ADMISSION HYPERGLYCEMIA IN CRITICALLY ILL PATIENTS WITH SEPSIS; HIGH IL6 AND ITS RELATION WITH OUTCOME

Document Type : Original Article

Authors

1 Departments of Internal Medicine, Faculty of Medicine, Al-Azhar University

2 Departments of Clinical Pathology, Faculty of Medicine, Al-Azhar University

Abstract

Background: Hyperglycemia has long been recognized as a common occurrence in critically ill patient, even without history of diabetes mellitus (D.M). Although there are few studies investigating the prevalence of stress hyperglycemia, one study reported that 38% of patients admitted to general hospitals had hyperglycemia episodes, 16% of which had no previous history of D.M.
Objective: To investigate the role of high IL6 in patients with sepsis admitted to medical I.C.U with acute hyperglycemia and its relation to 30 days outcome.
Patients and Methods: This study was conducted on 100 adult septic patients who were admitted to medical I.C.U at Al-Hussein University Hospital, the study was carried in the period between January 2018 and June 2019. 80 patients with evidence of hyperglycemia and 20 patients with euglycemic state.
Results: non-significant difference was found according to mean values of Na+, K+, creat, TLC, HB%, PLT, ALT, AST. On the other hand, the hyperglycemic group showed a significant increase regarding mean value of HbA1c compared to control group. The comparative study between the 2 groups revealed a significant increase of mean value of CRP in the hyperglycemic group compared to the control group. As regards the vital signs, the hyperglycemic group showed a significant increase in mean values of systolic blood pressure, diastolic blood pressure, MAP & HR compared to the control group. While there was no significant difference between the 2 groups regarding temperature and RR. This study showed statistically significant decrease in mean values of GCS in hyperglycemic group compared to control group, while APACHE II and qSOFA showed a significant increase in hyperglycemic group compared to control group. The mean values of ABG parameters revealed no statistically significant difference between the 2 groups. On the other hand, mean values of RBS and IL6 showed a statistically significant increase in hyperglycemic group compared to control group. The comparative study between the 2 groups showed a significant increase in mean values of hyperglycemic group compared to control group according to duration of ICU stay (days), Insulin therapy, AKI and Outcome  and non-significant difference according to ILD, CLD, CKD, stroke, pneumonia, IHD, COPD & HF.
Conclusion: Stress hyperglycemia with high IL6 is strongly associated with adverse outcomes in patients with sepsis who were admitted to the medical ICU. Sepsis patients with hyperglycemia showed increased incidence of mortality and AKI.

Keywords

Main Subjects


ADMISSION HYPERGLYCEMIA IN CRITICALLY ILL PATIENTS WITH SEPSIS; HIGH IL6 AND ITS RELATION WITH OUTCOME

By

Diaa A. Abd El-Monem, Gamal A. Badr, Farag k. Farag and Ashraf A. Ahmed*

Departments of Internal Medicine and Clinical Pathology*, Faculty of Medicine, Al-Azhar University

ABSTRACT

Background: Hyperglycemia has long been recognized as a common occurrence in critically ill patient, even without history of diabetes mellitus (D.M). Although there are few studies investigating the prevalence of stress hyperglycemia, one study reported that 38% of patients admitted to general hospitals had hyperglycemia episodes, 16% of which had no previous history of D.M.

Objective: To investigate the role of high IL6 in patients with sepsis admitted to medical I.C.U with acute hyperglycemia and its relation to 30 days outcome.

Patients and Methods: This study was conducted on 100 adult septic patients who were admitted to medical I.C.U at Al-Hussein University Hospital, the study was carried in the period between January 2018 and June 2019. 80 patients with evidence of hyperglycemia and 20 patients with euglycemic state.

Results: non-significant difference was found according to mean values of Na+, K+, creat, TLC, HB%, PLT, ALT, AST. On the other hand, the hyperglycemic group showed a significant increase regarding mean value of HbA1c compared to control group. The comparative study between the 2 groups revealed a significant increase of mean value of CRP in the hyperglycemic group compared to the control group. As regards the vital signs, the hyperglycemic group showed a significant increase in mean values of systolic blood pressure, diastolic blood pressure, MAP & HR compared to the control group. While there was no significant difference between the 2 groups regarding temperature and RR. This study showed statistically significant decrease in mean values of GCS in hyperglycemic group compared to control group, while APACHE II and qSOFA showed a significant increase in hyperglycemic group compared to control group. The mean values of ABG parameters revealed no statistically significant difference between the 2 groups. On the other hand, mean values of RBS and IL6 showed a statistically significant increase in hyperglycemic group compared to control group. The comparative study between the 2 groups showed a significant increase in mean values of hyperglycemic group compared to control group according to duration of ICU stay (days), Insulin therapy, AKI and Outcome  and non-significant difference according to ILD, CLD, CKD, stroke, pneumonia, IHD, COPD & HF.

