Nutrition in Intensive Care Richard Leonard St Mary’s Hospital, London
Slides and summary www.st-marys-anaesthesia.co.uk    ICU   Downloads
Resources www.evidencebased.net www.criticalcarenutrition.com   ACCEPT study Martin, CM et al CMAJ 2004;170:197-204 cluster RCT of nutrition algorithms intervention ICUs had lower mean hospital LOS 10% reduction in ICU mortality but p=0.1 no difference in attainment of most nutritional targets
Six simple questions Why do we feed ICU patients? Which patients should we feed? When should we start to feed them? Which route should we feed by? How much feed should we give? What should the feed contain?
Why feed ICU patients? few data directly compare feeding with no feeding – two trials and one meta-analysis suggest worse outcomes in un(der)fed patients catabolism of critical illness causes malnutrition malnutrition closely associated with poor outcomes many ICU patients are malnourished on admission
Aims of feeding ICU patients treat existing malnutrition minimise (but not prevent) the wasting of lean body mass that accompanies critical illness
Nutritional assessment important to identify existing malnutrition clinical evaluation is better than tests history weight loss, poor diet, reduced function examination loss of subcutaneous fat, muscle wasting, peripheral oedema, ascites
Which patients should we feed? which patients can safely be left to resume feeding themselves? 14 days’ starvation  -  dangerous depletion of lean body mass mortality rises in ICU patients with a second week of severe under-feeding 5 days without feed increases infections but not mortality one view is therefore that 5-7 days is the limit
Which patients should we feed? however ACCEPT study fed all patients not likely to eat within 24 hours one meta-analysis suggests reduced infections if patients are fed within 48 hours one meta-analysis of early TPN versus delayed EN found reduced mortality with early feeding
Which patients should we feed? all malnourished patients all patients who are unlikely to regain normal oral intake within either 2 or 5-7 days depending on your view
When should we start to feed? early feeding usually defined as starting within the first 48 hours of admission meta-analysis suggests reduced infections if patients are fed within 48 hours meta-analysis of early TPN versus delayed EN found reduced mortality with early feeding ACCEPT study aimed to start within 24 hours of ICU admission
When should we start to feed? surgical issues gastric, duodenal or high small bowel anastomoses critical mesenteric ischaemia
When should we start to feed? without undue delay once the patient is stable this will usually be within 48 hours of ICU admission
What route should we feed by? enteral feeding is claimed to be superior because it prevents gut mucosal atrophy  it reduces bacterial translocation and multi-organ failure lipid contained in TPN appears to be immuno-suppressive
Is enteral feeding really better? mucosal atrophy occurs far less in humans TPN is associated with increased gut permeability  bacterial translocation does occur in humans and may be associated with infections increased gut permeability never shown to cause translocation translocation has never been shown to be associated with multi-organ failure enteral nutrition has never been shown to prevent translocation
Outcome evidence does EN reduce infections? pancreatitis - probably abdominal trauma - probably (2 trials of 3) head injury - evenly balanced other conditions – no clear conclusion Lipman reviewed 31 trials and found no consistent effect meta-analysis by Heyland et al found reduced infections EN is definitely a risk factor for VAP
Outcome evidence does route of feeding affect mortality? Heyland’s meta-analysis showed no effect on mortality Doig and Simpson’s more robust meta-analysis found TPN reduced mortality when TPN and EN were directly compared; TPN versus early EN showed no difference
What route should we feed by? enteral feeding is cheaper easier and therefore preferable in most cases parenteral feeding is obviously necessary in some
A pragmatic approach Woodcock and MacFie Nutrition 2001 serious doubt about viability of enteral feeding within 7 days randomised to EN or TPN EN group no reduction in infections higher incidence of under-feeding and feed-related complications
What route should we feed by? EN preferred for majority on pragmatic grounds alone TPN obviously necessary for some if there is serious doubt that EN can be established in a reasonable time (ACCEPT study used 1 day; others would use 2 or 5 or 7…) commence TPN maintain at least minimal EN  keep trying to establish EN
