TPN

advertisement
การดแู ลผ้ ปู ่ วยทีไ่ ด้ รับสารอาหาร
ทางหลอดเลือดดาแบบสมบูรณ์
(TPN Patient Care Workshop)
1-3 กรกฎาคม 2552 รพ.พระมงกุฎเกล้า กทม.
Contents
1
Adults TPN
2
Pediatric and neonatal TPN
3
Complications of TPN
4
TPN in special population
การดูแลผู้ป่วยทีไ่ ด้ รับสารอาหารทางหลอดเลือดดาแบบสมบูรณ์
1.Adults TPN
- Physical and nutritional assessment
- Indication for TPN therapy
- Requirements of fluid, calorie, protein
and micronutrient
- Patient monitoring and formula
adjustment
- Patient education
การดูแลผู้ป่วยทีไ่ ด้ รับสารอาหารทางหลอดเลือดดาแบบสมบูรณ์
2.Pediatric and neonatal TPN
- Physical and nutritional assessment
- Indication for TPN therapy
- Requirements of fluid, calorie, protein
and micronutrient
- Patient monitoring and formula
adjustment
- Patient education
การดูแลผู้ป่วยทีไ่ ด้ รับสารอาหารทางหลอดเลือดดาแบบสมบูรณ์
 3.Complications of TPN
- Metabolic
- Infectious
- Mechanical/technical
 4.TPN in special population
Definition of
nutritional support
When normal diets
fail to meet the daily
requirements.
or
When assessment
documents deficiencies
Nutrition planning becomes
a part of medical therapeutics
Nutrition screening tools
Objective Measurement
* Anthropometry
* Laboratory
* Delayed cutaneous hypersensitivity
skin test
Subjective Measurement
* History-diet/medical/surgical/social
-functional/family/GI
* Nutrition focused physical assessment
* SGA, NRS (2002)
Subjective global assessment (SGA)

A.History
1.Weight change
Overall loss in past 6 mo: amount___kg, % loss =_____
Change in last 2 wk:_____Increase
_____No change
_____Decrease
2.Dietary intake change (relative to normal)
____No change
_____Change : duration____wks_____months
_____Type:_____sub-optimal solid diet
_____full liquid diet
_____hypocaloric diet
_____starvation
3.Gastrointestinal symptomps(that persisted > 2 wks)
_____None
_____Nausea
_____Vomiting
_____Diarrhea _____Anorexia
Subjective global assessment (SGA)
 A.History (cont.)
4.Functional capacity
_____No dysfunction (full capacity)
_____Dysfunction: duration____wks_____months
_____Type:______Working sub-optimally
______Ambulatory
______Bed ridden
5.Disease and its relationship to nutritional requirments
Primary diagnosis (specify)___________
Metabolic demand(stress): ______No stress
______Low stress
______Moderate stress
______High stress
Subjective global assessment (SGA)
 B.Physical (for each specify 0=normal, 1+=mild,
2+=moderate, 3+=severe)
_____Loss of subcutaneous fat (triceps, chest)
_____Muscle wasting (quadriceps, deltoids)
_____Ankle edema
_____Sacral edema
_____Ascites
 C.Subjective global assessment rating (select
one)
_____A=Well nourished
_____B=Moderate (or suspected) malnourished
_____C=Severely malnourished
Nutrition Risk Screening (NRS 2002)

Step 1 :Initial screening
1. Is BMI < 20.5 ?
2. Has the patient lost weight within the last 3 months ?
3. Has the patient had a reduced dietary intake in the last
week ?
4. Is the patient severely ill (e.g. in intensive therapy) ?
:If the answer is ‘Yes’ to any question, the screening in step
2 is performed.
:If the answer is ‘No’ to all questions the patient is rescreened weekly intervals.
;If the patient e.g. is scheduled for a major operation a
preventive nutritional care plan is considered to avoid
the associated risk status
Yes/No
Yes/No
Yes/No
Yes/No
Nutrition Risk Screening (NRS 2002)

Step 2 :Final screening
Impaired nutrition status
Severity of disease (=increase in
requirements)
Normal nutritional
Absent
requirement
Score=0
Absent
Score=0
Normal nutritional status
Mild
Score=1
Wt. loss > 5% in 3 mon. or
Food intake below 50-75%
of normal requirement in
preceding week
Mild
Score=1
Hip fracture, chronic
patients, in particular
acute complications:
cirrhosis, COPD, chronic
hemodialysis, DM,
Oncology
Moderate
Score=2
Wt loss > 5% in 2 mon. or
BMI 18.5-20.5 +Impaired
general condition or Food
intake 25-50% of normal
requirement in preceding
week
Moderate
Score=2
Major abdominal
surgery, stroke, severe
pneumonia,Hematologic
malignancy
Severe
Score 3
Wt loss > 5% in 1 mon.