Conclusion: Stress hyperglycemia with high IL6 is strongly associated with adverse outcomes in patients with sepsis who were admitted to the medical ICU. Sepsis patients with hyperglycemia showed increased incidence of mortality and AKI.

Key words: Hyperglycemia, sepsis, ICU, IL6.

 

 

INTRODUCTION

     Hyperglycemia has long been recognized as a common occurrence in critically ill patient, even without history of diabetes mellitus (D.M). Although there are few studies investigating the prevalence of stress hyperglycemia, one study reported that 38% of patients admitted to general hospitals had hyperglycemia episodes, 16% of which had no previous history of D.M (Fayed et al., 2015).

     Stress hyperglycemia is usually defined as nearly detected hyperglycemia > 200 mg/dl which resolve after resolution of acute illness. Two diagnostic categories of stress hyperglycemia have been reported: Hospital related hyperglycemia according to (ADA) consensus definition F.B.S ≥ 126 mg/dl or R.B.S ˃ 200 mg/dl without evidence of previous D.M. Pre-existing D.M with deterioration of pre-illness glycemic control (Pakhetra et al., 2016).

     Stress hyperglycemia is thought to be the body's adaptive response to stress on injury. However, recently it has been found that hyperglycemia in critically ill patients can pose a greater risk of mortality and morbidity. Furthermore, the evidence suggests that insulin therapy to control stress hyperglycemia can reduce mortality and improve overall patient outcome (Robba and Bilotta, 2016).

     Hospital related hyperglycemia results from activation of insulin counter regulatory hormones caused by stress. Glycemic control is further impaired by administration of drugs which increase insulin resistance such as catecholamines and steroids.

     Severe hyperglycemia is a catabolic state associated with adverse electrolytes and volume shifts. Mechanisms include high tissue and circulatory concentrations of inflammatory cytokines and reduction of glucose uptake capacity in peripheral tissues (Pakhetra et al., 2016).

     There is increased hepatic glucose production, depressed glycogenesis and glucose intolerance. Increased production of counter regulatory hormones lead to increased insulin resistance, thereby decreasing insulin action (Nakamura et al., 2012).

     TNF and IL6 have been shown to have a role in insulin resistance most likely via the modification of signaling properties of insulin receptor substrates.

     Insulin resistance ultimately promote a catabolic state leads to lipotoxins which further aggravate the inflammatory state especially in critical ill patients (Dellinger et al., 2013).

     The present work aimed to investigate the role of insulin resistance in patients with sepsis admitted to medical I.C.U with acute hyperglycemia and its relation to 30 days outcome.

PATIENTS AND METHODS

     This study was a prospective study, which was conducted on 100 adult sepsis patients who were admitted to medical I.C.U at Al-Hussein University Hospital, the study was carried in the period between January 2018 till June 2019.80 patients with evidence of hyperglycemia and 20 patients with euglycemic state. The study included patients ≥ 18 and < 65 years old; where patients receiving steroid therapy or/and already started steroid on admission.

     At enrollment, patients were subjected to the following: history taking and clinical examination, laboratory work-up, blood sugar level, C-peptide, IL6, Hb A1c, serum CRP, CBC, ABG, kidney function tests and liver function tests.

     The diagnosis of sepsis depended on the definition of a college of chest physician/ society of critical care medicine consensus conference (Chakraborty et al., 2020) by an identifiable site of infection and evidence of systemic inflammatory response.

     Admission hyperglycemia was defined as the first measurement of glucose within a time window of 4 hours before and up to 4 hours after admission. Blood glucose was categorized as: Euglycemia (70-140 mg/dl), mild hyperglycemia (141-199 mg/dl) and severe hyperglycemia ≥ 200 mg/dl (Pakhetra et al., 2016).

     Assessment of sepsis was done according to:

APACHE II score: (Park et al., 2010).

qSOFA score: (Raith et al., 2017).

IL6: Enzyme immunoassay for the quantitative determination of circulating IL6 concentrations in human serum (RIEDEL et al., 2005).

