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dc.contributor.authorBaravelli, Carl Michael
dc.contributor.authorAarsand, Aasne Karine
dc.contributor.authorSandberg, Sverre
dc.contributor.authorTollånes, Mette Christophersen
dc.date.accessioned2021-06-28T13:12:16Z
dc.date.available2021-06-28T13:12:16Z
dc.date.created2020-11-09T14:03:02Z
dc.date.issued2020
dc.identifier.issn1750-1172
dc.identifier.urihttps://hdl.handle.net/11250/2761699
dc.description.abstractBackground: Acute hepatic porphyria (AHP) consists of three rare metabolic disorders. We investigated the risk of long-term sick leave, disability pension, and premature death in individuals with AHP compared to the general population. Methods: In a nationwide cohort study from 1992 to 2017, records of 333 persons (total person-years = 6728) with a confirmed AHP diagnosis were linked to several national compulsory registries (reference population = 5,819,937). We conducted survival analyses to assess additional risk. Results: Persons with AHP had higher risks of accessing long-term sick leave (adjusted hazard ratio (aHR): 1.5, 95% confidence interval (CI): 1.3, 1.7) and disability pension (aHR: 1.9, CI: 1.5, 2.4). The risk was highest in persons who had been hospitalised for acute attacks, while no additional risk was observed in asymptomatic AHP gene mutation carriers. The median age when accessing disability pension was 45 years, 21 years younger than the general population. AHP was associated with increased risk of mortality due to hepatocellular carcinoma (adjusted mortality rate ratio (aMRR): 84.4, CI: 37.8, 188.2), but no overall increased risk of premature death was observed. Conclusions: Persons with symptomatic AHP were at increased risk of accessing long-term sick leave and disability pension but not of premature death.en_US
dc.language.isoengen_US
dc.publisherBioMed Centralen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleSick leave, disability, and mortality in acute hepatic porphyria: a nationwide cohort studyen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright the authorsen_US
dc.source.articlenumber56en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1186/s13023-019-1273-4
dc.identifier.cristin1846207
dc.source.journalOrphanet Journal of Rare Diseasesen_US
dc.identifier.citationOrphanet Journal of Rare Diseases. 2020, 15, 56.en_US
dc.source.volume15en_US


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