1
FLUID &
ELECTROLYTE
BALANCE
2
CONTENTS
 INTRODUCTION
 BODY FLUIDS & ELECTROLYTES
 METHODS OF FLUID AND ELECTROLYTE
MOVEMENTS
 DAILY INTAKE AND LOSS OF WATER
 REGULATION OF FLUID EXCHANGE AND
OSMOTIC EQUILIBRIUM
 APPLIED ASPECTS
 CONCLUSION
 REFERENCE
3
INTRODUCTION
 About 60 per cent of the adult
human body is fluid, mainly a water
solution of ions and other
substances.
 Most of this fluid is inside the cells
and is called intracellular fluid,
about one third is in the spaces
outside the cells and is called
extracellular fluid.
4
 The kidneys are essential for regulating the
volume and composition of bodily fluids.
 The relative constancy of the body fluids is
remarkable because there is continuous
exchange of fluid and solutes with the
external environment as well as within the
different compartments of the body.
5
 A most critical concept to understand
is how water and sodium regulation
are integrated to defend the body
against all possible disturbances in the
volume and osmolarity of bodily fluids.
 In addition to regulating total volume,
the osmolarity (the amount of solute
per unit volume) of bodily fluids is also
tightly regulated.
6
BODY FLUIDS & ELECTROLYTES
 BODY FLUIDS - 60% BODY WEIGHT
 WATER IS LARGEST SINGLE COMPONENT
 Variations based on age, gender & amt. of
body fat
 45-50 % body weight in elderly
 80% neonate is water
Major Compartments
for Fluids
 INTRACELLULAR FLUID
(ICF)
 Inside cell
 Most of body fluid
here - 40% weight
 Decreased in elderly
 EXTRACELLULAR FLUID
(ECF)
 Outside cell
 Intravascular fluid -
within blood vessels
(5%)
 Interstitial fluid -
between cells & blood
vessels (15%)
 Transcellular fluid -
cerebrospinal,
pericardial , synovial
8
Distribution of solutes in
body
 Electrolytes
 Non-Electrolytes
- glucose, urea, uric acid
- proteins ( albumin )
9
10
ELECTROLYTES
 Substance when dissolved in solution
separates into ions & is able to carry an
electrical current
 CATION - positively charged electrolyte
 ANION - negatively charged electrolyte
 Cations must be equal to anions for
homeostatsis to exist in each fluid
compartment
11
12
13
SODIUM (NA+)
 Dominant Extracellular Electrolyte
 Chief Base Of Blood
 Serum Level 135-145 m eq/L
 Main extracellular fluid (ECF) cation
 Helps govern normal ECF osmolality
 Helps maintain acid-base balance
 Activates nerve & muscle cells
 Influences water distribution (with
chloride)
POTASSIUM (K+)
 Dominant Intracellular Electrolyte
 Primary Buffer In Cell
 Serum Level 3.5-5.5 Meq/L
 Dominant cation in intracellular fluid
(ICF)
 Regulates cell excitability
 Permeates cell membranes, thereby
affecting cell’s electrical status
 Helps control ICF osmolality & ICF
osmotic pressure
16
METHODS OF FLUID &
ELECTROLYTE MOVEMENT
 Diffusion
 Osmosis
 Active Transport
 Filtration
DIFFUSION
 Process by which a solute in solution moves
Involves a gas or substance
 Molecules move from an area of higher
concentration to an area of lower
concentration
 Evenly distributes the solute in the solution
 Passive transport & requires no energy
18
OSMOSIS
 Osmosis is the net diffusion of water across
a selectively permeable membrane from a
region of high water concentration to one
that has a lower water concentration.
19
OSMOTIC PRESSURE
 Pull that draws solvent through the membrane
to the more concentrated side (or side with
solute )
 Amt. determined by relative number of
particles of solute on side of greater
concentration
 Proportional to number of particles per unit
volume solvent
20
COLLOID OSMOTIC PRESSURE
OR ONCOTIC PRESSURE
 Special kind of
osmotic pressure
 Created by
substances with a
high molecular
weight (like
albumin)
OSMOLALITY
 Measure of solution’s ability to create
osmotic pressure & thus affect movement
of water
 Number of osmotically active particles
per kilogram of water
 Plasma osmolality is 280-300 mOsm/ kg
 ECF osmolality is determined by sodium
 MEASURE used in clinical practice to
evaluate serum & urine
22
PLASMA PROTEINS
 Primarily Albumin
 Affect serum osmolarity
 Are main negatively charged intravascular fluid
anions
 Balance the positive charge of sodium in
osmolarity
 Create colloid osmotic pressure which pulls in &
holds water in the vascular bed as well as pulling
water from interstitial space into vascular bed -
“water magnet”
23
ACTIVE TRANSPORT
SYSTEM
 Moves molecules or ions uphill against
concentration & osmotic pressure
 Hydrolysis of adenosine triphosphate
(ATP) provides energy needed
 Requires specific “carrier” molecule as
well as specific enzyme (ATPase)
 Sodium, potassium, calcium, magnesium,
plus some sugars, & amino acids use it
24
FILTRATION
 Movement of fluid through a selectively
permeable membrane from an area of
higher hydrostatic pressure to an area of
lower hydrostatic pressure
 Arterial end of capillary has hydrostatic
pressure > than osmotic pressure so fluid
& diffusible solutes move out of capillary
25
HYPOTONIC & HYPERTONIC
 Solution of lower
osmotic pressure
 Less salt or more
water than isotonic
 If infused into blood,
RBCs draw water into
cells ( can swell &
burst )
 Solutions move into
cells causing them to
enlarge
 Solution of higher
osmotic pressure
 3% sodium chloride is
example
 If infused into blood,
water moves out of
cells & into solution
(cells wrinkle or
shrivel)
 Solutions pull fluid
from cells
26
27
Daily Intake of Water
 Water is added to the body by two major
sources:
(1) it is ingested in the form of liquids or water in
the food, which together normally add about
2100 ml/day to the body fluids, and
(2) it is synthesized in the body as a result of
oxidation of carbohydrates, adding about 200
ml/day.
