Public Defence: Anne Berit Bech
MSc Anne Berit Bech at Institute of Clinical Medicine will be defending the thesis “Mortality during opioid agonist treatment in Norway: a comprehensive study of the years 2014-2015” for the degree of PhD (Philosophiae Doctor).
Photo: Marte Goplen, Nasjonal kompetansetjeneste ROP
Due to copyright reasons, an electronic copy of the thesis must be ordered from the faculty. In order for the faculty to have time to process the order, it must be received by the faculty no later than 2 days prior to the public defence. Orders received later than 2 days before the defence will not be processed. Inquiries regarding the thesis after the public defence must be addressed to the candidate.
Trial Lecture – time and place
See Trial Lecture.
- First opponent: Professor Anders Håkansson, Lund University, Sweden
- Second opponent: Associate Professor Anne Høye, The Arctic University of Norway (UiT)
- Third member and chair of the evaluation committee: Asscoiate Professor Odd Martin Vallersnes, University of Oslo
Chair of the Defence
Professor Emeritus Øivind Larsen, University of Oslo
Researcher Ivar Skeie, Innlandet Hospital Trust
Although opioid agonist treatment (OAT) substantially reduces morbidity and mortality in individuals with opioid dependence, mortality is still higher than in the general population.
In this thesis, the main aim was to explore mortality and causes of death among patients receiving OAT who died during treatment in 2014 and 2015. The studies were cross-sectional, and data were collected from hospital records, the Cause of Death Registry, the Norwegian Patient Registry and autopsy reports.
Two-hundred patients died. The mean age at the time of death was 49 years, and 74% were men. The crude mortality rate was 1.4 per 100 person years. Physical diseases (e.g. cancer, and cardiovascular and pulmonary diseases) were the most common causes of death (45%), followed by drug-induced deaths (42%) and violent deaths (12%).
The most common organ pathologies detected post-mortem were chronic liver disease (84%), cardiovascular disease (68%) and pulmonary emphysema (41%). Pathological changes in two or more organ systems were common (65%).
A median of four substances was detected post-mortem. The pooled opioid (i.e. morphine-equivalent) concentration of various opioids was twice as high in drug-induced deaths compared with other causes of death (P < 0.001), while the pooled benzodiazepine (i.e., diazepam-equivalent) concentrations did not differ by cause of death (P = 0.353). In regression analysis, only pooled opioid concentration was independently associated with overdose as the cause of death (adjusted odds ratio = 1.003, 95% confidence interval = 1.001-1.006). Thus, the total opioid concentration seemed to play the most important role in overdose deaths.
To conclude, both somatic and drug-induced cause of death were common in patients receiving OAT. In addition to overdose prevention, improved screening, treatment and follow-up of physical diseases are therefore essential.
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