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DIALYSIS, ARTIFICIAL KIDNEY
AND RENAL TRANSPLANT
Pandian M.
DEPT. OF PHYSIOLOGY
D.Y. PATIL MEDICAL COLLEGE KOLHAPUR
OBJECTIVES
 INDICATIONS OF DIALYSIS
BASIC PRINCIPLES OF DIALYSIS WITH AN
ARTIFICIAL KIDNRY
PERITONEAL DIALYSIS
INDICATIONS OF RENAL TRANSPLANTION
DIALYSIS
The term dialysis refers to diffusion of solutes from
an area of higher concentration to the area of lower
concentration through a semipermeable
membrane.
This principle has been used to dialyse the blood of
patients with renal failure especially those
developing uremia.
Dialysis is the procedure to correct electrolyte
imbalances and to remove waste products in renal
failure.
It does not correct endocrine functions of kidney.
Hence dialysis is not a cure for renal failure.
INDICATIONS
The need for dialysis may be acute or chronic.
Acute dialysis is indicated :-
high & rising levels of serum potassium.
Fluid overload or impending edema.
Increasing acidosis
Pericarditis
Chronic dialysis is indicated :-
Chronic renal failure or end stage renal disease(ESRD)
Chronic kidney disease is defined as either kidney damage or
glomerular filtration rate < 60 ml/mim/1.73m2 for 3 months.
STAGE DESCRIPTION GFR
1 Kidney damage with
normal or raised GFR
> 90
2 Kidney damage with mildly
decreased GFR
60-89
3 Moderately decreased GFR 30-59
4 Severely decreased GFR 15-29
5 kidney failure <15
Uremia develops when more than 75% of nephrons are
damaged and is charecterised by :
Accumulation of nitrogenous waste products in the blood.
Metabolic acidosis.
Hyperkelemia.
Uremic coma is terminal event in chronic renal failure.
TYPES OF DIALYSIS
HEMODIALYSIS OR ARITIFICIAL KIDNEY.
PERITONEAL DIALYSIS.
HEMODAILYSIS OR ARTIFICIAL KIDNEY
It is most commonly used method of dialysis for patients
who are acutely ill and require short term dialysis (days
to week).
It can save the life in many types of acute renal failure
produced by reversible pathological process , specially
circulatory shock or mercury poisoning.
The intermittent dialysis may prolong the life of many
patients with chronic renal failure, which may lead for an
active life for many useful years.
REQUIREMENTS FOR HEMODIALYSIS
Access to patients circulation-
arterio venous fistula
arterio venous graft
central venous catheter
Dialysis machine & dialyzer with semipermeable
membrane.
Appropriate dialyzing fluid
PROCEDURE:
 Hemodialysis machine is also called as artificial kidney.
 Hemodialysis is done in hospitalized patient through IV line
for 3-5 hours.
 During hemodialysis the patient’s radial artery is connected
to the hemodialysis machine.
 Inside the hemodialysis machine the blood is passed through
a long coiled cellophone tube immersed in a dialysis fluid.
 Heparin is used as an anticoagulant while passing blood
through the machine.
COMPOSITION OF DILAZYING FLUID
The composition of dialyzing fluid is similar to that of
plasma, except it is free of waste products like urea, uric
acid, etc.
The fluid contains less amount of sodium , potassium
and chloride ions than in uremic blood.
But the quantity of glucose , bicarbonate and calcium
ions are more in the dialyzing fluid than in the uremic
blood.
CONSTITUENT UREMIC PLASMA DIALYZING FLUID
ELECTROLYTES(mEq/L)
-Na+
-K+
-Ca
-Mg
-Cl
-HCO
-Lactate
-HPO
-urate
-SO
NONELECTROLYTES
-Glucose
-urea
creatinine
142
7
2
1.5
103
14
1.2
9
2
3
100
200
6
142
4
3
1.5
107
27
1.2
0
0
0
125
0
0
PRINCIPLE OF HEMODIALYSIS
DIFFUSION- movement from higher concentration
(blood) to lower concentration (dialysate).
