MODERATOR: DR.C.S. PRAKASH H.O.D AND PROFESSOR DEPT OF ANAESTHESIA DR. RADHIKA ASSOCIATE PROFESSOR DEPT OF BIOCHEMISTRY PRESENTOR: DR. HARIHARAN. V II.

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MODERATOR: DR.C.S. PRAKASH H.O.D AND PROFESSOR DEPT OF ANAESTHESIA DR. RADHIKA ASSOCIATE PROFESSOR DEPT OF BIOCHEMISTRY PRESENTOR: DR. HARIHARAN. V II ND YR M.D. BIOCHEMISTRY

TOTAL BODY WEIGHT 40% SOLIDS 60% FLUIDS 2/3 RD ICF1/3 RD ECF 80% INTERSTITIAL FLUID 20% PLASMA DISTRIBUTION OF BODY WATER

SOLUTES:  ELECTROLYTES – Inorganic salts, acids, bases, and proteins  NON ELECTROLYTES – Glucose, urea, creatinine FUNCTIONS: Secretory activity Neuro muscular excitability Controlling fluid movements

CHIEF ELECTROLYTES IN BODY FLUID COMPARTMENTS INTRACELLULAREXTRACELLULAR POTASSIUMSODIUM PHOSPHATECHLORIDE MAGNESIUMBICARBONATE

Osmosis is the net movement of water molecules across a Partially-permeable membrane DUE TO CONCENTRATION DIFFERENCE OF SOLUTES.

 TO EXPRESS CONCENTRATION OF PARTICLES IN SOLUTION - OSMOLE  1 OSMOLE = 1 GRAM MOLECULAR WEIGHT OF OSMOTICALLY ACTIVE PARTICLES.  EX : 180 Gms OF GLUCOSE = 1 OSMOLE Gms OF NaCl = 2 OSMOLE.

OSMOLALITY Definition: Concentration of particles (osmotically active) in solution. It is usually expressed in millosmoles of solute per kg of solution.  Osmolality is independent of valency.  Osmolarity is expressed in milliosmoles of solute per litre of solution.  Plasma: mOsm/Kg  Same in all body compartments  Water distribution

 A property of a solution that depends on the osmotic force exerted across the membrane as influenced by the differing concentrations of solutes in and out of the cell.  Isotonic  Hypertonic  Hypotonic

HYPERTONIC SOLN

HYPOTONIC SOLN

Osmotic pressure 28 mmHg Arteriolar end Venous end Hydrostatic pressure (BP) 35 mm Hg Hydrostatic pressure (BP) 15 mm Hg Net inward pressure 6.7 mmHg Net outward pressure 13.3 mmHg FORCES THAT MAINTAIN FLUID BALANCE CAPILLARY Osmotic pressure 28 mm Hg Osmotic pressure 6.3 mm Hg

Total intake (2500ml)

Increased ECF water Restoration of ECF osmolality Increased water intake Stimulation of hypothalamic centre Renal water retention Redistribut ion of water from ICF Stimulation of vasopressin release Increased plasma osmolality Water loss

Loss of GI fluid-SI fistula, SI obstn(fluid accumulates in lumen) Isotonic contraction Addison's(aldosterone def), infusion of fluids with low Na eg. dextrose Hypotonic contraction Diarrhoea, vomiting, excessive sweating(has half Na as plasma) Diabetes insipidus Hypertonic contraction Cardiac failure Hypoalbuminemia Isotonic expansion Glomerular dysfunction(water retention), ADH excess Hypotonic expansion Conn’s and cushing’s syndrome(mineralocorticoid excess) Hypertonic expansion

SODIUM : DISTRIBUTION: TOTAL mmol/l Free ions - 70% major in ECF. Complexed in bone - 30% BALANCE: Input mmol/24 hr. Loss - < 10 mmol/24hr

 RENAL REGULATION:  GFR  ACTIVE REABSORPTION – PCT-70%  ALDOSTERONE - DCT <5%  ATRIAL NATRIURETIC PEPTIDE:  DECREASES DISTAL TUBULAR REABSORPTION  DECREASES RENIN SECRETION

