MR.J.G SAMBAD
IKDRC COLLEGE OF NURSING
 Fluid, electrolyte and acid base balance within
the body are necessary to maintain the health
and function in all the body systems. These
balance are maintain by the intake and output
of the water and electrolyte and regulation by
the renal and pulmonary systems.
 Approximately 60%of adult weight consist of
fluid (i.e. water ad electrolyte)
 Factors that influence the amount of body fluid
are age, gender and body fat.
4
Intracellular fluids (ICF)
Extracellular fluids (ECF)
 2/3 (65%) of TBW is intracellular (ICF)
 1/3 extra cellular water
-ECF is divided into small compartments
 25 % interstitial fluid (ISF)
 5- 8 % in plasma (IVF intravascular fluid)
 1- 2 % in Tran cellular fluids – CSF, intraocular
fluids, serous membranes, and in GI, respiratory,
urinary tracts and synovial fluid
5
6
 Electrolytes
Two types of electrolytes are
 Cations
e.g. Na+, K+, Ca+, H+
 Anions
e.g. Cl-, HCO3-,SO4-, P-
The unit of these ions are expressed in terms
of
Milliequivalent (mEq/l)
 Fluids and electrolytes constantly shift from
compartment to compartment to facilitate body
process such as tissue oxygenation, acid base
balance and urine formation.
Route for transporting materials to and from
intracellular compartments
 Osmosis,
 Diffusion,
 Active transport and
 Filtration.
 Osmosis is the movement of a pure
solvent, such as water through a
semipermeable membrane from an area
of lesser solute concentration to an area
of greater concentration
 Osmotic pressure - it is the amount of
the hydrostatic pressure needed to stop
the flow of water by osmosis
 Oncotic pressure
 Osmotic diuresis
 It is the movement of a solute (gas or substance) in
a solution across a semi permeable membrane
from an area of higher concentration to lower
concentration.
FILTRATION
 It is a process by which water and diffusible
substance move together in response to fluid
pressure, moving from an area of higher pressure
to lower pressure.
 It is a process that requires energy for
the movement of a substance through a
cell membrane from an area of lesser
solute concentration to higher
concentration.
 Kidneys
 Skins
 Lungs
 G. I. tract.
 Ingested liquids
 Water in food
 water in metabolic oxidation
 The physiological balance of the body fluid are
regulated by fluid intake , hormonal controls,
and fluid output is known as Homeostatic.
 Organs involved in homeostasis include the
Kidneys, Heart, Lungs, adrenal glands,
parathyroid glands and pituitary glands
 Regulation of ECF volume and osmolarity by
selective retention and excretion of body fluids
 Regulation of Ph of the ECF by retention of H+
HEART AND BLOOD VESSELS
- The pumping action of the heart circulates blood
through the kidney under sufficient pressure to allow
for urine formation
_ Failure of this pumping action interferes with renal
perfusion and hypovolemia by stimulating with
retention
 To correct metabolic acid base disturbance
regulates H+
concentration (pH) by controlling the
level of CO2 in the ECF
PITUITARY GLANDS
- Stores and release the antidiuretic hormone (ADH)
which makes the body retain water
ADRENAL GLANDS
- Regulate blood volume and Na and K balance by
secreting ALDOSTERONE
- Increase aldosterone secretion causes Na retention
and K loss
 Regulate Ca and PO4balance by means of
parathyroid hormone (PTH)
 PTH influence bone reabsorption Ca absorption
 Increase secretion of PTH causes
 A) elevated serum Ca concentration
 B) lower serum po4 concentration
 Inhibits and stimulates mechanism influencing
fluid balance, regulate Na and water intake and
excretion
 Regulates oral intake by acting at thirst centre
located in hypothalamus
ADH AND THIRST
- Maintaining Na concentration and oral intake of
fluid
- Oral intake is controlled by the thirst centre located
in hypothalamus
 Osmoresceptors are sensitive to change in the
concentration of ECF
 Sending appropriate impulses to the pituitary to
release ADH
 Acid
- An acid is a substance containing H+ that can
be liberated or release
 Base
-A base is a substance that can accept or trap H+
 Buffer system ,
 Respiratory mechanism and
 Renal mechanism
-A buffer is a substance that can
absorbed or released H+
to correct an
acid-base imbalance.
