بسم الله الرحمن الرحيم.

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Presentation transcript:

بسم الله الرحمن الرحيم

Nutritional assessment in hospitalized patients M. Safarian, MD PhD.

Nutrition Care Process Steps Nutrition Assessment Nutrition Diagnosis Nutrition Intervention Nutrition Monitoring and Evaluation The 4 quadrants around the core represent the four steps of the nutrition care process: nutrition assessment, nutrition diagnosis, nutrition intervention and nutrition monitoring and evaluation. Each of the steps is preceded by the word nutrition. This was a conscious decision to make the Nutrition Care Process unique and specific to dietetics professionals. Even though each step builds on the previous one, the process is not linear. Critical thinking and problem solving will frequently require that dietetics professionals revisit previous steps to reassess, add, or revise nutrition diagnoses; modify intervention strategies; and/or evaluate additional outcomes. The first step we’ll look at is the Nutrition Assessment

Nutritional care process Anthropometrics Nutritional assessment tools

Nutritional Assessment Anthropometric assessment Clinical evaluation Biochemical, laboratory assessment Dietary evaluation

ESPEN guidelines Questions to be answered: What is the condition now? Is the condition stable? Will the condition get worse? Will the disease process accelerate nutritional deterioration?

Anthropometric methods in ICU Weight Height estimation Mid-arm circumference Skin fold thickness Head circumference

Weight

Ideal Body Weight (kg) Men=48+ 2.3 for each inch over 152 m Women=45.3+2.3 for each inch over 152 cm Correction for skeletal size:

Ideal Body Weight (kg) Add 10% if SS is large Subtract 10% if SS is small

Adjusted body weight Used when actual body weight is more than 120% of IBW: ABW=IBW+ 25% of (actual body weight - IBW)

Height in ICU patients

Alternative measurements Estimating Height from ulna length

Estimations of height

Body composition (BIA) Very popular Safe Noninvasive Portable Rapid

Skin Fold Thickness معرف ميزان چربي زير پوستي و درنتيجه ميزان چاقي خواهد بود. محلهاي اندازه گيري: تريسپس، بايسپس،زير کتف و بالاي تيغه ايلياک . مشکلات عملي: خطاي در اندازه گيري. مشکلات اندازه گيري. وارياسيون توزيع چربي در افراد مختلف (فردي وجمعيتي). حساسيت کم.

Skin Fold Thickness

Mid arm circumference measured with a nonstretch measuring tape midway between the acromion and olecranon of the nondominant arm ≤ 15 cm: severe depletion of muscle mass 16–19 cm: moderate depletion 20–22 cm: mild depletion

Mid arm circumference

BMI estimation If MUAC is <23.5 cm, BMI is likely to be <20 kg/m2 If MUAC is >32.0 cm, BMI is likely to be >30 kg/m2

Clinical assessment

CLINICAL ASSESSMENT Detectiong of physical signs, (specific & non specific), that may be associated with malnutrition. Nutritional history General clinical examination, with special attention to organs like hair, angles of the mouth, gums, nails, skin, eyes, tongue, muscles, bones, & thyroid gland. Detection of relevant signs helps in establishing the nutritional diagnosis

CLINICAL ASSESSMENT

General: muscle wasting

Wasting in the hands 35

Wasting Clavicle 36

The Shoulder and Elbow The shoulder Normal: rounded or sloped Abnormal: square, can see acromion process The elbow well padded and not showing joint 37

The Arm Bend arm and pinch at triceps. Only pinch the fat, not the muscle. Normal: fingers don’t meet Abnormal: fingers meet 38

The Legs showing muscle wasting 39

Quadriceps and Knees 40

Flaky paint dermatosis: protein deficiency

Essential fatty acid deficiency syndromes (EFADs)

Zinc deficiency

Zinc deficiency

dermatitis dementia diarrhea death Pellagra niacin deficiency

Vitamin C deficiency Perifolicullar pitichea

Biochemical, laboratory assessment

The possibilities of biochemical monitoring On-line monitoring (cardiosurgery – pH, minerals (K), the electrodes are localized on central cateter, possibility to check parameters on-line. bed side monitoring (glycaemia, urine /protein, pH, blood../,oximeter O2 saturation, acidobasis, drugs /dg.strips) Biochemical analysis

