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Dept of Urology
Govt Royapettah Hospital and Kilpauk Medical College
Chennai
1
Moderators:
Professors:
 Prof. Dr. G. Sivasankar, M.S., M.Ch.,
 Prof. Dr. A. Senthilvel, M.S., M.Ch.,
Asst Professors:
 Dr. J. Sivabalan, M.S., M.Ch.,
 Dr. R. Bhargavi, M.S., M.Ch.,
 Dr. S. Raju, M.S., M.Ch.,
 Dr. K. Muthurathinam, M.S., M.Ch.,
 Dr. D. Tamilselvan, M.S., M.Ch.,
 Dr. K. Senthilkumar, M.S., M.Ch.
Dept Of Urology, KMC and GRH, Chennai 2
Definition
 Renal replacement therapy is a term used to
encompass life-supporting treatments for renal failure
 Treatment modalities: Dialysis and Transplantation
 First hemodialysis in human being was done by Dr.
HASS in 1924
 First to construct a working dialyzer was Dr .
WILLIAM KOLFF in 1943.
Dept Of Urology, KMC and GRH, Chennai 3
INDICATIONS FOR RRT
 Biochemical indications
 Refractory hyperkalemia> 6.5 mmol/L
 Serum urea > 50 mmol/L not due to hypovolemia
 Refractory metabolic acidosis pH ≤ 7.1
 Clinical indications
 End-organ damage: pericarditis, encephalopathy,
neuropathy, myopathy, uremic bleeding, weight loss
 Refractory volume overload
Dept Of Urology, KMC and GRH, Chennai 4
PRINCIPLES
 Whatever be the technique of RRT, the fundamental
principle is the removal of unwanted SOLUTES &
WATER through a semipermeable membrane and
maintain hemostasis
 WATER : Removal of water occurs through a process of
ULTRAFILTRATION
Dept Of Urology, KMC and GRH, Chennai 5
 It is achieved by generating a TRANS MEMBRANE
PRESSURE , which is greater than the plasma oncotic
pressure ( HF, IHD)
 By increasing the osmolarity of the dialysate ( PD)
Dept Of Urology, KMC and GRH, Chennai 6
SOLUTE REMOVAL
 It occurs by either DIFFUSION or by CONVECTION (
SOLVENT DRAG ).
 In diffusion an electro-chemical gradient is created
across the membrane with a dialysate solution.
Dept Of Urology, KMC and GRH, Chennai 7
Dept Of Urology, KMC and GRH, Chennai 8
Dialysis is any process that changes the concentration of
solutes in the plasma by exposure to a second solution
( the dialysis solution ) across a semipermeable membrane
.
Definition
Dept Of Urology, KMC and GRH, Chennai 9
Hemo dialysis
 The 3 essential components of HD are :
 Dialyzer
 Composition of dialysate
 Blood delivery system
Dept Of Urology, KMC and GRH, Chennai 10
DIALYZER
 Hollow-fiber dialyzer, the most commonly used type
of dialyzer
 composed of bundles of capillary tubes through which
blood circulates and the dialysate travels on the
outside of the fiber bundles.
 The blood and the dialysate may circulate in the same
or in opposite directions in co-current and
countercurrent techniques, respectively
Dept Of Urology, KMC and GRH, Chennai 11
Dialysis membrane
 It can be synthetic or biological.
 Cellulose :
 Has low flux
 poor in removing middle MW molecules.
 More complement and leucocyte activation.
 Not desirable in ICU patients.
 Worsening of the organ damage.
Dialysis membrane :
•
Dept Of Urology, KMC and GRH, Chennai 12
SYNTHETIC
 High flux membranes.
 Made up of PMMA, PAN, Polyamide, Polysulphone
(PS).
 Allows convective therapy and removal of middle MW
substances.
 Better biocompatibility, less leucocyte/complement
activation and end organ dysfunction
Dept Of Urology, KMC and GRH, Chennai 13
Dialysate
Dept Of Urology, KMC and GRH, Chennai 14
When to start dialysis
 To treat or to prevent life - threatening
hyperkalemia, acidosis, or hypervolemic pulmonary
edema,
or
 To treat complications of chronic renal failure
such as pericarditis, neuropathy, seizures, and
coma.
 Modern renal replacement uses dialysis to
remove unwanted solutes by diffusion and
hemofiltration to remove water, which carries
with it unwanted soluble substances.
Dept Of Urology, KMC and GRH, Chennai 15
Indications in AKI
Dept Of Urology, KMC and GRH, Chennai 16
Clinical indications to start dialysis
in CKD
 Pericarditis or pleuritis
 Progressive uremic encephalopathy or neuropathy
 A clinically significant bleeding diathesis attributable to
uremia
 Fluid overload refractory to diuretics
 Persistent metabolic disturbances that are refractory to
medical therapy; these include hyperkalemia, metabolic
acidosis, hypercalcemia, and hyperphosphatemia
 Persistent nausea and vomiting
 Hypertension poorly responsive to antihypertensive
medications
 Weight loss or signs of malnutrition
Dept Of Urology, KMC and GRH, Chennai 17
When not to dialyse?