1.Carbonic acid-sodium bicarbonate
buffers up to 90% of the H+
of (ECF)
 Acts like a base and binds free hydrogen
ions.
2.Phosphate Buffer System
 Active in intracellular fluid
 It converts alkaline sodium phosphate
(Na2HPO4) a week base to acid sodium
phosphate(NaH2PO4) in the kidneys.
 It is a mixture of the plasma protein and the
globins portion of the hemoglobin in RBC.
 It can combine with or liberate hydrogen ions
that tends to minimize change in PH and
serves as excellent buffering agent.
-Primary controller of the body’s carbonic acid
supply
-Carbon dioxide constantly produced by cellular
metabolism (Carbonic acid[H2CO3] yields CO2and
H2O), is excreted by exhalation.
 The concentration of bicarbonate in the plasma
is regulated by kidneys.
 Kidneys excrete or retain H+ and form or
excrete bicarbonate ion is responsible to the pH
of the blood.
Electrolyte imbalances: Sodium
 Hypernatremia (high levels of sodium)
 Plasma Na+
> 145 mEq / L
 Due to ↑ Na+
or ↓ water
 Water moves from ICF → ECF
 Cells dehydrate
28
 Hypertonic IV soln.
 Oversecretion of aldosterone
 Loss of pure water
 Long term sweating with chronic fever
 Respiratory infection → water vapor loss
 Diabetes – polyuria
 Insufficient intake of water (hypodipsia)
29
 Thirst
 Lethargy
 Neurological dysfunction due to dehydration of
brain cells
 Decreased vascular volume
30
 Lower serum Na+
 Isotonic salt-free IV fluid
 Oral solutions preferable
31
 Overall decrease in Na+
in ECF
 Two types: depletional and dilutional
 Depletional Hyponatremia
Na+
loss:
 diuretics, chronic vomiting
 Chronic diarrhea
 Decreased aldosterone
 Decreased Na+
intake
32
 Dilutional Hyponatremia:
 Renal dysfunction with ↑ intake of hypotonic
fluids
 Excessive sweating→ increased thirst → intake
of excessive amounts of pure water
 Syndrome of Inappropriate ADH (SIADH) or
oliguric renal failure, severe congestive heart
failure, cirrhosis all lead to:
 Impaired renal excretion of water
 Hyperglycemia – attracts water
33
 Neurological symptoms
 Lethargy, headache, confusion, apprehension,
depressed reflexes, seizures and coma
 Muscle symptoms
 Cramps, weakness, fatigue
 Gastrointestinal symptoms
 Nausea, vomiting, abdominal cramps, and diarrhea
 Tx – limit water intake or discontinue meds
34
 Serum K+
< 3.5 mEq /L
 Beware if diabetic
 Insulin gets K+
into cell
 Ketoacidosis – H+
replaces K+
, which is
lost in urine
 β – adrenergic drugs or
epinephrine
35
 Decreased intake of K+
 Increased K+
loss
 Chronic diuretics
 Trauma and stress
 Increased aldosterone
36
 Neuromuscular disorders
 Weakness, flaccid paralysis,
respiratory arrest, constipation
 Dysrhythmias, Postural hypotension
 Cardiac arrest
 Treatment-
 Increase K+
intake, but slowly, preferably by foods
37
 Serum K+
> 5.5 mEq / L
 Check for renal disease
 Massive cellular trauma
 Insulin deficiency
 Addison’s disease
 Potassium sparing diuretics
 Decreased blood pH
 Exercise causes K+ to move out of cells
38
 Early – hyperactive muscles , paresthesia
 Late - Muscle weakness, flaccid paralysis
 Change in ECG pattern
 Dysrhythmias
 Bradycardia , heart block, cardiac arrest
39
 If time, decrease intake and increase renal
excretion
 Insulin + glucose
 Bicarbonate
 Ca++
counters effect on heart
40
 Most in ECF
 Regulated by:
 Parathyroid hormone
 ↑Blood Ca++
by stimulating osteoclasts
 ↑GI absorption and renal retention