This provides a total water intake of about 2300
ml/day
28
Daily Loss of Body Water
 Insensible Water Loss- Some of the water losses
cannot be precisely regulated.
 For example, there is a continuous loss of water
by evaporation from the respiratory tract and
diffusion through the skin, which together
account for about 700 ml/day of water loss under
normal conditions.
 This is termed insensible water loss because we
are not consciously aware of it, even though it
occurs continually in all living humans.
29
 The insensible water loss through the skin
occurs independently of sweating and is
present even in people who are born
without sweat glands; the average water
loss by diffusion through the skin is about
300 to 400 ml/day.
 This loss is minimized by the cholesterol-
filled cornified layer of the skin, which
provides a barrier against excessive loss
by diffusion.
30
31
32
Regulation of Fluid Exchange and
Osmotic Equilibrium Between
Intracellular and Extracellular Fluid
 A frequent problem in treating seriously ill
patients is maintaining adequate fluids in one or
both of the intracellular and extracellular
compartments.
 The distribution of fluid between intracellular and
extracellular compartments, in contrast, is
determined mainly by the osmotic effect of the
smaller solutes— especially sodium, chloride,
and other electrolytes— acting across the cell
membrane.
33
 For maintenance of homeostasis, excretion of
water and electrolytes must precisely match
intake.
 If intake exceeds excretion, the amount of that
substance in the body will increase.
 If intake is less than excretion, the amount of
that substance in the body will decrease.
 Intake of water and many electrolytes is
governed mainly by a person’s eating and
drinking habits, requiring the kidneys to adjust
their excretion rates to match the intake of
various substances.
34
35
REGULATION OF WATER
INTAKE AND OUTPUT
 The hypothalamus in the brain contains
osmoreceptors that detect changes in the
osmolarity of bodyfluids.
 Osmolarity is the concentration of dissolved
materials present in a fluid.
 The normal plasma osmolality is 275 to 290
m.mol/kg
36
 The primary stimulus for water ingestion is thirst,
mediated either by an increase in effective
osmolality or a decrease in ECF volume or blood
pressure.
 Osmoreceptors, located in the anterolateral
hypothalamus, are stimulated by a rise in tonicity
37
 The hypothalamus is also involved in
water balance because of its production
of antidiuretic hormone (ADH), which is
stored in the posterior pituitary gland.
 In a state of dehydration, the
hypothalamus stimulates the release of
ADH from the posterior pituitary.
38
 Antidiuretic hormone then increases the
reabsorption of water by the kidney
tubules.
 Water is returned to the blood to preserve
blood volume, and urinary output
decreases.
39
40
41
THIRST
 Conscious desire for water
 It is the major factor that determines fluid
intake
 The osmo receptors in hypothalamus that
are stimulated by increase in osmotic
pressure of body fluids initiate thirst.
42
43
ADH (Antidiuretic Hormone)
 There is a powerful feedback system for
regulating plasma osmolarity and sodium
concentration that operates by altering renal
excretion of water independently of the rate of
solute excretion.
 A primary effector of this feedback is antidiuretic
hormone (ADH), also called vasopressin.
44
 Made in hypothalamus; water conservation
hormone
 Stored in posterior pituitary gland
 Acts on renal collecting tubule to regulate
reabsorption or elimination of water
 If blood volume decreases, then ADH is
released & water is reabsorbed by kidney.
 Urine output will be lower but concentration will
be increased.
45
46
47
ALDOSTERONE
 Produced by adrenal cortex
 Released as part of RAA mechanism
 Acts on renal distal convoluted tubule
 Regulates water reabsorption by
increasing sodium uptake from the
tubular fluid into the blood but potassium
is excreted
 Responsible for reabsorption of sodium &
water into the vascular compartment
48
RENIN
 Released by kidneys in response to
decreased blood volume
 Causes angiotensinogen (plasma
protein) to split & produce angiotensin I
 Lungs convert angiotensin I to
angiotensin II
 Angiotensin II stimulates adrenal gland to
release aldosterone & causes an increase
in peripheral vasoconstriction
49
50
51
Dehydration
 Disturbance of water balance
 Output greater than input
 Decrease in body water below normal
 May be the result of –
 pure water depletion
 pure salt depletion
 mixed
52
APPLIED ASPECTS
1-Pure water Depletion
 Occurs when water intake is not there and
there is no loss of salts in the secretions.
 CAUSES --- very weak or ill patient
- comatosed patient
- mentally upset
- dysphagia
- total inavailability of water
53
Pathophysiology and
Effects
 ECF becomes hypertonic
 Water flows from ICC to ECC and causes cellular
dehydration.
 There is Thirst, Oliguria due to the release of ADH.
BP may drop in late stage.
54
Biochemical findings
 ECF is hypertonic
 Blood urea may be slightly raised
 Plasma volume decreases in late stage
 Urine volume is scanty with raised specific
gravity
 Death occurs when water loss amounts to 15%
of body weight.
55
2- Pure Salt Depletion
 Due to the loss of fluids of high Na or Cl
content and replacement done by salt
deficient fluids.
 CAUSES : excessive sweating, loss of GI
fluids, urinary loss of Na, diuretics.
56
Pathophysiology and
effects
 ECF becomes hypotonic
 Decreased release of ADH and thus
diuresis
 Results in decrease in plasma and
interstitial fluid volume.
 Hypotonicity of ECF results in water entry
into the cells and further fall in ECF
volume.
57
 NO thirst
 Marked weakness and fainting
 Loss of interstitial fluid causes sunken eyes
and loss of skin elasticity
 Decreased cardiac output and fall in BP.
