Nutrition in Criticallyill
patient
Dr Arun m v
BSC (Zoology), MBBS, DGM (Geriatric Medicine),MSC (Psychology)DDT
Dialysis), CCPPM, GFPM (Pain and Pallative Medicine), FICCM (Critical Care
Medicine),PGDMH (Mental Health), CCEBDM (Diabetology)
2.
Malnutrition refers todeficiencies, excessive or imbalance
person's intake of energy and/or nutrients. (WHO definition)
3.
Nutrition support refersto enteral or parenteral provision of
• Calories
• Protein
• Electrolytes
• Vitamins
• Minerals
• Trace elements
• Fluids
Contraindications:
• Enteral Feeding:
1.Haemodynamically unstable patients where intravascular volume has
not been fully resuscitated(If volume resuscitation and tissue
perfusion is adequate, starting feeding early in patients on
vasopressors reduces ICU and hospital mortality(22.5% vs 28.3% and
34% vs 44%.
2. Intestinal obstruction
3. Major UGI Bleed.
4. Intractable vomiting or diarrhoea
5. Gl Ischemia
6. High output fistula
8.
Contraindications:
• Parenteral nutrition:
1.hyperosmolality
2. severe hyperglycemia
3. severe electrolyte abnormalities
4. volume overload
5. Inadequate IV access
6. Inadequate attempts to feed enterally.
9.
Nutritional requirement
A generalclinical assessment to be done to assess malnutrition in the
ICU until a specific tool is validated:
• SGA (Subjective global assessment)
• MNA (Mini-Nutrition Assessment) / MNA-SF
• NRS (Nutritional Risk Scoring) 2002
• NUTRIC (Nutritional risk in critically ill).
Type of nutrition:Timingof feeding
• Medical nutrition therapy is considered for all patients, staying for
more than 48 hours in ICU
• Patients who can eat orally, oral diet should be given.
• If oral diet is not possible, Early (within 48 hours) enteral feeds should
be initiated, if there is no contraindication, rather than delaying it.
• In case of contraindications to oral and EN, PN should be
implemented within three to seven days.
17.
Timing of feeding
•Early and progressive PN can be provided instead of no nutrition in
case of contraindications for EN in severely malnourished patients.
• To avoid overfeeding, early full EN and PN shall not be used in
critically ill patients but shall be prescribed within three to seven days.
Type of enteralfeeding (Formulations)
Standard formulation:
• Isotonic to serum
• Caloric density of approximately 1 kcal/mL
• Lactose-free
• Intact (nonhydrolyzed) protein content of about 40 g/1000 mL (40 g/1000 kcal)
• Nonprotein calorie to nitrogen ratio of approximately 130
• Mixture of simple and complex carbohydrates
• Long-chain fatty acids (although some are now including medium-chain and
omega-3 fats)
• Essential vitamins, minerals, and micronutrients
20.
Type of enteralfeeding (Formulations)
Concentrated formulation:
• Hyperosmolar
• Caloric density of approximately 1.2, 1.5 or 2 kcal/mL.
Pre-digested (elemental):
• Proteins are hydrolysed to peptides
• Carbohydrates are of less complex form
• Triglycerides are altered to fatty acids
• Disease specific: Renal / Diabetic formulations
• Thoracic duct leak
• Digestive defects
• Failure to tolerate
standard feeds
21.
Compositions of Enteralfeeds:
• Carbohydrate / Fat : 49-53% / 29-30% of Calories
• Protein:1.2 to 2 gm/kg body weight.
• Peptides
• Omega 3 fatty acid and antioxidants:No benefit
• Glutamine: No benefit. Potential harm
• Arginine: Not recommended
22.
Compositions of Enteralfeeds:
• Prebiotics and probiotics: No benefit. Harmful in Acute pancreatitis.
• Fiber:Routine use not beneficial in prevention of diarrhoea.Risk of
Bezoars in patient on vasopressors
• Vitamins and trace elements:
Reasonable to provide vitamins and trace elements in critically ill
patients(enteral or parenteral)
23.