(> 15% in 3 mon.) or
Severe
Score 3
BMI < 18.5 + Impaired
general condition or Food
intake 0-25% of normal
requirement in preceding
week
Score:
+ Score:
Head injury, Bone
marrow
transplantation,
Intensive care
patients
(APACHE > 10)
=Tol.score
Age: If ≥ 70 yrs; add 1 to total score above
Score ≥ 3: the patient is nutritionally at risk and a nutritional care plan is
initiated
Score < 3: weekly rescreening of the patient.If the patient, e.g., is
scheduled for a major operation, a preventive nutritional care
plan is considered to avoid the associated risk status
Severe Nutritional Risk
Presence of ≥ 1 criteria :
* Involuntary increase or decrease in weight
- ≥ 10 % usual weight over 6 months or
- ≥ 5 % of usual weight over 1 month
* BMI < 18.5 kg /m2
* SGA grade C or NRS ≥ 3
* Serum albumin < 3 g/dl (with no evidence
of hepatic or renal dysfunction)
Classification of Protein Energy
Malnutrition
Severity
Mild
Course
Acute
Main deficit
Energy
Moderate
Chronic
Protein
Severe
Both
Both
Kwashiorkor - predominantly protein deficiency
Marasmus - mainly energy deficiency
Marasmic kwashiorkor - combination of chronic energy deficiency
and chronic or acute protein deficit
Protein deficiency
Serum albumin < 3.5 g/dl
Absolute lymphocyte < 1,500 cell/mm3
Serum transferrin < 150 mg/dl
Loss of reactivity to common skin test
antigens
Lab. test for visceral protein
Protein
Albumin
Transferrin
Pre-albumin
Half-life
21 days
7 days
2 days
Normal value
3.5-5.5 g/dl
270-400 mg/dl
18-40 mg/dl
Pre-albumin
(mg/dl)
Albumin
(g/dl)
Transferrin
(mg/dl)
Mild
3.0-3.5
150-200
11-18
Moderate
2.1-3.0
100-150
5-10.9
Severe
< 2.1
< 100
<5
Severity
Serum albumin
(g/dl)
Total lymphocytes Status of visceral
(cell/mm3)
protein
3.0-3.5
1,500-1,800
2.5-3.0
900-1,500
< 2.5
< 900
Mildly depleted
Moderately
Severely
Creatinine-height index (CHI)
CHI=Actual 24 hr creatinine excretion x 100%
Ideal 24 hr creatinine excretion
CHI < 80%
=mild
60-80% =moderate
< 60% = severe
Nitrogen balance
= Protein-[24hr UUN(g) + 4]
6.25
Indication for TPN therapy
Length of expected NPO status
<3d
Premorbid BMI > 18.5
and < 10% Wt. loss
Dextrose containing IV
>3d
Premorbid BMI < 18.5
and > 10% Wt. loss
Perform complete
Nutrition assessment
- EN/PN
NPO > 3 d or change in clinical status
Disease diagnosis
GI tract function
No
Yes
Enteral feeding
NPO < 7 d
PPN
NPO > 7 d
TPN
Indication of PN
Adults
1. pt.มีปัญหาการทางานและการดูดซึมสารอาหารของ GI tract
* Massive small bowel resection
* GI fistula (high output; >500 ml)
* Inflammatory bowel diseases
* Bowel obstruction
* Persistent GI bleeding, GI ischemia
* Hyperemesis gravidarum
* Diarrheaอย่างรุนแรงและคาดว่าไม่สามารถรับอาหารทาง EN
หรืออาการไม่ดขี น้ึ ภายใน 5- 7 วัน
2. pt.CA ทีม่ ภ
ี าวะmalnutritionอย่างรุนแรง และGIผิดปกติ
จนไม่สามารถกินทางOral/รับทางENได้ เกินกว่า 1 wk
Indication of PN
 Adults (ต่อ)
3. Severe acute pancreatitis ไม่สามารถรับทางENได้เกินกว่า 1
wk e.g.ในpt.ปวดท้องอย่างรุนแรง, มี ascites,fistula output
4. Critical illness คาดว่า GI ทางานไม่ได้ 5-7 วัน e.g. major
surgery, trauma, sepsis
5. Catabolic state ระดับปานกลาง-รุนแรง e.g. pt. ตับ ไต ทางเดิน
หายใจล้มเหลว + malnutrition when GI tract is not
usable 5-7 days
6. Preoperative in severe malnourished without
functional GI tract
Indication of PN
Adults (ต่อ)
7. Anorexia nervosa ไม่สามารถทนรับทาง ENได้ดว้ ยเหตุผลทาง
กายภาพ/ทางอารมณ์
Indication of PN
 Pediatric and neonatal
1. pt.มีปัญหาการทางานและการดูดซึมสารอาหารของ GI tract
* Massive small bowel resection
* GI fistula e.g. esophageal, tracheosophageal
* Inflammatory bowel diseases e.g.
