2. • Total body fluid
• Fluid compartment composition
• Important Terminologies
• Approximate value of daily input and output
• Normal daily fluid loss
• Abnormal Fluid Loss
• Volume Changes
• Concentration Changes
• Composition Changes
6. • Example for a healthy 70 kg man,
• TBW=0.6x70=42L
• ICF=2/3 TBW = 0.66x42=28L
• ECF=1/3 TBW = 0.33x42= 14L
• Intravascular compartment= 0.25x 14 = 3.5L
• Interestitial compartment = 0.75x 14= 10.5 L
7. ECF ICF
MAJOR CATION SODIUM POTASSIUM AND
MAGNESSIUM
MAJOR ANION CHLORIDE AND
BICARBONATE
PHOSPHATE,
SULPHATE AND
PROTEIN
8. • Osmolarity:
• It is fluid capability to create osmotic pressure.
• It is concentration of osmotically active substance.
• Osmolality:
• It is number of particles/L of solution.
• Tonicity:
• Way of expressing effective osmolarity
9. • Fluid balance is an aspect of
the homeostasis of organisms in which the amount
of water in the organism needs to be controlled,
via osmoregulation and behavior, such that
the concentrations of electrolytes (salts in solution) in
the various body fluids are kept within healthy ranges.
10.
11. WATER GAIN ROUTE AVERAGE
DAILY
VOLUME (ml)
MINIMUM (ml) MAXIMUM (ml)
SENSIBLE ORAL FLUIDS 800-1500 0 1500/h
SOLID FOOD 500-700 0 1500
INSENSIBLE METABOLIC
WATER
250 125 800
12. WATER LOSS ROUTE AVERAGE
DAILY
VOLUME(ml)
SENSIBLE URINE 800-1500
INTESTINE 0-250
SWEAT 100
INSENSIBLE LUNGS 400
SKIN 500-1000
13. Insensible fluid input=300ml due to oxidation of water
Insensible fluid loss=500ml through skin
400ml through lungs
100ml through stool
Fluid loss –fluid input=1000-300=700ml
NORMAL DAILY INSENSIBLE FLUID
LOSS=700ML
15. There are seven means of abnormal means of fluid loss
which are:
• Vomiting
• Diarrhea
• Prespiration(moderate=500ml, severe=1-1.5L)
• Burns and open body cavity(laprotomy)=0.5-3 L
• Gastric suction
• Bleeding
• Diuretic drugs
• Fever:100ml/degree fever/day
• Tracheostomy (unhumidified air) :m ore than 1.5 litres
19. • Volume depletion generally results from a deficit in total
body Na+ content. This may result from renal or
extrarenal losses of Na+ from the ECF. Water losses
alone can also cause volume depletion, but the quantity
required to do so is large, as water is lost mainly from the
ICF and not the ECF, where volume contraction can be
assessed.
20. • Thirst
• Fatigue
• weakness,
• muscle cramps,
• and postural dizziness.
• Sometimes, syncope and coma can result with severe
volume depletion
21. • low jugular venous pressure,
• postural hypotension,
• postural tachycardia,
• and the absence of axillary sweat
• Diminished skin turgor and dry mucous membranes are
poor markers of decreased interstitial fluid. Mild degrees
of volume depletion are often not clinically detectable,
whereas larger fluid losses can lead to mental status
changes, oliguria(less than 0.5 L), and hypovolemic
shock.
22. • Laboratory studies are often helpful but must be used in
conjunction with the clinical picture
• Urine sodium
• Urine osmolality and serum bicarbonate -elevated.
• Hematocrit and serum albumin -increased
23. • Isotonic fluid, such as NS (0.9% NaCl), contains a Na+
content similar to that of plasma fluid in the ECF.
• BOLUS ADMINISTRATION:
• An initial bolus of lactated Ringer solution or normal
saline of 250-500ml (over 5-7 mins) of is given in an
adult (20 mL/kg in a pediatric patient), and the patient's
response is assessed.
• Hemorrhage or GI bleeding, blood transfusion.
24.
25. SIGNS:
• Expansion of the interstitial compartment may result in
peripheral edema, ascites, and pleural effusions.
Expansion of the intravascular compartment may result
in pulmonary rales, elevated jugular venous pressure,
hepatojugular reflux, an S3 gallop, and elevated blood
pressures.
• SYMPTOMS:
• dyspnea
• abdominal distention
• swelling of extremities
26. • Laboratory studies are generally not needed, and
hypervolemia is primarily a bedside diagnosis.
• The urine [Na+]
• CXR may show pulmonary edema or pleural effusions,
but clear lung fields do not exclude volume overload.
30. Acute hyponatremia:
• In acute hyponatremia (i.e., developing in <2 days),
approximately 125 mEq/L—NAUSEA AND MALAISE
• . As the plasma [Na+] falls further- headache, lethargy,
confusion, and obtundation.
• Stupor, seizures, and coma -below 115 mEq/L if falls
acutely.
• Chronic Hyponatremia (>3 days in duration)
32. • Three laboratory analyses, when used with a clinical
assessment of volume status, can narrow the differential
diagnosis of hyponatremia:
• (a) the plasma osmolality (<275 mOsm/L)
• (b) the urine osmolality (urine osmolality <100 mOsm/L
and specific gravity <1.003).
