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Dialytic Support for AKI
patients
By
Dr. Ahmed Mohammed Abd El Wahab
Lecturer of Internal Medicine(Nephrology)
Director of Critical Care and Convalescence Hospital
Mansoura Faculty of medicine
Classifications & Magnitude
RIFLE Strata
The 2nd International Consensus Conference of the Acute
Dialysis Quality Initiative (ADQI) Group
Where are we - too many
questions?
 What do we aim for?
 When should we start it?
 What therapy should we use?
 Which vascular access?
 How much therapy is enough?
 When do we stop/switch?
The Ideal Renal Replacement
Therapy
 Allows control of intra/extravascular
volume
 Corrects acid-base disturbances
 Corrects uraemia & effectively clears
“toxins”
 Promotes renal recovery
 Improves survival
 Is free of complications
 Clears drugs effectively (?)
Serum Creatinine as a trigger for RRT
When to initiate? Early vs
Late
Serum Urea as a trigger for RRT
When to initiate? Early vs
Late
UOP as a trigger for RRT
When to initiate? Early vs
Late
 To Consider RRT:
◦ Oliguria: urine output <100 ml in 6h
◦ Potassium >6.5 mmol/L
◦ pH <7.2
◦ BUN >70 mg/dl
◦ Creatinine >3.5 mg/dl
◦ Clinically significant organ edema
RENAL, Bellomo R, Cass A, Cole L, et al. N Engl J Med 2009; 361: 1627–1638.
 To Consider RRT:
◦ Urea  21 mmol/L
◦ Volume overload
◦ Persistent hyperkalemia (K+ > 6.2 mEq/L or ECG
changes)
◦ Severe metabolic acidosis (pH < 7.20)
◦ Uremic signs or symptoms
VA/NIH Acute Renal Failure Trial Network, Palevsky PM et al. N Engl J Med.
2008;359:7-20
Marlies Ostermann et al. Nephrol Dial Transplant (2012) 0: 1–7
A proposed
algorithm for
initiation RRT in
adult critically ill
patients
Whatever the criteria used to define ‘early’
versus ‘late’ RRT,
It is apparent that what may be ‘early’ for one
patient
could be ‘late’ for another patient depending on
the patient’s comorbidity and clinical course
Macedo E, Mehta R. Semin Dial 2011; 24: 132–137
Which Modality?
Major Renal Replacement
Techniques
Intermittent ContinuousHybrid
IHD
Intermittent
haemodialysis
IUF
Isolated
Ultrafiltration
SLEDD
Sustained (or
slow) low
efficiency daily
dialysis
SLEDD-
F
Sustained (or slow)
low efficiency daily
dialysis with
filtration
CVVH
Continuous veno-
venous haemofiltration
CVVHD
Continuous veno-
venous haemodialysis
CVVHDF
Continuous veno-
venous
haemodiafiltration
SCUF
Slow continuous
ultrafiltration
Intermittent Therapies - PRO
(Relatively) Inexpensive
Flexible timing allows for mobility/transport
Rapid correction of fluid overload
Rapid removal of dialyzable drugs
Rapid correction of acidosis & electrolyte
abnormality
Minimises anticoagulant exposure
Intermittent Therapies - CON
Hypotension 30-
60%
Cerebral
oedema
Limited therapy
duration
Renal injury &
ischaemia
Gut/coronary
ischaemia
Continuous Therapies - PRO
Haemodynamic stability => ?? better renal
recovery
Stable and predictable volume control
Stable and predictable control of chemistry
Stable intracranial pressure
Disease modification by cytokine removal
(CVVH)?
Continuous Therapies - CON
Anticoagulation requirements
Higher potential for filter
clotting
Expense – fluids etc.