necrotizing enterocolitis(NEC), ulcerative
colitis
* มีความผิดปกติของผนังหน้าท้องตัง้ แต่แรกคลอดและรับทางENไม่ได้
เช่น omphalocele, gastroschisis
* อาเจียนรุนแรง และคาดว่าไม่สามารถรับทางENได้มากกว่า 3 วัน
Indication of PN
Pediatric and neonatal (ต่อ)
*Diarrhea อย่างรุนแรง เช่นทารกอายุ < 3 เดือน ท้องเสีย > 2 wk
เมือ่ เพาะเชือ้ จากอุจจาระก็ไม่พบเชือ้ ก่อโรค และรับอาหารทางENแล้ว
อาการไม่ดขี น้ึ
* Bowel obstruction e.g. intestinal atresia,
imperforated anus, Hirschsprung’s disease
2.Very low birth weight <1,000 g ทีค่ าดว่า NPO/รับทาง
EN ไม่ได้ e.g. respiratory distress syndrome
(RDS)
3.pt. CA (เช่นเดียวกับผูใ้ หญ่)
4.Severe acute pancreatitis (เช่นเดียวกับผูใ้ หญ่)
5.Critical illness (เช่นเดียวกับผูใ้ หญ่)
Indication of PN
Pediatric and neonatal (ต่อ)
6.Catabolic state ระดับปานกลาง-รุนแรง (เช่นเดียวกับผูใ้ หญ่)
7.Preoperative in severe malnourished without
functional GI tract (เช่นเดียวกับผูใ้ หญ่)
8.Anorexia nervosa (เช่นเดียวกับผูใ้ หญ่)
9.Inborn error metabolism
Contraindication of PN
 Hemodynamic instability
 Severe fluid and electrolyte imbalance
 Renal failure without dialysis
 (Almost) complete functions of GI tract
 Patient’s refusal
 Terminal and hopeless illness
Parenteral Nutrition planning
Energy requirement
Macronutrients
Complication
Micronutrients
Monitoring
Energy requirement in adults
Total energy expenditure (TEE)
TEE=BEE x AF x SF
kcal/day
1.Basal energy expenditure (BEE)
จากสูตร Harris-Benedict equation
Men
= 66+(13.7xW)+(5xH)-(6.8xA)
Women = 665+(9.6xW)+(1.8xH)-(4.7xA)
*W=kg. (actual or usual wt.), H=cm.,A=yr.
*ไม่ใช้ในเด็กอายุ < 6 yr
*Obesity >120% IBW
*Marasmic/underweight
use adjust BW
actual BW
Energy requirement in adults
2.Activity Factor (AF)
- with respirator = 0.7-0.9
- bed rest
= 1.2
- ambulatory
= 1.3
3.Stress Factor (SF)=Metabolic Factor
Fever
Mild infection
Moderate infection
Minor operation
Moderate operation
Skeletal trauma
Major sepsis
e.g.
1+0.13/1 c Peritonitis
1.05-1.25
Cancer
1.0-1.25
1.0-1.2
Soft tissue trauma
1.0-1.3
1.2-1.4
Weight gain
1.1
1.2
Burns ; 10-30% BSA
1.5
1.2-1.4
; 30-50% BSA
1.75
1.35
; > 50% BSA
2.0
1.4-1.6
Energy requirement in adults
BEE x 1.4 (will cover the majority of pt.)
25-30 kcal/kg/day
Indirect calorimetry
-Resting energy expenditure (REE)
REE = [3.9(VO2)+1.1(VCO2)] x 1.44
VO2 =O2 consumption
VCO2=CO2 production
Energy requirement in Pediatric and neonatal
TEE=BMR (in 24 hr) x AF x SF
1.Basal metabolic rate (BMR)
-ดูจากตาราง /BEE/REE
2.Activity Factor (AF)
- นอนอยูแ่ ต่บนเตียง = 1.1
- จากัดการทากิจกรรม = 1.3
- มีกจิ กรรมปานกลาง = 1.5
- มีกจิ กรรมมาก
= 1.75
kcal/hr
3.Stress Factor (SF) (เช่นเดียวกับผูใ้ หญ่)
Holliday-Segar
10 kg แรก = 100 kcal/kg/day
10 kg ต่อมา = 50 kcal/kg/day
น้าหนักทีเ่ หลือ = 20 kcal/kg/day
(water 1 ml/calorie 1 kcal)
* ในกรณีทเ่ี ป็ นผูป้ ่ วยหนัก อาจไม่สามารถให้พลังงานได้ครบตามทีก่ าหนด
ในกรณีน้ใี นช่วงแรกควรได้รบั พลังงานอย่างน้อย 60% ของพลังงานที่
คานวณได้เพือ่ รักษาน้าหนักตัวให้คงที่

Age (y)
kcal/kg
0-1
90-120
1-7
7-12
12-18
> 18
75-90
60-75
30-60
25-30
It’s All about Nutrients
Macronutrients
 Energy sources
 Substrate sources
 Modulating functions
 CHO, Proteins, Lipids
Micronutrients
 Non-energy providing nutrients
 Regulatory functions
 Electrolytes, Trace element, Vitamins
Water
Carbohydrate (CHO)
Lipid
Protein
Macro
nutrients
Estimation of calories from PN
Nutrient
Kcal/g
CHO
Dextrose.H2O
3.4
Dextrose anhydrous
4.0
Glycerol
4.3
Fat source
Long chain fat emulsion
9
Medium chain fat emulsion 8.3
Protein
Amino acids
4
Carbohydrate
 Primary source of energy for normal healthy
person
 Principle energy substrate for brain, which
utilizes 130-140 g of glucose per day
 All CHO are absorbed in the form of glucose
 Reduce ketone production