Statistical analysis:

     Recorded data were analyzed using the statistical package for social sciences, version 20.0 (SPSS Inc., Chicago, Illinois, USA). Quantitative data were expressed as mean± standard deviation (SD). Qualitative data were expressed as frequency and percentage. Independent-samples t-test of significance was used when comparing between two means mann whitney U test. Chi-square (x2) test of significance was used in order to compare proportions between qualitative parameters. The confidence interval was set to 95% and the margin of error accepted was set to 5%. So, the p-value was considered significant when : P-value ≤ 0.05.


 

 

 

 

 

 

 

 

 

 

 

 

 

RESULTS

 

 

     This prospective study enrolled 100 adult sepsis patients who were admitted to medical I.C.U. They were divided into control group of 20 cases with euglycemic state, and study group of 80 cases with hyperglycemic state. Statistically significant difference was found between groups according to demographic data and ABG, but showed statistically significant increase in mean of hyperglycemia group compared to control group according to CRP (Table 1).


 

Table (1):   Comparison between control group and hyperglycemic group according to demographic data, CRP and ABG

Groups

Demographic

data

Control Group
(n=20)

Hyperglycemic
Group (n=80)

p-value

Age (years)#

 

 

 

Mean±SD

54.45±9.93

53.33±8.61

0.615

Range

33-64

23-65

Sex†

 

 

 

Female

11 (55.0%)

32 (40.0%)

0.226

Male

9 (45.0%)

48 (60.0%)

C-reactive protein‡

 

170 (65)

45-309

 

150 (90)

6-395

0.037

Median (IQR)

Range

Arterial blood gases

63 (15)

43-90

65 (19)

16-99

0.651

PaO2 (mmhg)‡

Median (IQR)

Range

PH#

 

 

 

Mean±SD

7.37±0.10

7.28±0.18

0.034

Range

7.14-7.47

6.8-7.69

Paco2 (mmhg)‡

 

 

 

Median (IQR)

37 (11)

38 (22)

0.929

Range

16-55

12-188

HCO3 (meq/L)‡

 

 

 

Median (IQR)

23 (8)

21 (7)

0.245

Range

14.9-40

4.3-36

Using: #Independent Sample t-test; †Chi-square test; ‡Mann-Whitney test

 

 

     A statistically significant increase was found in mean of hyperglycemic group compared to control group according to HbA1c (Table 2).

 

 

 

 

 

 

 

 

 

Table (2):   Comparison between control group and hyperglycemic group according to lab. Chemistery

Groups

Lab chemistery

Control Group
(n=20)

Hyperglycemic
Group (n=80)

p-value

Na+ (meq/L)#

 

 

 

Mean±SD

137.45±9.81

138.21±5.87

0.66

Range

128-172

128-150

K+ (meq/L)#

 

 

 

Mean±SD

3.94±0.55

4.20±1.36

0.407

Range

3.1-5.2

2.7-9.9

Creatinine (mg/100m)‡

 

 

 

Median (IQR)

3 (2)

3 (3)

0.671

Range

0.6-6.9

0.5-13

Total leukocytic count (TLC) (cmm3)#

 

 

 

Mean±SD

17.36±3.79

17.12±4.96

0.841

Range

13.3-28

12-34.5

Hb A1c

 

 

 

Median (IQR)

5 (1.5)

7 (2)

0.002

Range

3.9-6.3

2.4-10.5

HB%‡

 

 

 

Median (IQR)

10 (4)

10 (3)

0.823

Range

2.2-15

3.7-17

Platelets (cmm3) ‡

 

 

 

Median (IQR)

225 (111)

224 (110)

0.853

Range

85-490

70-435

Alanine transaminase (ALT) (U/L)‡

 

 

 

Median (IQR)

77 (80)

62 (101)

0.594

Range

10-319

10-450

Aspartate transaminase (AST) (U/L)‡

 

 

 

Median (IQR)

90 (140)

81 (115)

0.417

Range

16-452

10-466

Using: #Independent Sample t-test; ‡Mann-Whitney test

 

 

     A statistically significant decrease was found in mean of hyperglycemic group compared to control group according to GCS, while APACHE II and qSOFA showed a statistically significant increase in hyperglycemic group compared to control group (Table 3).