Enteral feeding underfeeding is a serious problem NJ tubes  probably do not reduce VAP probably increase proportion of target delivered prokinetic agents of unproven efficacy PEGs are not advisable in acutely ill patients
Diarrhoea use fibre-containing feed avoid drugs containing sorbitol and Mg exclude and treat  Clostridium difficile  infection faecal impaction consider malabsorption (pancreatic enzymes, elemental feed) lactose intolerance (lactose-free feed) using loperamide
TPN - complications catheter-related sepsis no benefit from single lumen catheters hyperchloraemic metabolic acidosis electrolyte imbalance - low Pi, K, Mg refeeding syndrome abnormal LFTs rebound hypoglycaemia on cessation deficiency of thiamine, vit K, folate
How much feed should we give? overfeeding is useless - upper limit to amounts of protein and energy that can be used dangerous hyperglycaemia and increased infection uraemia hypercarbia and failure to wean hyperlipidaemia hepatic steatosis
 
How much should we feed? underfeeding is also associated with malnutrition and worse outcomes
How much feed should we give? energy - 25 kCal/kg/day (ACCP) indirect calorimetry gold standard no evidence of benefit shows that other methods are inaccurate, especially as patients wean equations eg Schofield correct for disease, activity
How much feed should we give? nitrogen no benefit from measuring nitrogen balance nitrogen 0.15-0.2 g/kg/day protein 1-1.25 g/kg/day severely hypercatabolic patients (eg burns) may receive up to 0.3 g nitrogen/kg/day
What should the feed contain? carbohydrate EN: oligo- and polysaccharides PN: concentrated glucose lipid EN: long and medium chain triglycerides PN: soya bean oil, glycerol, egg phosphatides nitrogen EN: intact proteins PN: crystalline amino acid solutions water and electrolytes micronutrients
Nutrition in acute renal failure essentially normal CVVHD/F has meant fluid and protein restriction are no longer necessary or appropriate
Nutrition and liver disease chronic liver disease energy  requirement normal  lipolysis  increased so risk of hypertriglyceridaemia protein  restriction not normally needed, but in chronic encephalopathy intake should be built up from 0.5 g protein/kg/day BCAA -enriched feed may permit normal intake in the protein-intolerant acute liver failure gluconeogenesis  impaired, so hypoglycaemia a risk
Nutrition in respiratory failure avoid overfeeding at all costs energy given as 50% lipid may reduce PaCO 2  and improve weaning, but unproven
Nutrition in acute pancreatitis transpyloric feeding  shown to be safe reduce infection rate probably reduce mortality malabsorption  may require elemental feeds and pancreatic enzyme supplements TPN  no longer standard therapy - however, some patients do not tolerate enteral feeding
What else should the feed contain? glutamine? selenium? immunonutrition?
Glutamine primary fuel for enterocytes, lymphocytes and neutrophils; also involved in signal transduction and gene expression massive release from skeletal muscle during critical illness may then become ‘conditionally essential’ is not contained in most TPN preparations
Enteral glutamine reduces villus atrophy in animals and humans reduced pneumonia and bacteraemia in two studies - multiple trauma, sepsis one much larger study (unselected ICU patients) showed no effect difficult to give adequate dose enterally probably not worth it
Parenteral glutamine Liverpool study in ICU showed reduction in late mortality London study of all hospital TPN patients showed no benefit French trauma study showed reduced infection but no mortality effect German ICU study improved late survivial in patients fed for more than 9 days
Parenteral glutamine glutamine becomes conditionally essential in critical illness and is not given in standard TPN parenteral supplementation appears to be beneficial in patients requiring TPN for many days
Selenium regulates free-radical scavenging systems low levels common in normals and ICU patients several small studies inconclusive but suggest benefit one large, flawed recent study showed non-significant mortality benefit watch this space…
Immunonutrition omega-3 fatty acids produce less inflammatory eicosanoids arginine nitric oxide precursor enhances cell-mediated immunity in animals nucleotides DNA/RNA precursors deficiency suppresses cell-mediated immunity
