Insulin pump therapy and rapid acting insulin: What have we learned?

International Journal of Clinical Practice, Supplement

Volumn , Issue 123, 2001, Pages 47-50

  Zinman, B ^a  

^a UNIVERSITY OF TORONTO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYBUTYRIC ACID; FATTY ACID; GLUCOSE; INSULIN; INSULIN LISPRO;

CLINICAL TRIAL; CONFERENCE PAPER; CROSSOVER PROCEDURE; DIABETES CONTROL; DIABETES MELLITUS; DOUBLE BLIND PROCEDURE; FATTY ACID METABOLISM; GLUCOSE BLOOD LEVEL; HUMAN; HYPOGLYCEMIA; INFUSION PUMP; INSULIN DEPENDENT DIABETES MELLITUS; INSULIN INFUSION; INSULIN TREATMENT; METABOLIC REGULATION; POSTPRANDIAL STATE; PRIORITY JOURNAL;

DIABETES MELLITUS, TYPE 1; HUMANS; HYPOGLYCEMIA; HYPOGLYCEMIC AGENTS; INSULIN; INSULIN INFUSION SYSTEMS;

EID: 0034813156     PISSN: 1368504X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (11)

1. Acute complications associated with insulin infusion therapy
2. Stability of insulin lispro in insulin infusion systems
3. Insulin lispro in CSII: Results of a double blind cross-over study
4. Hypoglycemia in the Diabetes Control and Complications Trial
5. 1c and blood glucose stability in IDDM patients treated with lispro insulin analog in external pumps
6. Use of insulin lispro in continuous subcutaneous insulin infusion treatment: Results of a multicenter trial
7. Continuous subcutaneous insulin infusion (CSII): A study comparing lispro to regular human insulin
8. Efficacy, safety, and pump compatibility of human insulin aspart used in continuous subcutaneous insulin therapy in patients with type 1 diabetes
9. Effect of continuous subcutaneous insulin infusion with lispro on hepatic responsiveness to glucagon in type 1 diabetes
10. Catheter disconnection in type 1 diabetic patients treated with CSII: Comparison of insulin lispro and human regular insulin
11. Comparison of human regular and lispro insulins after interruption of continuous subcutaneous insulin infusion and in the treatment of acutely decompensated IDDM