Compositions of Enteralfeeds
• Immune modulators:
(Combination of glutamine, selenium, omega-3 fatty acids, and
antioxidants)
Not recommended
Increased 6 months mortality in Medical patients (54% vs 35%)
Amount and rateof feeding infusion
• A calorie goal of 18 to 25 kcal/kg/d is a reasonable initial range
• Trophic feed10 to 30 mL/hour
• initiate feeds at 25 to 30 percent of estimated goal rate
• In severely ill patients, not to increase further towards goal in next 5
to 7 days.
• In less severely ill patients, gradually rate to be increased towards
goal slowly provided patient tolerates feeds
• Gastric residual volume of 500 ml is taken as sign of intolerance.
26.
Complications of enteralfeeding: Prevention
& Managements
Aspiration:Backrest elevation- Questined
Post-pyloric feeding - doubtful benefit
Surgical / Percutaneous feeding (PEG)
Motility agents Metoclopramide, Erythromycin
Diarrhoea:15 - 18% vs 6% cases.
Cause to be searched
Fiber can be added.
27.
Complications of enteralfeeding: Prevention
& Managements
• Metabolic: Hyperglycaemia
Micronutrient deficiencies
Refeeding syndrome
• Fluid & water:Possibility of water deficit
Tube should be flushed with water.
• Mechanical:
Constipation and faecal impaction
Insertion into lung wrongly.
28.
The refeeding syndrome:
•Defined as the clinical complications that can occur as a result of fluid
and electrolyte shifts during aggressive nutritional rehabilitation of
malnourished patients.
• These complications are potentially fatal when not detected or
treated early during nutritional rehabilitation.
29.
The Refeeding Syndrome:
Hypophosphatemia
Starvation
andAnorexia
Feeding
Carbohydrate
Insulin
Lack of Phosphorylated
Intermediates
Use phosphate in ATP and 2,3
DPG, in the process of producing various molecules
Decrease in serum Phosphates
Increase in Cellular uptake of
Phosphate and Mg++ and K+
• Tissue Hypoxia
• Myocardial dysfunction
• Respiratoryfailure
• Haemolysis
• Rhabdomyolysis
• Seizures and Neurologic
• Gl and Hepatic dysfunction
30.
The refeeding syndrome:
Risksof Refeeding syndrome:
• Amount of weight loss(<70% of IBW / BMI <14kg/m2).
• Rapidity of weight restoration process
• High risk in the initial 2 weeks of nutritional rehabilitation.
Prevention and treatment:
• Electrolyte deficiencies to be corrected first
• Feeding to be initiated at low calories: 1400 to 1600 kcal/day
• Treatment of organ dysfunction
31.
Parenteral Nutrition
• Definition:Parenteral nutrition is a form of therapy in which
elemental nutrients are given as an intravenous infusion.
• Appropriate & safe prescribing of PN is a critical first step and an
essential component of PN-use process.
32.
Types
Peripheral parenteral nutrition(PPN)
• Administered through a peripheral intravenous catheter.
• Osmolarity - generally limited to 1,000 mOsm (to avoid phlebitis)
• Thus, large volumes (>2,500 mL) are needed
• Temporary nutritional supplementation may be useful
• Generally intended as supplement to oral feeding and is not optimal for critically ill pts
Total parenteral nutrition (TPN)
• Provides complete nutritional support
• The solution, volume of administration, and additives are individualized based on an
assessment of the nutritional requirements.
• Available in multiple single bags or Single bag multi chambered (premixed)
33.
Administration of TPN
•Use of protocols & nutrition support teams reduce risks.
• Hypo-caloric PN dosing (<20kcal/kg/day or 80% of estimated energy
needs with adequate protein (>1.2 g/kg/day)-should be considered
initially.
• TPN solutions are delivered most commonly as a continuous infusion.
• Additional maintenance intravenous fluids are unnecessary, and total
infused volume should be kept constant while nutritional content is
increased.
34.
Venous access
• Theinfusion of hyperosmoler nutrient solution requires a large bore,
high flow vessel to minimize vessel irritation and damage.
• Percutaneous subclavian vein catheterization and PICC are the most
commonly used techniques for parenteral nutrition
• Catheter can be placed via the subclavian vein, the jugular vein (less
desirable because of the high rate of associated infection), or a long
catheter placed in an arm vein and threaded into the central venous
system (a peripherally inserted central catheter line).
