ACA App
Annals of Cardiac Anaesthesia Annals of Cardiac Anaesthesia Annals of Cardiac Anaesthesia
Home | About us | Editorial Board | Search | Ahead of print | Current Issue | Archives | Submission | Subscribe | Advertise | Contact | Login 
Users online: 1252 Small font size Default font size Increase font size Print this article Email this article Bookmark this page
 


 

 
     
    Advanced search
 

 
 
     
  
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Email Alert *
    Add to My List *
* Registration required (free)  


    References

 Article Access Statistics
    Viewed233    
    Printed5    
    Emailed0    
    PDF Downloaded39    
    Comments [Add]    

Recommend this journal

 


 
Table of Contents
COMMENTARY  
Year : 2018  |  Volume : 21  |  Issue : 2  |  Page : 173-174
A Commentary: effects on glargine insulin on glycemic control in patients with diabetes mellitus type II undergoing off-pump coronary artery bypass graft


Department of Anaesthesiology and Critical Care, Dr. Ram Manohar Lohia Institute of Medical Sciences, Lucknow, Uttar Pradesh, India

Click here for correspondence address and email

Date of Web Publication12-Apr-2018
 

How to cite this article:
Nath SS, Das PK. A Commentary: effects on glargine insulin on glycemic control in patients with diabetes mellitus type II undergoing off-pump coronary artery bypass graft. Ann Card Anaesth 2018;21:173-4

How to cite this URL:
Nath SS, Das PK. A Commentary: effects on glargine insulin on glycemic control in patients with diabetes mellitus type II undergoing off-pump coronary artery bypass graft. Ann Card Anaesth [serial online] 2018 [cited 2019 Dec 14];21:173-4. Available from: http://www.annals.in/text.asp?2018/21/2/173/229934




The association between perioperative hyperglycemia and adverse outcomes after cardiac surgery is well established.[1] At present, in most of the cardiac centers, perioperative blood glucose is managed by continuous intravenous insulin infusion (CIII). However, CIII is fraught with the risks of fluctuations of blood glucose levels and risks of hypoglycemia.

Insulin glargine (IG) is a long-acting analogue of human insulin available for clinical use for more than a decade. Evidence from clinical trials suggests that IG has a lower risk of hypoglycemia. Unlike traditional insulin preparations that are absorbed rapidly from the abdomen than from the arm or leg, the site of administration does not influence IG's unique absorption kinetics, even when the insulin is injected into a working limb.[2] The main role of basal insulin secretion is to limit hepatic glucose production and lipolysis in the fasting state, particularly overnight, without impairing glucose availability for brain function. IG was specifically designed to provide basal insulin requirement.[3] IG lowered plasma glucose by a relatively hepatospecific action with greater suppression of endogenous glucose production compared with little or no increase in glucose disposal.[4]

Before the study by Gandhi et al.,[5] there had been only one study reported in literature by Forouzzannia et al.[6] which compared the effects of continuous insulin infusion with or without subcutaneous (s.c.) IG on glycemic control in diabetic patients undergoing coronary artery bypass grafts (CABG). Although they mentioned that good control of intraoperative blood glucose entails maintaining blood glucose level below 200 mg/dl, they kept a target of blood glucose level between 120 and 180 mg/dl.[6] Lazar HL (2012) compared aggressive glycemic control (90–120 mg/dl) against moderate control (120–180 mg/dl) in 82 patients undergoing CABG surgeries. In this report, there was no difference in the incidence of adverse effects between groups.[7] Furthermore, hypoglycemic events were more frequent in the aggressive group. This report supports the conclusion of NICE-SUGAR [8] trial and suggests that moderate control (120–180 mg/dl) may provide an appropriate balance between preventing adverse outcomes associated with perioperative hyperglycemia and avoiding dangerous hypoglycemia. Although there is still no consensus as to the best intraoperative blood glucose levels to be maintained, in general, the literature suggests maintaining blood glucose levels between 150 and 180 mg/dl.[9] Moreover, a study discovered that intraoperative hyperglycemia (blood glucose level >200 mg/dl) as well as relative normoglycemia (blood glucose level <140 mg/dl) was found to be associated significant morbidity and mortality.[10] Further, it found that blood glucose levels ranging from 140 to 170 mg/dl were associated with lowest risk of adverse outcomes.[10] Hence, probably, to minimize risk of hypoglycemia, we may be little more liberal with the intraoperative blood sugar target range.

