TY - JOUR
T1 - Multicenter, Randomized Trial of a Bionic Pancreas in Type 1 Diabetes
AU - Bionic Pancreas Research Group
AU - Russell, Steven J.
AU - Beck, Roy W.
AU - Damiano, Edward R.
AU - El-Khatib, Firas H.
AU - Ruedy, Katrina J.
AU - Balliro, Courtney A.
AU - Li, Zoey
AU - Calhoun, Peter
AU - Wadwa, R. Paul
AU - Buckingham, Bruce
AU - Zhou, Keren
AU - Daniels, Mark
AU - Raskin, Philip
AU - White, Perrin C.
AU - Lynch, Jane
AU - Pettus, Jeremy
AU - Hirsch, Irl B.
AU - Goland, Robin
AU - Buse, John B.
AU - Kruger, Davida
AU - Mauras, Nelly
AU - Muir, Andrew
AU - McGill, Janet B.
AU - Cogen, Fran
AU - Weissberg-Benchell, Jill
AU - Sherwood, Jordan S.
AU - Castellanos, Luz E.
AU - Hillard, Mallory A.
AU - Tuffaha, Marwa
AU - Putman, Melissa S.
AU - Sands, Mollie Y.
AU - Forlenza, Gregory
AU - Slover, Robert
AU - Messer, Laurel H.
AU - Cobry, Erin
AU - Shah, Viral N.
AU - Polsky, Sarit
AU - Lal, Rayhan
AU - Ekhlaspour, Laya
AU - Hughes, Michael S.
AU - Basina, Marina
AU - Hatipoglu, Betul
AU - Olansky, Leann
AU - Bhangoo, Amrit
AU - Forghani, Nikta
AU - Kashmiri, Himala
AU - Sutton, Francoise
AU - Choudhary, Abha
AU - Penn, Jimmy
AU - Jafri, Rabab
AU - Rayas, Maria
AU - Escaname, Elia
AU - Kerr, Catherine
AU - Favela-Prezas, Ruby
AU - Boeder, Schafer
AU - Trikudanathan, Subbulaxmi
AU - Williams, Kristen M.
AU - Leibel, Natasha
AU - Kirkman, M. Sue
AU - Bergamo, Kate
AU - Klein, Klara R.
AU - Dostou, Jean M.
AU - Machineni, Sriram
AU - Young, Laura A.
AU - Diner, Jamie C.
AU - Bhan, Arti
AU - Jones, J. Kimberly
AU - Benson, Matthew
AU - Bird, Keisha
AU - Englert, Kimberly
AU - Permuy, Joe
AU - Cossen, Kristina
AU - Felner, Eric
AU - Salam, Maamoun
AU - Silverstein, Julie M.
AU - Adamson, Samantha
AU - Cedeno, Andrea
AU - Meighan, Seema
AU - Dauber, Andrew
N1 - Publisher Copyright:
Copyright © 2022 Massachusetts Medical Society.
PY - 2022/9/29
Y1 - 2022/9/29
N2 - BACKGROUND Currently available semiautomated insulin-delivery systems require individualized insulin regimens for the initialization of therapy and meal doses based on carbohydrate counting for routine operation. In contrast, the bionic pancreas is initialized only on the basis of body weight, makes all dose decisions and delivers insulin autonomously, and uses meal announcements without carbohydrate counting. METHODS In this 13-week, multicenter, randomized trial, we randomly assigned in a 2:1 ratio persons at least 6 years of age with type 1 diabetes either to receive bionic pancreas treatment with insulin aspart or insulin lispro or to receive standard care (defined as any insulin-delivery method with unblinded, real-time continuous glucose monitoring). The primary outcome was the glycated hemoglobin level at 13 weeks. The key secondary outcome was the percentage of time that the glucose level as assessed by continuous glucose monitoring was below 54 mg per deciliter; the prespecified noninferiority limit for this outcome was 1 percentage point. Safety was also assessed. RESULTS A total of 219 participants 6 to 79 years of age were assigned to the bionic-pancreas group, and 107 to the standard-care group. The glycated hemoglobin level decreased from 7.9% to 7.3% in the bionic-pancreas group and did not change (was at 7.7% at both time points) in the standard-care group (mean adjusted difference at 13 weeks, -0.5 percentage points; 95% confidence interval [CI], -0.6 to -0.3; P<0.001). The percentage of time that the glucose level as assessed by continuous glucose monitoring was below 54 mg per deciliter did not differ significantly between the two groups (13-week adjusted difference, 0.0 percentage points; 95% CI, -0.1 to 0.04; P<0.001 for noninferiority). The rate of severe hypoglycemia was 17.7 events per 100 participant-years in the bionic-pancreas group and 10.8 events per 100 participant-years in the standard-care group (P = 0.39). No episodes of diabetic ketoacidosis occurred in either group. CONCLUSIONS In this 13-week, randomized trial involving adults and children with type 1 diabetes, use of a bionic pancreas was associated with a greater reduction than standard care in the glycated hemoglobin level.
AB - BACKGROUND Currently available semiautomated insulin-delivery systems require individualized insulin regimens for the initialization of therapy and meal doses based on carbohydrate counting for routine operation. In contrast, the bionic pancreas is initialized only on the basis of body weight, makes all dose decisions and delivers insulin autonomously, and uses meal announcements without carbohydrate counting. METHODS In this 13-week, multicenter, randomized trial, we randomly assigned in a 2:1 ratio persons at least 6 years of age with type 1 diabetes either to receive bionic pancreas treatment with insulin aspart or insulin lispro or to receive standard care (defined as any insulin-delivery method with unblinded, real-time continuous glucose monitoring). The primary outcome was the glycated hemoglobin level at 13 weeks. The key secondary outcome was the percentage of time that the glucose level as assessed by continuous glucose monitoring was below 54 mg per deciliter; the prespecified noninferiority limit for this outcome was 1 percentage point. Safety was also assessed. RESULTS A total of 219 participants 6 to 79 years of age were assigned to the bionic-pancreas group, and 107 to the standard-care group. The glycated hemoglobin level decreased from 7.9% to 7.3% in the bionic-pancreas group and did not change (was at 7.7% at both time points) in the standard-care group (mean adjusted difference at 13 weeks, -0.5 percentage points; 95% confidence interval [CI], -0.6 to -0.3; P<0.001). The percentage of time that the glucose level as assessed by continuous glucose monitoring was below 54 mg per deciliter did not differ significantly between the two groups (13-week adjusted difference, 0.0 percentage points; 95% CI, -0.1 to 0.04; P<0.001 for noninferiority). The rate of severe hypoglycemia was 17.7 events per 100 participant-years in the bionic-pancreas group and 10.8 events per 100 participant-years in the standard-care group (P = 0.39). No episodes of diabetic ketoacidosis occurred in either group. CONCLUSIONS In this 13-week, randomized trial involving adults and children with type 1 diabetes, use of a bionic pancreas was associated with a greater reduction than standard care in the glycated hemoglobin level.
UR - http://www.scopus.com/inward/record.url?scp=85138925143&partnerID=8YFLogxK
U2 - 10.1056/NEJMoa2205225
DO - 10.1056/NEJMoa2205225
M3 - Article
C2 - 36170500
AN - SCOPUS:85138925143
SN - 0028-4793
VL - 387
SP - 1161
EP - 1172
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 13
ER -