 Dementia
 Severe peripheral arterial disease
 Hypotensive heart failure
 Severe mental illness
 Malignant disease with poor prognosis
Dept Of Urology, KMC and GRH, Chennai 18
MODES OF RRT
 INTRACORPOREAL : Peritoneal dialysis
 EXTRACORPOREAL :
 Intermittent Hemodialysis
 Slow low efficiency dialysis (SLED)
 Continuous Hemo-filtration
 CAVH
 CVVH
 CAVHDF
 CVVHDF
Dept Of Urology, KMC and GRH, Chennai 19
Dept Of Urology, KMC and GRH, Chennai 20
Peritoneal dialysis
 Principle
Solute and fluid exchange occur between
peritoneal capillary blood and dialysis solution in the
peritoneal cavity
Dept Of Urology, KMC and GRH, Chennai 21
Anatomy
 Largest serosal surface
 Surface area is approximately equal to body surface
area 1-2sq.m in an adult
 Can hold appreciable quantity of fluid without overt
physiological alterations
 Parietal: more important in PD-blood supply from
the lumbar, intercostal and epigastric arteries and
drains into the IVC
 Blood flow 50-100ml/min
Dept Of Urology, KMC and GRH, Chennai 22
Fluid and molecules transfer
 Diffusion
 Osmosis
Dept Of Urology, KMC and GRH, Chennai 23
Three pore model
Ultrasmall pores (3–5 Å; water-selective pore), allowing
the transport of water but not solutes. About 50 per cent
of transcapillary UF occurs through these pores, inspite
of the surface area being only 1–2 per cent.
Small pores (40–50 Å; interendothelial clefts have been
considered the equivalent of small pores)—colloid
osmosis occurs at this level. (urea, creatinine, sodium,
potassium)
Large pores (>150 Å; probably less than 0.1 per cent of total
pore count), which are involved in macromolecular
transport
Dept Of Urology, KMC and GRH, Chennai 24
Dept Of Urology, KMC and GRH, Chennai 25
 In peritoneal dialysis, 1.5 – 3 L of peritoneal dialyzate
solution is infused into the peritoneal cavity and allowed to
dwell for a set period of time, usually 2 to 4 hours.
 The rate of diffusion diminishes with time and eventually
stops when equilibration between plasma and dialyzate is
reached
 Lactate is the preferred buffer
 Icodextrin, has been found to be associated with more
efficient ultrafiltration than dextrose-containing solutions.
 It may be associated with the complication of
ENCAPSULATING PERITONEAL SCLEROSIS.
Dept Of Urology, KMC and GRH, Chennai 26
Contraindications
 Absolute:-
Loss of peritoneal function producing inadequate
clearance
Adhesions blocking flow
Abdominal hernia
Stoma
Diaphragmatic fluid leak
Dept Of Urology, KMC and GRH, Chennai 27
Contraindications
 Relative:-
Fresh foreign body
Large polycystic kidneys
VP shunt
Morbid obesity
Severe malnutrition
Bowel disease
S.aureus carrier
Skin infections
Dept Of Urology, KMC and GRH, Chennai 28
Catheter placement
 Percutaneous Seldinger technique
 Laparoscopic
 Surgical
Dept Of Urology, KMC and GRH, Chennai 29
Dept Of Urology, KMC and GRH, Chennai 30
Modes of PD
Intermittent peritoneal dialysis
Continuous Ambulatory (CAPD)
– 3 exchanges during waking hours
Automated or Alternative (APD)
 Nocturnal Intermittent (NIPD)
- No exchange during day, 6-8 at night via cycling machine
 Nocturnal Tidal (NTPD)
No exchange during day, 6-8 at night each hour with a constant
volume of ≈ 1,500 mL in peritoneal cavity
 Continuous Cyclic (CCPD)
Dialysate instilled in AM, dwells during day, removed prior to bed
 Hybrid devices :Night exchange device
PD plus
Dept Of Urology, KMC and GRH, Chennai 31
Dept Of Urology, KMC and GRH, Chennai 32
Complications
 Mechanical
 Medical
 Infectious
Dept Of Urology, KMC and GRH, Chennai 33
Mechanical
 Kinking of catheter
 Early catheter malfunction
 Late catheter malfunction
Migration
Blood
Fibrin
Peritonitis
Dept Of Urology, KMC and GRH, Chennai 34