 Decreased glomerular filtration results in
raised urea level.
58
Biochemical findings
 ECF hypotonic
 Low plasma volume
 Decreased plasma sodium
 Raised blood urea
59
FLUID VOLUME DEFICIT
 Hypovolemia or FVD is result of water &
electrolyte loss
 Compensatory mechanisms include: Increased
sympathetic nervous system stimulation with an
increase in heart rate & cardiac contraction;
thirst; plus release of ADH & aldosterone
 Severe case may result in hypovolemic shock or
prolonged case may cause renal failure
60
CAUSES OF FVD
 Abnormal GI fluid loss
such as N&V or
drainage of GI tract
 Abnormal fluid loss
from skin such as high
temperature or burns
 Increased water
vapor from the lungs
such as hyperpnea
 Conditions that
increase renal
excretion of fluids
such as diuretics &
hypersomolar tube
feedings
 Decrease in fluid
intake
 Third-space shift such
as ascites
61
SIGNS & SYMPTOMS OF FVD
 Dry mucous membranes
 Weight loss -mild at 2%,moderate at 5%, &
severe deficit at 8%
 Orthostatic hypotension & increase in
pulse rate
 Body temperature usually subnormal
 Flat neck veins & decrease in CVP
 Decreased urinary output & altered
sensorium
62
MONITORING OF FVD
 Monitoring on a regular schedule depending on
the patient
 If urine output is below 30 mL / hr. notify the
physician
 May check urine specific gravity in 8hrs.
 Weigh patient daily at the same time &
recognize that a change of 2.2 lbs. represents a
loss of 1000 mL
63
FLUID VOLUME EXCESS
 Hypervolemia or FVE is result of expansion of
fluid compartment from an increase in total
sodium content
 Kidney receives signal to save sodium & water
to compensate for cirrhosis, CHF, renal failure,
excessive Na-containing fluid
 Labs may show decreased.:hematocrit, serum
Na, serum osmolality, urine sp. gravity
64
SIGNS & SYMPTOMS OF
FVE
 Orthopnea
 Edema & weight gain
 Distended neck veins & tachycardia
 Increased blood pressure
 Crackles & wheezes
 Maybe ascites & pleural effusion
 Increase in CVP
65
MONITORING OF FVE
 monitor for physical signs of hypervolemia
 Check for edema & weigh patient daily
 Restrict sodium intake as prescribed
 Limit intake of fluids
 Watch for signs of potassium imbalance
 Monitor for signs of pulmonary edema
 Place patient in semi-Fowler’s position
66
Clinical Abnormalities of
Fluid Volume Regulation: Hyponatremia
and Hypernatremia
 The primary measurement that is readily
available to the clinician for evaluating a
patient’s fluid status is the plasma sodium
concentration.
 When plasma sodium concentration is
reduced more than a few milliequivalents
below normal (about 142 mEq/L), a
person is said to have hyponatremia.
 When plasma sodium concentration is
elevated above normal, a person is said
to have hypernatremia.
67
Causes of Hyponatremia:
Excess Water or Loss of Sodium
 Decreased plasma sodium concentration
can result from loss of sodium chloride
from the extracellular fluid or addition of
excess water to the extracellular fluid.
 A primary loss of sodium chloride usually
results in hypo-osmotic dehydration and is
associated with decreased extracellular
fluid volume.
 Conditions that can cause hyponatremia
owing to loss of sodium chloride include
diarrhea and vomiting.
68
 Overuse of diuretics that inhibit the ability of the
kidneys to conserve sodium and certain types of
sodium-wasting kidney diseases can also cause
modest degrees of hyponatremia.
 Finally, Addison’s disease, which results from
decreased secretion of the hormone
aldosterone, impairs the ability of the kidneys to
reabsorb sodium and can cause a modest
degree of hyponatremia.
69
 Hyponatremia can also be associated
with excess water retention, which dilutes
the sodium in the extracellular fluid, a
condition that is referred to as
hypoosmotic overhydration.
 For example, excessive secretion of
antidiuretic hormone, which causes the
kidney tubules to reabsorb more water,
can lead to hyponatremia and
overhydration.
70
71
Causes of Hypernatremia:
Water Loss or Excess Sodium
 Increased plasma sodium concentration, which
also causes increased osmolarity, can be due to
either loss of water from the extracellular fluid,
which concentrates the sodium ions, or excess
sodium in the extracellular fluid.
 When there is primary loss of water from the
extracellular fluid, this results in hyperosmotic
dehydration.
 This condition can occur from an inability to
secrete antidiuretic hormone, which is needed for
the kidneys to conserve water.
72
 As a result of lack of antidiuretic hormone, the
kidneys excrete large amounts of dilute urine
(a disorder referred to as diabetes insipidus),
causing dehydration and increased
concentration of sodium chloride in the
extracellular fluid.
 In certain types of renal diseases, the kidneys
cannot respond to antidiuretic hormone, also
causing a type of nephrogenic diabetes insipidus.
73
 A more common cause of hypernatremia
associated with decreased extracellular fluid
volume is dehydration caused by water intake
that is less than water loss, as can occur with
sweating during prolonged, heavy exercise.
 Hypernatremia can also occur as a result of
excessive sodium chloride added to the
extracellular fluid.
 This often results in hyperosmotic overhydration
because excess extracellular sodium chloride is
usually associated with at least some degree of
water retention by the kidneys as well.
74
 For example, excessive secretion of the
sodium-retaining hormone aldosterone can
cause a mild degree of hypernatremia and
overhydration.
 The reason that the hypernatremia is not
more severe is that increased aldosterone
secretion causes the kidneys to reabsorb
greater amounts of water as well as sodium.
75
Edema: Excess Fluid
in the Tissues
 Edema refers to the presence of excess
fluid in the body tissues.