Biochemical parameters Na,K,Cl,Ca,P,Mg, osmolality - blood, urine Acidobasis, lactate urea, creatinin, creatinin clearence, Nitrogen balance bilirubine, ALT, AST, LDH, amylase, lipase cholesterol, triglycerides, glucose – blood, urine

Biochemical parameters Total protein, albumine, prealbumine CRP TSH Basic analysis are made at the first,must be done within 90minutes

Other biochemical parameters Trace elements /Zn,Se../ Vitamins Drugs /methotrexate, antiepileptics, antibiotics.../ Aminogram /glutamin../ Interleucins,TNF… Hormones /cortisol, glucagone, adrenaline../.

Biochemical Assessment

Serum Protein levels are not reliable during inflammation

Albumin Half-life - 20 days Under/over hydration, liver function Oncotic pressure, transport, nutritive reserve Determinants of synthesis Oncotic pressure, hormones, negative acute-phase reactant, nutrition support, aging, drugs

Transthyretin - TTY (Prealbumin) Half-life - 1-2 days Transports thyroid hormones and Vitamin A in Retinol Binding Protein Complex Negative acute-phase reactant  > 65% energy needs met,  <50% energy needs met Elevated in Renal Disease Elevated with steroid therapy

C-Reactive Protein Positive acute-phase protein Reacts with Somatic C Polysaccharide of Strep. Pneumoniae Half-life 5 hours Changes with acute & chronic inflammation Helps interpret Transthyretin and Albumin

MUST TOOL Is recommended by ESPEN for community 4 steps.

Biochemical markers of nutrition status: Plasmatic proteins with short biologic half-life Albumin -syntetizate in liver, half-life time is 21 days Normal: 35-45g/l. Decrease of alb: malnutrition Trends of changes alb.levels during realimentation are criterium of succesfull terapy. Acute decrease: acute phase response. 78

Biochemical markers of nutrition status: Transferin: syntesized in liver, biolog HL: 8days. Value 2-4g/l, RBP: syntesized in liver Biolog half-life : 12h., Normal value: 0,03-0,006g/l. Acute phase reactant (negative)

Biochemical markers of nutrition status: Prealbumin-syntesized in liver, biolog.half-life:1,5 days. Normal Value 0,15-0,4g/l. Decrease in failure of proteosyntesis-indicator of acute protein malnutrition.

NUTRITIONAL ASSESSMENT Urine urea nitrogen (UUN): to evaluate degree of hypermetabolism (stress level): 0 –5 g/d= normometabolism 5 – 10 g/d = mild hypermetabolism (level 1 stress) 10 – 15 = moderate (level 2 stress) >15 = severe (level 3 stress)

Nutrition Monitoring and Evaluation Monitor progress and determine if goals are met Identifies patient/client outcomes relevant to the nutrition diagnosis and intervention plans and goals Measure and compare to client’s previous status, nutrition goals, or reference standards

Other Outcomes Food and Nutrient Intake (FI) Energy intake Food and Beverage Enteral and parenteral Bioactive substances Macronutrients Micronutrients Physical Signs/Symptoms Anthropometric Biochemical and medical tests Physical examination

Monitoring

Enteral Nutrition Monitoring: Gastric Residuals Clinically assess the patient for abdominal distension, fullness, bloating, discomfort Place the pt on his/her right side for 15-20 minutes before checking a RV to avoid cascade effect Seek transpyloric access of feeding tube Raise threshold for RV to 200-300 mL Consider stopping RV checks in stable pts Rees Parrish C. Enteral Feeding: The Art and the Science. Nutr Clin Pract 2003; 18;75-85.

Some Lab tests

Na serum levels Hypernatremia: Na over 150 mmol/l hyperaldosteronism hypovolemia renin-angiot-aldost. Hypothalamic damage Hypertonic hyperhydration Diabetes insipidus Brain death

Na serum levels(136-145mEq/L) Hyponatremia: Na under 130 mEq/L Na in the third space - ascites, hydrothorax Cardiac failure – increase of extracellular volume Application of solutions without electrolytes Hypersecretion of ADH – water retention

K serum levels (3.5-5.3mEq/L) Hyperkalemia: K over 5,0 - 5,5 mEq/L pH dependent /acidosis increases K level Bigger intake, low output or both Acute renal failure Acute metabolic acidosis Infusion with K