• Position of catheter is confirmed by radiograph
35.
Central catheter (Non-tunneled)
ADVANTAGES
•Central access needed
• Multiple lumen can be used in acute emergency
• Hypertonic solutions can be given
• Can be placed for more than 6 weeks
DISADVANTAGES
• Increase infection rate
36.
Central catheter (Tunneled)
ADVANTAGES
•Convenient exit site
• Long lasting than non tunnels
• Hypertonic solutions can be given
DISADVANTAGES
• Removal needs surgical dissection
• Catheter related sepsis
• Other complications
37.
PICC line
ADVANTAGES
• Bedside technique
• Avoids complications: of central venous catheter
• Avoid multiple venous cannulations
• Hypertonic solutions can be given
DISADVANTAGES
• Trained personnel is needed
• Line blockage
• Mal position
• Phlebitis
• Line sepsis
• Thrombosis
38.
Clinical Data MonitoredDaily
• General sense of well-being.
• Vital signs including temperature, blood pressure, pulse, and
respiratory rate
• Fluid balance: weight at least several times weekly, fluid intake
(parenteral and enteral) vs. fluid output (urine, stool, gastric drainage,
wound, ostomy)
• Parenteral nutrition delivery equipment: tubing, pump, filter,
catheter, dressing
• Nutrient solution composition
39.
Labs
• Finger-stick glucose- Three times daily until stable
• Blood glucose,Na, K, Cl, НCO3, BUN - Daily until stable and fully
advanced, then twice weekly
• Serum creatinine, albumin, PO4,Ca,Mg, Hb, WBC - Baseline, then
twice weekly
• INR - Baseline, then weekly
• Micronutrient tests - As indicated
41.
Mechanical complications
• Airembolism
• pneumothorax
• hemothorax
• Cardiac tamponade
• Injuries to arteries and veins
• Injury to thoracic duct
• Brachial plexus injury
Infection
• Catheter related sepsisis most common lifethreateningcomplication
• Causes: staphepidermidis and staphaureus,enterococcus, candida, E
coli, psuedomonas,klebsiella etc. In immunocompromised pts
42.
Metabolic complications
Early ornutrient related
• Hyperglycemia
• Hypoglycemia
• Hyperlipidemia
• Refeeding syndrome
Late or related to long term administration
• Hepatic dysfunction
• Steatosis, steatohepatitis, lipidosis, cholestasis, cirrhosis
• Biliary complications: acalculous cholecystitis, cholelithiasis
• Metabolic bone disease: osteomalacia, osteopenia
• Fluid overload
• Hypo/hypernatremia
• Hypercalcemia
• Hypo/hyperkalemia
43.
Care of theparenteral nutrition (PN) mixture
• Store reconstituted PN bags in a refrigerator untiluse
• Always use aseptic techniques while connecting and infusing PN
• Always use an infusion set with in-built air vent and 0.2 m filter
• Never insert a needle for air venting in a PN bag
• Never add any medication to the PN bag
• Avoid frequent changes in the formulation of the PN solution
• Infuse the prescribed volume and avoid wastage of PN solution
44.
Discontinuation of TPN
•Discontinuation of TPN should take place when the patient can satisfy
75% of his or her caloric and protein needs with oral intake or enteral
feeding.
• To discontinue TPN, the infusion rate should be halved for 1 hour,
halved again the next hour, and then discontinued.
• Tapering in this manner prevents rebound hypoglycaemia from
hyperinsulinemia
• It is not necessary to taper the rate if the patient demonstrates
glycemic stability
45.
To summarize nutritiontherapy....
• Patients in ICU or for major surgery should be screened for pre-
existing malnutrition or nutrition risk (for nutrition related
complications).
• When nutrition risk is identified, it should be optimized by provision
of appropriate nutrition therapy
• Early EN provides both nutritional benefits as well as non-nutritional
benefits, but may be associated with poor tolerance due to the gut
dysfunction associated with critical illness.
• Early supplemental PN assures adequate delivery of energy, protein &
nutrients to minimize risk and improve outcomes.