OSMOSIS- excess water is removed from the blood by
osmosis, in which water moves from an area of higher
concentration to an area of lower concentration.
ULTAFILTRATION- Water moving under high pressure to
an area of lower pressure by negative pressure of a
suctioning force to the dialysis membrane.
DIALYZER
-Cannula in artery
-into vein
Uremic blood
from the person
Toxins diffuse through the membrane
Purified blood to the person
 During hemolysis , the semipermeable cellophane membrane
permits the free diffusion of constituents of plasma except proteins.
 In this way , the dialysis of patient’s blood removes the toxic waste
products and restores normal electrolyte concentration in plasma.
 The dialyzed blood is returned to the patient via peripheral vein.
 At a time about 500ml is passed through the artificial kidney.
 Hemodialysis is done usually thrice a week in severe uremia.
COMPLICATIONS OF
HEMODIALYSIS
During dialysis-hypotension, arrhythmias,
exsanguination, seziures, fever.
Between treatments-hyper/hypotension , edema ,
pulmonary edema , hyperkalemia , clotting.
Long term- hyperparathyroidism ,CHF , AV access
failure , pulmonary edema , neuropathy , anemia , GI
bleeding.
Others-infection , catheter clotting , central vein
thrombosis, stenosis, ischemia of hand, aneurysm.
PERITONEAL DIALYSIS
In this type of dialysis, the peritoneum is used as
semipermeable membrane.
Continuous ambulatory peritoneal dialysis is a form
of long-term dialysis done by patients at home or at
work.
INDICATIONS FOR PERITONEAL DIALYSIS
Vascular access failure.
Intolerance to hemodialysis.
Congestive heart failure.
Prosthetic valvular disease.
PROCEDURE
Under strict aseptic precautions 2 litres of dialyzing
fluid is introduced through a permanent intra
peritoneal catheter.
It is then kept in peritoneal cavity for exchange to
take place for a period of 15-20 minutes, called as
dwell time.
Strict input and output chart is maintained. The
whole procedure constitutes one cycle.
It is done at 6hours interval(4 cycles per day), even
when patient is ambulatory or mobile.
There is no need for hospitalization.
It is useful for young children and old patients with
cardiac disorders.
It prolongs survival in patients with chronic renal
failure for many years.
before medications are added, the dialysate is
warmed to body temperature to prevent patient
discomfort , abdominal pain and to dilate vessels of
peritoneum to increase urea clearance.
Solutions that are to cold cause pain and
vasoconstriction and reduce clearance. Solutions that
are too hot burn the peritoneum.
COMPLICATIONS
PERITONITIS
BLEEDING AT CATHETER SITE.
RESPIRATORY DIFFICULTY
PERITONEAL FLUID LEAK
CATHETER RELATED INFECTIONS
HYPER/HYPOVOLEMIA.
RENAL TRANSPLANT
Kidney transplant is the treatment of choice for end-
stage renal disease.
It provides better long term survival and improved
quality of life compared to dialysis.
INDICATIONS
ESRD GFR< 15ml/min.
Malignancy
 Hypertension
Diabetes mellitus
genetic diseases-
polycystic kidney disease
Metabolic disorders
CONTRAINDICATIONS
 Cardiac and pulmonary
insufficiency.
 Hepatic diseases.
 Concurrent tobacco use
and morbid obesity
 HIV
BENEFITS
 Significantly reduced risk of
mortality.
 Increased life expectancy
 Improved quality of life
 More likely to stay
employed
RISKS
 Acute rejection or failure
 Anti-rejection medication
effects—infection
--malignancies
--increased risk of
HTN/DM
-graft loss over time.
TYPES OF DONORS
LIVING DONORS-
Genetically related-parents , sibling, twin.
Living-unrelated.