 In most instances, edema occurs mainly
in the extracellular fluid compartment,
but it can involve intracellular fluid as
well.
76
Intracellular Edema
 Two conditions are especially prone to
cause intracellular swelling:
(1) depression of the metabolic systems of
the tissues, and
(2) lack of adequate nutrition to the cells.
77
Extracellular Edema
 Extracellular fluid edema occurs when there is
excess fluid accumulation in the extracellular
spaces.
 There are two general causes of extracellular
edema:
(1) abnormal leakage of fluid from the plasma to
the interstitial spaces across the capillaries
(2) failure of the lymphatics to return fluid from the
interstitium back into the blood.
78
 The most common clinical cause of interstitial
fluid accumulation is excessive capillary fluid
filtration.
79
Summary of Causes of
Extracellular Edema
80
81
Safety Factors That
Normally Prevent Edema
 Even though many disturbances can
cause edema, usually the abnormality
must be severe before serious edema
develops.
 The reason for this is that three major
safety factors prevent excessive fluid
accumulation in the interstitial spaces:
1. Low compliance of the interstitium when
interstitial fluid pressure is in the negative
pressure range
82
2. The ability of lymph flow to increase 10-
to 50-fold, and
3. washdown of interstitial fluid protein
concentration, which reduces interstitial
fluid colloid osmotic pressure as capillary
filtration increases.
83
Determination of Volumes of
Specific Body Fluid Compartments
84
Fluid and electrolyte
replacement
 done with 3 types of solutions
 ISOTONIC
 HYPOTONIC
 HYPERTONIC
85
ISOTONIC SOLUTIONS
 0.9% Sodium Chloride Solution
 Ringer’s Solution
 Lactated Ringer’s Solution
 Use- replace fluid losses, usually
extracellular losses, and to expand the
intravascular volume
HYPOTONIC SOLUTIONS
 5% DEXTROSE & WATER
 0.45% SODIUM CHLORIDE
 0.33% SODIUM CHLORIDE
 Use- They are commonly infused to
dilute extracellular fluid and rehydrate
the cells of patients who have
hypertonic fluid imbalances and to treat
gastric fluid loss and dehydration from
excessive diuresis.
HYPERTONIC SOLUTIONS
3% SODIUM CHLORIDE
5% SODIUM CHLORIDE
WHOLE BLOOD
ALBUMIN
TOTAL PARENTERAL NUTRITION
TUBE FEEDINGS
CONCENTRATED DEXTROSE (>10%)
Use- to treat patients who have severe
hyponatremia.
 Depending on the type of hypertonic fluid
infused, it can provide patients with calories, free
water, and some electrolytes.
Oral rehydration therapy
 Oral rehydration therapy (ORT) is a type of fluid
replacement used to prevent or
treat dehydration especially that due to
diarrhoea.
 It involves drinking water with modest amounts of
sugar and salt added (an oral rehydration
solution or ORS) while continuing to eat.
 Oral rehydration solution is on WHO's list of
essential medicines.
89
 WHO and UNICEF jointly have developed
official guidelines for the manufacture of ORS
and describe acceptable alternative
preparations, depending on material
availability.
 Commercial preparations are available as
either pre-prepared fluids or packets of oral
rehydration salts (ORS) ready for mixing with
water.
90
 The formula for the current WHO-ORS
(also known as low-osmolar
ORS or reduced-osmolarity ORS) is
 2.6 grams (0.092 oz) salt (NaCl),
 2.9 grams (0.10 oz) trisodium citrate dihydrate (C
6H5Na3O7,2H2O),
 1.5 grams (0.053 oz) potassium chloride (KCl),
 13.5 grams (0.48 oz)anhydrous glucose (C
6H12O6) per litre of fluid.
91
 It can be made using 6 level teaspoons
(25.2 grams) of sugar and 0.5 teaspoon
(2.1 grams) of salt in 1 litre of water.
92
Fluid and electrolyte
replacement in Dentistry
 In dentistry fluid and electrolyte replacement
implication is mainly related to oral and
maxilla facial surgery.
 Usually it is administered in clinical conditions
like
 Trauma
 During and after surgeries under GA
 Hypovolemic shock during minor surgical
procedures (eg - Injury to any artery)
 Hypogycemic shock during procedures
93
Conclusion
 To achieve homeostasis, the body
maintains strict control of water and
electrolyte distribution and of acid-base
balance.
 Methods of fluid & electrolyte movement
are diffusion, osmosis, active transport &
filtration
94
 The kidney is the primary organ that
maintains the total volume, pH, and
osmolarity of the extracellular fluid within
narrow limits.
 The kidney accomplishes this by altering
urine volume and osmolarity.
 The kidney, in turn, is regulated by neural,
hormonal, and local factors.
95
 Hormones like Renin, Angiotensin,
Aldosterone & Vassopressin play a key
role in regulation
 Assessment of body fluid is important to
determine causes of imbalance
 Interventions for imbalances are based
on the cause
96
REFERENCE
 GUYTON & HALL, TEXTBOOK OF MEDICAL
PHYSIOLOGY, ELEVENTH EDITION, ELSEVIER
PUBLISHERS
 K SEMBULINGAM, ESSENTIALS OF MEDICAL
PHYSIOLOGY, SIXTH EDITION, JAYPEE PUBLISHERS
 N GEETHA, TEXTBOOK OF MEDICAL PHYSIOLOGY,
THIRD EDITION, PARAS BOOKS
 LEONARD JOHNSON, ESSENTIAL MEDICAL
PHYSIOLOGY, THIRD EDITION
 THE TREATMENT OF DIARRHOEA, A MANUAL FOR
PHYSICIANS AND SENIOR HEALTH WORKERS-
WORLD HEALTH ORGANIZATION, 2005.
