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The impact of the severity of sepsis on the risk of hypoglycaemia and glycaemic variability
Critical Care volume 12, Article number: R129 (2008)
The purpose of this study was to assess the relation between glycaemic control and the severity of sepsis in a cohort of patients treated with intensive insulin therapy (IIT).
In a prospective, observational study, all patients in the intensive care unit (ICU) (n = 191) with sepsis, severe sepsis or septic shock were treated with IIT (target blood glucose (BG) level 80 to 140 mg/dl instead of strict normoglycaemia). BG values were analysed by calculating mean values, rate of BG values within different ranges, rate of patients experiencing BG values within different levels and standard deviation (SD) of BG values as an index of glycaemic variability.
The number of patients with hypoglycaemia and hyperglycaemia was highly dependent on the severity of sepsis (critical hypoglycaemia ≤ 40 mg/dl: sepsis: 2.1%, severe sepsis: 6.0%, septic shock: 11.5%, p = 0.1497; hyperglycaemia: >140 mg/dl: sepsis: 76.6%, severe sepsis: 88.0%, septic shock: 100%, p = 0.0006; >179 mg/dl: sepsis: 55.3%, severe sepsis: 73.5%, septic shock: 88.5%, p = 0.0005; >240 mg/dl: sepsis: 17.0%, severe sepsis: 48.2%, septic shock: 45.9%, p = 0.0011). Multivariate analyses showed a significant association of SD levels with critical hypoglycaemia especially for patients in septic shock (p = 0.0197). In addition, SD levels above 20 mg/dl were associated with a significantly higher mortality rate relative to those with SD levels below 20 mg/dl (24% versus 2.5%, p = 0.0195).
Patients with severe sepsis and septic shock who were given IIT had a high risk of hypoglycaemia and hyperglycaemia. Among these patients even with a higher target BG level, IIT mandates an increased awareness of the occurrence of critical hypoglycaemia, which is related to the severity of the septic episode.
Hyperglycaemia and insulin resistance are common in patients in the intensive care unit (ICU) and are associated with a substantial increase in mortality [1, 2]. Major causes of morbidity and death include severe infection, critical illness polyneuropathy and multi-organ failure . Intensive insulin therapy (IIT) aimed at achieving a blood glucose (BG) level between 80 and 110 mg/dl was shown to decrease morbidity (eg, reduced severe infections and organ failure) and mortality in adult surgical ICU patients . In medical ICU patients, the mortality rate was only decreased in the subgroup of patients that stayed in the ICU for three or more days .
Severe sepsis and septic shock are major causes of mortality in ICU patients [5, 6]. The impact and safety of IIT for these patients is controversial. The Surviving Sepsis Campaign Guidelines recommend a target BG level below 150 mg/dl . One of the most commonly mentioned and feared adverse effects of IIT is severe hypoglycaemia, which occurs significantly more often when using IIT compared with conventional insulin therapy [3, 4, 8]. The German multicentre Efficacy of Volume Substitution and Insulin Therapy in Severe Sepsis (VISEP) study of IIT for septic patients in multidisciplinary ICUs was prematurely stopped due to a higher risk of hypoglycaemia using IIT compared with conventional insulin therapy (17.0% versus 4.1%) .
Analysis of the actual BG levels of septic patients with target BG levels between 80 and 120 mg/dl revealed an increased risk of hypoglycaemia (BG levels < 80 mg/dl) . Recently, predisposing factors for hypoglycaemia in a mixed medical/surgical ICU population were identified; the risk factors include insulin use, sepsis, continuous renal replacement therapy (CRRT) with bicarbonate-based substitution fluid, diabetes, nutrition decrease without adjustment for insulin infusion and inotropic support [10, 11]. Previous studies have not differentiated between severe sepsis and septic shock, and they have used only the mean (morning) BG level per day as the parameter to evaluate BG dynamics. Therefore, it is unknown if the severity of sepsis is directly associated with a higher risk of hypoglycaemia and if analysis of the mean BG level per day is sufficient and appropriate for the analysis of BG dynamics.