Criteria:-
 AGE-18-70 yrs
 BMI<35
No cancer or active infection
Adequate renal function
Compatablity.
DECEASED DONORS
BRAIN DEAD DONORS
DONATION AFTER CARDIAC DEATH
COMPTABILITY
The patient has to be ABO compatible.
The recipient should share as many as HLA antigens
and minor antigens as possible.
Immunosupressent drugs are given to prevent anti
body reactions.
BLOOD GROUP , TISSUE TYPE AND CROSS
MATCHING TO BE DONE.
DRUGS USED IN RENAL TRANSPLANT
INDUCTION
 Monoclonal antibodies-
muromonab basiliximab
daclizimab
 Polyclonal antibodies
Antithymocyte globulin
(equine/rabbit)
MAINTENANCE
 Calcineurin inhibitors
cyclosporine tacrolimus
 Purine synthesis inhibitors
azathioprine
mycophenolate moeftil
Steroids -prednisolone
MTOR inhibitors-
sirolimus
PROCEDURE
 TIME-3HRS approx.
 Donor kidney is placed in the lower abdomen.
 Usually left kidney of donor is transplanted to right iliac fossa of
recipient.
 Arteries , veins from the recipient are connected to new kidney.
 Final step is to connect the ureter to new kidney.
 New kidney starts working immediately.
 Living kidney takes 3-5 days and cadaveric kidney upto7-15 days.
COMPLICATIONS
TRANSPLANT REJECTION
INFECTION AND SEPSIS
POST TRANSPLANT LYMPHOPROLIFERATIVE
DISORDER.
ELECTROLYTE IMBALANCE
IATROGENIC SIDE EFFECTS
REFRENCES
 1.Text book of medical physiology
-Guyton and hall, 12th edition.
 2.Ganong’s review of medical physiology
-23rd edition
 3.text of medical physiology
-2nd edition
 4.net sources (acknowledge for all online sources)
 5.text book of medical physiology
--A.K. JAIN
 6.text book of medical physiology
---indu khurana
Artificial kidney , dialysis and renal transplant by Pandian M

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Artificial kidney , dialysis and renal transplant by Pandian M

  • 1. DIALYSIS, ARTIFICIAL KIDNEY AND RENAL TRANSPLANT Pandian M. DEPT. OF PHYSIOLOGY D.Y. PATIL MEDICAL COLLEGE KOLHAPUR
  • 2. OBJECTIVES  INDICATIONS OF DIALYSIS BASIC PRINCIPLES OF DIALYSIS WITH AN ARTIFICIAL KIDNRY PERITONEAL DIALYSIS INDICATIONS OF RENAL TRANSPLANTION
  • 3. DIALYSIS The term dialysis refers to diffusion of solutes from an area of higher concentration to the area of lower concentration through a semipermeable membrane. This principle has been used to dialyse the blood of patients with renal failure especially those developing uremia.
  • 4. Dialysis is the procedure to correct electrolyte imbalances and to remove waste products in renal failure. It does not correct endocrine functions of kidney. Hence dialysis is not a cure for renal failure.
  • 5. INDICATIONS The need for dialysis may be acute or chronic. Acute dialysis is indicated :- high & rising levels of serum potassium. Fluid overload or impending edema. Increasing acidosis Pericarditis Chronic dialysis is indicated :- Chronic renal failure or end stage renal disease(ESRD)
  • 6. Chronic kidney disease is defined as either kidney damage or glomerular filtration rate < 60 ml/mim/1.73m2 for 3 months. STAGE DESCRIPTION GFR 1 Kidney damage with normal or raised GFR > 90 2 Kidney damage with mildly decreased GFR 60-89 3 Moderately decreased GFR 30-59 4 Severely decreased GFR 15-29 5 kidney failure <15
  • 7. Uremia develops when more than 75% of nephrons are damaged and is charecterised by : Accumulation of nitrogenous waste products in the blood. Metabolic acidosis. Hyperkelemia. Uremic coma is terminal event in chronic renal failure.
