Delays in Minimally Invasive Continuous Glucose Monitoring Devices: A Review of Current Technology

Through the use of enzymatic sensors—inserted subcutaneously in the abdomen or ex vivo by means of microdialysis fluid extraction—real-time minimally invasive continuous glucose monitoring (CGM) devices estimate blood glucose by measuring a patient's interstitial fluid (ISF) glucose concentrati...

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Published inJournal of diabetes science and technology Vol. 3; no. 5; pp. 1207 - 1214
Main Authors Keenan, D. Barry, Mastrototaro, John J., Voskanyan, Gayane, Steil, Garry M.
Format Journal Article
LanguageEnglish
Published United States Diabetes Technology Society 01.09.2009
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ISSN1932-2968
1932-3107
1932-3107
DOI10.1177/193229680900300528

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Summary:Through the use of enzymatic sensors—inserted subcutaneously in the abdomen or ex vivo by means of microdialysis fluid extraction—real-time minimally invasive continuous glucose monitoring (CGM) devices estimate blood glucose by measuring a patient's interstitial fluid (ISF) glucose concentration. Signals acquired from the interstitial space are subsequently calibrated with capillary blood glucose samples, a method that has raised certain questions regarding the effects of physiological time lags and of the duration of processing delays built into these devices. The time delay between a blood glucose reading and the value displayed by a continuous glucose monitor consists of the sum of the time lag between ISF and plasma glucose, in addition to the inherent electrochemical sensor delay due to the reaction process and any front-end signal-processing delays required to produce smooth traces. Presented is a review of commercially available, minimally invasive continuous glucose monitors with manufacturer-reported device delays. The data acquisition process for the Medtronic MiniMed (Northridge, CA) continuous glucose monitoring system—CGMS® Gold—and the Guardian® RT monitor is described with associated delays incurred for each processing step. Filter responses for each algorithm are examined using in vitro hypoglycemic and hyperglycemic clamps, as well as with an analysis of fast glucose excursions from a typical meal response. Results demonstrate that the digital filters used by each algorithm do not cause adverse effects to fast physiologic glucose excursions, although nonphysiologic signal characteristics can produce greater delays.
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Disclosure: D. Barry Keenan, John J. Mastrototaro, and Gayane Voskanyan are employees of Medtronic MiniMed. Garry M. Steil is no longer employed by Medtronic MiniMed but was an employee at the time this article was written.
ISSN:1932-2968
1932-3107
1932-3107
DOI:10.1177/193229680900300528