Miscellaneous Flashcards

1
Q

Describe typical stress and energy response in the body, as it relates to why TPN is needed during illness:

A

Increased metabolic needs > increased energy needs > increased calorie and nutrient needs > Gluconeogenesis > 1) Glycogen converted to glucose and urea for energy > 2) Fat stores mobilized for energy > 3) Protein stores mobilized for energy > Release of somatic and visceral proteins from muscle, tissue, etc. to create energy > Catabolic state > Negative nitrogen balance > Starvation

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2
Q

Define: Gluconeogenesis

A

Generation of glucose from certain non-carbohydrate carbon substrates

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3
Q

What does TPN promote?

A

Anabolism (synthesis of complex molecules for energy) to approximately the same ratio as a regular diet in a healthy person

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4
Q

Describe the neuroendocrine-mediated changes that can increase energy expenditure:

A

Stressor > NE mediated activation to stimulate tissue healing and preserve normal organ function > Few changes occur in first 24 hours > After, intense catabolic activation occurs > Stress hormones released > Increased energy expenditure, body protein breakdown, weight loss > Nitrogen excretion increases + K+ excretion increases + Glucose levels rise + Na+ and fluid retained + Decreased GI motility > Peak of catabolism > Anabolic recovery begins (stress hormones subside, glucose declines, nitrogen balance restored)

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5
Q

What are contraindications to parenteral nutrition support?

A
  • Catheter-related complications (e.g. occlusion, displacement)
  • Coagulopathies
  • Local and systemic complications associated with CVC
  • Pt noncompliance or refusal to eat
  • Pt with GI tracts expected to resume normal functioning within 7-10 days
  • Poor prognosis
  • Superior vena cava thrombosis
  • Terminal illness, comfort care only
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6
Q

How many calories do different types of intake provide?

A
  • Proteins = 4 cal/g
  • Carbs = 4 cal/g
  • Fats = 9 cal/g
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7
Q

What are some of the roles of protein?

A
  • Form immunoglobins to fight infection and disease
  • Form structure of tissues
  • Energy production
  • Maintain oncotic pressure (e.g. plasma proteins)
  • Promote tissue growth and repair
  • Synthesize compounds (e.g. thrombin, the clotting protein)
  • Synthesize essential bodily fluids and secretions (e.g. enzymes, hormones, neurotransmitters, bile acids, etc.)
  • Transportation (e.g. albumin transports free bilirubin, free fatty acids, and drugs)
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8
Q

Why is protein a key component of PN?

A
  • Adjunct in off-setting nitrogen loss or in treatment of negative nitrogen balance
  • Promotes anabolism
  • Prevents protein catabolism
  • Always administered concurrently with dextrose
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9
Q

Why are carbs a key component of PN?

A
  • Provide basic energy source (glucose) that can be stored in almost all body tissues (as glycogen)
  • Provides needed calories for energy
  • Spares protein and prevents gluconeogenesis
  • Needed to completely oxidize fat to prevent it being broken down into ketones
  • Dextrose has nitrogen sparing effect
  • Dextrose utilized type in TPN
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10
Q

Why are fats a key component of PN?

A
  • Most concentrated source of energy for all body tissue types (except CNS, fueled by glucose)
  • Supplies a non-carb and non-protein source of energy, causing an increase in heat production and decrease in respiratory quotient
  • Isotonic, can be either PIV or CVC
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11
Q

Why would pH related problems interfere with fat in PN?

A

The prime destabilizers of lipid emulsions are excessive acidity and inappropriate electrolyte content

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12
Q

Describe infusion rates of fats:

A
  • Initial rate 1 ml/min for first 15-30 minutes of infusion, may increase to 2 ml/min
  • No more than 500 cc in the first 24 hour of therapy
  • After 24 hours should not exceed 2.5 g/kg/day
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13
Q

What mineral CANNOT be mixed with other drugs and infusates?

