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Seda Banu Akıncı
Hacettepe University Hospital
Department of Anesthesiology
Critical Care Medicine
 Why pharmaconutrition/ immunonutrition
 New mechanisms
 Interrelation of nutrients
 Immunometer
 Update for critically ill patients
 Glutamine
 Arginine
 Antioxidants
 Omega-3 fatty acids
 Burns
 Trauma
 Future
 Why pharmaconutrition/ immunonutrition
 New mechanisms
 Interrelation of nutrients
 Immunometer
 Update for critically ill patients
 Glutamine
 Arginine
 Antioxidants
 Omega-3 fatty acids
 Burns
 Trauma
 Future
Cerrahi
Travma
Şok
Omega-3 yağ
asitleri
Arjinin
Glutamin
Dolaşım
yetmezliği
Doku
hipoksisi
İnflamatuar
cevap
IL-6, TNF-α
Hücresel
immünitenin
ciddi
baskılanması
Makrofaj
Enfeksiyon
Sepsis MODS
Ölüm
Lenfosit
Antiinflamatuar
cevap
IL-10, TGF-β,
Angele MK, 2005
 Why pharmaconutrition/ immunonutrition
 New mechanisms
 Interrelation of nutrients
 Immunometer
 Update for critically ill patients
 Glutamine
 Arginine
 Antioxidants
 Omega-3 fatty acids
 Burns
 Trauma
 Future
Elderly/diabetics/ obese
Immunosupression in patients who die of sepsis
Cytokins 
 Inhibitory mediators
 Suppressor cells
Sepsis
MODS
Wischmeyer, 2010
 BW, BMI
 Albumin, transthyretin, white blood cells counts, C-
reactive protein
 Nutritional Risk Index (NRI)
 Prognostic Inflammatory and Nutritional Index (PINI)
 Modified Glasgow Prognostic Score (mGPS)
 Neutrophil-to-lymphocyte ratio (NLR)
 CD4 & CD8 lymphocytes counts
 platelet-to-lymphocyte ratio (PLR)
 Prognostic Index(PI)
 Prognostic Nutritional Index (PNI) are prognostic factors
of outcome, but are not always correlated to
 Why pharmaconutrition/ immunonutrition
 New mechanisms
 Interrelation of nutrients
 Immunometer
 Update for critically ill patients
 Glutamine
 Arginine
 Antioxidants
 Omega-3 fatty acids
 Burns
 Trauma
 Future
 1223 patients 40 ICUs
 MOF, MV
 Glutamine + antioxidants
 Glutamine 0.35 g /kg/İBW/d iv (0.50 g/kg/day dipeptid
alanyl-glutamine [Dipeptiven, Fresenius Kabi]
 42.5 g alanyl-glutamin + glycine-glutamin dipeptid (30
g/gün glutamin, enteral
 500 μg of selenium iv (Selenase, Biosyn)
 Enteral: 300 μg selenium, 20 mg Zinc, 10 mg beta
carotene, 500 mg vitamin E, 1500 mg vitamin C.
 iv+ enteral within 24 hours
 28 day mortality
 32.4% / 27.2%; adjusted odds ratio, 1.28, 95% CI
1.00-1.64)
 Hospital mortality
 37.2% / 31%; P=0.02
 6 month mortality
 43.7% / 37.2%; P=0.02
 301 patients 14 ICUs
 Within 48 hrs- 28 days (GLN+3+antioxidants)
 65 gr glutamine %60 (910 kcal 45gr protein)
 Eaa /arg deficiencyhyperamonemia
 Low pro Low S homosistine
 Is it adaptive?
 Too early?
 Harmfull when excessive?
 Caution in renal
insufficiency
 Why pharmaconutrition/ immunonutrition
 New mechanisms
 Interrelation of nutrients
 Immunometer
 Update for critically ill patients
 Glutamine
Arginine
 Antioxidants
 Omega-3 fatty acids
 Burns
 Trauma
 Future
 Citrulline substition
Better gastrointestinal tolerance
Better absorption
No hepatic elimination, does not
increase urea
NO does not increase
Cellular transport is not inhibited
 5 g/kg mortality in rats
 0.09-0.2 g/kg/d (PE-EN)
 ICU >12 g/L arg (>%4 REE)
(Bistrian 2006)
 >3 days, optimum 3-10 gün
(Bistrian 2006)
 Why pharmaconutrition/ immunonutrition
 New mechanisms
 Interrelation of nutrients
 Immunometer
 Update for critically ill patients
 Glutamine
 Arginine
 Antioxidants
 Omega-3 fatty acids
 Burns
 Trauma
 Future
Dose?
