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Parenteral%20Nutrition

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Title: Parenteral%20Nutrition


1
Parenteral Nutrition
Graphic source http//www.rxkinetics.com/tpntutor
ial/1_4.html
2
Parenteral Nutrition (Definition)
  • Components are in elemental or pre-digested
    form
  • Protein as amino acids
  • CHO as dextrose
  • Fat as lipid emulsion
  • Electrolytes, vitamins and minerals

3
Parenteral Nutrition (PN) Definition
  • Delivery of nutrients intravenously, e.g. via the
    bloodstream.
  • Central Parenteral Nutrition often called Total
    Parenteral Nutrition (TPN) delivered into a
    central vein
  • Peripheral Parenteral Nutrition (PPN) delivered
    into a smaller or peripheral vein

A.S.P.E.N. Nutrition Support Practice Manual, 2nd
edition, 2005, p. 97
4
Indications for PN (ASPEN)
  • When Specialized Nutrition Support (SNS) is
    indicated, EN should generally be used in
    preference to PN. (B)
  • When SNS is indicated, PN should be used when the
    gastrointestinal tract is not functional or
    cannot be accessed and in patients who cannot be
    adequately nourished by oral diets or EN. (B)
  • The anticipated duration of PN should be gt7 days

ASPEN Board of Directors. JPEN 2619SA, 2002.
ASPEN Nutrition Support Practice Manual, 2005, p.
108
5
EN vs PN in Critical Care (EAL)
  • R.1. If the critically ill ICU patient is
    hemodynamically stable with a functional GI
    tract, then EN is recommended over PN.
  • Patients who received EN experienced less septic
    morbidity and fewer infectious complications than
    patients who received PN. Strong, Conditional

ADA Evidence Analysis Library, accessed 8/07
6
EN vs PN in Critical Care (EAL)
  • In the critically ill patient, EN is associated
    with significant cost savings when compared to
    PN. There is insufficient evidence to draw
    conclusions about the impact of EN or PN on LOS
    and mortality. Strong, Conditional

ADA Evidence Analysis Library, accessed 8/07
7
Common Indications for PN
  • Patient has failed EN with appropriate tube
    placement
  • Severe acute pancreatitis
  • Severe short bowel syndrome
  • Mesenteric ischemia
  • Paralytic ileus
  • Small bowel obstruction
  • GI fistula unless enteral access can be placed
    distal to the fistula or where volume of output
    warrants trial of EN

Adapted from Mirtallo in ASPEN, The Science and
Practice of Nutrition Support A Case-Based Core
Curriculum. 2001.
8
Contraindications
  • Functional and accessible GI tract
  • Patient is taking oral diet
  • Prognosis does not warrant aggressive nutrition
    support (terminally ill)
  • Risk exceeds benefit
  • Patient expected to meet needs within 14 days

9
PN Central Access
  • May be delivered via femoral lines, internal
    jugular lines, and subclavian vein catheters in
    the hospital setting
  • Peripherally inserted central catheters (PICC)
    are inserted via the cephalic and basilic veins
  • Central access required for infusions that are
    toxic to small veins due to medication pH,
    osmolarity, and volume

10
Venous Sites for Access to the Superior Vena Cava
11
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12
PICC Lines (peripherally inserted central
catheter)
  • PICC lines may be used in ambulatory settings or
    for long term therapy
  • Used for delivery of medication as well as PN
  • Inserted in the cephalic, basilic, median
    basilic, or median cephalic veins and threaded
    into the superior vena cava
  • Can remain in place for up to 1 year with proper
    maintenance and without complications

13
PN Peripheral Access
  • PN may be administered via peripheral access when
  • Therapy is expected to be short term (10-14 days)
  • Energy and protein needs are moderate
  • Formulation osmolarity is lt600-900 mOsm/L
  • Fluid restriction is not necessary

A.S.P.E.N. Nutrition Support Practice Manual,
2005 p. 94
14
Parenteral Nutrition
  • Macronutrients
  • Micronutrients

15
Macronutrients Carbohydrate
  • Source Monohydrous dextrose
  • Properties Nitrogen sparing Energy source
  • 3.4 Kcal/g
  • Hyperosmolar
  • Recommended intake
  • 2 5 mg/kg/min
  • 50-65 of total calories

16
Macronutrients Carbohydrate
  • Potential Adverse Effects
  • Increased minute ventilation
  • Increased CO2 production
  • Increased RQ
  • Increased O2 consumption
  • Lipogenesis and liver problems
  • Hyperglycemia