The aim of this study was to analyse the quality of BG control using different parameters and the risk for critical hypoglycaemia (≤ 40 mg/dl) in patients with sepsis, severe sepsis and septic shock receiving IIT with a target BG level of 80 to 140 mg/dl. In addition, potential predisposing factors for hypoglycaemia were analysed.
Materials and methods
The 'closed' 42-bed ICU at the University hospital of Goettingen receives patients mainly from surgical departments, but also from medical and neurology units. Most patients are admitted because of cardiac, neurological, abdominal or trauma-related surgery. The nurse:patient ratio ranges from 1:2 to 1:3. The local ethics committee approved the study and waived patients' informed consent. Data collection began after an eight-week introduction period. All patients admitted from July to September 2004 or from November to December 2004 (n = 191) and who fulfilled the criteria of sepsis either on admission or at any time during their ICU stay were included in the study. They were sequentially treated with one of two different nurse-driven IIT protocols for four months. The assignment to a specific protocol depended on the date of admission. No randomisation was performed. The study design was strictly observational, and the members of our study group who performed data assessment were completely separate from the regular ICU staff.
Sepsis data assessment and analysis
The assessment of sepsis severity was retrospectively performed day by day according to the classification criteria set forth by the German Sepsis Society  by one investigator (RW) after a two-month training period. Septic patients were assigned to one of the following three categories after discharge from the ICU according to the most severe degree of sepsis observed during the entire ICU stay.
Sepsis was defined as the presence of two or more of the following systemic inflammatory response syndrome (SIRS) criteria associated with infection: tachycardia (≥ 90 beats/minute); tachypnoea (≥ 20 breaths/minute) or hyperventilation (pCO2 ≤ 4.3 kPa/≤ 33 mmHg); leucocytosis (≥ 12,000 cells/mm3), leucocytopenia (≤ 4000 cells/mm3) or normal white blood cell (WBC) count with 10% of more immature cells; and fever (core temperature ≥ 38.0°C) or hypothermia (core temperature ≤ 36.0°C) .
Severe sepsis was defined as secondary organ failure due to sepsis. Criteria for secondary organ failure were: acute encephalopathy, relative or absolute thrombocytopenia (≤ 100,000 platelets/mm3 or reduction of more than 30% within 24 hours), arterial hypoxaemia (PaO2 ≤ 10 kPa/≤ 75 mmHg on natural air or PaO2/FiO2 ≤ 33 kPa/≤ 250 mmHg), impaired renal function (urine output ≤ 0.5 ml/kg/hour or serum creatinine more than twice normal value) or metabolic acidosis (base excess ≤ -5 or hyperlactataemia more than 1.5 times normal value).
Septic shock was defined as persistent hypotension (systolic BP < 90 mmHg/mean BP < 65 mmHg) unresponsive to volume resuscitation with the need for vasopressor therapy .
The treatment of sepsis was carried out according to the guidelines of the Surviving Sepsis Campaign .
In addition, all patient data, including vital parameters and laboratory results, were collected in the electronic patient data management system (PDMS) of the ICU. Furthermore, parameters defining SIRS  and secondary organ failure, the assessment of infectious status, as well as Simplified Acute Physiology Score (SAPS) II  and Sepsis-Related Organ Failure Assessment (SOFA)  scores were prospectively collected on a daily basis and processed in an Access database, Office 2003, Microsoft, USA.
Intensive insulin therapy
The target BG level for both therapy protocols was 80 to 140 mg/dl. This higher range compared with the study protocol of Van den Berghe and colleagues [3, 4] and was chosen because of the concern for hypoglycaemia in a 'real life', non-study setting. Protocol 1 was a 'sliding scale' protocol with a combination of continuous insulin infusion (50 IU Actrapid in 50 ml of 0.9% sodium chloride using an infusion pump (Braun, Germany)) and an additional IV bolus application using a specified treatment algorithm based on the actual glucose value (additional file 1). Using a sliding scale, a predefined amount of insulin was given according to the range of the actual BG value .
Protocol 2 was a 'dynamic scale' protocol with continuous insulin infusion (without any bolus application) based on the protocol of Kanji and colleagues  (additional file 2). Using a dynamic scale, the dosage of the continuous insulin infusion was increased or decreased by an amount that was dependent on the range of the previous BG value compared with the actual BG level . It is important to note that the second protocol did not include a bolus insulin application and the rate of continuous insulin infusion was not limited.
