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dc.contributor.authorÅm, Marte Kierulf
dc.contributor.authorTeigen, Ingrid Anna
dc.contributor.authorRiaz, Misbah
dc.contributor.authorFougner, Anders Lyngvi
dc.contributor.authorChristiansen, Sverre Christian
dc.contributor.authorCarlsen, Sven Magnus
dc.date.accessioned2023-11-08T14:42:00Z
dc.date.available2023-11-08T14:42:00Z
dc.date.created2023-09-01T13:24:35Z
dc.date.issued2023
dc.identifier.issn0391-4097
dc.identifier.urihttps://hdl.handle.net/11250/3101489
dc.description.abstractIntroduction Diabetes mellitus type 1 is a chronic disease that implies mandatory external insulin delivery. The patients must monitor their blood glucose levels and administer appropriate insulin boluses to keep their blood glucose within the desired range. It requires a lot of time and endeavour, and many patients struggle with suboptimal glucose control despite all their efforts. Materials and methods This narrative review combines existing knowledge with new discoveries from animal experiments. Discussion In the last decade, artificial pancreas (AP) devices have been developed to improve glucose control and relieve patients of the constant burden of managing their disease. However, a feasible and fully automated AP is yet to be developed. The main challenges preventing the development of a true, subcutaneous (SC) AP system are the slow dynamics of SC glucose sensing and particularly the delay in effect on glucose levels after SC insulin infusions. We have previously published studies on using the intraperitoneal space for an AP; however, we further propose a novel and potentially disruptive way to utilize the vasodilative properties of glucagon in SC AP systems. Conclusion This narrative review presents two lesser-explored viable solutions for AP systems and discusses the potential for improvement toward a fully automated system: A) using the intraperitoneal approach for more rapid insulin absorption, and B) besides using glucagon to treat and prevent hypoglycemia, also administering micro-boluses of glucagon to increase the local SC blood flow, thereby accelerating SC insulin absorption and SC glucose sensor site dynamics.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectVasodilatasjonen_US
dc.subjectVasodilationen_US
dc.subjectIntraperitoneal insulininfusjonen_US
dc.subjectIntraperitoneal insulin infusionen_US
dc.subjectType 1 diabetesen_US
dc.subjectType 1 diabetesen_US
dc.subjectGlukagoninfusjonen_US
dc.subjectGlucagon infusionen_US
dc.titleThe Artificial Pancreas: Two Alternative Approaches to Achieve a Fully Closed Loop System with Optimal Glucose Controlen_US
dc.title.alternativeThe Artificial Pancreas: Two Alternative Approaches to Achieve a Fully Closed Loop System with Optimal Glucose Controlen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.subject.nsiVDP::Medisinsk teknologi: 620en_US
dc.subject.nsiVDP::Medical technology: 620en_US
dc.source.journalJournal of Endocrinological Investigationen_US
dc.identifier.doi10.1007/s40618-023-02193-2
dc.identifier.cristin2171680
dc.relation.projectNorges forskningsråd: 294828en_US
dc.relation.projectNorges forskningsråd: 248872en_US
dc.relation.projectNorges forskningsråd: 332850en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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