 

 

 

 

 

 

 

 

 

 

Table (3):   Comparison between control group and hyperglycemic group according to scoring system

Groups

Scoring system

Control Group
(n=20)

Hyperglycemic
Group (n=80)

p-value

Glasgow Coma Score (GCS) #

 

 

 

Mean±SD

12.25±0.97

9.85±1.63

<.0001

Range

11-14

5-12

APACHE II#

 

 

 

Mean±SD

15.75±2.63

22.85±4.31

<.0001

Range

12-21

10-37

qSOFA#

 

 

 

Mean±SD

1.75±0.72

2.75±0.44

<.0001

Range

1-3

2-3

Using: #Independent Sample t-test

 

 

     There was a statistically significant increase in mean of hyperglycemic group compared to control group according to RBS and serum level of IL6 (Table 4).

 

 

Table (4):   Comparison between control group and hyperglycemic group according to RBS and IR

Groups

Variables

Control Group
(n=20)

Hyperglycemic
Group (n=80)

p-value

Random blood sugar (RBS) (g/dL) ‡

 

 

 

Median (IQR)

106 (16)

410 (115)

<0.001

Range

76-136

180-605

Serum level of  (IL6) ‡

 

 

 

Median (IQR)

0.06 (0.45)

1.3 (1.5)

<0.001

Range

0.0099-0.1

0.04-4.6

Using: #Independent Sample t-test; ‡Mann-Whitney test

 

 

     A statistically significant increase was found in mean of hyperglycemic group compared to control group according to duration of ICU stay (days), Insulin therapy, AKI and hypoglycemia and outcome (Table 5).

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Table (5):   Comparison between control group and hyperglycemic group according to outcome

Groups

Outcome†

Control Group
(n=20)

Hyperglycemic
Group (n=80)

p-value

Duration of ICU stay (days)#

 

 

 

Mean±SD

9.80±4.24

14.74±6.90

0.003

Range

1-21

6-67

Insulin therapy

2 (10.0%)

32 (40.0%)

0.023

Acute kidney injury (AKI)

0 (0%)

14 (17.5%)

0.039

Interstitial lung disease (ILD)

1 (5.0%)

15 (18.8%)

0.134

Chronic lung disease (CLD)

2 (10.0%)

19 (23.8%)

0.177

Chronic kidney disease (CKD)

4 (20.0%)

6 (7.5%)

0.096

Stroke

1 (5.0%)

5 (6.3%)

0.833

Pneumonia

2 (10.0%)

1 (1.3%)

0.04

Ischemic heart disease (IHD)

1 (5.0%)

9 (11.3%)

0.405

Chronic obstructive pulmonary

disease (COPD)

1 (5.0%)

9 (11.3%)

0.405

Heart failure (HF)

1 (5.0%)

0 (0.0%)

0.144

Outcome

 

 

 

Alive

19 (95.0%)

56 (70.0%)

0.021

Died

1 (5.0%)

24 (30.0%)

Normal

9 (45.0%)

2 (2.5%)

<0.001

Using: #Independent Sample t-test; †Chi-square test

 

 

DISCUSSION

     Hyperglycemia has long been recognized as a common occurrence in critically ill patient, even without history of D.M. Stress hyperglycemia is usually defined as nearly detected hyperglycemia> 200 mg/dl which resolve after resolution of acute illness (Fayed et al., 2015).

     This study demonstrated that there was no statistically significant difference between groups according to age and sex. On the other hand, the study group showed a significant increase regarding CRP compared to the control group. Dellinger et al. (2013) showed that inflammatory markers such as CRP have been related to the development of insulin resistance and type 2 diabetes (Sourris et al., 2012). Ford E. had also established that CRP levels are higher in people with diabetes and associated with increased HbA1c in people without diabetes.

     Dellinger et al. (2013) go a step further with the finding that among people with established diabetes, at successively higher levels of HbA1c the percent of people with CRP> 0.30 mg/dl is significantly higher. The mean implications of these findings are that inflammation may not only be implicated in the development of diabetes, but also in ongoing levels of hyperglycemia once diabetes is established.

     Jozwiak et al. (2011) found links between CRP and insulin resistance, other study has related hyperglycemia to inflammation by demonstrating simultaneous inflammation, endothelial dysfunction and insulin resistance at the physiologic level.

     In the current study, hemodynamic parameters, presence of risk factors and comorbid diseases, revealed those patients with hyperglycemia had lower SBP and DBP. These results were in agreement with Schmitz et al. (2012) who found that when the severity of disease increases in sepsis, the variability in the values of both SBP and DBP are increased. Also he found that APACHE II score was positively correlated with variability in the values of both SBP and DBP. This indicated that when APACHE II increased, blood pressure varied too.