 Calcitonin from the thyroid gland
 Promotes bone formation
 ↑ renal excretion
41
 Results from:
 Hyperparathyroidism
 Hypothyroid states
 Renal disease
 Excessive intake of vitamin D
 Malignant tumors – hypercalcemia of malignancy
 Tumor products promote bone breakdown
 Tumor growth in bone causing Ca++
release
42
 Effects:
 Many nonspecific – fatigue, weakness, lethargy
 Increases formation of kidney stones and pancreatic
stones
 Muscle cramps
 Bradycardia, cardiac arrest
 Pain
 GI activity also common
 Nausea, abdominal cramps
 Diarrhea / constipation
 Metastatic calcification
43
 Hyperactive neuromuscular reflexes and tetany
differentiate it from hypercalcemia
 Convulsions in severe cases
 Caused by:
 Lack of vitamin D
 Suppression of parathyroid function
 Hypersecretion of calcitonin
 Malabsorption states
 Widespread infection or peritoneal inflammation
 Pancreatitis – produce fatty acid that combine with
calcium , iron decreasing serum Ca level
44
 Diagnosis:
 Chvostek’s sign
 Trousseau’s sign
 Treatment
 IV calcium for acute
 Oral calcium and vitamin D for chronic
45
 It refers to a magnesium excess.
 It depress the skeletal muscles and nerve
function.
 The depression of acetylcholine leads to a
sedative effect, which can lead to bradycardia,
cardiac arrhythmia, and decreased respiratory
rate and depth.
 Occurs in end stage renal failure.
46
47
 Renal failure.
 Excess oral or parenteral intake of
magnesium.
SIGN and SYMPTOMS:
 Hypoactive deep tendon reflexes
 Decrease depth and rate of respiration,
 Hypotension and flushing.
LAB FINDINGS
 Serum magnesium level > 2.5 mEq/L
 Magnesium deficit.
 Occurs with malnutrition and malasorption disease
and sign and symptoms related to neuromuscular
disorders.
CAUSES
 Inadequate intake: malnutrition and alcoholism.
 Inadequate absorption: diarrhea, vomiting, fistulas,
disease of small intestine.
 Aldosterone excess
 Polyuria.
48
 Muscular tremor,
 Hyperactive deep tendon reflexes,
 Confusion and disorientation,
 Dysrhythmia and positive chvosliks and
 Trousseasis sign.
LAB FINDINGS
 Srrum magnesium level < 1.5 mEq/L
49
ISOTONIC IMBALANCE :
i) Fluid volume deficit (Hypovolemia)
ii) Fluid volume excess (Hypervolemia)
OSMOLAR IMBALANCE :
i) Hyper osmolar imbalance (Dehydration)
ii) Hypoosmolar imbalance (Water excess)
50
 Diarrhea
 Vomiting
 Drainage from fistula and tubes.
 Loss of plasma or whole blood eg. Burns and
hemorrhage
 Excessive perspiration
 Decreased oral intake of fluids
 Fever
 Use of diuretics.
51
 Postural hypotention
 Tachycardia
 Dry mucous membranes
 Poor skin turgor, thirst
 Confusion, lethargy
 Rapid weight loss and weak pulse
LAB FINDINGS
 Urine sepecific gravity >1.030
 Increased hematocrit level and BUN level
 FVE refers to an isotonic expansion of ECF
caused by the abnormal retention of water
and sodium near normal proportion which
are normally exist in ECF.
CAUSES
 Congestive heart failure
 Renal failure
 Increased serum aldosterone and steroid
level
 Excessive sodium intake or administration.
 Rapid weight gain, edema
 Hypertension and polyuria
 Neck vein distention
 Increased venous pressure
LAB FINDINGS
 Decreased hematocrit level
HYPEROSMOLAR IMBALANCE
(DEHYDRATION)
 It refers only to a decreased volume of water
alone with increased serum sodium level.
CAUSES:
 Diabetic ketoacidosis
 Osmotic diuresis
 Administration of hypertonic parenteral
fluid .
