Language
English
Publication Date
3-4-2023
Journal
Endocrine Reviews
DOI
10.1210/endrev/bnac022
PMID
36066457
PMCID
PMC9985411
PubMedCentral® Posted Date
9-6-2022
PubMedCentral® Full Text Version
Post-print
Abstract
The significant and growing global prevalence of diabetes continues to challenge people with diabetes (PwD), healthcare providers, and payers. While maintaining near-normal glucose levels has been shown to prevent or delay the progression of the long-term complications of diabetes, a significant proportion of PwD are not attaining their glycemic goals. During the past 6 years, we have seen tremendous advances in automated insulin delivery (AID) technologies. Numerous randomized controlled trials and real-world studies have shown that the use of AID systems is safe and effective in helping PwD achieve their long-term glycemic goals while reducing hypoglycemia risk. Thus, AID systems have recently become an integral part of diabetes management. However, recommendations for using AID systems in clinical settings have been lacking. Such guided recommendations are critical for AID success and acceptance. All clinicians working with PwD need to become familiar with the available systems in order to eliminate disparities in diabetes quality of care. This report provides much-needed guidance for clinicians who are interested in utilizing AIDs and presents a comprehensive listing of the evidence payers should consider when determining eligibility criteria for AID insurance coverage.
Keywords
Humans, Insulin, Hypoglycemic Agents, Diabetes Mellitus, Type 1, Consensus, Blood Glucose, Blood Glucose Self-Monitoring, automated insulin delivery, closed-loop, type 1 diabetes, consensus recommendations
Published Open-Access
yes
Recommended Citation
Phillip, Moshe; Nimri, Revital; Bergenstal, Richard M; et al., "Consensus Recommendations for the Use of Automated Insulin Delivery Technologies in Clinical Practice" (2023). Faculty, Staff and Students Publications. 6441.
https://digitalcommons.library.tmc.edu/baylor_docs/6441
Graphical Abstract