     Also, the comparison between the two groups revealed that HR was higher in patients of the hyperglycemic group. These results agreed with Knaus et al. (2010) who concluded that, variability in HR was correlated with increased illness severity as calculated using APACHE II score.

     In agreement with Shigeki et al. (2013), our results illustrated that elevated temperature was not associated with an increase in disease severity or risk of mortality.

     According to RR and ABG, this study showed no significant difference between the two groups. These results were explained by Ganesh et al. (2016) who mentioned that in patients with sepsis and septic shock, high anion gap metabolic acidosis is the dominant blood gas anomaly in addition to lactate.

     This study also showed that patients with hyperglycemia had a significant lower GCS which may be explained by severity of sepsis in those patients. This was in agreeing with John and Bryan (2011) who proved that advanced sepsis can cause brain damage. Milder cases may recover without neurological problem; these cases may be related to the reversible mechanisms of what is called sepsis- associated encephalopathy (SAE), however more advanced cases of sepsis may have neuron- killing complications.

     In this study, data of disease severity which is represented by hemodynamic parameters, need of mechanical ventilation and vasoactive support were significantly worse in hyperglycemic group which was reflected also in worse APACHE II score. This was in agree with James (2010) who proved that sepsis ultimately leads to tissue injury and multi-organ dysfunction for example, circulatory shock and acute lung injury.

     The present study showed a significant increase in the level of plasma IL6 in the hyperglycemic patients compared to the control group this also what was proved by Nakamura et al. (2012) who made a study on 40 patients with sepsis admitted to ICU. In this study he noticed elevation in serum IL-6 level in SIRS/ sepsis patients and the levels were extremely high in patients with severe hyperglycaemia and severe septic shock Nakamura et al. (2012) concluded that measurement of serum Il-6 level is useful in evaluating the severity and in predicting the outcome of patients with sepsis Jozwiak et al. (2011).

     Our study showed statistically significant increase mean of hyperglycemia group compared to control group according duration of ICU stay. In support, Marik and Bellomo (2013) mentioned that the median duration of ICU and hospital length of stay was longer in patients with stress hyperglycemia. They added that severe stress hyperglycemia may be harmful due to its effects on serum osmolarity. In addition, severe hyperglycemia exceeds the renal threshold, resulting in an osmotic diuresis and volume depletion.

     In terms of AKI, this study reported a higher incidence in hyperglycemic patients. This was in agree with Wang et al. (2017) who explained that stress hyperglycemia can impair renal function by increased activation of NF-kappa B and oxidant levels with the stages of sepsis, which leads to a much higher incidence of AKI.

     Our study clarified that septic patients with hyperglycemia had a significant higher mortality rate. Several studies have demonstrated that sepsis is associated with the activation of inflammation and coagulation, and the activation of coagulation accounts for a large proportion of deaths. In addition, stress hyperglycemia is associated with abnormal coagulation and fibrinolysis to a certain extent Wang et al. (2017).

     Venot et al. (2015) showed higher mortality in hyperglycemic patients. The functions of leucocytes, especially polymorphonuclear leukocytes (PMN), are impaired by hyperglycemia. It was reported by several studies that membrane fluidity of PMN were significantly lower in hyperglycemic patients, resulting in the decrease of multiple functions, such as impaired migration, reduced phagocytosis, and intracellular killing capacity, as well as altered chemotaxis.

 

CONCLUSION

     The results of our study suggested that stress hyperglycemia with high IL6 is strongly associated with adverse outcomes in patients with sepsis who were admitted to the medical ICU. Septic patients with hyperglycemia showed increased incidence of mortality and AKI.