17
Macronutrients Amino Acids
  • Source Crystalline amino acids standard or
    specialty
  • Properties 4.0 Kcal/g
  • EAA 4050 NEAA 50- 60
  • Glutamine / Cysteine
  • Recommended intake
  • 0.8-2.0 g/kg/day
  • 15-20 of total calories

18
Macronutrients Amino Acids
  • Potential Adverse Effects
  • Increased renal solute load
  • Azotemia

19
Macronutrients Amino Acids
  • Specialized Amino Acid Solutions
  • Branched chain amino acids (BCAA)
  • Essential amino acids (EAA)
  • Not shown to improve patient outcome
  • More expensive than standard solutions

20
Macronutrients Lipid
  • Source Safflower and/or soybean oil
  • Properties Long chain triglycerides
  • Isotonic or hypotonic
  • Stabilized emulsions 10 Kcals/g
  • Prevents essential fatty acid
    deficiency
  • Recommended intake
  • 0.5 1.5 g/kg/day (not gt2 g/kg) 12 24 hour
    infusion rate

21
Macronutrients Lipids
  • Requirements
  • 4 to 10 kcals given as lipid meets EFA
    requirements or 2 to 4 kcals given as linoleic
    acid
  • Generally 500 mL of 10 fat emulsion given two
    times weekly or 500 mL of 20 lipids given once
    weekly will prevent EFAD
  • Usual range 25 to 35 of total kcals
  • Max. 60 of kcal or 2 g fat/kg

22
Macronutrients Lipids
  • Potential Adverse Effects
  • Egg allergy
  • Hypertriglyceridemia
  • Decreased cell-mediated immunity (limit to lt1
    g/kg/day in critically ill immunosuppressed
    patients)
  • Abnormal LFTs

23
Parenteral Base Solutions
  • Carbohydrate
  • Available in concentrations from 5 to 70
  • D30, D50 and D70 used for manual mixing
  • Amino acids
  • Available in 3, 3.5, 5, 7, 8.5, 10, 15, 20
    solutions
  • 8.5 and 10 generally used for manual mixing
  • Fat
  • 10 emulsions 1.1 kcal/ml
  • 20 emulsions 2 kcal/ml
  • 30 emulsions 3 kcal/ml (used only in mixing
    TNA, not for direct venous delivery)

The A.S.P.E.N. Nutrition Support Practice Manual,
2nd edition, 2005, p. 97 Barber et al. In ASPEN,
The Science and Practice of Nutrition Support A
Case-Based Core Curriculum. 2001.
24
Other Requirements
  • Fluid30 to 50 ml/kg (1.5 to 3 L/day)
  • Sterile water is added to PN admixture to meet
    fluid requirements
  • Electrolytes
  • Use acetate or chloride forms to manage metabolic
    acidosis or alkalosis
  • Vitamins multivitamin formulations
  • Trace elements

25
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26
Electrolytes/Vitamins/Trace Elements
  • Because parenterally-administered vitamins and
    trace elements do not go through
    digestion/absorption, recommendations are lower
    than DRIs
  • Salt forms of electrolytes can affect acid-base
    balance

27
Adult Parenteral Multivitamins
  • New FDA requirements published in 2000 replacing
    NAG-AMA guidelines
  • Increased B1, B6, vitamin C, folic acid, added
    Vitamin K
  • MVI Adult (Mayne Pharma) and Infuvite (MVI-13)
    from Baxter contain Vitamin K and are consistent
    with the new FDA guidelines
  • MVI-12 (Mayne Pharma) does not contain Vitamin K

28
Parenteral Nutrition Vitamin Guidelines
Vitamin FDA Guidelines
A IU 3300 IU
D IU 200 IU
E IU 10 IU
K mcg 150 mcg
C mg 200
Folate mcg 600
Niacin mg 40
Vitamin FDA Guidelines
B2 mg 3.6
B1 mg 6
B6 mg 6
B12 mg 5.0
Biotin mcg 60
B5 dexpanthenol mg 15
Federal Register 66(77) April 20, 2000
29
Daily Trace Element Supplementation for Adult PN
TRACE ELEMENT INTAKE
Chromium 10-15 mcg
Copper 0.3-0.5 mg
Manganese 60-100 mcg
Zinc 2.5-5.0 mg
ASPEN Safe practices for parenteral nutrition
formulations. JPEN 22(2) 49, 1998
30
Daily Electrolyte Requirements Adult PN
Electrolyte PN Equiv RDA Standard Intake
Calcium 10 mEq 10-15 mEq
Magnesium 10 mEq 8-20 mEq
Phosphate 30 mmol 20-40 mmol
Sodium N/A 1-2 mEq/kg replacement
Potassium N/A 1-2 mEq/kg
Acetate N/A As needed for acid-base
Chloride N/A As needed for acid-base
ASPEN Safe practices for parenteral nutrition
formulations. JPEN 22(2) 49, 1998
31
PN Contaminants
  • Components of PN formulations have been found to
    be contaminated with trace elements
  • Most common contaminants are aluminum and
    manganese
  • Aluminum toxicity a problem in pts with renal
    compromise on long-term PN and in infants and
    neonates
  • Can cause osteopenia in long term adult PN
    patients