 Facilitates storage of TG in fat tissue
 Preserve body protein ( gluconeogenesis)
Carbohydrate
Dextrose = Glucose
*adult ; oxidize glucose = 4-7 mg/kg/min
* load > 7 mg/kg/min;
- glycogen, lipid syn.,metabolic complications
(hyperglycemia, excess CO2, lipogenesis,
LFT สูง
fatty liver)
* แนะนา ≤ 5 mg/kg/min
*neonate ; oxidize glucose = 6-8 mg/kg/min
max.=10-14 mg/kg/min
*preterm (very low birth wt.); oxidize glucose =
max. 12-15 mg/kg/min
*infant & child
max. 15-20 mg/kg/min
Carbohydrate
*ในเด็กค่อยๆ ให้ทลี ะน้อย
hyperglycemia,
hyperosmolarity
*เริม่ conc.10%, 10 g/kg/day max. 25 g/kg/day
*pt.sepsis/stress
hyperglycemia
*closely monitored and adjusted in the
postoperative period in neonates and children
to avoid hyperglycemia
* อาจต้อง add insulin
*Provide 50-60% of total energy in adults
*Provide 40-50% of total energy in infants and
children
Carbohydrate
Age
(year)
Energy
(kcal/kg/d)
Glucose
(mg/kg/min)
Preterm
Term
1-3
4-6
7-10
11-18
80-120
90-120
75-90
65-75
55-75
40-55
10-18
11-18
9-14
8-11
7-11
7-8.5
Lipids
Source of energy
Carries of fat-soluble vitamins
Precursors of eicosanoids, modulate
immune function
Substrate for fat formation in adipose
tissue
High energy content in
a low volume:
9 kcal/g lipids
Lipids
 Lipids Classification-chain length
1. Short chain FA (C1-5);not used in PN
2. Medium chain FA (C6-11);water
soluble, good energy source
3. Long chain FA (C12-22);energy,
membrane structure, most of the
biologic activity
Lipids
 Lipids Classification-number and
position of double bonds
1. Saturated fatty acids
2. Monounsaturated fatty acids (MUFA)
3. Polyunsaturated fatty acids (PUFA)
Lipids
C/=
FA
C8:0
C10:0
C12:0
C14:0
C16:0
C18:0
C18:1
C18:2
C18;3
Caprylic acid
Capric acid
Lauric acid
Myristic acid
Palmitic acid
Stearic acid
Oleic acid
Linoleic acid
Alpha-Lionlenic
acid
ω-3
Intralipid
Data expressed in weight percent
0.1
11.0
4.3
22.5
53.8
6.9
LCT/MCT
29.6
19.1
0.3
0.1
6.5
2.0
1.3
35.0
5.8
ClinOleic
0.1
13.5
2.9
59.5
18.5
2.0
Lipids
1st
2nd
Soy bean +
safflower oil,
very rich in ω 6 PUFA(LCT)
e.g. Intralipid®
• 50% Soy
bean+50%
Coconut(MCT)oil
e.g. Lipofundin
MCT/LCT®
• 80% Olive oil
+20% Soy bean
oil e.g.
ClinOleic®
Mixture soy bean
LCT+MCT+Olive
oil+Fish oil e.g.
SMOFlipid®
Lipids
 Contents
- lipid emulsion based on soybean oil + safflower
oil
- egg phospholipid = emulsifier
- glycerol = isotonic
 10% fat emulsion = 1.1 kcal/ml
 20% fat emulsion = 2.0 kcal/ml
 Source of EFA –linoleic acid(ω-6), linolenic
acid(ω-3)
PUFA (LCT)
เด็ก start 0.5 g/kg/day hypertriglyceridemia
max. 3-3.5 g/kg/day, 50% of total energy
Lipids
เด็กทีม่ ปี ั ญหารุนแรงของระบบหายใจ/sepsis
lipid intolerance
ระบบทาลายเชือ้ ของร่างกายลดลง
 add heparin 0.5-1.0 unit/ml of TPN เพือ่
ช่วยกระตุน้ endothelial lipoprotein lipase
ป้ องกันการอุดตันในสาย catheter
 The first days ;infused as slowly as possible
< 0.1 g/kg/h with LCT
< 0.15 g/kg/h with LCT+MCT
 Provide 30-40% of total energy in adults
max. = 60%
ketosis
Lipids
 Recommendations for Fat emulsion
1. Prevent EFA deficiency
- 10% fat emulsion 500 ml x 3 times/wk
- 20% fat emulsion 500 ml weekly
2. Acceptable Triglyceride
- serum TG < 250 mg/dl 4hr after lipid
infusion
- serum TG < 400 mg/dl for continues
infusion
Proteins
Tissue synthesis
Constitutes of hair, skin, nails, tendon,
bones,ligaments,major organs, muscle
Precursors of neurotransmitters
Major part of antibodies, enzymes,
transports of ions and substrates in
blood
Initiators of muscle contraction
Amino acids
 First to introduce, last to withdraw
 Protein deficiency VS Energy deficiency
 Amino acids as fuel VS as substrate
 Infusion of glucose along with amino acids
 0.5-3.0 g/kg/day
 Tritration
- clinical symptoms and signs
- Biochemistry
Amino acids

1.