97
98

Fluid and electrolyte balance

  • 1.
  • 2.
  • 3.
    CONTENTS  INTRODUCTION  BODYFLUIDS & ELECTROLYTES  METHODS OF FLUID AND ELECTROLYTE MOVEMENTS  DAILY INTAKE AND LOSS OF WATER  REGULATION OF FLUID EXCHANGE AND OSMOTIC EQUILIBRIUM  APPLIED ASPECTS  CONCLUSION  REFERENCE 3
  • 4.
    INTRODUCTION  About 60per cent of the adult human body is fluid, mainly a water solution of ions and other substances.  Most of this fluid is inside the cells and is called intracellular fluid, about one third is in the spaces outside the cells and is called extracellular fluid. 4
  • 5.
     The kidneysare essential for regulating the volume and composition of bodily fluids.  The relative constancy of the body fluids is remarkable because there is continuous exchange of fluid and solutes with the external environment as well as within the different compartments of the body. 5
  • 6.
     A mostcritical concept to understand is how water and sodium regulation are integrated to defend the body against all possible disturbances in the volume and osmolarity of bodily fluids.  In addition to regulating total volume, the osmolarity (the amount of solute per unit volume) of bodily fluids is also tightly regulated. 6
  • 7.
    BODY FLUIDS &ELECTROLYTES  BODY FLUIDS - 60% BODY WEIGHT  WATER IS LARGEST SINGLE COMPONENT  Variations based on age, gender & amt. of body fat  45-50 % body weight in elderly  80% neonate is water
  • 8.
    Major Compartments for Fluids INTRACELLULAR FLUID (ICF)  Inside cell  Most of body fluid here - 40% weight  Decreased in elderly  EXTRACELLULAR FLUID (ECF)  Outside cell  Intravascular fluid - within blood vessels (5%)  Interstitial fluid - between cells & blood vessels (15%)  Transcellular fluid - cerebrospinal, pericardial , synovial 8
  • 9.
    Distribution of solutesin body  Electrolytes  Non-Electrolytes - glucose, urea, uric acid - proteins ( albumin ) 9
  • 10.
  • 11.
    ELECTROLYTES  Substance whendissolved in solution separates into ions & is able to carry an electrical current  CATION - positively charged electrolyte  ANION - negatively charged electrolyte  Cations must be equal to anions for homeostatsis to exist in each fluid compartment 11
  • 12.
  • 13.
  • 14.
    SODIUM (NA+)  DominantExtracellular Electrolyte  Chief Base Of Blood  Serum Level 135-145 m eq/L  Main extracellular fluid (ECF) cation  Helps govern normal ECF osmolality  Helps maintain acid-base balance  Activates nerve & muscle cells  Influences water distribution (with chloride)
  • 15.
    POTASSIUM (K+)  DominantIntracellular Electrolyte  Primary Buffer In Cell  Serum Level 3.5-5.5 Meq/L  Dominant cation in intracellular fluid (ICF)  Regulates cell excitability  Permeates cell membranes, thereby affecting cell’s electrical status  Helps control ICF osmolality & ICF osmotic pressure
  • 16.
  • 17.
    METHODS OF FLUID& ELECTROLYTE MOVEMENT  Diffusion  Osmosis  Active Transport  Filtration
  • 18.
    DIFFUSION  Process bywhich a solute in solution moves Involves a gas or substance  Molecules move from an area of higher concentration to an area of lower concentration  Evenly distributes the solute in the solution  Passive transport & requires no energy 18
  • 19.
    OSMOSIS  Osmosis isthe net diffusion of water across a selectively permeable membrane from a region of high water concentration to one that has a lower water concentration. 19
  • 20.
    OSMOTIC PRESSURE  Pullthat draws solvent through the membrane to the more concentrated side (or side with solute )  Amt. determined by relative number of particles of solute on side of greater concentration  Proportional to number of particles per unit volume solvent 20
  • 21.
    COLLOID OSMOTIC PRESSURE ORONCOTIC PRESSURE  Special kind of osmotic pressure  Created by substances with a high molecular weight (like albumin)
  • 22.
    OSMOLALITY  Measure ofsolution’s ability to create osmotic pressure & thus affect movement of water  Number of osmotically active particles per kilogram of water  Plasma osmolality is 280-300 mOsm/ kg  ECF osmolality is determined by sodium  MEASURE used in clinical practice to evaluate serum & urine 22
  • 23.
    PLASMA PROTEINS  PrimarilyAlbumin  Affect serum osmolarity  Are main negatively charged intravascular fluid anions  Balance the positive charge of sodium in osmolarity  Create colloid osmotic pressure which pulls in & holds water in the vascular bed as well as pulling water from interstitial space into vascular bed - “water magnet” 23
  • 24.
    ACTIVE TRANSPORT SYSTEM  Movesmolecules or ions uphill against concentration & osmotic pressure  Hydrolysis of adenosine triphosphate (ATP) provides energy needed  Requires specific “carrier” molecule as well as specific enzyme (ATPase)  Sodium, potassium, calcium, magnesium, plus some sugars, & amino acids use it 24
  • 25.
    FILTRATION  Movement offluid through a selectively permeable membrane from an area of higher hydrostatic pressure to an area of lower hydrostatic pressure  Arterial end of capillary has hydrostatic pressure > than osmotic pressure so fluid & diffusible solutes move out of capillary 25
  • 26.
    HYPOTONIC & HYPERTONIC Solution of lower osmotic pressure  Less salt or more water than isotonic  If infused into blood, RBCs draw water into cells ( can swell & burst )  Solutions move into cells causing them to enlarge  Solution of higher osmotic pressure  3% sodium chloride is example  If infused into blood, water moves out of cells & into solution (cells wrinkle or shrivel)  Solutions pull fluid from cells 26
  • 27.
  • 28.