Medical
 Glucose overload
 Malnutrition – protein loss
 Hypo / hypercalcemia
 Idiopathic ascites
 Haemoperitoneum
 Eosinophilic peritonitis
Dept Of Urology, KMC and GRH, Chennai 35
Medical
 Glucose overload
 Malnutrition – protein loss
 Hypo / hypercalcemia
 Idiopathic ascites
 Haemoperitoneum
 Eosinophilic peritonitis
Dept Of Urology, KMC and GRH, Chennai 36
Other complications
 Hernias (15-20%); any existing hernia should be
repaired pre PD
 Fluid leaks
 Prolapse
 Back pain
Dept Of Urology, KMC and GRH, Chennai 37
Dept Of Urology, KMC and GRH, Chennai 38
Principle
The use of a semipermeable membrane that will
allow the passage of water and small molecular weight
(MW) solutes, but not large molecules (e.g. proteins)
MW of urea = 60, creatinine = 113, vitamin B12 =
1355, albumin = 60 000, IgG = 140 000 Da
Dept Of Urology, KMC and GRH, Chennai 39
Mechanisms of solute clearance
 Diffusive transport
 Along concentration gradient
 Small solutes
 Convective transport
 Smaller and larger solutes are effectively dragged along
with fluid
 Depends on pore size
 Ultrafiltration
 Pressure gradient
 Fluid and small molecules
Dept Of Urology, KMC and GRH, Chennai 40
Types of vascular access
 AV fistula
 AV graft
 Central venous catheters
Dept Of Urology, KMC and GRH, Chennai 41
AV fistula
 Constructed in subcutaneous
plane between an artery and
vein (side of artery to side or
end of vein)
 Advantages
 Excellent patency
 Lower rates of complications
(infection, steal, stenosis)
 Disadvantages
 Long maturation time
 Occasional failure to
develop
Dept Of Urology, KMC and GRH, Chennai 42
AV graft
 Synthetic conduit, usually polytetrafluoroethylene (PTFE, also known
as Gortex), between an artery and vein
 Advantages
 Short maturation time
 Easy cannulation and large surface area
 Easier surgical handling
 Disadvantages
 Inferior long term patency
 High infection rate than native AVF
 Good alternative in patients in whom adequate AVF cannot be created
Dept Of Urology, KMC and GRH, Chennai 43
Dept Of Urology, KMC and GRH, Chennai 44
Central venous catheters
 Temporary catheters
(Vascath)
 ARF requiring dialysis
 ESRD but without
alternative access
 Tunneled cuffed catheters
 Alternative form of long
term vascular access for
patients in whom AV
access cannot readily be
created
Dept Of Urology, KMC and GRH, Chennai 45
The circuit
Dept Of Urology, KMC and GRH, Chennai 46
Blood and dialysate flow
Dept Of Urology, KMC and GRH, Chennai 47
Dialysate
Dept Of Urology, KMC and GRH, Chennai 48
Water
 Dialysate diluted in sterile water
 Ratio of 1:34
 Standard 4 hour session, flow rate 500ml/min – 120 L
of water
Dept Of Urology, KMC and GRH, Chennai 49
Contraindications
Absolute
 No vascular access possible
Relative
 Difficult access
 Needle phobia
 Cardiac failure
 Coagulopathy
Dept Of Urology, KMC and GRH, Chennai 50
ANTI-COAGULANTS IN DIALYSIS
 Interacting of blood with dialyzing membrane causes
activation of clotting cascade – thrombosis-dysfunction.
 Commonly used anti-coagulant is HEPARIN .
 SYSTEMIC ANTICOAGULATION :
 Administered in doses of 50-100u/kg at the initiation
followed by a bolus of 100u/hr
 REGIONAL ANTICOAGULATION :
 circuit alone is anti-coagulated by administering 500-750
u/hr intothe arterial line and by parallel administration of
protamine 1mg/100u of heparin.
Dept Of Urology, KMC and GRH, Chennai 51
 VARIANT OF REGIONAL ANTI-COAGULANT :
 uses sodium citrate with dialysate containing no
calcium, Used for patients with high risk of bleeding.
 DIALYSIS WITHOUT ANTI-COAGULANTS :
 Uses the saline flush technique
 HD is initiated at a higher rate to reduce the
thrombogenicity and dialyzer is flushed every 15-
20min with 50ml of saline.