In all patients, a balanced full electrolyte crystalloid solution containing 5% glucose (1 mg/kg/hour Sterofundin BG-5 (Braun, Germany)) was started on admission. Enteral or parenteral nutrition was started on day two after admission. Nutritional support was not further controlled by our study protocol; it was prescribed by the attending physicians. BG levels were measured predominantly in arterial blood on admission and at least every three hours thereafter (every 30 to 60 minutes in the case of hypoglycaemic values; if an arterial line was not in place, central venous blood was sampled) using an ABL 700 blood sample analyser (Radiometer Medical, Copenhagen).
Blood glucose level
The quality of BG control by IIT was evaluated measurement of the overall mean BG level; the morning BG level; the number of patients who had at least one BG value within indicated BG ranges (hypoglycaemia ≤ 40 mg/dl, 41 to 60 mg/dl, 61 to 79 mg/dl, normoglycaemia 80 to 40 mg/dl and hyperglycaemia 141 to 179 mg/dl, 180 to 239 mg/dl and ≥ 240 mg/dl); the number of critical hypoglycaemic episodes (≤ 40 mg/dl) and the rate of those episodes per 100 hours of IIT. In addition, the rate of BG values within different levels, which were divided into the indicated groups, and the median number of BG measurements obtained per day were analyed. As an index of glycaemic variability, we calculated the standard deviation (SD) of all BG values for each patient. The time to reach the BG target was defined as the interval from the first insulin application to the first BG value inside the target range. The incidence of critical hypoglycaemia (≤ 40 mg/dl) was compared during days with and without sepsis. In addition, the time interval from the previous BG measurement to the following critical hypoglycaemic episode itself and the time intervals between all BG measurements within the 24 hours before a hypoglycaemic episode were analysed. All analyses were performed separately for septic episodes; for the entire ICU stay; for each IIT protocol; and for the groups stratified by the severity of sepsis.
The duration of continuous insulin application, the duration of overall insulin therapy (interval from the first to the last insulin application), and the given insulin dose per day were compared.
Morbidity and mortality
In order to assess morbidity and mortality, the following factors were analysed: the rate of acute renal failure, rate of patients with CRRT (using primarily bicarbonate-based replacement fluids), frequency of readmission to the ICU during the same hospital admission, duration of the septic episode for the groups stratified by the severity of sepsis, length of mechanical ventilation, length of stay (LOS), and mean SAPS II and SOFA scores for each patient. In addition, 28-day, ICU and hospital mortality rates were analysed. Acute renal failure was defined as a creatinine level of more than twice the normal upper limit, an increase of creatinine to twice the value on admission, and/or acute oliguria for at least two hours (urine output < 0.5 ml/kg/hour). IIT seems to improve the mortality rates of patients with prolonged ICU stays [3, 4], so the 28-day and ICU mortality rates were analysed separately for patients with a LOS of more than three days and more than five days.
Predisposing factors for hypoglycaemia
We studied the following possible predisposing factors for critical hypoglycaemia (BG level ≤ 40 mg/dl): age, gender, type of admission (medical, scheduled surgery and unscheduled surgery), IIT protocol, SAPS II and SOFA scores on the first day of sepsis, history of diabetes, acute renal failure, CRRT, inotropic/vasopressor therapy, hydrocortisone therapy, LOS and duration of ventilation.
Pearson chi-squares 2 × 2 contingency table, Mann-Whitney U test and student's t-test (to compare parameters between the different treatment groups) or a chi-squares test, Kruskal–Wallis analysis of variance (ANOVA) and univariate ANOVA (to compare parameters within the different sepsis level groups) were used as appropriate. To define predisposing factors, chi-squared tests were used for categorical parameters and odds ratios (OR) and 95% confidence intervals (CI) were used for binary parameters. For single parameters, mean/SD or median/interquartile range (IQR) values are given. Multivariable logistic regression analyses were performed using advanced linear/nonlinear models.
