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. 2016 Sep;18(9):517-24.
doi: 10.1089/dia.2016.07281.sf. Epub 2016 Aug 15.

Insulin Infusion Set Use: European Perspectives and Recommendations

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Insulin Infusion Set Use: European Perspectives and Recommendations

Dorothee Deiss et al. Diabetes Technol Ther. 2016 Sep.

Abstract

Insulin pump users worldwide depend on insulin infusion sets (IISs) for predictable delivery of insulin to the subcutaneous tissue. Yet emerging data indicates that IISs are associated with many pump-related adverse events and may contribute to potentially life-threatening problem of unexplained hyperglycemia. The relative scarcity of published research on IISs to date, the heterogeneity of regional IIS practices, and the increasing demand for international standards guiding their use prompted convening of a panel of diabetologists and diabetes nurse educators last February, in Milan, Italy, to discuss a framework for optimizing IIS practice in Europe. The multinational panel was tasked, first, with identifying the often-overlooked IIS issues that can affect patients' experience of pump therapy-e.g., partial or complete blockage of the cannula, skin pathologies, unpredictable variations in insulin absorption, dislodgment, and the demands of site rotation and set changes-and, second, with establishing direction for developing cohesive protocols to assure long-term success. As reported in this article, the panel examined IIS-related complications of pump therapy encountered in clinical practice, considered country-wide policies to prevent and mitigate such complications, and updated priorities for improving IIS education on issues of device selection, skin care, and troubleshooting unexplained hyperglycemia. These recommendations may be more relevant with the possibility of closed-loop systems available in the near future.

Keywords: Insulin infusion sets; artificial pancreas; insulin pumps; lipohypertrophy; unexplained hyperglycemia.

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Conflict of interest statement

Author Disclosures D.D. has received research support from BD, DexCom, Medtronic, and Roche. P.A. has received lecture honoraria from Novo Nordisk, Eli Lilly, Sanofi, Roche, Medtronic, Dexcom, Menarini, and Abbott, and participated in Advisory Boards for Eli Lilly, Abbott, Roche and Sanofi. P.A. is one of the founders and board member of Diasend Inc. M.A.Z. has no disclosures to report. G.B.B. has received honoraria for consultation and advice from Sanofi, Eli Lilly, Menarini. G.C. has no disclosures to report. C.C. has patent applications related to glucose sensors and the artificial pancreas; he has received non-financial support from Roche and Dexcom, and received research support, managed by University of Padova, from Dexcom, Sanofi, Adocia; he is a consultant/advisor for Novo Nordisk. T.D. has received research support or served as a consultant for Abbott, AstraZeneca, Bayer, BD, Boehringer, DexCom, Eli Lilly, Medtronic, Novo Nordisk, Roche, Sanofi, and Ypsomed. A.G. has no disclosures to report. H.M. is a consultant for Medtronic (German-Switzerland-Austria), Eli Lilly (Germany), Sanofi (Germany), Bayer Healthcare, and all regional German pharmacists associations. E.R. is a consultant/advisor for Menarini Diagnostics, Abbott, BD, Cellnovo, Dexcom, Eli Lilly, Johnson & Johnson (Animas, LifeScan), Medtronic, Novo Nordisk, Roche Diagnostics and Sanofi, and has received research grant/material support from Abbott, Dexcom, Insulet and Roche Diagnostics. C.A.V. has no disclosures to report.

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