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 Polyuria
 Nocturia
 Urinary frequency
 Normal urine output ? 800 – 2500 ML/Day
 Physiological - primary polydipsia
 Pathological – diabetes insipidus
 Burning micturition
 Increased frequency
 increased Urgency
 A/W disorders of urinary tract
 Inability to retain urine in bladder
 Neurogenic incontinence
 Stress incontinence
 Mechanical incontinence
 Overflow incontinence
 Psychogenic incontinence
 Functional incontinence
 Enuresis
 Oliguria
 Anuria
 Diuresis
 Natriuresis
 Deterioration of renal functions resulting in
reduced GFR leading to accumulation of
urea ,creatinine , electrolytes ,and non
nitrogenous substances
 ARF
 CRF
 Oliguria
 Anuria
 Volume overload
 Hyperkalemia
 Metabolic acidosis
 Hypoalcemia
 Anorexia , nausea , vomiting , muscle
twitching , fits , coma
 Sudden reduction in function of kidney A/w
rapid rise in urea and creatinine
 Pre renal
 Renal
 Post renal
 Pre renal – severe hemorrhage , shock ,
hypovolemia , burns , septicaemia
 Renal – glomerulonephritis , acute tubular
necrosis
 Post renal – urinary tract obstruction
 Slow insidious onset
 Irreversible loss of renal functions
 Leading to uremia
 Manifesting as excretory , metabolic ,
hematological , endocrinal functional
abnormalities
 Maintenance of adequate water and
electrolyte balance
 Control of infection
 Control of BP
 Acid base balance
 Diet
 Dialysis
 Congenital disorders
 Vascular disorders
 Glomerular disorders
 Tubulointestitial disorders
 Obstructive disorders
 Massive proteinuria and associated
complications
 Hypoalbuminemia
 Edema
 Hyperlipidemia
 Lipiduria
 Hypercoagulability
 Haemodialysis
 Peritoneal dialysis
 Functions as artificial kidney in patients with
non functional kidneys
 To treat patients in uremic coma
 Uses the principle of diffusion of solutes
through a semi-permeable membrane
 Can never replace a normal kidney
 Does not provide endocrinal , hematological
function of kidney
 Dialyzing fluid
 Uses heparin as an anti-coagulent
 Drains blood from the patient through AV
fistula or large veins
 Semi-permeable membrane allows passage
of all solutes except proteins
 At any given time artificial kidney contains
500ml of blood
 Used in both ARF and CRF
 Needs hospitalization and monitoring
 Needs AV fistula in CRF for repeated uses
 One cycle runs for 4- 6 hours
 Clears urea at the rate of 100 – 225 ml/min
 Peritoneal membrane is used as dialyzing
membrane
 No need for hospitalization
 Used in young children and older individuals
 Also known as CAPD
 Two liters of dialyzing fluid is injected into the
peritoneum
 Placement of permanent peritoneal catheter
 Exchange happens for 15 min
 Dialyzing fluid drained out and measured
 One cycle for every 6 hours
 Strict i/o chart is maintained
 Irreversible or terminally damaged kidneys
 ESRD
 Donor – cadaveric
sibling
 isogenic or allogenic
 Left kidney is preferred
 Rt iliac fossa is preferred
 Immunosupression needed- prednisolone ,
cyclosporine
 Substances increasing urine output
 By increasing water excretion
 Diuresis occurs along with natriuresis
 Loss of both water and solutes
 Used to reduce ECF volume
 Depending upon their ability (effectiveness)
they are classified under
 High efficacy diuretics - Loop diuretics
 Medium efficacy – Thiazides
 Weak diuretic -
 Osmotic diuretic
 Carbonic anhydrase inhibitors
 Aldosterone antagonist
 Sodium channel blockers
 Diuretics acting on PCT
 Diuretics acting on loop of henle
 Diuretics acting on DCT and CD
 Potassium sparing diuretics
 Acting on loop of TAL
 Inhibiting Na- k- 2cl symporter
 High efficacy diuretiics
 Furosemide , bumetanide
 Acts on early DCT
 Inhibits Na –Cl symport
 Medium efficacy drugs
 Hydrochlorthiazide
 Site of action is PCT
 Inhibits H+ secretion thro Na H antiport
 Causes loss of Na and bicarbonate
 Acetazolamide ..
 Mannitol , glycerol , isosorbide
 Major site of action PCT
 Causes increased osmolarity in the tubules
 Loss of water through diffusion
 Aldosterone antagonist
 EnaC inhibitors
 Acts on DT ,CD
 Spironolactone , amiloride ,
Pathophysiology of common renal diseases and diurectics
Pathophysiology of common renal diseases and diurectics

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Pathophysiology of common renal diseases and diurectics

