- Poster presentation
- Published:
Blood glucose amplitude variation: effects of intensive insulin therapy and relative association with mortality
Critical Care volume 14, Article number: P575 (2010)
Introduction
There is growing evidence that not only blood glucose (BG) level but also BG amplitude variation (BGAV) is associated with mortality in critically ill patients [1].
Methods
Retrospective analysis of the data of the Leuven intensive insulin therapy (IIT) trial in 1,200 MICU patients, randomized to receive either IIT or conventional insulin therapy [2]. The hyperglycemic index (HGI) and hypoglycemic index (HoGI) were used as measures of BG level, the standard deviation of all BG readings per patient (SD BG) as a measure of BGAV. The univariable effect of IIT on these indices was analyzed, the independent association with hospital mortality was assessed by multivariable logistic regression (MVR), corrected for baseline risks.
Results
IIT reduced the median HGI from 3.2 to 0.8 mmol/l (P < 0.0001), increased the median HoGI from 0.005 to 0.048 mmol/l (P < 0.0001), and did not affect median SD BG (conventional: 2.12; IIT: 1.99 mmol/l (P = 0.161)). The results of the MVR are summarized in Table 1. HGI, HoGI and SD BG were independently associated with mortality.
Conclusions
BGAV was associated with mortality in MICU patients, independent of baseline risks and BG level. IIT reduced HGI, increased HoGI, and did not affect BGAV. Reducing BGAV, in addition to IIT, may theoretically increase its potential for clinical benefit.
References
Krinsley , et al: Crit Care Med. 2008, 36: 3008-3013. 10.1097/CCM.0b013e31818b38d2.
Berghe Van den , et al: N Engl J Med. 2006, 354: 449-461. 10.1056/NEJMoa052521.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Bekaert, E., Wouters, P., Wilmer, A. et al. Blood glucose amplitude variation: effects of intensive insulin therapy and relative association with mortality. Crit Care 14 (Suppl 1), P575 (2010). https://doi.org/10.1186/cc8807
Published:
DOI: https://doi.org/10.1186/cc8807