SAFE AND SIMPLE EMERGENCY DEPARTMENT DISCHARGE THERAPY FOR PATIENTS WITH TYPE 2 DIABETES MELLITUS AND SEVERE HYPERGLYCEMIA

被引:24
作者
Babu, Ambika [1 ]
Mehta, Avinder [3 ]
Guerrero, Pilar [4 ]
Chen, Zhen [5 ]
Meyer, Peter M. [2 ]
Koh, Chung Kay [6 ]
Roberts, Rebecca [4 ]
Schaider, Jeffrey [4 ]
Fogelfeld, Leon [1 ]
机构
[1] John H Stroger Jr Hosp Cook Cty, Dept Endocrinol & Metab, Chicago, IL USA
[2] Rush Univ, Med Ctr, Dept Prevent Med & Biostat, Chicago, IL 60612 USA
[3] Lutheran Med Ctr, Dept Family Med, Brooklyn, NY USA
[4] John H Stroger Jr Hosp Cook Cty, Dept Emergency Med, Chicago, IL USA
[5] Univ Michigan, Sch Publ Hlth, Dept Biostat, Ann Arbor, MI 48109 USA
[6] Rush Univ, Med Ctr, Dept Endocrinol, Chicago, IL 60612 USA
关键词
BETA-CELL FUNCTION; MARKEDLY SYMPTOMATIC PATIENTS; HIGH GLUCOSE-CONCENTRATIONS; INSULIN GENE-EXPRESSION; FASTING PLASMA-GLUCOSE; CHRONIC EXPOSURE; HIT CELLS; SECRETION; TOXICITY; HIT-T15;
D O I
10.4158/EP09117.ORR
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To investigate the safety and effectiveness of 2 simple discharge regimens for use in patients with type 2 diabetes mellitus (DM2) and severe hyperglycemia, who present to the emergency department (ED) and do not need to be admitted. Methods: We conducted an 8-week, open-label, randomized controlled trial in 77 adult patients with DM2 and blood glucose levels of 300 to 700 mg/dL seen in a public hospital ED. Patients were randomly assigned to receive glipizide XL, 10 mg orally daily (G group), versus glipizide XL, 10 mg orally daily, plus insulin glargine, 10 U daily (G+G group). The primary outcome was to maintain safe fasting glucose and random glucose levels of <350 and <500 mg/dL up to 4 weeks and <300 and <400 mg/dL, respectively, thereafter and to have no return ED visits (responders). Results: Baseline characteristics were similar between the 2 treatment groups. The primary outcome was achieved in 87% of patients in both treatment groups. The enrollment mean blood glucose values of 440 and 467 mg/dL in the G and G+G groups, respectively, declined by the end 0 of week 1 to 298 and 289 mg/dL and by week 8 to 140 and 135 mg/dL, respectively. Homeostasis model assessment of beta-cell function and early insulin response improved 7-fold and 4-fold, respectively, in responders at the end of the 8-week study. Conclusion: Sulfonylurea with and without use of a small dose of insulin glargine rapidly improved blood glucose levels and beta-cell function in patients with DM2. Use of sulfonylurea alone once daily can be considered a safe discharge regimen for such patients and an effective bridge between ED intervention and subsequent follow-up. (Endocr Pract. 2009;15:696-704)
引用
收藏
页码:696 / 704
页数:9
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