2.
3.
4.
5.
6.
7.
8.
Essential
Isoleucine
Leucine
Lysine
Methionine
Phenylalanine
Threonine
Trytophan
Valine
• Conditionally essential
1. Arginine
2. Cysteine
3. Glutamine
4. Histidine
5. Taurine
6. Tyrosine
• Non- essential
1. Alanine
6. Ornithine
2. Asparagine 7. Proline
3. Aspartic acid 8. Serine
4. Glutamic acid
5. Glycine
Amino acids
 Specialized amino acid solutions
1. Branch chain amino acids;



Isoleucine, Leucine, Valine
Increased metabolic stress
Hepatic failure with encephalopathy
2. Higher concentrations of essential
amino acids;


Renal failure not receiving dialysis
Benefit have not been proven in controlled trials
Amino acids
3. Conditionally essential amino acids in
infants

Histidine for neonates and infants up to 6
mon.
CHO+AA+Lipid
 Suggested pediatric parenteral substrate
provision
Nutrition
Initiation
CHO
AA
Lipid
Advancement
CHO
AA
Lipid
Usual upper limit CHO
-Peripheral
-Central
AA
Amount
10% D (6-8 mg/kg/min)
50-100% of goal
0.5-1.0 g/kg/d
5% D/day (2-4 mg/kg/min)
100% of goal
0.5-1.0 g/kg/d
8-18 mg/kg/min
12.5% D
25-35% D
3.0g/kg/d
Non-protein calories : Nitrogen (NPC:N)
 NPC:N =
calories from glucose+calories from fat emulsion x 6.25
amino acid (g)
Status
NPC:N
Adult
Pediatric
Minor catabolic
Moderate stress
Severe catabolic state
Renal failure
50-250:1
150-200:1
125-180:1
150:1
80-100:1
250-400:1
Electrolytes
Trace elements
Vitamins
Micro
nutrients
Sodium
Chloride, Acetate
Magnesium
Potassium
Electrolytes
Calcium
Phosphate
Electrolytes
Suggested
electrolytes in adults
(per L)
Na
60-150 mEq
K
40-120 mEq
Cl
60-120 mEq
PO4
10-30 mM
Conditions that require
alteration of amount
provided
-Renal function, Fluid status,
GI loss, Traumatic brain injury
-Renal function, GI loss,
Metabolic acidosis, Refeeding
-Renal function, GI loss, Acidbase status
-Renal function, Refeeding,
Bone disease, Hypercalcemia,
Rapid healing,Hepatic function
Electrolytes
Suggested
electrolytes in adults
(per L)
Acetate 10-40 mEq
Ca
4.5-9.2 mEq
Mg
8.1-24.3 mEq
Conditions that require
alteration of amount
provided
-Renal function, GI loss, Acidbase status, Hepatic function
-Hyperparathyroidism,
Malignancy, Bone disease,
Immobilization, Acute
pancreatitis
-Renal function, Refeeding,
Hypokalemia
Electrolytes in Pediatrics
Electrolytes
Na (mEq/kg/d)
K
(mEq/kg/d)
Cl
Ca
P
(mEq/kg/d)
(mg/kg/d)
(mg/kg/d)
Mg
(mg/kg/d)
Preterm
Term
> 1 year
3
2
5
80-100
43-62
3-6
3
2
5
60-90
48-68
6-10.5
3
2
5
24-60
18-45
2.4-6.0
Trace Elements
Prosthetic groups of enzymes
Routine addition of zinc, copper,
selenium, chromium, and manganese
recommended
Addition of molybdenum probable
Vitamin and trace element levels should
be monitored periodically during longterm PN administration
Requirement of Trace element in
PN
Trace elements
Trace elements
Requirement/day (adult)
Zn (mg)
Cr (μg)
Cu (mg)
Mn (μg)
Fe (mg)
I (μg/kg)
Mo (μg)
Se (μg)
2.5-4.0
10-15
0.3-0.5
60-100
1.0-2.0
1.0-2.0
20-130
20-40
Trace Elements
Trace Elements
Zn
Cu
Cr
Mn
Mo
Comments
-Increase dose with catabolic
state, intestinal loss
12.2 mg/L small bowel fluid loss
17.1 mg/kg stool/ileostomy
-Reduce or hold dose with biliary
disease
-Increase to 20 μg with intestinal
losses, reduce in renal disease
-Reduce dose with biliary disease
-Reduce dose with biliary disease
Vitamins
Vitamin requirements
- Vitamin requirements during PN
therapy are uncertain because they are
not based on balance studies.