• (c) the urine [Na+]: discriminate between extrarenal
and renal losses of Na+
33.
34.
35. • Hypernatremia is defined as a plasma [Na+] >145 mEq/L
and represents a state of hyperosmolality.
• • Asymptomatic
• • Symptomatic (Na>160 meq/L)
• CNS manifestations : due to dehydration of brain cells
36. Body system Signs & symptoms
Central nervous system Restlessness, lethargy, ataxia,
irritability, tonic spasms, delirium,
seizures, coma
Musculoskeletal Weakness
Cardiovascular Tachycardia, hypotension, syncope
Tissue Dry sticky mucous membranes, red
swollen tongue,
decreased saliva and tears
Renal Oliguria
Metabolic Fever
39. • Increased renal excretion
• Administration of potassium free fluids
• Parentral nutrition without potassium
• Fistulas
• Direct loss of potassium from gastrointestinal fluid
(diarrhea), (gastric fluid, either as vomiting or high
nasogastric output)
41. • Oral therapy. Oral doses of 40 mEq are generally well
tolerated and can be given as often as every 4 hours.
Traditionally, 10 mEq of potassium salts are given for
each 0.10mEq/L decrement in serum [K+].
• IV THERAPY : The maximum concentration of
administered of K+ should be no more than 40 mEq/L
via a peripheral vein or 100 mEq/L via a central vein.
• Kdeficit (in mmol) = (Knormal lower limit − Kmeasured) × kg body
weight × 0.4.
43. Body system Signs & symptoms
Gastrointestinal Nausea/vomiting ,colic diarrhea
Neuromuscular weakness, paralysis, respiratory
failure
Cardiovascular Arrhythmia, arrest
ECG changes Peaked T waves (early change)
Flattened P wave
Prolonged PR interval (first-degree
block)
Widened QRS complex
Ventricular fibrillation
44.
45. • Majority of the 1000 to 1200g of calcium in the average-
sized adult is found in the bone .
• Normal daily intake of calcium is 1 to 3 gm.
• Normal serum level = 8.8-10.5 mg/dl
• Albumin Bound = 40-60%
• Ionized portion (1.2 mg/dl) is responsible for
neuromuscular stability
• Most is excreted via the GI tract
Corrected calcium = 4 – albumin x 0.8 + serum calcium
47. Hypocalcemia S/S Hypercalcemia S/S
1. Hypotension
2. Anxiety
3. Psychosis
4. Paresthesia
5. Laryngeal spasm
6. Numbness and tingling of the
circumoral region and the tips of
the
fingers and toes
7. tetany with carpopedal spasm,
convulsions (with severe deficit),
8. Chvosteck & trousseau’s signs
1. Hypertension
2. Bradycardia
3. Constipation
4. Anorexia
5. nausea, vomiting
6. Nephrolithiasis
7. Pain
8. Psychosis
9. Pruritis
10. weight loss, thirst, polydipsia,
and
polyuria
11. easy fatigue, weakness,
stupor,and
coma
48. HYPOCALCEMIA HYPERCALCEMIA
• (IV) calcium gluconate-
ACUTE
• oral calcium and vitamin
D supplements-CHRONIC
• 0.9% NORMAL SALINE
THEN FUROSEMIDE.
Notas do Editor
Osmotic pressure(created by dissolved electrolyte in body fluids) and hydrostatic pressure (created by the water in body fluids) are the main forces behind any molecular movement between body compartments.
Renal losses may be
secondary to enhanced diuresis,
salt-wasting nephropathies,
Mineralocorticoid deficiency
resolution of obstructive renal disease.
Extrarenal losses include fluid loss from the GI tract (vomiting, nasogastric suction, fistula drainage,
diarrhea), respiratory losses, skin losses (especially with burns), hemorrhage, and severe third spacing of fluid in critically ill patients
Urine sodium is a marker for Na+ avidity in the kidney.
Urine Na+ <15 mEq is consistent with volume depletion, as is a fractional excretion of sodium (FeNa) <1%.
Urine osmolality and serum bicarbonate levels may also be elevated.
Hematocrit and serum albumin may be increased from hemoconcentration
Mild volume contraction can usually be corrected via the oral route. However, the presence of hemodynamic instability, symptomatic fluid loss, or intolerance to oral administration requires IV therapy
The primary therapeutic goal is to protect hemodynamic stability and replenish intravascular volume with fluid that will preferentially expand the ECF compartment. This can be accomplished with Na+-based solutions, because the Na+ will be retained in the ECF.
and thus remains entirely in the ECF space. It is the initial fluid of choice for replenishing intravascular volume.
hemorrhage or GI bleeding, blood transfusion can accomplish both volume expansion and concomitant correction of anemia
The clinical manifestations of hypervolemia result from a surplus of total body Na+. It can be caused by a primary disorder of renal Na+ retention. Alternatively, it may be secondary to decreased effective circulating volume, as in heart failure, cirrhosis, or profound hypoalbuminemia
Because overt signs of hypervolemia may not manifest until 3-4 L of fluid retention, a gradual rise in water weight is often the earliest indication of Na+ retention