K serum levels Hypokalemia: K under 3,5mEq/L Low intake, bigger uptake, or both Emesis, diarrhoe / intestinal loss/ Diuretics Chemotherapy, antimycotics /renal tubules failure/ Anabolic phasis Hyperaldosteronism Acute metabolic alcalosis

BUN (5-20 mg/dl) Consider hydration and Nutrition. High level of urea high intake of N, increase catabolism polytrauma-muscele loss GIT bleeding dehydration low output- renal failure, Low level – malnutrition,serious hepatic failure- ureosyntetic cycle and gluconeogenesis dysfunction, pregnancy- increase ECF

BUN (5-20 mg/dl) Low level – malnutrition, serious hepatic failure- ureosyntetic cycle and gluconeogenesis dysfunction, pregnancy- increase ECF

Urea Urea in urine Increase – catabolism, prerenal failure Decrease – chronic malnutrition, acute renal failure

Creatinine(0.5-1.1 mg/dl) Serum levels of creatinine evaluation together with muscle mass, age, gender Increase bigger offer- destruction of muscle mass, low output-renal failure Decrease- low offer-low muscle mass malnutrition Creatinine clearence, excretion fraction -renal function N-balance – catabolism – the need of nitrogen Uratic acid – cell damage, arthritis uratica

ALT(SGPT) N V: M: 7-46 F:4-35 U/L High level – hepatopathologia, steatosis, hepatitis, cell damage,

AST(SGOT) High level – hypoperfusion, hepatitis, cell necrosis, muscles damage both aminotransferases increase during damage of hepatic cells during inf.hepatitis.

TG(10-190 mg/dl) TG-increase Glycemia, serum, urine, during sepsis, mainly on the begining, monitorate during parenterál nutrition with lipid emulsion Glycemia, serum, urine, Hypoglycemia below 2,5mmol/l-vital danger hyperglycemia- insulin.rezistence, recomendation level of glycemia 4,5-8,2 /2006/ better survive in ICU patient

Glucose Glycemia, serum, urine, Hypoglycemia below 2,5mmol/l-(45 mg/dl) vital danger hyperglycemia- insulin.rezistence Recomendation level of glycemia 4,5-8,2 (80-150 mg/dl)

P– serum levels(2.7-4.5 mg/dl) Hypophosphataemia: under 1,9 mg/dl Acute wastage of energy after succesfully resuscitation, overfeeding sy, anabolism (energetic substrates without K,Mg,P). Hyperphosphataemia – over 5,8 mg/dl Renal failure Cell damage

Mg – serum levels (1,3-2,5 mEq/L) Mg – together with potassium Hypomagnesaemia – under 1,2 mEq/L / renal failure low intake.

Monitoring of EN For formula intolerance, Hydration status, Electrolyte status, Nutritional status,

Monitoring

Monitoring in PN therapy Weight (on a daily basis,initialy and ) Blood Daily Electrolytes (Na+, K+, Cl-) Glucose Acid-base status 3 times/week BUN Ca+, P Plasma transaminases NOTES FOR PRESENTERS Once a person has been screened, the decision of whether to give nutrition support can be made. Nutrition support should be considered for people who are malnourished or at risk of malnourishment. All healthcare professionals involved in starting or stopping nutrition support should be aware of the ethical and legal considerations surrounding patient consent and withdrawing or withholding support, bearing in mind that the provision of nutrition support is not always appropriate. Guidance issued by the General Medical Council and the Department of Health should be followed. You can see their websites for details (www.gmc-uk.org and www.dh.gov.uk).

Monitoring in PN therapy Variable to be monitored Initial Later period Clinical status Daily Catetheter site Temperature Intake &Output NOTES FOR PRESENTERS Once a person has been screened, the decision of whether to give nutrition support can be made. Nutrition support should be considered for people who are malnourished or at risk of malnourishment. All healthcare professionals involved in starting or stopping nutrition support should be aware of the ethical and legal considerations surrounding patient consent and withdrawing or withholding support, bearing in mind that the provision of nutrition support is not always appropriate. Guidance issued by the General Medical Council and the Department of Health should be followed. You can see their websites for details (www.gmc-uk.org and www.dh.gov.uk).