REFERENCES

  1. Dellinger RP, Levy MM and Rhodes A (2013): Surviving Sepsis Campaign: International Guidelines for Management of Severe Sepsis and Septic Shock. Crit Care Med., 41: 580-637.
  2. Fayed AM, El-sawy MM, Mahrous AA-E and Soliman ME (2015): IL-6 and ITS correlation to stress hyperglycemia in diabetic and non-diabetic critically ill septic patients intensive care mwdicine. Experimental, 3(1):304-307.
  3. Ganesh K, Sharma RN, Varghese J and Pillai MG. (2016): A profile of metabolic acidosis in patients with sepsis in an Intensive Care Unit setting. Int J Crit Illn Inj Sci., 6(4):178-181.
  4. James AR (2010): Management of Sepsis. N Engl J Med., 355:1699-1713.
  5. John X W and Bryan Y (2011): Sepsis-associated encephalopathy: Evolving concepts. Neurol J Southeast Asia, 8: 65–76.
  6. Jozwiak M, Persichini R and Monnet X. (2011): Management of Myocardial Dysfunction in Severe Sepsis. Semin Respir Crit Care Med., 32(2):206-214.
  7. Knaus WA, Draper EA and Wagner DP. (2010): APACHE II: a severity of disease classification system. Crit Care Med., 13(10):818-29.
  8. Marik PE and Bellomo R. (2013): Stress hyperglycemia: an essential survival response. Crit Care Med., 41(6): 93-4.
  9. Nakamura M, Oda S, sadhir T, Watanabe E, Abe R, Nakada T, Morita and Hirasawa H (2012): Correlation between high blood IL6 level, hyperglycemia and glucose control in sebtic patients. Critical Care, 16(58):1-9.

10. Pakhetra LCR, Grag CMK and Suryanarawana AMKM (2016): Management of hyperglycemia in critical illness: review of targets strategies. Med J Armed Forces India, 67(1): 53–57.

11. Park, S. K., Chun, H. J., Kim, D. W., Im, T. H., Hong, H. J., and Yi, H. J. (2010): Acute Physiology and Chronic Health Evaluation II and Simplified Acute Physiology Score II in predicting hospital mortality of neurosurgical intensive care unit patients. Journal of Korean medical science, 24(3), 420-426.‏

12. Raith, E. P., Udy, A. A., Bailey, M., McGloughlin, S., MacIsaac, C., Bellomo, R., and Pilcher, D. V. (2017): Prognostic accuracy of the SOFA score, SIRS criteria, and qSOFA score for in-hospital mortality among adults with suspected infection admitted to the intensive care unit. Jama, 317(3), 290-300.‏

13. RIEDEL, F., ZAISS, I., HERZOG, D., GÖTTE, K., NAIM, R., and HÖRMANN, K. (2005): Serum levels of interleukin-6 in patients with primary head and neck squamous cell carcinoma. Anticancer research, 25(4), 2761-2765.‏

14. Robba C and Bilotta F (2016): Admission hyperglycemia and outcome in ICU patients with sepsis.  J thorac Dis., 8(7):581-583.

15. Schmitz D, Kobbe P and Lendemanns S. (2012): Survival and cellular immune functions in septic mice treated with growth hormone (GH) and insulin-like growth factor-I (IGF-I). Growth Horm IGF Res., 18(3):245-52.

16. Shigeki K, Satoshi G and Daizoh S (2013): The impact of body temperature abnormalities on the disease severity and outcome in patients with severe sepsis: an analysis from a multicenter, prospective survey of severe sepsis. Critical Care, 17:271-75.

17. Sourris KC, Lyons JG and de Courten MP. (2012): c-Jun NH2-terminal kinase activity in subcutaneous adipose tissue but not nuclear factor-kappaB activity in peripheral blood mononuclear cells is an independent determinant of insulin resistance in healthy individuals. Diabetes, 58(6):1259-65.

18. Spindler MP, HO AM, Tridgell D, McCulloch-Oslon M, Gersuk V, NI C, Greenbaum C and Sanda S (2016): Acute hyperglycemia, IL6 expression in humans. Immunity, Inflammation and Disease, 4(1):91-97.

19. Venot M, Weis L, Clec'h C, Darmon M, Allaouchiche B, Goldgran-Tolédano D, Garrouste-Orgeas M, Adrie C, Timsit JF and Azoulay E. (2015): Acute kidney injury in severe sepsis and septic shock in patients with and without diabetes mellitus: A multicenter study. PLoS One, 10(5): 127-133.

20. Wang Z, Ren J, Wang G, Liu Q, Guo K and Li J (2017): Association Between Diabetes Mellitus and Outcomes of Patients with Sepsis: A Meta-Analysis. Med Sci Monit., 23: 3546-3555.

 

إرتفاع سکر الدم الحاد ومستوي الانترلوکين السادس في الحالات الحرجة لمرضى التسمم الدموى وعلاقته بالنتائج

ضياء عبد المنعم، جمال بدر، فرج فرج, أشرف أحمد*

قسمي الأمراض الباطنة والباثولوجيا الإکلينيکية*، کلية الطب جامعة الأزهر

خلفية البحث: فرط سکر الدم لفترة طويلة حدث شائع في المرضى المصابين بأمراض حرجة، حتى بدون تاريخ مرضى للإصابة بمرض السکر.