  • 8. TYPES OF DIALYSIS HEMODIALYSIS OR ARITIFICIAL KIDNEY. PERITONEAL DIALYSIS.
  • 9. HEMODAILYSIS OR ARTIFICIAL KIDNEY It is most commonly used method of dialysis for patients who are acutely ill and require short term dialysis (days to week). It can save the life in many types of acute renal failure produced by reversible pathological process , specially circulatory shock or mercury poisoning. The intermittent dialysis may prolong the life of many patients with chronic renal failure, which may lead for an active life for many useful years.
  • 10. REQUIREMENTS FOR HEMODIALYSIS Access to patients circulation- arterio venous fistula arterio venous graft central venous catheter Dialysis machine & dialyzer with semipermeable membrane. Appropriate dialyzing fluid
  • 11.
  • 12. PROCEDURE:  Hemodialysis machine is also called as artificial kidney.  Hemodialysis is done in hospitalized patient through IV line for 3-5 hours.  During hemodialysis the patient’s radial artery is connected to the hemodialysis machine.  Inside the hemodialysis machine the blood is passed through a long coiled cellophone tube immersed in a dialysis fluid.  Heparin is used as an anticoagulant while passing blood through the machine.
  • 13. COMPOSITION OF DILAZYING FLUID The composition of dialyzing fluid is similar to that of plasma, except it is free of waste products like urea, uric acid, etc. The fluid contains less amount of sodium , potassium and chloride ions than in uremic blood. But the quantity of glucose , bicarbonate and calcium ions are more in the dialyzing fluid than in the uremic blood.
  • 14. CONSTITUENT UREMIC PLASMA DIALYZING FLUID ELECTROLYTES(mEq/L) -Na+ -K+ -Ca -Mg -Cl -HCO -Lactate -HPO -urate -SO NONELECTROLYTES -Glucose -urea creatinine 142 7 2 1.5 103 14 1.2 9 2 3 100 200 6 142 4 3 1.5 107 27 1.2 0 0 0 125 0 0
  • 15. PRINCIPLE OF HEMODIALYSIS DIFFUSION- movement from higher concentration (blood) to lower concentration (dialysate). OSMOSIS- excess water is removed from the blood by osmosis, in which water moves from an area of higher concentration to an area of lower concentration. ULTAFILTRATION- Water moving under high pressure to an area of lower pressure by negative pressure of a suctioning force to the dialysis membrane.
  • 16. DIALYZER -Cannula in artery -into vein Uremic blood from the person Toxins diffuse through the membrane Purified blood to the person
  • 17.
  • 18.  During hemolysis , the semipermeable cellophane membrane permits the free diffusion of constituents of plasma except proteins.  In this way , the dialysis of patient’s blood removes the toxic waste products and restores normal electrolyte concentration in plasma.  The dialyzed blood is returned to the patient via peripheral vein.  At a time about 500ml is passed through the artificial kidney.  Hemodialysis is done usually thrice a week in severe uremia.
  • 19. COMPLICATIONS OF HEMODIALYSIS During dialysis-hypotension, arrhythmias, exsanguination, seziures, fever. Between treatments-hyper/hypotension , edema , pulmonary edema , hyperkalemia , clotting. Long term- hyperparathyroidism ,CHF , AV access failure , pulmonary edema , neuropathy , anemia , GI bleeding. Others-infection , catheter clotting , central vein thrombosis, stenosis, ischemia of hand, aneurysm.
  • 20. PERITONEAL DIALYSIS In this type of dialysis, the peritoneum is used as semipermeable membrane. Continuous ambulatory peritoneal dialysis is a form of long-term dialysis done by patients at home or at work.
  • 21. INDICATIONS FOR PERITONEAL DIALYSIS Vascular access failure. Intolerance to hemodialysis. Congestive heart failure. Prosthetic valvular disease.
