Open questions on basal insulin therapy in T2D: a Delphi consensus

Author:

,Alberto Aglialoro,Roberto Anichini,Angelo Avogaro,Cristiana Baggiore,Cesare Berra,Riccardo Bonadonna,Giuseppe Corrao Salvatore Maria,Andrea Da Porto,Lorenzo De Candia,Alessandro De Cosmo Salvatore,Graziano Di Cianni,Gloria Formoso,Gabriella Garrapa,Mariangela Ghiani,Francesco Giorgino,Giacomo Guaita,Ida Maiorino Maria,Stefano Masi,Monica Modugno,Nicola Morea,Lelio Morviducci,Nicola Napoli,Raffaele Napoli,Margherita Occhipinti,Emanuela Orsi,Gianluca Perseghin,Salvatore Piro,Giovanni Sartore,Giorgio Sesti,Francesco Tassone,Roberto Trevisan,Buzzetti Raffaella,Candido Riccardo,Esposito Katherine,Giaccari Andrea,Mannucci Edoardo,Nicolucci AntonioORCID,Russo Giuseppina T.

Abstract

Abstract Aims The revolution in the therapeutic approach to type 2 diabetes (T2D) requires a rethinking of the positioning of basal insulin (BI) therapy. Given the considerable number of open questions, a group of experts was convened with the aim of providing, through a Delphi consensus method, practical guidance for doctors. Methods A group of 6 experts developed a series of 29 statements on: the role of metabolic control in light of the most recent guidelines; BI intensification strategies: (1) add-on versus switch; (2) inertia in starting and titrating; (3) free versus fixed ratio combination; basal-bolus intensification and de-intensification strategies; second generation analogues of BI (2BI). A panel of 31 diabetologists, by accessing a dedicated website, assigned each statement a relevance score on a 9-point scale. The RAND/UCLA Appropriateness Method was adopted to assess the existence of disagreement among participants. Results Panelists showed agreement for all 29 statements, of which 26 were considered relevant, one was considered not relevant and two were of uncertain relevance. Panelists agreed that the availability of new classes of drugs often allows the postponement of BI and the simplification of therapy. It remains essential to promptly initiate and titrate BI when required. BI should always, unless contraindicated, be started in addition to, and not as a replacement, for ongoing treatments with cardiorenal benefits. 2BIs should be preferred for their pharmacological profile, greater ease of self-titration and flexibility of administration. Conclusion In a continuously evolving scenario, BI therapy still represents an important option in the management of T2D patients.

Funder

The project was funded by Sanofi S.r.l., Milan, Italy.

Publisher

Springer Science and Business Media LLC

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