Efficacy and Safety of Mini-Dose Glucagon for Treatment of Nonsevere Hypoglycemia in Adults With Type 1 Diabetes

被引:35
作者
Haymond, Morey W. [1 ]
DuBose, Stephanie N. [2 ]
Rickels, Michael R. [3 ]
Wolpert, Howard [4 ]
Shah, Viral N. [5 ]
Sherr, Jennifer L. [6 ]
Weinstock, Ruth S. [7 ]
Agarwal, Shivani [3 ]
Verdejo, Alandra S. [2 ]
Cummins, Martin J. [8 ]
Newswanger, Brett [8 ]
Beck, Roy W. [2 ]
机构
[1] Baylor Coll Med, Houston, TX 77030 USA
[2] Jaeb Ctr Hlth Res, 15310 Amberly Dr,Suite 350, Tampa, FL 33647 USA
[3] Univ Penn, Rodebaugh Diabet Ctr, Perelman Sch Med, Philadelphia, PA 19104 USA
[4] Harvard Med Sch, Joslin Diabet Ctr, Boston, MA 02215 USA
[5] Univ Colorado, Barbara Davis Ctr Diabet, Anschutz Med Campus, Aurora, CO 80045 USA
[6] Yale Sch Med, New Haven, CT 06510 USA
[7] SUNY Upstate Med Univ, Syracuse, NY 13210 USA
[8] Xeris Pharmaceut Inc, Austin, TX 78705 USA
关键词
MILD HYPOGLYCEMIA; CHILDREN; RESCUE;
D O I
10.1210/jc.2017-00591
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
7 Context: Standard treatment of hypoglycemia is oral carbohydrate, but it often results in hyper-glycemia and entails extra caloric intake. Objective: To evaluate low-dose glucagon to treat mild hypoglycemia in ambulatory adults with type 1 diabetes (T1D). Design: Randomized crossover trial (two 3-week periods). Setting: Five U.S. diabetes clinics. Patients: Twenty adults with T1D using an insulin pump and continuous glucose monitor (CGM) and experiencing frequent mild hypoglycemia. Intervention: Nonaqueous mini-dose glucagon (MDG) (150 mu g) to treat nonsevere hypoglycemia. Main Outcome Measures: Successful treatment was defined as blood glucose (BG) >= 50 mg/dL 15minutes and >= 70mg/dL 30minutes after intervention, on the studymeter. Two authors, blinded to treatment arm, independently judged each event as a clinical success or failure. Results: Sixteen participants (mean age 39 years, 75% female, mean diabetes duration 23 years, mean hemoglobin A1c 7.2%) had 118 analyzable events with initial BG of 50 to 69 mg/dL. Successful treatment criteria were met for 58 (94%) of 62 events during the MDG period and 53 (95%) of 56 events during the glucose tablets (TABS) period (adjusted P = 0.99). Clinical assessments of success for these events were 97% and 96%, respectively. CGM-measured time in range did not differ between treatment groups during the 2 hours after events, but TABS resulted in higher maximum glucose (116 vs 102 mg/dL; P = 0.01) over the first hour. Conclusions: Low-dose glucagon can successfully treat mild hypoglycemia and may be a useful alternative to treatment with oral carbohydrate when trying to avoid unnecessary caloric intake.
引用
收藏
页码:2994 / 3001
页数:8
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