 Dry and sticky mucous membranes
 Flushed and dry skins
 Thirst and irritability
 Elevated body temperature
 Convulsion and coma.
LAB FINDINGS
 Increased serum sodium level above
145mEq/L
 It refers only to above normal amounts of
water in extracellular space.
CAUSES:
 Excess water intake
 Malfunction of the kidneys causing inability
to excrete the excesses.
SIGNS AND SYMPTOMS:
 Decreased level of consciousness
 Edema around eyes, fingers, ankles .
 Decreased serum sodium level below 135mEq/L.
ACID-BASE IMBALANCE
 Acid base imbalances occur when the carbonic
acid or bicarbonate levels become
disproportionate.
FOUR MAIN TYPES OF ACID BASE IMBALANCE
 Respiratory acidosis
 Respiratory alkalosis
 Metabolic acidosis
 Metabolic alkalosis
 Respiratory acidosis is a clinical disorder in
which the pH is less than 7.35 and the PaCO2
is greater then 42 mmHg.
 Respiratory acidosis = high PaCO2 because
of alveolar hypoventilation.
 Respiratory alkalosis is a clinical condition in
which the arterial pH is greater than 7.45 and
the PaCO2 is less than 38 mmHg.
 Respiratory alkalosis = low PaCO2 because of
alveolar hyperventilation.
 Metabolic acidosis is a clinical disturbance
characterized by a low pH ( increased H+
concentration) and a low bicarbonate concentration. It
can be produced by again of hydrogen ion or a loss of
bicarbonate.
Metabolic acidosis = low bicarbonate or
HCO3
-
is loss in similar amount.
ABG<7.35
Paco2 <35 mm of Hg.
 Metabolic alkalosis is a clinical disturbance
characterized by a high pH ( decreased H+
concentration) and a high bicarbonate
concentration.
 Metabolic alkalosis = high bicarbonate.
ABG>7.45
Paco2>45mm of Hg.
3 TYPES OF IV FLUIDS
i) Isotonic fluids
ii) Hypotonic fluids
iii) Hypertonic fluids
THANK YOU

Fluid and electrolyte imbalance

  • 1.
  • 2.
     Fluid, electrolyteand acid base balance within the body are necessary to maintain the health and function in all the body systems. These balance are maintain by the intake and output of the water and electrolyte and regulation by the renal and pulmonary systems.
  • 3.
     Approximately 60%ofadult weight consist of fluid (i.e. water ad electrolyte)  Factors that influence the amount of body fluid are age, gender and body fat.
  • 4.
    4 Intracellular fluids (ICF) Extracellularfluids (ECF)  2/3 (65%) of TBW is intracellular (ICF)  1/3 extra cellular water -ECF is divided into small compartments  25 % interstitial fluid (ISF)  5- 8 % in plasma (IVF intravascular fluid)  1- 2 % in Tran cellular fluids – CSF, intraocular fluids, serous membranes, and in GI, respiratory, urinary tracts and synovial fluid
  • 5.
  • 6.
  • 7.
     Electrolytes Two typesof electrolytes are  Cations e.g. Na+, K+, Ca+, H+  Anions e.g. Cl-, HCO3-,SO4-, P- The unit of these ions are expressed in terms of Milliequivalent (mEq/l)
  • 8.
     Fluids andelectrolytes constantly shift from compartment to compartment to facilitate body process such as tissue oxygenation, acid base balance and urine formation. Route for transporting materials to and from intracellular compartments  Osmosis,  Diffusion,  Active transport and  Filtration.
  • 9.
     Osmosis isthe movement of a pure solvent, such as water through a semipermeable membrane from an area of lesser solute concentration to an area of greater concentration
  • 10.
     Osmotic pressure- it is the amount of the hydrostatic pressure needed to stop the flow of water by osmosis  Oncotic pressure  Osmotic diuresis
  • 11.
     It isthe movement of a solute (gas or substance) in a solution across a semi permeable membrane from an area of higher concentration to lower concentration. FILTRATION  It is a process by which water and diffusible substance move together in response to fluid pressure, moving from an area of higher pressure to lower pressure.
  • 12.
