Continuous subcutaneous glucose monitoring improved metabolic control in pediatric patients with type 1 diabetes: A controlled crossover study

被引:142
作者
Ludvigsson, J
Hanas, R
机构
[1] Univ Hosp, Dept Pediat, Linkoping, Sweden
[2] Cent Hosp, Uddevalla, Sweden
关键词
type; 1; diabetes; children; glucose sensing; Continuous Glucose Monitoring System; metabolic control; hypoglycemia; Dawn phenomenon; Somogyi phenomenon; rebound phenomenon;
D O I
10.1542/peds.111.5.933
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective. To improve metabolic control and prevent complications, both acute and late, we need to adjust treatment on the basis of the blood glucose (BG) profile, as not even the most active BG self-monitoring gives sufficient information. Design. We have used Continuous Glucose Monitoring System (CGMS; Medtronic MiniMed, Northridge, CA) in a controlled crossover study including 27 diabetic patients aged 12.5 +/- 3.3 (mean; standard deviation; range: 5-19) years. All patients were treated with intensive insulin therapy, 14 with multiple injections, and 13 with pumps. The patients were randomized into an open or blind study arm. Both arms wore the CGMS sensor for 3 days every 2 weeks. CGMS profiles were used in the open study arm to adjust insulin therapy at follow-up visits every 6 weeks. Both the patients and the diabetes team were masked to the CGMS profiles in the blinded arm, and insulin therapy adjustments were based solely on 7-point BG profiles performed by the patients. At 3 months the 2 study arms were crossed over. Results. Despite initial problems with a device new to both patients and the diabetes team, hemoglobin A(1)C decreased significantly in the open arm (from 7.70%-7.31%) but not in the blind arm (7.75%-7.65%). A total of 26/27 patients experienced daytime low subcutaneous glucose (<3.0 mmol/L; .8 episodes/day; duration 58 +/- 29 minutes; 5.5% of total time), and 27/27 patients had at least 1 nocturnal episode of low subcutaneous glucose (. 4 episodes/ night; duration 132 +/- 81 minutes; 10.1% of total time). Conclusions. Use of CGMS facilitated an improved treatment, and patients received new insight and increased motivation. In this study, we found CGMS to be a useful tool for education and improving metabolic control.
引用
收藏
页码:933 / 938
页数:6
相关论文
共 20 条
[1]  
Arnqvist H, 1997, Lakartidningen, V94, P4789
[2]   Continuous glucose monitoring used to adjust diabetes therapy improves glycosylated hemoglobin: a pilot study [J].
Bode, BW ;
Gross, TM ;
Thornton, KR ;
Mastrototaro, JJ .
DIABETES RESEARCH AND CLINICAL PRACTICE, 1999, 46 (03) :183-190
[3]   DECLINING INCIDENCE OF NEPHROPATHY IN INSULIN-DEPENDENT DIABETES-MELLITUS [J].
BOJESTIG, M ;
ARNQVIST, HJ ;
HERMANSSON, G ;
KARLBERG, BE ;
LUDVIGSSON, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (01) :15-18
[4]   Limitations of conventional methods of self-monitoring of blood glucose - Lessons learned from 3 days of continuous glucose sensing in pediatric patients with type 1 diabetes [J].
Boland, E ;
Monsod, T ;
Delucia, M ;
Brandt, CA ;
Fernando, S ;
Tamborlane, WV .
DIABETES CARE, 2001, 24 (11) :1858-1862
[5]  
Boyne MS, 2000, DIABETES, V49, pA99
[6]   Continuous subcutaneous glucose monitoring in children with type 1 diabetes [J].
Chase, HP ;
Kim, LM ;
Owen, SL ;
MacKenzie, TA ;
Klingensmith, GJ ;
Murtfeldt, R ;
Garg, SK .
PEDIATRICS, 2001, 107 (02) :222-226
[7]   Persistent differences among centers over 3 years in glycemic control and hypoglycemia in a study of 3,805 children and adolescents with type 1 diabetes from the Hvidore Study Group [J].
Danne, T ;
Mortensen, HB ;
Hougaard, P ;
Lynggaard, H ;
Aanstoot, HJ ;
Chiarelli, F ;
Daneman, D ;
Dorchy, H ;
Garandeau, P ;
Greene, SA ;
Hoey, H ;
Holl, RW ;
Kaprio, EA ;
Kocova, M ;
Martul, P ;
Matsuura, N ;
Robertson, KJ ;
Schoenle, EJ ;
Sovik, O ;
Swift, PGF ;
Tsou, RM ;
Vanelli, M ;
Åman, J .
DIABETES CARE, 2001, 24 (08) :1342-1347
[9]   A pilot study of the continuous glucose monitoring system - Clinical decisions and glycemic control after its use in pediatric type 1 diabetic subjects [J].
Kaufman, FR ;
Gibson, LC ;
Halvorson, M ;
Carpenter, S ;
Fisher, LK ;
Pitukcheewanont, P .
DIABETES CARE, 2001, 24 (12) :2030-2034
[10]  
Kerr D, 2001, DIABETOLOGIA, V44, pA239