We created a model to predict mortality, including rate of critical hypoglycaemia (≤40 mg/dl), median SD of BG levels for each patient, IIT protocol and a model to predict the occurrence of severe hypoglycaemia, including median SD of BG levels, severity of sepsis, IIT protocol, history of diabetes, CRRT, catecholamine therapy, mechanical ventilation, rate of critical hypoglycaemia and mortality. The significance level was set at p = 0.05. All analyses were performed using the Statistica 8.0 software (StatSoft Inc., USA).
Comparison of the severity of sepsis
Table 1 shows the baseline characteristics according to the severity of sepsis and table 2 shows the corresponding outcome parameters. The differentiation into the sepsis groups led to a significant distinction of outcome parameters.
The rate of patients with critical hypoglycaemia (≤ 40 mg/dl) tended to be higher in the group of patients who developed severe sepsis, especially septic shock, during septic episodes (sepsis: 2.1%, severe sepsis: 6.0%, septic shock: 11.5%, p = 0.1497, Figure 1); however, this association did not hold true when the entire ICU stay was analysed (sepsis: 12.8%, severe sepsis: 14.5%, septic shock: 13.1%, p = 0.9551). Figure 1 shows the percentage of patients who had at least one BG value within the indicated BG ranges across the different sepsis groups.
The rate of hyperglycaemic BG values was also higher for patients with severe sepsis and septic shock compared with patients with sepsis (rate of BG values > 140 mg/dl: sepsis: 30.8%, severe sepsis: 40.2%, septic shock: 41.9%, p < 0.0001). Figure 2 details the distribution of all measured BG values in the following categories: hypoglycaemia ≤ 40 mg/dl, 41 to 59 mg/dl, 60 to 79 mg/dl; normoglycaemia 80 to 99 mg/dl, 100 to 119 mg/dl, 120 to 140 mg/dl; and hyperglycaemia 141 to 179 mg/dl, 180 to 239 mg/dl, ≥ 240 mg/dl). The SD of all measured BG values for each patient was significantly higher for patients with severe sepsis relative to the other groups with sepsis and septic shock (SD median (IQR): sepsis: 29.5 mg/dl (19.2 to 35.9 mg/dl), severe sepsis: 38.5 mg/dl (26.0 to 52.1 mg/dl), septic shock: 31.1 mg/dl (25.2 to 46.9 mg/dl); p = 0.0090).
Table 3 shows the median number of BG measurements collected per day and the number of hypoglycaemic episodes. Patients with critical hypoglycaemia during sepsis also had a significantly higher risk of critical hypoglycaemia outside of septic episodes (hypoglycaemic patients during sepsis: 30.8% of patients with hypoglycaemia outside sepsis, non-hypoglycaemic patients during sepsis: 8.3% of patients with hypoglycaemia outside sepsis, p = 0.0323). Table 3 lists the different time intervals from BG measurements to each hypoglycaemic episode. Figure 3 details the mean BG levels measured per day.
Patients with septic shock had an increased duration of continuous and overall insulin therapy (duration of continuous therapy in median (IQR): sepsis: 83.4 hours (50.3 to 166.4 hours), severe sepsis: 101.1 hours (18.4 to 199.7 hours), septic shock: 217.6 hours (110.8 to 466.1 hours), p = 0.0001; duration of overall insulin therapy: sepsis: 134.0 hours (72.1 to 251.4 hours), severe sepsis: 184.3 hours (93.7 to 310.7 hours), septic shock: 320.2 hours (158.0 to 789.9 hours), p < 0.0001). Similarly, the median insulin dose per day applied over the entire ICU stay was higher for patients with septic shock (median (IQR) insulin dose per day: sepsis: 33.2 IU (22.7 to 47.6 IU), severe sepsis: 36.3 IU (21.4 to 48.7 IU), septic shock: 45.0 IU (34.6 to 68.9 IU), p = 0.0005).
Comparison of the two IIT protocols
No differences were observed when comparing baseline characteristics and outcome parameters, with the exception of age (median years; protocol 1: 67.0, protocol 2: 70.0, p = 0.0336) and gender (female; protocol 1: 41.0%, protocol 2: 27.5%, p = 0.0496). Table 4 shows further comparisons between the two protocols. Additional file 2 details the mean BG levels per day.
Figure 4 summarises ORs and CIs for the analysed predisposing factors of hypoglycaemia.
