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dc.contributor.authorÅm, Marte Kierulf
dc.contributor.authorKölle, Konstanze
dc.contributor.authorFougner, Anders Lyngvi
dc.contributor.authorDirnena-Fusini, Ilze
dc.contributor.authorBösch, Patrick Christian
dc.contributor.authorEllingsen, Reinold
dc.contributor.authorHjelme, Dag Roar
dc.contributor.authorStavdahl, Øyvind
dc.contributor.authorCarlsen, Sven Magnus
dc.contributor.authorChristiansen, Sverre
dc.date.accessioned2019-03-28T09:58:28Z
dc.date.available2019-03-28T09:58:28Z
dc.date.created2018-09-28T13:39:38Z
dc.date.issued2018
dc.identifier.citationPLoS ONE. 2018, 13:e0205447 (10), 1-21.nb_NO
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/11250/2592136
dc.description.abstractIn diabetes research, the development of the artificial pancreas has been a major topic since continuous glucose monitoring became available in the early 2000’s. A prerequisite for an artificial pancreas is fast and reliable glucose sensing. However, subcutaneous continuous glucose monitoring carries the disadvantage of slow dynamics. As an alternative, we explored continuous glucose sensing in the peritoneal space, and investigated potential spatial differences in glucose dynamics within the peritoneal cavity. As a secondary outcome, we compared the glucose dynamics in the peritoneal space to the subcutaneous tissue. Material and methods: Eight-hour experiments were conducted on 12 anesthetised non-diabetic pigs. Four commercially available amperometric glucose sensors (FreeStyle Libre, Abbott Diabetes Care Ltd., Witney, UK) were inserted in four different locations of the peritoneal cavity and two sensors were inserted in the subcutaneous tissue. Meals were simulated by intravenous infusions of glucose, and frequent arterial blood and intraperitoneal fluid samples were collected for glucose reference. Results: No significant differences were discovered in glucose dynamics between the four quadrants of the peritoneal cavity. The intraperitoneal sensors responded faster to the glucose excursions than the subcutaneous sensors, and the time delay was significantly smaller for the intraperitoneal sensors, but we did not find significant results when comparing the other dynamic parameters.nb_NO
dc.language.isoengnb_NO
dc.publisherPublic Library of Sciencenb_NO
dc.relation.urihttps://doi.org/10.1371/journal.pone.0205447
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectGlukosemålingnb_NO
dc.subjectGlucose sensingnb_NO
dc.subjectDiabetesnb_NO
dc.subjectKunstig bukspyttkjertelnb_NO
dc.subjectArtificial Pancreasnb_NO
dc.titleEffect of sensor location on continuous intraperitoneal glucose sensing in an animal modelnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.subject.nsiVDP::Medisinske fag: 700nb_NO
dc.subject.nsiVDP::Midical sciences: 700nb_NO
dc.source.pagenumber1-21nb_NO
dc.source.volume13:e0205447nb_NO
dc.source.journalPLoS ONEnb_NO
dc.source.issue10nb_NO
dc.identifier.doi10.1371/journal.pone.0205447
dc.identifier.cristin1615744
dc.relation.projectNorges forskningsråd: 248872nb_NO
dc.relation.projectSamarbeidsorganet mellom Helse Midt-Norge og NTNU: 2014/23166nb_NO
dc.description.localcode© 2018 Åm et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.nb_NO
cristin.unitcode194,65,15,0
cristin.unitcode194,63,25,0
cristin.unitcode194,63,35,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.unitnameInstitutt for teknisk kybernetikk
cristin.unitnameInstitutt for elektroniske systemer
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.fulltextpostprint
cristin.qualitycode1


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