Fluid and Electrolyte Prescribing Flashcards

1
Q

Identify the main kinds of IV fluids.

A

1) Glucose 5%
2) Sodium Chloride 0.18% and glucose 4%
3) Saline 0.9%
4) Balanced crystalloids
5) Colloids

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2
Q

How well does colloid fluid pass through semi-permeable membrane ? 5% dextrose ? Saline ? Crystalloids ? NaCl 0.18% and glucose 4% ?

A

-Colloid- large proteins in it, will not pass (in intravascular space, stays there)
-Dextrose 5%- passes through (Initially distributes through ISF and plasma; glucose
metabolised so effectively adding just water. Further distributes into cells as well as ISF and plasma)
-Saline and crystalloids- Similar to extracellular fluid, passes through and disperse into other extracellular compartments
-Sodium 0.18% and dextrose 4%- passes through (disperses into other compartments including both extra and intracellular)

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3
Q

Identify the major fluid divisions. State the Volumes ff each.

A

INTRACELLULAR (28)

EXTRACELLULAR (14)

  • Plasma (3)
  • Interstitial (11)

Total (for an average 70 kg male)= 42 L

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4
Q

Why are UandE results always good indicators of K+ levels ?

A

Intracellular potassium acts as a reservoir (attenuates change, so low K+ may not appear in plasma).

HENCE, low K+ reflects VERY significant loss of total body K+

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5
Q

What is the barrier between plasma and interstitial fluid ? To what extent can ions, water, and proteins pass freely ?

A

Capillary wall (water and ions can pass freely, but not proteins)

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6
Q

What is the barrier between extracellular and intracellular fluid ? To what extent can ions, water, and proteins pass freely ?

A

Plasma membrane (water can pass freely, ions have to pass through channels, proteins cannot pass)

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7
Q

Describe exchange of fluid across the capillary membrane.

A

Arterial end: hydrostatic force larger, will push fluid out

Venous end: Oncotic force will force fluid back into plasma from interstitial space

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8
Q

State the following for the intracellular compartment:

K+ 
Na+
Mg2+ 
Cl-
pH
A
INTRACELLULAR
K+: 150 mM
Na+: 10 mM
Mg2+: 2.5 mM
Cl-: 10 mM
pH: around 7.0
EXTRACELLULAR
Interstitial 
K+: 4.5 mM
Na+: 130 mM
Mg2+: 0.85 mM
Cl-: 110 mM
pH: 7.4
Plasma
K+: 4.5 mM
Na+: 130 mM
Mg2+: 0.85 mM
Cl-: 110 mM
pH: 7.4
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9
Q

What is the main difference between plasma and ISF in terms of composition ?

A

Proteins (oncotic P higher in plasma)

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10
Q

Intracellularly, where does most of the negative charge come from ? Extracellularly ?

A

INTRA
Negatively charged proteins
Phosphate

EXTRA
Chloride

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11
Q

Identify the main gains, and losses of total body fluid, and the V of fluid lost through each of these on average per day.

A

GAINS
Food and water intake; oxidation of food

LOSSES

  • Urine(variable; average 1500ml)
  • Faeces (variable; average 100 ml)
  • Sweat (variable; average 50mls)
  • Insensible losses (variable; average 900ml)
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12
Q

How much fluid do we lose on average per day ?

A

2250 mmL

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13
Q

Identify examples of insensible water losses.

A
  • Transepidermal diffusion: water that passes through the skin and is lost by evaporation
  • Evaporation loss from the respiratory tract

Insensible losses are solute free

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14
Q

What is the difference between the role of sweat and insensible fluid loss.

A

SWEAT
Body temperature regulation

INSENSIBLE FLUID
Cannot be prevented
Evaporation of insensible fluid is a major source of heat loss from body but is NOT under regulatory control

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15
Q

Identify respiratory disease processes, and iatrogenic processes which can result in increased fluid loss.

A

RESPIRATORY

Disease process: anything which increases respiratory rate, will increase insensible losses via respiratory route (e.g. asthma, pneumonia)

Iatrogenic: Oxygen mask (dry air, takes up more humidity, increases sensible losses)

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16
Q

Identify GI disease processes, and iatrogenic processes which can result in increased fluid loss.