Multivariate logistic regression analyses
The SD of BG values was positively associated with critical hypoglycaemia regardless of the severity of sepsis (p = 0.0043). More specifically, the SD was significantly associated with critical hypoglycaemia only for patients with septic shock (p = 0.0197). Catecholamine therapy was not confirmed as a risk factor for critical hypoglycaemia (p = 0.2950). CRRT remained significant as a risk factor (p = 0.0476). Critical hypoglycaemia was not associated with mortality (p = 0.3211). An SD above 20 was associated with mortality (mortality rate; SD > 20 mg/dl: 24.0%, SD < 20 mg/dl: 2.5%; p = 0.0195). All patients with severe sepsis and septic shock who died had SD values above 20 mg/dl.
The risks and benefits of IIT are controversial. Major arguments are centred on the risk of hypoglycaemia in critically ill patients and the undefined impact on morbidity and mortality in different patient subgroups .
Our comparison of different sepsis levels revealed a tendency towards a higher rate of critical hypoglycaemia in patients with severe sepsis and septic shock (p = 0.1497) despite a higher upper target BG level compared with other studies. Interestingly, this effect was observed even though the median number of BG measurements per day was significantly higher for patients with septic shock. In addition, we observed a continuous increase in the rate of critical hypoglycaemia from patients with sepsis (lowest rate of hypoglycaemia) to severe sepsis to septic shock (highest rate of hypoglycaemia). This observation supports the hypothesis that, with an increased severity of illness, there is a corresponding increase in metabolic instability. Even though the increase was not significant, the occurrence of critical hypoglycaemia among 11.5% of patients with septic shock is quite high and deserves attention, especially as critical hypoglycaemia is independently associated with an increased risk of mortality .
In addition, a higher rate of critical hypoglycaemia among patients with severe sepsis and septic shock was reported by the results of the VISEP study from the German Sepsis Society . This multicentre trial, which compared conventional insulin therapy to IIT among septic patients, was stopped prematurely because of an increased risk of critical hypoglycaemic episodes among septic patients receiving IIT. This study did not differentiate by grade and combined patients with severe sepsis and septic shock. Compared with the VISEP trial, which was conducted in surgical as well as non-surgical ICUs, our study population differs with regard to reason for admission (percentage of non-surgical patients: VISEP 46.9% versus 17.0% among our patients). Moreover the study population varies because of the different inclusion criteria (VISEP study was severe sepsis/septic shock excluding sepsis with a lesser degree of severity; mean SOFA (95% CI): VISEP 7.8 (7.4 to 8.1) versus 7.3 (6.8 to 7.7) in our patients). Using IIT, 17% of patients with severe sepsis and septic shock developed critical hypoglycaemia compared with 4.1% in the conventional treatment group . The lower rate observed among our patients with either severe sepsis or septic shock (8.3%) was probably due to the higher target range utilised in our study (80 to 140 mg/dl; German Sepsis Society BG target range: 80 to 110 mg/dl). This finding was confirmed by the results of the Glucontrol trial, which compared two different target BG levels (72 to 110 mg/dl versus 141 to 180 mg/dl) for IIT in the ICU. This study was also stopped prematurely because of a higher rate of hypoglycaemia in the group randomised to the 72 to 110 mg/dl target range (publication in preparation) .
Other recent publications have demonstrated a higher risk of hypoglycaemia among septic patients irrespective of the severity of sepsis [11, 19]. In one of these studies  950 septic patients were analysed in a post hoc analysis of the surgical and medical patients from the two major Leuven studies [3, 4]. The effect of IIT on outcome in patients with sepsis and a prolonged LOS was similar to the effects observed in other patients .
The rate of hyperglycaemia was higher in patients with severe sepsis and septic shock compared with patients with sepsis, but the rate did not differ between the group of patients with severe sepsis and the one with septic shock, even though hydrocortisone replacement therapy (200 mg/24 hours) was performed in 57.4% of patients during septic shock compared with only 4.8% of patients with severe sepsis.
