were men. Somatic disease was the most common cause of death (45%), followed by drug-induced death (42%), and violent death (12%). In general, CMRs increased with age, and they were higher in men and in patients taking methadone compared with buprenorphine. Increasing somatic comorbidity, measured by the Charlson comorbidity index, reduced the odds of dying of a drug-induced cause of death compared with other causes of death. CONCLUSIONS: Both somatic and drug-induced causes of death were common during OAT. Improved treatment and follow-up of chronic diseases, especially in patients aged > 40 years, and continuous measures to reduce drug-induced deaths appear to be essential to reduce future morbidity and mortality burdens in this population.en_US
dc.description.sponsorshipThe study was funded by Innlandet Hospital Trust (grant no. 150351). The funder had no involvement in the design of the study or in the collection, analysis and interpretation of data or in the writing of the manuscript.en_US
dc.language.isoengen_US
dc.relation.urihttps://bmchealthservres.biomedcentral.com/articles/10.1186/s12913-019-4282-z
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectBuprenorphine;en_US
dc.subjectCause of death;en_US
dc.subjectMethadone;en_US
dc.subjectMortality;en_US
dc.subjectMultimorbidity;en_US
dc.subjectOpioid agonist treatment;en_US
dc.subjectOverdoseen_US
dc.titleMortality and causes of death among patients with opioid use disorder receiving opioid agonist treatment: A national register studyen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2019 The Author(s). This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.en_US
dc.source.pagenumber10en_US
dc.source.volume19en_US
dc.source.journalBMC Health Services Researchen_US
dc.source.issue1en_US
dc.identifier.doi10.1186/s12913-019-4282-z
dc.identifier.cristin1717515
cristin.unitcode1991,9,2,0
cristin.unitcode1991,3,0,0
cristin.unitnameAvd Rusrelatert psykiatri og avhengighet
cristin.unitnameDiv Gjøvik
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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