Immobility & Transport
issues
Increased bleeding risk
High heparin
exposure
Solute Clearance - Diffusion
 Small (< 500d)
molecules cleared
efficiently
 Concentration gradient
critical
 Gradient achieved by
countercurrent flow
 Principal clearance
mode of dialysis
techniques
Solute Clearance – Ultrafiltration &
Convection (Haemofiltration)
 Water movement “drags” solute
across membrane
 At high UF rates (> 1L/hour)
enough solute is dragged to
produce significant clearance
 Convective clearance dehydrates
the blood passing through the filter
 If filtration fraction > 30% there is
high risk of filter clotting*
 Also clears larger molecular
weight substances (e.g. B12, TNF,
inulin)
* In post-dilution haemofiltration
SCUF
• High flux membranes
• Up to 24 hrs per day
• Objective VOLUME control
• Not suitable for solute
clearance
• Blood flow 50-200 ml/min
• UF rate 2-8 ml/min
CA/VVH
• Extended duration up to
weeks
• High flux membranes
• Mainly convective clearance
• UF > volume control amount
• Excess UF replaced
• Replacement pre- or post-
filter
• Blood flow 50-200 ml/min
• UF rate 10-60 ml/min
CA/VVHD
• Mid/high flux membranes
• Extended period up to weeks
• Diffusive solute clearance
• Countercurrent dialysate
• UF for volume control
• Blood flow 50-200 ml/min
• UF rate 1-8 ml/min
• Dialysate flow 15-60 ml/min
CVVHDF
• High flux membranes
• Extended period up to weeks
• Diffusive & convective
solute
clearance
• Countercurrent dialysate
• UF exceeds volume control
• Replacement fluid as
required
• Blood flow 50-200 ml/min
• UF rate 10-60 ml/min
• Dialysate flow 15-30 ml/min
• Replacement 10-30 ml/min
SLED(D) & SLED(D)-F : Hybrid therapy
 Conventional dialysis equipment
 Online dialysis fluid preparation
 Excellent small molecule detoxification
 Cardiovascular stability as good as
CRRT
 Reduced anticoagulation requirement
 11 hrs SLED comparable to 23 hrs
CVVH
 Decreased costs compared to CRRT
 Phosphate supplementation requiredFliser, T & Kielstein JT. Nature Clin Practice Neph 2006; 2: 32-39
Berbece, AN & Richardson, RMA. Kidney International 2006; 70: 963-968
Uraemia Control
Liao, Z et al. Artificial Organs 2003; 27: 802-807
Large molecule clearance
Liao, Z et al. Artificial Organs 2003; 27: 802-807
Outcome with IRRT vs CRRT
Tonelli, M et al. Am J Kidney Dis 2002; 40: 875-885
• No mortality difference between therapies
• No renal recovery difference between
therapies
• Unselected patient populations
• Majority of studies were unpublished
2004-2014
5.6.2: We suggest using CRRT, rather
than standard intermittent RRT, for
hemodynamically unstable patients.
(2B)
Dialysis Interventions for Treatment of AKI
KDIGO® AKI Guideline March 2012
5.6.3: We suggest using CRRT, rather than intermittent RRT, for
AKI patients with acute brain injury or other causes of increased
intracranial pressure or generalized brain edema. (2B)
Using what?
 5.4.1: We suggest initiating RRT in patients with AKI
via an uncuffed nontunneled dialysis catheter,
rather than a tunneled catheter. (2D)
 5.4.2: When choosing a vein for insertion of a
dialysis catheter in patients with AKI, consider these
preferences (Not Graded):
 First choice: right jugular vein;
 Second choice: femoral vein;
 Third choice: left jugular vein;
 Last choice: subclavian vein with preference for the dominant
side.
Vascular
access
KDIGO® AKI Guideline March 2012
Bicarbonate versus lactatebased fluid replacement in CVVH
Prospective, randomized study
 Results :
 Serum lactate concentration was
significantly higher and the
bicarbonate was lower in patients
treated with lactatebased solutions
 Increased incidence of CVS events
in pts ttt with lactate solution
◦ Hypotension
◦ Increased dose of inotropic
support
barenborck and colleague
Barenbrock M et al; Kidney Int (2000)
Solutions for CRRT
cardiovascular
complications
hypotensive episodes
5.7.3: We suggest using bicarbonate, rather
than lactate, as a buffer in dialysate and
replacement fluid for RRT in patients with AKI
and liver failure and/or lactic acidemia. (2B)
Dialysis Interventions for Treatment of AKI
KDIGO® AKI Guideline March 2012
The Membrane
 High Flux membrane , synthetic , biocompatable ,
acting by providing both methods of detoxications:
a) Diffusion : for low molecular weight toxins.
b) Convection : for large molecules.