Monitoring in PN therapy Variable to be monitored Initial Later period Weight Daily Weekly serum glucose 3/wk Electrolytes (Na+, K+, Cl-) 1-2//wk BUN Ca+, P,mg Liver function Enzymes Serum triglycerides weekly CBC NOTES FOR PRESENTERS Once a person has been screened, the decision of whether to give nutrition support can be made. Nutrition support should be considered for people who are malnourished or at risk of malnourishment. All healthcare professionals involved in starting or stopping nutrition support should be aware of the ethical and legal considerations surrounding patient consent and withdrawing or withholding support, bearing in mind that the provision of nutrition support is not always appropriate. Guidance issued by the General Medical Council and the Department of Health should be followed. You can see their websites for details (www.gmc-uk.org and www.dh.gov.uk).

Problems Catheter sepsis Placement problems Metabolic complications

Complications Dehydration Possible cause: Management: Inadequate fluid support; Unaccounted fluid loss (e.g. diarrhea, fistulae, persistent high fever). Management: Start second infusion of appropriate fluid, such as D5W, 1/2NS, NS. Estimate fluid requirement and adjust PN accordingly. NOTES FOR PRESENTERS Once a person has been screened, the decision of whether to give nutrition support can be made. Nutrition support should be considered for people who are malnourished or at risk of malnourishment. All healthcare professionals involved in starting or stopping nutrition support should be aware of the ethical and legal considerations surrounding patient consent and withdrawing or withholding support, bearing in mind that the provision of nutrition support is not always appropriate. Guidance issued by the General Medical Council and the Department of Health should be followed. You can see their websites for details (www.gmc-uk.org and www.dh.gov.uk).

Complications Overhydration Possible cause: Management: Excess fluid administration; Compromised renal or cardiac function. Management: Consider D70 (can’t use with PPN) or 20% lipid as calorie source Initiate diuretics. Limit volume. NOTES FOR PRESENTERS Once a person has been screened, the decision of whether to give nutrition support can be made. Nutrition support should be considered for people who are malnourished or at risk of malnourishment. All healthcare professionals involved in starting or stopping nutrition support should be aware of the ethical and legal considerations surrounding patient consent and withdrawing or withholding support, bearing in mind that the provision of nutrition support is not always appropriate. Guidance issued by the General Medical Council and the Department of Health should be followed. You can see their websites for details (www.gmc-uk.org and www.dh.gov.uk).

Complications Alkalosis Possible cause: Management: Inadequate K to compensate for cellular uptake during glucose transport Excessive GI or renal K losses. Inadequate Cl- in patients undergoing gastric decompression. Management: KCl to PN. Assure adequate hydration. Discontinue acetate. NOTES FOR PRESENTERS Once a person has been screened, the decision of whether to give nutrition support can be made. Nutrition support should

Complications Acidosis Possible cause: Management: Excessive renal or GI losses of base Excessive Cl- in PN. Management: Rule out DKA and sepsis. Add acetate to PN. NOTES FOR PRESENTERS Once a person has been screened, the decision of whether to give nutrition support can be made. Nutrition support should be considered for people who are malnourished or at risk of malnourishment. All healthcare professionals involved in starting or stopping nutrition support should be aware of the ethical and legal considerations surrounding patient consent and withdrawing or withholding support, bearing in mind that the provision of nutrition support is not always appropriate. Guidance issued by the General Medical Council and the Department of Health should be followed. You can see their websites for details (www.gmc-uk.org and www.dh.gov.uk).

Complications Hypercarbia Possible cause: Management: Excessive calorie or carbohydrate load. Management: Decrease total calories or CHO load. NOTES FOR PRESENTERS Once a person has been screened, the decision of whether to give nutrition support can be made. Nutrition support should be considered for people who are malnourished or at risk of malnourishment. All healthcare professionals involved in starting or stopping nutrition support should be aware of the ethical and legal considerations surrounding patient consent and withdrawing or withholding support, bearing in mind that the provision of nutrition support is not always appropriate. Guidance issued by the General Medical Council and the Department of Health should be followed. You can see their websites for details (www.gmc-uk.org and www.dh.gov.uk).