ASPEN Nutrition Support Practice Manual 2005 p.
109
32
PN Contaminants
  • FDA requires disclosure of aluminum content of PN
    components
  • Safe intake of aluminum in PN is set at 5
    mcg/kg/day

33
PN Contaminants
  • Manganese toxicity has been reported in long term
    home PN patients
  • May lead to neurological symptoms
  • Manganese concentrations of 8 to 22 mcg/daily
    volume have been reported in formulations with no
    added manganese
  • May need to switch to single-unit trace elements
    that dont include manganese

ASPEN Nutrition Support Practice Manual 2005 p.
98-99
34
Calculating Nutrient Needs
  • Provide adequate calories so protein is not used
    as an energy source
  • Avoid excess kcal (gt35 kcal/kg)
  • Determine energy and protein needs using usual
    methods (kcals/kg, Ireton-Jones 1992,
    Harris-Benedict)
  • Use specific PN dosing guides for electrolytes,
    vitamins, and minerals

35
Protein Requirements
  • 1.2 to 1.5 g protein/kg IBW mild or moderate
    stress
  • Up to 2.5 g protein/kg IBW burns or severe trauma

36
Peripheral Parenteral Nutrition
  • Hyperosmolar solutions cause thrombophlebitis in
    peripheral veins
  • Limited to 800 to 900 mOsm/kg (MHS uses 1150
    mOsm/kg w/ lipid in the solution)
  • Dextrose limited to 5-10 final concentration and
    amino acids 3 final concentration
  • Electrolytes may also be limited
  • Use lipid to protect veins and increase calories

37
Peripheral Parenteral Nutrition
  • New catheters allow longer support via this
    method
  • In adults, requires large fluid volumes to
    deliver adequate nutrition support (2.5-3L)
  • May be appropriate in mild to moderate
    malnutrition (lt2000 kcal required or lt14 days)
  • More commonly used in infants and children
  • Controversial

38
Contraindications to Peripheral Parenteral
Nutrition
  • Significant malnutrition
  • Severe metabolic stress
  • Large nutrition or electrolyte needs (potassium
    is a strong vascular irritant)
  • Fluid restriction
  • Need for prolonged PN (gt2 weeks)
  • Renal or liver compromise

From Mirtallo. In ASPEN, The Science and Practice
of Nutrition Support A Case-Based Core
Curriculum. 2001, 222.
39
Compounding Methods
  • Total nutrient admixture (TNA) or 3-in-1
  • Dextrose, amino acids, lipid, additives are mixed
    together in one container
  • Lipid is provided as part of the PN mixture on a
    daily basis and becomes an important energy
    substrate
  • 2-in-1 solution of dextrose, amino acids,
    additives
  • Typically compounded in 1-liter bags
  • Lipid is delivered as piggyback daily or
    intermittently as a source of EFA

40
Advantages of TNA
  • Decreased nursing time
  • Decreased risk of touch contamination
  • Decreased pharmacy prep time
  • Cost savings
  • Easier administration in home PN
  • Better fat utilization in slow, continuous
    infusion of fat
  • Physiological balance of macronutrients

41
Disadvantages of TNA
  • Diminished stability and compatibility
  • IVFE (IV fat emulsions) limits the amount of
    nutrients that can be compounded
  • Limited visual inspection of TNA reduced ability
    to detect precipitates