 DIRECT THROMBIN INHIBITORS :
 Hirudin, lepirudin, Argatroban
Dept Of Urology, KMC and GRH, Chennai 52
Complications
 Dialysis reactions
 Cardiovascular
 Neuromuscular
 Haematologic
 Pulmonary
 Technical
Dept Of Urology, KMC and GRH, Chennai 53
Dialysis reactions
 Anaphylaxis
 Microbial contamination
Dept Of Urology, KMC and GRH, Chennai 54
Hypotension
 10-30%
 Asymptomatic to organ hypoperfusion
 Trendelenburg position
 Stop dialysis
 Normal saline
 Cool dialysate
Dept Of Urology, KMC and GRH, Chennai 55
Other cardiovascular
 Hypertension
 Arrythmias
 Sudden death
Dept Of Urology, KMC and GRH, Chennai 56
Neuromuscular
 Cramps
5-20%
Legs
Hypo-osmolality & hypomagnesemia
 Restless leg syndrome
 Seizures
Dept Of Urology, KMC and GRH, Chennai 57
Dialysis disequilibrium syndrome
 Neurologic symptoms of varying severity that are thought
to be due primarily to cerebral edema
 Reverse osmotic shift
 Intracerebral acidosis
 Early findings
 Headache, nausea, disorientation, restlessness, blurred vision
 Late findings
 Confusion, seizures, coma, and even death
 Prevention
 The initial dialysis should be gentle, but repeated frequently
 The aim is a gradual reduction in BUN
Dept Of Urology, KMC and GRH, Chennai 58
Haematologic
 Complement activation, neutropenia
 Haemolysis
 Haemorrhage
Dept Of Urology, KMC and GRH, Chennai 59
Pulmonary
 Dialysis-Associated hypoxemia
 PaO2 decreases by 5-20mmHg
 Clinically not significant
 Important in patients with respiratory compromise
Dept Of Urology, KMC and GRH, Chennai 60
Technical
 Air embolism
 Altered dialysate composition
 Line disconnection
Dept Of Urology, KMC and GRH, Chennai 61
Other complications
 Post-dialysis syndrome
 Pruritus
 Priapism
 Hearing & visual loss
Dept Of Urology, KMC and GRH, Chennai 62
HD or PD
 Ideally should be patient’s choice
 Resource limitation
 Physician’s prejudice
Dept Of Urology, KMC and GRH, Chennai 63
Dept Of Urology, KMC and GRH, Chennai 64
Advantages Disadvantages
Haemodialysis Short treatment
Efficient removal
Specialised staff
and equipment
Heparinisation
Protein loss
Peritoneal
dialysis
Can be
performed
manually
No heparinisation
Longer treatment
period
Continuous
Risk of peritonitis
May cause
respiratory
compromise
Dept Of Urology, KMC and GRH, Chennai 65
Goals of dialysis
 Achieve desired dry weight
 Adequate removal of waste products
 Prevent sequelae of electrolyte disturbances
 Reduce morbidity and mortality
Dept Of Urology, KMC and GRH, Chennai 66
SLOW LOW- EFFICIENCY DIALYSIS
 Conventional dialysis treatment .
 Uses dialysate flow rates of 300 ml/min & low blood
flow pump speeds of 200ml/min for 6 – 12 hrs a day.
 Excellent small molecule detoxification.
 Reduced anticoagulant requirement.
 11 hrs SLED is comparable to 24 hrs of CHD .
Dept Of Urology, KMC and GRH, Chennai 67
Haemofiltration
 Solute clearance purely by convection – dragged along
with water
 Large volumes removed – replace
 Replacement fluid directly administered to patient
 Highly permeable large membranes
 High flow rate
Dept Of Urology, KMC and GRH, Chennai 68
Dept Of Urology, KMC and GRH, Chennai 69
Dept Of Urology, KMC and GRH, Chennai 70
CONTINUOUS VENO-VENOUS HEMOFILTRATION
 Solute clearance occurs by convection.
 No dialysate , 1-2 l/hr of ultrafiltration rates used.
 Replacement fluid provided to replace the excess
volume that is being removed and replenish desired
solutes
 Effective method of solute removal
 Major advantage is that solute can be removed in large
quantities ,maintaining a net zero or even a positive
fluid balance
Dept Of Urology, KMC and GRH, Chennai 71
CONTINUOUS VENO-VENOUS HEMODIAFILTRATION
 Involves the ultrafiltration of fluid across a high-flux
dialyzer with compensatory reinfusion of ultrapure
dialysate
 increases middle-sized molecule clearances
 Benefits of both diffusion and convection for solute
removal
 Use of replacement fluid allows for adequate removal
of solutes with zero or positive net fluid balance
Dept Of Urology, KMC and GRH, Chennai 72
SLOW CONTINUOUS ULTRAFILTRATION
 Ultrafiltration at a rate of 100-300ml/hr is performed
to maintain fluid balance.
 No fluids are administered either as dialysate or
replacement fluids.