5.5.1: We suggest to use dialyzers with a biocompatible membrane
for IHD and CRRT in patients with AKI. (2C)
KDIGO® AKI Guideline March 2012
Anticoagulation
Modality Advantages Disadvantages
Heparin Good anticoagulation Thrombocytopenia bleeding
LMWH Less thrombocytopenia bleeding
Citrate Lowest risk of bleeding
Metabolic alkalosis,
hypocalcemia special dialysate
Regional Heparin Reduced bleeding Complex management
Saline flushes No bleeding risk Poor efficacy
Prostacycline Reduced bleeding risk Hypotension poor efficacy
5.3.2.1: For anticoagulation in intermittent RRT, we
recommend using either unfractionated or
low-molecular weight heparin, rather than
other anticoagulants. (1C)
5.3.2.2: For anticoagulation in CRRT, we suggest using
regional citrate anticoagulation rather than
heparin in patients who do not have
contraindications for citrate. (2B)
KDIGO® AKI Guideline March 2012
How much therapy?
Kidney International Supplements (2012) 2, 89–115
RENAL, Bellomo R, Cass A, Cole L, et al. N Engl J Med 2009; 361: 1627–1638.
Kidney International Supplements (2012) 2, 89–115
Kidney International Supplements (2012) 2, 89–115
When To Stop/Switch?
Recovery
Uchino S, Bellomo R, Morimatsu H, et al. Crit Care Med 2009; 37: 2576–
Uchino S, Bellomo R, Morimatsu H, et al. Crit Care Med 2009; 37: 2576–
Uchino S, Bellomo R, Morimatsu H, et al. Crit Care Med 2009; 37: 2576–
When to Stop?
Kidney International Supplements (2012) 2, 89–115
It is also important to acknowledge that there
may be patients with a futile prognosis in whom
RRT would not be appropriate and where
withholding RRT constitutes good end-of-life
careLassnigg A, Schmidlin D, Mouhieddine M et al. J Am Soc Nephrol 2004; 15:1597–1605
How to improve outcome?
Early Detection
Contd.,
 Special AE
 Lack of resources (finances-
equipment-trained medical staff).
 Lack of awareness
 Data quality and accuracy
 Lack of continuous therapies
 Special cultures
 Natural remedies
Implications of the available
data
ARF is not an innocent bystander in ICU
We must ensure adequate dosing of RRT
Choice of RRT mode may not be critical
Septic ARF may be a different beast
We must strive to avert acute renal failure
Thank You

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Dialytic Support for AKI Patients

  • 1. Dialytic Support for AKI patients By Dr. Ahmed Mohammed Abd El Wahab Lecturer of Internal Medicine(Nephrology) Director of Critical Care and Convalescence Hospital Mansoura Faculty of medicine
  • 3. RIFLE Strata The 2nd International Consensus Conference of the Acute Dialysis Quality Initiative (ADQI) Group
  • 4.
  • 5.
  • 6.
  • 7. Where are we - too many questions?  What do we aim for?  When should we start it?  What therapy should we use?  Which vascular access?  How much therapy is enough?  When do we stop/switch?
  • 8. The Ideal Renal Replacement Therapy  Allows control of intra/extravascular volume  Corrects acid-base disturbances  Corrects uraemia & effectively clears “toxins”  Promotes renal recovery  Improves survival  Is free of complications  Clears drugs effectively (?)
  • 9.
  • 10.
  • 11.
  • 12. Serum Creatinine as a trigger for RRT When to initiate? Early vs Late
  • 13. Serum Urea as a trigger for RRT When to initiate? Early vs Late
  • 14. UOP as a trigger for RRT When to initiate? Early vs Late
  • 15.  To Consider RRT: ◦ Oliguria: urine output <100 ml in 6h ◦ Potassium >6.5 mmol/L ◦ pH <7.2 ◦ BUN >70 mg/dl ◦ Creatinine >3.5 mg/dl ◦ Clinically significant organ edema RENAL, Bellomo R, Cass A, Cole L, et al. N Engl J Med 2009; 361: 1627–1638.
  • 16.  To Consider RRT: ◦ Urea  21 mmol/L ◦ Volume overload ◦ Persistent hyperkalemia (K+ > 6.2 mEq/L or ECG changes) ◦ Severe metabolic acidosis (pH < 7.20) ◦ Uremic signs or symptoms VA/NIH Acute Renal Failure Trial Network, Palevsky PM et al. N Engl J Med. 2008;359:7-20
  • 17.
  • 18.
  • 19.
  • 20.
  • 21.