Most studies of IIT have restricted their analyses to mean (morning) BG levels [3, 4, 8, 20] and the rate of hypoglycaemic episodes [3, 4, 8]. Recently different studies evaluated other parameters than the mean BG level to analyse the changes of BG. They focused on glycaemic variability and its association with mortality in ICU patients showing that increasing glycaemic variability is a strong independent risk factor of mortality [21–24]. Among our patients the SD of all BG values for each patient, as an index of glycaemic variability, was significantly higher for patients with severe sepsis compared with patients with sepsis and septic shock. So no clear relation between SD and severity of sepsis was found. Further analyses showed a significant association with critical hypoglycaemia, especially for patients with septic shock. Interestingly SD levels above 20 mg/dl were associated with a significantly higher mortality rate relative to those with SD levels below 20 mg/dl (24.0% versus 2.5%).
In addition, all patients with severe sepsis and septic shock and a fatal outcome had SD levels above 20 mg/dl. So BG variability is highly associated with mortality as was also shown by the VISEP study . This data suggest a positive association of the severity of disease and the variability of BG levels. Other parameters for BG variability were evaluated. Another interesting approach was introduced by Van Herpe and colleagues with the glycaemic penalty index which analyses BG variability according to the severity of BG changes . Further studies with higher patient numbers are needed to evaluate the validity and reliability of different parameters for BG variability.
The following predisposing factors for hypoglycaemia were identified in this study using univariate analyses: diabetes, CRRT and inotropic combined with vasopressor therapy. In a multivariate model including several parameters, only CRRT was significantly associated with critical hypoglycaemia. Some of these predisposing factors were confirmed by other studies: diabetes, CRRT and haemodynamic shock [10, 11]. Consequently, the coexistence of predisposing factors, which are also influenced by the severity of sepsis, could increase the risk of critical hypoglycaemia among these patients.
Risk factors and outcomes of critical hypoglycaemia were recently evaluated in a retrospective analysis of 102 patients with BG levels below 40 mg/dl. In this study, even a single episode of critical hypoglycaemia was independently associated with an increased risk of mortality .
One major limitation of our study was lack of randomisation and the significantly different rate of patients with diabetes within the different sepsis groups. Another limitation of our study was its observational study design to evaluate the implementation of an IIT protocol under real ICU conditions without the influence of the members of the study group. Also, better control of BG values with dynamic scaled IIT may have been facilitated by a learning effect of the ICU staff during the study period. To minimise this effect, an eight-week introduction period for the sliding scale protocol was performed and strict treatment protocols were used. Additionally, we did not monitor the daily calorie intake. Finally, this study is underpowered to detect differences in morbidity or mortality. Therefore, further studies are needed to confirm our results with a randomised study protocol. Further research will permit analysis of additional parameters to evaluate BG profiles and BG variability, which will improve the quality of studies on IIT. In addition, identification of additional predisposing factors for hypoglycaemia, evaluation of the consequences of hypoglycaemia in ICU patients and determination of the effects of IIT on morbidity and mortality among these patients can be undertaken in further studies.
Patients with severe sepsis and septic shock treated with IIT have a high risk for hypoglycaemia and hyperglycaemia. Our results confirm those of other studies showing a higher risk of hypoglycaemia using IIT, even though we used a higher target range of 80 to 140 mg/dl. Therefore an increased awareness during IIT in patients with severe sepsis and septic shock is mandatory in order to enhance patient safety. A higher rate of BG measurements would be indicated in these patients but might be difficult to achieve outside controlled studies as long as continuous measurements are not available. Glycaemic variability, reflected by the SD of the mean BG level for each patient, was independently associated with both risk of severe hypoglycaemia and the risk of mortality.
The risks and benefits of IIT are controversial; more specifically the risk of hypoglycaemia and its undefined impact on morbidity and mortality in patients with severe sepsis and septic shock are debated.
Patients with severe sepsis and septic shock treated with IIT have a high incidence of critical hypoglycaemia, even with a higher target BG range of 80 and 140 mg/dl.
Glycaemic variability, reflected by the SD of the mean BG level for each patient, was independently associated with both the risk of severe hypoglycaemia and the risk of mortality.
Predisposing factors for critical hypoglycaemia were continuous renal therapy and combined inotropic and vasopressor therapy.