Immunonutrition few studies in ICU populations some found reduced infection in elective surgery one unblinded study has shown reduced mortality in unselected ICU patients; benefit in least ill (CCM 2000; 28:643) another showed increased mortality on re-analysis which barely failed to reach statistical significance (CCM 1995; 23:436)
Immunonutrition first meta-analysis (Ann Surg 1999; 229: 467) no effect on pneumonia reduced other infections and length of hospital stay increased mortality only just missing statistical significance did not censor for death second meta-analysis (CCM 1999; 27:2799) reduced infection reduced length of ventilation and hospital stay no effect on mortality
Immunonutrition third meta-analysis (JAMA 2001; 286:944) benefit in elective surgery increased mortality in ICU patients with sepsis large Italian RCT (ICM 2003; 29:834) compared enteral immunonutrition with TPN stopped early because interim analysis showed increased mortality in septic patients 44.4% vs 14.3%; p=0.039
Immunonutrition arbitrary doses random mixture of agents mutually antagonistic effects diverse case mix individual components need proper evaluation
Why do we feed ICU patients? to treat existing malnutrition to minimise the wasting of lean body mass that accompanies critical illness
Which patients should we feed? all malnourished patients all patients who are unlikely to regain normal oral intake within 2 days
When should we start to feed? without undue delay once the patient is stable within 2 days
What route should we feed by? EN preferred for majority on pragmatic grounds alone TPN obviously necessary for some if there is serious doubt that EN can be established in 2 (or 5, 7…) days commence TPN maintain at least minimal EN  keep trying to establish EN
How much feed should we give? 25 kCal/kg/day equations indirect calorimetry
What should the feed contain? carbohydrate lipid nitrogen water and electrolytes micronutrients

Nutrition in Intensive Care

  • 1.
    Nutrition in IntensiveCare Richard Leonard St Mary’s Hospital, London
  • 2.
    Slides and summarywww.st-marys-anaesthesia.co.uk  ICU  Downloads
  • 3.
    Resources www.evidencebased.net www.criticalcarenutrition.com ACCEPT study Martin, CM et al CMAJ 2004;170:197-204 cluster RCT of nutrition algorithms intervention ICUs had lower mean hospital LOS 10% reduction in ICU mortality but p=0.1 no difference in attainment of most nutritional targets
  • 4.
    Six simple questionsWhy do we feed ICU patients? Which patients should we feed? When should we start to feed them? Which route should we feed by? How much feed should we give? What should the feed contain?
  • 5.
    Why feed ICUpatients? few data directly compare feeding with no feeding – two trials and one meta-analysis suggest worse outcomes in un(der)fed patients catabolism of critical illness causes malnutrition malnutrition closely associated with poor outcomes many ICU patients are malnourished on admission
  • 6.
    Aims of feedingICU patients treat existing malnutrition minimise (but not prevent) the wasting of lean body mass that accompanies critical illness
  • 7.
    Nutritional assessment importantto identify existing malnutrition clinical evaluation is better than tests history weight loss, poor diet, reduced function examination loss of subcutaneous fat, muscle wasting, peripheral oedema, ascites
  • 8.
    Which patients shouldwe feed? which patients can safely be left to resume feeding themselves? 14 days’ starvation - dangerous depletion of lean body mass mortality rises in ICU patients with a second week of severe under-feeding 5 days without feed increases infections but not mortality one view is therefore that 5-7 days is the limit
  • 9.
    Which patients shouldwe feed? however ACCEPT study fed all patients not likely to eat within 24 hours one meta-analysis suggests reduced infections if patients are fed within 48 hours one meta-analysis of early TPN versus delayed EN found reduced mortality with early feeding
  • 10.
    Which patients shouldwe feed? all malnourished patients all patients who are unlikely to regain normal oral intake within either 2 or 5-7 days depending on your view
  • 11.
    When should westart to feed? early feeding usually defined as starting within the first 48 hours of admission meta-analysis suggests reduced infections if patients are fed within 48 hours meta-analysis of early TPN versus delayed EN found reduced mortality with early feeding ACCEPT study aimed to start within 24 hours of ICU admission
  • 12.
    When should westart to feed? surgical issues gastric, duodenal or high small bowel anastomoses critical mesenteric ischaemia
  • 13.