الهدف من البحث: التحقيق في دور الانترلوکين السادس في المرضى الذين يعانون من تسمم الدم المعترف بهم في وحدة العناية المرکزة الطبية مع ارتفاع السکر في الدم الحاد وعلاقته بنتيجة 30 يومًا.

المرضى وطرق البحث: أجريت هذه الدراسة على 100 مريض بالغ مصاب بتسمم الدم تم إدخالهم إلى وحدة العناية المرکزة الطبية، و80 مريضاً لديهم دليل على ارتفاع السکر في الدم و20 مريضاً يعانون من حالة سکر الدم.

نتائج البحث: هناک اختلاف غير ذي دلالة وفقًا لمتوسط القيم للصوديوم والبوتاسيوم والکرياتينين وعدد کرات الدم البيضاء والنسبة المئوية للهيموجلوبين وعدد الصفائح الدموية وإنزيمات الکبد. من ناحية أخرى، أظهرت مجموعة ارتفاع السکر في الدم زيادة کبيرة فيما يتعلق بالقيمة المتوسطة للهيموجلوبين السکرى مقارنة بالمجموعة الضابطة. کشفت الدراسة المقارنة بين المجموعتين زيادة کبيرة في متوسط القيمة للبروتين التفاعلي سى في مجموعة ارتفاع السکر في الدم مقارنة بالمجموعة الضابطة. فيما يتعلق بالعلامات الحيوية، أظهرت مجموعة فرط سکر الدم زيادة کبيرة في متوسط القيم لضغط الدم الانقباضي وضغط الدم الانبساطي ومتوسط الضغط الشريانى ومعدل نبض القلب مقارنة بالمجموعة الضابطة. بينما لم يکن هناک فرق کبير بين المجموعتين فيما يتعلق بدرجة الحرارة ومقاومة الإنسولين.

         وقد اظهرت هذه الدراسة انخفاضًا مهمًا إحصائيًا في متوسط القيم على مقياس جلاسکو للغيبوبة في مجموعة ارتفاع السکر في الدم مقارنة بالمجموعة الضابطة، في حين أظهرت الدرجات على مقياس وظائف الأعضاء الحادة و الصحة المزمنة ومقياس سريع لتقييم فشل الأعضاء المرتبط بتسمم الدم زيادة کبيرة في مجموعة ارتفاع السکر في الدم مقارنة بالمجموعة الضابطة. لم تکشف القيم المتوسطة لغازات الدم الشريانى عن فرق ذي دلالة إحصائية بين المجموعتين. من ناحية أخرى، أظهرت قيم متوسط مستوى السکر العشوائي بالدم ومستوي الانترلوکين السادس بالدم زيادة ذات دلالة إحصائية في مجموعة ارتفاع السکر في الدم مقارنة بالمجموعة الضابطة. أظهرت الدراسة المقارنة بين المجموعتين زيادة کبيرة في متوسط القيم لمجموعة ارتفاع السکر في الدم مقارنة بالمجموعة الضابطة وفقًا لمدة بقاء وحدة العناية المرکزة (أيام) والعلاج بالإنسولين والفشل الکلوى الحاد والنتائج وفرق غير مهم وفقًا لالتهاب رئوى خلوى مزمن  والأمراض الرئوية المزمنة وأمراض الکلى المزمنة والسکتة الدماغية والالتهاب الرئوي ومرض القلب الإقفاري وفشل عضلة القلب المزمن والانسداد الرئوي المزمن.

الاستنتاج: فرط سکر الدم مع ارتفاع مستوي الانترلوکين السادس بالدم يرتبطان بقوة بالنتائج السلبية في المرضى الذين يعانون من تسمم الدم الذين تم إدخالهم إلى وحدة العناية المرکزة الطبية. وأظهر مرضى تسمم الدم الذين يعانون من ارتفاع السکر في الدم زيادة في حدوث الوفيات وفشل کلوى حاد.

الکلمات الدالة : إرتفاع سکر الدم – التسمم الدموى – إنترليوکين 6- العناية المرکزة .