Increased awareness for critical hypoglycaemia during IIT of patients with severe sepsis and septic shock is mandatory in order to enhance patient safety.
analysis of variance
body mass index
continuous renal replacement therapy
Glasgow Coma Scale
intensive care unit
intensive insulin therapy
length of stay
patient data management system
Simplified Acute Physiology Score
systemic inflammatory response syndrome
Sepsis-Related Organ Failure Assessment
Efficacy of Volume Substitution and Insulin Therapy in Severe Sepsis
white blood cells.
Krinsley JS: Association between hyperglycemia and increased hospital mortality in a heterogeneous population of critically ill patients. Mayo Clin Proc 2003, 78: 1471-1478.
Lewis KS, Kane-Gill SL, Bobek MB, Dasta JF: Intensive insulin therapy for critically ill patients. Ann Pharmacother 2004, 38: 1243-1251. 10.1345/aph.1D211
Berghe G, Wouters P, Weekers F, Verwaest C, Bruyninckx F, Schetz M, Vlasselaers D, Ferdinande P, Lauwers P, Bouillon R: Intensive insulin therapy in the critically ill patients. New Engl J Med 2001, 345: 1359-1367. 10.1056/NEJMoa011300
Berghe G, Wilmer A, Hermans G, Meersseman W, Wouters PJ, Milants I, Van Wijngaerden E, Bobbaers H, Bouillon R: Intensive insulin therapy in the medical ICU. N Engl J Med 2006, 354: 449-461. 10.1056/NEJMoa052521
Russell JA: Management of sepsis. N Engl J Med 2006, 355: 1699-1713. 10.1056/NEJMra043632
Sablotzki A, Muhling J, Czeslick E: [Sepsis and multiple organ failure – update of current therapeutic concepts]. Anasthesiol Intensivmed Notfallmed Schmerzther 2005, 40: 511-520. 10.1055/s-2005-870104
Dellinger RP, Levy MM, Carlet JM, Bion J, Parker MM, Jaeschke R, Reinhart K, Angus DC, Brun-Buisson C, Beale R, Calandra T, Dhainaut JF, Gerlach H, Harvey M, Marini JJ, Marshall J, Ranieri M, Ramsay G, Sevransky J, Thompson BT, Townsend S, Vender JS, Zimmerman JL, Vincent JL: Surviving Sepsis Campaign: international guidelines for management of severe sepsis and septic shock: 2008. Crit Care Med 2008, 36: 296-327. 10.1097/CCM.0b013e31817d7ee4
Brunkhorst FM, Engel C, Bloos F, Meier-Hellmann A, Ragaller M, Weiler N, Moerer O, Gruendling M, Oppert M, Grond S, Olthoff D, Jaschinski U, John S, Rossaint R, Welte T, Schaefer M, Kern P, Kuhnt E, Kiehntopf M, Hartog C, Natanson C, Loeffler M, Reinhart K: Intensive insulin therapy and pentastarch resuscitation in severe sepsis. N Engl J Med 2008, 358: 125-139. 10.1056/NEJMoa070716
Clayton SB, Mazur JE, Condren S, Hermayer KL, Strange C: Evaluation of an intensive insulin protocol for septic patients in a medical intensive care unit. Crit Care Med 2006, 34: 2974-2978.
Krinsley JS, Grover A: Severe hypoglycemia in critically ill patients: risk factors and outcomes. Crit Care Med 2007, 35: 2262-2267.
Vriesendorp TM, van Santen S, DeVries JH, de Jonge E, Rosendaal FR, Schultz MJ, Hoekstra JB: Predisposing factors for hypoglycemia in the intensive care unit. Crit Care Med 2006, 34: 96-101. 10.1097/01.CCM.0000194536.89694.06
Reinhart K, Brunkhorst FM, Bone HG, Gerlach H, Grundling M, Kreymann G, Kujath P, Marggraf G, Mayer K, Meier-Hellmann A, Peckelsen C, Putensen C, Quintel M, Ragaller M, Rossaint R, Stüber F, Weiler N, Welte T, Werdan K: [Diagnosis and Therapy of Sepsis: Guidelines of the German Sepsis Society Inc. and the German Interdisciplinary Society for Intensive and Emergency Medicine.]. Internist (Berl) 2006, 47: 356-373. 10.1007/s00108-006-1595-x
American College of Chest Physicians/Society of Critical Care Medicine Consensus Conference: definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis Crit Care Med 1992, 20: 864-874.