Complications Hypocalcemia Possible cause: Management: Excessive PO4 salts Low serum albumin. Inadequate Ca in PN. Management: Slowly increase calcium in PN prescription. NOTES FOR PRESENTERS Once a person has been screened, the decision of whether to give nutrition support can be made. Nutrition support should be considered for people who are malnourished or at risk of malnourishment. All healthcare professionals involved in starting or stopping nutrition support should be aware of the ethical and legal considerations surrounding patient consent and withdrawing or withholding support, bearing in mind that the provision of nutrition support is not always appropriate. Guidance issued by the General Medical Council and the Department of Health should be followed. You can see their websites for details (www.gmc-uk.org and www.dh.gov.uk).

Complications Hypercalcemia Possible cause: Management: Excessive Ca in PN Administration of vitamin A in patients with renal failure. Can lead to pancreatitis. Management: Decrease calcium in PN. Ensure adequate hydration. Limit vitamin supplements in patients with renal failure to vitamin C and B vitamins. NOTES FOR PRESENTERS Once a person has been screened, the decision of whether to give nutrition support can be made. Nutrition support should be considered for people who are malnourished or at risk of malnourishment. All healthcare professionals involved in starting or stopping nutrition support should be aware of the ethical and legal considerations surrounding patient consent and withdrawing or withholding support, bearing in mind that the provision of nutrition support is not always appropriate. Guidance issued by the General Medical Council and the Department of Health should be followed. You can see their websites for details (www.gmc-uk.org and www.dh.gov.uk).

Complications Hyperglycemia Possible cause: Stress response. Occurs approximately 25% of cases. Management: Rule out infection. Decrease carbohydrate in PN. Provide adequate insulin. NOTES FOR PRESENTERS Once a person has been screened, the decision of whether to give nutrition support can be made. Nutrition support should be considered for people who are malnourished or at risk of malnourishment. All healthcare professionals involved in starting or stopping nutrition support should be aware of the ethical and legal considerations surrounding patient consent and withdrawing or withholding support, bearing in mind that the provision of nutrition support is not always appropriate. Guidance issued by the General Medical Council and the Department of Health should be followed. You can see their websites for details (www.gmc-uk.org and www.dh.gov.uk).

Complications Hypoglycemia Possible cause: Management: Sudden withdrawal of concentrated glucose. More common in children. Management: Taper PN. Start D10. NOTES FOR PRESENTERS Once a person has been screened, the decision of whether to give nutrition support can be made. Nutrition support should be considered for people who are malnourished or at risk of malnourishment. All healthcare professionals involved in starting or stopping nutrition support should be aware of the ethical and legal considerations surrounding patient consent and withdrawing or withholding support, bearing in mind that the provision of nutrition support is not always appropriate. Guidance issued by the General Medical Council and the Department of Health should be followed. You can see their websites for details (www.gmc-uk.org and www.dh.gov.uk).

Complications Cholestasis Possible cause: Management: Lack of GI stimulation. Sludge present in 50% of patients on PN for 4-6 weeks; resolves with resumption of enteral feeding. Management: Promote enteral feeding. NOTES FOR PRESENTERS Once a person has been screened, the decision of whether to give nutrition support can be made. Nutrition support should be considered for people who are malnourished or at risk of malnourishment. All healthcare professionals involved in starting or stopping nutrition support should be aware of the ethical and legal considerations surrounding patient consent and withdrawing or withholding support, bearing in mind that the provision of nutrition support is not always appropriate. Guidance issued by the General Medical Council and the Department of Health should be followed. You can see their websites for details (www.gmc-uk.org and www.dh.gov.uk).

Complications Hepatic tissue damage and fat infiltration Possible cause: Unclear etiology. May be related to excessive glucose or energy administration; L-carnitine deficiency. Management: Rule out all other causes of liver failure. Increase fat intake relative to CHO. Enteral feeding. NOTES FOR PRESENTERS Once a person has been screened, the decision of whether to give nutrition support can be made. Nutrition support should be considered for people who are malnourished or at risk of malnourishment. All healthcare professionals involved in starting or stopping nutrition support should be aware of the ethical and legal considerations surrounding patient consent and withdrawing or withholding support, bearing in mind that the provision of nutrition support is not always appropriate. Guidance issued by the General Medical Council and the Department of Health should be followed. You can see their websites for details (www.gmc-uk.org and www.dh.gov.uk).

Nutritional screening tools

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