The Nutrition Care Process Flashcards

1
Q

The nutrition care process

A

Nutrition assessment/reassessment

  • ABCDE model
  • interpret with evidence based standards
  • record all social/environmental info and acknowledge correct reference ranges

Nutrition diagnosis

  • identify and label problem
  • determine cause and contributing factors
  • cluster signs/ symptoms/ defining characteristics and document

Nutrition intervention

  • plan nutrition intervention and plan of action
  • formulate goals
  • Document

Nutrition monitoring and evaluation

  • monitor progress
  • measure outcome indicators
  • evaluate outcomes
  • document
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2
Q

ABCDE model

A
Anthropometry 
- weight, height, weight history, body composition 
Biochemistry
- blood tests 
Clinical 
- nutrition impact symptoms 
Dietary
- diet history, quantitative/ qualitative analysis 
Exercise
- type, duration
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3
Q

Why we measure body size and composition

A

Detect deficiencies and excesses that may be related to health or disease
Eg. Length and weight in infants- assessing growth patterns, is feeding adequate? Screen for conditions which impact on growth and development
Eg. Measurement of body fat levels- nutritional diagnosis with appropriate interventions
Eg. Monitoring weight and body fat levels in athletes- pre season training, competition targets

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4
Q

5 level model of compartmentalisation

A
Whole body
Tissue
Organ
Cellular
Molecular 
Atomic
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5
Q

Whole body

A
  • Weight-
  • Height- good report development. Quick, easy, non invasive, reference data
  • BMI- WHO healthy weight ranges, classify as underweight, healthy weight, obese. Relies on assumption excess weight = excess fat.
  • Childhood growth charts- monitors growth and development
  • Circumferences- waist:hip obesity, head circumference for child growth.
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6
Q

Limitations of height and weight

A

Patient cannot stand or sit- visual estimate, use circumference, need to use surrogate measures such as ulna length and knee height

Curvature of spine- underestimated height and overestimated BMI

Altered hydration status- eg, oedema. Hydration status leads to over/underestimation

No info on body tissue composition- won’t diagnose muscle washing or XS adiposity- consider body comp measurement

Don’t distinguish excess fat and muscle bulk, or what type of tissue makes up body weight

Malnutrition- which sites are depleted, muscle, fat or both?

Changing weight- what tissue is gained or lost

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7
Q

Atomic

A

Total body potassium counter- can calculate body cell mass from total body K. Only one in Vic
In Vivo neutron activation analysis

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8
Q

Molecular

A
Fat free mass 
- skeleton muscle- strength 
- skeleton 
- cell, tissue and organ structure and function 
Metabolically active tissue 

Fat mass

  • adipose tissue, energy store
  • visceral fat

Can be measured via dexa

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9
Q

Dual energy X- ray absorptiometry (DXA)

A

X-ray: attenuation of 2 beams of different energy
Different body tissues attenuate the beams differently
- distinguish soft tissue from bone mineral content (BMC)
- divide the soft tissue into lean tissue mass (LTM) and fat mass
- fat free mass = BMC + LTM
- fat mass- % fat
- can also provide bone mineral density and fracture risk, regional body composition
- Less accessibility for body composition- no Medicare rebate available

Quick, non invasive, not dependent on height and weight
requires trained operator, exposure to ionising radiation, not suitable for subjects who cannot lie still, strict protocol required- glycogen depleted and hydrated.
Precision: 1-2% for BMC, 1-3% FFN, 2-4% fat mass.
Accuracy: 1-3% difference bw scanner models

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10
Q

Bioelectrical impedance analysis (BIA)

A

Weak electric current passed through body which encounters resistance: fatty tissues- watery tissues (FFM)
Resistance and reactance measurements are used to calculate FFM or TBW using prediction equations
Quick, easy, inexpensive after purchase, non invasive, no radiation, small inter observer variability
Inaccurate if hydration altered, serum Na temp and posture may influence. Influenced by recent caffeine, alcohol and strenuous exercise
Precision: high
Accuracy: approx 3-5% for body fat; approx 2-8% for FFM

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11
Q

Densiometry

A

If we can measure density of the body we can calculate % body fat
From weight + % fat we can calculate fat mass and FFM

Underwater weighing

Need specialised equipment, not portable, subject cooperation, tolerable for some illnesses?

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12
Q

BOD POD

A

Air displacement plethsymography
Same principles as underwater weighting - density- % fat
Closed air chamber rather than water chamber.
Pea pod for young ones

Specialised equipment, not portable, subject cooperation, more tolerable than UWW

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13
Q

Other methods of weighing

A

Many limited availability more involved in research
Isotope dilution-
CT scanning- can examine quality of body tissue
MRI scanning- intramuscular fat
Ultrasound

When assessing il patients (acute/ chronic disease) interpret data with caution: assumptions based on data in health may not hold true in disease

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14
Q

Height measurement

A
<2 years 
Recumbent length 
Specialised equipment
Correct positioning essential 
Monitoring growth- small changes to be detected, important to be confident change is real not an error. Height cannot decrease. Plotted against charts

> 2 years: standing height
Stadiometer or wall mounted
Correct positioning important
How does height change across the day? (Shrink a bit at night)
Surrogate measures of height: knee height, arm span, ulna length (prediction eqn)
Decide which surrogate measure to use: can subject spread arms out? If not, ulna length is only suitable measure

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15
Q

Weight measurement

A

Poorly calibrated equipment main source of error- poor preparation of client such as shoes, phone in pocket
Consider hydration status: oedema, full bladder, dehydration
Visual estimate if bed bound

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16
Q

Weight history

A

Look for trends over time- family, dentures loose, losing muscle mass, previous weight from gp etc

Non invasive, inexpensive, quick, collect and record serial data, can use part of nutrition screening as assessment

Bed bound patients, correctly prepare subject
Doesn’t give quantification of body composition

17
Q

Circumferences

A

Head- young children
Waist- abdominal
Hip/ gluteal
Mid arm- useful for monitoring muscle stores (combine with triceps skinfold)
Waist and hip- indicator of disease risk, body fat distribution(as important as total body fat)
Central obesity- increased CVD risk
Waist circumference and waist to hip ratio more strongly associate with metabolic risk factors, incident CVS events and death than BMI

18
Q

Precision

A

How reproducible is the measurement?
- can test observer/ operator obtain the SAME results when they truly are the same
Ie. when no biological change has occurred, repeat result on same day
Aka reproducibility, reliability and repeatability
Person influenced by characteristics inherent to the technique
The procedures used: strictly followed or not

19
Q

Inter observer variability

A

How likely it is you get the same result with two or more different operators/ observers
Higher with techniques such as skinfolds
Lower with techniques such as weight, BIA
Importance of strictly adhering to procedures and aiming to use same staff over time

20
Q

Accuracy

A

Aka validity
How close measurement is to true value
May not be possible to be 100% certain of a true value in human measurement - best estimate of truth
Accuracy impacted by nature of technique, assumptions underlying technique, patient characteristics (do assumptions hold true to this age, race etc), the operator

21
Q

Waist circumferences references

A
High risk: 
males >102cm (40 inches) 
Asian makes >85cn (33.5 inches) 
Females >88cm (35 inches) 
Asian females >80cm (31.5 inches)
22
Q

BMI risks

A
Underweight <18.5
Normal 18.5-25 
Overweight 25-30 
Obesity class 1 30-35
Obesity class 2 35-40 
Obesity class 3 above 40