 Indicated in CCF refractory to diuretics and in volume
overload
Dept Of Urology, KMC and GRH, Chennai 73
Advanatges
 Better removal of large substances
 Improved clearance of uremic toxins
 Better cardiovascular stability
 Less inflammatory reactions
 Suitable for patients planned for long term dialysis
Dept Of Urology, KMC and GRH, Chennai 74
Thank you…
Dept Of Urology, KMC and GRH, Chennai 75

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Renal transplant esrd & rrt

  • 1. Dept of Urology Govt Royapettah Hospital and Kilpauk Medical College Chennai 1
  • 2. Moderators: Professors:  Prof. Dr. G. Sivasankar, M.S., M.Ch.,  Prof. Dr. A. Senthilvel, M.S., M.Ch., Asst Professors:  Dr. J. Sivabalan, M.S., M.Ch.,  Dr. R. Bhargavi, M.S., M.Ch.,  Dr. S. Raju, M.S., M.Ch.,  Dr. K. Muthurathinam, M.S., M.Ch.,  Dr. D. Tamilselvan, M.S., M.Ch.,  Dr. K. Senthilkumar, M.S., M.Ch. Dept Of Urology, KMC and GRH, Chennai 2
  • 3. Definition  Renal replacement therapy is a term used to encompass life-supporting treatments for renal failure  Treatment modalities: Dialysis and Transplantation  First hemodialysis in human being was done by Dr. HASS in 1924  First to construct a working dialyzer was Dr . WILLIAM KOLFF in 1943. Dept Of Urology, KMC and GRH, Chennai 3
  • 4. INDICATIONS FOR RRT  Biochemical indications  Refractory hyperkalemia> 6.5 mmol/L  Serum urea > 50 mmol/L not due to hypovolemia  Refractory metabolic acidosis pH ≤ 7.1  Clinical indications  End-organ damage: pericarditis, encephalopathy, neuropathy, myopathy, uremic bleeding, weight loss  Refractory volume overload Dept Of Urology, KMC and GRH, Chennai 4
  • 5. PRINCIPLES  Whatever be the technique of RRT, the fundamental principle is the removal of unwanted SOLUTES & WATER through a semipermeable membrane and maintain hemostasis  WATER : Removal of water occurs through a process of ULTRAFILTRATION Dept Of Urology, KMC and GRH, Chennai 5
  • 6.  It is achieved by generating a TRANS MEMBRANE PRESSURE , which is greater than the plasma oncotic pressure ( HF, IHD)  By increasing the osmolarity of the dialysate ( PD) Dept Of Urology, KMC and GRH, Chennai 6
  • 7. SOLUTE REMOVAL  It occurs by either DIFFUSION or by CONVECTION ( SOLVENT DRAG ).  In diffusion an electro-chemical gradient is created across the membrane with a dialysate solution. Dept Of Urology, KMC and GRH, Chennai 7
  • 8. Dept Of Urology, KMC and GRH, Chennai 8
  • 9. Dialysis is any process that changes the concentration of solutes in the plasma by exposure to a second solution ( the dialysis solution ) across a semipermeable membrane . Definition Dept Of Urology, KMC and GRH, Chennai 9
  • 10. Hemo dialysis  The 3 essential components of HD are :  Dialyzer  Composition of dialysate  Blood delivery system Dept Of Urology, KMC and GRH, Chennai 10
  • 11. DIALYZER  Hollow-fiber dialyzer, the most commonly used type of dialyzer  composed of bundles of capillary tubes through which blood circulates and the dialysate travels on the outside of the fiber bundles.  The blood and the dialysate may circulate in the same or in opposite directions in co-current and countercurrent techniques, respectively Dept Of Urology, KMC and GRH, Chennai 11
  • 12. Dialysis membrane  It can be synthetic or biological.  Cellulose :  Has low flux  poor in removing middle MW molecules.  More complement and leucocyte activation.  Not desirable in ICU patients.  Worsening of the organ damage. Dialysis membrane : • Dept Of Urology, KMC and GRH, Chennai 12
  • 13. SYNTHETIC  High flux membranes.  Made up of PMMA, PAN, Polyamide, Polysulphone (PS).  Allows convective therapy and removal of middle MW substances.  Better biocompatibility, less leucocyte/complement activation and end organ dysfunction Dept Of Urology, KMC and GRH, Chennai 13
  • 14. Dialysate Dept Of Urology, KMC and GRH, Chennai 14
  • 15. When to start dialysis  To treat or to prevent life - threatening hyperkalemia, acidosis, or hypervolemic pulmonary edema, or  To treat complications of chronic renal failure such as pericarditis, neuropathy, seizures, and coma.  Modern renal replacement uses dialysis to remove unwanted solutes by diffusion and hemofiltration to remove water, which carries with it unwanted soluble substances. Dept Of Urology, KMC and GRH, Chennai 15
  • 16. Indications in AKI Dept Of Urology, KMC and GRH, Chennai 16
