Glycemic Control in the ICU

       Steven Podnos MD
Hyperglycemia
• Occurs in up to 50% of ICU patients due to
  underlying DM , steroids, and/or stress of
  illness
• Is a MARKER of worse outcomes in many
  different ICU illnesses
Control of Glucose in ICU
• One early study (van den Berghe) found a
  decreased mortality with intensive control of
  glucose (IIT), but was limited to Cardiac
  Surgery patients , often on TPN
• Two large recent trials of IIT were stopped due
  to 1) lack of benefit with IIT and 2) increased
  hypoglycemia
Stress Hormones and Hyperglycemia
•   Glucagon,Glucocorticoids,Norepinephrine
•   Epinephrine
•   Tumor Necrosis factor
•   All these hormones are secreted with stress
    of illness and produce elevated glucose
    through various methods
Ill Effects of Hyperglycemia
• Direct Immune suppression
• Excess insulin causes cellular damage
• Direct cellular toxicity and release of
  inflammatory mediators in presence of
  hyperglycemia
Hypoglycemia
• Brain requires adequate glucose levels or
  coma/death results in minutes
Why is Consensus Changing?
• Early studies suggested benefit to Intensive
  Insulin Therapy (IIT)
• Later studies do not-some show harm from
  hypoglycemia and no mortality benefit
• Studies differ in many variables: SICU vs
  MICU, parenteral vs enteral nutrition, degree
  of illness (APACHE 2 scores), intensity of
  control
• More studies pending
Recommendations
• Current consensus seems to be liberalizing
  glucose control to 140-180.
• Evidence weak of benefit
• Some suggest it is swings in glucose levels that
  may be harmful rather than absolute levels.
• May be more appropriate to use constant
  insulin drip to keep levels higher than sliding
  scale which has more glucose fluctuations
  (unproven)

Glycemic control in_the_icu

  • 1.
    Glycemic Control inthe ICU Steven Podnos MD
  • 2.
    Hyperglycemia • Occurs inup to 50% of ICU patients due to underlying DM , steroids, and/or stress of illness • Is a MARKER of worse outcomes in many different ICU illnesses
  • 3.
    Control of Glucosein ICU • One early study (van den Berghe) found a decreased mortality with intensive control of glucose (IIT), but was limited to Cardiac Surgery patients , often on TPN • Two large recent trials of IIT were stopped due to 1) lack of benefit with IIT and 2) increased hypoglycemia
  • 4.
    Stress Hormones andHyperglycemia • Glucagon,Glucocorticoids,Norepinephrine • Epinephrine • Tumor Necrosis factor • All these hormones are secreted with stress of illness and produce elevated glucose through various methods
  • 5.
    Ill Effects ofHyperglycemia • Direct Immune suppression • Excess insulin causes cellular damage • Direct cellular toxicity and release of inflammatory mediators in presence of hyperglycemia
  • 6.
    Hypoglycemia • Brain requiresadequate glucose levels or coma/death results in minutes
  • 7.
    Why is ConsensusChanging? • Early studies suggested benefit to Intensive Insulin Therapy (IIT) • Later studies do not-some show harm from hypoglycemia and no mortality benefit • Studies differ in many variables: SICU vs MICU, parenteral vs enteral nutrition, degree of illness (APACHE 2 scores), intensity of control • More studies pending
  • 8.
    Recommendations • Current consensusseems to be liberalizing glucose control to 140-180. • Evidence weak of benefit • Some suggest it is swings in glucose levels that may be harmful rather than absolute levels. • May be more appropriate to use constant insulin drip to keep levels higher than sliding scale which has more glucose fluctuations (unproven)