Le Gall JR, Lemeshow S, Saulnier F: A new Simplified Acute Physiology Score (SAPS II) based on a European/North American multicenter study. JAMA 1993, 270: 2957-2963. 10.1001/jama.270.24.2957
Vincent JL, Moreno R, Takala J, Willatts S, De Mendonca A, Bruining H, Reinhart CK, Suter PM, Thijs LG: The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the Working Group on Sepsis-Related Problems of the European Society of Intensive Care Medicine. Intensive Care Med 1996, 22: 707-710. 10.1007/BF01709751
Meijering S, Corstjens AM, Tulleken JE, Meertens JH, Zijlstra JG, Ligtenberg JJ: Towards a feasible algorithm for tight glycaemic control in critically ill patients: a systematic review of the literature. Crit Care 2006, 10: R19. 10.1186/cc3981
Kanji S, Singh A, Tierney M, Meggison H, McIntyre L, Hebert PC: Standardization of intravenous insulin therapy improves the efficiency and safety of blood glucose control in critically ill adults. Intensive Care Med 2004, 30: 804-810. 10.1007/s00134-004-2252-2
Devos P, Preiser JC: Current controversies around tight glucose control in critically ill patients. Curr Opin Clin Nutr Metab Care 2007, 10: 206-209.
Van Cromphaut S, Wilmer A, Berghe G: Management of sepsis. N Engl J Med 2007, 356: 1179-1181.
Krinsley JS: Effect of an intensive glucose management protocol on the mortality of critically ill adult patients. Mayo Clin Proc 2004, 79: 992-1000.
Ali NA, O'Brien JM Jr, Dungan K, Phillips G, Marsh CB, Lemeshow S, Connors AF Jr, Preiser JC: Glucose variability and mortality in patients with sepsis. Crit Care Med 2008, 36: 2316-2321. 10.1097/CCM.0b013e318170f5ba
Dossett LA, Cao H, Mowery NT, Dortch MJ, Morris JM Jr, May AK: Blood glucose variability is associated with mortality in the surgical intensive care unit. Am Surg 2008, 74: 679-685. discission 685.
Egi M, Bellomo R, Stachowski E, French CJ, Hart G: Variability of blood glucose concentration and short-term mortality in critically ill patients. Anesthesiology 2006, 105: 244-252. 10.1097/00000542-200608000-00006
Krinsley JS: Glycemic variability: A strong independent predictor of mortality in critically ill patients. Crit Care Med 2008.
Van Herpe T, De Brabanter J, Beullens M, De Moor B, Berghe G: Glycemic penalty index for adequately assessing and comparing different blood glucose control algorithms. Critical Care 2008, 12: R24. 10.1186/cc6800
We would like to thank the physicians and nurses of the ICU for their compassionate efforts to put the different therapeutic approaches into daily practice, which made this study possible. In addition, we would like to thank Dr Thomas Renner for performing data extraction from our electronic PDMS.
The authors declare that they have no competing interests.
RW participated in the conception and design of the study, carried out the data collection and data analysis, and drafted the manuscript. OM participated in the conception and design of the study and drafting of the manuscript. RH performed the statistical analysis and participated in the drafting of the manuscript. PH participated in the programming data analysis. PN participated in the design of the study and drafting of the manuscript. MQ conceived the study, participated in its design, was involved in its coordination, and helped to draft and revise the manuscript.
Electronic supplementary material
Additional file 2: A pdf file containing a figure showing the mean BG level per day over the time for the two therapy protocols used. Each column represents the mean BG level of all patients at the first 28 days after admission. The numbers above the error bars indicate the number of patients involved. (PDF 47 KB)
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Waeschle, R.M., Moerer, O., Hilgers, R. et al. The impact of the severity of sepsis on the risk of hypoglycaemia and glycaemic variability. Crit Care 12, R129 (2008). https://doi.org/10.1186/cc7097
- Septic Shock
- Severe Sepsis
- Continuous Renal Replacement Therapy
- Simplify Acute Physiology Score
- Intensive Insulin Therapy