    When should westart to feed? without undue delay once the patient is stable this will usually be within 48 hours of ICU admission
  • 14.
    What route shouldwe feed by? enteral feeding is claimed to be superior because it prevents gut mucosal atrophy it reduces bacterial translocation and multi-organ failure lipid contained in TPN appears to be immuno-suppressive
  • 15.
    Is enteral feedingreally better? mucosal atrophy occurs far less in humans TPN is associated with increased gut permeability bacterial translocation does occur in humans and may be associated with infections increased gut permeability never shown to cause translocation translocation has never been shown to be associated with multi-organ failure enteral nutrition has never been shown to prevent translocation
  • 16.
    Outcome evidence doesEN reduce infections? pancreatitis - probably abdominal trauma - probably (2 trials of 3) head injury - evenly balanced other conditions – no clear conclusion Lipman reviewed 31 trials and found no consistent effect meta-analysis by Heyland et al found reduced infections EN is definitely a risk factor for VAP
  • 17.
    Outcome evidence doesroute of feeding affect mortality? Heyland’s meta-analysis showed no effect on mortality Doig and Simpson’s more robust meta-analysis found TPN reduced mortality when TPN and EN were directly compared; TPN versus early EN showed no difference
  • 18.
    What route shouldwe feed by? enteral feeding is cheaper easier and therefore preferable in most cases parenteral feeding is obviously necessary in some
  • 19.
    A pragmatic approachWoodcock and MacFie Nutrition 2001 serious doubt about viability of enteral feeding within 7 days randomised to EN or TPN EN group no reduction in infections higher incidence of under-feeding and feed-related complications
  • 20.
    What route shouldwe feed by? EN preferred for majority on pragmatic grounds alone TPN obviously necessary for some if there is serious doubt that EN can be established in a reasonable time (ACCEPT study used 1 day; others would use 2 or 5 or 7…) commence TPN maintain at least minimal EN keep trying to establish EN
  • 21.
    Enteral feeding underfeedingis a serious problem NJ tubes probably do not reduce VAP probably increase proportion of target delivered prokinetic agents of unproven efficacy PEGs are not advisable in acutely ill patients
  • 22.
    Diarrhoea use fibre-containingfeed avoid drugs containing sorbitol and Mg exclude and treat Clostridium difficile infection faecal impaction consider malabsorption (pancreatic enzymes, elemental feed) lactose intolerance (lactose-free feed) using loperamide
  • 23.
    TPN - complicationscatheter-related sepsis no benefit from single lumen catheters hyperchloraemic metabolic acidosis electrolyte imbalance - low Pi, K, Mg refeeding syndrome abnormal LFTs rebound hypoglycaemia on cessation deficiency of thiamine, vit K, folate
  • 24.
    How much feedshould we give? overfeeding is useless - upper limit to amounts of protein and energy that can be used dangerous hyperglycaemia and increased infection uraemia hypercarbia and failure to wean hyperlipidaemia hepatic steatosis
  • 25.
  • 26.
    How much shouldwe feed? underfeeding is also associated with malnutrition and worse outcomes
  • 27.
    How much feedshould we give? energy - 25 kCal/kg/day (ACCP) indirect calorimetry gold standard no evidence of benefit shows that other methods are inaccurate, especially as patients wean equations eg Schofield correct for disease, activity
  • 28.
    How much feedshould we give? nitrogen no benefit from measuring nitrogen balance nitrogen 0.15-0.2 g/kg/day protein 1-1.25 g/kg/day severely hypercatabolic patients (eg burns) may receive up to 0.3 g nitrogen/kg/day
  • 29.
    What should thefeed contain? carbohydrate EN: oligo- and polysaccharides PN: concentrated glucose lipid EN: long and medium chain triglycerides PN: soya bean oil, glycerol, egg phosphatides nitrogen EN: intact proteins PN: crystalline amino acid solutions water and electrolytes micronutrients
  • 30.
    Nutrition in acuterenal failure essentially normal CVVHD/F has meant fluid and protein restriction are no longer necessary or appropriate
  • 31.