A

GASTROINTESTINAL

Disease process: Chorea, other causes of vomiting and diarrhea

Iatrogenic: Industrial strength laxative given before bowel surgery will cause marked fluid depletion

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17
Q

Identify urinary disease processes, and iatrogenic processes which can result in increased fluid loss.

A

URINARY

Disease process: Uncontrolled diabetes (glucose is osmotic diuretic, will be lost in urine and pull water with it)

Iatrogenic: Diuretic

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18
Q

Identify skin disease processes, and iatrogenic processes which can result in increased fluid loss.

A

SKIN

Disease process: Fever (insensible losses), burns

Iatrogenic: Surgery on abdomen with large SA of bowel exposed, moisture evaporates

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19
Q

How is total body fluid controlled ?

A

Sensors/ Central controller/ Effectors

Changes to gains/ losses result in a change in osmolality
and/or volume

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20
Q

Identify the main sensors of the body.

A

SENSORS

  • osmoreceptors in the hypothalamus (daily housekeeping, sense osmolality in blood)
  • low pressure baroreceptors in right atria and great veins (when dramatic event occurs e.g. shock)
  • high pressure sensors (carotid sinus / aorta)
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21
Q

How do osmoreceptors respond to water shortages (i.e. effectors).

A

In times of water shortage, blood osmolality increases, sensed by osmoreceptors resulting in:

  • Increased thirst (for increased water input)
  • ADH secretion (for decreased water output)
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22
Q

What is the key driver of total volume ? How so ?

A

Total sodium

  • If total sodium drops and osmolality (tightly regulated) stays the same, the total volume falls (including plasma volume)
  • If total sodium rises and osmolality stays the same, the total volume will rise
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23
Q

Identify the compensatory mechanisms linked to low V and high V.

A

Compensatory mechanisms are really linked to low volume (low GFR, stimulation of JGA ) or high volume (increased GFR and release of ANP)

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24
Q

Identify the main gains and losses of NaCl.

A
  • Gains: food and drink

- Losses: sweat (0.25g), faeces (0.25g), urine (10g)

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25
Q

How may your body compensate for too much/too little Sodium ?

A
  • If you eat too much/ too little salt, the only controllable route of loss is via urine: hormonal control
  • May increase losses via the other routes in a non- hormonally controlled way (exercise/heat etc causing increased sweating; diarrhoea causing increased loss via faeces)
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26
Q

Why is intake of sodium in excess of need ?

A

Hedonistic

27
Q

Describe hormonal control of urine output in the context of too high/low Sodium.

A
  • DCT is the area of control in the nephron
  • No receptors detecting Na+, controlled indirectly via volume sensors (changes in Na+ lead to changes in BV)
  • Net Sodium excretion = Na+ filtered (changed via GFR) - Na+ reabsorbed (changed via rate of flow, aldosterone, ANP)
28
Q

Describe responses if osmolality rises, and falls.

A

IF OSMOLALITY RISES (Na+ increase):

  • Increase in thirst
  • Increase in release of ADH
  • Increase in water intake/retention (take in more water, retain more water)
  • Increase in V

IF OSMOLALITY FALLS (Na+ falls):

  • Decrease in thirst
  • Decrease in release of ADH
  • Decrease in water intake/retention
  • Decrease in V
29
Q

Describe responses if volume increases. When might this occur ?

A

Increase in V may occur when heading towards Heart Failure

Increase in stretch of vascular system

  • Baroreceptors (high pressure areas; low pressure areas)
  • Decrease in renin release
  • Decrease in aldosterone release (aldosterone normally retains sodium so if not released, lose sodium and water)
  • Increased release of ANP (cardiac myocytes)
  • Decreased sodium and water retention
30
Q

Describe responses if volume decreases. When might this occur ?

A

Decrease in V may occur when heading towards shock (e.g. hypoV due to loss in GI, or trauma)

Decrease in stretch of vascular system

  • Baroreceptors (high pressure areas; low pressure areas)
  • If pressure (from decreased volume) falls, also influences ADH release and thirst centres
  • Increase in renin release
  • Increased levels of AII
  • Increase in aldosterone release
  • Decreased release of ANP
  • Increased sodium and water retention
31
Q

What are the main gains and losses of K+ ?

A

Gains via food/drink

Losses: predominantly via urine, little is lost in sweat or
faeces in normal conditions

32
Q

How may your body compensate for too much Potassium ?