A

Iron

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14
Q

What is the difference between minerals and vitamins?

A

Minerals are inorganic elements, and vitamins are organic substances

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15
Q

What are some hepatic and renal compromise considerations with PN?

A

LIVER:
- Pt’s with liver disease (cirrhosis, encephalopathy, coma) have LOW levels of branched chain amino acids and high levels of aromatic amino acids, which makes them intolerant of crystalline amino acid preparations
= intolerant of crystalline amino acid preparations
- When intolerant of crystalline solutions, require amino acids with HIGH levels of branched chain amino acids (with encephalopathy, will improve mental status and EEG patterns)

RENAL:

  • TPN solutions contain both essential and non-essential amino acids, BUT renal restrictions = should have ONLY essential amino acids
  • Only minimal quantities of ESSENTIAL amino acids will be beneficial (enhance urea utilization, promote protein synthesis, improve metabolic balance [decrease electrolyte imbalances])
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16
Q

What are some guidelines for TPN administration?

A
  • If next dose not yet available, hang a 10% dextrose infuse with 50% dextrose added to prevent rebound hypoglycemia
  • Remove refrigerated mixtures ~1 hour before administering (otherwise cold and uncomfortable)
  • Introduce TPN relatively slow to preclude hyperglycemia (50 cc/hr)
  • Never “catch up” if fallen behind, only adjusted within a 10% margin
  • Pt’s need to be weaned off to prevent rebound hypoglycemia (4-48 hours, gradually decreasing and evaluating patient response)
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17
Q

Why is TPN susceptible to microbial growth?

A

Their high dextrose content is attractive to microbes

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18
Q

What are S&S of metabolic acidosis?

A
  • Confusion
  • Headache
  • INCREASED RR and depth
  • N/v
  • Warm and flushed skin
  • Decreased pH
  • Decreased HCO3
  • Increased serum chloride
  • Increased serum bicarbonate
19
Q

What are S&S of metabolic alkalosis?

A
  • Paresthesia
  • Muscle hypertonia
  • DEPRESSED RR
  • Hypokalemia
  • Vertigo
  • Decreased serum chloride
  • Increased serum bicarbonate
20
Q

What are S&S of hypoglycemia?

A
  • Diaphoresis
  • Irritability
  • Nervousness
  • Shakiness
21
Q

What are S&S of hyperglycemia?

A
  • Increased serum glucose
  • Fruity breath
  • Anxiety/confusion
  • Dehydration
  • Polydipsia
  • Polyuria
  • Malaise
22
Q

What are S&S of hypocalcemia?

A
  • CNS irritability **
  • Tingling/numbness
  • Muscle cramping/spasms
  • Tetany
  • Seizures
  • Chvostek’s and Trousseau’s signs
23
Q

What are S&S of hypokalemia?

A
  • Slight glucose elevation d/t insulin suppression
  • Anorexia
  • Fatigue
  • Muscle weakness
  • Decreased gastric motility
  • EKG changes
24
Q

What are S&S of hyperkalemia?

A
  • Acidosis
  • EKG changes
  • Ventricular dysrhythmias
  • Cardiac arrest
  • Muscle weakness
  • Flaccid muscular paralysis
  • Paresthesia
25
Q

What is refeeding syndrome?

A
  • Complication that may occur during initial TPN
  • Body, during starvation, has adapted somewhat to being nutritionally deprived
  • Aggressive initiation of nutritional support can result in electrolyte shift from plasma to intracellular fluid
  • Can be very dangerous and fatal d/t cardiorespiratory complications
  • May manifest as edema; hypernatremia; hypokalemia; hypomagesemia; and hypophosphatemia
26
Q

Why does TPN IV sets have filters?

A

Filters allow for various particles to be removed before infusion, preventing catheter-related complications such as infection

27
Q

What is a 3:1 solution?