- The requirements for an adult TPN:
FDA 2003 (increase in vitamin B1, B6,
C and folic acid and include 150 μg of
vitamin K)
Vitamins in PN
Vitamin
Amount
Thiamine B1
Riboflavin B2
Pyridoxine B6
Cyanocobalamin B12
Niacin
Folic acid
Pantothenic acid
Biotin
Ascorbic acid
Vit. A
Vit. D
Vit. E
Vit. K
6 mg (3)
3.6 mg
6 mg (4)
5 μg
40 mg
600 μg (400)
15 mg
60 μg
200 mg (100)
3300 IU
5 μg
10 IU
150 μg
Fluid requirement
 Adults
* 30-35 ml/kg
* 1 ml/1 kcal
* 100 ml/kg for first 10 kg of wt. plus
50 ml/kg of wt. from 11-20 kg plus
Age ≤ 50 y.;20 ml/kg over 20 kg or
Age > 50 y.;15 ml/kg over 20 kg
 Pediatrics
* Holliday-Segar formula
* 1,500-1,700 ml/m2 of BSA
* 1 ml/1 kcal
 Fluid need should be calculated with fluid loss
(diarrhea, fistula)
Fluid and Electrolytes
Variations depending on clinical status
PN not meant to correct severe fluid
and electrolytes imbalance
Water and electrolyte requirements
should be adjusted in pediatric patients
undergoing surgical procedures or who
have on-going losses from stomas or
other sites
Monitoring
Efficacy of therapy
Complication detection and prevention
Clinical condition evaluation
Clinical outcome determination
Growth
Metabolic
Clinical observations
Monitoring
 Growth
 Weight
 Height/Length
 Head circumference
 Metabolic
 E’lytes, BUN, Cr, Ca, PO4, Mg, acid-base
 Albumin, pre-albumin
 CBC, glucose, triglycerides, LFTs, PT/PTT
 Urine markers; specific gravity, glucose,
ketones, UUN
Monitoring
Clinical observations
 Vital signs
 Intake and output
 Catheter site/dressing
 Administration system
 Growth and development
Monitoring
 Malnourished patients at risk for refeeding
syndrome should have serum P, Mg, K and
glucose levels monitored closely at initiation of
SNS.
 In pt.with diabetes or risk factors for glucose
intolerance, SNS should be initiated with a low
dextrose infusion rate and blood and urine
glucose monitored closely
 Blood glucose should be monitored frequently
upon initiation of SNS, after any change in
insulin dose, and until measurements are
stable
 Serum electrolytes (Na, K, Cl,HCO3) should be
monitored frequently upon initiation of SNS
until measurements are stable
Monitoring
 Pts. receiving IV fat emulsion should have
serum triglyceride levels monitored until
stable and when changes are made in the
amount of fat administerd
 Liver function tests should be monitored
periodically in patients receiving PN
 Bone densitometry should be performed upon
initiation of long-term SNS and periodically
thereafter
 Postpyloric placement of feeding tubes should
be considered in pts. At high risk for aspiration
who are receiving EN
Follow up : parenteral feeding
Parameter
Initial
Follow up
Electrolytes
BUN/Cr
Ca, P, Mg
Acid-base
Albumin/pre-albumin
Glucose
Triglyceride
LFTs
CBC
Platelets,PT/PTT
Daily to weekly
Weekly
Twice weekly
Until stable
Weekly
Daily to weekly
Daily
Weekly
Weekly
Weekly
Weekly to
Monthly
Weekly to
Weekly to
Weekly to
Weekly to
Weekly to
Weekly to
monthly
monthly
monthly
monthly
monthly
monthly
monthly
Weekly to monthly
As indicated
Monitoring for Adult Patients on PN
Baseline
Critically ill pateints
Stable patients
Chemistry screen
(Ca, P, Mg, LFTs)
Yes
2-3x/week
Weekly
Electrolytes, BUN, Cr
Yes
Daily
1-2x/week
Serum triglyceride
Yes
Weekly
Weekly
CBC with differential
Yes
Weekly
Weekly
PT,PTT
Yes
Weekly
Weekly
Parameter
Capillary glucose
3x/day
3x/day
(until consistently
<200 mg/dl)
3x/day
(until consistently <200
mg/dl)
If possible
Daily
2-3x/weekly
Daily
Daily
Daily unless fluid status is
assessed by physical exam
Nitrogen balance
As needed
As needed
As needed
Indirect calorimetry
As needed
As needed
As needed
Weight
Intake& output
Patient education
1. อธิบายให้ผรู้ บั บริการเข้าใจถึงความจาเป็ น และวิธปี ฏิบตั ใิ นการแทงเข็ม
สอดสายเข้าหลอดเลือดดาส่วนกลาง เพือ่ ผูร้ บั บริการให้การยอมรับและ
ร่วมมือ
2. อธิบายความจาเป็ นในการให้สารอาหารทางหลอดเลือดดา
3. ประโยชน์ของการให้สารอาหาร
4. ความจาเป็ นในการตรวจวัดสัญญาณชีพ การตรวจประเมินเป็ นระยะๆ
รวมทัง้ การตรวจเลือด
5. ความเสีย่ ง/ภาวะแทรกซ้อน
PN Complications
Metabolic
Infectious
Mechanical
1.
