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A comparison of two insulin infusion protocols in the medical intensive care unit by continuous glucose monitoring.
De Block, Christophe E M; Rogiers, Peter; Jorens, Philippe G; Schepens, Tom; Scuffi, Cosimo; Van Gaal, Luc F.
Afiliação
  • De Block CEM; Department of Endocrinology, Diabetology and Metabolism, Faculty of Medicine, Antwerp University Hospital and University of Antwerp, Wilrijkstraat 10, 2650, Edegem, Belgium. christophe.deblock@uantwerpen.be.
  • Rogiers P; Intensive Care Unit, ZNA, General Hospital Middelheim, Antwerp, Belgium.
  • Jorens PG; Intensive Care Unit, Antwerp University Hospital, University of Antwerp, Edegem, Belgium.
  • Schepens T; Intensive Care Unit, Antwerp University Hospital, University of Antwerp, Edegem, Belgium.
  • Scuffi C; A. Menarini Diagnostics, Scientific and Technology Affairs, Florence, Italy.
  • Van Gaal LF; Department of Endocrinology, Diabetology and Metabolism, Faculty of Medicine, Antwerp University Hospital and University of Antwerp, Wilrijkstraat 10, 2650, Edegem, Belgium.
Ann Intensive Care ; 6(1): 115, 2016 Dec.
Article em En | MEDLINE | ID: mdl-27878572
ABSTRACT

BACKGROUND:

Achieving good glycemic control in intensive care units (ICU) requires a safe and efficient insulin infusion protocol (IIP). We aimed to compare the clinical performance of two IIPs (Leuven versus modified Yale protocol) in patients admitted to medical ICU, by using continuous glucose monitoring (CGM). This is a pooled data analysis of two published prospective randomized controlled trials. CGM monitoring was performed in 57 MICU patients (age 64 ± 12 years, APACHE-II score 28 ± 7, non-diabetic/diabetic 36/21). The main outcome measures were percentage of time in normoglycemia (80-110 mg/dl) and in hypoglycemia (<60 mg/dl), and glycemic variability (standard deviation, coefficient of variation, mean amplitude of glucose excursions, mean of daily differences).

RESULTS:

Twenty-two subjects were treated using the Leuven protocol and 35 by the Yale protocol; >63,000 CGM measurements were available. The percentage of time in normoglycemia (80-110 mg/dl) was higher (37 ± 15 vs. 26 ± 11%, p = 0.001) and percentage of time spent in hypoglycemia was lower (0[0-2] vs. 5[1-8]%, p = 0.001) in the Yale group. Median glycemia did not differ between groups (118[108-128] vs. 128[106-154] mg/dl). Glycemic variability was less pronounced in the Yale group (median SD 28[21-37] vs. 47[31-71] mg/dl, p = 0.001; CV 23[19-31] vs. 36[26-50]%, p = 0.001; MODD 35[26-41] vs. 60[33-94] mg/dl, p = 0.001). However, logistic regression could not identify type of IIP, diabetes status, age, BMI, or APACHE-II score as independent parameters for strict glucose control.

CONCLUSIONS:

The Yale protocol provided better average glycemia, more time spent in normoglycemia, less time in hypoglycemia, and less glycemic variability than the Leuven protocol, but was not independently associated with strict glycemic control.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Idioma: En Revista: Ann Intensive Care Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Idioma: En Revista: Ann Intensive Care Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Bélgica