ASPEN Nutrition Support Practice Manual 2005 p.
98-99
42
Two-in-One PN
43
PN Compounding Machines Automix
44
PN Compounding Machines Micromix
45
PN SOLUTION COMPONENTSA
Central Peripheral ---Solutions--- Solutions
Lipid- Dextrose- based based
Dextrose 14.5 35.0 lt10.0 Amino Acids 5.5 5.0 lt4.25 Fat 5.0 250 ml/ 3.0 - 8.0 20 fat q M,Th a Final Concentration Courtesy of Marian, MJ.
46
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48
Initiation of PN
  • Adults should be hemodynamically stable, able to
    tolerate the fluid volume necessary to deliver
    significant support, and have central venous
    access
  • If central access is not available, PPN should be
    considered (more commonly used in neonatal and
    peds population)
  • Start slowly(1 L 1st day 2 L 2nd day)

ASPEN Nutrition Support Practice Manual 2005 p.
98-99
49
Initiation of PN formulation
  • As protein associated with few metabolic side
    effects, maximum amount of protein can be given
    on the first day, up to 60-70 grams/liter
  • Maximum CHO given first day 150-200 g/day or a
    15-20 final dextrose concentration
  • In pts with glucose intolerance, 100-150 g
    dextrose or 10-15 glucose concentration may be
    given initially

ASPEN Nutrition Support Practice Manual 2005 p.
98-99
50
Initiation of PN Formulation
  • Generally energy and protein needs can be met in
    adults by day 2 or 3
  • In neonates and peds, time to reach full support
    relates inversely to age, may be 3-5 days

51
Initiation of PN Formulation
  • Dextrose content of PN can be increased if
    capillary blood glucose levels are consistently
    lt180 mg/dL
  • IVFE in PN can be increased if triglycerides are
    lt400 mg/dL

ASPEN Nutrition Support Practice Manual 2005 p.
109
52
PN AdministrationTransition to Enteral Feedings
in Adults
  • Controversial
  • In adults receiving oral or enteral nutrition
    sufficient to maintain blood glucose, no need to
    taper PN
  • Reduce rate by half every 1 to 2 hrsor switch to
    10 dextrose IV) may prevent rebound hypoglycemia
    (not necessary in PPN)
  • Monitor blood glucose levels 30-60 minutes after
    cessation

53
PN AdministrationTransition to Enteral Feedings
in Pediatrics
  • Generally tapered more slowly than in adults as
    oral or enteral feedings are introduced and
    advanced
  • Generally PN is continued until 75-80 of energy
    needs are met enterally

ASPEN Nutrition Support Practice Manual 2005 p.
109
54
Medications That May Be Added to Total Nutrient
Admixture (TNA)
  • Phytonadione
  • Selenium
  • Zinc chloride
  • Levocarnitine
  • Insulin
  • Metoclopromide
  • Ranitidine
  • Sodium iodide
  • Heparin
  • Octreotide

55
Parenteral Nutrition
  • Infusion Schedules

56
Infusion Schedules
  • Continuous PN
  • Non-interrupted infusion of a PN solution over
    24 hours via a central or peripheral venous access

57
Continuous PN
  • Advantages
  • Well tolerated by most patients
  • Requires less manipulation
  • decreased nursing time
  • decreased potential for touch contamination

58
Continuous PN
  • Disadvantages
  • Persistent anabolic state
  • altered insulin glucagon ratios
  • increased lipid storage by the liver
  • Reduces mobility in ambulatory patients

59
Infusion Schedules
  • Cyclic PN
  • The intermittent administration of PN via a
    central or peripheral venous access, usually over
    a period of 12 18 hours
  • Patients on continuous therapy may be converted
    to cyclic PN over 24-48 hours

60
Cyclic PN
  • Advantages
  • Approximates normal physiology of intermittent
    feeding
  • Maintains
  • Nitrogen balance
  • Visceral proteins
  • Ideal for ambulatory patients
  • Allows normal activity
  • Improves quality of life

61
Cyclic PN
  • Disadvantages
  • Incorporation of N2 into muscle stores may be
    suboptimal
  • Nutrients administered when patient is less
    active
  • Not tolerated by critically ill patients
  • Requires more nursing manipulation
  • Increased potential for touch contamination
  • Increased nursing time

62
Parenteral Nutrition
  • Home TPN

63
Home TPN
  • Safety and efficacy
  • depend on
  • Proper selection of patients
  • Adequate discharge planning/education
  • Home monitoring protocols

64
Home TPN
  • Patient selection
  • Reasonable life expectancy
  • Demonstrates motivation, competence, compliance
  • Home environment conducive to sterile technique

65
Home TPN Discharge Planning
  • Determination whether patient meets payer
    criteria for PN completion of CMN forms
  • Identification of home care provider and DME
    supplier
  • Identification of monitoring team for home
  • Conversion of 24-hour infusion schedule to cyclic
    infusion with monitoring of patient response

