Treatment Satisfaction With Omnipod DASH in Adults With Type 1 Diabetes: A Nonblinded 1:1 Randomized Controlled Trial

被引:0
|
作者
Kong, Yee Wen [1 ,2 ]
Yuan, Cheng Yi [1 ,2 ]
Kiburg, Katerina [1 ,2 ]
Brown, Katrin [1 ,2 ]
Trawley, Steven [1 ,3 ,4 ]
Partovi, Andi [5 ]
Roem, Kerryn [1 ]
Pham, Cecilia [4 ,6 ,7 ]
Harrison, Natalie [8 ]
Fourlanos, Spiros [4 ,7 ,9 ]
Ekinci, Elif, I [4 ,6 ,7 ]
O'Neal, David N. [1 ,2 ,4 ,7 ,10 ]
机构
[1] Univ Melbourne, Diabet Technol Res Grp, Melbourne, Vic 3065, Australia
[2] St Vincents Hosp Melbourne, Dept Endocrinol & Diabet, Melbourne, Vic 3065, Australia
[3] Cairnmillar Inst, Dept Psychol, Camberwell, Vic 3124, Australia
[4] Univ Melbourne, Dept Med, Melbourne, Vic 3065, Australia
[5] Keylead Hlth, Melbourne, Vic 3065, Australia
[6] Austin Hlth, Dept Endocrinol, Heidelberg, Vic 3084, Australia
[7] Univ Melbourne, Australian Ctr Accelerating Diabet Innovat ACADI, Melbourne, Vic 3010, Australia
[8] Geelong Endocrinol & Diabet, Geelong, Vic 3220, Australia
[9] Royal Melbourne Hosp, Dept Diabet & Endocrinol, Melbourne, Vic 3052, Australia
[10] Univ Melbourne, St Vincents Hosp Melbourne, Dept Med, 4th Fl,Clin Sci Bldg,29 Regent St, Fitzroy, Vic 3065, Australia
来源
关键词
Omnipod DASH system; tubeless insulin pump therapy; treatment satisfaction; quality of life; INSULIN MANAGEMENT-SYSTEM; QUALITY-OF-LIFE; PATIENT PERCEPTIONS; PUMP THERAPY; YOUNG-ADULTS; GLUCOSE; ASSOCIATION; ADOLESCENTS; INJECTIONS; PREFERENCE;
D O I
10.1210/clinem/dgae088
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Omnipod DASH Insulin Management System is a tubeless insulin pump that overcomes the physical inconveniences of conventional tubed insulin pump therapy (IPT). Objective: We compared treatment satisfaction with Omnipod DASH System to usual care (multiple daily injections [MDIs] or tubed IPT) in adults with type 1 diabetes using self-monitoring blood glucose (SMBG). Methods: Adults with type 1 diabetes on MDI (n = 40) or IPT (n = 25) from 4 diabetes centers in Australia were randomly assigned in a 1:1 nonblinded manner to Omnipod DASH System (Omnipod group) or continue usual care (Usual Care group) for 12 weeks, followed by a further 12-week extension during which all participants used the device. The primary outcome was treatment satisfaction assessed by change in Diabetes Technology Questionnaire "current" (Delta DTQ-current) score at 12 weeks (study end). Secondary outcomes included Delta DTQ-current following extension and other participant-reported outcomes (PROs) measuring quality of life, burden of disease treatment, and glycemic and device-related outcomes at 12 weeks (study end) and 24 weeks (end extension). Results: Treatment satisfaction improved more in the Omnipod group vs the Usual Care group (Delta DTQ-current score of 16.4 [21.2] vs 0.0 [12.8]; P < .001) at study end. Significantly greater improvements in other PROs and glycated hemoglobin A(1c) were also observed. Improvements in DTQ-current and other PROs comparing study end and end extension were similar. While percentage in time in range change from baseline did not differ at study end (-2.0 [12.7] %), it was significantly greater at end extension (5.6 [10.9] %; P = .016). Conclusion: The Omnipod DASH System resulted in greater treatment satisfaction at 12 weeks in adults with type 1 diabetes using SMBG that was sustained after 24 weeks of device use without compromising sleep quality and fear of hypoglycemia. Improvements in glycemia were also observed.
引用
收藏
页码:1984 / 1995
页数:12
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