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LiMON in Intensive Care Medicine

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LiMON provides an easy, fast and non-invasive monitoring of liver and splanchnic perfusion. ... Optimize splanchnic inflow by - Optimizing cardiac preload ... – PowerPoint PPT presentation

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Title: LiMON in Intensive Care Medicine


1
LiMON in Intensive Care Medicine
2
Basics
  • The Plasma Disappearance Rate of ICG-PULSION
    (PDR) is influenced by liver function and liver
    perfusion.
  • Changes of ICG-PDR within a short period of time
    are reflecting liver respectively splanchnic
    perfusion, as the function of liver cells does
    not change rapidly.
  • LiMON provides an easy, fast and non-invasive
    monitoring of liver and splanchnic perfusion.

3
Scientific facts I
  • PDR as parameter of prognosis of survival
  • ICG-PDR is perfectly suited as parameter for
    prognosis of survival of surgical intensive care
    patients compared to the complex scores SAPS II
    and APACHE II.

Sakka S, Reinart K, Meier-Hellmann A Chest 122
(5), 1715-1720, 2002
4
Scientific facts II
  • PDR and mortality
  • 2/3 of surgical intensive care patients qualified
    for advanced hemodynamic monitoring exhibit
    reduced ICG-PDR values, accompanied with a
    significantly increased mortality.


  • PDR threshold value
  • An ICG-PDR ? 16 /min requires intervention.

Sakka S, Reinart K, Meier-Hellmann A Chest 122
(5), 1715-1720, 2002
5
Scientific facts III
  • PDR in septic shock
  • Patients in septic shock will not survive if a
    reduced ICG elimination can not be increased
    within the first 120 hours.

According to Kimura S, Yoshioka T, Shibuya M,
Sakano T, Tanaka R, Matsuyama S Crit Care Med 29
(6), 1159-1163, 2001
6
Scientific facts IV
  • Multi-Organ-Management
  • The combination of PiCCO and LiMON enables
    optimized volume therapy. In case of volume
    withdrawal due to increased lung water,
    splanchnic perfusion can be monitored and a
    cut-off point for volume withdrawal can be
    defined.

Sakka S, Meier-Hellmann A Int J Intensive Care 9
(2), 66-72, 2002
7
Recommendations for application in intensive care
  • ICG-PDR monitoring
  • In all critically ill patients at least once per
    day
  • In patients undergoing volume withdrawal or
    inotropic/vasoactive therapy a more frequent
    monitoring is recommended
  • Therapeutic recommendations (please refer to
    check list)
  • Reduction of hepatotoxic substances
  • Optimization of hemodynamics
  • Liver support therapy
  • ICG-PDR target value
  • ICG-PDR gt 16/min
  • Measurement site
  • Disposable sensor at the ear lobe
  • ICG dosage
  • 0.25 mg/kg body weight per measurement

8
LiMON Therapeutic check list
ICG-PDR ? 16 /min
RESULT
Optimize global hemodynamic situation
Reduce/stop hepatotoxic drugs
Liver support therapy
? Advanced hemodynamic monitoring (PiCCO
Technology) ? Optimize splanchnic inflow by -
Optimizing cardiac preload - Positive
inotropic or vasoactive drugs1
? Contact liver specialist
T H E R A P Y
? Treatment of alcoholic hepatitis3
? Optimize venous return by - Reduction of
intrathoracic pressure - Reduction of intra
abdominal pressure - Improvement of (right)
heart function2
? Install extracorporal support system (MARS)
ICG-PDR gt 16 /min
TARGET
1 dobutamine, phosphodiesterase III inhibitor,
prostaglandin 2 dobutamine, phosphodiesterase
III inhibitor, adrenaline, prostaglandin, NO
inhalation 3 steroids, pentoxyfylline
9
Conclusion
  • Routine monitoring of ICG-PDR (minimum once
    daily) may contribute to an early detection or
    prevention of reduced liver/splanchnic perfusion.
  • Previous studies demonstrated that ICG-PDR values
    ? 16/min are requiring intervention. Thus, a
    goal-directed therapy to achieve an ICG-PDR gt
    16/min is recommended.
  • An early detection and, if necessary, a
    goal-directed therapy of a reduced splanchnic
    perfusion contributes to a prevention of
    complications and therewith to cost reduction.

10
Appendix
  • ICG dosage
  • ICG-PDR can be measured accurately with a reduced
    ICG dosage of 0.25 mg/kg body weight.

Sakka S, Koeck H, Meier-Hellmann A Intensive
Care Med 30 (3) 506-509, 2004
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