  • 17. Clinical indications to start dialysis in CKD  Pericarditis or pleuritis  Progressive uremic encephalopathy or neuropathy  A clinically significant bleeding diathesis attributable to uremia  Fluid overload refractory to diuretics  Persistent metabolic disturbances that are refractory to medical therapy; these include hyperkalemia, metabolic acidosis, hypercalcemia, and hyperphosphatemia  Persistent nausea and vomiting  Hypertension poorly responsive to antihypertensive medications  Weight loss or signs of malnutrition Dept Of Urology, KMC and GRH, Chennai 17
  • 18. When not to dialyse?  Dementia  Severe peripheral arterial disease  Hypotensive heart failure  Severe mental illness  Malignant disease with poor prognosis Dept Of Urology, KMC and GRH, Chennai 18
  • 19. MODES OF RRT  INTRACORPOREAL : Peritoneal dialysis  EXTRACORPOREAL :  Intermittent Hemodialysis  Slow low efficiency dialysis (SLED)  Continuous Hemo-filtration  CAVH  CVVH  CAVHDF  CVVHDF Dept Of Urology, KMC and GRH, Chennai 19
  • 20. Dept Of Urology, KMC and GRH, Chennai 20
  • 21. Peritoneal dialysis  Principle Solute and fluid exchange occur between peritoneal capillary blood and dialysis solution in the peritoneal cavity Dept Of Urology, KMC and GRH, Chennai 21
  • 22. Anatomy  Largest serosal surface  Surface area is approximately equal to body surface area 1-2sq.m in an adult  Can hold appreciable quantity of fluid without overt physiological alterations  Parietal: more important in PD-blood supply from the lumbar, intercostal and epigastric arteries and drains into the IVC  Blood flow 50-100ml/min Dept Of Urology, KMC and GRH, Chennai 22
  • 23. Fluid and molecules transfer  Diffusion  Osmosis Dept Of Urology, KMC and GRH, Chennai 23
  • 24. Three pore model Ultrasmall pores (3–5 Å; water-selective pore), allowing the transport of water but not solutes. About 50 per cent of transcapillary UF occurs through these pores, inspite of the surface area being only 1–2 per cent. Small pores (40–50 Å; interendothelial clefts have been considered the equivalent of small pores)—colloid osmosis occurs at this level. (urea, creatinine, sodium, potassium) Large pores (>150 Å; probably less than 0.1 per cent of total pore count), which are involved in macromolecular transport Dept Of Urology, KMC and GRH, Chennai 24
  • 25. Dept Of Urology, KMC and GRH, Chennai 25
  • 26.  In peritoneal dialysis, 1.5 – 3 L of peritoneal dialyzate solution is infused into the peritoneal cavity and allowed to dwell for a set period of time, usually 2 to 4 hours.  The rate of diffusion diminishes with time and eventually stops when equilibration between plasma and dialyzate is reached  Lactate is the preferred buffer  Icodextrin, has been found to be associated with more efficient ultrafiltration than dextrose-containing solutions.  It may be associated with the complication of ENCAPSULATING PERITONEAL SCLEROSIS. Dept Of Urology, KMC and GRH, Chennai 26
  • 27. Contraindications  Absolute:- Loss of peritoneal function producing inadequate clearance Adhesions blocking flow Abdominal hernia Stoma Diaphragmatic fluid leak Dept Of Urology, KMC and GRH, Chennai 27
  • 28. Contraindications  Relative:- Fresh foreign body Large polycystic kidneys VP shunt Morbid obesity Severe malnutrition Bowel disease S.aureus carrier Skin infections Dept Of Urology, KMC and GRH, Chennai 28
  • 29. Catheter placement  Percutaneous Seldinger technique  Laparoscopic  Surgical Dept Of Urology, KMC and GRH, Chennai 29
  • 30. Dept Of Urology, KMC and GRH, Chennai 30
  • 31. Modes of PD Intermittent peritoneal dialysis Continuous Ambulatory (CAPD) – 3 exchanges during waking hours Automated or Alternative (APD)  Nocturnal Intermittent (NIPD) - No exchange during day, 6-8 at night via cycling machine  Nocturnal Tidal (NTPD) No exchange during day, 6-8 at night each hour with a constant volume of ≈ 1,500 mL in peritoneal cavity  Continuous Cyclic (CCPD) Dialysate instilled in AM, dwells during day, removed prior to bed  Hybrid devices :Night exchange device PD plus Dept Of Urology, KMC and GRH, Chennai 31
  • 32. Dept Of Urology, KMC and GRH, Chennai 32
  • 33. Complications  Mechanical  Medical  Infectious Dept Of Urology, KMC and GRH, Chennai 33