  • 22. Marlies Ostermann et al. Nephrol Dial Transplant (2012) 0: 1–7 A proposed algorithm for initiation RRT in adult critically ill patients
  • 23. Whatever the criteria used to define ‘early’ versus ‘late’ RRT, It is apparent that what may be ‘early’ for one patient could be ‘late’ for another patient depending on the patient’s comorbidity and clinical course Macedo E, Mehta R. Semin Dial 2011; 24: 132–137
  • 24.
  • 26. Major Renal Replacement Techniques Intermittent ContinuousHybrid IHD Intermittent haemodialysis IUF Isolated Ultrafiltration SLEDD Sustained (or slow) low efficiency daily dialysis SLEDD- F Sustained (or slow) low efficiency daily dialysis with filtration CVVH Continuous veno- venous haemofiltration CVVHD Continuous veno- venous haemodialysis CVVHDF Continuous veno- venous haemodiafiltration SCUF Slow continuous ultrafiltration
  • 27. Intermittent Therapies - PRO (Relatively) Inexpensive Flexible timing allows for mobility/transport Rapid correction of fluid overload Rapid removal of dialyzable drugs Rapid correction of acidosis & electrolyte abnormality Minimises anticoagulant exposure
  • 28. Intermittent Therapies - CON Hypotension 30- 60% Cerebral oedema Limited therapy duration Renal injury & ischaemia Gut/coronary ischaemia
  • 29. Continuous Therapies - PRO Haemodynamic stability => ?? better renal recovery Stable and predictable volume control Stable and predictable control of chemistry Stable intracranial pressure Disease modification by cytokine removal (CVVH)?
  • 30. Continuous Therapies - CON Anticoagulation requirements Higher potential for filter clotting Expense – fluids etc. Immobility & Transport issues Increased bleeding risk High heparin exposure
  • 31. Solute Clearance - Diffusion  Small (< 500d) molecules cleared efficiently  Concentration gradient critical  Gradient achieved by countercurrent flow  Principal clearance mode of dialysis techniques
  • 32. Solute Clearance – Ultrafiltration & Convection (Haemofiltration)  Water movement “drags” solute across membrane  At high UF rates (> 1L/hour) enough solute is dragged to produce significant clearance  Convective clearance dehydrates the blood passing through the filter  If filtration fraction > 30% there is high risk of filter clotting*  Also clears larger molecular weight substances (e.g. B12, TNF, inulin) * In post-dilution haemofiltration
  • 33. SCUF • High flux membranes • Up to 24 hrs per day • Objective VOLUME control • Not suitable for solute clearance • Blood flow 50-200 ml/min • UF rate 2-8 ml/min
  • 34. CA/VVH • Extended duration up to weeks • High flux membranes • Mainly convective clearance • UF > volume control amount • Excess UF replaced • Replacement pre- or post- filter • Blood flow 50-200 ml/min • UF rate 10-60 ml/min
  • 35. CA/VVHD • Mid/high flux membranes • Extended period up to weeks • Diffusive solute clearance • Countercurrent dialysate • UF for volume control • Blood flow 50-200 ml/min • UF rate 1-8 ml/min • Dialysate flow 15-60 ml/min
  • 36. CVVHDF • High flux membranes • Extended period up to weeks • Diffusive & convective solute clearance • Countercurrent dialysate • UF exceeds volume control • Replacement fluid as required • Blood flow 50-200 ml/min • UF rate 10-60 ml/min • Dialysate flow 15-30 ml/min • Replacement 10-30 ml/min
  • 37. SLED(D) & SLED(D)-F : Hybrid therapy  Conventional dialysis equipment  Online dialysis fluid preparation  Excellent small molecule detoxification  Cardiovascular stability as good as CRRT  Reduced anticoagulation requirement  11 hrs SLED comparable to 23 hrs CVVH  Decreased costs compared to CRRT  Phosphate supplementation requiredFliser, T & Kielstein JT. Nature Clin Practice Neph 2006; 2: 32-39 Berbece, AN & Richardson, RMA. Kidney International 2006; 70: 963-968
  • 38. Uraemia Control Liao, Z et al. Artificial Organs 2003; 27: 802-807
  • 39. Large molecule clearance Liao, Z et al. Artificial Organs 2003; 27: 802-807
  • 40.
  • 41.
  • 42. Outcome with IRRT vs CRRT Tonelli, M et al. Am J Kidney Dis 2002; 40: 875-885 • No mortality difference between therapies • No renal recovery difference between therapies • Unselected patient populations • Majority of studies were unpublished
  • 43.
  • 44.
  • 45.
  • 46.