Forouzzannia et al. administered 15 U of IG in all patients irrespective of body weight, which is likely to be <0.3 U/kg (they have mentioned body mass index (BMI) of about 26 kg/m2 and not the weight).[6] Wang et al. examined the pharmacokinetic and pharmacodynamic dose-response effects of single (s.c.) injections of IG in obese type 2 diabetic individuals and observed that over a dose range of 0.5–2.0 units/kg, circulating plasma insulin levels increased modestly despite large (s.c.) IG doses.[4] Silinskie KM et al. compared the efficacy and safety of dosing IG by weight versus percentage of total daily insulin (TDI) in cardiac surgery patients transitioning from continuous insulin infusion to (s.c.) insulin. Patients received either 50% of their TDI requirement or 0.5 units/kg of glargine as a one-time dose, 2 h before stopping the continuous insulin infusion.[11] The percentage of blood glucose measurements in target range (80–140 mg/dl) was similar between the weight-based group and the percentage-based group. In this small cohort, dosing IG by weight at the dose of 0.5 U/kg proved to be safe.[11] We ought to remember that IG is supposed to deliver the basal insulin requirements and not the entire insulin requirement. We are of the opinion that for patients with normal BMI or till 30 kg/m2, IG dose of 0.3 U/kg and those who are overweight a dose of 0.5 U/kg may suffice for the basal insulin requirement.

In the study by Forouzzannia et al., patients undergoing both on-pump and off-pump CABGs were included.[6] However, the number of patients who underwent on-pump procedures was significantly more in the group who received only CIII (P = 0.031)! Hence, strictly speaking, the groups were not comparable. Moreover, significantly more patients in CIII group needed inotropic agents (P = 0.039)! On-pump CABGs are often associated with mild-to-moderate hypothermia and use of inotropes. Higher percentage of blood glucose levels above 200 mg/dl in CIII reported in the study could be attributed to hypothermia and/or use of inotropes. In the study by Gandhi et al., all patients underwent off-pump CABG, and they reported better perioperative glycemic control with significant reduction in postoperative morbidity.[5] Data regarding use of inotropes, an important piece of information, whenever we are dealing with blood glucose level, if presented, would have enhanced our understanding in a more clear manner.

To conclude, although the idea of (s.c.) IG seems novel, we ought to remember that this has been tried only in a small study. How the attributes of IG differ intraoperatively in CABG patients needs to be studied further and the dose of IG needs to be standardized before we embrace IG wholeheartedly for intraoperative control of blood glucose in patients undergoing CABG.



 
   References Top

1.
Reddy P, Duggar B, Butterworth J. Blood glucose management in the patient undergoing cardiac surgery: A review. World J Cardiol 2014;6:1209-17.  Back to cited text no. 1
    
2.
Powers CA, D'Alessio D. Endocrine pancreas and pharmacotherapy of diabetes mellitus and hypoglycemia. In: Bruntan L, Chamber B, Knollman B, editors. Goodman Gilman's The Pharmacological Basis of Therapeutics. 12th ed. New York: McGraw Hill Books; 2011. p. 1237-73.  Back to cited text no. 2
    
3.
Hilgenfeld R, Seipke G, Berchtold H, Owens DR. The evolution of insulin glargine and its continuing contribution to diabetes care. Drugs 2014;74:911-27.  Back to cited text no. 3
    
4.
Wang Z, Hedrington MS, Gogitidze Joy N, Briscoe VJ, Richardson MA, Younk L, et al. Dose-response effects of insulin Glargine in type 2 diabetes. Diabetes Care 2010;33:1555-60.  Back to cited text no. 4
    
5.
Gandhi H, Sarvaia A, Malhotra A, Acharya H, Shah K, Rajavat J. Effects of glargine insulin on glycemic control in patients with diabetes mellitus type II undergoing off pump coronary artery bypass graft. Ann Card Anaesth 2018;21:167-72.  Back to cited text no. 5
  [Full text]  
6.
Forouzzannia SK, Mohammadi SM, Mirhosseini SJ, Abdollahi MH, Mostaghion SH, Hosseini H, et al. Comparing effects of continuous insulin infusion with or without subcutaneous glargine insulin on glycemic control in diabetic patients undergoing coronary artery bypass graft. Iran J Diabet Obes 2009;1:5-10.  Back to cited text no. 6
    
7.
Lazar HL. Glycemic control during coronary artery bypass graft surgery. ISRN Cardiol 2012;2012:292490.  Back to cited text no. 7
    
8.
NICE-SUGAR Study Investigators, Finfer S, Chittock DR, Su SY, Blair D, Foster D, et al. Intensive versus conventional glucose control in critically ill patients. N Engl J Med 2009;360:1283-97.  Back to cited text no. 8
    
9.
Sudhakaran S, Surani SR. Guidelines for perioperative management of the diabetic patient. Surg Res Pract 2015;2015:284063.  Back to cited text no. 9
    
10.
Duncan AE, Abd-Elsayed A, Maheshwari A, Xu M, Soltesz E, Koch CG, et al. Role of intraoperative and postoperative blood glucose concentrations in predicting outcomes after cardiac surgery. Anesthesiology 2010;112:860-71.  Back to cited text no. 10
    
11.
Silinskie KM, Kirshner R, Hite MS. Converting continuous insulin infusion to subcutaneous insulin glargine after cardiac surgery using percentage-based versus weight-based dosing: A pilot trial. Ann Pharmacother 2013;47:20-8.  Back to cited text no. 11
    

Top
Correspondence Address:
Pravin Kumar Das
Dr. Ram Manohar Lohia Institute of Medical Sciences, Lucknow - 226 010, Uttar Pradesh
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/aca.ACA_213_17

Rights and Permissions




 

Top