Introduction and Objective: Technologies such as continuous glucose monitors (CGM), continuous subcutaneous insulin infusion (CSII) and automated insulin delivery systems (AID) enhance diabetes management. While this may improve long-term survival, how this translates into the more acute experience of persons w/ diabetes (PwD) may be variable. We assessed how diabetes technology use is associated w/ the acute living experience of PwD and whether it differently affects certain groups defined by race/ethnicity. Methods: Participants aged 14 to 40 (n=724) were invited complete online surveys about diabetes technology use (techuse), life threatening diabetic ketoacidosis (DKA) and severe hypoglycemia in the past yr, and the following: T1D distress (T1DD), Diabetes Self Monitoring (DSM), Glucose Management Experience (GME), and Insulin Treatment Satisfaction (ITS) Questionnaires. Techuse was defined as the combined use of CGM + CSII, or AID. Results: Techuse was reported in 79% of Non-Hispanic White (NHW), 66% of Non-Hispanic Black (NHB), and 67% of Hispanic Americans. Most recent HbA1c was lower in techusers overall (p=0.007). The greatest differences were observed in NHB Americans (p-interaction=0.04). Mean HbA1c (%) by techuse was as follows: 6.9 vs 7.3 (p=0.007) for NHW; 7.8 vs 9.2 (p=0.07) for NHB; and 8.0 vs 8.5 (p=.23) for Hispanic participants. Techuse was associated w/ lower odds of DKA in NHW (OR=0.32, 0.15-0.71), a marginally higher odds in NHB (OR=1.95, 0.36-10.46) and no differences in Hispanic participants (OR=1.02, 0.31-3.39), (p-interaction=0.03). Techuse was linked to a significantly lower odds of hypoglycemia (OR=0.44, 0.21-0.92) overall w/ no variation by race. Techuse was not linked w/ T1DD, DSM score, or GME (all p-values0.05), but was associated w/ increased ITS (p0.001); these relationships did not vary by race. Conclusion: Diabetes technology use is linked to lower HbA1c, hypoglycemia and DKA, those this varies by race, w/ greater reductions in HbA1c in NHB and DKA in NHW Americans, and increased insulin treatment satisfaction in all races. Disclosure R. Conway: None. K. Valdez: None. P.A. Mensah: None. C. Chartier-Logan: None. J. Snell-Bergeon: None. Funding American Diabetes Association (11-22-ICTSHD-03)
CONWAY et al. (Fri,) studied this question.
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