66
Home TPN
  • Cost effective
  • Quicker discharge from hospital
  • Improved rehabilitation in the home
  • Reduced hospital readmissions

67
Common Indications for PN in Peds
  • Surgical GI disorders
  • Intractable diarrhea of infancy
  • Short bowel syndrome
  • Inflammatory bowel disease
  • Intractable chylothorax
  • Intensive cancer treatment

68
Pediatric Energy Needs in PN
  • No consensus exists as to how to determine energy
    needs of hospitalized children
  • RDAs are intended for healthy children but can
    use for healthy/acutely ill children and monitor
    response
  • Can estimate REE using WHO equation and add
    stress factors, monitor clinical course
  • Indirect calorimetry recommended in difficult
    cases

69
RDAs for Energy and Protein
Category Age (yr) Energy (kcal/kg/d) Protein (g/kg/d)
Infants 0.0-0.5 108 2.2
Children 1-3 102 1.2
4-6 90 1.1
7-10 70 1.0
Females 11-14 47 1.0
15-18 40 0.8
Males 11-14 44 1.0
15-18 45 0.9
Recommended Dietary Allowances, 10th ed. 1989.
National Academy Press, Washington, DC
70
WHO Equations to predict REE from body weight
Sex/Age Range (years) Equation to Derive REE (kcal/d)
Males 0-3 (60.0 x wt) 54
Males 3-10 (22.7 x wt) 495
Males 10-18 (17.5 x wt) 651
Females 0-3 (6.1 x wt) 51
Females 3-10 (22.5 x wt) 499
Females 10-18 (12.2 x wt) 746
71
Increase WHO REE by stress factors
Fever Increase 13 per degree C
Cardiac Failure 15-25
Traumatic Injury 20-30
Severe respiratory distress or broncho-pulmonary dysplasia 25-30
Severe sepsis 45-50
Olson, D. Pediatric Parenteral Nutrition. In
Sharpening your skills as a nutrition support
dietitian. DNS, 2003.
72
Trauma/Critically Ill Peds
Age in years Kcals/kg G/pro/kg
0-1 90-120 2.0-3.5
1-6 75-90 1.8-3.0
7-12 50-75 1.5-2.5
13-18 30-60 1.0-2.0
73
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74
Pediatric PN Fluids
  • Standard calculation
  • 100 kcal/kg for infant 3-10 kg
  • 1000 kcal 50 kcal/kg for every kg over 10 kg
    for a child 10-20 kg
  • 1500 kcal 20 kcal/kg for every kg over 20 kg
    for a child over 20 kg
  • 1 mL fluid/kcal/d adjustments for fever,
    diarrhea, stress, etc.

ASPEN BOD Guidelines for the use of parenteral
and enteral nutrition in adult and pediatric
patients. JPEN 2626SA, 2001
75
Pediatric PN Carbohydrate
  • Carbohydrate should comprise 45-50 of caloric
    intake in infants and children (C)
  • For neonates, CHO delivery in PN should begin at
    6-8 mg/kg/minute of dextrose and advanced to
    10-14 mg/kg/minute. (B)

ASPEN BOD Guidelines for the use of parenteral
and enteral nutrition in adult and pediatric
patients. JPEN 2628-29SA, 2001
76
Pediatric PN Lipid
  • Preterm start at .5 g/kg/day and increase by
    .5g/kg q day
  • Infants Start at 1 g/kg and increase by .5
    g/kg/day until the maximum or desired dose is
    reached need 0.5 to 1 g/kg/day for EFA needs
  • Maximum is 3 g/kg for lt24 months old and 2.5g/kg
    for 24 months and older

77
Daily Electrolyte and Mineral Requirements for
Peds Pts
Electrolyte Infants/Children Adolescents
Sodium 2-6 mEq/kg Individualized
Chloride 2-5 mEq/kg Individualized
Potassium 2-3 mEq/kg Individualized
Calcium 1-2.5 mEq/kg 10-20 mEq
Phosphorus 0.5-1 mmol/kg 10-40 mmol
Magnesium 0.3-0.5 mEq/kg 10-30 mEq
National Advisory Group. Safe practices for
parenteral nutrition formulations JPEN
19982249-66
78
Document in Chart
  • Type of feeding formula and tube
  • Method (bolus, drip, pump)
  • Rate and water flush
  • Intake energy and protein
  • Tolerance, complications, and corrective actions
  • Patient education
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