    Daily Intake ofWater  Water is added to the body by two major sources: (1) it is ingested in the form of liquids or water in the food, which together normally add about 2100 ml/day to the body fluids, and (2) it is synthesized in the body as a result of oxidation of carbohydrates, adding about 200 ml/day. This provides a total water intake of about 2300 ml/day 28
  • 29.
    Daily Loss ofBody Water  Insensible Water Loss- Some of the water losses cannot be precisely regulated.  For example, there is a continuous loss of water by evaporation from the respiratory tract and diffusion through the skin, which together account for about 700 ml/day of water loss under normal conditions.  This is termed insensible water loss because we are not consciously aware of it, even though it occurs continually in all living humans. 29
  • 30.
     The insensiblewater loss through the skin occurs independently of sweating and is present even in people who are born without sweat glands; the average water loss by diffusion through the skin is about 300 to 400 ml/day.  This loss is minimized by the cholesterol- filled cornified layer of the skin, which provides a barrier against excessive loss by diffusion. 30
  • 31.
  • 32.
  • 33.
    Regulation of FluidExchange and Osmotic Equilibrium Between Intracellular and Extracellular Fluid  A frequent problem in treating seriously ill patients is maintaining adequate fluids in one or both of the intracellular and extracellular compartments.  The distribution of fluid between intracellular and extracellular compartments, in contrast, is determined mainly by the osmotic effect of the smaller solutes— especially sodium, chloride, and other electrolytes— acting across the cell membrane. 33
  • 34.
     For maintenanceof homeostasis, excretion of water and electrolytes must precisely match intake.  If intake exceeds excretion, the amount of that substance in the body will increase.  If intake is less than excretion, the amount of that substance in the body will decrease.  Intake of water and many electrolytes is governed mainly by a person’s eating and drinking habits, requiring the kidneys to adjust their excretion rates to match the intake of various substances. 34
  • 35.
  • 36.
    REGULATION OF WATER INTAKEAND OUTPUT  The hypothalamus in the brain contains osmoreceptors that detect changes in the osmolarity of bodyfluids.  Osmolarity is the concentration of dissolved materials present in a fluid.  The normal plasma osmolality is 275 to 290 m.mol/kg 36
  • 37.
     The primarystimulus for water ingestion is thirst, mediated either by an increase in effective osmolality or a decrease in ECF volume or blood pressure.  Osmoreceptors, located in the anterolateral hypothalamus, are stimulated by a rise in tonicity 37
  • 38.
     The hypothalamusis also involved in water balance because of its production of antidiuretic hormone (ADH), which is stored in the posterior pituitary gland.  In a state of dehydration, the hypothalamus stimulates the release of ADH from the posterior pituitary. 38
  • 39.
     Antidiuretic hormonethen increases the reabsorption of water by the kidney tubules.  Water is returned to the blood to preserve blood volume, and urinary output decreases. 39
  • 40.
  • 41.
  • 42.
    THIRST  Conscious desirefor water  It is the major factor that determines fluid intake  The osmo receptors in hypothalamus that are stimulated by increase in osmotic pressure of body fluids initiate thirst. 42
  • 43.
  • 44.
    ADH (Antidiuretic Hormone) There is a powerful feedback system for regulating plasma osmolarity and sodium concentration that operates by altering renal excretion of water independently of the rate of solute excretion.  A primary effector of this feedback is antidiuretic hormone (ADH), also called vasopressin. 44
  • 45.
     Made inhypothalamus; water conservation hormone  Stored in posterior pituitary gland  Acts on renal collecting tubule to regulate reabsorption or elimination of water  If blood volume decreases, then ADH is released & water is reabsorbed by kidney.  Urine output will be lower but concentration will be increased. 45
  • 46.
  • 47.
  • 48.
    ALDOSTERONE  Produced byadrenal cortex  Released as part of RAA mechanism  Acts on renal distal convoluted tubule  Regulates water reabsorption by increasing sodium uptake from the tubular fluid into the blood but potassium is excreted  Responsible for reabsorption of sodium & water into the vascular compartment 48
  • 49.
    RENIN  Released bykidneys in response to decreased blood volume  Causes angiotensinogen (plasma protein) to split & produce angiotensin I  Lungs convert angiotensin I to angiotensin II  Angiotensin II stimulates adrenal gland to release aldosterone & causes an increase in peripheral vasoconstriction 49
  • 50.
  • 51.
  • 52.
    Dehydration  Disturbance ofwater balance  Output greater than input  Decrease in body water below normal  May be the result of –  pure water depletion  pure salt depletion  mixed 52 APPLIED ASPECTS
  • 53.
    1-Pure water Depletion Occurs when water intake is not there and there is no loss of salts in the secretions.  CAUSES --- very weak or ill patient - comatosed patient - mentally upset - dysphagia - total inavailability of water 53
  • 54.
    Pathophysiology and Effects  ECFbecomes hypertonic  Water flows from ICC to ECC and causes cellular dehydration.  There is Thirst, Oliguria due to the release of ADH. BP may drop in late stage. 54
  • 55.
    Biochemical findings  ECFis hypertonic  Blood urea may be slightly raised  Plasma volume decreases in late stage  Urine volume is scanty with raised specific gravity  Death occurs when water loss amounts to 15% of body weight. 55
  • 56.
    2- Pure SaltDepletion  Due to the loss of fluids of high Na or Cl content and replacement done by salt deficient fluids.  CAUSES : excessive sweating, loss of GI fluids, urinary loss of Na, diuretics. 56
  • 57.
    Pathophysiology and effects  ECFbecomes hypotonic  Decreased release of ADH and thus diuresis  Results in decrease in plasma and interstitial fluid volume.  Hypotonicity of ECF results in water entry into the cells and further fall in ECF volume. 57
  • 58.