  1. REFERENCES

    1. Dellinger RP, Levy MM and Rhodes A (2013): Surviving Sepsis Campaign: International Guidelines for Management of Severe Sepsis and Septic Shock. Crit Care Med., 41: 580-637.
    2. Fayed AM, El-sawy MM, Mahrous AA-E and Soliman ME (2015): IL-6 and ITS correlation to stress hyperglycemia in diabetic and non-diabetic critically ill septic patients intensive care mwdicine. Experimental, 3(1):304-307.
    3. Ganesh K, Sharma RN, Varghese J and Pillai MG. (2016): A profile of metabolic acidosis in patients with sepsis in an Intensive Care Unit setting. Int J Crit Illn Inj Sci., 6(4):178-181.
    4. James AR (2010): Management of Sepsis. N Engl J Med., 355:1699-1713.
    5. John X W and Bryan Y (2011): Sepsis-associated encephalopathy: Evolving concepts. Neurol J Southeast Asia, 8: 65–76.
    6. Jozwiak M, Persichini R and Monnet X. (2011): Management of Myocardial Dysfunction in Severe Sepsis. Semin Respir Crit Care Med., 32(2):206-214.
    7. Knaus WA, Draper EA and Wagner DP. (2010): APACHE II: a severity of disease classification system. Crit Care Med., 13(10):818-29.
    8. Marik PE and Bellomo R. (2013): Stress hyperglycemia: an essential survival response. Crit Care Med., 41(6): 93-4.
    9. Nakamura M, Oda S, sadhir T, Watanabe E, Abe R, Nakada T, Morita and Hirasawa H (2012): Correlation between high blood IL6 level, hyperglycemia and glucose control in sebtic patients. Critical Care, 16(58):1-9.

    10. Pakhetra LCR, Grag CMK and Suryanarawana AMKM (2016): Management of hyperglycemia in critical illness: review of targets strategies. Med J Armed Forces India, 67(1): 53–57.

    11. Park, S. K., Chun, H. J., Kim, D. W., Im, T. H., Hong, H. J., and Yi, H. J. (2010): Acute Physiology and Chronic Health Evaluation II and Simplified Acute Physiology Score II in predicting hospital mortality of neurosurgical intensive care unit patients. Journal of Korean medical science, 24(3), 420-426.‏

    12. Raith, E. P., Udy, A. A., Bailey, M., McGloughlin, S., MacIsaac, C., Bellomo, R., and Pilcher, D. V. (2017): Prognostic accuracy of the SOFA score, SIRS criteria, and qSOFA score for in-hospital mortality among adults with suspected infection admitted to the intensive care unit. Jama, 317(3), 290-300.‏

    13. RIEDEL, F., ZAISS, I., HERZOG, D., GÖTTE, K., NAIM, R., and HÖRMANN, K. (2005): Serum levels of interleukin-6 in patients with primary head and neck squamous cell carcinoma. Anticancer research, 25(4), 2761-2765.‏

    14. Robba C and Bilotta F (2016): Admission hyperglycemia and outcome in ICU patients with sepsis.  J thorac Dis., 8(7):581-583.

    15. Schmitz D, Kobbe P and Lendemanns S. (2012): Survival and cellular immune functions in septic mice treated with growth hormone (GH) and insulin-like growth factor-I (IGF-I). Growth Horm IGF Res., 18(3):245-52.

    16. Shigeki K, Satoshi G and Daizoh S (2013): The impact of body temperature abnormalities on the disease severity and outcome in patients with severe sepsis: an analysis from a multicenter, prospective survey of severe sepsis. Critical Care, 17:271-75.

    17. Sourris KC, Lyons JG and de Courten MP. (2012): c-Jun NH2-terminal kinase activity in subcutaneous adipose tissue but not nuclear factor-kappaB activity in peripheral blood mononuclear cells is an independent determinant of insulin resistance in healthy individuals. Diabetes, 58(6):1259-65.

    18. Spindler MP, HO AM, Tridgell D, McCulloch-Oslon M, Gersuk V, NI C, Greenbaum C and Sanda S (2016): Acute hyperglycemia, IL6 expression in humans. Immunity, Inflammation and Disease, 4(1):91-97.

    19. Venot M, Weis L, Clec'h C, Darmon M, Allaouchiche B, Goldgran-Tolédano D, Garrouste-Orgeas M, Adrie C, Timsit JF and Azoulay E. (2015): Acute kidney injury in severe sepsis and septic shock in patients with and without diabetes mellitus: A multicenter study. PLoS One, 10(5): 127-133.

    20. Wang Z, Ren J, Wang G, Liu Q, Guo K and Li J (2017): Association Between Diabetes Mellitus and Outcomes of Patients with Sepsis: A Meta-Analysis. Med Sci Monit., 23: 3546-3555.