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65 Cards in this Set

  • Front
  • Back
key to when to use PTN
GUT MUST NOT BE WORKING
PN definition
 Parenteral Nutrition (PN)- any type of item that provides nutrition (can be just like a bag of potassium)
Total Nutrient Admixture (TNA) vs. TPN
 Total Parenteral Nutrition (TPN)- we are trying to provide all nutrients

TNA- same, but term used when we've added fats to nutrition as well
Peripheral Parenteral Nutrition (PPN)-
can be any nutrition administered peripherally (not central)
5 disease indications for TPN
GI obstruction
Severe mucositis
Ileus (dysmotility)
Intractable nausea/vomiting
Severe diarrhea
7 non-disease related indications for TPN
Inability to obtain enteral access
GI rest (pancreatitis, GI fistula, wounds)
Poor GI perfusion
Short gut
High metabolic rates
Multiple OR trips- too many surgeries requiring fasting
TPN CI (when not to use) (4)
 GI tract that is functioning
 Inability to obtain IV access
 Estimated need for treatment less than 5 days
 Prognosis not warranting aggressive therapy- end of life care, DNR
peripheral parenteral nutrition- need what type of veins?

site changes? if so how often?

short or long term? (give max duration)
Need high quality veins!
 Site change every 48 hours
 Short term therapy (No more than 2 weeks)
peripheral parenteral nutrition- kcal and mOsm req
 < 1800 kcals
 < 900 mOsm
% conc of dextrose and AA max that can be used for peripheral
 5 – 10% dextrose
concentration max
 3% amino acid (AA)
concentration max
size of volume with peripheral infusions- why?

usually higher in ____
 More dilute, so larger volume
 Usually higher fat formulas
PN is considered hypo or hypertonic to body fluids?
HYPERTONIC DUUHHH BLOOD OSM IS LIKE 290
3 issues if PN is given inappropriately
Phlebitis, thrombosis
and extravasation if
give inappropriately
mOsm per gram of dextrose
per g AA
per mEq
5 mOsm/g dextrose
10 mOsm/g amino acid
1 mOsm/mEq
central PN dilutional factor in superior vena cava
Dilutional factor of 3600:1- super diluted so can't cause dmg to vessels!!YAYY
benefit of central PN over peripheral
Can provide PN that meets ALL
nutritional requirements
placement of WHAT is important when determining proper central venous placement

what vein?
TIP PLACEMENT
is Key!!!

Superior vena cava
Percutaneous Nontunneled Catheter- when used?
access through which veins (4)
Used more in acute care setting for short duration therapies

Access through subclavian, jugular,
femoral or antecubital but ULTIMATELY routed through vessel and tip goes into superior VC
why is percutaneous nontunneled catheter called "nontunneled"
nontunneled means it doesn't tunnel through skin , but may be
sutured at exit site
from skin- just goes right into vein
Peripherally Inserted Central Venous Catheter (PICC) - tunneled or non tunneled

venous access where? (3 examples)

common where? (2)
Type of nontunneled catheter

Access and placement
through a peripheral
vein, such as basilic,
cephalic and brachial

Common both in
acute care and in
home care
Tunneled Central Venous Catheter- venipuncture site, exit site
Percutaneous exit site under breast area (pt can see where shit is hooked up)

Actual venipuncture site into subclavian or
jugular veins
tunneled central venous catheter- reason for using this one
Concept is to separate venipuncture and exit sites to decrease risk it'll get into blood for infections so can use for long term care
Implanted Port for Central Venous
Access- what is it

# of times you can access port
Catheter attached to disk with self-sealing
silicone elastomer septum

Can access port up to 1000 to 2000 times
Implanted Port for Central Venous
Access- placed where?

benefits (2)
Placed into subcutaneous pocket
in anterior chest

Lower rates infection and thrombosis
catheter complications (3) on insertion
 Pneumothorax
 Nerve damage
 Malposition- at placement or it migrates- have to xray after placement to make sure it's in the right place
catheter complications- occlusions (3)
Kink
Fibrin sheath
Thrombus (clot)
catheter complications- infection issues (2 locations)
 At site
 Sepsis
3 CHO for TPN
 Dextrose most commoon
 Fructose
 Glycerin
3 micronutrients for TPN
 Electrolytes
 Vitamins
 Trace Minerals
other shit you can add to TPN (6)
 Insulin
 H2R2s
 Iron
 Heparin
 Albumin
 Additional vitamins
for fixed TPN formulations (premade)- how would you adjust cals
 Adjust calories by adjusting the infusion
rate
std formulations can be used for which pt (2)
if pt only needs to use for a few weeks- prob won't need adjustments

Can be used for patient with normal
daily nutrition needs
stock solutions- never do what?

only use for what?
 NEVER administered directly to a patient
 Only used to manufacture more
dilute infusions- ex) 30% fat emulsion
fat emulsions- tonicity-->exception

implications
All fat emulsions are isotonic EXCEPT 30% so don't ever infuse this peripherally

so can be infused peripherally
due to _____ we can't use 9kcal/g for fat emulsion
Due to glycerin, cannot use 9 kcals/gram we use for fat
order of nutrient calculations - (9)
1.Calories- how many do they need
2.Fluids - how much do they need
3.Amino Acids- how much of kcal will be AA
4.Lipids- % of kcal
5.Carbohydrates – use to QS to total calories needed
6.Electrolytes- normal or are labs off?
7.Vitamins- deficiency or no?
8.Trace Elements
9.Other ingredients

QS to total fluids
pt with what 2 disease states may be sodium restricted
 Pts with CHF or fluid overload may be restricted
pt with what conditions may have larger sodium needs (3)
 Pts with fistulas, NG tubes, small bowel losses may have large needs
potassium needs will be affected by...
acid base status
Ca++ bound to what?