 No differene with
PE Glutamine
 Selenium 500/d
≥ 5 d PE decrease
infection without
a change in
mortality
 Why pharmaconutrition/ immunonutrition
 New mechanisms
 Interrelation of nutrients
 Immunometer
 Update for critically ill patients
 Glutamine
 Arginine
 Antioxidants
 Omega-3 fatty acids
 Burns
 Trauma
 Future
 No difference in mortality
 OMEGA study
 Study was terminated early
 N3 suplement increases 60
day mortality
(%26.6 X %16.3)
 Study is unique due to
 Infüsion X bolus
 High n6Xn9 X carbohydrates
 Lung protectice strategy
 Fluid restriction
 Why pharmaconutrition/ immunonutrition
 New mechanisms
 Interrelation of nutrients
 Immunometer
 Update for critically ill patients
 Glutamine
 Arginine
 Antioxidants
 Omega-3 fatty acids
 Burns
 Trauma
 Future
 4 RKÇ, 155 hasta
 Glutamine decreases LOS in burns
 Why pharmaconutrition/ immunonutrition
 New mechanisms
 Interrelation of nutrients
 Immunometer
 Update for critically ill patients
 Glutamine
 Arginine
 Antioxidants
 Omega-3 fatty acids
 Burns
Trauma
 Future
 0.5g/kg/BW/d dipeptid form iv
 5 day inefficient
 6. day GLN still low
 Worse prognosis if GLN 6. day levels are low
No neurologic deterioration
 Pharmaconutrition (drug, dose, route, duration)
 According to serum levels
 Adjustment for organ insufficiency
 Other aa, calori, protein ratios
 Management(calori, nitrogen, other parameters)
 Immunometer

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İmmun nutri̇syonda son duru mkısaing

  • 1. Seda Banu Akıncı Hacettepe University Hospital Department of Anesthesiology Critical Care Medicine
  • 2.  Why pharmaconutrition/ immunonutrition  New mechanisms  Interrelation of nutrients  Immunometer  Update for critically ill patients  Glutamine  Arginine  Antioxidants  Omega-3 fatty acids  Burns  Trauma  Future
  • 3.
  • 4.
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  • 6.  Why pharmaconutrition/ immunonutrition  New mechanisms  Interrelation of nutrients  Immunometer  Update for critically ill patients  Glutamine  Arginine  Antioxidants  Omega-3 fatty acids  Burns  Trauma  Future
  • 7.
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  • 11.  Why pharmaconutrition/ immunonutrition  New mechanisms  Interrelation of nutrients  Immunometer  Update for critically ill patients  Glutamine  Arginine  Antioxidants  Omega-3 fatty acids  Burns  Trauma  Future
  • 12. Elderly/diabetics/ obese Immunosupression in patients who die of sepsis Cytokins   Inhibitory mediators  Suppressor cells
  • 14.  BW, BMI  Albumin, transthyretin, white blood cells counts, C- reactive protein  Nutritional Risk Index (NRI)  Prognostic Inflammatory and Nutritional Index (PINI)  Modified Glasgow Prognostic Score (mGPS)  Neutrophil-to-lymphocyte ratio (NLR)  CD4 & CD8 lymphocytes counts  platelet-to-lymphocyte ratio (PLR)  Prognostic Index(PI)  Prognostic Nutritional Index (PNI) are prognostic factors of outcome, but are not always correlated to
  • 15.  Why pharmaconutrition/ immunonutrition  New mechanisms  Interrelation of nutrients  Immunometer  Update for critically ill patients  Glutamine  Arginine  Antioxidants  Omega-3 fatty acids  Burns  Trauma  Future
  • 16.  1223 patients 40 ICUs  MOF, MV  Glutamine + antioxidants  Glutamine 0.35 g /kg/İBW/d iv (0.50 g/kg/day dipeptid alanyl-glutamine [Dipeptiven, Fresenius Kabi]  42.5 g alanyl-glutamin + glycine-glutamin dipeptid (30 g/gün glutamin, enteral  500 μg of selenium iv (Selenase, Biosyn)  Enteral: 300 μg selenium, 20 mg Zinc, 10 mg beta carotene, 500 mg vitamin E, 1500 mg vitamin C.  iv+ enteral within 24 hours
  • 17.