    Nutrition and liverdisease chronic liver disease energy requirement normal lipolysis increased so risk of hypertriglyceridaemia protein restriction not normally needed, but in chronic encephalopathy intake should be built up from 0.5 g protein/kg/day BCAA -enriched feed may permit normal intake in the protein-intolerant acute liver failure gluconeogenesis impaired, so hypoglycaemia a risk
  • 32.
    Nutrition in respiratoryfailure avoid overfeeding at all costs energy given as 50% lipid may reduce PaCO 2 and improve weaning, but unproven
  • 33.
    Nutrition in acutepancreatitis transpyloric feeding shown to be safe reduce infection rate probably reduce mortality malabsorption may require elemental feeds and pancreatic enzyme supplements TPN no longer standard therapy - however, some patients do not tolerate enteral feeding
  • 34.
    What else shouldthe feed contain? glutamine? selenium? immunonutrition?
  • 35.
    Glutamine primary fuelfor enterocytes, lymphocytes and neutrophils; also involved in signal transduction and gene expression massive release from skeletal muscle during critical illness may then become ‘conditionally essential’ is not contained in most TPN preparations
  • 36.
    Enteral glutamine reducesvillus atrophy in animals and humans reduced pneumonia and bacteraemia in two studies - multiple trauma, sepsis one much larger study (unselected ICU patients) showed no effect difficult to give adequate dose enterally probably not worth it
  • 37.
    Parenteral glutamine Liverpoolstudy in ICU showed reduction in late mortality London study of all hospital TPN patients showed no benefit French trauma study showed reduced infection but no mortality effect German ICU study improved late survivial in patients fed for more than 9 days
  • 38.
    Parenteral glutamine glutaminebecomes conditionally essential in critical illness and is not given in standard TPN parenteral supplementation appears to be beneficial in patients requiring TPN for many days
  • 39.
    Selenium regulates free-radicalscavenging systems low levels common in normals and ICU patients several small studies inconclusive but suggest benefit one large, flawed recent study showed non-significant mortality benefit watch this space…
  • 40.
    Immunonutrition omega-3 fattyacids produce less inflammatory eicosanoids arginine nitric oxide precursor enhances cell-mediated immunity in animals nucleotides DNA/RNA precursors deficiency suppresses cell-mediated immunity
  • 41.
    Immunonutrition few studiesin ICU populations some found reduced infection in elective surgery one unblinded study has shown reduced mortality in unselected ICU patients; benefit in least ill (CCM 2000; 28:643) another showed increased mortality on re-analysis which barely failed to reach statistical significance (CCM 1995; 23:436)
  • 42.
    Immunonutrition first meta-analysis(Ann Surg 1999; 229: 467) no effect on pneumonia reduced other infections and length of hospital stay increased mortality only just missing statistical significance did not censor for death second meta-analysis (CCM 1999; 27:2799) reduced infection reduced length of ventilation and hospital stay no effect on mortality
  • 43.
    Immunonutrition third meta-analysis(JAMA 2001; 286:944) benefit in elective surgery increased mortality in ICU patients with sepsis large Italian RCT (ICM 2003; 29:834) compared enteral immunonutrition with TPN stopped early because interim analysis showed increased mortality in septic patients 44.4% vs 14.3%; p=0.039
  • 44.
    Immunonutrition arbitrary dosesrandom mixture of agents mutually antagonistic effects diverse case mix individual components need proper evaluation
  • 45.
    Why do wefeed ICU patients? to treat existing malnutrition to minimise the wasting of lean body mass that accompanies critical illness
  • 46.
    Which patients shouldwe feed? all malnourished patients all patients who are unlikely to regain normal oral intake within 2 days
  • 47.
    When should westart to feed? without undue delay once the patient is stable within 2 days
  • 48.
    What route shouldwe feed by? EN preferred for majority on pragmatic grounds alone TPN obviously necessary for some if there is serious doubt that EN can be established in 2 (or 5, 7…) days commence TPN maintain at least minimal EN keep trying to establish EN
  • 49.
    How much feedshould we give? 25 kCal/kg/day equations indirect calorimetry
  • 50.
    What should thefeed contain? carbohydrate lipid nitrogen water and electrolytes micronutrients