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DR MARIA FATIMA
PGT, GMT-1
 Renal replacement therapy (RRT) replaces the
normal blood filtering functions of the kidney
in patients with renal failure.
 Refractory hyperkalemia
 Refractory metabolic acidosis
 Signs of uremia
 Fluid overload unresponsive to diuresing
agents
 Anuria
 Overdose of dialysable toxin e.g Lithium
 GFR <15ml/min/1.73m2
 Severe hyperkalemia
 Severe metabolic acidosis
 Intractable intravascular fluid overload
 Urine output <200ml in 12 hours
 Uremic Pericarditis/Encephalopathy
 Failure to thrive
 HEMODIALYSIS
 HEMOFILTRATION
 HEMODIAFILTRATION
 PERITONEAL DIALYSIS
 KIDNEY TRANSPLANT
 Diffusion
 Ultrafiltration
 Hemodialysis:
Solute passively moves down a concentration
gradient between the dialysate and the
capillaries.
 Hemofiltration
Plasma water and solute move down a
concentration gradient by ultrafiltration and
convection induced by hydrostatic pressure,
 3 essential components:
 Dialyser
 Dialysate
 Blood filtering system
 Hollow fiber dialyser, most commonly used.
 Contains bundles of capillary tubes through
which blood flows, while the dialysate
circulates outside it.
 Dialysate flows countercurrent to the blood,
 Urea, Creatinine and Potassium flow from
Blood to Dialysate.
 Calcium and Bicarbonate flow from Dialysate
to Blood.
 Easy access to blood
 Prevention of stenosis and thrombosis
 Low risk of infection
 Sites:
 Internal Jugular vein
 Subclavian vein
 Femoral vein
• Vein cross cut and
attached end to side
with artery.
• Takes 2-4 months to
mature.
• Low infectious risk,
durable.
 Biocompatible tube
attached from end to
side on artery and vein.
 Requires 2 weeks till
swelling resolves.
 Higher risk of
stenosis/thrombosis,
high infection risk.
 Tunelled under skin to
reduce contamination.
 Can be used
immediately.
 High risk of
thrombosis, infection.
• Arm veins suitable for access should be
preserved.
• Wear Medic bracelet.
• Save the non-dominant arm
 No B.P measurement
 No I/V cannula
 No blood draws
• Place vascular access within ayear of
hemodialysis anticipation.
 To maintain patency of vascular access.
 Unfractionated/LMW Heparin may be used
@40-70U/Kg bolus dose follwed by 0.5-
1.0U/kg/hour in infusion.
 C/I to anticoagulation in dialysis?
• Line sepis
• Air emboli
• Blood loss
• Platelet consumption
• Hemodynamic instability
• Electrolyte imbalance
• Hypothermia
• Heparin induced thrombocytopenia
 Dialysate infused into peritoneal cavity,
followed by slow diffusion of solutes e.g
urea, creatinine.
 The vascular peritoneal membrane acts as a
semi-permeable membrane.
 Ultrafiltration due to osmotic gradient
generated by glucose in dialysate.
 Peritonitis
 Catheter associated infections
 Protein loss
 Residual uremia
 Interference with diaphragm function
• Low dialysate & blood flow rates.
• Small molecule detoxification
• Reduced anti-coagulant requirement
• 11 hours SLED equally efficient to CRRT
• Reduced cost
 During or immediately after dialysis.
 Caused by acute rapid increase in water
content in the brain cells and change in pH of
CSF.
 Anorexia, vomiting, headache, hypotension,
blurred vision, cramps, tremors.
 May cause psychosis, confusion, seizures
 Stop dialysis
 Protect airway
 Correct hypoglycemia
 Inj Valium/Phenytoin for seizures
 May be avoided by short dialysis session, low
sodium dialysate.
 GFR < 20ml/kg/min
 GFR 15-19ml/kg/min: live donor with 6
antigen matches
 GFR <15ml/kg/min: any donor
 Active malignancy
 Advanced lung disease
 Liver Cirrhosis
 Ongoing infection
 Life expectancy <2 years
 Ischemic cardiac disease
 Severe peripheral vascular disease
 BMI >40
 Acute transplant rejection
 Graft vs host disease
 Post transplant malignancy
 Diabetes
 Recurrent infections
 Anemia
 Hypocalcemia
 Serum Vit D deficiency
 Hyperphosphatemia
 Metabolic acidosis
 Caused due to decreased erythropoietin
production.
 Erythropoietin stimulating agents e.g Epoietin
alfa or Darbepoietin alfa may be used if Hb
<10g/dL.
 Calcium salts e.g Calcium acetate, Calcium
carbonate may be given with or without
Calcitriol.
 Vitamin D analogues e.g Calcitriol (1,25
dihydroxycholecalciferol) or Doxercalciferol
(1-alphahydroxyergocalciferol) may be given
in case of elevated or rising PTH levls.
 Calcium salts
 Calcimimetics e.g
 Cinacalcet by increasing sensitivity of calcium
receptors on parathyroid gland to
extracellular calcium
 Etelcalcitide by enhancing calcium receptor
activation by extracellular calcium.
 Phosphate binders e.g calcium acetate,
lanthanum carbonate, Sevelamer.
 Insoluble salts excreted in feces.
 Oral alkali supplements
Renal Replacement Therapy

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Renal Replacement Therapy

  • 1.
  • 2.