     NO thirst Marked weakness and fainting  Loss of interstitial fluid causes sunken eyes and loss of skin elasticity  Decreased cardiac output and fall in BP.  Decreased glomerular filtration results in raised urea level. 58
  • 59.
    Biochemical findings  ECFhypotonic  Low plasma volume  Decreased plasma sodium  Raised blood urea 59
  • 60.
    FLUID VOLUME DEFICIT Hypovolemia or FVD is result of water & electrolyte loss  Compensatory mechanisms include: Increased sympathetic nervous system stimulation with an increase in heart rate & cardiac contraction; thirst; plus release of ADH & aldosterone  Severe case may result in hypovolemic shock or prolonged case may cause renal failure 60
  • 61.
    CAUSES OF FVD Abnormal GI fluid loss such as N&V or drainage of GI tract  Abnormal fluid loss from skin such as high temperature or burns  Increased water vapor from the lungs such as hyperpnea  Conditions that increase renal excretion of fluids such as diuretics & hypersomolar tube feedings  Decrease in fluid intake  Third-space shift such as ascites 61
  • 62.
    SIGNS & SYMPTOMSOF FVD  Dry mucous membranes  Weight loss -mild at 2%,moderate at 5%, & severe deficit at 8%  Orthostatic hypotension & increase in pulse rate  Body temperature usually subnormal  Flat neck veins & decrease in CVP  Decreased urinary output & altered sensorium 62
  • 63.
    MONITORING OF FVD Monitoring on a regular schedule depending on the patient  If urine output is below 30 mL / hr. notify the physician  May check urine specific gravity in 8hrs.  Weigh patient daily at the same time & recognize that a change of 2.2 lbs. represents a loss of 1000 mL 63
  • 64.
    FLUID VOLUME EXCESS Hypervolemia or FVE is result of expansion of fluid compartment from an increase in total sodium content  Kidney receives signal to save sodium & water to compensate for cirrhosis, CHF, renal failure, excessive Na-containing fluid  Labs may show decreased.:hematocrit, serum Na, serum osmolality, urine sp. gravity 64
  • 65.
    SIGNS & SYMPTOMSOF FVE  Orthopnea  Edema & weight gain  Distended neck veins & tachycardia  Increased blood pressure  Crackles & wheezes  Maybe ascites & pleural effusion  Increase in CVP 65
  • 66.
    MONITORING OF FVE monitor for physical signs of hypervolemia  Check for edema & weigh patient daily  Restrict sodium intake as prescribed  Limit intake of fluids  Watch for signs of potassium imbalance  Monitor for signs of pulmonary edema  Place patient in semi-Fowler’s position 66
  • 67.
    Clinical Abnormalities of FluidVolume Regulation: Hyponatremia and Hypernatremia  The primary measurement that is readily available to the clinician for evaluating a patient’s fluid status is the plasma sodium concentration.  When plasma sodium concentration is reduced more than a few milliequivalents below normal (about 142 mEq/L), a person is said to have hyponatremia.  When plasma sodium concentration is elevated above normal, a person is said to have hypernatremia. 67
  • 68.
    Causes of Hyponatremia: ExcessWater or Loss of Sodium  Decreased plasma sodium concentration can result from loss of sodium chloride from the extracellular fluid or addition of excess water to the extracellular fluid.  A primary loss of sodium chloride usually results in hypo-osmotic dehydration and is associated with decreased extracellular fluid volume.  Conditions that can cause hyponatremia owing to loss of sodium chloride include diarrhea and vomiting. 68
  • 69.
     Overuse ofdiuretics that inhibit the ability of the kidneys to conserve sodium and certain types of sodium-wasting kidney diseases can also cause modest degrees of hyponatremia.  Finally, Addison’s disease, which results from decreased secretion of the hormone aldosterone, impairs the ability of the kidneys to reabsorb sodium and can cause a modest degree of hyponatremia. 69
  • 70.
     Hyponatremia canalso be associated with excess water retention, which dilutes the sodium in the extracellular fluid, a condition that is referred to as hypoosmotic overhydration.  For example, excessive secretion of antidiuretic hormone, which causes the kidney tubules to reabsorb more water, can lead to hyponatremia and overhydration. 70
  • 71.
  • 72.
    Causes of Hypernatremia: WaterLoss or Excess Sodium  Increased plasma sodium concentration, which also causes increased osmolarity, can be due to either loss of water from the extracellular fluid, which concentrates the sodium ions, or excess sodium in the extracellular fluid.  When there is primary loss of water from the extracellular fluid, this results in hyperosmotic dehydration.  This condition can occur from an inability to secrete antidiuretic hormone, which is needed for the kidneys to conserve water. 72
  • 73.
     As aresult of lack of antidiuretic hormone, the kidneys excrete large amounts of dilute urine (a disorder referred to as diabetes insipidus), causing dehydration and increased concentration of sodium chloride in the extracellular fluid.  In certain types of renal diseases, the kidneys cannot respond to antidiuretic hormone, also causing a type of nephrogenic diabetes insipidus. 73
  • 74.
     A morecommon cause of hypernatremia associated with decreased extracellular fluid volume is dehydration caused by water intake that is less than water loss, as can occur with sweating during prolonged, heavy exercise.  Hypernatremia can also occur as a result of excessive sodium chloride added to the extracellular fluid.  This often results in hyperosmotic overhydration because excess extracellular sodium chloride is usually associated with at least some degree of water retention by the kidneys as well. 74
  • 75.
     For example,excessive secretion of the sodium-retaining hormone aldosterone can cause a mild degree of hypernatremia and overhydration.  The reason that the hypernatremia is not more severe is that increased aldosterone secretion causes the kidneys to reabsorb greater amounts of water as well as sodium. 75
  • 76.
