Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2015 Jun 22;19(1):270.
doi: 10.1186/s13054-015-0959-9.

Influence of a strict glucose protocol on serum potassium and glucose concentrations and their association with mortality in intensive care patients

Affiliations
Observational Study

Influence of a strict glucose protocol on serum potassium and glucose concentrations and their association with mortality in intensive care patients

Esther V Uijtendaal et al. Crit Care. .

Abstract

Introduction: Tight glucose control therapy (TGC) has been implemented to control hyperglycemia in ICU patients. TGC may also influence serum potassium concentrations. We therefore investigated the influence of TGC on both serum glucose and serum potassium concentrations and associated mortality.

Method: We performed a retrospective analysis including all patients admitted to the ICU of a tertiary hospital for 24 hours or more and with at least three serum glucose and serum potassium concentrations between 1999-2001 (conventional period), 2002-2006 (implementation period) or 2007-2009 (TGC period). Segmented regression analysis was used to estimate changes in outcomes that occurred after the intervention controlling for pre-intervention trends. Means and standard deviations (SDs) of serum glucose and serum potassium concentrations, and rate of severe hypoglycemia (≤ 2.2 mmol/L) and hypokalemia (≤ 3 mmol/L), were compared between the TGC and conventional period.

Results: Although mean serum glucose concentrations dropped 2.1 mmol/L (95% CI =-1.8 to -2.3 mmol/L, p<0.002), mean serum potassium concentrations did not change (absolute increase 0.02 mmol/L; 95% CI = -0.06 to 0.09 mmol/L, p=0.64). The rate of severe hypoglycemia increased with 5.9% (95% CI=-3.0 to -8.9, p<0.002), but the rate of hypokalemia remained equal (absolute reduction 4.8%; 95% CI = -11.1% to 1.5%, p=0.13). The SD of serum glucose concentrations within a patient did not change, while the SD of serum potassium concentrations even decreased 0.04 mmol/L (95% CI = -0.01 to -0.07, p = 0.01). ICU mortality decreased but this decrease was not significant (absolute difference -3.63%; 95% CI = -9.33 to 2.09, p = 0.20). Mean serum glucose concentrations, mean serum potassium concentrations and SDs of both serum glucose and serum potassium concentrations were all independently associated with ICU mortality. Highest mortality rates were seen at both the lowest and highest mean values (U/J-shaped association) and mortality rates increased with increasing variability (SDs) for both serum glucose and serum potassium concentrations.

Conclusion: Our study shows that a TGC was not associated with an increased risk of serum potassium related events. Low and high mean values and high variability of both serum glucose and serum potassium concentrations are predictors for high ICU mortality.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Inclusion of study patients
Fig. 2
Fig. 2
Mean serum glucose concentrations during the study period. y = 8.720875 - 0.00002*time1 - 0.0011*time2 + 0.001605*time3
Fig. 3
Fig. 3
Percentage of patients with a period of severe hypoglycemia (≤2.2 mmol/L) during the study period. y = 2.268667 - 0.00056*time1 + 0.003807*time2 - 0.00659*time3
Fig. 4
Fig. 4
Means of individual standard deviations for serum glucose concentrations during the study period. y = 2.085461 - 0.00019*time1 + 0.000133*time2 + 1.342228*time3
Fig. 5
Fig. 5
Mean serum potassium concentrations during the study period. y = 4.117654 - 0.0000025*time1 + 0.0000114*time2 + 0.0000374*time3
Fig. 6
Fig. 6
Percentage of patients with a period of hypokalemia (≤3 mmol/L) during the study period. y = 24.14247 - 0.00029*time1 - 0.00236*time2 - 0.004526*time3
Fig. 7
Fig. 7
Means of individual standard deviations for serum potassium concentrations during the study period. y = 0.493879 - 0.000021*time1 - 0.000033*time2 - 0.0000311*time3
Fig. 8
Fig. 8
ICU mortality during the study period. y = 18.3116 + 0.000695*time1 - 0.00268*time2 + 0.0000777*time3
Fig. 9
Fig. 9
Relationship between mean serum glucose concentrations and adjusted* ODDs ratio on ICU mortality during TGC period. * adjusted for age, gender, length of ICU stay and mean serum potassium concentrations
Fig. 10
Fig. 10
Relationship between mean serum potassium concentrations and adjusted* ODDs ratio on ICU mortality during TGC period. * adjusted for age, gender, length of ICU stay and mean serum glucose concentrations
Fig. 11
Fig. 11
Relationship between SD for serum glucose concentrations and adjusted* ODDs ratio on ICU mortality during TGC period. * adjusted for age, gender, length of ICU stay and SD for serum potassium concentrations
Fig. 12
Fig. 12
Relationship between SD for serum potassium concentrations and adjusted* ODDs ratio on ICU mortality during TGC period. * adjusted for age, gender, length of ICU stay and SD for serum glucose concentrations

Similar articles

Cited by

References

    1. Lepper PM, Ott S, Nüesch E, Von Eynatten M, Schumann C, Pletz MW, et al. Serum glucose levels for predicting death in patients admitted to hospital for community acquired pneumonia: prospective cohort study. BMJ. 2012;344:e3397. doi: 10.1136/bmj.e3397. - DOI - PMC - PubMed
    1. Brownlee M. Biochemistry and molecular cell biology of diabetic complications. Nature. 2001;414:813–820. doi: 10.1038/414813a. - DOI - PubMed
    1. Weekers F, Giulietti AP, Michalaki M, Coopmans W, Van Herck E, Mathieu C, et al. Metabolic, endocrine and immune effects of stress hyperglycemia in a rabbit model of prolonged critical illness. Endocrinology. 2003;144:5329–5338. doi: 10.1210/en.2003-0697. - DOI - PubMed
    1. Mizock BA. Alterations in carbohydrate metabolism during stress: A review of the literature. Am J Med. 1995;98:75–84. doi: 10.1016/S0002-9343(99)80083-7. - DOI - PubMed
    1. Van Cromphaut SJ. Hyperglycaemia as part of the stress response: the underlying mechanisms. Best Pract Res Clin Anaesthesiol. 2009;23:375–386. doi: 10.1016/j.bpa.2009.08.005. - DOI - PubMed

Publication types