  • 34. Mechanical  Kinking of catheter  Early catheter malfunction  Late catheter malfunction Migration Blood Fibrin Peritonitis Dept Of Urology, KMC and GRH, Chennai 34
  • 35. Medical  Glucose overload  Malnutrition – protein loss  Hypo / hypercalcemia  Idiopathic ascites  Haemoperitoneum  Eosinophilic peritonitis Dept Of Urology, KMC and GRH, Chennai 35
  • 36. Medical  Glucose overload  Malnutrition – protein loss  Hypo / hypercalcemia  Idiopathic ascites  Haemoperitoneum  Eosinophilic peritonitis Dept Of Urology, KMC and GRH, Chennai 36
  • 37. Other complications  Hernias (15-20%); any existing hernia should be repaired pre PD  Fluid leaks  Prolapse  Back pain Dept Of Urology, KMC and GRH, Chennai 37
  • 38. Dept Of Urology, KMC and GRH, Chennai 38
  • 39. Principle The use of a semipermeable membrane that will allow the passage of water and small molecular weight (MW) solutes, but not large molecules (e.g. proteins) MW of urea = 60, creatinine = 113, vitamin B12 = 1355, albumin = 60 000, IgG = 140 000 Da Dept Of Urology, KMC and GRH, Chennai 39
  • 40. Mechanisms of solute clearance  Diffusive transport  Along concentration gradient  Small solutes  Convective transport  Smaller and larger solutes are effectively dragged along with fluid  Depends on pore size  Ultrafiltration  Pressure gradient  Fluid and small molecules Dept Of Urology, KMC and GRH, Chennai 40
  • 41. Types of vascular access  AV fistula  AV graft  Central venous catheters Dept Of Urology, KMC and GRH, Chennai 41
  • 42. AV fistula  Constructed in subcutaneous plane between an artery and vein (side of artery to side or end of vein)  Advantages  Excellent patency  Lower rates of complications (infection, steal, stenosis)  Disadvantages  Long maturation time  Occasional failure to develop Dept Of Urology, KMC and GRH, Chennai 42
  • 43. AV graft  Synthetic conduit, usually polytetrafluoroethylene (PTFE, also known as Gortex), between an artery and vein  Advantages  Short maturation time  Easy cannulation and large surface area  Easier surgical handling  Disadvantages  Inferior long term patency  High infection rate than native AVF  Good alternative in patients in whom adequate AVF cannot be created Dept Of Urology, KMC and GRH, Chennai 43
  • 44. Dept Of Urology, KMC and GRH, Chennai 44
  • 45. Central venous catheters  Temporary catheters (Vascath)  ARF requiring dialysis  ESRD but without alternative access  Tunneled cuffed catheters  Alternative form of long term vascular access for patients in whom AV access cannot readily be created Dept Of Urology, KMC and GRH, Chennai 45
  • 46. The circuit Dept Of Urology, KMC and GRH, Chennai 46
  • 47. Blood and dialysate flow Dept Of Urology, KMC and GRH, Chennai 47
  • 48. Dialysate Dept Of Urology, KMC and GRH, Chennai 48
  • 49. Water  Dialysate diluted in sterile water  Ratio of 1:34  Standard 4 hour session, flow rate 500ml/min – 120 L of water Dept Of Urology, KMC and GRH, Chennai 49
  • 50. Contraindications Absolute  No vascular access possible Relative  Difficult access  Needle phobia  Cardiac failure  Coagulopathy Dept Of Urology, KMC and GRH, Chennai 50
  • 51. ANTI-COAGULANTS IN DIALYSIS  Interacting of blood with dialyzing membrane causes activation of clotting cascade – thrombosis-dysfunction.  Commonly used anti-coagulant is HEPARIN .  SYSTEMIC ANTICOAGULATION :  Administered in doses of 50-100u/kg at the initiation followed by a bolus of 100u/hr  REGIONAL ANTICOAGULATION :  circuit alone is anti-coagulated by administering 500-750 u/hr intothe arterial line and by parallel administration of protamine 1mg/100u of heparin. Dept Of Urology, KMC and GRH, Chennai 51
  • 52.  VARIANT OF REGIONAL ANTI-COAGULANT :  uses sodium citrate with dialysate containing no calcium, Used for patients with high risk of bleeding.  DIALYSIS WITHOUT ANTI-COAGULANTS :  Uses the saline flush technique  HD is initiated at a higher rate to reduce the thrombogenicity and dialyzer is flushed every 15- 20min with 50ml of saline.  DIRECT THROMBIN INHIBITORS :  Hirudin, lepirudin, Argatroban Dept Of Urology, KMC and GRH, Chennai 52
  • 53. Complications  Dialysis reactions  Cardiovascular  Neuromuscular  Haematologic  Pulmonary  Technical Dept Of Urology, KMC and GRH, Chennai 53
  • 54. Dialysis reactions  Anaphylaxis  Microbial contamination Dept Of Urology, KMC and GRH, Chennai 54