     It isa process that requires energy for the movement of a substance through a cell membrane from an area of lesser solute concentration to higher concentration.
  • 13.
     Kidneys  Skins Lungs  G. I. tract.
  • 14.
     Ingested liquids Water in food  water in metabolic oxidation
  • 16.
     The physiologicalbalance of the body fluid are regulated by fluid intake , hormonal controls, and fluid output is known as Homeostatic.  Organs involved in homeostasis include the Kidneys, Heart, Lungs, adrenal glands, parathyroid glands and pituitary glands
  • 17.
     Regulation ofECF volume and osmolarity by selective retention and excretion of body fluids  Regulation of Ph of the ECF by retention of H+ HEART AND BLOOD VESSELS - The pumping action of the heart circulates blood through the kidney under sufficient pressure to allow for urine formation _ Failure of this pumping action interferes with renal perfusion and hypovolemia by stimulating with retention
  • 18.
     To correctmetabolic acid base disturbance regulates H+ concentration (pH) by controlling the level of CO2 in the ECF PITUITARY GLANDS - Stores and release the antidiuretic hormone (ADH) which makes the body retain water ADRENAL GLANDS - Regulate blood volume and Na and K balance by secreting ALDOSTERONE - Increase aldosterone secretion causes Na retention and K loss
  • 19.
     Regulate Caand PO4balance by means of parathyroid hormone (PTH)  PTH influence bone reabsorption Ca absorption  Increase secretion of PTH causes  A) elevated serum Ca concentration  B) lower serum po4 concentration
  • 20.
     Inhibits andstimulates mechanism influencing fluid balance, regulate Na and water intake and excretion  Regulates oral intake by acting at thirst centre located in hypothalamus ADH AND THIRST - Maintaining Na concentration and oral intake of fluid - Oral intake is controlled by the thirst centre located in hypothalamus
  • 21.
     Osmoresceptors aresensitive to change in the concentration of ECF  Sending appropriate impulses to the pituitary to release ADH
  • 22.
     Acid - Anacid is a substance containing H+ that can be liberated or release  Base -A base is a substance that can accept or trap H+
  • 23.
     Buffer system,  Respiratory mechanism and  Renal mechanism -A buffer is a substance that can absorbed or released H+ to correct an acid-base imbalance.
  • 24.
    1.Carbonic acid-sodium bicarbonate buffersup to 90% of the H+ of (ECF)  Acts like a base and binds free hydrogen ions. 2.Phosphate Buffer System  Active in intracellular fluid  It converts alkaline sodium phosphate (Na2HPO4) a week base to acid sodium phosphate(NaH2PO4) in the kidneys.
  • 25.
     It isa mixture of the plasma protein and the globins portion of the hemoglobin in RBC.  It can combine with or liberate hydrogen ions that tends to minimize change in PH and serves as excellent buffering agent.
  • 26.
    -Primary controller ofthe body’s carbonic acid supply -Carbon dioxide constantly produced by cellular metabolism (Carbonic acid[H2CO3] yields CO2and H2O), is excreted by exhalation.
  • 27.
     The concentrationof bicarbonate in the plasma is regulated by kidneys.  Kidneys excrete or retain H+ and form or excrete bicarbonate ion is responsible to the pH of the blood.
  • 28.
    Electrolyte imbalances: Sodium Hypernatremia (high levels of sodium)  Plasma Na+ > 145 mEq / L  Due to ↑ Na+ or ↓ water  Water moves from ICF → ECF  Cells dehydrate 28
  • 29.
     Hypertonic IVsoln.  Oversecretion of aldosterone  Loss of pure water  Long term sweating with chronic fever  Respiratory infection → water vapor loss  Diabetes – polyuria  Insufficient intake of water (hypodipsia) 29
  • 30.
     Thirst  Lethargy Neurological dysfunction due to dehydration of brain cells  Decreased vascular volume 30
  • 31.
     Lower serumNa+  Isotonic salt-free IV fluid  Oral solutions preferable 31
  • 32.
     Overall decreasein Na+ in ECF  Two types: depletional and dilutional  Depletional Hyponatremia Na+ loss:  diuretics, chronic vomiting  Chronic diarrhea  Decreased aldosterone  Decreased Na+ intake 32
  • 33.
