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dc.contributor.authorChristiansen, Sverre
dc.contributor.authorFougner, Anders Lyngvi
dc.contributor.authorStavdahl, Øyvind
dc.contributor.authorKölle, Konstanze
dc.contributor.authorEllingsen, Reinold
dc.contributor.authorCarlsen, Sven Magnus
dc.date.accessioned2017-11-15T12:44:57Z
dc.date.available2017-11-15T12:44:57Z
dc.date.created2017-05-15T12:03:11Z
dc.date.issued2017
dc.identifier.citationDiabetes Therapy. 2017, 8 1-18.nb_NO
dc.identifier.issn1869-6961
dc.identifier.urihttp://hdl.handle.net/11250/2466458
dc.description.abstractIntroduction Patients with diabetes type 1 (DM1) struggle daily to achieve good glucose control. The last decade has seen a rush of research groups working towards an artificial pancreas (AP) through the application of a double subcutaneous approach, i.e., subcutaneous (SC) continuous glucose monitoring (CGM) and continuous subcutaneous insulin infusion. Few have focused on the fundamental limitations of this approach, especially regarding outcome measures beyond time in range. Methods Based on insulin physiology, the limitations of CGM, SC insulin absorption, meal challenge, and physical activity in DM1 patients, we discuss the limitations of the double SC approach. Finally, we discuss safety measures and the achievements reported in some recent AP studies that have utilized the double SC approach. Results Most studies show that a double SC AP increases the time in range compared to a sensor-augmented insulin pump and shortens the time in hypoglycemia. Despite these achievements, the proportion of time spent in hyperglycemia is still roughly 20–40%, and hypoglycemia is still present 1–4% of the time. The main factors limiting further progress are the latency of SC CGM (at least 5–10 min) and the slow pharmacokinetics of SC-delivered fast-acting insulin. The maximum blood insulin level is reached after 45 min and the maximum glucose-lowering effect is observed after 1.5–2 h, while the glucose-lowering effect lasts for at least 5 h. Conclusions Although using a double SC AP leads to significant improvements in glucose control, the SC approach has severe limitations that hamper further progress towards a robust AP.nb_NO
dc.language.isoengnb_NO
dc.publisherSpringer Verlagnb_NO
dc.relation.urihttp://dx.doi.org/10.1007/s13300-017-0263-6
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.titleA Review of the Current Challenges Associated with the Development of an Artificial Pancreas by a Double Subcutaneous Approachnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber1-18nb_NO
dc.source.volume8nb_NO
dc.source.journalDiabetes Therapynb_NO
dc.identifier.doi10.1007/s13300-017-0263-6
dc.identifier.cristin1470224
dc.relation.projectSamarbeidsorganet mellom Helse Midt-Norge og NTNU: 46075403nb_NO
dc.relation.projectSamarbeidsorganet mellom Helse Midt-Norge og NTNU: 46075401nb_NO
dc.relation.projectNorges forskningsråd: 248872nb_NO
dc.description.localcode© The Author(s) 2017. This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/)nb_NO
cristin.unitcode194,65,15,0
cristin.unitcode194,63,25,0
cristin.unitcode194,63,35,0
cristin.unitnameInstitutt for kreftforskning og molekylær medisin
cristin.unitnameInstitutt for teknisk kybernetikk
cristin.unitnameInstitutt for elektronikk og telekommunikasjon
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse-Ikkekommersiell 4.0 Internasjonal