when would you calculate adjusted Ca
Bound to albumin

Calculate adjusted Ca if
albumin levels low
purpose of Cl and acetate in TPN
Chloride and Acetate used to
balance formula
Factors Affecting Calcium Phosphate **** KNOW THIS precipitation (4)
pH of the solution- the lower the pH, the more is solubilized
Concentration of calcium and phosphate- As concentrations increase, risk for precipitation rises
Salt form of calcium-
 Type of phosphate- Potassium phosphate has high pH, so adding large quantities can increase pH of final solution
CaCl vs. Ca gluconate- which is better? why?
Calcium chloride has much higher % dissociation and more
risk for precipitation than calcium gluconate
AA effect on ca phos precipitation (2)

dextrose effect

others (2)
concentration of AA- AA have acidic pH (4.5-6.5) and buffer TPN so phosphate does not increase pH
composition of AA- AA may already contain phosphate or other lytes
concentration of dextrose- dextrose buffers- higher conc. better
temp of solution- higher temp = higher risk for precipitation
order of mixing- phosphate first, calcium last
For fairly acidic amino acids (pH
around 4.5 like Aminosyn etc.)
and... AA Conc > 2% (FINAL CONC. in g/100mL)- rule of thumb for CaPhos precipitation- how to determine if it will precipitate
Phosphate mMol+ Calcium (mEq) ≤ 30
should be fine

Amounts > 30 should raise a Big
Red Flag
how to decrease risk of precipitates killing pt in TPN- (7)

general advice, TNA volume size, mixing order, minimum AA conc.
 Follow compounder’s protocol!
 Use software or references to
check Ca-Phos compatibility
 Add phosphate before calcium
 Minimum AA concentration 3%
 Use minimum volumes for TNA
 Use EVA containers- DEHP may leach lipids
 Filtration of all parenteral
nutrition
size filter to use for 2-in-1 TPN and 3-in-1 TPN
 0.22 micron filter for all 2-in-1 (piggyback lipids)
 1.2 micron filter for 3-in-1
lipid stability major issue and how it happens


what to do if this happens

what increases risk of this happening
Negative charges in lipid emulsions keep fat particles in emulsion

If ionic forces broken down, fat particles
begin to clump and cause “cracking”

Cracked or marbled products must be
discarded!

Divalent and trivalent cations (calcium and shit in TPN) increase risk
when compounding- order you should add lipids and dextrose and AA

why?
When compounding, never add lipids directly to dextrose as too acidic pH

Add dextrose to amino acids and then add lipids
when choosing something for GERD in TPN- what is compatible and what is not?
all H2R2s

NOT PPIs
2 compatible additives often added to TPN
insulin
additional vitamins/trace minerals
Iron and albumin addition to TPN- issues
 Iron- Strongly ionized and can
crack lipid emulsions
Albumin- Strongly ionized and can
crack lipid emulsions
things to be careful of when adding more shit to TPN (2)
Additives may change pH and affect chance for calcium-phosphate
precipitation

Additives may cause creaming or cracking of lipid emulsions
major contaminant of TPN

where is it found (2)
Aluminum is a contaminant of many
ingredients utilized in manufacture of PN

 Phosphate products typically contain
 Amount on product labels and in package inserts
Why is aluminum such a horrible contaminant- what does it do? concern for whom in particular (3)

keep total amount below what level
Can be deposited in bone and in brain
 Concern for neonates, people in renal failure and people on long-term TPN
 Keep total amount in PN below 25mcg per liter
continuous admin of TPN- what does this mean

typical in what setting

rate/conc when initiating
 All ingredients administered over 24 hours
 Typical of acute care settings

 When initiate, start with lower concentration OR lower rate for initial 24 to 72 hours
cyclic admin of TPN- admin over what duration/how to taper on and off (2)

setting
 Nutrition administered over 12 to 14 hours

Taper patient on and off by using lower infusion rates

Typical of home care settings- don't have to always be attached to tubes

Total administered must
meet patient’s daily nutrition needs
routine monitoring for TPN- what to monitor? also mention frequency (5)
 Temperature daily
 Weight daily
 Glucose q 4- 6 hrs until
stable- to make sure pancreas can handle
 Electrolytes daily until
stable, then 2-3 x week
 I/O- inputs outputs
4 nutritional labby protein things to monitor
 Prealbumin/ albumin- assessment of nutrition status
 Transferrin
 Retinol binding protein
 Nitrogen balance- 24 hour urine collection
TPN use by date - risk (when prepared in ISO class 5 LAFH) - why?
Parenteral nutrition solutions involve multiple additives and complex
manipulations

Medium risk when prepared
in ISO Class 5 LAFH
Medium Risk Use-By date RT and refrigeration (TPN without lipids: 2-in-1)
 30 hours room temp
 9 days refrigerated
TPN with LIPIDS use by dates at RT

hang time of lipids if admin separately
 24 hours room temp when added to PN
 12 hours hang time when administered separately
how often do you have to change sets?? and lines for 3-in-1 vs. 2-in-1
 Every 24 hours for TNA (3-in-1)
 Every 72 hours for 2-in-1
7 things that have to be on label
pharmacy info/pt info
date/time to be administrated
base formula (amt of dextrose and shit) + electrolytes
route of admin (Central line?) and rate
volume/overfill
beyond use date
storage conditions
4 things to inspect in the final check
Visual inspection- against lighted white and/or black bg, look for visual defects within solution or container

compounding accuracy- weighing, checks

sterility testing- media fill test??

comparison of doc order to compounding worksheet to product to label