  • 4.  Renal replacement therapy (RRT) replaces the normal blood filtering functions of the kidney in patients with renal failure.
  • 5.  Refractory hyperkalemia  Refractory metabolic acidosis  Signs of uremia  Fluid overload unresponsive to diuresing agents  Anuria  Overdose of dialysable toxin e.g Lithium
  • 6.  GFR <15ml/min/1.73m2  Severe hyperkalemia  Severe metabolic acidosis  Intractable intravascular fluid overload  Urine output <200ml in 12 hours  Uremic Pericarditis/Encephalopathy  Failure to thrive
  • 7.
  • 8.  HEMODIALYSIS  HEMOFILTRATION  HEMODIAFILTRATION  PERITONEAL DIALYSIS  KIDNEY TRANSPLANT
  • 9.
  • 11.  Hemodialysis: Solute passively moves down a concentration gradient between the dialysate and the capillaries.  Hemofiltration Plasma water and solute move down a concentration gradient by ultrafiltration and convection induced by hydrostatic pressure,
  • 12.
  • 13.
  • 14.  3 essential components:  Dialyser  Dialysate  Blood filtering system
  • 15.  Hollow fiber dialyser, most commonly used.  Contains bundles of capillary tubes through which blood flows, while the dialysate circulates outside it.
  • 16.
  • 17.  Dialysate flows countercurrent to the blood,  Urea, Creatinine and Potassium flow from Blood to Dialysate.  Calcium and Bicarbonate flow from Dialysate to Blood.
  • 18.
  • 19.  Easy access to blood  Prevention of stenosis and thrombosis  Low risk of infection  Sites:  Internal Jugular vein  Subclavian vein  Femoral vein
  • 20. • Vein cross cut and attached end to side with artery. • Takes 2-4 months to mature. • Low infectious risk, durable.
  • 21.  Biocompatible tube attached from end to side on artery and vein.  Requires 2 weeks till swelling resolves.  Higher risk of stenosis/thrombosis, high infection risk.
  • 22.  Tunelled under skin to reduce contamination.  Can be used immediately.  High risk of thrombosis, infection.
  • 23. • Arm veins suitable for access should be preserved. • Wear Medic bracelet. • Save the non-dominant arm  No B.P measurement  No I/V cannula  No blood draws • Place vascular access within ayear of hemodialysis anticipation.
  • 24.  To maintain patency of vascular access.  Unfractionated/LMW Heparin may be used @40-70U/Kg bolus dose follwed by 0.5- 1.0U/kg/hour in infusion.  C/I to anticoagulation in dialysis?
  • 25.
  • 26. • Line sepis • Air emboli • Blood loss • Platelet consumption • Hemodynamic instability • Electrolyte imbalance • Hypothermia • Heparin induced thrombocytopenia
  • 27.
  • 28.  Dialysate infused into peritoneal cavity, followed by slow diffusion of solutes e.g urea, creatinine.  The vascular peritoneal membrane acts as a semi-permeable membrane.  Ultrafiltration due to osmotic gradient generated by glucose in dialysate.
  • 29.
  • 30.
  • 31.  Peritonitis  Catheter associated infections  Protein loss  Residual uremia  Interference with diaphragm function
  • 32. • Low dialysate & blood flow rates. • Small molecule detoxification • Reduced anti-coagulant requirement • 11 hours SLED equally efficient to CRRT • Reduced cost
  • 33.  During or immediately after dialysis.  Caused by acute rapid increase in water content in the brain cells and change in pH of CSF.  Anorexia, vomiting, headache, hypotension, blurred vision, cramps, tremors.  May cause psychosis, confusion, seizures
  • 34.  Stop dialysis  Protect airway  Correct hypoglycemia  Inj Valium/Phenytoin for seizures  May be avoided by short dialysis session, low sodium dialysate.
  • 35.
  • 36.
  • 37.  GFR < 20ml/kg/min  GFR 15-19ml/kg/min: live donor with 6 antigen matches  GFR <15ml/kg/min: any donor
  • 38.  Active malignancy  Advanced lung disease  Liver Cirrhosis  Ongoing infection  Life expectancy <2 years  Ischemic cardiac disease  Severe peripheral vascular disease  BMI >40
  • 39.
  • 40.  Acute transplant rejection  Graft vs host disease  Post transplant malignancy  Diabetes  Recurrent infections
  • 41.
  • 42.  Anemia  Hypocalcemia  Serum Vit D deficiency  Hyperphosphatemia  Metabolic acidosis
  • 43.  Caused due to decreased erythropoietin production.  Erythropoietin stimulating agents e.g Epoietin alfa or Darbepoietin alfa may be used if Hb <10g/dL.
  • 44.  Calcium salts e.g Calcium acetate, Calcium carbonate may be given with or without Calcitriol.  Vitamin D analogues e.g Calcitriol (1,25 dihydroxycholecalciferol) or Doxercalciferol (1-alphahydroxyergocalciferol) may be given in case of elevated or rising PTH levls.
  • 45.  Calcium salts  Calcimimetics e.g  Cinacalcet by increasing sensitivity of calcium receptors on parathyroid gland to extracellular calcium  Etelcalcitide by enhancing calcium receptor activation by extracellular calcium.
  • 46.  Phosphate binders e.g calcium acetate, lanthanum carbonate, Sevelamer.  Insoluble salts excreted in feces.
  • 47.  Oral alkali supplements