    Edema: Excess Fluid inthe Tissues  Edema refers to the presence of excess fluid in the body tissues.  In most instances, edema occurs mainly in the extracellular fluid compartment, but it can involve intracellular fluid as well. 76
  • 77.
    Intracellular Edema  Twoconditions are especially prone to cause intracellular swelling: (1) depression of the metabolic systems of the tissues, and (2) lack of adequate nutrition to the cells. 77
  • 78.
    Extracellular Edema  Extracellularfluid edema occurs when there is excess fluid accumulation in the extracellular spaces.  There are two general causes of extracellular edema: (1) abnormal leakage of fluid from the plasma to the interstitial spaces across the capillaries (2) failure of the lymphatics to return fluid from the interstitium back into the blood. 78
  • 79.
     The mostcommon clinical cause of interstitial fluid accumulation is excessive capillary fluid filtration. 79
  • 80.
    Summary of Causesof Extracellular Edema 80
  • 81.
  • 82.
    Safety Factors That NormallyPrevent Edema  Even though many disturbances can cause edema, usually the abnormality must be severe before serious edema develops.  The reason for this is that three major safety factors prevent excessive fluid accumulation in the interstitial spaces: 1. Low compliance of the interstitium when interstitial fluid pressure is in the negative pressure range 82
  • 83.
    2. The abilityof lymph flow to increase 10- to 50-fold, and 3. washdown of interstitial fluid protein concentration, which reduces interstitial fluid colloid osmotic pressure as capillary filtration increases. 83
  • 84.
    Determination of Volumesof Specific Body Fluid Compartments 84
  • 85.
    Fluid and electrolyte replacement done with 3 types of solutions  ISOTONIC  HYPOTONIC  HYPERTONIC 85
  • 86.
    ISOTONIC SOLUTIONS  0.9%Sodium Chloride Solution  Ringer’s Solution  Lactated Ringer’s Solution  Use- replace fluid losses, usually extracellular losses, and to expand the intravascular volume
  • 87.
    HYPOTONIC SOLUTIONS  5%DEXTROSE & WATER  0.45% SODIUM CHLORIDE  0.33% SODIUM CHLORIDE  Use- They are commonly infused to dilute extracellular fluid and rehydrate the cells of patients who have hypertonic fluid imbalances and to treat gastric fluid loss and dehydration from excessive diuresis.
  • 88.
    HYPERTONIC SOLUTIONS 3% SODIUMCHLORIDE 5% SODIUM CHLORIDE WHOLE BLOOD ALBUMIN TOTAL PARENTERAL NUTRITION TUBE FEEDINGS CONCENTRATED DEXTROSE (>10%) Use- to treat patients who have severe hyponatremia.  Depending on the type of hypertonic fluid infused, it can provide patients with calories, free water, and some electrolytes.
  • 89.
    Oral rehydration therapy Oral rehydration therapy (ORT) is a type of fluid replacement used to prevent or treat dehydration especially that due to diarrhoea.  It involves drinking water with modest amounts of sugar and salt added (an oral rehydration solution or ORS) while continuing to eat.  Oral rehydration solution is on WHO's list of essential medicines. 89
  • 90.
     WHO andUNICEF jointly have developed official guidelines for the manufacture of ORS and describe acceptable alternative preparations, depending on material availability.  Commercial preparations are available as either pre-prepared fluids or packets of oral rehydration salts (ORS) ready for mixing with water. 90
  • 91.
     The formulafor the current WHO-ORS (also known as low-osmolar ORS or reduced-osmolarity ORS) is  2.6 grams (0.092 oz) salt (NaCl),  2.9 grams (0.10 oz) trisodium citrate dihydrate (C 6H5Na3O7,2H2O),  1.5 grams (0.053 oz) potassium chloride (KCl),  13.5 grams (0.48 oz)anhydrous glucose (C 6H12O6) per litre of fluid. 91
  • 92.
     It canbe made using 6 level teaspoons (25.2 grams) of sugar and 0.5 teaspoon (2.1 grams) of salt in 1 litre of water. 92
  • 93.
    Fluid and electrolyte replacementin Dentistry  In dentistry fluid and electrolyte replacement implication is mainly related to oral and maxilla facial surgery.  Usually it is administered in clinical conditions like  Trauma  During and after surgeries under GA  Hypovolemic shock during minor surgical procedures (eg - Injury to any artery)  Hypogycemic shock during procedures 93
  • 94.
    Conclusion  To achievehomeostasis, the body maintains strict control of water and electrolyte distribution and of acid-base balance.  Methods of fluid & electrolyte movement are diffusion, osmosis, active transport & filtration 94
  • 95.
     The kidneyis the primary organ that maintains the total volume, pH, and osmolarity of the extracellular fluid within narrow limits.  The kidney accomplishes this by altering urine volume and osmolarity.  The kidney, in turn, is regulated by neural, hormonal, and local factors. 95
  • 96.
     Hormones likeRenin, Angiotensin, Aldosterone & Vassopressin play a key role in regulation  Assessment of body fluid is important to determine causes of imbalance  Interventions for imbalances are based on the cause 96
  • 97.
    REFERENCE  GUYTON &HALL, TEXTBOOK OF MEDICAL PHYSIOLOGY, ELEVENTH EDITION, ELSEVIER PUBLISHERS  K SEMBULINGAM, ESSENTIALS OF MEDICAL PHYSIOLOGY, SIXTH EDITION, JAYPEE PUBLISHERS  N GEETHA, TEXTBOOK OF MEDICAL PHYSIOLOGY, THIRD EDITION, PARAS BOOKS  LEONARD JOHNSON, ESSENTIAL MEDICAL PHYSIOLOGY, THIRD EDITION  THE TREATMENT OF DIARRHOEA, A MANUAL FOR PHYSICIANS AND SENIOR HEALTH WORKERS- WORLD HEALTH ORGANIZATION, 2005. 97
  • 98.