2.
3.
Metabolic complications
Substrate intolerance
Fluids & Electrolytes imbalance
Acid-Base abnormalities
Substrate intolerance
 Hyperglycemia
 Traditional > 220 mg/dl
 Cardiac surgery pts., BS > 150 mg/dl
 Surgical critical care pts., maintaining BS
80-110 mg/dl
 Pt. sepsis, trauma, burn, CA, Cr deficiency
 Tx - add Insulin ;aware in neonate
hypoglycemia
 Blood and urine glucose monitored closely
Substrate intolerance
Hyperosmolar hyperglycemic nonketotic
dehydration
 ได้รับ glucose
osmotic diuresis
(from glucosuria), dehydrate/fluid
deficit, coma
 TX - Isotonic/hypotonic saline
Substrate intolerance
Excess CO2 production

CHO
 Pt. respiratory distress
คัง่ CO2
 Tx -Dextrose ≤ 5 mg/kg/min
Substrate intolerance
Refeeding syndrome
 Refers to the metabolic and physiological
shifts of fluid, E’lytes and minerals e.g. P,
Mg, K
 Occur in malnourished pts. during rapid
nutritional replacement
 Risk factor; starvation, alcoholism,
anorexia, morbid obesity with massive wt.
loss
Substrate intolerance
 Aggressive nutrition support delivery of
calories in the form of CHO
 CHO delivery stimulates insulin secretion
during starvation
 CHO stimulates the release of insulin
 Causes an intracellular shift of these E’lytes
and minerals
 Insulin shifts K,P into cells
 Potential for severe hypo P, Mg, K
 Na retention leads to fluid overload,
pulmonary edema and cardiac
decompensation
Substrate intolerance
Symtoms of refeeding syndrome is
characterizied
 Generalized fatique, lethargy muscle
weakness, edema, cardiac arrhythmia, and
hemolysis
Calories should be initialed and
advanced slowly in pt. who are at risk
for refeeding syndrome
Substrate intolerance
Preventation;
 start low and go slow
 Gradual provision of calories over 3
to 5 days
 Thaimine replacement
 E’lytes replacement: K, Mg, P
Substrate intolerance
Hypoglycemia
 Abrupt discontinuation of PN can lead
to rebound hypoglycemia
 Excessive or erroneous insulin
administration
 Pts. requiring large doses of insulin
have a greater risk for rebound
hypoglycemia
Substrate intolerance
Prevention
 10% dextrose should be infused for 1 or 2
hrs following PN discontinuation avoid a
possible rebound hypoglycemia
 Infusion 1 to 2 hrs taper down in
susceptible pts.
 Obtaining a capillary blood glucose conc. 30
min. to 1 hr after the PN solution is
discontinuation will help identify rebound
hypoglycemia
Substrate intolerance
TX -Initiation of a 10% dextrose
infusion
-Administer 50% dextrose
-Stopping any source of insulin
administration
Substrate intolerance
Hypertriglyceridemia
 Serum triglyceride > 220 mg/dL
 Risk;neonate , very low birth wt, sepsis
 Tx - Heparin 0.5-1 unit/1ml of PN
solution
กระตุน้ enzyme phospholipase
Substrate intolerance
Hypercholesterolemia
 Phospholipid/triglycerides ratio
 10% fat emulsion = 0.12
 20% fat emulsion = 0.06
 Pts ;very low birth wt
Substrate intolerance
Essential fatty acid deficiency (EFAD)
 Biochemical evidence of EFAD
 Triene:tetraene ratio > 0.4
 Linoleic acid (EFA) M
arachidonic acid
(tetraene)
 Oleic acid M eicosatrienoic acid(triene)
 Risk; immature ถ้าไม่ได้รบั fat 1-2wks
 Scaly dermatitis, alopecia, anemia, fatty
liver, hepatomegaly, thrombocytopenia
Substrate intolerance
Prevention;
 1-2% of daily energy requirement should
be derived from linoleic acid
 0.5% of energy from linolenic acid
 Approximately; twice weekly of
- 500 ml of 10% fat emulsion
- 250 ml of 20% fat emulsion
 Alternately; 500 ml of a 20% fat emulsion
once a week
Substrate intolerance
Azotemia
 Excessive protein intake
 Increased BUN
 Pts. With hepatic or renal disease are
prone to developing azotemia
 Osmotic diuresis, dehydration, coma
Substrate intolerance
Hyperammonemia
 Hepatic immaturity in low birth
weight infants
 Pts . Renal failure ได้รับเฉพาะ EAA ขาด
arginine
 Tx- ลด protein in PN
Substrate intolerance
Hepatobiliary complications
 Disorders of the liver and biliary
system are common in pts. receiving
PN, long term support
 Types of Hepatobiliary disoders
- Steatosis
- Cholestasis
- Gallbladder sludge/stones
*disorders may coexist
Substrate intolerance
Steatosis-Hepatic Fat
 Dose related
 Dextrose infusion rates > max.