A

INCREASED K+ IN PLASMA
-Increases activity of basolateral sodium pump (i.e. more K+ enters the cell)
- Increased secretion of K+ across simple diffusion channels on apical membrane
-Increased secretions of aldosterone (NOT driven by AII, but by direct detection of raised K+ levels by the aldosterone-secreting cells of the adrenal cortex), which does the following:
• Increases activity of sodium pump (basolateral)
• Increases the number of sodium pumps (basolateral)
• Increases the number of sodium and potassium channels in apical membrane
• Result: increased reabsorption of sodium and increased secretion of potassium

33
Q

Describe normal excretion of K+ at the kidney.

A

K+ is freely filtered, then predominantly reabsorbed again in the PCT with controlled secretion at the DCT. This secretion is linked to Na+ reabsorption (sodium pump).

34
Q

What is Conn’s syndrome ?

A

Hyperaldosteronism leading to a) hypertension from increased

fluid volume, and b) hypokalaemia

35
Q

What are the main risks with IV fluids ?

A
  • Peripheral Vascular Catheter (PVC) required
  • Easy to give too much fluid (especially in sick people)
  • Errors in prescribing
36
Q

Should you encourage patients to take oral fluids rather than IV fluids if possible ?

A

YES

37
Q

How may history help determine fluid status of a patient ?

A
  1. Limited intake?
  2. Abnormal losses?
    - How much?
    - What kind of fluid?
    - Ongoing? Can you treat the cause?
  3. Comorbidities?
  4. Current illness?
  5. Symptomatic?
  6. Fluid balance charts?
38
Q

Identify signs and symptoms of hyperV.

A
  • Shortness of breath when lying flat
  • Peripheral oedema
  • Orthopnea
  • PND
  • History of cardiac or renal problems
  • Raised JVP
  • Inspiratory crackles at lung bases (e.g. pulmonary edema)
  • HyperT
39
Q

Identify signs and symptoms of hypoV.

A
  • Dry mouth, dry eyes
  • Postural hypoT (sensitive marker of HypoV)
  • Systolic BP: <100 mmHg
  • HR: >90 bpm
  • Capillary refill: >2 secs
  • Respiratory rate: 20 breaths/min
  • Urine output/color: <0.5 mLs/kg/hr
  • Decreased skin turgor
  • Responsive to passive leg raising (HR decreases and BP increases as a result of lifting legs)
40
Q

Identify investigations which may be helpful in assessing volume status of a patient (after history and examination).

A
 Full Blood Count
 Urea and Electrolytes 
 Chest x-ray
 Lactate
 Urine biochemistry
41
Q

What are the daily electrolyte requirements of Sodium, Potassium and calories in IV fluids ?

A

Sodium: 1mmol/kg/24hours
Potassium: 1mmol/kg/24hours
Calories: minimum of 400kcal/24hours

ALSO keep an eye on Magnesium, Calcium and Phosphate

42
Q

Identify the main kinds of fluids given for different kinds of fluid losses.

A

Maintenance fluids: Patient does not have excess losses (may be supplementing oral intake)

Replacement fluid: of previous and/or current abnormal losses (in addition to maintenance fluid)

Resuscitation fluid: the patient is hypovolaemic and requires urgent correction of intravascular depletion (with BOLUS)

43
Q

How much maintenance fluids are needed if no other intake ? If there are oral intakes ?

A

If no other intake approximately 30mls / kg/ 24hours. May only need part of this IV if some oral intake

44
Q

In the case where abnormal losses have taken place, what factor determines the replacement fluid used ?

A

Use fluid which mirrors ion content of abnormal losses

45
Q

How often should peripheral venous catheters be changed ?

A

Every 72 hours

46
Q

Identify examples of cystalloid IV fluids. When is each of these used ?

A
  • 5% dextrose
  • 0.18% NaCl 4%dextrose: used as maintenance fluid
  • 0.9% NaCl (isotonic saline): used when losing ion rich fluid, including as bolus as resuscitation fluid
  • Plasmalyte: used when losing ion rich fluid, or as resuscitation fluids (as bolus)

0.9% NaCl and Plasmalyte mirror contents of ECF so when given into intravascular space, expand ECF

47
Q

How well does Plasmalyte distribute in different compartments ?

A

Distributes through ISF and plasma; does not enter cells

48
Q

Identify examples of colloid IV fluid. How good is each of these at distributing around different compartments ?