A
  • Aka. TNA
  • Amino acids, dextrose AND fats (fats may be done separate, if not it is a 3:1)
  • Caution must be taken to minimize pH related problems that might occur in a 3:1 solution (follow proper combining protocols)
28
Q

According to the course overview, what advantages does CVC have over peripheral lines?

A
  • Administration of solutions that would be irritating to small veins
  • Access to individuals with inaccessible peripheral veins
  • Rapid administration of large solutions
  • Uninterrupted administration of several solutions at one time
  • Drawing of blood samples
  • Monitoring central venous pressure
29
Q

Why is TPN typically separate from fat infusions?

A
  • Conventional TPN administration sets and bags contain PVC (synthetic plastic) and have DEHP as a plasticizer (solvent promoting flexibility and promote elasticity), but lipids extract hese
  • Recommended to have separate administration sets, glass containers or special non-PVC bags
  • infuse lipids via Y-connector or separate lumen
30
Q

Why can’t regular filters be used with fat emulsions?

A
  • Regular porosity filters contain filters too small for lipids to pass through (0.2 compared to 0.4-0.5)
  • Generally uses a 1.2 size
31
Q

When do we need to exercise caution while administering fat emulsions?

A
  • Patients with anemia, coagulopathies, severe liver damage, or any danger of fat embolism
  • Pt ability to eliminate infused fat from circulation needs monitoring via routine triglyceride levels and LFT’s
32
Q

Proteins are _____ compounds

A
  • Nitrogenous
  • This means that when there is increased energy expenditure and breakdown of body protein, there is a break down of nitrogen, which is not being replaced (nitrogen has to be ingested), so cannot replace and balance nitrogen levels without proteins!
  • Remember that there are essential amino acids
  • Biologic value of amino acids = % of absorbed nitrogen (from ingested amino acids)
33
Q

Define: Crystalline preparation

A

Crystalline solids consist of atoms, ions and molecules arranged in definite and repeating three-dimensional patterns

34
Q

Carbs are necessary to completely oxidize ______ so that it is not broken down into ______

A

fat; ketones

35
Q

Define: Uremia

A

a raised level in the blood of urea and other nitrogenous waste compounds that are normally eliminated by the kidneys.

36
Q

If a patient is in a hypercatabolic state, how should their TPN be altered?

A
  • Increased nitrogen excretion d/t altered protein metabolism = need to increase protein compared to conventional TPN
  • Mixture of essential and nonessential amino acids with high amounts of branched chain acids
37
Q

When is stress formula TPN contradinciated?

A
  • Anuria (failure to produce urine)
  • Severe uncorrected acid-base and electrolyte
  • Hepatic coma
38
Q

When is hepatic TPN formulas contraindicated?

A

Anuria (remember that patients with renal impairment NEED to have NO NON-essential amino acids, but hepatic patients have both)

39
Q

What estimates caloric needs?

A

Calorimetry (measure of heat loss or gain, determines oxygen expenditure and carbon dioxide production)

40
Q

What is Essential Fatty Acid Deficiency?

A
  • Etiology: Deficient intake (remember that there are essential fats for life!)
  • Defining: Increased BUN; alopecia; dry, cracked skin with dermatitis; CNS aberrations; pulmonary dysfunction
  • Interventions: Fat emulsion supplementation in TPN or with intermittent infusions
  • Prevention: accurate calculation of protein, fat and CHO ratios to maintain positive nitrogen balance
41
Q

How do we know when refeeding is reversed?

A

Once body has reestablished normal albumin and electrolyte imbalances

42
Q

How do we avert refeeding syndrome?

A
  • Initiate TPN slowly
  • Gradually increase TPN rate
  • Carefully monitor patient response and electrolyte levels
43
Q

What are the five key signs of refeeding syndrome?

A
  • Edema
  • Hypernatremia
  • Hypokalemia
  • Hypomagnesemia
  • Hypophosphatemia
  • Electrolyte shift from PLASMA to INTRA-CELLULAR fluid*