     Dilutional Hyponatremia: Renal dysfunction with ↑ intake of hypotonic fluids  Excessive sweating→ increased thirst → intake of excessive amounts of pure water  Syndrome of Inappropriate ADH (SIADH) or oliguric renal failure, severe congestive heart failure, cirrhosis all lead to:  Impaired renal excretion of water  Hyperglycemia – attracts water 33
  • 34.
     Neurological symptoms Lethargy, headache, confusion, apprehension, depressed reflexes, seizures and coma  Muscle symptoms  Cramps, weakness, fatigue  Gastrointestinal symptoms  Nausea, vomiting, abdominal cramps, and diarrhea  Tx – limit water intake or discontinue meds 34
  • 35.
     Serum K+ <3.5 mEq /L  Beware if diabetic  Insulin gets K+ into cell  Ketoacidosis – H+ replaces K+ , which is lost in urine  β – adrenergic drugs or epinephrine 35
  • 36.
     Decreased intakeof K+  Increased K+ loss  Chronic diuretics  Trauma and stress  Increased aldosterone 36
  • 37.
     Neuromuscular disorders Weakness, flaccid paralysis, respiratory arrest, constipation  Dysrhythmias, Postural hypotension  Cardiac arrest  Treatment-  Increase K+ intake, but slowly, preferably by foods 37
  • 38.
     Serum K+ >5.5 mEq / L  Check for renal disease  Massive cellular trauma  Insulin deficiency  Addison’s disease  Potassium sparing diuretics  Decreased blood pH  Exercise causes K+ to move out of cells 38
  • 39.
     Early –hyperactive muscles , paresthesia  Late - Muscle weakness, flaccid paralysis  Change in ECG pattern  Dysrhythmias  Bradycardia , heart block, cardiac arrest 39
  • 40.
     If time,decrease intake and increase renal excretion  Insulin + glucose  Bicarbonate  Ca++ counters effect on heart 40
  • 41.
     Most inECF  Regulated by:  Parathyroid hormone  ↑Blood Ca++ by stimulating osteoclasts  ↑GI absorption and renal retention  Calcitonin from the thyroid gland  Promotes bone formation  ↑ renal excretion 41
  • 42.
     Results from: Hyperparathyroidism  Hypothyroid states  Renal disease  Excessive intake of vitamin D  Malignant tumors – hypercalcemia of malignancy  Tumor products promote bone breakdown  Tumor growth in bone causing Ca++ release 42
  • 43.
     Effects:  Manynonspecific – fatigue, weakness, lethargy  Increases formation of kidney stones and pancreatic stones  Muscle cramps  Bradycardia, cardiac arrest  Pain  GI activity also common  Nausea, abdominal cramps  Diarrhea / constipation  Metastatic calcification 43
  • 44.
     Hyperactive neuromuscularreflexes and tetany differentiate it from hypercalcemia  Convulsions in severe cases  Caused by:  Lack of vitamin D  Suppression of parathyroid function  Hypersecretion of calcitonin  Malabsorption states  Widespread infection or peritoneal inflammation  Pancreatitis – produce fatty acid that combine with calcium , iron decreasing serum Ca level 44
  • 45.
     Diagnosis:  Chvostek’ssign  Trousseau’s sign  Treatment  IV calcium for acute  Oral calcium and vitamin D for chronic 45
  • 46.
     It refersto a magnesium excess.  It depress the skeletal muscles and nerve function.  The depression of acetylcholine leads to a sedative effect, which can lead to bradycardia, cardiac arrhythmia, and decreased respiratory rate and depth.  Occurs in end stage renal failure. 46
  • 47.
    47  Renal failure. Excess oral or parenteral intake of magnesium. SIGN and SYMPTOMS:  Hypoactive deep tendon reflexes  Decrease depth and rate of respiration,  Hypotension and flushing. LAB FINDINGS  Serum magnesium level > 2.5 mEq/L
  • 48.