oxidation rate = steatosis, excessive
glycogen deposition in liver
 Elevated liver function tests
 Can progress to severe dysfunction
Substrate Intolerance
Steatosis-Hepatic Fat
 Steatosis is the condition of hepatic fat
accumulation
 Predominant in adults and is generally
benign
 Modest elevations of serum
aminotransferase conc. (AST,ALT)that occur
within 2 wks. of PN therapy
 Most pts. are asymptomic
 Steatosis is a complication of overfeeding
Substrate intolerance
Cholestasis
 Cholestasis is a condition of impaired bile
secretion or frank biliary obstruction
- Predominant in children
- May also occur in adult pts. receiving
long–term PN
 Cholestasis is a serious complication
- it may progress to cirrhosis and liver
failure
Substrate intolerance
Cholestasis
 Elevation of;
- Alkaline phosphatase (ALP)
- Gamma-glutamyl transpeptidase(GGT)
- Conjugated (direct) bilirubin conc.>2
mg/dL
- With or without jaundice
Substrate intolerance
Gallbladder sludge/stones
 Gallbladder stasis during PN therapy lead to
gallstones or gallbladder sludge with
subsequent cholecystitis
 Related more to the lack of enteral
stimulation > PN infusion
 The lack of oral intake results in decreased
cholecystokinin (CCK) release
- impaired bile flow and gallbladder
contractility
Substrate intolerance
Gallbladder sludge/stones
 The duration of PN therapy seems to
correlate with the development of biliary
sludge
 Biliary sludge may progress to acute
cholecystitis in the absence of gallstones
 This condition is also referred to as
acalculous cholecystitis
Fluids & Electrolytes imbalance
Fluid overload
 พบ fluid overload > fluid deficit




Pts. e.g. Critically ill
Intake/output
Weight gain
Osmolarity, Na, Hematocrit
effect
dilution
Fluids & Electrolytes imbalance
Fluid deficit or Dehydration
 พบร่ วมกับ Hyperosmolar hyperglycemic
nonketotic dehydration
Fluids & Electrolytes imbalance
Hyponatremia/ Hypernatremia
Hypokalemia/ Hyperkalemia
Hypophosphatemia/ Hyperphosphatemia
Hypocalcemia/ Hypercalcemia
Hypomagnesemia/ Hypermagnesemia
Acid-Base abnormalities
Metabolic acidosis
 Hyperchloremic metabolic acidosis
 Metabolic acidosis
anion gap
Metabolic alkalosis
Others
Vitamins
Trace elements
Metabolic bone disease
Routine Monitoring Parameters
 Base line; E’lytes, Glucose, Ca, Mg,
P, Albumin, TG, LFTs, PT, CBC, BUN,
Cr
 Daily; E’lytes, Glucose q6h
 2-3 times/week; Ca, Mg ,P
 Weekly; Prealbumin, LFTs, PT, CBC
Infectious complications
Sepsis is a serious complication in PN
Cause;
 Catheters ; PVC > Silicone rubber,
multilumen
 compounding PN-Rx
 Pts. care-Nurse
 Staphylococcus epidermis,
Staphylococcus aureus, Candida
albicans, Bacteria gram negative
Infectious complications
Prevention;
 Aseptic techniques; QC in PN, catheters
access, dressing
 Amino acid/glucose infusion giving sets and
extensions can be left 48-72 hrs. inbetween changing.
 Lipid sets should be changed every 24 hrs.
 PN solution should be changed every 24 hrs
 Carers should be taught about the signs of
catheter related sepsis
Infectious complications
Diagnostic criteria;
 Fever >38.5 c or rise in temp. of >1 c
 White blood count สูง
 พบเชือ้ ในเลือดและ catheter tip
Infectious complications
1.ซักประวัตแิ ละตรวจร่างกายเพือ่ หาตาแหน่งและ source
2.การอักเสบของแผล ถ้ามีหนองให้ทา gram stain, C/S
3.CBC, UA, Hemoculture, PN solution culture
4.เปลี่ยนขวดสารละลาย และ IV line
5.Fat emulsion-off
6.Tx-IV antibiotics
Infectious complications
 Indication to remove the catheters
1. Pts.-Septic shock
2. Persistent pyrexia with positive blood
cultures after 48 hrs. of appropriate
antibiotics
3. fungemia
Mechanical/technical complications
e.g. catheter occlusion, pneumothorax,
subcutaneous emphysema, thrombosis,
arterial injury, air embolism, catheter
tear or break
TPN in special population
1.
2.
3.
4.
5.
6.
Critical illness
Renal failure
Hepatic disease
Pancreatitis
Pulmonary disease
Heart failure
PHARMACY PRACTICE
Experience in the U.S.
Clinical Pharmacist
Chart review
Drug information
Medication group
Pharmacy to dose orders
Drug utilization review
Formulary review
Patient care conference
PHARMACY PRACTICE
Experience in the U.S.
Clinical Pharmacist (cont.)
CE and presentation
Response to code blue
Drug monitor
Preceptor and teaching
ADR
Activity report
Download