  • 47.
  • 49.
  • 50.
  • 51. 5.6.2: We suggest using CRRT, rather than standard intermittent RRT, for hemodynamically unstable patients. (2B) Dialysis Interventions for Treatment of AKI KDIGO® AKI Guideline March 2012 5.6.3: We suggest using CRRT, rather than intermittent RRT, for AKI patients with acute brain injury or other causes of increased intracranial pressure or generalized brain edema. (2B)
  • 53.  5.4.1: We suggest initiating RRT in patients with AKI via an uncuffed nontunneled dialysis catheter, rather than a tunneled catheter. (2D)  5.4.2: When choosing a vein for insertion of a dialysis catheter in patients with AKI, consider these preferences (Not Graded):  First choice: right jugular vein;  Second choice: femoral vein;  Third choice: left jugular vein;  Last choice: subclavian vein with preference for the dominant side. Vascular access KDIGO® AKI Guideline March 2012
  • 54. Bicarbonate versus lactatebased fluid replacement in CVVH Prospective, randomized study  Results :  Serum lactate concentration was significantly higher and the bicarbonate was lower in patients treated with lactatebased solutions  Increased incidence of CVS events in pts ttt with lactate solution ◦ Hypotension ◦ Increased dose of inotropic support barenborck and colleague Barenbrock M et al; Kidney Int (2000) Solutions for CRRT cardiovascular complications hypotensive episodes
  • 55. 5.7.3: We suggest using bicarbonate, rather than lactate, as a buffer in dialysate and replacement fluid for RRT in patients with AKI and liver failure and/or lactic acidemia. (2B) Dialysis Interventions for Treatment of AKI KDIGO® AKI Guideline March 2012
  • 56. The Membrane  High Flux membrane , synthetic , biocompatable , acting by providing both methods of detoxications: a) Diffusion : for low molecular weight toxins. b) Convection : for large molecules. 5.5.1: We suggest to use dialyzers with a biocompatible membrane for IHD and CRRT in patients with AKI. (2C) KDIGO® AKI Guideline March 2012
  • 57. Anticoagulation Modality Advantages Disadvantages Heparin Good anticoagulation Thrombocytopenia bleeding LMWH Less thrombocytopenia bleeding Citrate Lowest risk of bleeding Metabolic alkalosis, hypocalcemia special dialysate Regional Heparin Reduced bleeding Complex management Saline flushes No bleeding risk Poor efficacy Prostacycline Reduced bleeding risk Hypotension poor efficacy
  • 58. 5.3.2.1: For anticoagulation in intermittent RRT, we recommend using either unfractionated or low-molecular weight heparin, rather than other anticoagulants. (1C) 5.3.2.2: For anticoagulation in CRRT, we suggest using regional citrate anticoagulation rather than heparin in patients who do not have contraindications for citrate. (2B) KDIGO® AKI Guideline March 2012
  • 60.
  • 61.
  • 62. Kidney International Supplements (2012) 2, 89–115 RENAL, Bellomo R, Cass A, Cole L, et al. N Engl J Med 2009; 361: 1627–1638.
  • 63. Kidney International Supplements (2012) 2, 89–115
  • 64.
  • 65. Kidney International Supplements (2012) 2, 89–115
  • 67. Recovery Uchino S, Bellomo R, Morimatsu H, et al. Crit Care Med 2009; 37: 2576–
  • 68. Uchino S, Bellomo R, Morimatsu H, et al. Crit Care Med 2009; 37: 2576–
  • 69. Uchino S, Bellomo R, Morimatsu H, et al. Crit Care Med 2009; 37: 2576–
  • 70. When to Stop? Kidney International Supplements (2012) 2, 89–115 It is also important to acknowledge that there may be patients with a futile prognosis in whom RRT would not be appropriate and where withholding RRT constitutes good end-of-life careLassnigg A, Schmidlin D, Mouhieddine M et al. J Am Soc Nephrol 2004; 15:1597–1605
  • 71. How to improve outcome?
  • 74.
  • 75.
  • 76.  Special AE  Lack of resources (finances- equipment-trained medical staff).  Lack of awareness  Data quality and accuracy  Lack of continuous therapies  Special cultures  Natural remedies
  • 77. Implications of the available data ARF is not an innocent bystander in ICU We must ensure adequate dosing of RRT Choice of RRT mode may not be critical Septic ARF may be a different beast We must strive to avert acute renal failure