  • 1.
  • 2.
  • 3.  Polyuria  Nocturia  Urinary frequency  Normal urine output ? 800 – 2500 ML/Day
  • 4.  Physiological - primary polydipsia  Pathological – diabetes insipidus
  • 5.  Burning micturition  Increased frequency  increased Urgency  A/W disorders of urinary tract
  • 6.  Inability to retain urine in bladder  Neurogenic incontinence  Stress incontinence  Mechanical incontinence  Overflow incontinence  Psychogenic incontinence  Functional incontinence
  • 7.  Enuresis  Oliguria  Anuria  Diuresis  Natriuresis
  • 8.  Deterioration of renal functions resulting in reduced GFR leading to accumulation of urea ,creatinine , electrolytes ,and non nitrogenous substances  ARF  CRF
  • 9.  Oliguria  Anuria  Volume overload  Hyperkalemia  Metabolic acidosis  Hypoalcemia  Anorexia , nausea , vomiting , muscle twitching , fits , coma
  • 10.  Sudden reduction in function of kidney A/w rapid rise in urea and creatinine  Pre renal  Renal  Post renal
  • 11.  Pre renal – severe hemorrhage , shock , hypovolemia , burns , septicaemia  Renal – glomerulonephritis , acute tubular necrosis  Post renal – urinary tract obstruction
  • 12.  Slow insidious onset  Irreversible loss of renal functions  Leading to uremia  Manifesting as excretory , metabolic , hematological , endocrinal functional abnormalities
  • 13.  Maintenance of adequate water and electrolyte balance  Control of infection  Control of BP  Acid base balance  Diet  Dialysis
  • 14.  Congenital disorders  Vascular disorders  Glomerular disorders  Tubulointestitial disorders  Obstructive disorders
  • 15.
  • 16.  Massive proteinuria and associated complications  Hypoalbuminemia  Edema  Hyperlipidemia  Lipiduria  Hypercoagulability
  • 17.
  • 19.  Functions as artificial kidney in patients with non functional kidneys  To treat patients in uremic coma  Uses the principle of diffusion of solutes through a semi-permeable membrane  Can never replace a normal kidney  Does not provide endocrinal , hematological function of kidney
  • 20.  Dialyzing fluid  Uses heparin as an anti-coagulent  Drains blood from the patient through AV fistula or large veins  Semi-permeable membrane allows passage of all solutes except proteins  At any given time artificial kidney contains 500ml of blood
  • 21.  Used in both ARF and CRF  Needs hospitalization and monitoring  Needs AV fistula in CRF for repeated uses  One cycle runs for 4- 6 hours  Clears urea at the rate of 100 – 225 ml/min
  • 22.
  • 23.
  • 24.  Peritoneal membrane is used as dialyzing membrane  No need for hospitalization  Used in young children and older individuals  Also known as CAPD  Two liters of dialyzing fluid is injected into the peritoneum  Placement of permanent peritoneal catheter
  • 25.  Exchange happens for 15 min  Dialyzing fluid drained out and measured  One cycle for every 6 hours  Strict i/o chart is maintained
  • 26.  Irreversible or terminally damaged kidneys  ESRD  Donor – cadaveric sibling  isogenic or allogenic  Left kidney is preferred  Rt iliac fossa is preferred  Immunosupression needed- prednisolone , cyclosporine
  • 27.  Substances increasing urine output  By increasing water excretion  Diuresis occurs along with natriuresis  Loss of both water and solutes  Used to reduce ECF volume
  • 28.  Depending upon their ability (effectiveness) they are classified under  High efficacy diuretics - Loop diuretics  Medium efficacy – Thiazides  Weak diuretic -  Osmotic diuretic  Carbonic anhydrase inhibitors  Aldosterone antagonist  Sodium channel blockers
  • 29.  Diuretics acting on PCT  Diuretics acting on loop of henle  Diuretics acting on DCT and CD  Potassium sparing diuretics
  • 30.  Acting on loop of TAL  Inhibiting Na- k- 2cl symporter  High efficacy diuretiics  Furosemide , bumetanide
  • 31.  Acts on early DCT  Inhibits Na –Cl symport  Medium efficacy drugs  Hydrochlorthiazide
  • 32.  Site of action is PCT  Inhibits H+ secretion thro Na H antiport  Causes loss of Na and bicarbonate  Acetazolamide ..
  • 33.
  • 34.  Mannitol , glycerol , isosorbide  Major site of action PCT  Causes increased osmolarity in the tubules  Loss of water through diffusion
  • 35.  Aldosterone antagonist  EnaC inhibitors  Acts on DT ,CD  Spironolactone , amiloride ,

Editor's Notes

  1. physiology of abnormal states the disordered physiological processes associated with disease or injury