HYPONATREMIA NORMAL/HIGH PL.OSMOLALITY LOW PLASMA OSMOLALITY TRANSLOCATIONAL GLUCOSE MANNITOL MALTOSE PSEUDO HYPONATREMIA PROTEIN LIPID URINE OSMOLALITY <100mosm/kg WATER INTAKE EXCEEDS URINARY DILUTION LOW SOLUTE INTAKE CORRECTION PHASE OF HYPONATREMIA URINE OSMOLALITY >100mosm/kg HYPOVOLEMIA EUVOLEMIA HYPERVOLEMIA TBW TOTAL BODY Na TBW NO CHANGE IN TOTAL BODY Na TBW TOTAL BODY Na URINARY Na >20mmol/L DIURETIC EXCESS MINERALOCORTICOID DEFI PROXIMAL RTA URINARY Na <10mmol/l VOMITTING DIARRHOEA BURNS SWEATING URINARY Na >20mmol/L GLUCOCORTICOID DEF HYPOTHYROIDISM DIURETICS SIADH URINARY Na >20mmol/l ACUTE / CHRONIC RENAL FAILURE PREGNANCY <10mmol/l NEPHROTIC SYNDROME CIRRHOSIS HEART FAILURE

HYPERNATREMIA ASSESS VOLUME HYPOVOLEMIA HYPERVOLEMIA T B W T B Na URINARY Na > 20mmol/l PRIMARY HYPER ALDOSTERONISM CUSHING HYPERTONIC DIALYSIS T B W T B Na URINARY Na > 20 mmol/L URINARY Na <20mmol/L EUVOLEMIA T B W T B Na NO CHANGE RENAL LOSS 1)OSMOTIC /LOOP DIURETIC 2) POST OBSTRUCTION 3)INTRINSIC RENAL DISEASE EXTRA RENAL LOSS 1)EXCESS SWEATING 2) BURNS 3) DIARRHOEA URINARY Na INVARIABLE RENAL LOSS 1)DIABETES INSIPIDUS EXTRA RENAL LOSS INSENSIBLE LOSS

POTASSIUM: PREDOMINANT INTRACELLULAR ION DISTRIBUTION: FREE - 90% BOUND FORM – 10% ECF - 2% REGULATION: RENAL: REABSORPTION – PROXIMAL TUBULES SECRETION – DISTAL TUBULE- ALDOSTERONE GIT: SECRETED IN GASTRIC JUICE REABSORBED –SMALL INTESTINE SECRETED – COLON – ALDOSTERONE

 MAJOR ANION OF ECF.  SECRETED IN GASTRIC JUICE  99% REABSORBED UNDER NORMAL PH CONDITIONS.  CHLORIDE SHIFT  DECREASED IN ACIDOSIS

 PRESENT IN ECF  BUFFERING ACTION  REABSORBED IN TUBULE AS CO2 FOR HYDROGEN ION.

 CALCITONIN- decreases bone resorption

PTH play important role in regulating phosphate concentration through 2 effects: 1) PTH promotes bone resorption, thereby dumping large amounts of phosphate ions into the ECF from bones salts 2) PTH decreases the transport maximum for phosphate by the renal tubules

Control of Renal Magnesium Excretion and Extracellular Magnesium Ion Concentration Total plasma magnesium concentration is about 1.8 mEq/L, more than one half bound to plasma proteins Regulation of magnesium excretion is achieved by mainly changing tubular reabsorption.

 COLLECTION OF BLOOD  STORAGE  TIME OF ANALYSIS  HEMOLYSIS

Normal Laboratory Values ParametersValues Sodium meq/L Potassium meq/L Chloride meq/L Bicarbonate meq/L Calcium 9-11 mg/dL or mmo/l ( mmol/l*4 =mg/l) Phosphate mg/dL or mmol/l (mmol/l*3=mg/l) Glucose mg/dL ( mg/dl/18 = mmol/dl) BUN 8-18 mg/dL or mmol/l ( mmol/l* 6= mg/l) Creatinine mg/dL or µmol/l (µmol/l* 0.011=mg/dl) PLASMA Osmolality mOsm/kg URINE Osmolality mOsm/kg

 Tietz- clinical chemistry  Vasudevan- textbook of biochemistry  Harrison’s internal medicine  Pubmed.com