A

•4.5% albumin:
Tends to stay in plasma; does not enter cells (expands intravascular space)

•Hydrolysed gelatin:
Initially tends to stay in plasma; does not enter cells. Protein metabolised over time so then equivalent to 0.9% NaCl

•Blood:
Stays in the vasculature and increases blood volume

49
Q

How are 4.5M albumin and hydrolysed gelatin infused as fluids ?

A

Both supplied in 0.9% NaCl

50
Q

How are maintenance fluid prescribed ?

A

Prescribed in mls/hour

51
Q

True or False: Maintenance Fluid are available with additional K+ (10 or 20mmol/500mls) if required

A

TRUE

52
Q

What is a possible side effect of colloid IV fluids ?

A

May expose patients to anaphylaxis

53
Q

When should resuscitation fluids be given ? How are they given ?

A

Fluid challenge:

  • Oligouria or hypotension and no sign of overload
  • Given in 500 mLs balanced salt solution, QUICKLY (<15 mns), then re-assess and can repeat up to 2000 mLs
54
Q

Explain what happens when a fluid challenge is given to a hypotensive patient.

A

Underfilled patient will be both tachycardic and hypotensive.
By infusing 500 mL into intravascular space, increase CO, so increase BP and decreased HR

(refer to slide 47)

55
Q

Identify cautions of fluid challenges.

A
  • Obese patients (used ideal body weight)
  • Elderly or frail
  • Renal impairment
  • Cardiac failure (may want to cut down to 250 mL bolus)
  • Malnourished or at risk of refeeding syndrome
56
Q

Identify monitoring techniques when the heart is not working adequately despite IV fluids.

A

1) CVP line (measures R atrial P, target is 8-12 mmHg)

2) Point of care USS (look at IVC to see how full venous compartment is) or ECHO (determine ejection fraction of heart)

57
Q

Describe the principles involved in managing a patient with DKA.

A

ACTRAPID

-Airway, breathing, circulation
-Commence fluid resuscitation
-Treat K+
-Replace insulin
-Acidosis management
-Prevent complications
Information for patients
-Discharge

58
Q

What is the effect of DKA on K+ ? Effect of insulin treatment ?

A

OVERALL TOTAL POTASSIUM LOSS
-Because since Potassium is present in the blood it may be excreted by kidneys, and may be additional losses if vomiting

But serum K+ may be normal or even high (because shifted out of cells, into plasma) can be excreted by kidneys and possible addition losses if vomitting)

HOWEVER, INSULIN INFUSION
Plasma K+ will fall and will have to start supplementing K+

59
Q

Identify the main clinical features of DKA.

A

Hyperglycaemia

  • Dehydration (i.e insignificant urine output)
  • Tachycardia
  • Hypotension
  • Clouding of conciousness

Acidosis

  • Air hunger (Kussmaul’s respiration)
  • Acetone on breath
  • Abdominal pain
  • Vomiting
  • May be present with Gastroparesis

+ features related to precipitating factors (e.g. sepsis)

60
Q

Why are DKA patients dehydrated ?

A
  • Hyperglycaemia
  • Vomiting
  • Kaussmaul respiration
  • Altered conscious level (reduced intake)
61
Q

What is the total body deficit of water in DKA ?

A

Up to 7 liters in 70 kg adult

62
Q

What hormones may be produced in DKA ?

A

Stress response hormones: glucagon, cortisol, growth hormone, adrenaline

63
Q

Describe the IV fluids given to a patient in DKA.

A

In an adult start by giving 1000mls 0.9% saline over first hour (may require 4-6 L over 24 hrs), and subsequently Dextrose 5% (to replace water losses)
+
IV Insulin infusion 6 units/hour (for hyperG)
+
Possible IV K+ (slowly)

64
Q

At which ranges of K+ should K+ be infused IV ?

A

If K+ is high (i.e. above 5.3 mmol/L), do not give K+ but monitor it every 2 hrs (anticipating that it will be driven into cells by insulin and will drop)

If K+ is within normal (3.3-5.3 mmol/L), give 20-30 mmol K+/hr in each L of IV fluid to keep K+ between 4 and 5 mmol/L

If K+ is low (i.e. below 3.3 mmol/L), hold insulin (don’t want to push more K+ into cells) and give 20-30 mmol K+/hr until K+ > 3.3 mmol/L