     Magnesium deficit. Occurs with malnutrition and malasorption disease and sign and symptoms related to neuromuscular disorders. CAUSES  Inadequate intake: malnutrition and alcoholism.  Inadequate absorption: diarrhea, vomiting, fistulas, disease of small intestine.  Aldosterone excess  Polyuria. 48
  • 49.
     Muscular tremor, Hyperactive deep tendon reflexes,  Confusion and disorientation,  Dysrhythmia and positive chvosliks and  Trousseasis sign. LAB FINDINGS  Srrum magnesium level < 1.5 mEq/L 49
  • 50.
    ISOTONIC IMBALANCE : i)Fluid volume deficit (Hypovolemia) ii) Fluid volume excess (Hypervolemia) OSMOLAR IMBALANCE : i) Hyper osmolar imbalance (Dehydration) ii) Hypoosmolar imbalance (Water excess) 50
  • 51.
     Diarrhea  Vomiting Drainage from fistula and tubes.  Loss of plasma or whole blood eg. Burns and hemorrhage  Excessive perspiration  Decreased oral intake of fluids  Fever  Use of diuretics. 51
  • 52.
     Postural hypotention Tachycardia  Dry mucous membranes  Poor skin turgor, thirst  Confusion, lethargy  Rapid weight loss and weak pulse LAB FINDINGS  Urine sepecific gravity >1.030  Increased hematocrit level and BUN level
  • 53.
     FVE refersto an isotonic expansion of ECF caused by the abnormal retention of water and sodium near normal proportion which are normally exist in ECF. CAUSES  Congestive heart failure  Renal failure  Increased serum aldosterone and steroid level  Excessive sodium intake or administration.
  • 54.
     Rapid weightgain, edema  Hypertension and polyuria  Neck vein distention  Increased venous pressure LAB FINDINGS  Decreased hematocrit level
  • 55.
    HYPEROSMOLAR IMBALANCE (DEHYDRATION)  Itrefers only to a decreased volume of water alone with increased serum sodium level. CAUSES:  Diabetic ketoacidosis  Osmotic diuresis  Administration of hypertonic parenteral fluid .
  • 56.
     Dry andsticky mucous membranes  Flushed and dry skins  Thirst and irritability  Elevated body temperature  Convulsion and coma. LAB FINDINGS  Increased serum sodium level above 145mEq/L
  • 57.
     It refersonly to above normal amounts of water in extracellular space. CAUSES:  Excess water intake  Malfunction of the kidneys causing inability to excrete the excesses. SIGNS AND SYMPTOMS:  Decreased level of consciousness  Edema around eyes, fingers, ankles .
  • 58.
     Decreased serumsodium level below 135mEq/L. ACID-BASE IMBALANCE  Acid base imbalances occur when the carbonic acid or bicarbonate levels become disproportionate. FOUR MAIN TYPES OF ACID BASE IMBALANCE  Respiratory acidosis  Respiratory alkalosis  Metabolic acidosis  Metabolic alkalosis
  • 59.
     Respiratory acidosisis a clinical disorder in which the pH is less than 7.35 and the PaCO2 is greater then 42 mmHg.  Respiratory acidosis = high PaCO2 because of alveolar hypoventilation.
  • 60.
     Respiratory alkalosisis a clinical condition in which the arterial pH is greater than 7.45 and the PaCO2 is less than 38 mmHg.  Respiratory alkalosis = low PaCO2 because of alveolar hyperventilation.
  • 61.
     Metabolic acidosisis a clinical disturbance characterized by a low pH ( increased H+ concentration) and a low bicarbonate concentration. It can be produced by again of hydrogen ion or a loss of bicarbonate. Metabolic acidosis = low bicarbonate or HCO3 - is loss in similar amount. ABG<7.35 Paco2 <35 mm of Hg.
  • 62.
     Metabolic alkalosisis a clinical disturbance characterized by a high pH ( decreased H+ concentration) and a high bicarbonate concentration.  Metabolic alkalosis = high bicarbonate. ABG>7.45 Paco2>45mm of Hg.
  • 63.
    3 TYPES OFIV FLUIDS i) Isotonic fluids ii) Hypotonic fluids iii) Hypertonic fluids
  • 67.