  • 22. PROCEDURE Under strict aseptic precautions 2 litres of dialyzing fluid is introduced through a permanent intra peritoneal catheter. It is then kept in peritoneal cavity for exchange to take place for a period of 15-20 minutes, called as dwell time. Strict input and output chart is maintained. The whole procedure constitutes one cycle.
  • 23. It is done at 6hours interval(4 cycles per day), even when patient is ambulatory or mobile. There is no need for hospitalization. It is useful for young children and old patients with cardiac disorders. It prolongs survival in patients with chronic renal failure for many years.
  • 24. before medications are added, the dialysate is warmed to body temperature to prevent patient discomfort , abdominal pain and to dilate vessels of peritoneum to increase urea clearance. Solutions that are to cold cause pain and vasoconstriction and reduce clearance. Solutions that are too hot burn the peritoneum.
  • 25.
  • 26. COMPLICATIONS PERITONITIS BLEEDING AT CATHETER SITE. RESPIRATORY DIFFICULTY PERITONEAL FLUID LEAK CATHETER RELATED INFECTIONS HYPER/HYPOVOLEMIA.
  • 27. RENAL TRANSPLANT Kidney transplant is the treatment of choice for end- stage renal disease. It provides better long term survival and improved quality of life compared to dialysis.
  • 28. INDICATIONS ESRD GFR< 15ml/min. Malignancy  Hypertension Diabetes mellitus genetic diseases- polycystic kidney disease Metabolic disorders CONTRAINDICATIONS  Cardiac and pulmonary insufficiency.  Hepatic diseases.  Concurrent tobacco use and morbid obesity  HIV
  • 29. BENEFITS  Significantly reduced risk of mortality.  Increased life expectancy  Improved quality of life  More likely to stay employed RISKS  Acute rejection or failure  Anti-rejection medication effects—infection --malignancies --increased risk of HTN/DM -graft loss over time.
  • 30. TYPES OF DONORS LIVING DONORS- Genetically related-parents , sibling, twin. Living-unrelated. Criteria:-  AGE-18-70 yrs  BMI<35 No cancer or active infection Adequate renal function Compatablity.
  • 31. DECEASED DONORS BRAIN DEAD DONORS DONATION AFTER CARDIAC DEATH
  • 32. COMPTABILITY The patient has to be ABO compatible. The recipient should share as many as HLA antigens and minor antigens as possible. Immunosupressent drugs are given to prevent anti body reactions. BLOOD GROUP , TISSUE TYPE AND CROSS MATCHING TO BE DONE.
  • 33. DRUGS USED IN RENAL TRANSPLANT INDUCTION  Monoclonal antibodies- muromonab basiliximab daclizimab  Polyclonal antibodies Antithymocyte globulin (equine/rabbit) MAINTENANCE  Calcineurin inhibitors cyclosporine tacrolimus  Purine synthesis inhibitors azathioprine mycophenolate moeftil Steroids -prednisolone MTOR inhibitors- sirolimus
  • 34. PROCEDURE  TIME-3HRS approx.  Donor kidney is placed in the lower abdomen.  Usually left kidney of donor is transplanted to right iliac fossa of recipient.  Arteries , veins from the recipient are connected to new kidney.  Final step is to connect the ureter to new kidney.  New kidney starts working immediately.  Living kidney takes 3-5 days and cadaveric kidney upto7-15 days.
  • 35. COMPLICATIONS TRANSPLANT REJECTION INFECTION AND SEPSIS POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER. ELECTROLYTE IMBALANCE IATROGENIC SIDE EFFECTS
  • 36. REFRENCES  1.Text book of medical physiology -Guyton and hall, 12th edition.  2.Ganong’s review of medical physiology -23rd edition  3.text of medical physiology -2nd edition  4.net sources (acknowledge for all online sources)  5.text book of medical physiology --A.K. JAIN  6.text book of medical physiology ---indu khurana