malnutrition Flashcards

1
Q

define malnutrition

A

deficiency, excess or imbalance nutrients, results in a measurable adverse effect on body function and clinical outcome

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

cause of malnutrition in hospital

A

reduced intake
-NBM
-depression

maldigestion/malabsorption
-function
-length

altered metabolism
1. injury
2.catabolism- cover metabolic need
3.anabolism- muscle recovery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

impact on malnutrition

A

-poorer clinical outcome- increase mortality/decrease wound healing

-NHS cost

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

how to diagnose malnutrition

A
  1. screen: MUST (malnutrition universal screening tool)
  2. assess- dietitian
    3.diagnose
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

nutritional support should be considered in people who are either:

A

malnourished//

at risk of malnutrition

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what is considered malnourished

A

BMI < 18.5 kg/m2 or

Unintentional weight loss >10 % past 3-6/12 or

BMI < 20 kg/m2 + unintentional weight loss > 5 % past 3 –6/12 month.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what is considered at risk of malnutrition

A

Have eaten little/nothing for > 5 days +/- are likely to eat little or nothing for the next 5 days+ or

poor absorptive capacity, +/- high nutrient losses +/- increased nutritional needs ie. catabolism.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Oral Nutrition Support- examples and who is it for

A

-Tailored dietary counselling,
-Oral nutritional supplements (ONS)
-Fortification of meals and snacks

any patient with inadequate food and fluid intakes,
unless they cannot swallow safely, impaired GI function or if no benefit is anticipated e.g. end of life care.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Q. What is artificial nutrition support?

A

The provision of enteral or parenteral nutrients to treat or prevent malnutrition.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what are the 2 types of artificial nutrition support

A

enteral

parenteral

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

order of feeding preferences and to return to preferred ones as soon as clinically possible

A
  1. oral nutrition support
  2. enteral nutrition support
  3. parenteral nutrition support
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

enteral nutrition access: is gastric feeding possible? yes/no- what tube is used?

long term: 3 months+ access?

A

yes= naso-gastric tube (NGT)

no= naso-duodenal (NDT)/naso-jejunal tube(NJT)

LT= gastrostomy/ jejunostomy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what to do if there is Gastric outlet obstruction? In terms of access using enteral feeding

A

cannot use NGT feeding.
use NJT

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the complications associated with enteral feeding? Mechanical, metabolic and GI

A

Mechanical: misplacement, blockage

Metabolic: hypergylcaemia, electrolytes imbalance

GI: Aspiration, nasopharyngeal pain, laryngeal ulceration, V+D

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what to do when NGT is misplaced

A

-Aspirate pH ≤5.5
-pH > 5.5 → chest x-ray

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Artificial Nutrition Support: Parenteral- how are the nutrients delivered

A

The delivery of nutrient directly into venous blood.

17
Q

when to use parenteral nutrition support

A

inadequate/ unsafe oral +/- enteral nutritional intake

OR

impaired gastrointestinal tract

18
Q

parenteral feed access:

A

Central venous catheter (CVC): tip at superior vena cava and right atrium.

19
Q

What are the complications associated with parenteral nutrition?

A

-catheter related infections

-metabolic: electrolyte imbalance, hyperglycaemia

-mechanical- pneumothorax, thrombosis, catheter occlusion

20
Q

Albumin- where it’s synthesised, what does hypoalbuminaemia mean?

A

-liver
-poor prognosis
-negative acute phase protein -> low albumin= high inflammation

21
Q

albumin-what is the acute phase response

A

Inflammatory stimulus → activation of monocytes → release cytokines.

Cytokines act on liver -> proteins synthesis e.g. CRP, whilst downregulating production of others e.g. albumin.

22
Q

Is albumin a valid marker of malnutrition in the acute hospital setting?

A

No. Albumin synthesis ↓es in response to inflammation ∴ poor predictor of malnutrition during acute phase.

23
Q

what is refeeding syndrome

A

biochemical shifts & clinical symptoms occurring in malnourished/starved individual on the reintroduction of oral, enteral or parenteral nutrition

24
Q

Consequences of RFS:

A

-Arrhythmia, tachycardia, CHF → Cardiac arrest, sudden death

-Respiratory depression
-Encephalopathy, coma, seizures
-Wernicke’s encephalopy

25
Q

RFS: what are the criteria for: at risk, high risk and extremely high risk

A

At risk:
Very little or no food intake for > 5 days

High risk: ≥1 of the following:
-BMI < 16 kg/m2
-Unintentional weight loss > 15 % 3 – 6 /12
-Very little / no nutrition > 10 days.
-Low K+, Mg2+, PO4 prior to feeding

Or ≥2 of the following:
-BMI < 18.5 kg/m2
-Unintentional weight loss > 10% 3 – 6 / 12
-Very little / no nutrition > 5 days
-PMHx alcohol abuse or drugs (insulin, chemotherapy, antacids, diuretics)

Extremely high risk:
-BMI < 14 kg/m2
-Negligible intake > 15 days

26
Q

RFS management

A

refer to dietitians
1. administer thiamine 30 mins before + first 10 days of feeding

2.correct and monitor electrolyte

  1. start 10-20kcal/kg
    carb-40-50%
    micronutrients from feeding
  2. monitor fluid shifts and minimise risk of fluid and Na+ Overload