  • 55. Hypotension  10-30%  Asymptomatic to organ hypoperfusion  Trendelenburg position  Stop dialysis  Normal saline  Cool dialysate Dept Of Urology, KMC and GRH, Chennai 55
  • 56. Other cardiovascular  Hypertension  Arrythmias  Sudden death Dept Of Urology, KMC and GRH, Chennai 56
  • 57. Neuromuscular  Cramps 5-20% Legs Hypo-osmolality & hypomagnesemia  Restless leg syndrome  Seizures Dept Of Urology, KMC and GRH, Chennai 57
  • 58. Dialysis disequilibrium syndrome  Neurologic symptoms of varying severity that are thought to be due primarily to cerebral edema  Reverse osmotic shift  Intracerebral acidosis  Early findings  Headache, nausea, disorientation, restlessness, blurred vision  Late findings  Confusion, seizures, coma, and even death  Prevention  The initial dialysis should be gentle, but repeated frequently  The aim is a gradual reduction in BUN Dept Of Urology, KMC and GRH, Chennai 58
  • 59. Haematologic  Complement activation, neutropenia  Haemolysis  Haemorrhage Dept Of Urology, KMC and GRH, Chennai 59
  • 60. Pulmonary  Dialysis-Associated hypoxemia  PaO2 decreases by 5-20mmHg  Clinically not significant  Important in patients with respiratory compromise Dept Of Urology, KMC and GRH, Chennai 60
  • 61. Technical  Air embolism  Altered dialysate composition  Line disconnection Dept Of Urology, KMC and GRH, Chennai 61
  • 62. Other complications  Post-dialysis syndrome  Pruritus  Priapism  Hearing & visual loss Dept Of Urology, KMC and GRH, Chennai 62
  • 63. HD or PD  Ideally should be patient’s choice  Resource limitation  Physician’s prejudice Dept Of Urology, KMC and GRH, Chennai 63
  • 64. Dept Of Urology, KMC and GRH, Chennai 64
  • 65. Advantages Disadvantages Haemodialysis Short treatment Efficient removal Specialised staff and equipment Heparinisation Protein loss Peritoneal dialysis Can be performed manually No heparinisation Longer treatment period Continuous Risk of peritonitis May cause respiratory compromise Dept Of Urology, KMC and GRH, Chennai 65
  • 66. Goals of dialysis  Achieve desired dry weight  Adequate removal of waste products  Prevent sequelae of electrolyte disturbances  Reduce morbidity and mortality Dept Of Urology, KMC and GRH, Chennai 66
  • 67. SLOW LOW- EFFICIENCY DIALYSIS  Conventional dialysis treatment .  Uses dialysate flow rates of 300 ml/min & low blood flow pump speeds of 200ml/min for 6 – 12 hrs a day.  Excellent small molecule detoxification.  Reduced anticoagulant requirement.  11 hrs SLED is comparable to 24 hrs of CHD . Dept Of Urology, KMC and GRH, Chennai 67
  • 68. Haemofiltration  Solute clearance purely by convection – dragged along with water  Large volumes removed – replace  Replacement fluid directly administered to patient  Highly permeable large membranes  High flow rate Dept Of Urology, KMC and GRH, Chennai 68
  • 69. Dept Of Urology, KMC and GRH, Chennai 69
  • 70. Dept Of Urology, KMC and GRH, Chennai 70
  • 71. CONTINUOUS VENO-VENOUS HEMOFILTRATION  Solute clearance occurs by convection.  No dialysate , 1-2 l/hr of ultrafiltration rates used.  Replacement fluid provided to replace the excess volume that is being removed and replenish desired solutes  Effective method of solute removal  Major advantage is that solute can be removed in large quantities ,maintaining a net zero or even a positive fluid balance Dept Of Urology, KMC and GRH, Chennai 71
  • 72. CONTINUOUS VENO-VENOUS HEMODIAFILTRATION  Involves the ultrafiltration of fluid across a high-flux dialyzer with compensatory reinfusion of ultrapure dialysate  increases middle-sized molecule clearances  Benefits of both diffusion and convection for solute removal  Use of replacement fluid allows for adequate removal of solutes with zero or positive net fluid balance Dept Of Urology, KMC and GRH, Chennai 72
  • 73. SLOW CONTINUOUS ULTRAFILTRATION  Ultrafiltration at a rate of 100-300ml/hr is performed to maintain fluid balance.  No fluids are administered either as dialysate or replacement fluids.  Indicated in CCF refractory to diuretics and in volume overload Dept Of Urology, KMC and GRH, Chennai 73
  • 74. Advanatges  Better removal of large substances  Improved clearance of uremic toxins  Better cardiovascular stability  Less inflammatory reactions  Suitable for patients planned for long term dialysis Dept Of Urology, KMC and GRH, Chennai 74
  • 75. Thank you… Dept Of Urology, KMC and GRH, Chennai 75