  • 18.  28 day mortality  32.4% / 27.2%; adjusted odds ratio, 1.28, 95% CI 1.00-1.64)  Hospital mortality  37.2% / 31%; P=0.02  6 month mortality  43.7% / 37.2%; P=0.02
  • 19.
  • 20.  301 patients 14 ICUs  Within 48 hrs- 28 days (GLN+3+antioxidants)
  • 21.
  • 22.  65 gr glutamine %60 (910 kcal 45gr protein)  Eaa /arg deficiencyhyperamonemia  Low pro Low S homosistine
  • 23.
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  • 26.
  • 27.  Is it adaptive?  Too early?  Harmfull when excessive?
  • 28.  Caution in renal insufficiency
  • 29.
  • 30.  Why pharmaconutrition/ immunonutrition  New mechanisms  Interrelation of nutrients  Immunometer  Update for critically ill patients  Glutamine Arginine  Antioxidants  Omega-3 fatty acids  Burns  Trauma  Future
  • 31.  Citrulline substition Better gastrointestinal tolerance Better absorption No hepatic elimination, does not increase urea NO does not increase Cellular transport is not inhibited
  • 32.  5 g/kg mortality in rats  0.09-0.2 g/kg/d (PE-EN)  ICU >12 g/L arg (>%4 REE) (Bistrian 2006)  >3 days, optimum 3-10 gün (Bistrian 2006)
  • 33.
  • 34.  Why pharmaconutrition/ immunonutrition  New mechanisms  Interrelation of nutrients  Immunometer  Update for critically ill patients  Glutamine  Arginine  Antioxidants  Omega-3 fatty acids  Burns  Trauma  Future
  • 35. Dose?
  • 36.  No differene with PE Glutamine  Selenium 500/d ≥ 5 d PE decrease infection without a change in mortality
  • 37.
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  • 41.
  • 42.  Why pharmaconutrition/ immunonutrition  New mechanisms  Interrelation of nutrients  Immunometer  Update for critically ill patients  Glutamine  Arginine  Antioxidants  Omega-3 fatty acids  Burns  Trauma  Future
  • 43.
  • 44.
  • 45.  No difference in mortality
  • 47.  Study was terminated early
  • 48.  N3 suplement increases 60 day mortality (%26.6 X %16.3)  Study is unique due to  Infüsion X bolus  High n6Xn9 X carbohydrates  Lung protectice strategy  Fluid restriction
  • 49.  Why pharmaconutrition/ immunonutrition  New mechanisms  Interrelation of nutrients  Immunometer  Update for critically ill patients  Glutamine  Arginine  Antioxidants  Omega-3 fatty acids  Burns  Trauma  Future
  • 50.  4 RKÇ, 155 hasta
  • 51.
  • 52.  Glutamine decreases LOS in burns
  • 53.
  • 54.
  • 55.
  • 56.
  • 57.
  • 58.  Why pharmaconutrition/ immunonutrition  New mechanisms  Interrelation of nutrients  Immunometer  Update for critically ill patients  Glutamine  Arginine  Antioxidants  Omega-3 fatty acids  Burns Trauma  Future
  • 59.  0.5g/kg/BW/d dipeptid form iv  5 day inefficient  6. day GLN still low  Worse prognosis if GLN 6. day levels are low
  • 60.
  • 61.
  • 62.
  • 64.
  • 65.
  • 66.  Pharmaconutrition (drug, dose, route, duration)  According to serum levels  Adjustment for organ insufficiency  Other aa, calori, protein ratios  Management(calori, nitrogen, other parameters)  Immunometer